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. 2022 Jul 25;19(7):e1004055. doi: 10.1371/journal.pmed.1004055

Implementation research on noncommunicable disease prevention and control interventions in low- and middle-income countries: A systematic review

Celestin Hategeka 1,*, Prince Adu 2, Allissa Desloge 3, Robert Marten 4, Ruitai Shao 5, Maoyi Tian 6,7, Ting Wei 6, Margaret E Kruk 1
Editor: Elvin Hsing Geng8
PMCID: PMC9359585  PMID: 35877677

Abstract

Background

While the evidence for the clinical effectiveness of most noncommunicable disease (NCD) prevention and treatment interventions is well established, care delivery models and means of scaling these up in a variety of resource-constrained health systems are not. The objective of this review was to synthesize evidence on the current state of implementation research on priority NCD prevention and control interventions provided by health systems in low- and middle-income countries (LMICs).

Methods and findings

On January 20, 2021, we searched MEDLINE and EMBASE databases from 1990 through 2020 to identify implementation research studies that focused on the World Health Organization (WHO) priority NCD prevention and control interventions targeting cardiovascular disease, cancer, diabetes, and chronic respiratory disease and provided within health systems in LMICs. Any empirical and peer-reviewed studies that focused on these interventions and reported implementation outcomes were eligible for inclusion. Given the focus on this review and the heterogeneity in aims and methodologies of included studies, risk of bias assessment to understand how effect size may have been compromised by bias is not applicable. We instead commented on the distribution of research designs and discussed about stronger/weaker designs. We synthesized extracted data using descriptive statistics and following the review protocol registered in PROSPERO (CRD42021252969). Of 9,683 potential studies and 7,419 unique records screened for inclusion, 222 eligible studies evaluated 265 priority NCD prevention and control interventions implemented in 62 countries (6% in low-income countries and 90% in middle-income countries). The number of studies published has been increasing over time. Nearly 40% of all the studies were on cervical cancer. With regards to intervention type, screening accounted for 49%, treatment for 39%, while prevention for 12% (with 80% of the latter focusing on prevention of the NCD behavior risk factors). Feasibility (38%) was the most studied implementation outcome followed by adoption (23%); few studies addressed sustainability. The implementation strategies were not specified well enough. Most studies used quantitative methods (86%). The weakest study design, preexperimental, and the strongest study design, experimental, were respectively employed in 25% and 24% of included studies. Approximately 72% of studies reported funding, with international funding being the predominant source. The majority of studies were proof of concept or pilot (88%) and targeted the micro level of health system (79%). Less than 5% of studies report using implementation research framework.

Conclusions

Despite growth in implementation research on NCDs in LMICs, we found major gaps in the science. Future studies should prioritize implementation at scale, target higher levels health systems (meso and macro levels), and test sustainability of NCD programs. They should employ designs with stronger internal validity, be more conceptually driven, and use mixed methods to understand mechanisms. To maximize impact of the research under limited resources, adding implementation science outcomes to effectiveness research and regional collaborations are promising.


Celestin Hategeka and colleagues evaluate the current state of implementation research on Non-Communicable Disease prevention and control interventions in low-and middle-income countries (LMICs).

Author summary

Why was the study done?

  • While the evidence for the clinical effectiveness of most noncommunicable disease (NCD) prevention and treatment interventions is well established, care delivery models and means of scaling these up to entire populations in need in heterogeneous and resource-constrained health systems are not.

  • Implementation research on NCD program delivery can illuminate what does and does not work in preventing NCDs or achieving NCD control. This can promote faster, more efficient, and more effective scale-up of life-saving and health-preserving health system strategies.

  • Evidence needed on the current state of implementation research on World Health Organization (WHO) priority NCD prevention and control interventions to help inform research priority.

What did the researchers do and find?

  • We performed a systematic review search in MEDLINE and EMBASE databases from 1990 through 2020 to identify implementation research studies that focused on the WHO priority NCD prevention and control interventions targeting cardiovascular disease, cancer, diabetes, and chronic respiratory disease and provided within health systems in low- and middle-income countries (LMICs).

  • We identified 222 eligible studies that evaluated 265 priority NCD prevention and control interventions implemented in 62 countries (6% in low-income countries and 90% in middle-income countries). The number of studies published has been increasing over time. The majority of interventions were focused on either screening (49%) or treatment (39%), while prevention accounted for only 12%.

  • Reviewed studies emphasized a few health areas, such as cervical cancer, with many other high-burden conditions little researched. The majority of studies were proof of concept or pilot, quantitative using weaker study designs and targeted the micro level of health system.

What do these findings mean?

  • While implementation research on priority NCDs has grown substantially, from under 10 studies per year in early 2000s to 51 studies in 2020, this is still vastly incommensurate with the health burden of NCDs.

  • Future studies should prioritize implementation at scale, target higher levels health systems (meso and macro levels), and test sustainability of NCD programs. They should employ designs with stronger internal validity, be more conceptually driven, and use mixed methods to understand mechanisms.

  • To maximize impact of the research under limited resources, adding implementation science outcomes to effectiveness research and regional collaborations are promising.

Introduction

Noncommunicable diseases (NCDs) have become the leading contributors to morbidity and mortality worldwide. They are now responsible for 74% of all global deaths, 77% of which occur in low- and middle-income countries (LMICs) [1,2]. Approximately 85% of NCD deaths among people aged 30 and 69 years occur in LMICs [1]. Cardiovascular diseases are the leading causes of NCD mortality, followed by cancers, respiratory diseases, and diabetes [1]. Together, these 4 NCDs are responsible of over 80% of all premature NCD deaths [1]. Risk factors such as tobacco and alcohol use, physical inactivity, and unhealthy diets result in significantly greater risk of dying from NCDs. Primary, secondary, and tertiary prevention strategies are vital in addressing NCD burden [1]. Sustainable Development Goal (SDG) target 3.4 commits countries to reduce premature mortality from NCDs by a third by 2030 relative to 2015 levels. Recent analysis shows that no LMIC is on track to meet this target for both men and women if they maintain their 2010 to 2016 average rates of decline [3].

NCD prevention and control should not be regarded as a vertical issue separated from other health conditions. The ongoing Coronavirus Disease 2019 (COVID-19) pandemic has put a spotlight on NCDs, as these increased the risk of death for people with COVID infection. Similarly, NCDs increase mortality risk among people with other infectious diseases such as tuberculosis and HIV. It further highlighted the economic and social inequities in who is afflicted with NCDs, in both high-income countries and LMICs. While primary prevention relies on public health, taxation, and other public policy measures, mitigating the health consequences of NCDs also requires strong health systems. Health systems that recognize this challenge and address modifiable risk factors and prioritize the management of NCDs will be better positioned to promote and maintain health. Data from the 2019 World Health Organization (WHO) NCD Country Capacity surveys reveal that only half of 160 countries have national guidelines for NCDs, half have the 6 essential technologies for early detection, diagnosis, and monitoring of NCDs available in primary care facilities of the public health sector, and 20% of countries have 6 (or fewer) of the 11 essential medicines available [4]. Greater prioritization of NCDs within health systems and high-quality care are essential to achieving SDG 3.4 [3]. Beyond this lies an important agenda for tackling the cumulatively large group of rarer NCDs that afflict the world’s poorest people [5].

To support countries in crafting effective NCD strategies, the WHO Assembly endorsed the Global Action Plan for the Prevention and Control of Noncommunicable Diseases 2013–2020 (GAP-NCD) in May 2013 together with a set of evidence-based interventions (best-buys) and policy options in its appendix 3 that was updated in 2016 and provides 84 interventions or policy options [6,7]. Furthermore, WHO has developed a compendium including all available health interventions. The list and compendium aim to assist Member States, as appropriate in specific national contexts, in implementing measures to achieve the 9 global voluntary targets for NCDs and Target 3.4 of the SDGs. Despite recent calls for a new commitment to implementation research for NCDs, a mid-point evaluation of the WHO NCD Global Action Plan 2013–2030 (NCD-GAP) found that “research has been the weakest NCD-GAP objective in terms of implementation and that progress in implementing research linked to the NCD-GAP has been slow and incremental” [8,9].

While the evidence for the clinical effectiveness of most NCD prevention and treatment interventions is well established, care delivery models and means of scaling these up to entire populations in need in heterogeneous and resource-constrained health systems are not. Implementation research on NCD program delivery, including cost effectiveness in various regions, can illuminate what does and does not work in achieving NCD control [8,1012]. This can promote faster, more efficient, and more effective scale-up of life-saving and health-preserving health system strategies [13,14]. In this systematic review, we aim to synthesize evidence on the current state of implementation research on WHO priority NCD prevention and control interventions provided within health systems in LMICs [6,7,1517].

Methods

This systematic review was conducted according to a study protocol registered in PROSPERO (#CRD42021252969) [18].

Search strategy

Following the Systematic Reviews and Meta-Analyses (PRISMA) checklist [19], we searched for implementation research studies that focused on relevant NCD prevention and control interventions (Table A in S1 Appendix) provided within health systems in LMICs and were published in peer-reviewed journals indexed in MEDLINE and EMBASE databases from 1990 to 2020. The databases were last searched on January 20, 2021. Our search terms included medical subject heading (MeSH) terms and/or key words for 4 key themes (implementation research; NCDs; NCD interventions; LMICs) that were adjusted for each database:

  • Implementation research (e.g., implementation research, implementation science, diffusion of innovations, implementation strategies, dissemination science, implementation outcomes).

  • NCDs (e.g., cardiovascular disease, cancer, diabetes, chronic respiratory disease).

  • Interventions (e.g., smoking cessation, management of hypertension, treatment of acute myocardial infarction, cervical and colorectal cancer screening).

  • LMICs as defined by the World Bank in 2019 (Table C in S1 Appendix).

Language restrictions were not applied. Full details of the search strategy are provided in Table B in S1 Appendix.

Inclusion and exclusion criteria

Table 1 summarizes our review’s specific eligibility criteria. This review includes peer-reviewed, empirical quantitative, qualitative, and mixed method study designs conducted in LMICs that described the implementation of relevant NCD preventive and/or control interventions provided within health systems. Using the updated Appendix 3 of the WHO Global NCD Action Plan 2013–2020, we identified the WHO priority NCD prevention and control interventions [6]. Of these interventions, we selected those that are specifically provided by health systems. This was achieved through discussions and consensus. Table 2 summarizes the intervention categories across eligible NCD risk factors (i.e., tobacco and alcohol use, physical inactivity, and unhealthy diets) and NCDs (i.e., cardiovascular disease, diabetes, cancer, and chronic respiratory disease), and full details are provided in Table A in S1 Appendix. While our search in databases was not restricted to any language, during study screening/review processes, we only retained eligible studies that were in 6 official languages of the United Nations (i.e., Arabic, Chinese, English, French, Russian, and Spanish). We drew on Proctor and colleagues and Glasgow and colleagues to define implementation outcomes eligible for inclusion [20,21]. Nonempirical/primary research studies are not eligible for inclusion (Table 1).

Table 1. Inclusion and exclusion criteria.

Inclusion criteria Exclusion criteria
Population Human beings with or without NCDs. Human beings with or without NCD risk factors. Subjects are not human beings.
Intervention NCD prevention and/or control interventions that are provided within health systems (see Table A in S1 Appendix). Interventions that are not specified in the inclusion criteria.
Outcome Implementation outcomes as defined by Proctor and colleagues and Glasgow and colleagues [20,21]
    • Acceptability
    • Adoption
    • Appropriateness
    • Feasibility
    • Fidelity
    • Penetration
    • Sustainability
    • Implementation costs
    • Reach
    • Implementation
    • Maintenance
Outcomes other than those specified in the inclusion criteria.
Study design Quantitative, qualitative, or mixed method.
Quantitative study designs included experimental and observational.
    • Experimental designs:
      ○ Randomized controlled trial,
      ○ Cluster randomized trial,
      ○ Randomized step wedge,
    • Observational designs:
      ○ Quasi-experimental designs:
        ▪ Single interrupted time series,
        ▪ Controlled interrupted time series,
        ▪ Pre-post with comparison group,
        ▪ Regression discontinuity,
        ▪ Nonrandomized stepped wedge
      ○ Preexperimental designs (no control group or no repeated measures):
        ▪ Pre-post
        ▪ Post-only design
      ○ Other observational designs include:
        ▪ Cohort studies
        ▪ Cross-sectional studies
        ▪ Case-control studies
Nonempirical/primary research including:
    • Review
    • Meta-analysis
    • Editorial
    • Commentary
    • Letter to editor
    • Opinion paper
    • Newspaper
    • Protocols
    • Case report
    • Epidemiological/descriptive studies (e.g., nonintervention association studies including knowledge, attitude, discrete choice experiment, awareness, willingness, and perception (including perceived barriers) studies) and not in the context of implementation of NCD interventions.
    • Instrument/screening or diagnostic test validation studies
    • Call to action
    • Sharing experience/lessons learned on the field if not resulting from research
    • (Descriptive) cost-effectiveness studies based on modeling (and not in the context of implementation of NCD interventions)
Geographic Scope LMICs (see Table C in S1 Appendix) Areas other than LMICs
Time frame 1990–2020 Studies published before 1990

LMIC, low- and middle-income country; NCD, noncommunicable disease.

Table 2. Summary of eligible NCD preventive and control interventions.

Conditions Intervention categories
NCD risk factors
Tobacco use Individual smoking cessation
Mass media campaign smoking cessation
Harmful use of alcohol Alcohol reduction counseling for at risk individuals
Treatment for alcohol use disorder
Unhealthy diet Mass media or other behavior change program to reduce salt intake
Nutrition education in institutions
Salt reduction public institutions
Interventions to promote exclusive breastfeeding
Physical inactivity Community environmental program increase physical activity
Mass media campaign promote physical activity
Physical activity counseling
NCDs
Cardiovascular disease Treatment of hypertension
Rehabilitation of post-acute CVD event (myocardial infarction, stroke)
Treatment of high-risk CVD event
Treatment of acute ischemic stroke
Treatment of acute myocardial infarction
Treatment of heart failure
Antibiotic treatment of streptococcal pharyngitis (rheumatic fever prevention)
Treatment for secondary prevention of stroke (e.g., anticoagulation for atrial fibrillation, aspirin)
Diabetes Glycemic control among people with diabetes
Screening to prevent complications among people with diabetes
Treatment of diabetes
Preconception care for women with diabetes
Influenza vaccination for people with diabetes
Cancer Breast cancer screening
Cervical cancer screening
HPV vaccination for teen girls
Colorectal cancer screening
Treatment of breast and colorectal cancer
Hepatitis B immunization for liver cancer prevention
Screening for oral cancer in high-risk groups
Chronic respiratory disease Treatment of asthma and COPD
Influenza vaccination for patients with COPD

COPD, chronic obstructive pulmonary disease; CVD, cardiovascular disease; HPV, human papilloma virus; NCD, noncommunicable disease.

Data extraction and analysis

The titles and abstracts of unique results from the databases were reviewed independently by 2 researchers for potential inclusion using COVIDENCE review software [22]. The full texts of studies retained at the title and abstract screening stage were retrieved and independently assessed for inclusion. Any discrepancies were resolved through discussion and consensus. Data extraction on each included study was conducted by a single researcher using a data extraction tool, developed and piloted a priori (Table D in S1 Appendix). Data elements included study characteristics (e.g., publication year, country of implementation, study funding), NCD conditions (risk factors and disease), intervention details (e.g., type of intervention, level of health system), methods (e.g., research approach, study design), implementation outcomes (e.g., fidelity, feasibility), and equity lens (e.g., disaggregated by key SES stratifiers, targeted vulnerable population). We also extracted data on implementation strategies including actor (i.e., who delivered the intervention), action target, and recipients; details of other implementation strategies were not sufficiently described to permit extraction [23]. The recipients of the action/strategy were further aggregated by demographic subgroup (e.g., people eligible for cancer screening including cervical and colorectal), disease risk subgroup (e.g., patients with myocardial infarction, patients with diabetes or hypertension, people who smoke), general population, healthcare workers (e.g., physicians, nurses, pharmacists, and midwives), and community health workers. We synthesize extracted data using descriptive statistics and following the review protocol registered in PROSPERO. Specifically, we provide an overview of NCD priority intervention implementation study characteristics across NCD conditions to shed light on the current state of implementation research of priority NCD prevention and control interventions in LMICs. Given this review does not focus on effect size of NCD interventions, we did not perform a meta-analysis.

Risk of bias assessment

This review focuses on implementation of multiple interventions across various NCDs, rather than effectiveness of any single set of interventions. Further, studies with heterogenous aims and methodologies (including qualitative methodology) were included. Therefore, risk of bias assessment to understand how effect size may have been compromised by bias is not applicable in this review. We instead commented on the distribution of research designs and discussed about stronger/weaker designs.

Results

Our search strategy implemented in MEDLINE and EMBASE identified 9,683 publications, of which 7,419 unique records were screened for inclusion. Abstract and full-text screening identified 222 studies that met our inclusion criteria (Tables 1 and 2) [24245]. A summary of this process is presented in the PRISMA flow diagram in Fig 1.

Fig 1. PRISMA flow chart.

Fig 1

Intervention refers to studies excluded because they studied the implementation of interventions that did not meet the eligible criteria. Study design refers to studies excluded because they used study designs that did not meet eligibility criteria (e.g., nonempirical studies including reviews and commentaries). Outcomes refer to studies excluded based on not having focused on relevant implementation outcomes. Settings refer to studies excluded because they were not conducted in LMICs. Full text means that studies were excluded because full text was not available. Time refers to studies that were excluded because they were published before/conducted before 1990.

The 222 studies included in this review evaluated 265 priority NCD prevention and control interventions implemented in 62 countries, of which 6% were in low-income countries (LICs), 45% in LMICs, and 46% in upper middle-income countries (UMICs) (Table 3 and Figs 2, 3, and 4A and Table E in S1 Appendix). The NCD conditions targeted varied by income groups of countries (Fig A in S1 Appendix). Eight of the included studies were multicountry studies. The number of studies published has been increasing over time (Fig 5A). Overall, the majority of interventions were focused on either screening (49%) or treatment (39%), while prevention accounted for only 12%, with nearly 80% of these tackling prevention of the shared NCD behavioral risk factors—tobacco use, unhealthy diet, physical inactivity, and harmful use of alcohol. The NCD interventions varied by conditions and type (prevention, screening, and treatment) (Figs 2, B, and C in S1 Appendix). Notably, over one-third of the interventions studied (37%) were for cervical cancer (Fig 2), which accounts for 0.35% of DALYs lost and 0.5% of deaths globally, with similar figures for LMICs (https://vizhub.healthdata.org/gbd-compare/). Diabetes was the focus of nearly one-quarter of the research with hypertension the topic of another 9% (Fig 2). Each of the other recommended interventions represented 5% or less of the implementation research output. Chronic respiratory disease was understudied relative to its prevalence: less than 1% of the studies examined chronic respiratory disease treatment and only 3% smoking cessation programs. The intervention focus appears to vary by income groups of countries (Fig D in S1 Appendix). Feasibility was the most studied implementation outcome followed by adoption (Fig 6). Most of the actors were researchers, which accounted for 58%; whereas government/ministry of health, providers, and NGOs accounted for 18%, 10%, and 6%, respectively. The majority of intervention targeted improvement in health outcomes (45%) followed by change in behavior (34%).

Table 3. Overview of study characteristics.

NCDs and risk factors Intervention categories N Distribution of priority NCD interventions (N = 265)
Country’s income classification, N Methods approach, N Major study design, N Health system level*, N Level of scale-up, N Implementation outcomes, N Considered equity†, N Implementation strategies
Actor, N Action target, N Recipients, N
Tobacco use Individual smoking cessation 6 LMICs = 5
UMICs = 1
Quantitative = 5
Mixed = 1
Experimental = 2
Multiple = 1
Preexperimental = 2
Other Observational = 1
Micro = 4
Meso = 2
Pilot† = 5
Scale-up = 1
Adoption = 1
Appropriateness = 1
Feasibility = 3
Multiple = 1
4 Researchers = 4
Providers = 2
Behavior = 6 Disease risk subgroup = 6
Mass media campaign smoking cessation 2 UMICs = 2 Quantitative = 2 Experimental = 1
Observational = 1
Macro = 2 Scale-up = 2 Adoption = 1
Penetration = 1
1 Researchers = 1
MOH = 1
Behavior = 2 Disease risk subgroup = 2
Harmful use of alcohol Alcohol reduction 1 LMICs = 1 Quantitative = 1 Experimental = 1 Micro = 1 Pilot = 1 Multiple = 1 0 Researchers = 1 Behavior = 1 Disease risk subgroup = 1
Unhealthy diet Mass media or other behavior change program to reduce salt intake 3 LMICs = 2
UMICs = 1
Quantitative = 3 Experimental = 2
Other observational = 1
Micro = 1
Meso = 1
Macro = 1
Pilot = 1
Scale-up = 2
Adoption = 1
Penetration = 1
Multiple = 1
2 Researchers = 1
MOH = 2
Behavior = 3 General population = 2
Disease risk subgroup = 1
Nutrition education in institutions 5 LMICs = 1
UMICs = 3
Multiple = 1
Quantitative = 4
Mixed method = 1
Quasi-experimental designs = 3
Preexperimental = 1
Other observational = 1
Micro = 1
Meso = 3
Macro = 1
Pilot = 2
Scale-up = 3
Acceptability = 1
Adoption = 2
Feasibility = 1
Penetration = 1
3 Researchers = 4
MOH = 1
Behavior = 3
Behavior, health outcomes = 2
Demographic subgroup = 2
Disease risk subgroup = 3
Salt reduction public institutions 2 UMICs = 2 Quantitative = 2 Other observational = 2 Macro = 2 Pilot = 1
Scale-up = 1
Adoption = 1
Penetration = 1
1 Researchers = 1
MOH = 1
Behavior = 2 Demographic subgroup = 2
Physical inactivity Community environmental program increase physical activity 4 LMICs = 3
UMICs = 1
Quantitative = 4 Experimental = 2
Preexperimental = 1
Other observational = 1
Micro = 1
Meso = 1
Macro = 2
Pilot = 1
Scale-up = 3
Feasibility = 1
Penetration = 1
Multiple = 2
2 Researchers = 3
MOH = 1
Behavior = 2
Behavior and knowledge = 2
Demographic subgroup = 3
Disease risk subgroup = 1
Mass media campaign promote physical activity 2 UMCIs = 2 Quantitative = 2 Experimental = 1
Other observational = 1
Macro = 2 Scale-up = 2 Adoption = 1
Penetration = 1
1 Researchers = 1
MOH = 1
Behavior = 1
Behavior and knowledge = 1
Demographic subgroup = 1
Disease risk subgroup = 1
CVD Rehabilitation post-acute CVD event 1 UMICs = 1 Quantitative = 1 Experimental = 1 Micro = 1 Pilot = 1 Feasibility = 1 0 Researchers = 1 Health outcomes = 1 Disease risk subgroup = 1
Treatment of high-risk CVD event 5 LMICs = 2
UMICs = 3
Quantitative = 5 Experimental = 2
Quasi-experimental designs = 2
Other observational = 1
Micro = 5 Pilot = 5 Acceptability = 1
Adoption = 2
Feasibility = 1
Maintenance = 1
3 Researchers = 4
Providers = 1
Behavior = 3
Health outcomes = 1
Demographic subgroup = 1
Disease risk subgroup = 3
HCWs = 1
Treatment of acute ischemic stroke 10 LMICs = 5
UMICs = 5
Quantitative = 10 Experimental = 2
Preexperimental = 7
Other observational = 1
Micro = 6
Meso = 4
Pilot = 8
Scale-up = 2
Adoption = 4
Feasibility = 4
Fidelity = 1
1 Researchers = 5
MOH = 4
Providers = 1
Health outcomes = 10 Disease risk subgroup = 10
Treatment of acute myocardial infarction 12 LMICs = 2
UMICs = 10
Quantitative = 11
Qualitative = 1
Experimental = 3
Quasi-experimental designs = 2
Preexperimental = 4
Other observational = 3
Micro = 6
Macro = 6
Pilot = 10
Scale-up = 1
Adoption = 5
Feasibility = 5
Fidelity = 1
Penetration = 1
3 Researchers = 4
MOH = 4
Providers = 4
Health outcomes = 11
Behavior = 1
Disease risk subgroup = 11
HCWs = 1
Treatment of heart failure 5 LMICs = 2
UMICs = 3
Quantitative = 5 Experimental = 2
Quasi-experimental designs = 1
Preexperimental = 2
Micro = 5 Pilot = 5 Adoption = 2
Feasibility = 3
1 Researchers = 3
Providers = 2
Health outcomes = 5 Disease risk subgroup = 5
Treatment of hypertension 23 LMICs = 10
Multiple = 2
UMICs = 11
Quantitative = 16
Qualitative = 1
Mixed method = 6
Experimental = 7
Quasi-experimental designs = 4
Preexperimental = 2
Other observational = 5
Multiple = 5
Micro = 20
Meso = 2
Macro = 1
Pilot = 22
Scale-up = 1
Adoption = 1
Feasibility = 18
Fidelity = 3
Multiple = 1
10 Researchers = 10
MOH = 5
NGO = 1
Providers = 6
NC = 1
Behavior = 10
Health outcomes = 8
Behavior and health outcomes = 5
Demographic subgroup = 1
Disease risk subgroup = 22
Diabetes Glycemic control among people with diabetes 7 LMICs = 3
UMICs = 2
Multiple = 2
Quantitative = 5
Mixed method = 2
Experimental = 2
Quasi-experimental designs = 4
Multiple = 1
Micro = 4
Meso = 2
Macro = 1
Pilot = 6
Scale-up = 1
Adoption = 1
Appropriateness = 2
Feasibility = 2
Multiple = 2
4 Researchers = 5
MOH = 1
NGO = 1
Behavior = 4
Health outcomes = 2
Behavior and health outcomes = 1
Demographic subgroup = 1
Disease risk subgroup = 6
Screening to prevent complications among people with diabetes 17 LMICs = 10
UMICs = 7
Quantitative = 16
Mixed method = 1
Experimental = 1
Quasi-experimental designs = 1
Preexperimental = 6
Other observational = 8
Multiple = 1
Micro = 16
Meso = 1
Pilot = 1 Acceptability = 1
Adoption = 2
Feasibility = 10
Multiple = 1
Reach = 3
6 Researchers = 8
MOH = 1
NGO = 3
Providers = 4
NC = 1
Behavior = 5
Health outcomes = 12
Disease risk subgroup = 16
CHWs = 1
Diabetes management 39 LMICs = 22
UMICs = 14
Multiple = 3
Quantitative = 33
Qualitative = 1
Mixed method = 5
Experimental = 8
Quasi-experimental designs = 6
Preexperimental = 9
Other observational = 12
Multiple = 4
Micro = 34
Meso = 3
Macro = 2
Pilot = 38
Scale-up = 1
Acceptability Adoption = 1
Appropriateness = 2
Feasibility = 21
Fidelity = 1
Reach = 3
Multiple = 4
16 Researchers = 22
MOH = 6
NGO = 4
Providers = 6
NC = 1
Behavior = 11
Behavior and knowledge = 3
Health outcomes = 20
Behavior and health outcomes = 4
Knowledge and health outcomes = 1
Demographic subgroup = 3
Disease risk subgroup = 35
CHWs = 1
Influenza vaccination for people with diabetes 1 UMICs = 1 Quantitative = 1 Other observational = 1 Micro = 1 Pilot = 1 Adoption = 1 0 Researchers = 1 Health outcomes = 1 Disease risk subgroup = 1
Cancer Breast cancer screening 9 LMICs = 5
UMICs = 4
Quantitative = 9 Experimental = 1
Quasi-experimental designs = 2
Preexperimental = 2
Other observational = 4
Micro = 6
Macro = 9
Pilot = 7
Scale-up = 1
Acceptability = 1
Adoption = 1
Feasibility = 4
Implementation cost = 1
Reach = 1
Multiple = 1
7 Researchers = 4
MOH = 4
NC/NA = 1
Behavior = 4
Health outcomes = 5
Demographic subgroup = 9
Cervical cancer screening 93 LICs = 13
LMICs = 42
UMICs = 34
Multiple = 4
Quantitative = 78
Qualitative = 8
Mixed method = 7
Experimental = 16
Quasi-experimental designs = 4
Preexperimental = 20
Other observational = 47
Multiple = 6
Micro = 78
Meso = 10
Macro = 5
Pilot = 78
Scale-up = 12
Acceptability = 22
Adoption = 23
Feasibility = 22
Implementation cost = 4
Maintenance = 1
Reach = 10
Sustainability = 2
Multiple = 9
40 Researchers = 56
MOH = 13
NGO = 10
Providers = 2
NC = 6
NA = 6
Behavior = 30
Health outcomes = 41
Knowledge = 5
Knowledge and behavior = 4
Knowledge, behavior, health outcome = 2
Knowledge and health outcomes = 3
NC/NA = 8
Demographic subgroup = 80
Disease risk subgroup = 2
HCWs = 3
CHWs = 2
HPV vaccination for teen girls 5 LMICs = 2
UMICs = 2
Multiple = 1
Quantitative = 4
Qualitative = 1
Preexperimental = 2
Other observational = 3
Micro = 3
Macro = 2
Pilot = 3
Scale-up = 2
Adoption = 3
Feasibility = 1
Multiple = 1
1 Researchers = 3
MOH = 1
NGO = 1
Behavior = 2
Health outcomes = 3
Demographic subgroup = 5
Colorectal cancer screening 11 LMICs = 1
UMICs = 10
Quantitative = 10
Mixed method = 1
Experimental = 2
Quasi-experimental designs = 1
Preexperimental = 1
Other observational = 6
Multiple = 1
Micro = 7
Meso = 4
Pilot = 9
Scale-up = 2
Acceptability = 1
Adoption = 4
Feasibility = 3
Implementation cost = 1
Reach = 1
Multiple = 1
4 Researchers = 7
MOH = 4
Behavior = 5
Health outcomes = 5
Knowledge and behavior = 1
Demographic subgroup = 10
Disease risk subgroup = 1
Chronic respiratory disease Treatment of asthma 2 LMICs = 2 Mixed method = 2 Multiple = 2 Micro = 1
Macro = 1
Pilot = 1
Scale-up = 1
Acceptability = 1 1 Researchers = 1
MOH = 1
Health outcomes = 2 Disease risk subgroup = 2

*Micro level refers to the point where the care providers interact with the patient; micro-level interventions aim to directly influence the performance of the staff or the operations of a facility [11,264]. Meso level refers to the level responsible for service areas/clinical programs providing care for a similar group of patients, typically part of a larger organization (e.g., subnational intervention targeting improvement of a network of facilities and communities) [11,264]. Macro level is the highest (strategic) level of the system, an umbrella including all intersecting areas, departments, providers, and staff (e.g., boards, healthcare network, integrated health system that includes several organizations); macro-level interventions are best able to directly tackle the social, political, economic, and organizational structures that shape a health system [11,264].

†Equity lens used if studies disaggregated by SES stratifiers (e.g., age, sex, education, income, and rural vs. urban) and/or targeted vulnerable population.

CHW, community health workers include ASHAs in India; CVD, cardiovascular disease; HCW, healthcare worker; HPV, human papilloma virus; LIC, low-income country; LMIC, lower middle-income country; MOH, Ministry of Health/Government; N, number of NCD interventions; NC/NA, not clear/not applicable; NCDs, noncommunicable disease; NGO, nongovernmental organization; UMIC, upper middle-income country.

Fig 2. Distribution of priority NCD prevention and control interventions by type of NCD and their risk factors (N = 265).

Fig 2

Fig 3. Distribution of studies per 1 million population by country of implementation.

Fig 3

We used country population size in 2020 (https://data.worldbank.org/indicator/SP.POP.TOTL) to standardized estimates expressed as number of studies per 1 million population. We used “rworldmap” package (https://cran.r-project.org/web/packages/rworldmap/rworldmap.pdf) available in R software to present these standardized estimates across countries where interventions were implemented. Country borders in this package are derived from Natural Earth data. Table E in S1 Appendix shows number of included studies per country.

Fig 4. Distribution of study countries, funding, and authorship (N = 222).

Fig 4

Fig 5.

Fig 5

Growth of research over time (A) and distributions of NCD interventions by type (B). Fig 5A shows number of studies published each year (N = 222 studies); Fig 5B shows distributions by type of interventions (N = 265 NCD interventions evaluated in studied included in the review).

Fig 6. Distribution of implementation outcomes.

Fig 6

Most studies used quantitative methods, which accounted for 86%, whereas mixed methods and qualitative methods accounted for 9% and 5%, respectively (Table 2). The majority of studies used observational designs, with cross-sectional designs used in 45 studies. Among evaluations, preexperimental studies (such as pre-post without a comparison group or post-only) was the most frequently employed (n = 56 or 25% of all studies); experimental designs were used in a quarter of studies (n = 53 or 24% of all studies); quasi-experimental evaluation designs (such as pre-post comparison group or time series) were used in 15 papers (7% of all studies) (Fig 7). Study designs also appear to vary by NCD conditions targeted (Fig E in S1 Appendix). The sample size among included studies varied, ranging from 11 to 350,581, with median of 658. Most studies were standalone implementation studies (85%), with some variations by NCD conditions (Fig F in S1 Appendix). Hybrid implementation and effectiveness studies accounted only for 15%. Less than 5% of studies reported they were guided by widely known implementation science framework. Majority of studies were proof of concept or pilot versus scale-up studies (88% versus 12%), with variations by NCD conditions (Fig G in S1 Appendix). The level of health system targeted most often was micro level, accounting for 79% of studies, with variations by NCD conditions. The meso and macro levels of health systems were targeted by 14% and 7% of studies, respectively (Fig H in S1 Appendix). Approximately 42% of studies employed an equity lens—i.e., studies disaggregated by SES stratifiers (e.g., age, sex, education, income, and rural versus urban) and/or targeted vulnerable population.

Fig 7. Study designs.

Fig 7

A majority of studies (72%) reported funding, with international funding being the predominant source (Fig 4B). There seems to be some variations by NCD conditions (Figs I–K in S1 Appendix). For example, while 78% of studies focused on cervical cancer reported funding, of which 77% were from international sources, those focused on colorectal cancer and treatment of acute myocardial infarction received most of their funding from the countries where implementation research was conducted (Fig K in S1 Appendix). Majority of reported funding was provided by government/universities (43.6%), 35% reported multiple funders, 16% were foundations/NGOs, and 6% were private funders (e.g., pharmaceutical companies, professional associations) (Fig L in S1 Appendix). Approximately 62% of corresponding authors were from the country of implementation (Fig 4C); however, this varied by funding sources, with studies funded by international funders having the highest number of international corresponding authors.

Discussion

We conducted a systematic review of implementation research studies on NCD prevention and control strategies in LMICs published between 1990 and 2020. We focused our analysis on WHO-recommended NCD interventions carried out by the health system rather than through policy, legislation, or public health approaches [6,7]. These studies therefore represent the state of the implementation science in prevention and control of NCDs by health systems in the countries bearing the bulk of disease burden from noncommunicable conditions.

Of the 222 implementation science studies included in this review, 94% were conducted in middle-income countries (evenly split between lower- and upper-middle) and 6% in LICs. UMICs were slightly overrepresented compared to their share of the LMIC population (approximately 40%). Only 8 of the studies were multicountry studies, suggesting that cross-national generalizability is not the primary motivation for this type of research. India and China, with 43% of the population of LMICs, comprised one-third of the studies. South Africa, Brazil, Iran, Kenya, and Nigeria, were well represented, each contributing more than 3% of the research.

The studies described 265 different NCD interventions, ranging from screening to prevention to treatment and palliation. Conditions studied varied substantially by region. All 13 of the interventions studied in LICs were for cervical cancer screening. In low-middle income countries, cervical cancer accounted for 37%, diabetes for 29%, and hypertension for 8% of interventions. There was a larger variety of conditions studied in UMICs: while cervical cancer and diabetes comprised half the studies, hypertension, myocardial infarction, colorectal cancer, other cardiovascular diseases, and unhealthy diet each comprised more than 5% of studies. The 2 countries with the largest research output and populations, China and India, differed substantially in focus. In India over 70% of studies were on 2 conditions: diabetes (51%) and cervical cancer (19%), whereas the research was more evenly distributed across the NCDs in China.

Half of all studied interventions in this review evaluated screening for disease, nearly 40% treatment and 12% prevention. Over 70% of all screening studies were for cervical cancer, with less research on other conditions for which screening can be cost effective, such as diabetes, colorectal cancer, and breast cancer. Primary and secondary prevention can reduce incidence of disease and forestall disease progression and disability. We found that only 31 (12%) of the studied interventions addressed prevention with nearly 80% of these tackling prevention of the NCD behavior risk factors (e.g., tobacco use, inactivity, unhealthy diet). Less than 10% of the interventions evaluated in this review focused on management of hypertension (the leading metabolic risk factor worldwide, accounting for approximately 19% of global deaths) [246]. This suggests a substantial implementation research gap in secondary prevention, a critical function of primary care and other levels of health systems. Primary care services such as hypertension management and glucose control play a major role in reducing mortality, thus insufficient research on their optimal implementation is a major missed opportunity. Recent work shows that treatment and control rates for hypertension were below 25% and 10%, respectively, in many countries in South Asia and sub-Saharan Africa. These countries also showed the slowest rates of improvement from 1990 [247].

The preponderance of interventions studied was in pilot phase, with fewer than 15% studying large-scale implementation. Along the same lines, feasibility and adoption were the most studied implementation outcomes, suggesting the research is focused on introduction of new approaches. While proof of concept studies is vital with new implementation strategies, arguably WHO-proposed interventions are well established and evidence on (clinical) effectiveness abound. To provide useful guidance to health system planners and realize population health gains, there needs to be a greater investment in large-scale NCD implementation research to promote sustainability of evidence-based interventions. To best scale scarce research resources and accelerate impact, countries could join regional consortia to study interventions and undertake factorial designs that compare locally adapted implementation approaches.

Over three-quarters of the studies were situated at the micro level of the health system—targeting patient, provider, or clinic levels. Nearly 1 in 5 tested a new technology, despite evidence that technology adoption without substantial integration into policies, data, and workflows is typically ineffective in transforming care [248,249]. Education was another common target featuring in 3 of 10 studies; researchers accounted for the majority of the actors. While micro-level approaches are the most “researchable,” as they are easiest to implement and analyze; positive results are difficult to scale and sustain in the absence of systemic health system change. The Lancet Commission on High Quality Health Systems notes that high-quality care results from structures that align system aims and policies with strong governance, management, and appropriately trained workforce [250]. In this context, micro-level innovation cannot raise quality system wide and is only effective if undertaken as part of a learning health system that can determine whether it offers sufficient benefit over current practice in complexity, cost, and health benefit, and if so, how to best integrate into the health system [251].

Nearly 9 in 10 studies were stand-alone implementation research. This also points to an opportunity to add implementation research to ongoing effectiveness trials. Integrated or hybrid effectiveness-implementation studies are increasingly being used in high-income countries to shed light on both the outcome and extent and quality of service/program delivery [252]. Notably, fewer than 5% of studies cited use of an implementation science framework consistent with prior research showing that the use of implementation science framework is substantially lower in LMICs compared with high-income countries [253]. The use of a tested conceptual framework can improve the rigor of the research and promote comparability of results. Of the studies that reported a funding source, 60% was from international sources, 33% from the country of the research, and the remaining from both local and international sources. This reflects the low spending for health research and especially for health systems and implementation research in LMICs. The lack of domestic support is unlikely to be offset by global funding going forward; a recent analysis showed that NCDs were under prioritized in bilateral agency portfolios relative to their health impacts [254]. Over 40% of development assistance for health in LICs for NCDs came from NGOs and philanthropies, which are less inclined to support research than operations [254]. Indeed, we found that only 16% of studies with funding information reviewed were supported by philanthropies or NGOs, while the other remaining studies reported funding sources from government, private, and/or multiple sources.

Scarcity of funding for research is a key constraint to needed implementation research for NCDs. While there are proposals for coordinating and increasing global support, it is unrealistic to expect this to meet the scale of needed research without a substantial increase in countries’ investment in research [255]. Such an investment is likely to pay off in better health and higher quality, more efficient service delivery [256]. To make best use of research funds, implementation science should strive to be as generalizable as possible—at minimum at a regional level where health systems share similarities. International and regional institutions can play an important role in supporting research consortia and partnerships to promote efficiency of and accelerate the pace of research and, ultimately its uptake into routine care at scale.

Over 50 of the 222 included studies used an experimental research design. While this is the strongest design to yield causal inference, it is not always feasible to implement. Quasi-experimental designs, such as pretest, posttest comparison group designs, and interrupted time series, which can offer robust information were used in only 15 studies. Preexperimental designs that do not include a comparison group or tracking over time, comprised nearly a quarter of the studies. These designs have very low internal validity and should generally be avoided. The remainder of the studies used cross-sectional descriptions, cohort studies, and qualitative research or multiple study types. Given the disproportionate health harms of NCDs among the poor and other vulnerable groups within countries, disaggregated or stratified analysis is crucial. Forty percent of the assessed studies included stratification by age, sex, education, or urbanicity. Going forward, greater use of quasi-experimental designs, hybrid implementation studies and mixed methods approaches, would benefit the field. An expanded focus on equity of implementation outcomes is also needed.

Strengths and limitations

Our study had several strengths, notably the extensive scope for the search that covered LMICs, a wide range of outcomes and study types, and a large contingent of conditions and health services. We had no language restrictions permitting a comprehensive assessment of the published literature. The review also had several limitations. We focused on WHO-recommended interventions, which at present do not include guidance for some prevalent conditions such as mental health problems and kidney disease [6,12]. Mental health is a major contributor to the global burden of disease and future work should assess the implementation science for the growing range of mental health interventions that appear to be effective in lower-income settings [257,258]. The studies we assessed used differing definitions of implementation outcomes (e.g., acceptability was measured in some studies by self-report and in others by behavior change). This limits direct comparison of study outcomes. Greater use of implementation science frameworks can promote coherence in the research approaches and terminology used to the benefit of end users. Similarly, given the implementation strategies were not specified well enough in the included studies, we elected to focus on actors, action target, and recipients in our description of implementation strategies. Clearly, reporting empirical implementation studies using existing framework to describe implementation strategies would help bolster uptake of implementation research in NCDs.

We also did not search the gray literature and as such, some relevant studies may have been missed. However, studies in gray literature that were not peer reviewed would have not have been eligible for inclusion in this review. Despite using rigorous search strategies without language restrictions, studies published in journals not indexed in MEDLINE and EMBASE were not captured [259263]. Given the focus on this review and the heterogeneity in aims and methodologies of included studies, risk of bias assessment to understand how effect size may have been compromised by bias is not applicable. As such, we only commented on the distribution of research designs and discussed about stronger/weaker designs. Lastly, we reported year of publication and not time of when study/implementation was conducted.

Conclusions

High-quality implementation science can play a key role in informing effective delivery of health system interventions to mitigate the burden of NCDs and avoiding expensive mistakes. While implementation research on priority NCDs has grown substantially, from under 10 studies per year in early 2000s to 51 studies in 2020, this is still vastly incommensurate with the health importance of the topic. Further, the concentration of studies in a few geographies and a few health areas, such as cervical cancer, highlights the dearth of research for other key conditions. We found a major gap in research on secondary prevention, i.e., management of risk factors or early disease to prevent disease progression and premature death. Research on ways in which health systems can be strengthened, including primary care levels, to provide optimal care for NCDs is critically needed. Future studies should use implementation science frameworks, and, when testing interventions, strong research designs with strong internal validity, including well-designed quasi-experimental studies. Opportunities exist for adding implementation science studies to planned effectiveness research.

Supporting information

S1 PRISMA Checklist. PRISMA 2020 checklist.

(DOCX)

S1 Appendix. Appendix tables and figures.

Table A in S1 Appendix. Interventions provided within health systems. Table B in S1 Appendix. Sample of the search strategy used in the MEDLINE database. Table C in S1 Appendix. List of low- and middle-income countries. Table D in S1 Appendix. Data extraction tool. Table E in S1 Appendix. Distribution of studies by countries where they were implemented. Fig A in S1 Appendix. Variation of conditions evaluated by income group. Fig B in S1 Appendix. Priority NCD interventions (n = 265) identified in 222 studies included in the review. Fig C in S1 Appendix. Distribution of included studies by NCD. Fig D in S1 Appendix. Distribution of intervention type by income group. Fig E in S1 Appendix. Distributions by research designs. Fig F in S1 Appendix. Distributions by standalone implementation studies vs. embedded or hybrid effectiveness-implementation studies. Fig G in S1 Appendix. Distributions by pilot vs. scale-up project. Fig H in S1 Appendix. Variation by level of health system. Fig I in S1 Appendix. Studies that reported funding (vs. those that did not) by NCD conditions. Fig J in S1 Appendix. Distributions by funding type. Fig K in S1 Appendix. Distribution of funding sources by NCDs and their risk factors. Fig L in S1 Appendix. Types of reported funding sources (N = 222 included studies).

(DOCX)

Abbreviation

COVID-19

Coronavirus Disease 2019

LIC

low-income country

LMIC

low- and middle-income country

NCD

noncommunicable disease

SDG

Sustainable Development Goal

UMIC

upper middle-income country

Data Availability

All relevant data are within the manuscript and its supporting information files.

Funding Statement

The Alliance for Policy and Health Systems Research and The World Health Organization funded the study. CH received support through a Banting Postdoctoral Fellowship from the Canadian Institutes of Health Research. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

References

  • 1.World Health Organization. Noncommunicable diseases: World Health Organization. 2021. [cited 2021 Sep 7]. Available from: https://www.who.int/news-room/fact-sheets/detail/noncommunicable-diseases. [Google Scholar]
  • 2.World Health Organization. Global health estimates. 2020. [Google Scholar]
  • 3.Countdown NCD. NCD Countdown 2030: pathways to achieving Sustainable Development Goal target 3.4. Lancet. 2020. doi: 10.1016/S0140-6736(20)31761-X [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.World Health Organization. Assessing national capacity for the prevention and control of noncommunicable diseases. Report of 2019 Global Survey WHO. 2020. [Google Scholar]
  • 5.Bukhman G, Mocumbi AO, Atun R, Becker AE, Bhutta Z, Binagwaho A, et al. The Lancet LancetNCDI Poverty Commission: bridging a gap in universal health coverage for the poorest billion. Lancet. 2020;396(10256):991–1044. Epub 2020/09/18. doi: 10.1016/S0140-6736(20)31907-3 ; PubMed Central PMCID: PMC7489932. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.World Health Organization. Updated appendix 3 of the who global Ncd action plan 2013–2020. Technical Annex 2017. [Google Scholar]
  • 7.World Health Organization. Global action plan for the prevention and control of noncommunicable diseases 2013–2020: World Health Organization. 2013. [Google Scholar]
  • 8.Marten R, Mikkelsen B, Shao R, Dal Zennaro L, Berdzuli N, Fernando T, et al. Committing to implementation research for health systems to manage and control non-communicable diseases. Lancet Glob Health. 2021;9(2):e108–e109. doi: 10.1016/S2214-109X(20)30485-X [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.World Health Organization. Mid-point evaluation of the implementation of the WHO global action plan for the prevention and control of noncommunicable diseases 2013–2020 (NCD-GAP). 2020. [Google Scholar]
  • 10.Alonge O, Rodriguez DC, Brandes N, Geng E, Reveiz L, Peters DH. How is implementation research applied to advance health in low-income and middle-income countries? BMJ Glob Health. 2019;4(2):e001257. doi: 10.1136/bmjgh-2018-001257 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Kruk ME, Gage AD, Arsenault C, Jordan K, Leslie HH, Roder-DeWan S, et al. High-quality health systems in the Sustainable Development Goals era: time for a revolution. Lancet Glob Health. 2018;6(11):e1196–e1252. doi: 10.1016/S2214-109X(18)30386-3 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Isaranuwatchai W, Teerawattananon Y, Archer RA, Luz A, Sharma M, Rattanavipapong W, et al. Prevention of non-communicable disease: best buys, wasted buys, and contestable buys. BMJ. 2020;368. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Madon T, Hofman KJ, Kupfer L, Glass RI. Public Health: Implementation Science. Science. 2007;318(5857):1728–1729. doi: 10.1126/science.1150009 [DOI] [PubMed] [Google Scholar]
  • 14.Geng EH, Peiris D, Kruk ME. Implementation science: Relevance in the real world without sacrificing rigor. PLoS Med. 2017;14(4):e1002288. Epub 2017/04/26. doi: 10.1371/journal.pmed.1002288 ; PubMed Central PMCID: PMC5404833. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Allen LN, Pullar J, Wickramasinghe KK, Williams J, Roberts N, Mikkelsen B, et al. Evaluation of research on interventions aligned to WHO ‘Best Buys’ for NCDs in low-income and lower-middle-income countries: a systematic review from 1990 to 2015. BMJ Glob Health. 2018;3(1):e000535. doi: 10.1136/bmjgh-2017-000535 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Allen LN, Nicholson BD, Yeung BY, Goiana-da-Silva F. Implementation of non-communicable disease policies: a geopolitical analysis of 151 countries. Lancet Glob Health. 2020;8(1):e50–e58. doi: 10.1016/S2214-109X(19)30446-2 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Allen LN, Wigley S, Holmer H. Implementation of non-communicable disease policies from 2015 to 2020: a geopolitical analysis of 194 countries. Lancet Glob Health. 2021;9(11):e1528–e1538. doi: 10.1016/S2214-109X(21)00359-4 [DOI] [PubMed] [Google Scholar]
  • 18.Systematic Review of NCD Implementation Research in Low- and Middle-Income Countries. [Internet]. PROSPERO 2021. [cited 2021 Oct 2]. Available from: https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42021252969.
  • 19.Moher D, Liberati A, Tetzlaff J, Altman DG. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Ann Intern Med. 2009;151(4):264–269. doi: 10.7326/0003-4819-151-4-200908180-00135 [DOI] [PubMed] [Google Scholar]
  • 20.Proctor E, Silmere H, Raghavan R, Hovmand P, Aarons G, Bunger A, et al. Outcomes for implementation research: conceptual distinctions, measurement challenges, and research agenda. Adm Policy Ment Health. 2011;38(2):65–76. doi: 10.1007/s10488-010-0319-7 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Glasgow RE, Vogt TM, Boles SM. Evaluating the public health impact of health promotion interventions: the RE-AIM framework. Am J Public Health. 1999;89(9):1322–1327. doi: 10.2105/ajph.89.9.1322 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Veritas Health Innovation. Covidence systematic review software. 2020 [cited 2021 Nov 5]. Available from: https://get.covidence.org/systematic-review?campaignid=11343712044&adgroupid=114130876511&gclid=Cj0KCQjwtrSLBhCLARIsACh6RmjH6RwcJalTVCaL76kpSCeqErC2sP8uX4Vj8wZYdEQWQxdXWVwD0eMaAsz1EALw_wcB.
  • 23.Proctor EK, Powell BJ, McMillen JC. Implementation strategies: recommendations for specifying and reporting. Implement Sci. 2013;8(1):1–11. doi: 10.1186/1748-5908-8-139 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Abdullah F, Su TT. Enhancement of the cervical cancer screening program in Malaysia: a qualitative study. Asian Pac J Cancer Prev. 2010;11(5):1359–66. . [PubMed] [Google Scholar]
  • 25.Abdullah NN, Daud S, Wang SM, Mahmud Z, Mohd Kornain NK, Al-Kubaisy W. Human Papilloma Virus (HPV) self-sampling: do women accept it? J Obstet Gynaecol. 2018;38(3):402–7. doi: 10.1080/01443615.2017.1379061 . [DOI] [PubMed] [Google Scholar]
  • 26.Abu SH, Woldehanna BT, Nida ET, Tilahun AW, Gebremariam MY, Sisay MM. The role of health education on cervical cancer screening uptake at selected health centers in Addis Ababa. PLoS ONE [Electronic Resource]. 2020;15(10):e0239580. doi: 10.1371/journal.pone.0239580 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Abuadas FH, Petro-Nustas WJ, Abuadas MH. The Effect of a Health Education Intervention on Jordanian Participants’ Colorectal Cancer Knowledge, Health Perceptions, and Screening Practices. Cancer Nurs. 2018;41(3):226–37. doi: 10.1097/NCC.0000000000000480 . [DOI] [PubMed] [Google Scholar]
  • 28.Abuelo CE, Levinson KL, Salmeron J, Sologuren CV, Fernandez MJ, Belinson JL. The Peru Cervical Cancer Screening Study (PERCAPS): the design and implementation of a mother/daughter screen, treat, and vaccinate program in the Peruvian jungle. J Community Health. 2014;39(3):409–15. doi: 10.1007/s10900-013-9786-6 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Adefuye PO, Dada OA, Adefuye BO, Shorunmu TO, Akinyemi BO, Idowu-Ajiboye BO. Feasibility, acceptability, and effectiveness of visual inspection of the cervix with acetic acid and cryotherapy for dysplasia in Nigeria. Int J Gynaecol Obstet. 2015;129(1):62–6. doi: 10.1016/j.ijgo.2014.10.032 . [DOI] [PubMed] [Google Scholar]
  • 30.Adsul P, Srinivas V, Gowda S, Nayaka S, Pramathesh R, Chandrappa K, et al. A community-based, cross-sectional study of hrHPV DNA self-sampling-based cervical cancer screening in rural Karnataka, India. Int J Gynaecol Obstet. 2019;146(2):170–6. doi: 10.1002/ijgo.12859 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Ajay VS, Jindal D, Roy A, Venugopal V, Sharma R, Pawar A, et al. Development of a Smartphone-Enabled Hypertension and Diabetes Mellitus Management Package to Facilitate Evidence-Based Care Delivery in Primary Healthcare Facilities in India: The mPower Heart Project. J Am Heart Assoc. 2016;5(12). doi: 10.1161/JAHA.116.004343 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Alexander T, Mullasari AS, Joseph G, Kannan K, Veerasekar G, Victor SM, et al. A system of care for patients with ST-segment elevation myocardial infarction in India: The Tamil Nadu-ST-segment elevation myocardial infarction program. JAMA Cardiol. 2017;2(5):498–505. doi: 10.1001/jamacardio.2016.5977 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Alfaro K, Maza M, Felix JC, Gage JC, Castle PE, Alonzo TA, et al. Outcomes for Step-Wise Implementation of a Human Papillomavirus Testing-Based Cervical Screen-and-Treat Program in El Salvador. JCO Glob Oncol. 2020;6:1519–30. doi: 10.1200/GO.20.00206 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Allende G, Surriabre P, Caceres L, Bellot D, Ovando N, Torrico A, et al. Evaluation of the self-sampling for cervical cancer screening in Bolivia. BMC Public Health. 2019;19(1):80. doi: 10.1186/s12889-019-6401-5 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Allerton J, Mash R. The impact of intensified clinical care on glycaemic control in patients with type 2 diabetes at Khayelitsha Community Health Centre, South Africa: Quasi-experimental study. Prim Care Diabetes. 2020;14(2):97–103. doi: 10.1016/j.pcd.2019.08.006 . [DOI] [PubMed] [Google Scholar]
  • 36.Amir Khan M, Ahmar Khan M, Walley JD, Khan N, Imtiaz Sheikh F, Ali S, et al. Feasibility of delivering integrated COPD-asthma care at primary and secondary level public healthcare facilities in Pakistan: a process evaluation. BJGP Open. 2019;3(1):bjgpopen18X101632. doi: 10.3399/bjgpopen18X101632 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Arief M, Harika B, Nilugal K, Syed IA. Clinical pharmacist interventions in managing cardiovascular risk factors. Int J Pharm Sci Rev Res. 2015;35(1):63–6. [Google Scholar]
  • 38.Arrossi S, Thouyaret L, Herrero R, Campanera A, Magdaleno A, Cuberli M, et al. Effect of self-collection of HPV DNA offered by community health workers at home visits on uptake of screening for cervical cancer (the EMA study): a population-based cluster-randomised trial. Lancet Glob Health. 2015;3(2):e85–94. doi: 10.1016/S2214-109X(14)70354-7 . [DOI] [PubMed] [Google Scholar]
  • 39.Asgary R, Adongo PB, Nwameme A, Cole HV, Maya E, Liu M, et al. mHealth to Train Community Health Nurses in Visual Inspection With Acetic Acid for Cervical Cancer Screening in Ghana. J Low Genit Tract Dis. 2016;20(3):239–42. doi: 10.1097/LGT.0000000000000207 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Austad K, Chary A, Xocop SM, Messmer S, King N, Carlson L, et al. Barriers to Cervical Cancer Screening and the Cervical Cancer Care Continuum in Rural Guatemala: A Mixed-Method Analysis. J Glob Oncol. 2018;4:1–10. doi: 10.1200/JGO.17.00228 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.Awolude OA, Oyerinde SO, Akinyemi JO. Screen and triage to facilitate screen and treat by community health extension workers: Task-sharing strategy to achieve universal cervical cancer screening in Nigeria. J Glob Oncol. 2018;4(Supplement 1):14S. doi: 10.1200/JGO.18.00023 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42.Aye LL, Tripathy JP, Maung Maung T, Oo MM, Nwe ML, Thu HMM, et al. Experiences from the pilot implementation of the Package of Essential Non-communicable Disease Interventions (PEN) in Myanmar, 2017–18: A mixed methods study. PLoS ONE [Electronic Resource]. 2020;15(2):e0229081. doi: 10.1371/journal.pone.0229081 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43.Aziz Z, Mathews E, Absetz P, Sathish T, Oldroyd J, Balachandran S, et al. A group-based lifestyle intervention for diabetes prevention in low- and middle-income country: implementation evaluation of the Kerala Diabetes Prevention Program. Implement Sc. 2018;13(1):97. doi: 10.1186/s13012-018-0791-0 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.Balagopal P, Kamalamma N, Patel TG, Misra R. A community-based diabetes prevention and management education program in a rural village in India. Diabetes Care. 2008;31(6):1097–104. doi: 10.2337/dc07-1680 . [DOI] [PubMed] [Google Scholar]
  • 45.Bansil P, Wittet S, Lim JL, Winkler JL, Paul P, Jeronimo J. Acceptability of self-collection sampling for HPV-DNA testing in low-resource settings: a mixed methods approach. BMC Public Health. 2014;14:596. doi: 10.1186/1471-2458-14-596 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 46.Bao HL, Zhao ZP, Zhang M, Wang LM, Cong S, Fang LW, et al. [The impact of five-year Chinese rural area cervical cancer screening program on screening rate]. Chung-Hua Yu Fang i Hsueh Tsa Chih [Chinese Journal of Prev Med]. 2018;52(3):260–4. doi: 10.3760/cma.j.issn.0253-9624.2018.03.008 . [DOI] [PubMed] [Google Scholar]
  • 47.Barasheh N, Shakerinejad G, Nouhjah S, Haghighizadeh MH. The effect of educational program based on the precede-proceed model on improving self-care behaviors in a semi-urban population with type 2 diabetes referred to health centers of Bavi, Iran. Diabetes Metab Syndr. 2017;11(Supplement 2):S759–S65. [DOI] [PubMed] [Google Scholar]
  • 48.Barfar E, Rashidian A, Hosseini H, Nosratnejad S, Barooti E, Zendehdel K. Cost-effectiveness of mammography screening for breast cancer in a low socioeconomic group of Iranian women. Arch Iran Med. 2014;17(4):241–5. . [PubMed] [Google Scholar]
  • 49.Berner A, Hassel SB, Tebeu PM, Untiet S, Kengne-Fosso G, Navarria I, et al. Human papillomavirus self-sampling in Cameroon: women’s uncertainties over the reliability of the method are barriers to acceptance. J Low Genit Tract Dis. 2013;17(3):235–41. doi: 10.1097/LGT.0b013e31826b7b51 . [DOI] [PubMed] [Google Scholar]
  • 50.Bernstein M, Hari A, Aggarwal S, Lee D, Farfel A, Patel P, et al. Implementation of a human papillomavirus screen-and-treat model in Mwanza, Tanzania: training local healthcare workers for sustainable impact. Int Health. 2018;10(3):197–201. doi: 10.1093/inthealth/ihy014 . [DOI] [PubMed] [Google Scholar]
  • 51.Bhatt S, Isaac R, Finkel M, Evans J, Grant L, Paul B, et al. Mobile technology and cancer screening: Lessons from rural India. J Glob Health. 2018;8(2):020421. doi: 10.7189/jogh.08.020421 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 52.Blumenthal PD, Gaffikin L, Deganus S, Lewis R, Emerson M, Adadevoh S, et al. Cervical cancer prevention: safety, acceptability, and feasibility of a single-visit approach in Accra, Ghana. Am J Obstet Gynecol. 2007;196(4):407.e1–8; discussion. e8. doi: 10.1016/j.ajog.2006.12.031 . [DOI] [PubMed] [Google Scholar]
  • 53.Botha MH, Van Der Merwe FH, Snyman L, Dreyer G. The vaccine and cervical cancer screen (VACCS) project-acceptance of human papilloma virus vaccination in a school based program. Int J Gynecol Cancer. 2014;24(9):821. .26046162 [Google Scholar]
  • 54.Bouchlaka A, Ben Abdallah M, Ben Aissa R, Smida S, Ouechtati A, Boussen H, et al. [Practice of large scale mammography in the Ariana area of Tunisia: prelude to a mass screening?]. Tunis Med. 2009;87(7):426–31. . [PubMed] [Google Scholar]
  • 55.Broquet C, Triboullier D, Untiet S, Schafer S, Petignat P, Vassilakos P. Acceptability of self-collected vaginal samples for HPV testing in an urban and rural population of Madagascar. Afr Health Sci. 2015;15(3):755–61. doi: 10.4314/ahs.v15i3.8 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 56.Busingye P, Nakimuli A, Nabunya E, Mutyaba T. Acceptability of cervical cancer screening via visual inspection with acetic acid or Lugol’s iodine at Mulago Hospital, Uganda. Int J Gynaecol Obstet. 2012;119(3):262–5. doi: 10.1016/j.ijgo.2012.06.015 . [DOI] [PubMed] [Google Scholar]
  • 57.Cai SR, Zhu HH, Huang YQ, Li QL, Ma XY, Zhang SZ, et al. Cost-Effectiveness between Double and Single Fecal Immunochemical Test(s) in a Mass Colorectal Cancer Screening. Biomed Res Int. 2016;2016:6830713. doi: 10.1155/2016/6830713 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 58.Campbell C, Kafwafwa S, Brown H, Walker G, Madetsa B, Deeny M, et al. Use of thermo-coagulation as an alternative treatment modality in a ‘screen-and-treat’ programme of cervical screening in rural Malawi. Int J Cancer. 2016;139(4):908–15. doi: 10.1002/ijc.30101 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 59.Chalapati W, Chumworathayi B. Can a home-visit invitation increase Pap smear screening in Samliem, Khon Kaen, Thailand? Asian Pac J Cancer Prev. 2007;8(1):119–23. . [PubMed] [Google Scholar]
  • 60.Chariwala RA, Shukla R, Gajiwala UR, Gilbert C, Pant H, Lewis MG, et al. Effectiveness of health education and monetary incentive on uptake of diabetic retinopathy screening at a community health center in South Gujarat, India. Indian J Ophthalmol. 2020;68(Suppl 1):S52–S5. doi: 10.4103/ijo.IJO_2118_19 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 61.Chary AN, Rohloff PJ. Major challenges to scale up of visual inspection-based cervical cancer prevention programs: the experience of Guatemalan NGOs. Glob Health Sci Pract. 2014;2(3):307–17. doi: 10.9745/GHSP-D-14-00073 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 62.Chigbu C, Onyebuchi A, Onyeka T, Odugu B, Dim C. Impact of community health educators on uptake of cervical/ breast cancer prevention services. Int J Gynaecol Obstet. 2018;143(Supplement 3):443. . [DOI] [PubMed] [Google Scholar]
  • 63.Chinula L, Mapanje C, Varela A, Chapola J, Limarzi L, Bulla A, et al. Uptake of a community-based screen-and-treat cervical cancer prevention strategy in rural malawi. Int J Gynaecol Obstet. 2018;143(Supplement 3):456. .33687746 [Google Scholar]
  • 64.Chong HY, Roslani AC, Law CW. Colonoscopic prioritization in colorectal carcinoma screening using quantitative immunochemical faecal occult blood test: a pilot study. Med J Malaysia. 2013;68(1):30–3. . [PubMed] [Google Scholar]
  • 65.Chumworathayi B, Yuenyao P, Luanratanakorn S, Pattamadilok J, Chalapati W, Na-Nhongkai C. Can an appointment-letter intervention increase pap smear screening in Samliem, Khon Kaen, Thailand? Asian Pac J Cancer Prev. 2007;8(3):353–6. . [PubMed] [Google Scholar]
  • 66.Chutinet A, Keosodsay S, Vorasayan P, Samajarn J, Akarathanawat W, Kijpaisalratana N, et al. The First 10 Thrombolysis for Acute Ischemic Stroke in Lao People’s Democratic Republic under Teleconsultation from Thailand. J Stroke Cerebrovasc Dis. 2019;28(11):104327. doi: 10.1016/j.jstrokecerebrovasdis.2019.104327 . [DOI] [PubMed] [Google Scholar]
  • 67.Crofts V, Flahault E, Tebeu PM, Untiet S, Fosso GK, Boulvain M, et al. Education efforts may contribute to wider acceptance of human papillomavirus self-sampling. Int J Womens Health. 2015;7:149–54. doi: 10.2147/IJWH.S56307 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 68.Dandge S, Jeemon P, Reddy PS. Technology enabled non-physician health workers extending telemedicine to rural homes to control hypertension and diabetes (TETRA): A pre-post demonstration project in Telangana, India. PLoS ONE. 2019;14(2). doi: 10.1371/journal.pone.0211551 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 69.de Villiers A, Steyn NP, Draper CE, Hill J, Dalais L, Fourie J, et al. Implementation of the HealthKick intervention in primary schools in low-income settings in the Western Cape Province, South Africa: a process evaluation. BMC Public Health. 2015;15:818. doi: 10.1186/s12889-015-2157-8 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 70.Do TNP, Do QH, Cowie MR, Ha NB, Do VD, Do TH, et al. Effect of the Optimize Heart Failure Care Program on clinical and patient outcomes—The pilot implementation in Vietnam. Int J Cardiol Heart Vasc. 2019;22:169–73. doi: 10.1016/j.ijcha.2019.02.010 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 71.Dorje T, Zhao G, Tso K, Wang J, Chen Y, Tsokey L, et al. Smartphone and social media-based cardiac rehabilitation and secondary prevention in China (SMART-CR/SP): a parallel-group, single-blind, randomised controlled trial. Lancet Digit Health. 2019;1(7):e363–e74. doi: 10.1016/S2589-7500(19)30151-7 . [DOI] [PubMed] [Google Scholar]
  • 72.Dorji T, Tshomo U, Phuntsho S, Tamang TD, Tshokey T, Baussano I, et al. Introduction of a National HPV vaccination program into Bhutan. Vaccine. 2015;33(31):3726–30. doi: 10.1016/j.vaccine.2015.05.078 . [DOI] [PubMed] [Google Scholar]
  • 73.Elnaem MH, Nik Mohamed MH, Huri HZ. Pharmacist-led academic detailing improves statin therapy prescribing for Malaysian patients with type 2 diabetes: Quasi-experimental design. PLoS ONE [Electronic Resource]. 2019;14(9):e0220458. doi: 10.1371/journal.pone.0220458 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 74.Erwin E, Aronson KJ, Day A, Ginsburg O, Macheku G, Feksi A, et al. SMS behaviour change communication and eVoucher interventions to increase uptake of cervical cancer screening in the Kilimanjaro and Arusha regions of Tanzania: a randomised, double-blind, controlled trial of effectiveness. BMJ Innov. 2019;5(1):28–34. doi: 10.1136/bmjinnov-2018-000276 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 75.Escosteguy CC, Teixeira AB, Portela MC, Guimaraes AE, Lima SM, Ferreira VM, et al. Implementing clinical guidelines on acute myocardial infarction care in an emergency service. Arq Bras Cardiol. 2011;96(1):18–25. doi: 10.1590/s0066-782x2010005000142 . [DOI] [PubMed] [Google Scholar]
  • 76.Fall NS, Tamalet C, Diagne N, Fenollar F, Raoult D, Sokhna C, et al. Feasibility, Acceptability, and Accuracy of Vaginal Self-Sampling for Screening Human Papillomavirus Types in Women from Rural Areas in Senegal. Am J Trop Med Hyg. 2019;100(6):1552–5. doi: 10.4269/ajtmh.19-0045 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 77.Fallala MS, Mash R. Cervical cancer screening: Safety, acceptability, and feasibility of a single-visit approach in Bulawayo, Zimbabwe. Afr J Prim Health Care Fam Med. 2015;7(1):05. doi: 10.4102/phcfm.v7i1.742 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 78.Flor LS, Wilson S, Bhatt P, Bryant M, Burnett A, Camarda JN, et al. Community-based interventions for detection and management of diabetes and hypertension in underserved communities: a mixed-methods evaluation in Brazil, India, South Africa and the USA. BMJ Glob Health. 2020;5(6):06. doi: 10.1136/bmjgh-2019-001959 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 79.Fokom Domgue J, Futuh B, Ngalla C, Kakute P, Manjuh F, Manga S, et al. Feasibility of a community-based cervical cancer screening with “test and treat” strategy using self-sample for an HPV test: Experience from rural Cameroon, Africa. Int J Cancer. 2020;147(1):128–38. doi: 10.1002/ijc.32746 . [DOI] [PubMed] [Google Scholar]
  • 80.Fong J, Gyaneshwar R, Lin S, Morrell S, Taylor R, Brassil A, et al. Cervical screening using visual inspection with acetic acid (VIA) and treatment with cryotherapy in Fiji. Asian Pac J Cancer Prev. 2014;15(24):10757–62. doi: 10.7314/apjcp.2014.15.24.10757 . [DOI] [PubMed] [Google Scholar]
  • 81.Fort MP, Murillo S, Lopez E, Dengo AL, Alvarado-Molina N, de Beausset I, et al. Impact evaluation of a healthy lifestyle intervention to reduce cardiovascular disease risk in health centers in San Jose, Costa Rica and Chiapas, Mexico. BMC Health Serv Res. 2015;15:577. doi: 10.1186/s12913-015-1248-7 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 82.Gagliardino JJ, Etchegoyen G, Pendid-La Research G. A model educational program for people with type 2 diabetes: a cooperative Latin American implementation study (PEDNID-LA). Diabetes Care. 2001;24(6):1001–7. doi: 10.2337/diacare.24.6.1001 . [DOI] [PubMed] [Google Scholar]
  • 83.Geng W, Tian X, Fu X, Wang P, Wang Y, Wang X, et al. Early routine angioplasty versus selective angioplasty after successful thrombolysis in acute ST-segment elevation myocardial infarction. Coron Artery Dis. 2013;24(3):238–43. doi: 10.1097/MCA.0b013e32835e5c67 . [DOI] [PubMed] [Google Scholar]
  • 84.Ghosh K, Segura A, Crispen C, Montz FJ. Use of the ‘see and treat’ technique for the management of high-risk abnormal Pap smears in a Third World country. Int J Gynecol Cancer. 1997;7(2):144–50. [Google Scholar]
  • 85.Gottschlich A, Rivera-Andrade A, Grajeda E, Alvarez C, Mendoza Montano C, Meza R. Acceptability of Human Papillomavirus Self-Sampling for Cervical Cancer Screening in an Indigenous Community in Guatemala. J Glob Oncol. 2017;3(5):444–54. doi: 10.1200/JGO.2016.005629 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 86.Greenwald ZR, Fregnani JH, Longatto-Filho A, Watanabe A, Mattos JSC, Vazquez FL, et al. The performance of mobile screening units in a breast cancer screening program in Brazil. Cancer Causes Control. 2018;29(2):233–41. doi: 10.1007/s10552-017-0995-7 . [DOI] [PubMed] [Google Scholar]
  • 87.Gulayin PE, Lozada A, Beratarrechea A, Gutierrez L, Poggio R, Chaparro RM, et al. An Educational Intervention to Improve Statin Use: Cluster RCT at the Primary Care Level in Argentina. Am J Prev Med. 2019;57(1):95–105. doi: 10.1016/j.amepre.2019.02.018 . [DOI] [PubMed] [Google Scholar]
  • 88.Gurav SK, Zirpe KG, Wadia RS, Naniwadekar A, Pote PU, Tungenwar A, et al. Impact of “Stroke Code”-Rapid Response Team: An Attempt to Improve Intravenous Thrombolysis Rate and to Shorten Door-to-Needle Time in Acute Ischemic Stroke. Indian J Crit Care Med. 2018;22(4):243–8. doi: 10.4103/ijccm.IJCCM_504_17 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 89.Haikel RL, Mauad EC, Silva TB, Mattos J, Chala LF, Longatto-Filho A, et al. Mammography-based screening program: Preliminary results from a first 2-year round in a Brazilian region using mobile and fixed units. BMC Womens Health. 2012;12(no pagination). . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 90.Hasandokht T, Farajzadegan Z, Siadat ZD, Paknahad Z, Rajati F. Lifestyle interventions for hypertension treatment among Iranian women in primary health-care settings: Results of a randomized controlled trial. J Res Med Sci. 2015;20(1):54–61. . [PMC free article] [PubMed] [Google Scholar]
  • 91.Hassan ZM. Mobile phone text messaging to improve knowledge and practice of diabetic foot care in a developing country: Feasibility and outcomes. Int J Nurs Pract. 2017;23(1). doi: 10.1111/ijn.12546 . [DOI] [PubMed] [Google Scholar]
  • 92.He M, Wang J, Gong L, Dong Q, Ji N, Xing H, et al. Community-based stroke system of care for Chinese rural areas. Stroke. 2014;45(8):2385–90. doi: 10.1161/STROKEAHA.114.006030 . [DOI] [PubMed] [Google Scholar]
  • 93.Hebert K, Quevedo HC, Gogichaishvili I, Nozadze N, Sagirashvili E, Trahan P, et al. Feasibility of a heart failure disease management program in eastern Europe: Tbilisi, Georgia. Circ Heart Fail. 2011;4(6):763–9. doi: 10.1161/CIRCHEARTFAILURE.111.962431 . [DOI] [PubMed] [Google Scholar]
  • 94.Heydari G, Jianfar G, Alvanpour A, Hesami Z, Talischi F, Masjedi MR. Efficacy of telephone quit-line for smokers in Iran: 12 months follow up results. Tanaffus. 2011;10(3):42–8. . [PMC free article] [PubMed] [Google Scholar]
  • 95.Hua W, Cao S, Cui J, Maberley D, Matsubara J. Analysis of reasons for noncompliance with laser treatment in patients of diabetic retinopathy. Can J Ophthalmol. 2017;52(Suppl 1):S34–S8. doi: 10.1016/j.jcjo.2017.09.025 . [DOI] [PubMed] [Google Scholar]
  • 96.Huang S, Hu X, Chen H, Xie D, Gan X, Wu Y, et al. The positive effect of an intervention program on the hypertension knowledge and lifestyles of rural residents over the age of 35 years in an area of China. Hypertens Res. 2011;34(4):503–8. doi: 10.1038/hr.2010.265 . [DOI] [PubMed] [Google Scholar]
  • 97.Huang X, Liu L, Song Y, Gao L, Zhao M, Bao H, et al. Achieving blood pressure control targets in hypertensive patients of rural China—A pilot randomized trial. Trials. 2020;21(1). doi: 10.1186/s13063-020-04368-1 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 98.Huchko MJ, Ibrahim S, Blat C, Cohen CR, Smith JS, Hiatt RA, et al. Cervical cancer screening through human papillomavirus testing in community health campaigns versus health facilities in rural western Kenya. Int J Gynaecol Obstet. 2018;141(1):63–9. doi: 10.1002/ijgo.12415 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 99.Huchko MJ, Olwanda E, Choi Y, Kahn JG. HPV-based cervical cancer screening in low-resource settings: Maximizing the efficiency of community-based strategies in rural Kenya. Int J Gynaecol Obstet. 2020;148(3):386–91. doi: 10.1002/ijgo.13090 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 100.Ibrahim HO, Stapar D, Mash B. Is screening for microalbuminuria in patients with type 2 diabetes feasible in the Cape Town public sector primary care context? A cost and consequence study. S Afr Fam Pract. 2013;55(4):367–72. [Google Scholar]
  • 101.Isaac R, Finkel M, Olver I, Annie IK, Prashanth HR, Subhashini J, et al. Translating evidence into practice in low resource settings: cervical cancer screening tests are only part of the solution in rural India. Asian Pac J Cancer Prev. 2012;13(8):4169–72. doi: 10.7314/apjcp.2012.13.8.4169 . [DOI] [PubMed] [Google Scholar]
  • 102.Jafar TH, Silva A, Naheed A, Jehan I, Liang F, Assam PN, et al. Control of blood pressure and risk attenuation: a public health intervention in rural Bangladesh, Pakistan, and Sri Lanka: feasibility trial results. J Hypertens. 2016;34(9):1872–81. doi: 10.1097/HJH.0000000000001014 . [DOI] [PubMed] [Google Scholar]
  • 103.Jahic E. Experience and Outcomes of Primary Percutaneous Coronary Intervention for Patients with ST-Segment Elevation Myocardial Infarction of Tertiary Care Center in Bosnia and Herzegovina. Med Arh. 2017;71(3):183–7. doi: 10.5455/medarh.2017.71.183-187 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 104.Jeyapaul S, Oommen AM, Cherian AG, Marcus TA, Malini T, Prasad JH, et al. Feasibility, uptake and real-life challenges of a rural cervical and breast cancer screening program in Vellore, Tamil Nadu, South India. Indian J Cancer. 2020;02:02. doi: 10.4103/ijc.IJC_271_19 . [DOI] [PubMed] [Google Scholar]
  • 105.Jin H, Qu Y, Guo ZN, Yan XL, Sun X, Yang Y. Impact of Jilin Province Stroke Emergency Maps on Acute Stroke Care Improvement in Northeast China. Front Neurol [electronic resource]. 2020;11:734. doi: 10.3389/fneur.2020.00734 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 106.Joshi R, Agrawal T, Fathima F, Usha T, Thomas T, Misquith D, et al. Cardiovascular risk factor reduction by community health workers in rural India: A cluster randomized trial. Am Heart J. 2019;216:9–19. doi: 10.1016/j.ahj.2019.06.007 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 107.Juan Z, Rongrong J, Juanjuan L, Jinlei L, Xiawen S, Guijuan D, et al. Study on the effectiveness of implementation: The National Demonstration Areas for Comprehensive Prevention and Control of Non-communicable Diseases. [Chinese]. Zhonghua Liu Xing Bing Xue Za Zhi. 2018;39(4):394–400. doi: 10.3760/cma.j.issn.0254-6450.2018.04.002 . [DOI] [PubMed] [Google Scholar]
  • 108.Junling G, Yang L, Junming D, Pinpin Z, Hua F. Evaluation of group visits for Chinese hypertensives based on primary health care center. Asia Pac J Public Health. 2015;27(2):NP350–60. doi: 10.1177/1010539512442566 . [DOI] [PubMed] [Google Scholar]
  • 109.Kamal AK, Khalid W, Muqeet A, Jamil A, Farhat K, Gillani, et al. Making prescriptions “talk” to stroke and heart attack survivors to improve adherence: Results of a randomized clinical trial (The Talking Rx Study). PLoS ONE [Electronic Resource]. 2018;13(12):e0197671. doi: 10.1371/journal.pone.0197671 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 110.Khan N, Walley JD, Khan SE, Hicks J, Sheikh FI, Khan MA, et al. Enhanced hypertension care through private clinics in Pakistan: A cluster randomised trial. BJGP Open. 2019;3(1). doi: 10.3399/bjgpopen18X101617 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 111.Khetan AK, Zullo MZ, Gupta RG, Agarwal SA, Mohan SM, Josephson RJ. Effect of a community health worker based approach to integrated cardiovascular risk factor control in India: A cluster randomized, controlled, parallel-group trial (SEHAT). Eur Heart J. 2018;39(Supplement 1):646–7. [Google Scholar]
  • 112.Khuhaprema T, Sangrajrang S, Lalitwongsa S, Chokvanitphong V, Raunroadroong T, Ratanachu-Ek T, et al. Organised colorectal cancer screening in Lampang Province, Thailand: preliminary results from a pilot implementation programme. BMJ Open. 2014;4(1):e003671. doi: 10.1136/bmjopen-2013-003671 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 113.Klassen SL, Miller RJH, Hao R, Warnica JW, Fine NM, Carpen M, et al. Implementation of a Multidisciplinary Inpatient Cardiology Service to Improve Heart Failure Outcomes in Guyana. J Card Fail. 2018;24(12):835–41. doi: 10.1016/j.cardfail.2018.07.002 . [DOI] [PubMed] [Google Scholar]
  • 114.Ku GM, Kegels G. Effects of the First Line Diabetes Care (FiLDCare) self-management education and support project on knowledge, attitudes, perceptions, self-management practices and glycaemic control: a quasi-experimental study conducted in the Northern Philippines. BMJ Open. 2014;4(8):e005317. doi: 10.1136/bmjopen-2014-005317 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 115.Kundury KK, Hathur B. Intervention through Short Messaging System (SMS) and phone call alerts reduced HbA1C levels in ~47% type-2 diabetics-results of a pilot study. PLoS ONE [Electronic Resource]. 2020;15(11):e0241830. doi: 10.1371/journal.pone.0241830 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 116.Kurt G, Akyuz A. Evaluating the Effectiveness of Interventions on Increasing Participation in Cervical Cancer Screening. J Nurs Res. 2019;27(5):e40. doi: 10.1097/jnr.0000000000000317 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 117.Kushwaha S, Talwar P, Chandel N, Anthony A, Maheshwari S, Khurana S. Saving the brain initiative—Developing an effective hub-and-spoke model to improve the acute stroke management pathways in urban India. J Neurol Sci. 2018;393:83–7. doi: 10.1016/j.jns.2018.08.012 . [DOI] [PubMed] [Google Scholar]
  • 118.Laatikainen T, Inglin L, Collins D, Ciobanu A, Curocichin G, Salaru V, et al. Implementing Package of Essential Non-communicable Disease Interventions in the Republic of Moldova-a feasibility study. Eur J Public Health. 2020;16. doi: 10.1093/eurpub/ckaa037 . [DOI] [PubMed] [Google Scholar]
  • 119.Latina J, Fernandez-Jimenez R, Bansilal S, Sartori S, Vedanthan R, Lewis M, et al. Grenada Heart Project-Community Health ActioN to EncouraGe healthy BEhaviors (GHP-CHANGE): A randomized control peer group-based lifestyle intervention. Am Heart J. 2020;220:20–8. doi: 10.1016/j.ahj.2019.08.022 . [DOI] [PubMed] [Google Scholar]
  • 120.Lee H, Mtengezo JT, Kim D, Makin MS, Kang Y, Malata A, et al. Exploring Complicity of Cervical Cancer Screening in Malawi: The Interplay of Behavioral, Cultural, and Societal Influences. Asia Pac J Oncol Nurs. 2020;7(1):18–27. doi: 10.4103/apjon.apjon_48_19 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 121.Legood R, Gray AM, Mahe C, Wolstenholme J, Jayant K, Nene BM, et al. Screening for cervical cancer in India: How much will it cost? A trial based analysis of the cost per case detected. Int J Cancer. 2005;117(6):981–7. doi: 10.1002/ijc.21220 . [DOI] [PubMed] [Google Scholar]
  • 122.Levinson KL, Abuelo C, Chyung E, Salmeron J, Belinson SE, Sologuren CV, et al. The Peru cervical cancer prevention study (PERCAPS): community-based participatory research in Manchay, Peru. Int J Gynecol Cancer. 2013;23(1):141–7. doi: 10.1097/IGC.0b013e318275b007 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 123.Levinson KL, Abuelo C, Salmeron J, Chyung E, Zou J, Belinson SE, et al. The Peru Cervical Cancer Prevention Study (PERCAPS): the technology to make screening accessible. Gynecol Oncol. 2013;129(2):318–23. doi: 10.1016/j.ygyno.2013.01.026 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 124.Li M, Nyabigambo A, Navvuga P, Nuwamanya E, Nuwasiima A, Kaganda P, et al. Acceptability of cervical cancer screening using visual inspection among women attending a childhood immunization clinic in Uganda. Papillomavirus Res. 2017;4:17–21. doi: 10.1016/j.pvr.2017.06.004 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 125.Lidofsky A, Miller A, Jorgensen J, Tajik A, Tendeu K, Pius D, et al. Development and Implementation of a Culturally Appropriate Education Program to Increase Cervical Cancer Screening among Maasai Women in Rural Tanzania. Ann Glob Health. 2019;85(1):127. doi: 10.5334/aogh.2503 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 126.Lieber M, Afzal O, Shaia K, Mandelberger A, Du Preez C, Beddoe AM. Cervical Cancer Screening in HIV-Positive Farmers in South Africa: Mixed-Method Assessment. Ann Glob Health. 2019;85(1):15. doi: 10.5334/aogh.37 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 127.Liebermann EJ, VanDevanter N, Shirazian T, Frias Guzman N, Niles M, Healton C, et al. Barriers to Cervical Cancer Screening and Treatment in the Dominican Republic: Perspectives of Focus Group Participants in the Santo Domingo Area. J Transcult Nurs. 2020;31(2):121–7. doi: 10.1177/1043659619846247 . [DOI] [PubMed] [Google Scholar]
  • 128.Lima ST, da Silva Nalin de Souza B, Franca AK, Salgado Filho N, Sichieri R. Dietary approach to hypertension based on low glycaemic index and principles of DASH (Dietary Approaches to Stop Hypertension): a randomised trial in a primary care service. Br J Nutr. 2013;110(8):1472–9. doi: 10.1017/S0007114513000718 . [DOI] [PubMed] [Google Scholar]
  • 129.Lin G, Feng Z, Liu H, Li Y, Nie Y, Liang Y, et al. Mass screening for colorectal cancer in a population of two million older adults in Guangzhou, China. Sci Rep. 2019;9(1):10424. doi: 10.1038/s41598-019-46670-2 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 130.Linde DS, Andersen MS, Mwaiselage J, Manongi R, Kjaer SK, Rasch V. Effectiveness of One-Way Text Messaging on Attendance to Follow-Up Cervical Cancer Screening Among Human Papillomavirus-Positive Tanzanian Women (Connected2Care): Parallel-Group Randomized Controlled Trial. J Med Internet Res. 2020;22(4):e15863. doi: 10.2196/15863 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 131.Liyanage IK, Wickramasinghe K, Katulanda P, Jayawardena R, Karunathilake I, Friel S, et al. Integrating the development agenda with noncommunicable disease prevention in developing countries: A quasi-experimental study on inter-sectoral action and its impact on self-reported salt consumption-the INPARD study. Cardiovasc Diagn Ther. 2019;9(2):120–8. doi: 10.21037/cdt.2018.10.19 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 132.Lizbeth NCF, Cristina CAL, Jessica ZC, Eduardo TOL, de Dios ALJ, Leticia CSM. Individualized nutritional and pharmaceutical therapy consultation as a new strategy for the management of chronic diseases in actopan, Hidalgo. Int Res J Pharm. 2019;10(12):37–44. [Google Scholar]
  • 133.Luo JG, Han L, Chen LW, Gao Y, Ding XJ, Li Y, et al. Effect of Intensive Personalized “5As+5Rs” Intervention on Smoking Cessation in Hospitalized Acute Coronary Syndrome Patients Not Ready to Quit Immediately: A Randomized Controlled Trial. Nicotine Tob Res. 2018;20(5):596–605. doi: 10.1093/ntr/ntx126 . [DOI] [PubMed] [Google Scholar]
  • 134.Lynch A, Sobuwa S, Castle N. Barriers to the implementation of prehospital thrombolysis in the treatment of ST-segment elevation myocardial infarction in South Africa: An exploratory inquiry. Afr J Emerg Med. 2020. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 135.Ma GX, Yin L, Gao W, Tan Y, Liu R, Fang C, et al. Workplace-based breast cancer screening intervention in China. Cancer Epidemiol Biomarkers Prev. 2012;21(2):358–67. doi: 10.1158/1055-9965.EPI-11-0915 . [DOI] [PubMed] [Google Scholar]
  • 136.Marino BCA, Ribeiro ALP, Alkmim MB, Antunes AP, Boersma E, Marcolino MS. Coordinated regional care of myocardial infarction in a rural area in Brazil: Minas Telecardio Project 2. Eur Heart J Qual Care Clin Outcomes. 2016;2(3):215–24. doi: 10.1093/ehjqcco/qcw020 . [DOI] [PubMed] [Google Scholar]
  • 137.Martin CE, Tergas AI, Wysong M, Reinsel M, Estep D, Varallo J. Evaluation of a single-visit approach to cervical cancer screening and treatment in Guyana: feasibility, effectiveness and lessons learned. J Obstet Gynaecol Res. 2014;40(6):1707–16. doi: 10.1111/jog.12366 . [DOI] [PubMed] [Google Scholar]
  • 138.Mash B, Powell D, du Plessis F, van Vuuren U, Michalowska M, Levitt N. Screening for diabetic retinopathy in primary care with a mobile fundal camera—evaluation of a South African pilot project. S Afr Med J. 2007;97(12):1284–8. . [PubMed] [Google Scholar]
  • 139.Matenge TG, Mash B. Barriers to accessing cervical cancer screening among HIV positive women in Kgatleng district, Botswana: A qualitative study. PLoS ONE [Electronic Resource]. 2018;13(10):e0205425. doi: 10.1371/journal.pone.0205425 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 140.Mathers LJ, Wigton TR, Leonhardt JG. Screening for cervical neoplasia in an unselected rural Guatemalan population using direct visual inspection after acetic acid application: a pilot study. J Low Genit Tract Dis. 2005;9(4):232–5. doi: 10.1097/01.lgt.0000179864.59951.91 . [DOI] [PubMed] [Google Scholar]
  • 141.Mauad EC, Nicolau SM, Moreira LF, Haikel RL Jr., Longatto-Filho A, Baracat EC. Adherence to cervical and breast cancer programs is crucial to improving screening performance. Rural Remote Health. 2009;9(3):1241. . [PubMed] [Google Scholar]
  • 142.Maza M, Melendez M, Masch R, Alfaro K, Chacon A, Gonzalez E, et al. Acceptability of self-sampling and human papillomavirus testing among non-attenders of cervical cancer screening programs in El Salvador. Prev Med. 2018;114:149–55. doi: 10.1016/j.ypmed.2018.06.017 . [DOI] [PubMed] [Google Scholar]
  • 143.Megevand E, Van Wyk W, Knight B, Bloch B. Can cervical cancer be prevented by a see, screen, and treat program? A pilot study. Am J Obstet Gynecol. 1996;174(3):923–8. doi: 10.1016/s0002-9378(96)70327-7 . [DOI] [PubMed] [Google Scholar]
  • 144.Mehndiratta A, Mishra SC, Bhandarkar P, Chhatbar K, Cluzeau F, PrimaryCareDoctors T. Increasing identification of foot at risk of complications in patients with diabetes: a quality improvement project in an urban primary health centre in India. BMJ Open Qual. 2020;9(3):08. doi: 10.1136/bmjoq-2019-000893 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 145.Memon S, Ahsan S, Alvi R, Fawwad A, Basit A, Shera S, et al. Retinal Screening Acceptance, Laser Treatment Uptake and Follow-up Response in Diabetics Requiring Laser Therapy in an Urban Diabetes Care Centre. J Coll Physicians Surg Pak. 2015;25(10):743–6. doi: 10.2015/JCPSP.743746 . [DOI] [PubMed] [Google Scholar]
  • 146.Mendoza Montano C, Fort M, deRamirez M, Cruz J, Ramirez-Zea M. Evaluation of a pilot hypertension management programme for Guatemalan adults. Health Promot Int. 2016;31(2):363–74. doi: 10.1093/heapro/dau117 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 147.Meng W, Bi XW, Bai XY, Pan HF, Cai SR, Zhao Q, et al. Barrier-focused intervention to increase colonoscopy attendance among nonadherent high-risk populations. World J Gastroenterol. 2009;15(31):3920–5. doi: 10.3748/wjg.15.3920 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 148.Mishra SI, Bastani R, Crespi CM, Chang LC, Luce PH, Baquet CR. Results of a randomized trial to increase mammogram usage among Samoan women. Cancer Epidemiol Biomarkers Prev. 2007;16(12):2594–604. doi: 10.1158/1055-9965.EPI-07-0148 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 149.Mittal S, Mandal R, Banerjee D, Das P, Ghosh I, Panda C, et al. HPV detection-based cervical cancer screening program in low-resource setting: lessons learnt from a community-based demonstration project in India. Cancer Causes Control. 2016;27(3):351–8. doi: 10.1007/s10552-015-0708-z . [DOI] [PubMed] [Google Scholar]
  • 150.Modibbo F, Iregbu KC, Okuma J, Leeman A, Kasius A, de Koning M, et al. Randomized trial evaluating self-sampling for HPV DNA based tests for cervical cancer screening in Nigeria. Infect Agent Cancer [Electronic Resource]. 2017;12:11. doi: 10.1186/s13027-017-0123-z . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 151.Moon TD, Silva-Matos C, Cordoso A, Baptista AJ, Sidat M, Vermund SH. Implementation of cervical cancer screening using visual inspection with acetic acid in rural Mozambique: successes and challenges using HIV care and treatment programme investments in Zambezia Province. J Int AIDS Soc. 2012;15(2):17406. doi: 10.7448/IAS.15.2.17406 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 152.Moreira J, Figueroa MM, Anselmi M, Prandi R, Montano CC, Bell D, et al. Long-Term Outcomes of a Cohort of Hypertensive Subjects in Rural Ecuador. Glob Heart. 2019;14(4):373–8. doi: 10.1016/j.gheart.2019.09.001 . [DOI] [PubMed] [Google Scholar]
  • 153.Morrison J, Akter K, Jennings HM, Nahar T, Kuddus A, Shaha SK, et al. Participatory learning and action to address type 2 diabetes in rural Bangladesh: a qualitative process evaluation. BMC Endocr Disord. 2019;19(1):118. doi: 10.1186/s12902-019-0447-3 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 154.Muffih TP, Claudettea C, Manjuha F, DeGregoriob G, Mangaa S, Nulaha K, et al. Implementing a fee-for-service cervical cancer screening and treatment program in cameroon: Challenges and opportunities. J Glob Oncol. 2018;4(Supplement 2):73s. . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 155.Murthy GVS, Gilbert C, Shukla R, Bala V, Anirudh GG, Mukpalkar S, et al. Overview and project highlights of an initiative to integrate diabetic retinopathy screening and management in the public health system in India. Indian J Ophthalmol. 2020;68(Suppl 1):S12–S5. doi: 10.4103/ijo.IJO_1964_19 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 156.Nakalembe M, Makanga P, Kambugu A, Laker-Oketta M, Huchko MJ, Martin J. A public health approach to cervical cancer screening in Africa through community-based self-administered HPV testing and mobile treatment provision. Cancer Med. 2020;9(22):8701–12. doi: 10.1002/cam4.3468 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 157.Ndikom CM, Ofi BA, Omokhodion FO, Adedokun BO. Effects of educational intervention on women’s knowledge and uptake of cervical cancer screening in selected hospitals in Ibadan, Nigeria. Int J Health Promot Educ. 2017;55(5–6):259–71. [Google Scholar]
  • 158.Ng N, Nichter M, Padmawati RS, Prabandari YS, Muramoto M, Nichter M. Bringing smoking cessation to diabetes clinics in Indonesia. Chronic Illn. 2010;6(2):125–35. doi: 10.1177/1742395310364253 . [DOI] [PubMed] [Google Scholar]
  • 159.Ngichabe SK, Muthaura PN, Murungi C, Muyoka J, Omenge E, Muchiri L. Cryotherapy Following Visual Inspection with Acetic Acid and Lugol’s Iodine (Via/Vili) in Khwisero, Western Kenya: Lesson from the Field Affecting Policy and Practice. East Afr Med J. 2013;90(10):316–23. . [PubMed] [Google Scholar]
  • 160.Nguyen HL, Ha DA, Goldberg RJ, Kiefe CI, Chiriboga G, Ly HN, et al. Culturally adaptive storytelling intervention versus didactic intervention to improve hypertension control in Vietnam- 12 month follow up results: A cluster randomized controlled feasibility trial. PLoS ONE. 2018;13(12). doi: 10.1371/journal.pone.0209912 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 161.Nguyen QN, Pham ST, Nguyen VL, Wall S, Weinehall L, Bonita R, et al. Implementing a hypertension management programme in a rural area: local approaches and experiences from Ba-Vi district, Vietnam. BMC Public Health. 2011;11:325. doi: 10.1186/1471-2458-11-325 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 162.Obioha KC, Dim CC, Ugwu EO, Chigbu CO, Enebe JT, Ozumba BC. Acceptability and outcome of cervical cytology in postnatal women and other nonpregnant women in Enugu, Nigeria: A cross-sectional study. J Clin Diagn Res. 2020;14(4):QC07–QC10. [Google Scholar]
  • 163.Ogilvie GS, Mitchell S, Sekikubo M, Biryabarema C, Byamugisha J, Jeronimo J, et al. Results of a community-based cervical cancer screening pilot project using human papillomavirus self-sampling in Kampala, Uganda. Int J Gynaecol Obstet. 2013;122(2):118–23. doi: 10.1016/j.ijgo.2013.03.019 . [DOI] [PubMed] [Google Scholar]
  • 164.Ogola EN, Okello FO, Herr JL, Macgregor-Skinner E, Mulvaney A, Yonga G. Healthy Heart Africa-Kenya: A 12-Month Prospective Evaluation of Program Impact on Health Care Providers’ Knowledge and Treatment of Hypertension. Glob Heart. 2019;14(1):61–70. doi: 10.1016/j.gheart.2019.02.002 . [DOI] [PubMed] [Google Scholar]
  • 165.Oranratanaphan S, Termrungruanglert W, Khemapech N. Acceptability of self-sampling HPV testing among Thai women for cervical cancer screening. Asian Pac J Cancer Prev. 2014;15(17):7437–41. doi: 10.7314/apjcp.2014.15.17.7437 . [DOI] [PubMed] [Google Scholar]
  • 166.Ouedraogo Y, Furlane G, Fruhauf T, Badolo O, Bonkoungou M, Pleah T, et al. Expanding the Single-Visit Approach for Cervical Cancer Prevention: Successes and Lessons From Burkina Faso. Glob Health Sci Pract. 2018;6(2):288–98. doi: 10.9745/GHSP-D-17-00326 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 167.Page CM, Ibrahim S, Park LP, Huchko MJ. Systems-level barriers to treatment in a cervical cancer prevention program in Kenya: Several observational studies. PLoS ONE [Electronic Resource]. 2020;15(7):e0235264. doi: 10.1371/journal.pone.0235264 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 168.Palanuwong B. Alternative cervical cancer prevention in low-resource settings: Experiences of visual inspection by acetic acid with single-visit approach in the first five provinces of Thailand. Aust N Z J Obstet Gynaecol. 2007;47(1):54–60. doi: 10.1111/j.1479-828X.2006.00680.x . [DOI] [PubMed] [Google Scholar]
  • 169.Pantano NP, Fregnani JH, Resende JC, Zeferino LC, Fonseca BO, Antoniazzi M, et al. Evaluation of human papillomavirus self-collection offered by community health workers at home visits among under-screened women in Brazil. J Med Screen. 2020:969141320941056. doi: 10.1177/0969141320941056 . [DOI] [PubMed] [Google Scholar]
  • 170.Paolino M, Gago J, Le Pera A, Cinto O, Thouyaret L, Arrossi S. Adherence to triage among women with HPV-positive self-collection: A study in a middle-low income population in Argentina. Ecancermedicalscience. 2020;14(no pagination). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 171.Parham GP, Mwanahamuntu MH, Kapambwe S, Muwonge R, Bateman AC, Blevins M, et al. Population-level scale-up of cervical cancer prevention services in a low-resource setting: development, implementation, and evaluation of the cervical cancer prevention program in Zambia. PLoS ONE [Electronic Resource]. 2015;10(4):e0122169. doi: 10.1371/journal.pone.0122169 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 172.Pastakia SD, Manyara SM, Vedanthan R, Kamano JH, Menya D, Andama B, et al. Impact of Bridging Income Generation with Group Integrated Care (BIGPIC) on Hypertension and Diabetes in Rural Western Kenya. J Gen Intern Med. 2017;32(5):540–8. doi: 10.1007/s11606-016-3918-5 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 173.Patel A, Praveen D, Maharani A, Oceandy D, Pilard Q, Kohli MPS, et al. Association of Multifaceted Mobile Technology-Enabled Primary Care Intervention with Cardiovascular Disease Risk Management in Rural Indonesia. JAMA Cardiol. 2019;4(10):978–86. doi: 10.1001/jamacardio.2019.2974 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 174.Patel S, Klein RM, Patel A, Klein RB, Aung M, Hoe W. Diabetic retinopathy screening and treatment in Myanmar: a pilot study. BMJ Open Ophthalmol. 2017;1(1):e000084. doi: 10.1136/bmjophth-2017-000084 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 175.Paul P, Winkler JL, Bartolini RM, Penny ME, Huong TT, Nga le T, et al. Screen-and-treat approach to cervical cancer prevention using visual inspection with acetic acid and cryotherapy: experiences, perceptions, and beliefs from demonstration projects in Peru, Uganda, and Vietnam. Oncologist. 2013;18(12):1278–84. doi: 10.1634/theoncologist.2013-0253 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 176.Paz-Soldan VA, Bayer AM, Nussbaum L, Cabrera L. Structural barriers to screening for and treatment of cervical cancer in Peru. Reprod Health Matters. 2012;20(40):49–58. doi: 10.1016/S0968-8080(12)40680-2 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 177.Pazoki R, Nabipour I, Seyednezami N, Imami SR. Effects of a community-based healthy heart program on increasing healthy women’s physical activity: a randomized controlled trial guided by Community-based Participatory Research (CBPR). BMC Public Health. 2007;7:216. doi: 10.1186/1471-2458-7-216 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 178.Pfaendler KS, Mwanahamuntu MH, Sahasrabuddhe VV, Mudenda V, Stringer JS, Parham GP. Management of cryotherapy-ineligible women in a “screen-and-treat” cervical cancer prevention program targeting HIV-infected women in Zambia: lessons from the field. Gynecol Oncol. 2008;110(3):402–7. doi: 10.1016/j.ygyno.2008.04.031 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 179.Phongsavan K, Phengsavanh A, Wahlstrom R, Marions L. Safety, feasibility, and acceptability of visual inspection with acetic acid and immediate treatment with cryotherapy in rural Laos. Int J Gynaecol Obstet. 2011;114(3):268–72. doi: 10.1016/j.ijgo.2011.03.009 . [DOI] [PubMed] [Google Scholar]
  • 180.Pillay A, Trieu K, Santos JA, Sukhu A, Schultz J, Wate J, et al. Assessment of a Salt Reduction Intervention on Adult Population Salt Intake in Fiji. Nutrients. 2017;9(12):12. doi: 10.3390/nu9121350 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 181.Pimple S, Pednekar M, Mazumdar P, Goswami S, Shastri S. Predictors of quitting tobacco—results of a worksite tobacco cessation service program among factory workers in Mumbai, India. Asian Pac J Cancer Prev. 2012;13(2):533–8. doi: 10.7314/apjcp.2012.13.2.533 . [DOI] [PubMed] [Google Scholar]
  • 182.Prabhakaran D, Jeemon P, Mohanan PP, Govindan U, Geevar Z, Chaturvedi V, et al. Management of acute coronary syndromes in secondary care settings in Kerala: impact of a quality improvement programme. Natl Med J India. 2008;21(3):107–11. . [PubMed] [Google Scholar]
  • 183.Praveen PA, Venkatesh P, Tandon N. Screening model for diabetic retinopathy among patients with type 1 diabetes attending a tertiary care setting in India. Indian J Ophthalmol. 2020;68(Suppl 1):S96–S9. doi: 10.4103/ijo.IJO_1830_19 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 184.Queiroz MS, de Carvalho JX, Bortoto SF, de Matos MR, das Gracas Dias Cavalcante C, Andrade EAS, et al. Diabetic retinopathy screening in urban primary care setting with a handheld smartphone-based retinal camera. Acta Diabetol. 2020;57(12):1493–9. doi: 10.1007/s00592-020-01585-7 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 185.Raj P, Singh S, Lewis MG, Shukla R, Murthy GVS, Gilbert C. Diabetic retinopathy screening uptake after health education with or without retinal imaging within the facility in two AYUSH hospitals in Hyderabad, India: A nonrandomized pilot study. Indian J Ophthalmol. 2020;68(Suppl 1):S56–S8. doi: 10.4103/ijo.IJO_2119_19 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 186.Rajalakshmi R, Shanthirani CS, Anandakumar A, Anjana RM, Murthy GVS, Gilbert C, et al. Assessment of diabetic retinopathy in type 1 diabetes in a diabetes care center in South India-Feasibility and awareness improvement study. Indian J Ophthalmol. 2020;68(Suppl 1):S92–S5. doi: 10.4103/ijo.IJO_1851_19 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 187.Ramachandran A, Kumar R, Nanditha A, Raghavan A, Snehalatha C, Krishnamoorthy S, et al. MDiabetes initiative using text messages to improve lifestyle and health-seeking behaviour in India. BMJ Innov. 2018;4(4):155–62. [Google Scholar]
  • 188.Ramagiri R, Kannuri NK, Lewis MG, Murthy GVS, Gilbert C. Evaluation of whether health education using video technology increases the uptake of screening for diabetic retinopathy among individuals with diabetes in a slum population in Hyderabad. Indian J Ophthalmol. 2020;68(Suppl 1):S37–S41. doi: 10.4103/ijo.IJO_2028_19 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 189.Ramogola-Masire D, de Klerk R, Monare B, Ratshaa B, Friedman HM, Zetola NM. Cervical cancer prevention in HIV-infected women using the “See and Treat” approach in Botswana. J Acquir Immune Defic Syndr. 2011;30. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 190.Rashid RM, Ramli S, John J, Dahlui M. Cost effective analysis of recall methods for cervical cancer screening in Selangor—results from a prospective randomized controlled trial. Asian Pac J Cancer Prev. 2014;15(13):5143–7. doi: 10.7314/apjcp.2014.15.13.5143 . [DOI] [PubMed] [Google Scholar]
  • 191.Rosenbaum AJ, Gage JC, Alfaro KM, Ditzian LR, Maza M, Scarinci IC, et al. Acceptability of self-collected versus provider-collected sampling for HPV DNA testing among women in rural El Salvador. Int J Gynaecol Obstet. 2014;126(2):156–60. doi: 10.1016/j.ijgo.2014.02.026 . [DOI] [PubMed] [Google Scholar]
  • 192.Rosser JI, Njoroge B, Huchko MJ. Changing knowledge, attitudes, and behaviors regarding cervical cancer screening: The effects of an educational intervention in rural Kenya. Patient Educ Couns. 2015;98(7):884–9. doi: 10.1016/j.pec.2015.03.017 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 193.Sadeghi-Hokmabadi E, Farhoudi M, Taheraghdam A, Hashemilar M, Savadi-Osguei D, Rikhtegar R, et al. Intravenous recombinant tissue plasminogen activator for acute ischemic stroke: a feasibility and safety study. Int J Gen Med. 2016;9:361–7. doi: 10.2147/IJGM.S112430 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 194.Salamanca O, Geary A, Suarez N, Benavent S, Gonzalez M. Implementation of a diabetic retinopathy referral network, Peru. Bull World Health Organ. 2018;96(10):674–81. doi: 10.2471/BLT.18.212613 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 195.Salimzadeh H, Delavari A. Effectiveness of a theory-based intervention to increase colorectal cancer screening among Iranian. J Gastroenterol Hepatol. 2013;28:567–8. doi: 10.1007/s10865-013-9533-6 . [DOI] [PubMed] [Google Scholar]
  • 196.Sanghvi H, Limpaphayom KK, Plotkin M, Charurat E, Kleine A, Lu E, et al. Cervical cancer screening using visual inspection with acetic acid: operational experiences from Ghana and Thailand. Reprod Health Matters. 2008;16(32):67–77. doi: 10.1016/S0968-8080(08)32401-X . [DOI] [PubMed] [Google Scholar]
  • 197.Sankaranarayanan R, Rajkumar R, Esmy PO, Fayette JM, Shanthakumary S, Frappart L, et al. Effectiveness, safety and acceptability of ‘see and treat’ with cryotherapy by nurses in a cervical screening study in India. Br J Cancer. 2007;96(5):738–43. doi: 10.1038/sj.bjc.6603633 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 198.Saraf DS, Gupta SK, Pandav CS, Nongkinrih B, Kapoor SK, Pradhan SK, et al. Effectiveness of a School Based Intervention for Prevention of Non-communicable Diseases in Middle School Children of Rural North India: A Randomized Controlled Trial. Indian J Pediatr. 2015;82(4):354–62. doi: 10.1007/s12098-014-1562-9 . [DOI] [PubMed] [Google Scholar]
  • 199.Sartorelli DS, Sciarra EC, Franco LJ, Cardoso MA. Beneficial effects of short-term nutritional counselling at the primary health-care level among Brazilian adults. Public Health Nutr. 2005;8(7):820–5. doi: 10.1079/phn2005737 . [DOI] [PubMed] [Google Scholar]
  • 200.Scepanovic M, Jovanovic O, Keber D, Jovanovic I, Miljus D, Nikolic G, et al. Faecal occult blood screening for colorectal cancer in Serbia: a pilot study. Eur J Cancer Prev. 2017;26(3):195–200. doi: 10.1097/CEJ.0000000000000247 . [DOI] [PubMed] [Google Scholar]
  • 201.Scott LaMontagne D, Barge S, Le NT, Mugisha E, Penny ME, Gandhi S, et al. Human papillomavirus vaccine delivery strategies. Bull World Health Organ 2011;89(11):821–30. doi: 10.2471/BLT.11.089862 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 202.Sharma SR, Sharma N. Hyperacute thrombolysis with recombinant tissue plasminogen activator of acute ischemic stroke: feasibility and effectivity from an Indian perspective. Ann Indian Acad Neurol. 2008;11(4):221–4. doi: 10.4103/0972-2327.44556 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 203.Shastri SS, Mittra I, Mishra GA, Gupta S, Dikshit R, Singh S, et al. Effect of VIA screening by primary health workers: randomized controlled study in Mumbai, India. J Natl Cancer Inst. 2014;106(3):dju009. doi: 10.1093/jnci/dju009 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 204.Shen J, Olwanda E, Kahn JG, Huchko MJ. Cost of HPV screening at community health campaigns (CHCs) and health clinics in rural Kenya. BMC Health Serv Res. 2018;18(1):378. doi: 10.1186/s12913-018-3195-6 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 205.Shiferaw N, Salvador-Davila G, Kassahun K, Brooks MI, Weldegebreal T, Tilahun Y, et al. The Single-Visit Approach as a Cervical Cancer Prevention Strategy Among Women With HIV in Ethiopia: Successes and Lessons Learned. Glob Health Sci Pract. 2016;4(1):87–98. doi: 10.9745/GHSP-D-15-00325 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 206.Singh S, Shukla AK, Sheikh A, Gupta G, More A. Effect of health education and screening location on compliance with diabetic retinopathy screening in a rural population in Maharashtra. Indian J Ophthalmol. 2020;68(Suppl 1):S47–S51. doi: 10.4103/ijo.IJO_1976_19 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 207.Singla S, Mathur S, Kriplani A, Agarwal N, Garg P, Bhatla N. Single visit approach for management of cervical intraepithelial neoplasia by visual inspection & loop electrosurgical excision procedure. Indian J Med Res. 2012;135(5):614–20. . [PMC free article] [PubMed] [Google Scholar]
  • 208.Snyman LC, Dreyer G, Botha MH, van der Merwe FH, Becker PJ. The Vaccine and Cervical Cancer Screen (VACCS) project: Linking cervical cancer screening to HPV vaccination in the South-West District of Tshwane, Gauteng, South Africa. S Afr Med J. 2015;105(2):115–20. doi: 10.7196/samj.8418 . [DOI] [PubMed] [Google Scholar]
  • 209.Solla DJ, Paiva Filho Ide M, Delisle JE, Braga AA, Moura JB, Moraes X Jr., et al. Integrated regional networks for ST-segment-elevation myocardial infarction care in developing countries: the experience of Salvador, Bahia, Brazil. Circ Cardiovasc Qual Outcomes. 2013;6(1):9–17. doi: 10.1161/CIRCOUTCOMES.112.967505 . [DOI] [PubMed] [Google Scholar]
  • 210.Souza GF, Figueira RM, Alkmim MB, Sousa LAP, Bonisson L, Ribeiro ALP, et al. Teleophthalmology Screening for Diabetic Retinopathy in Brazil: Applicability and Economic Assessment. Telemed J E Health. 2020;26(3):341–6. doi: 10.1089/tmj.2018.0241 . [DOI] [PubMed] [Google Scholar]
  • 211.Sui Y, Luo J, Dong C, Zheng L, Zhao W, Zhang Y, et al. Implementation of regional Acute Stroke Care Map increases thrombolysis rates for acute ischaemic stroke in Chinese urban area in only 3 months. Stroke Vasc Neurol. 2020;24:24. doi: 10.1136/svn-2020-000332 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 212.Swaddiwudhipong W, Chaovakiratipong C, Nguntra P, Mahasakpan P, Tatip Y, Boonmak C. A mobile unit: an effective service for cervical cancer screening among rural Thai women. Int J Epidemiol. 1999;28(1):35–9. doi: 10.1093/ije/28.1.35 . [DOI] [PubMed] [Google Scholar]
  • 213.Tamin NSI, Razalli KA, Sallahuddin SN, Chan HK, Hassan MRA. A 5-year evaluation of using stool-based test for opportunistic colorectal cancer screening in primary health institutions across Malaysia. Cancer Epidemiol. 2020;69(no pagination). doi: 10.1016/j.canep.2020.101829 . [DOI] [PubMed] [Google Scholar]
  • 214.Tankumpuan T, Anuruang S, Jackson D, Hickman LD, DiGiacomo M, Davidson PM. Improved adherence in older patients with hypertension: An observational study of a community-based intervention. Int J Older People Nurs. 2019;14(3):e12248. doi: 10.1111/opn.12248 . [DOI] [PubMed] [Google Scholar]
  • 215.Teguete I, Muwonge R, Traore CB, Dolo A, Bayo S, Sankaranarayanan R. Can visual cervical screening be sustained in routine health services? Experience from Mali, Africa. BJOG. 2012;119(2):220–6. doi: 10.1111/j.1471-0528.2011.03122.x . [DOI] [PubMed] [Google Scholar]
  • 216.Tetra Dewi FS, Stenlund H, Marlinawati VU, Ohman A, Weinehall L. A community intervention for behaviour modification: an experience to control cardiovascular diseases in Yogyakarta, Indonesia. BMC Public Health. 2013;13:1043. doi: 10.1186/1471-2458-13-1043 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 217.Tian M, Yin X, Dunzhu D, Liu Z, Li C, Sun H, et al. A qualitative evaluation of a simplified cardiovascular management program in Tibet, China. Global Health. 2018;14(1):24. doi: 10.1186/s12992-018-0342-0 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 218.Todo MC, Bergamasco CM, Azevedo PS, Minicucci MF, Inoue RMT, Okoshi MP, et al. Impact of coronary intensive care unit in treatment of myocardial infarction. Rev Assoc Med Bras. 2017;63(3):242–7. doi: 10.1590/1806-9282.63.03.242 . [DOI] [PubMed] [Google Scholar]
  • 219.Torres KL, Marino JM, Pires Rocha DA, de Mello MB, de Melo Farah HH, Reis RDS, et al. Self-sampling coupled to the detection of HPV 16 and 18 E6 protein: A promising option for detection of cervical malignancies in remote areas. PLoS ONE [Electronic Resource]. 2018;13(7):e0201262. doi: 10.1371/journal.pone.0201262 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 220.Tran VD, Jancey J, Lee A, James A, Howat P, Thi Phuong Mai L. Physical activity and nutrition program for adults with metabolic syndrome: Process evaluation. Eval Program Plann. 2017;61:128–33. doi: 10.1016/j.evalprogplan.2016.12.012 . [DOI] [PubMed] [Google Scholar]
  • 221.Tsvetanova Dimova R, Dimitrova Dimitrova D, Angelova Levterova B, Stoyanov Dimov R, Atanasova Semerdjieva M, Frantova Tarnovska M, et al. Feasibility of immunochemical faecal occult blood testing for colorectal cancer screening in Bulgaria. J BUON. 2015;20(2):413–20. . [PubMed] [Google Scholar]
  • 222.Tutino GE, Yang WY, Li X, Li WH, Zhang YY, Guo XH, et al. A multicentre demonstration project to evaluate the effectiveness and acceptability of the web-based Joint Asia Diabetes Evaluation (JADE) programme with or without nurse support in Chinese patients with Type 2 diabetes. Diabet Med. 2017;34(3):440–50. doi: 10.1111/dme.13164 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 223.Uivarosan D, Bungau S, Tit DM, Moisa C, Fratila O, Rus M, et al. Financial Burden of Stroke Reflected in a Pilot Center for the Implementation of Thrombolysis. Medicina. 2020;56(2):28. doi: 10.3390/medicina56020054 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 224.Vinitha R, Nanditha A, Snehalatha C, Satheesh K, Susairaj P, Raghavan A, et al. Effectiveness of mobile phone text messaging in improving glycaemic control among persons with newly detected type 2 diabetes. Diabetes Res Clin Pract. 2019;158(no pagination). doi: 10.1016/j.diabres.2019.107919 . [DOI] [PubMed] [Google Scholar]
  • 225.Walley JD, Khan N, Khan MA, Ali S, King R, Khan SE, et al. Delivering integrated hypertension care at private health facilities in urban pakistan: A process evaluation. BJGP Open. 2018;2(4):1–12. doi: 10.3399/bjgpopen18X101613 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 226.Wan LH, Zhang XP, You LM, Ruan HF, Chen SX. The Efficacy of a Comprehensive Reminder System to Improve Health Behaviors and Blood Pressure Control in Hypertensive Ischemic Stroke Patients: A Randomized Controlled Trial. J Cardiovasc Nurs. 2018;33(6):509–17. doi: 10.1097/JCN.0000000000000496 . [DOI] [PubMed] [Google Scholar]
  • 227.Wang B, Wang Y, Ye T, Xiao G, Chang H, Wen H, et al. [Integrated regional network construction for ST-segment elevation myocardial infarction care]. Chung-Hua Hsin Hsueh Kuan Ping Tsa Chih [Chinese Journal of Cardiology]. 2014;42(8):650–4. . [PubMed] [Google Scholar]
  • 228.Wang X, Liu D, Du M, Hao R, Zheng H, Yan C. The role of text messaging intervention in Inner Mongolia among patients with type 2 diabetes mellitus: a randomized controlled trial. BMC Med Inform Decis Mak. 2020;20(1):90. doi: 10.1186/s12911-020-01129-7 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 229.Wang YH, Ye KY, Wang SY, Wu F, Yan QH, Cheng MN, et al. Real world study of influenza vaccination intervention among key population of chronic disease management in Shanghai community. Chung-Hua Yu Fang i Hsueh Tsa Chih [Chinese Journal of Prev Med]. 2020;54(4):425–9. doi: 10.3760/cma.j.cn112150-20191031-00828 . [DOI] [PubMed] [Google Scholar]
  • 230.Webb EM, Rheeder P. A cluster-randomized trial to estimate the effect of mobile screening and treatment feedback on HbA1c and diabetes-related complications in Tshwane primary health care clinics, South Africa. Prim Care Diabetes. 2017;11(6):546–54. doi: 10.1016/j.pcd.2017.05.010 . [DOI] [PubMed] [Google Scholar]
  • 231.Wei X, Walley JD, Zhang Z, Zou G, Gong W, Deng S, et al. Implementation of a comprehensive intervention for patients at high risk of cardiovascular disease in rural China: A pragmatic cluster randomized controlled trial. PLoS ONE [Electronic Resource]. 2017;12(8):e0183169. doi: 10.1371/journal.pone.0183169 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 232.Wu Y, Li S, Patel A, Li X, Du X, Wu T, et al. Effect of a Quality of Care Improvement Initiative in Patients with Acute Coronary Syndrome in Resource-Constrained Hospitals in China: A Randomized Clinical Trial. JAMA Cardiol. 2019;4(5):418–27. doi: 10.1001/jamacardio.2019.0897 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 233.Wu Y, Liang Y, Zhou Q, Liu H, Lin G, Cai W, et al. Effectiveness of a short message service intervention to motivate people with positive results in preliminary colorectal cancer screening to undergo colonoscopy: A randomized controlled trial. Cancer. 2019;125(13):2252–61. doi: 10.1002/cncr.32043 . [DOI] [PubMed] [Google Scholar]
  • 234.Xiao M, Lei X, Zhang F, Sun Z, Harris VC, Tang X, et al. Home Blood Pressure Monitoring by a Mobile-Based Model in Chongqing, China: A Feasibility Study. Int J Environ Res Public Health [Electronic Resource]. 2019;16(18):10. doi: 10.3390/ijerph16183325 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 235.Yazdanpanah B, Safari M, Yazdanpanah S, Angha P, Karami M, Emadi M, et al. The effect of participatory community-based diabetes cares on the control of diabetes and its risk factors in western suburb of Yasouj, Iran. Health Educ Res. 2012;27(5):794–803. doi: 10.1093/her/cys079 . [DOI] [PubMed] [Google Scholar]
  • 236.Yeates KE, Sleeth J, Hopman W, Ginsburg O, Heus K, Andrews L, et al. Evaluation of a Smartphone-Based Training Strategy Among Health Care Workers Screening for Cervical Cancer in Northern Tanzania: The Kilimanjaro Method. J Glob Oncol. 2016;2(6):356–64. doi: 10.1200/JGO.2015.001768 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 237.You J, Wang S, Li J, Luo Y. Usefulness of a nurse-led program of care for management of patients with chronic heart failure. Med Sci Monit. 2020;26(no pagination). doi: 10.12659/MSM.920469 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 238.Yu R, Yan LL, Wang H, Ke L, Yang Z, Gong E, et al. Effectiveness of a community-based individualized lifestyle intervention among older adults with diabetes and hypertension, Tianjin, China, 2008–2009. Prev Chronic Dis. 2014;11:E84. doi: 10.5888/pcd11.120333 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 239.Yu Y, Lv Y, Yao B, Duan L, Zhang X, Xie L, et al. A novel prescription pedometer-assisted walking intervention and weight management for Chinese occupational population. PLoS ONE [Electronic Resource]. 2018;13(1):e0190848. doi: 10.1371/journal.pone.0190848 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 240.Zhang Q, Zhang RY, Qiu JP, Zhang JF, Wang XL, Jiang L, et al. Prospective multicenter randomized trial comparing physician versus patient transfer for primary percutaneous coronary intervention in acute ST-segment elevation myocardial infarction. Chin Med J (Engl). 2008;121(6):485–91. . [PubMed] [Google Scholar]
  • 241.Zhang X, Zhao G, Bi H, Zhou M, Wang X, Juan J. Exploring an Appropriate Method of Cervical Cancer Screening in Rural China. Asia Pac J Public Health. 2019;31(7):652–8. doi: 10.1177/1010539519876411 . [DOI] [PubMed] [Google Scholar]
  • 242.Zhao Y, Liao Q, Mi X, Li MZ, Zhao C, Cui SH, et al. [Survey of the acceptance status of HPV self-sampling screening in female population for cervical cancer]. Chung-Hua Fu Chan Ko Tsa Chih [Chinese Journal of Obstetrics & Gynecology]. 2019;54(5):312–7. doi: 10.3760/cma.j.issn.0529-567x.2019.05.005 . [DOI] [PubMed] [Google Scholar]
  • 243.Zheng X, Spatz ES, Bai X, Huo X, Ding Q, Horak P, et al. Effect of Text Messaging on Risk Factor Management in Patients With Coronary Heart Disease: The CHAT Randomized Clinical Trial. Circ Cardiovasc Qual Outcomes. 2019;12(4):e005616. doi: 10.1161/CIRCOUTCOMES.119.005616 . [DOI] [PubMed] [Google Scholar]
  • 244.Zhong X, Potemans B, Zhang L, Oldenburg B. Getting a Grip on NCDs in China: an Evaluation of the Implementation of the Dutch-China Cardiovascular Prevention Program. Int J Behav Med. 2015;22(3):393–403. doi: 10.1007/s12529-014-9453-z . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 245.Zhong X, Wang Z, Fisher EB, Tanasugarn C. Peer Support for Diabetes Management in Primary Care and Community Settings in Anhui Province, China. Ann Fam Med. 2015;13(Suppl 1):S50–8. doi: 10.1370/afm.1799 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 246.Forouzanfar MH, Afshin A, Alexander LT, Anderson HR, Bhutta ZA, Biryukov S, et al. Global, regional, and national comparative risk assessment of 79 behavioural, environmental and occupational, and metabolic risks or clusters of risks, 1990–2015: a systematic analysis for the Global Burden of Disease Study 2015. Lancet. 2016;388(10053):1659–1724. doi: 10.1016/S0140-6736(16)31679-8 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 247.Collaboration NCDRF. Worldwide trends in hypertension prevalence and progress in treatment and control from 1990 to 2019: a pooled analysis of 1201 population-representative studies with 104 million participants. Lancet. 2021. Epub 2021/08/28. doi: 10.1016/S0140-6736(21)01330-1 . [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 248.Tomlinson M, Rotheram-Borus MJ, Swartz L, Tsai AC. Scaling up mHealth: where is the evidence? PLoS Med. 2013;10(2):e1001382. Epub 2013/02/21. doi: 10.1371/journal.pmed.1001382 ; PubMed Central PMCID: PMC3570540. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 249.Vedanthan R, Bernabe-Ortiz A, Herasme OI, Joshi R, Lopez-Jaramillo P, Thrift AG, et al. Innovative Approaches to Hypertension Control in Low- and Middle-Income Countries. Cardiol Clin. 2017;35(1):99–115. Epub 2016/11/26. doi: 10.1016/j.ccl.2016.08.010 ; PubMed Central PMCID: PMC5131527. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 250.Kruk ME, Pate M, Mullan Z. High quality health systems—time for a revolution: Report of Lancet Glob Health Commission on High Quality Health Systems in the SDG Era Lancet. Global Health. 2018. [DOI] [PubMed] [Google Scholar]
  • 251.Sheikh K, Abimbola S, Organization WH. Learning health systems: pathways to progress: flagship report of the Alliance for Health Policy and Systems Research. 2021. [Google Scholar]
  • 252.Curran GM, Bauer M, Mittman B, Pyne JM, Stetler C. Effectiveness-implementation hybrid designs: combining elements of clinical effectiveness and implementation research to enhance public health impact. Med Care. 2012;50(3):217–26. Epub 2012/02/09. doi: 10.1097/MLR.0b013e3182408812 ; PubMed Central PMCID: PMC3731143. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 253.Kirk MA, Kelley C, Yankey N, Birken SA, Abadie B, Damschroder L. A systematic review of the use of the consolidated framework for implementation research. Implement Sc. 2015;11(1):1–13. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 254.Jailobaeva K, Falconer J, Loffreda G, Arakelyan S, Witter S, Ager A. An analysis of policy and funding priorities of global actors regarding noncommunicable disease in low- and middle-income countries. Global Health. 2021;17(1):68. Epub 2021/07/01. doi: 10.1186/s12992-021-00713-4 ; PubMed Central PMCID: PMC8240078. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 255.Beyeler N, Fewer S, Yotebieng M, Yamey G. Improving resource mobilisation for global health R&D: a role for coordination platforms? BMJ Glob Health. 2019;4(1):e001209. Epub 2019/03/23. doi: 10.1136/bmjgh-2018-001209 ; PubMed Central PMCID: PMC6407558. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 256.Kruk ME, Yamey G, Angell SY, Beith A, Cotlear D, Guanais F, et al. Transforming Global Health by Improving the Science of Scale-Up. PLoS Biol. 2016;14(3):e1002360. Epub 2016/03/05. doi: 10.1371/journal.pbio.1002360 ; PubMed Central PMCID: PMC4775018. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 257.Patel S, Craigen G, Pinto da Costa M, Inkster B. Opportunities and Challenges for Digital Social Prescribing in Mental Health: Questionnaire Study. J Med Internet Res. 2021;23(3):e17438. Epub 2021/03/10. doi: 10.2196/17438 ; PubMed Central PMCID: PMC7988390. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 258.Daniel M, Maulik PK, Kallakuri S, Kaur A, Devarapalli S, Mukherjee A, et al. An integrated community and primary healthcare worker intervention to reduce stigma and improve management of common mental disorders in rural India: protocol for the SMART Mental Health programme. Trials. 2021;22(1):179. Epub 2021/03/04. doi: 10.1186/s13063-021-05136-5 ; PubMed Central PMCID: PMC7923507. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 259.Asubiaro T. Sub-Saharan Africa’s Biomedical Journal Coverage in Scholarly Databases: A comparison of Web of Science, Scopus, EMBASE, PubMed, African Index Medicus and African Journals Online. 2021. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 260.Kieling C, Herrman H, Patel V, Mari JdJ. Indexation of psychiatric journals from low- and middle-income countries: a survey and a case study. World Psychiatry. 2009;8(1):40. doi: 10.1002/j.2051-5545.2009.tb00209.x [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 261.Pilkington K, Boshnakova A, Clarke M, Richardson J. “No language restrictions” in database searches: what does this really mean? J Altern Complement Med. 2005;11(1):205–207. doi: 10.1089/acm.2005.11.205 [DOI] [PubMed] [Google Scholar]
  • 262.Shenderovich Y, Eisner M, Mikton C, Gardner F, Liu J, Murray J. Methods for conducting systematic reviews of risk factors in low-and middle-income countries. BMC Med Res Methodol. 2016;16(1):1–8. doi: 10.1186/s12874-016-0134-2 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 263.Sheriff RJS, Adams CE, Tharyan P, Jayaram M, Duley L. Randomised trials relevant to mental health conducted in low and middle-income countries: a survey. BMC Psychiatry. 2008;8(1):1–9. doi: 10.1186/1471-244X-8-69 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 264.Beard P, Greenall J, Hoffman C, Nettleton S, Popescu I, Ste-Marie M. Incident Analysis Collaborating Parties. Canadian Incident Analysis Framework. Edmonton, AB: Canadian Patient Safety Institute; 2012. [Google Scholar]

Decision Letter 0

Beryne Odeny

10 Dec 2021

Dear Dr Hategeka,

Thank you for submitting your manuscript entitled "Systematic Review of Implementation Research on Non-Communicable Disease Care in Low- and Middle-Income Countries" for consideration by PLOS Medicine.

Your manuscript has now been evaluated by the PLOS Medicine editorial staff and I am writing to let you know that we would like to send your submission out for external peer review.

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Please re-submit your manuscript within two working days, i.e. by Dec 14 2021 11:59PM.

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Feel free to email us at plosmedicine@plos.org if you have any queries relating to your submission.

Kind regards,

Beryne Odeny

PLOS Medicine

Decision Letter 1

Beryne Odeny

28 Jan 2022

Dear Dr. Hategeka,

Thank you very much for submitting your manuscript "Implementation Research on Non-Communicable Disease Care in Low- and Middle-Income Countries: A Systematic Review" (PMEDICINE-D-21-05057R1) for consideration at PLOS Medicine.

Your paper was evaluated by a senior editor and discussed among all the editors here. It was also sent to independent reviewers, including a statistical reviewer. The reviews are appended at the bottom of this email and any accompanying reviewer attachments can be seen via the link below:

[LINK]

In light of these reviews, I am afraid that we will not be able to accept the manuscript for publication in the journal in its current form, but we would like to consider a revised version that addresses the reviewers' and editors' comments. Obviously we cannot make any decision about publication until we have seen the revised manuscript and your response, and we plan to seek re-review by one or more of the reviewers.

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We look forward to receiving your revised manuscript.

Sincerely,

Beryne Odeny,

PLOS Medicine

plosmedicine.org

-----------------------------------------------------------

Requests from the editors:

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Comments from the reviewers:

Reviewer #1: See attachment

Michael Dewey

Reviewer #2: Reviewer Comments

Title: Systematic Review of Implementation Research on Non-Communicable Disease Care

in Low- and Middle-Income Countries

Authors: Hategeka C, et al.

Overview

The investigators conducted a systematic review of evidence on the current state of implementation research (IR) for NCD prevention and control in low-and middle-income countries (LMICs) using MEDLINE and EMBASE databases from 1990 through 2020. They used standard search terms for this topic that are detailed in their documentation. Among more than 9600 potential studies they found 222 eligible studies from 63 countries. Most studies were on cervical cancer and were for proof of concept or pilots targeted at a micro-level of the healthcare system. Most studies used quantitative methods and weak study designs were common. Study publications increase dramatically over their study timeframe. Major gaps in IR were noted and that published studies were mostly funded by international sources.

General Comments

This is a very well written study that is very important and timely. IR is currently vastly underused in LMICs, and the authors highlight this challenge and the need for more efforts and resources. While they do show convincingly that the number of IR studies annually has increased over their 30-year study timeframe, efforts in this area fall short of what is needed.

There are several areas where the manuscript could be improved. The results seem to be in both the results section some are also in the discussion section. There are many figures and tables and some of the findings could be moved into the text with a concise description and allowing for deletion of some figures/tables. Better description of the inclusion/exclusion criteria would be helpful. A brief clear description of the working definition of screening, treatment and prevention would be useful.

Some discussion on why so few studies were multinational would be helpful. Also, a brief description of micro, meso and macro health system interventions would be useful. In the discussion, using high income country comparable statistics might be useful to give the context of what is currently the situation (e.g., use of implementation science framework for studies in HIC vs LMIC, etc.). While not the ideal comparator is could help under the challenges in the LMIC context. In the discussion/conclusion, it would be helpful to present some of the challenges and barriers conducting IR in LMICs. This could be very insightful. Finally, a better description of why descriptive epidemiological studies were excluded is needed. These may contain barriers and facilitators to implementation and be key in designing IR intervention strategies.

Specific Comments

Funding source section.

While the statement is made that the funders have no involvement in the study, it does not state who the funders were. Suggest including them.

Page 8 first para

…"country of implementation" is a bit unclear. Suggest making it "county where the IR is being conducted" - it seems that is what you are communicating.

Figure 1.

More description of the exclusion categories is needed. For example, intervention, and full text are not entirely clear.

Figure 2

How were studies that had multiple interventions in this graphic? Were they included in all the categories that had interventions?

Figure 3.

This plot is driven by county size. Consider a metric that uses a standardization method such as studies per 100,000 population. This may allow for better comparisons, etc.

Figure 5.

Seems that A and B should have the same total numbers but in B 2020 is lower than 2020 in A. Please explain/reconcile.

Figure 7.

Same issue as for Fig 2. How were studies with multiple interventions handled. Some studies may have a N >1. Please clarify.

Table 1.

See above comment about exclusion of epidemiology descriptive studies. They may have barriers and facilitates for IR intervention development.

Appendix Table 3.

Should have a date on it because LMIC countries change their status over time (e.g., move from LIC to LMIC, etc.)

Appendix Figure 1.

Diabetes is misspelled

Appendix Figure 5.

See above comments. Macro, Meso, and Micro need short descriptions.

Appendix Figure 7.

The legend is off the page.

Appendix Figure 8.

Legend is confusing as a standalone. Suggest: Funding, no funding (at least none noted in the published report). However, for the study to happen, it must have been funded at some level - so 'no funding" may not work. More detail would be interesting.

Reviewer #3: Thank you for this interesting and useful review of the literature focusing on implementation research on 33 WHO recommended interventions to prevent and control non-communicable diseases in low- and middle-income countries.

General comments

Overall, the study is well written and easy to follow. I have a series of more specific suggestions and comments below, but my main concern is that you only present descriptive statistics regarding some key characteristics of the identified studies, rather than the narrative synthesis which you planned to do according to the study protocol in PROSPERO. Such a narrative synthesis could have provided the reader with a richer understanding of what included studies found and other aspects beyond the narrower quantitative approach used. If you can, including a narrative synthesis would likely be very interesting. If this is not feasible, you should at least comment on this departure from the study protocol and throughout the paper more clearly state the narrow quantitative scope of the study.

Another key aspect which is missing from the paper is an assessment of the quality and usefulness of the included studies. Indeed, you stress the importance of good quality implementation research in several places in the manuscript, yet it is difficult from this study to say anything about the current quality of implementation research on NCD interventions in LMICs.

Specific comments

-- Title

Since the study focuses on NCD prevention and control interventions and not only care, you could consider replacing "Care" with "prevention and control interventions" in the manuscript title: "Implementation Research on Non-Communicable Disease Prevention and Control Interventions in Low- and Middle-Income Countries: A Systematic Review"

-- Abstract

I would not mention the protocol in the abstract.

"We synthesize extracted data narratively using descriptive statistics" - generally narrative synthesis refers to "the use of words and text to summarise and explain the findings of the synthesis", whereas descriptive statistics is a quantitative approach to describe or summarize the characteristics of a sample or data set. Actually, in this study you only present descriptive statistics, no narrative summary or synthesis. Please revise the abstract accordingly.

It would be useful if you could mention something about inclusion and exclusion criteria in methods.

"…approximately similar to their proportion of global population…" while this is a nice idea, it does not make sense to make this sort of comparison since you are missing the high-income countries in your review and they would very likely distort these proportions. Also, your assessment isn't quite correct since LICs are home to about 9% of the global population and about 73% live in MICs.

"Slightly more studies used the weakest study design, pre-experimental, than the strongest design, experimental (25% versus 24%)" - in my view, it would be more correct to state that these two categories were (almost exactly) equal as the difference is something like 2 studies out of 222.

"Despite growth in implementation research on NCDs in LMICs" - this statement is not supported by the findings in the abstract, suggest adding a line supporting this.

"Future studies should prioritize implementation at scale". One could argue that studying interventions at the pilot stage should be prioritized in order to assess whether to take an intervention to scale in the first place. Is there a risk that advocating for a priority on studying implementation at scale could lead to less well studied interventions going to scale?

"stronger internal validity, be more conceptually-driven and use mixed- methods to understand mechanisms" - while interesting, these conclusions are not supported by the findings stated in the abstract. Note that it should be possible to read the abstract without reading the full manuscript.

"To maximize impact of the research under limited resources, adding implementation science outcomes to effectiveness research and regional collaborations are promising." Could you clarify what you mean by this statement, and consider whether this conclusion is supported by the findings of the present study?

-- Research in context

The text provided under "Added value of this study" does not seem to correspond to this heading. I would suggest beginning the paragraph with something like "This study provides the first comprehensive review of implementation research on NCD interventions…"

The text provided under "Implications of all the available evidence" does not seem to be supported by the findings of the present study. Please review this paragraph.

-- Introduction

In the first paragraph, you only mention NCD mortality. I would encourage you to also mention the significant NCD morbidity and its consequences.

You mention COVID-19 and the interlinkages between NCD morbidity and COVID-19. You could consider also making a similar link to other infectious diseases such as TB and HIV to drive home the point that NCD prevention and control should not be regarded as a vertical issue separated from other health issues.

You write that "…the evidence for the clinical effectiveness of most NCD prevention and treatment interventions is well established…" - would you agree with Isaranuwatchai et al. (BMJ 2020;368:m141) who argue that the clinical effectiveness of some NCD prevention and treatment interventions may indeed be contestable or even wasted in some contexts?

Please consider explicitly stating the study aim and/or research question of the study.

Given the limited scope of this study, consider rephrasing "In this systematic review, we synthesize evidence on the current state of implementation research" to better reflect that you present descriptive statistics of key characteristics of peer-reviewed publications on implementation research on 33 specific interventions in LMICs in 1990-2020.

-- Methods

According to the information registered on the PROSPERO database, the study protocol was technically not pre-specified as the start date (Dec 1, 2020) was seven months before the protocol was registered (July 30, 2021), and the anticipated completion date was only one day later (July 31, 2021).

Could you clarify in the methods how you selected the included interventions and specifically how you define "relevant" interventions and "within health systems"? For example, in Table 2 / Appendix table 1 you list "mass media campaigns that educate the public about the harms of smoking/tobacco use and second hand smoke" as an intervention within the health system, whereas it seems like you have excluded other interventions such as taxation and plain packaging.

"Low- and middle-income countries as defined by the World Bank." - please specify which version you use as the classification is modified each year and the list has changed a fair bit since 1990. For example, in 1990 both China and India were classified as low-income countries.

Throughout, I would recommend making the reference to the updated Appendix 3 of the WHO Global NCD Action Plan 2013-2020 more explicit to avoid the perception that you came up with your own list of interventions.

The list of data elements you extracted, presented in appendix table 4, plays a central role in defining the focus of your study. Please describe how you arrived at the 29 included parameters.

The following sentence is redundant since the information is provided in table 1: "Non-empirical/primary research including reviews meta-analyses, editorials, commentaries, letters to editors, opinion papers, newspaper and protocols, are not eligible for inclusion."

As noted in the abstract: As far as I can see, you do not present any narrative summary or synthesis of findings, only some basic descriptive statistics.

The heading "Risk of bias assessment" could be removed from methods since it was not done, unless it is explicitly required by editors. The corresponding paragraph could be moved to the limitations section.

Table 1. This table is unnecessarily unwieldy. Specifically I would recommend removing the row for "population" as your review focuses on interventions and not populations (that non-humans are excluded can be left implicit in my opinion), and significantly shorten the study design section - it is not necessary to list all existing study designs here.

-- Results

Perhaps I am missing something, but I would normally expect there to be a table with the full list of included studies and their characteristics (either in manuscript or in appendix). Currently, there is just a reference to Table 1 (which should not be referenced here as it belongs to methods), followed by references "20-241". In my view, this is not a sufficient way to list the included studies.

I would recommend using the same number of decimal points throughout (you now mix between 1 and 0 decimal points).

You refer to a grand total of 12 figures in the Appendix, all of which are simple bar or pie charts. In my opinion, this information would be far more easily digested if you could present it as one or two tables instead.

According to table 2 you have only 33 eligible interventions in this study - how could you find 265 interventions? Per the study design, you should only be able to find a maximum of 33 interventions. Could you clarify this? (According to Appendix figure 1, you found studies covering 32 of the 33 eligible interventions, and in total there were 265 instances across the 32 interventions).

Appendix figure 1. The figure says "Fiabetes management", please review.

How do figure 2 and appendix figure 1 relate? The numbers seem not to match.

Appendix table 5 should have a column with country income category. The column entitled "proportion" should read "percentage".

Sorry to make an editorial comment, but please make sure the order of figures and tables are correct (for example, Appendix figure 2 appears in the text before Appendix figure 1).

You state that "The NCD conditions targeted varied by countries" and refer to Appendix Figure 3, but the figure only shows how the number of interventions targeting each condition (though you write number of conditions evaluated) varied by country income category. Please revise the text and figure.

Could you clarify what you mean by "The NCD interventions varied by conditions and type" - in what way did interventions vary? Perhaps you mean that the number of identified interventions varied?

When you state "The intervention focus appears to vary by countries" you again seem to be referring to the country income category rather than country.

The three types of intervention focus brought up in results (screening, treatment and prevention) do not appear to be presented neither in the methods nor in the appendix - where Appendix table 4, row 22. "intervention type" refers back to Appendix table 1, where in column "category of interventions" you only have primary, secondary or tertiary prevention. Please make sure that all methods used are presented in the methods and that the same terminology is used throughout.

Please include a definition and reference for what you mean by "level of health system" (micro, meso, macro) in the methods as this is not clear to the reader.

Each time you write that study characteristics varied by income category or condition etc. I wonder whether you did any simple statistical test to assess whether there were significant differences, or did you decide against this?

I would suggest mentioning the equity lens in the methods since you bring it up in the results (even though it is presented in Appendix table 4).

Figure 5A presents the number of publications by year, but it generally takes years from research to publication - do you have any sense of when research was carried out, not only when it was published?

-- Discussion

I am not sure I agree with this statement: "These studies therefore represent the state of the science today on how to scale up the response of the health system to the growing burden of NCDs in the countries bearing the bulk of disease burden from non-communicable conditions." - nowhere in your study design do you mention a focus on "how to scale up the response of the health system", or is this implicit somehow?

Please rephrase as discussed above: "The studies described 265 different NCD interventions, ranging from screening to prevention to treatment and palliation."

The comparison between number of studies and disease prevalence is interesting but I would recommend adding it to results (and methods) rather than introducing this analysis in the discussion.

Some of the statements in the discussion appear to be new information, i.e. "We found that only 31 of the studied interventions addressed prevention with nearly 80% of these tackling primary prevention (e.g., tobacco use, inactivity, unhealthy diet)." - could you please make sure that you do not introduce new information in the discussion?

You write: "arguably WHO- proposed interventions are well established and a range of implementation models abound" - please see my earlier comment about the fact that the list of interventions has been questioned in its own right. I also note that you contradict yourself when you write that "a range of implementation models abound", while in the introduction you noted that "care delivery models and means of scaling these up to entire populations in need in heterogeneous and resource-constrained health systems are not".

"the micro-level of the health system— targeting patient, provider, or clinic levels", this is the first time in tha manuscript that you explain what you mean by the micro level, see comment above.

"Nearly one in five tested a new technology, despite evidence that technology adoption without substantial integration into policies, data, and workflows is typically ineffective in transforming care" - are you here implying that this was not the case in the included studies?

"The lack of domestic support is unlikely to be offset by global funding going forward; a recent analysis showed that NCDs were under prioritized in bilateral agency portfolios relative to their health impacts." - I would argue that this situation is changing, besides, it may be more useful to think about this in terms of health systems strengthening than as a vertical NCD silo. You may want to touch on that aspect in the discussion.

You write "We had no language restrictions permitting a comprehensive assessment of the published literature" - did you do any searches in other languages? Did you include studies in other languages?

I would suggest adding a few sentences to the limitations about the fact that you did not assess quality or usefulness of the included studies. (Indeed, you begin the conclusion by stating that "High quality implementation science can play a key role in informing effective delivery of health system interventions", yet your study only quantifies the number of studies, not their quality.)

Limitations should also, importantly, discuss the fact that there may be significant implementation research conducted which is never published which may introduce important selection bias in your study.

The paragraph starting with "Over 50 of the 222 included studies used an experimental research design." seems misplaced after the "strength and limitations" section.

-- Conclusion

You should generally avoid adding new arguments and references in the conclusion, but rather conclude what you found, relating back to your study aim. Your current conclusion reads more like a conclusion about the usefulness and need for implementation more broadly, rather than about your study findings. Several of the conclusions are not supported by the study findings and should be brought up in the discussion rather than the conclusion. Please revise the conclusion accordingly.

Any attachments provided with reviews can be seen via the following link:

[LINK]

Attachment

Submitted filename: hategeka.pdf

Decision Letter 2

Beryne Odeny

29 Mar 2022

Dear Dr. Hategeka,

Thank you very much for submitting your manuscript "Implementation Research on Non-Communicable Disease Prevention and Control Interventions in Low- and Middle-Income Countries: A Systematic Review" (PMEDICINE-D-21-05057R2) for consideration at PLOS Medicine.

Your paper was evaluated by a senior editor and discussed among all the editors here. It was also discussed with an academic editor with relevant expertise, and sent to independent reviewers, including a statistical reviewer. The reviews are appended at the bottom of this email and any accompanying reviewer attachments can be seen via the link below:

[LINK]

In light of these reviews, I am afraid that we will not be able to accept the manuscript for publication in the journal in its current form, but we would like to consider a revised version that addresses the reviewers' and editors' comments. Obviously we cannot make any decision about publication until we have seen the revised manuscript and your response, and we plan to seek re-review by one or more of the reviewers.

In revising the manuscript for further consideration, your revisions should address the specific points made by each reviewer and the editors. Please also check the guidelines for revised papers at http://journals.plos.org/plosmedicine/s/revising-your-manuscript for any that apply to your paper. In your rebuttal letter you should indicate your response to the reviewers' and editors' comments, the changes you have made in the manuscript, and include either an excerpt of the revised text or the location (eg: page and line number) where each change can be found. Please submit a clean version of the paper as the main article file; a version with changes marked should be uploaded as a marked up manuscript.

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We look forward to receiving your revised manuscript.

Sincerely,

Beryne Odeny,

PLOS Medicine

plosmedicine.org

-----------------------------------------------------------

Requests from the academic editor:

This is an interesting study, but I think two things are missing and could make it much better.

First, there is a notable lack of attention in systematically capturing categorizing the strategies. While the categorization of strategies is a moving target in implementation science, it is nevertheless a crucial "ingredient" in implementation science and our limited ability to describe the strategy (which is the exposure or treatment if you will in this field) limits what we learn from it. There are many different ways of classifying strategies, that range from the original Proctor Actor-Action etc., to ERIC to Cochrane EPOC to Waltz et al. - none of them are perfect but they can still be useful. At a minimum, who in the health system is carrying out the strategy, what are the actions, and who are the actions meant to target are critical. In truth, some of the strategies are going to be difficult to categorize because the primary sources do not say what they are, but it would nevertheless be of interest say how many did or did not. The authors are undoubtedly familiar with both the challenges and the importance of describing strategies used in these studies, so whatever direction they take, some discussion and justification of it in the discussion would be helpful.

Some additional analysis of the implementation outcomes might be useful, with more description on where in the health system (at the patient, the hcw, the organization, the system) etc., the strategies targeted. How has this changed over time? does it differ by disease condition? what about by donor? Likewise this could be done with the strategies as well, but understanding what kind of targets implementation science addressing NCD's seek would be helpful. What I would be concerned about in general is the phenomenon where clinical research and patient level outcomes in clinical medicine drive outcome selection and measurement, and even though much of the action is above the level of the patient, the outcomes - even those considered implementation outcomes - are reported at the level of the patient, and if so would be of limited informativeness.

Comments from the reviewers:

Reviewer #1: The authors have met most of my points especially about the figures although I still think Figure 4 is not really a good use of ink and space.

I thank the authors for the offprint about comparison of databases but I do not draw the same optimistic message from it as they do. Unfortunately it does not give us the breakdown of the intersections of the coverage so we cannot tell if searching a new database would give us additional references. Just because Embase has, say 10%, and AIM 5% does not imply the 5% are a proper subset of the 10%. They might all be different. I still think the search is rather limited.

Michael Dewey

Reviewer #3: Thank you for your thorough and thoughtful responses to reviewers' and editors' comments. As this is a re-review, I present my remaining concerns below.

You state that "We have already clarified in our methods section and in the protocol that narrative descriptive analysis that would be used in this review refers to descriptive statistics including summary statistics of type of interventions, study designs, and implementation outcomes". My point is that you cannot do descriptive statistics and call it narrative synthesis as those are two different things. Please revise the manuscript accordingly, possibly including an explanation why you did not do a narrative synthesis as you had planned to do according to the study protocol.

You state that "Table 2 shows a list of unique interventions that were eligible for inclusion. In the results, we report total number (instead of unique type of interventions) of NCD interventions evaluated in 222 included studies. We found that 265 interventions were evaluated across 222 included studies, meaning that there were some studies that evaluated more than one intervention.". I do not think you have addressed the problem I raised regarding the terminology used, namely that you use the word "intervention" to mean both the 33 priority NCD interventions included in this study and the 265 studied instances of those interventions being used. This is particularly confusing since you actually found 222 studies covering 32 of the 33 interventions. I suggest you consider an alternative terminology which separates between the 33 priority interventions and the 265 instances of interventions being used.

Regarding your comment that "We reported year of publication and not time of when study/implementation was conducted." I would suggest you make a comment about this in the limitations.

Any attachments provided with reviews can be seen via the following link:

[LINK]

Decision Letter 3

Beryne Odeny

1 Jun 2022

Dear Dr. Hategeka,

Thank you very much for re-submitting your manuscript "Implementation Research on Non-Communicable Disease Prevention and Control Interventions in Low- and Middle-Income Countries: A Systematic Review" (PMEDICINE-D-21-05057R3) for review by PLOS Medicine.

I have discussed the paper with my colleagues and the academic editor. I am pleased to say that provided the remaining editorial and production issues are dealt with we are planning to accept the paper for publication in the journal.

The remaining issues that need to be addressed are listed at the end of this email. Any accompanying reviewer attachments can be seen via the link below. Please take these into account before resubmitting your manuscript:

[LINK]

***Please note while forming your response, if your article is accepted, you may have the opportunity to make the peer review history publicly available. The record will include editor decision letters (with reviews) and your responses to reviewer comments. If eligible, we will contact you to opt in or out.***

In revising the manuscript for further consideration here, please ensure you address the specific points made by each reviewer and the editors. In your rebuttal letter you should indicate your response to the reviewers' and editors' comments and the changes you have made in the manuscript. Please submit a clean version of the paper as the main article file. A version with changes marked must also be uploaded as a marked up manuscript file.

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We ask every co-author listed on the manuscript to fill in a contributing author statement. If any of the co-authors have not filled in the statement, we will remind them to do so when the paper is revised. If all statements are not completed in a timely fashion this could hold up the re-review process. Should there be a problem getting one of your co-authors to fill in a statement we will be in contact. YOU MUST NOT ADD OR REMOVE AUTHORS UNLESS YOU HAVE ALERTED THE EDITOR HANDLING THE MANUSCRIPT TO THE CHANGE AND THEY SPECIFICALLY HAVE AGREED TO IT.

Please ensure that the paper adheres to the PLOS Data Availability Policy (see http://journals.plos.org/plosmedicine/s/data-availability), which requires that all data underlying the study's findings be provided in a repository or as Supporting Information. For data residing with a third party, authors are required to provide instructions with contact information for obtaining the data. PLOS journals do not allow statements supported by "data not shown" or "unpublished results." For such statements, authors must provide supporting data or cite public sources that include it.

To enhance the reproducibility of your results, we recommend that you deposit your laboratory protocols in protocols.io, where a protocol can be assigned its own identifier (DOI) such that it can be cited independently in the future. Additionally, PLOS ONE offers an option to publish peer-reviewed clinical study protocols. Read more information on sharing protocols at https://plos.org/protocols?utm_medium=editorial-email&utm_source=authorletters&utm_campaign=protocols

Please review your reference list to ensure that it is complete and correct. If you have cited papers that have been retracted, please include the rationale for doing so in the manuscript text, or remove these references and replace them with relevant current references. Any changes to the reference list should be mentioned in the rebuttal letter that accompanies your revised manuscript.

Please note, when your manuscript is accepted, an uncorrected proof of your manuscript will be published online ahead of the final version, unless you've already opted out via the online submission form. If, for any reason, you do not want an earlier version of your manuscript published online or are unsure if you have already indicated as such, please let the journal staff know immediately at plosmedicine@plos.org.

If you have any questions in the meantime, please contact me or the journal staff on plosmedicine@plos.org.  

We look forward to receiving the revised manuscript by Jun 08 2022 11:59PM.   

Sincerely,

Beryne Odeny,

PLOS Medicine

plosmedicine.org

------------------------------------------------------------

Requests from Editors:

1) Figure 3 - At the top of each column, please indicate the meaning of numbers in each cell/ row (e.g., “=5”). If this is the N of studies, please clearly indicate this at the top of each column.

2) References

a) Please ensure that journal name abbreviations consistently match those found in the National Center for Biotechnology Information (NCBI) databases. https://journals.plos.org/plosmedicine/s/submission-guidelines#loc-references.

b) Please ensure that an access date is provided for all references with weblinks.

Comments from Reviewers:

Any attachments provided with reviews can be seen via the following link:

[LINK]

Decision Letter 4

Beryne Odeny

16 Jun 2022

Dear Dr. Hategeka,

Thank you very much for re-submitting your manuscript "Implementation Research on Non-Communicable Disease Prevention and Control Interventions in Low- and Middle-Income Countries: A Systematic Review" (PMEDICINE-D-21-05057R4) for review by PLOS Medicine.

I have discussed the paper with my colleagues and the academic editor. I am pleased to say that provided the remaining editorial and production issues are dealt with we are planning to accept the paper for publication in the journal.

The remaining issues that need to be addressed are listed at the end of this email. Any accompanying reviewer attachments can be seen via the link below. Please take these into account before resubmitting your manuscript:

[LINK]

***Please note while forming your response, if your article is accepted, you may have the opportunity to make the peer review history publicly available. The record will include editor decision letters (with reviews) and your responses to reviewer comments. If eligible, we will contact you to opt in or out.***

In revising the manuscript for further consideration here, please ensure you address the specific points made by each reviewer and the editors. In your rebuttal letter you should indicate your response to the reviewers' and editors' comments and the changes you have made in the manuscript. Please submit a clean version of the paper as the main article file. A version with changes marked must also be uploaded as a marked up manuscript file.

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Please review your reference list to ensure that it is complete and correct. If you have cited papers that have been retracted, please include the rationale for doing so in the manuscript text, or remove these references and replace them with relevant current references. Any changes to the reference list should be mentioned in the rebuttal letter that accompanies your revised manuscript.

Please note, when your manuscript is accepted, an uncorrected proof of your manuscript will be published online ahead of the final version, unless you've already opted out via the online submission form. If, for any reason, you do not want an earlier version of your manuscript published online or are unsure if you have already indicated as such, please let the journal staff know immediately at plosmedicine@plos.org.

If you have any questions in the meantime, please contact me or the journal staff on plosmedicine@plos.org.  

We look forward to receiving the revised manuscript by Jun 23 2022 11:59PM.   

Sincerely,

Beryne Odeny,

PLOS Medicine

plosmedicine.org

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Requests from Editors:

- In the abstract, methods and discussion sections, please clearly mention that the implementation strategies are not specified well enough. This should be highlighted as one of the limitations.

Any attachments provided with reviews can be seen via the following link:

[LINK]

Decision Letter 5

Beryne Odeny

21 Jun 2022

Dear Dr Hategeka, 

On behalf of my colleagues and the Academic Editor, Dr Elvin Hsing Geng, I am pleased to inform you that we have agreed to publish your manuscript "Implementation Research on Non-Communicable Disease Prevention and Control Interventions in Low- and Middle-Income Countries: A Systematic Review" (PMEDICINE-D-21-05057R5) in PLOS Medicine.

Before your manuscript can be formally accepted you will need to complete some formatting changes, which you will receive in a follow up email. Please be aware that it may take several days for you to receive this email; during this time no action is required by you. Once you have received these formatting requests, please note that your manuscript will not be scheduled for publication until you have made the required changes.

In the meantime, please log into Editorial Manager at http://www.editorialmanager.com/pmedicine/, click the "Update My Information" link at the top of the page, and update your user information to ensure an efficient production process. 

PRESS

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We also ask that you take this opportunity to read our Embargo Policy regarding the discussion, promotion and media coverage of work that is yet to be published by PLOS. As your manuscript is not yet published, it is bound by the conditions of our Embargo Policy. Please be aware that this policy is in place both to ensure that any press coverage of your article is fully substantiated and to provide a direct link between such coverage and the published work. For full details of our Embargo Policy, please visit http://www.plos.org/about/media-inquiries/embargo-policy/.

To enhance the reproducibility of your results, we recommend that you deposit your laboratory protocols in protocols.io, where a protocol can be assigned its own identifier (DOI) such that it can be cited independently in the future. Additionally, PLOS ONE offers an option to publish peer-reviewed clinical study protocols. Read more information on sharing protocols at https://plos.org/protocols?utm_medium=editorial-email&utm_source=authorletters&utm_campaign=protocols

Thank you again for submitting to PLOS Medicine. We look forward to publishing your paper. 

Sincerely, 

Beryne Odeny 

PLOS Medicine

Associated Data

    This section collects any data citations, data availability statements, or supplementary materials included in this article.

    Supplementary Materials

    S1 PRISMA Checklist. PRISMA 2020 checklist.

    (DOCX)

    S1 Appendix. Appendix tables and figures.

    Table A in S1 Appendix. Interventions provided within health systems. Table B in S1 Appendix. Sample of the search strategy used in the MEDLINE database. Table C in S1 Appendix. List of low- and middle-income countries. Table D in S1 Appendix. Data extraction tool. Table E in S1 Appendix. Distribution of studies by countries where they were implemented. Fig A in S1 Appendix. Variation of conditions evaluated by income group. Fig B in S1 Appendix. Priority NCD interventions (n = 265) identified in 222 studies included in the review. Fig C in S1 Appendix. Distribution of included studies by NCD. Fig D in S1 Appendix. Distribution of intervention type by income group. Fig E in S1 Appendix. Distributions by research designs. Fig F in S1 Appendix. Distributions by standalone implementation studies vs. embedded or hybrid effectiveness-implementation studies. Fig G in S1 Appendix. Distributions by pilot vs. scale-up project. Fig H in S1 Appendix. Variation by level of health system. Fig I in S1 Appendix. Studies that reported funding (vs. those that did not) by NCD conditions. Fig J in S1 Appendix. Distributions by funding type. Fig K in S1 Appendix. Distribution of funding sources by NCDs and their risk factors. Fig L in S1 Appendix. Types of reported funding sources (N = 222 included studies).

    (DOCX)

    Attachment

    Submitted filename: Response to the PLOS Medicine Staff.docx

    Attachment

    Submitted filename: hategeka.pdf

    Attachment

    Submitted filename: Hategeka et al. Responses to EditorsReviewers FEB25.docx

    Attachment

    Submitted filename: Responses to editors and reviewers May 02.docx

    Attachment

    Submitted filename: Responses to Requests from Editors JUN01.docx

    Attachment

    Submitted filename: Responses to Requests from Editors.docx

    Data Availability Statement

    All relevant data are within the manuscript and its supporting information files.


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