Skip to main content
PLOS One logoLink to PLOS One
. 2020 Nov 24;15(11):e0242801. doi: 10.1371/journal.pone.0242801

Alcohol consumption increases non-adherence to ART among people living with HIV enrolled to the community-based care model in rural northern Uganda

Norbert Adrawa 1,2,3, John Bosco Alege 3, Jonathan Izudi 3,4,*
Editor: Tim Mathes5
PMCID: PMC7685449  PMID: 33232369

Abstract

Background

Non-adherence to anti-retroviral therapy (ART) is associated with considerable morbidity and mortality among people living with Human Immunodeficiency Virus (PLHIV). Community-based ART delivery model offers a decentralized and patient-centered approach to care for PLHIV, with the advantage of improved adherence to ART hence good treatment outcomes. However, data are limited on the magnitude of non-adherence to ART among PLHIV enrolled to the community-based ART model of care. In this study, we determined the frequency of non-adherence to ART and the associated factors among PLHIV enrolled to the community-based ART delivery model in a large health facility in rural northern Uganda.

Methods

This analytic cross-sectional study randomly sampled participants from 21 community drug distribution points at the AIDS Support Organization (TASO) in Gulu district, northern Uganda. Data were collected using a standardized and pre-tested questionnaire, entered in Epi-Data and analyzed in Stata at univariate, bivariate, and multivariate analyses levels. Binary logistic regression analysis was used to determine factors independently associated with non-adherence to ART, reported using odds ratio (OR) and 95% confidence level (CI). The level of statistical significance was 5%.

Results

Of 381 participants, 25 (6.6%) were non-adherent to ART and this was significantly associated with alcohol consumption (Adjusted (aOR), 3.24; 95% CI, 1.24–8.34). Other factors namely being single/or never married (aOR, 1.97; 95% CI, 0.62–6.25), monthly income exceeding 27 dollars (aOR, 1.36; 95% CI, 0.52–3.55), being on ART for more than 5 years (aOR, 0.60; 95% CI, 0.23–1.59), receipt of health education on ART side effects (aOR, 0.36; 95% CI, 0.12–1.05), and disclosure of HIV status (aOR, 0.37; 95% CI, 0.04–3.20) were not associated with non-adherence in this setting.

Conclusion

Non-adherence to ART was low among PLHIV enrolled to community-based ART delivery model but increases with alcohol consumption. Accordingly, psychosocial support programs should focus on alcohol consumption.

Introduction

An estimated 37.9 million people are living with Human Immunodeficiency Virus (HIV) globally [1]. The highest burden of HIV is in sub-Saharan Africa, particularly the East and Southern African region where 20.7 (54.0%) million people were living with HIV by the end of 2019 [2]. HIV is treatable with life-long Anti-retroviral therapy (ART) [3]. The goal of ART is to suppress the level of viral load among people living with HIV (PLHIV) to undetectable levels, to reduce the risk of morbidity and mortality, and to reduce transmission [4]. To achieve these goals, good adherence to ART is critical because it ensures reduced risk of drug resistance, improved overall health, quality of life, and long term survival [4]. Previous epidemiological studies showed that ART adherence is influenced by several factors namely patient, treatment regimen, disease characteristics, healthcare provider relationships, and clinic setting [57]. Poor ART adherence tends to result into treatment failure and therefore ART adherence should be routinely assessed and reinforced by every member of the clinical team namely physicians, counselors, nurses, pharmacists, and peer educators amongst others and at all levels of patient care [8].

One approach to addressing the challenges of ART adherence is to ensure the health system provides patient-centered approaches to ART delivery [8], a strategy termed as differentiated service delivery models. A differentiated HIV treatment and care is a strategic mix of approaches to address specific requirements of a subgroup of PLHIV and basically entails approaches that modify client flow, schedules and location of HIV treatment and care services for improved access, coverage, and quality of care. In Uganda, the recommended approaches to differentiated HIV treatment and care include facility and community-based models, both for stable and unstable persons living with HIV [8]. The AIDS Support Organization (TASO) Gulu provides ART through three main models namely health facility, home, and community [9]. Under the community-based ART delivery model, there are designated sites in the community known as community-based drug distribution points where PLHIV come twice or thrice to receive drug refills, clinical evaluation, and psychosocial support [9].

TASO has implemented the community-based drug distribution points approach since 2006 and this approach is considered appropriate in overcoming barriers to retention in care and achieving good rates of viral load suppression [10]. However, this evidence used data from a relatively stable urban setting and the findings may not be generalizable to our setting, a rural and post-conflict region that has suffered at least 2 decades of civil war under the Lord’s Resistance Army. In addition, anecdotal evidence reports that some PLHIV enrolled to the community-based ART model of care have failed to suppress their viral load despite ongoing psychosocial support. One of the reasons for failure to achieve viral load suppression is non-adherence to ART. However, data are limited on non-adherence to ART among PLHIV enrolled to the community-based ART delivery model in our setting. Accordingly, we conducted this study to determine the frequency of non-adherence to ART and the associated patient, clinical, and health systems related factors among PLHIV enrolled to the community-based ART delivery model at TASO Gulu. This study thus provides information that healthcare providers, health planners, health policy makers, and health managers amongst others can use to improve the quality of HIV service provision to PLHIV at TASO Gulu and similar settings in developing countries.

Materials and methods

Study design and setting

We used an analytic cross-sectional study design since the outcome (non-adherence to ART) and the associated factors (exposures) were assessed at the same point in time. The study setting was TASO Gulu in Gulu district, northern Uganda.

TASO is one of the largest and the first local organizations to respond to the HIV epidemic in sub-Saharan Africa and it has 11 service centers spread across Uganda and 1 training center known as TASO College of Health Sciences located in Kampala, Uganda [11]. Gulu district is located about 335 kilometers by road away from Kampala, Uganda’s Capital City. With respect to community-based ART delivery model, there are community drug distribution points, which are sites within the community chosen by PLHIV as being convenient, appropriate, and accessible points for their monthly drug refills. PLHIV who are eligible for community-based ART delivery model are those assessed and deemed stable namely: 1) children, adolescents, pregnant mothers, and adults who have been on their current ART regimen for more than 12 months; 2) those virally suppressed, with viral load less than 1000 copies per ml at the most recent viral load test in the last 12 months; 3) those in the World Health Organization (WHO) clinical stages 1 or 2; 4) those on first or second line ART regimens; and, 5) those with demonstrated good adherence thus over 95% ART adherence in the last 6 consecutive months [8]. For TASO Gulu, there are about 80 community drug distribution points (sites for delivery of community-based ART) spread across the 6 districts of Gulu, Nwoya, Amuru, Pader, Oyam, and Omoro, all in northern Uganda. Elsewhere [12], we have described the setting of TASO Gulu.

Study population: Eligibility criteria, sample size, and sampling

Eligible participants were PLHIV aged 18 years and beyond enrolled to the community-based ART delivery model. The eligibility criteria for enrollment to the model has already been described under the study setting [8]. Using Yamane’s formula shown below [13], we estimated that 381 participants were needed for this study based on the following assumptions: 95% confidence limit, 5% precision (sampling error), and an estimated 8,000 PLHIV enrolled to the community-based ART delivery model.

Sample size (n) = N/1+N(e)2, where N is the total number of PLHIV enrolled to the community-based ART delivery model = 8,000 PLHIV and e is the maximum allowable error = 5% or 0.05. Accordingly, n = 8000/1+8000(0.05)2 = 380.9 ≈ 381.

The sample size was distributed proportionally to size of each of the 21 community-based drug distribution points. We conducted sampling in 2 phases. In the first phase, we sampled 21 community-based drug distribution points through simple random sampling approach without replacement to ensure unbiased selection of the study sites. In the second phase, at each of the selected community-based drug distribution points, we used a systematic random sampling approach to establish a sampling interval by dividing the number of participants scheduled for drug refill by the sample size for the study site. From the established sampling interval, we employed simple random sampling to select a participants until the required number of participants for the site was reached.

Measurements

The outcome variable was non-adherence to ART measured on binary scale (no or yes), defined according to the Uganda Ministry of Health standard as the number of pills taken divided by the number of pills expected to have been taken, expressed as a percentage. To determine participants who were non-adherent versus those adherent to ART, we used a cut-off of 95%. Participants below this cut-off were considered non-adherent to ART and all the rest were taken as adherent to ART. In addition, we asked the non-adherent participants to provide reasons for missing to take their medications.

The independent variables included age in years, sex, tribe, religion, marital status, level of income in Ugandan shillings and later converted to United States dollars, employment status, level of education, duration on ART, waiting time in hours at the community-based drug distribution point, disclosure of HIV status, years lived with HIV since diagnosis, current consumption of alcohol, receipt of health education on the benefits of ART, current ART side effects, current ART regimen, knowledge of need for life-long HIV treatment; use of reminders to enhance ART adherence, and receipt of counseling in the past 3 months.

Data collection and quality control measures

Data were collected through researcher administered questionnaire which consisted of both open and closed ended questions in the local language “Luo”, a predominantly spoken language in the study setting. The questionnaire was forwarded and backward translated, thus from English to Luo language and back translated from Luo to English language by 2 independent fluent speakers and writers in both languages. The original and translated English versions of the questionnaire were compared and any discrepancies were harmonized by the 2 translators and a final questionnaire was then generated. The final questionnaire was pretested in the neighboring districts of Amuru, Nwoya and Oyam to assess its appropriateness after which some questions were modified appropriately prior to data collection. Data were then collected by research assistants who were trained on the study protocol and supervised by team lead. During data collection, all completed questionnaires were reviewed in real time to ensure data integrity.

Statistical analysis

Data (S1 File) were single-entered in Epi-Data (Epi-Data Association, Odense, Denmark) [14] impregnated with quality control measures namely skips, range and legal values, and alerts.

We used the Chi-squared test to assess differences in proportions of non-adherence to ART with categorical variables such as sex when the cell count was ≥5 and the Fisher’s exact test when the cell count was <5. We used the Student’s t-test to asses mean differences in non-adherence to ART with numerical variables like age when data were normally distributed, otherwise the Mann-Whitney U test was used for skewed data. Variables that demonstrated statistical significance at bivariate analysis and those deemed clinically relevant were considered for unadjusted and adjusted binary logistic regression analyses. In the multivariate regression analysis, we included tribe, marital status, level of income, current alcohol consumption, duration on ART, health education on ART related side effects, and HIV status disclosure. We stated the logistic regression analyses results using odds ratio (OR) and 95% confidence interval (CI). The reasons for non-adherence to ART were sorted, categorized, and tabulated, and then used to triangulate the quantitative findings. The overall analysis was performed in Stata version 15.1 [15], at 5% significance level.

Ethical issues

Participants who could read and write provided a written informed consent under no due influence of coercion. However, for participants who cannot read and write (those with no formal education), informed consent was obtained through thumb print. Prior to the acquisition of informed consent, the participants were provided information on the purpose of the study, benefits and possible psychological, social, and physical harms if any, and the reasons for their participation in the study. Ethical review and approval was obtained from Clarke International University Research Ethics Committee while administrative approval was obtained from TASO Gulu Institutional Review Board.

Study reporting

We followed the Strengthening of the Reporting of Observational Studies in Epidemiology (STROBE) guidelines [16, 17] and the ESPACOMP Medication Adherence Reporting Guidelines (EMERGE) [18] to report the study findings.

Results

Participants’ characteristics

Table 1 shows participant characteristics cross-tabulated by ART adherence. The mean age of all the participants was 42.5 years (standard deviation = 9.7 years). Participants adherent to ART were on average older than those who were non-adherent to ART: 42.5±9.7 versus 40.5±9.0 years, respectively (p = 0.314). There were statistically significant differences in non-adherence to ART with respect to ethnicity (p = 0.005), marital status (p = 0.004), household income (p = 0.020), duration on ART (p = 0.036), and current alcohol consumption (p<0.001). We observed no statistically significant difference in non-adherence to ART with regards to sex, educational level, employment status, time taken to reach the community-based drug distribution point, and disclosure of HIV status (all p>0.05).

Table 1. Characteristics of participants.

Non-adherent to ART
Participant characteristics No (n = 356, 93.4%) Yes (n = 25, 6.6%) Total (n = 381) P-value
Age category (years) 0.469
< 50 268 (92.7) 21 (7.3) 289
≥ 50 88 (95.7) 4 (4.3) 92
Mean ± SD 42.5±9.7 40.5±9.0 42.4±9.7 0.314
Sex 0.281
Male 119 (91.5) 11 (8.5) 130
Female 237 (94.4) 14 (5.6) 251
Tribe 0.005
Acholi 295 (95.2) 15 (4.8) 310
None Acholi 61 (85.9) 10 (14.1) 71
Current marital status 0.004
Married 178 (94.7) 10 (5.3) 188
Single 41 (82.0) 9 (18.0) 50
Separated 137 (95.8) 6 (4.2) 143
Educational level 0.473
None 95 (96.0) 4 (4.0) 99
Primary 197 (92.1) 17 (7.9) 214
Above primary 64 (94.1) 4 (5.9) 68
Employment type 0.067
Peasant 257 (94.5) 15 (5.5) 272
Self 82 (93.2) 6 (6.8) 90
Formal 17 (80.9) 4 (19.1) 21
Income per month (Ugandan Shillings) 0.020
≤100,000 273 (95.1) 14 (4.9) 287
>100,000 83 (88.3) 11 (11.7) 94
Duration on ART at time of study 0.036
≤5 years 179 (90.9) 18 (9.1) 197
>5 years 177 (96.2) 7 (3.8) 184
Time to reach the community drug distribution point in hours 1.000
≤ 1 102 (93.5) 7 (6.4) 109
>1 254 (93.4) 18 (6.6) 272
Current alcohol consumption <0.001
No 314 (95.4) 15 (4.6) 329
Yes 42 (80.8) 10 (19.2) 52
Ever disclosed HIV status 0.071
No 5 (71.4) 2 (28.6) 7
Yes 351 (93.9) 23 (6.2) 374

Level of ART adherence and reasons for non-adherence to ART

The data shows that 25 (6.6%, 93.5%; 4.3–9.5) participants were non-adherent to ART (Table 1). The reasons for non-adherence to ART is shown in Table 2, with the most common reason being forgetfulness, stress, and travels.

Table 2. Reasons for non-adherence to ART among patients.

Reasons Frequency Percentage
Forgetfulness 45 51.7
Gender based violence 3 3.4
Ran out of pills 4 4.6
Life stresses 12 13.8
On safari (travel to somewhere) 9 10.3
Medication fatigue 5 5.7
Admitted in hospital 5 5.7
Lacked transport to come for refill 4 4.6

Bivariate analysis of differences in non-adherence to ART

Table 3 shows differences in participant characteristics stratified by non-adherence to ART. No statistically significant difference was observed with respect to years lived with HIV, education on ART benefits and the need for lifelong ART, knowledge of present ART regimen, disclosure of HIV status, receipt of counseling in the past 3 months, and use of reminders to maximize ART adherence (all p>0.05).

Table 3. Bivariate analysis of differences in non-adherence to ART among PLHIV enrolled to community-based ART delivery model with health services related factors.

Non-adherent to ART
Participant characteristics No (n = 356, 93.4%) Yes (n = 25, 6.6%) Total (n = 381) P-value
Years alive since diagnosed with HIV 0.849
≤3 years 52 (92.9) 4 (7.1) 56
>3 years 304 (93.5) 21 (6.5) 325
Mean ± SD 7.8±3.40 6.9±3.25 7.8±3.39 0.197
Educated on benefits of taking ARVs 1.000
No 5 (100.0) 0 (0.0) 5
Yes 351 (93.3) 25 (6.7) 376
Knows ART is lifelong 0.612
No 14 (100.0) 0 (0.0) 14
Yes 342 (93.2) 25 (6.8) 367
Knows his/her current regimen 0.176
No 150 (91.5) 14 (8.5) 164
Yes 206 (94.9) 11 (5.1) 217
Attitude of health workers 0.422
Receptive 349 (93.6) 24 (6.4) 373
None receptive 7 (87.5) 1 (12.5) 8
Perceived waiting time at the community drug distribution point 0.154
Short/just okay 318 (94.1) 20 (5.9) 338
Long/longer 38 (88.4) 5 (11.6) 43
Received counseling in the past 3 months 0.750
No 275 (93.2) 20 (6.8) 295
Yes 81 (94.2) 5 (5.8) 86
Use reminders for ART adherence 0.652
No 99 (92.5) 8 (7.5) 107
Yes 257 (93.8) 17 (6.2) 274

Multivariate analysis of factors associated with non-adherence to ART

Table 4 summarized the unadjusted and adjusted analyses results. In the unadjusted analysis, non-adherence to ART was more likely among the non-Acholi (Unadjusted OR (uOR), 3.22; 95% CI, 1.38–752) and single or never married (uOR, 3.91, 95% CI, 1.49–10.23) participants. Also, income exceeding 100,000 Ugandan shillings (equivalent to 27 dollars) per month (uOR, 2.58; 95% CI, 1.13–5.91) and alcohol consumption (uOR, 4.98; 95% CI, 2.10–11.81) were associated with increased likelihood of non-adherence to ART. On the other hand, non-adherence to ART was less likely when the participant had separated (uOR, 0.78; 95% CI, 0.28–2.20), had been on ART for at least 5 years (uOR, 0.39; 95% CI, 0.16–0.96), had ever received health education about ART side effects (uOR, 0.24; 95% CI, 0.09–0.61), and had disclosed his/her HIV status (uOR, 0.16; 95% CI, 0.03–0.89).

Table 4. Results of logistic regression analysis of factors associated with non-adherence to ART among people living with HIV enrolled to community-based ART delivery model.

Binary logistic regression analysis
Participant characteristics Unadjusted analysis Adjusted analysis
OR 95% CI aOR 95% CI
Tribe
Acholi 1 1
None Acholi 3.22** (1.38,7.52) 1.49 (0.52,4.27)
Current marital status
Married 1 1
Single 3.91** (1.49,10.23) 1.97 (0.62,6.25)
Separated 0.78 (0.28,2.20) 0.76 (0.26,2.26)
Income per month (Ugandan Shillings)
≤100,000 1 1
>100,000 2.58* (1.13,5.91) 1.36 (0.52,3.55)
Current alcohol consumption
No 1 1
Yes 4.98*** (2.10,11.81) 3.24* (1.26,8.34)
Duration on ART at time of study
≤5 years 1 1
>5 years 0.39* (0.16,0.96) 0.60 (0.23,1.59)
Educated on ART side effects
No 1 1
Yes 0.24** (0.09,0.61) 0.36 (0.12,1.05)
Disclosed HIV status
No 1 1
Yes 0.16* (0.03,0.89) 0.37 (0.04,3.20)

Note: 1) * p < 0.05,

** p < 0.01,

*** p < 0.001 at 5% significance level; 2) All odds ratios (OR) are exponentiated with the 95% confidence intervals in brackets.

In the adjusted analysis, non-adherence to ART was significantly associated with alcohol consumption (Adjusted odds ratio (aOR), 3.24; 95% CI, 1.26–8.34). However, non-adherence to ART was not significantly associated with being a non-Acholi (aOR, 1.49; 95% CI, 0.52–4.27), single or never married (aOR, 1.97; 95% CI, 0.62–6.25) or separated (aOR, 0.76; 95% CI, 0.26–2.26), having monthly income exceeding 100,000 Ugandan shillings (aOR, 1.36; 95% CI, 0.52–3.55), being on ART for more than 5 years (aOR, 0.60; 95% CI, 0.23–1.59), ever receiving health education on ART side effects (aOR, 0.36; 95% CI, 0.12–1.05), and disclosure of HIV status (aOR, 0.37; 95% CI, 0.04–3.20).

Discussion

This study determined the prevalence of non-adherence to ART and the associated factors among PLHIV enrolled to the community-based ART delivery model in northern Uganda. Our data shows that 6.6% of PLHIV are non-adherent to ART and alcohol consumption increases ART non-adherence. The prevalence of non-adherence to ART in this study is slightly lower than the prevalence observed in previous observational studies [1921] but similar to another previous study in Uganda [22]. Our findings suggest that a small proportion of PLHIV enrolled to the community-based ART delivery model did not achieve the desired perfect adherence to ART of ≥95% [23]. The community-based ART delivery model therefore appears to have overcome most of the barriers to ART adherence due to improved access to HIV care to ≤5 km radius to one’s homestead. The model has made ART delivery more efficient and effective for both the health system and PLHIV. Besides this, the model provides appropriate support to PLHIV that promotes their long-term retention [9]. However, there is also the possibility that the low prevalence of non-adherence to ART is a reflection of enrolling participants who were likely to be adherent to ART. This further implies that non-adherence to ART cannot be ignored even amongst PLHIV who have proven record of good adherence to ART. Accordingly, strengthening adherence to ART through measures such as treatment supporter, continuous counseling on benefits of perfect ART adherence, use of personal reminders such as alarms and calendars among others is important. One of the main reasons cited for non-adherence to ART is forgetfulness and this is consistent with previous studies [24, 25]. The other reasons included shortage of pills, transportation challenges, and gender-based violence. Previous study medication fatigue [26], which is inconsistent with the reasons reported in this study.

The finding that alcohol consumption increases the likelihood of non-adherence to ART is consistent with several studies elsewhere [2729]. Indeed, alcohol consumption is a frequent problem among PLHIV [30, 31], more so among those on long term ART (≥6 years).Alcohol consumption has been reported to contribute to substantial number of deaths among PLHIV [32]. Our finding is thus not surprising because alcohol has a disinhibitory effect on cognitive functioning thus disrupting an individual’s normal behavior and reasoning. Alcohol consumption is a central cause of forgetfulness, non-adherence to clinical and counseling advice, and disruption of normal social life among others. These effects compromise adherence to ART. It is important to recognize that in our setting, many households brew alcohol to earn a living and access to alcohol is unrestricted provided one is able to buy. Accordingly, with no healthy public policies to regulate alcohol consumption in place, many PLHIV continue to access and drink alcohol. The community-based ART program therefore needs to strengthen the ongoing counseling to focus on the dangers of alcohol consumption namely possible interactions with anti-retroviral drugs, physical and mental health damage, and adverse socio-economic consequences such as loss of income and unemployment among others.

Our study has several strengths and limitations to consider. In terms of strengths, this is one of the few studies to underscore non-adherence to ART among PLHIV enrolled to the community-based ART delivery model in northern Uganda. We assessed non-adherence to ART across a representative sample of community drug distribution points, making these results generalizable to similar settings in Uganda and elsewhere. We used the Uganda Ministry of Health standard definition to distinguish adherence from non-adherence to ART. However, one of the limitations in this study is that adherence to ART was assessed through pill counts and the possibility of participants returning with incomplete number of pills during routine visits to the community drug distribution points cannot be ignored.

This study was conducted in a predominantly rural setting and the findings might not apply to an urban setting due to differences in socio-economic profiles and geographical access to health services. Another limitation is that alcohol consumption was measured as a self-reported response so social desirability bias remains a possibility. One study conducted in Southwestern Uganda showed that PLHIV tend to under report alcohol consumption [24]. Besides this, we did not use the alcohol use disorder identification test tool to grade alcohol consumption and to determine the association with non-adherence to ART. Lastly, since we conducted a cross-sectional study, our findings demonstrate association but not causation. Despite these limitations, our findings underscore that near perfect adherence to ART is possible among PLHIV enrolled to community-based ART delivery model in Uganda and possibly in similar settings.

In conclusion, our data shows that a small proportion of PLHIV enrolled to the community-based ART delivery model in northern Uganda are non-adherent to ART, suggesting the model has lessened most of the barriers to perfect ART adherence. However, alcohol consumption increases non-adherence to ART so ongoing psychosocial support is critical. These findings strengthens the evidence base for scaling up community-based ART delivery model in similar settings across developing countries.

Supporting information

S1 File. Dataset.

(DTA)

Acknowledgments

We thank the entire staff of TASO for providing routine clinical and psychosocial support to people living with HIV. We also thank people living with HIV for accepting to take part in this research. We are indebted to Clarke International University Research Ethics Committee for providing timely and quality review of the study protocol.

Data Availability

All relevant data are within the manuscript and its Supporting Information files.

Funding Statement

The authors received no specific funding for this work.

References

  • 1.UNAIDS. 90-90-90: Treatment for all 2020 [cited 2020 Jan 22]. Available from: https://www.unaids.org/en/resources/909090.
  • 2.Centers for Diseases Control and Prevention (CDC). Global statistics: the global HIV/AIDS epidemic 2020 [updated July 07, 2020; cited 2020 Oct 15]. Available from: https://www.hiv.gov/hiv-basics/overview/data-and-trends/global-statistics.
  • 3.AVERT. Is there a cure for HIV? 2019 [cited 2020 22 Jan]. Available from: https://www.avert.org/about-hiv-aids/cure.
  • 4.HIV/AIDS JUNPo. 90-90-90: an ambitious treatment target to help end the AIDS epidemic. Geneva: Joint United Nations Programme on HIV. AIDS. 2014:33.
  • 5.Mannheimer S, Friedland G, Matts J, Child C, Chesney M, AIDS TBCPfCRo. The consistency of adherence to antiretroviral therapy predicts biologic outcomes for Human Immunodeficiency Virus infected persons in clinical trials. Clinical Infectious Diseases. 2002;34(8):1115–21. 10.1086/339074 [DOI] [PubMed] [Google Scholar]
  • 6.Bartlett JA, DeMasi R, Quinn J, Moxham C, Rousseau F. Overview of the effectiveness of triple combination therapy in antiretroviral-naive HIV-1 infected adults. Acquired Immune Deficiency Syndromes. 2001;15(11):1369–77. 10.1097/00002030-200107270-00006 [DOI] [PubMed] [Google Scholar]
  • 7.Wagner GJ. Predictors of antiretroviral adherence as measured by self-report, electronic monitoring, and medication diaries. AIDS Patient Care and STDs. 2002;16(12):599–608. 10.1089/108729102761882134 [DOI] [PubMed] [Google Scholar]
  • 8.Republic of Uganda. Consolidated guidelines for prevention and treatment of HIV in Uganda. Kampala, Uganda: Ministry of Health, 2018.
  • 9.Okoboi S, Ssali L, Yansaneh IA, Bakanda C, Birungi J, Nantume S, et al. Factors associated with long-term antiretroviral therapy attrition among adolescents in rural Uganda: a retrospective study. Journal of International AIDS Society. 2016;19(Suppl 4):20841 10.7448/IAS.19.5.20841 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Okoboi S, Ding E, Persuad S, Wangisi J, Birungi J, Shurgold S, et al. Community-based ART distribution system can effectively facilitate long-term program retention and low-rates of death and virologic failure in rural Uganda. AIDS Research and Therapy. 2015;12(1):37 10.1186/s12981-015-0077-4 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.The AIDS Support Organization (TASO). TASO Gulu 2015 [cited 2015 Dec 3]. Available from: http://www.tasouganda.org/index.php/component/content/article?id=79.
  • 12.Izudi J, Adrawa N, Amongin D. Precancerous Cervix in Human Immunodeficiency Virus Infected Women Thirty Years Old and above in Northern Uganda. Journal of Oncology. 2016;2016:7 10.1155/2016/5473681 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Arya R, Antonisamy B, Kumar S. Sample size estimation in prevalence studies. Indian J Pediatr. 2012. November;79(11):1482–8. 10.1007/s12098-012-0763-3 [DOI] [PubMed] [Google Scholar]
  • 14.Lauritsen J, Bruus M. EpiData (version 3). A comprehensive tool for validated entry and documentation of data Odense: EpiData Association. 2003.
  • 15.StataCorp. Stata statistical software: Release 15. College Station, TX: StataCorp LLC. 2017;10:733.
  • 16.Vandenbroucke JP, Von Elm E, Altman DG, Gøtzsche PC, Mulrow CD, Pocock SJ, et al. Strengthening the Reporting of Observational Studies in Epidemiology (STROBE): explanation and elaboration. PLoS Medicine. 2007;4(10):e297 10.1371/journal.pmed.0040297 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Von Elm E, Altman DG, Egger M, Pocock SJ, Gøtzsche PC, Vandenbroucke JP, et al. The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) Statement: guidelines for reporting observational studies. International Journal of Surgery. 2014;12(12):1495–9. 10.1016/j.ijsu.2014.07.013 [DOI] [PubMed] [Google Scholar]
  • 18.De Geest S, Zullig LL, Dunbar-Jacob J, Helmy R, Hughes DA, Wilson IB, et al. ESPACOMP Medication Adherence Reporting Guideline (EMERGE). Ann Intern Med. 2018;169(1):30–5. 10.7326/M18-0543 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Bangsberg DR, Perry S, Charlebois ED, Clark RA, Roberston M, Zolopa AR, et al. Non-adherence to highly active antiretroviral therapy predicts progression to AIDS. Acquired Immune Deficiency Syndromes. 2001;15(9):1181–3. 10.1097/00002030-200106150-00015 [DOI] [PubMed] [Google Scholar]
  • 20.Paterson DL, Swindells S, Mohr J, Brester M, Vergis EN, Squier C, et al. Adherence to protease inhibitor therapy and outcomes in patients with HIV infection. Annals of Internal Medicine. 2000;133(1):21–30. 10.7326/0003-4819-133-1-200007040-00004 [DOI] [PubMed] [Google Scholar]
  • 21.Low-Beer S, Chan K, Yip B, Wood E, Montaner J, O'Shaughnessy MV, et al. Depressive symptoms decline among persons on HIV protease inhibitors. Journal of Acquired Immune Deficiency Syndromes. 2000;23(4):295–301. 10.1097/00126334-200004010-00003 [DOI] [PubMed] [Google Scholar]
  • 22.Oyugi J, Byakika-Tusiime J, Mugyenyi P, Mugerwa R, Guzman D, Charlebois E, et al., editors. Self-reported adherence measures are feasible and valid compared to multiple objective measures in Kampala, Uganda. Abstract presented at the Second IAS Conference on HIV Pathogenesis and Treatment, Paris; 2003.
  • 23.Republic of Uganda. Consolidated guidelines for the prevention and treatment of HIV and AIDS in Uganda. 2020.
  • 24.Bajunirwe F, Haberer JE, Boum Y II, Hunt P, Mocello R, Martin JN, et al. Comparison of Self-Reported Alcohol Consumption to Phosphatidylethanol Measurement among HIV-Infected Patients Initiating Antiretroviral Treatment in Southwestern Uganda. PloS One. 2014;9(12):e113152 10.1371/journal.pone.0113152 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Walsh JC, Horne R, Dalton M, Burgess AP, Gazzard BG. Reasons for non-adherence to antiretroviral therapy: patients’ perspectives provide evidence of multiple causes. AIDS Care. 2011;13:709–20. [DOI] [PubMed] [Google Scholar]
  • 26.Byakika-Tusiime J, Oyugi J, Tumwikirize W, Katabira E, Mugyenyi P, Bangsberg D. Adherence to HIV antiretroviral therapy in HIV+ Ugandan patients purchasing therapy. International Journal of STD & AIDS. 2005;16(1):38–41. 10.1258/0956462052932548 [DOI] [PubMed] [Google Scholar]
  • 27.Gordillo V, del Amo J, Soriano V, González-Lahoz J. Sociodemographic and psychological variables influencing adherence to antiretroviral therapy. Acquired Immune Deficiency Syndromes. 1999;13(13):1763–9. 10.1097/00002030-199909100-00021 [DOI] [PubMed] [Google Scholar]
  • 28.Ickovics JR, Cameron A, Zackin R, Bassett R, Chesney M, Johnson VA, et al. Consequences and determinants of adherence to antiretroviral medication: results from Adult AIDS Clinical Trials Group protocol 370. Antiviral Therapy. 2002;7(3):185–93. [DOI] [PubMed] [Google Scholar]
  • 29.Morojele NK, Kekwaletswe CT, Nkosi S. Associations between alcohol use, other psychosocial factors, structural factors and antiretroviral therapy (ART) adherence among South African ART recipients. AIDS and Behavior. 2014;18(3):519–24. 10.1007/s10461-013-0583-0 [DOI] [PubMed] [Google Scholar]
  • 30.McNabb J, Ross JW, Abriola K, Turley C, Nightingale CH, Nicolau DP. Adherence to highly active antiretroviral therapy predicts virologic outcome at an inner-city human immunodeficiency virus clinic. Clinical Infectious Diseases. 2001;33(5):700–5. 10.1086/322590 [DOI] [PubMed] [Google Scholar]
  • 31.Arnsten JH, Demas PA, Farzadegan H, Grant RW, Gourevitch MN, Chang C-J, et al. Antiretroviral therapy adherence and viral suppression in HIV-infected drug users: comparison of self-report and electronic monitoring. Clinical Infectious Diseases. 2001;33(8):1417–23. 10.1086/323201 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Mbonye M, Seeley J, Ssembajja F, Birungi J, Jaffar S. Adherence to antiretroviral therapy in Jinja, Uganda: a six-year follow-up study. PloS One. 2013;8(10):e78243 10.1371/journal.pone.0078243 [DOI] [PMC free article] [PubMed] [Google Scholar]

Decision Letter 0

Tim Mathes

9 Oct 2020

PONE-D-20-22867

Alcohol consumption increases non-adherence to ART among people living with HIV enrolled to the community-based care model in rural northern Uganda

PLOS ONE

Dear Dr. Izudi,

Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process.

Please submit your revised manuscript by Nov 23 2020 11:59PM. If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at plosone@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pone/ and select the 'Submissions Needing Revision' folder to locate your manuscript file.

Please include the following items when submitting your revised manuscript:

  • A rebuttal letter that responds to each point raised by the academic editor and reviewer(s). You should upload this letter as a separate file labeled 'Response to Reviewers'.

  • A marked-up copy of your manuscript that highlights changes made to the original version. You should upload this as a separate file labeled 'Revised Manuscript with Track Changes'.

  • An unmarked version of your revised paper without tracked changes. You should upload this as a separate file labeled 'Manuscript'.

If you would like to make changes to your financial disclosure, please include your updated statement in your cover letter. Guidelines for resubmitting your figure files are available below the reviewer comments at the end of this letter.

If applicable, we recommend that you deposit your laboratory protocols in protocols.io to enhance the reproducibility of your results. Protocols.io assigns your protocol its own identifier (DOI) so that it can be cited independently in the future. For instructions see: http://journals.plos.org/plosone/s/submission-guidelines#loc-laboratory-protocols

We look forward to receiving your revised manuscript.

Kind regards,

Tim Mathes

Academic Editor

PLOS ONE

Additional Editor Comments:

- STROBE is just a reporting guideline. So you cannot follow STROBE in “the design, conduct, and analysis of this study” (line 194). Please report all results according STROBE and ESPACOMP (https://www.equator-network.org/reporting-guidelines/espacomp-medication-adherence-reporting-guideline-emerge/).

- It should be described more clearly which predictors you included in the multivariate regression.

Journal Requirements:

When submitting your revision, we need you to address these additional requirements.

1. Please ensure that your manuscript meets PLOS ONE's style requirements, including those for file naming. The PLOS ONE style templates can be found at

https://journals.plos.org/plosone/s/file?id=wjVg/PLOSOne_formatting_sample_main_body.pdf and

https://journals.plos.org/plosone/s/file?id=ba62/PLOSOne_formatting_sample_title_authors_affiliations.pdf

2. Please include additional information regarding the survey or questionnaire used in the study and ensure that you have provided sufficient details that others could replicate the analyses. For instance, if you developed a questionnaire as part of this study and it is not under a copyright more restrictive than CC-BY, please include a copy, in both the original language and English, as Supporting Information.  If the original language is written in non-Latin characters, for example Amharic, Chinese, or Korean, please use a file format that ensures these characters are visible.

[Note: HTML markup is below. Please do not edit.]

Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: Partly

Reviewer #2: Partly

**********

2. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: No

Reviewer #2: Yes

**********

3. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

Reviewer #2: Yes

**********

4. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: No

Reviewer #2: Yes

**********

5. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: 1. I found the authors digressing away from their research questions in the discussion and taking away more value from the study. The discussion should have focused on the effects of alcohol consumption on adherence.

2. Assumptions made in the determination of the sample size are unclear.

3. Yes

4. There are a lot of grammatical areas in the manuscript.

Reviewer #2: 1. Could you check out the entire manuscript for typos and missing words eg line 85?

Introduction

1.The second sentence of the introduction grossly misrepresents facts on the population in the east and Southern Africa.

2. Literature about factors associated with ART non adherence seem to be readily available. The value of this paper could be on how the community based ART delivery model helps to improve adherence to ART or why this model fails to address alcohol as a barrier to ART adherence. This is because previous studies have reported being single/never married, poverty/less income, fatigue/side effects as reasons/factors associated with non adherence to ART. Health education and disclosure as facilitators of ART. Your study maintains disclosure and health education as being associated with ART adherence in addition to turning previously reported barriers of being single/never married, side effects and less income to not being associated with non adherence. Could the previously reported barriers now turned into being not associated with non adherence be attributed to community ART delivery model?

3. The authors term this study as cross sectional though on further reflection, one wonders whether this was really the right study design. The fact that the authors refer to a drug refill prior to data collection and that at the point of data collection when non adherence was determined, leave one wondering whether this was not a cohort study with a retrospective /prospective start. with cross sectional design, the exposure and outcome happen at the same time. For the current study, the exposure which were the drugs were given earlier and the outcome which was non adherence was determined later. this is typical of cohort Alternatively, this could be a case control study design. Participants were recruited by virtual of being cases/non adherent and worked backwards to determine what could have been the exposure. Considering the above, the manuscript will require reanalysis.

4.Abreviations like CDPPS ought to be written out prior to their use see line 120

5. Prior description of TASO Gulu need to be referenced too.

6. It is not clear why authors did not use non adherence to ART in earlier studies in sample size estimation when the subject is heavily researched.

7. How did the 99 participants with zero education give a written informed consent?

8. Isn't low prevalence of none adherence in this study a reflection of the eligibility criteria to start accessing ART through the community based ART delivery model? This brings in focus the study having been carried out among participants that are likely to be adherent to ART. Also this should have been discussed in the discussion section.

9.The discussion section ought to be structured in such a way that reflects how the community based ART delivery model helps to overcome non adherence to ART than the current format that reproduces what we already know.

10. The conclusion too should reflect to what extent does the community based ART delivery model overcomes barriers to ART non adherence.

**********

6. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

If you choose “no”, your identity will remain anonymous but your review may still be made public.

Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #1: Yes: Dr Munyaradzi Madhombiro

Reviewer #2: No

[NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files.]

While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Registration is free. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email PLOS at figures@plos.org. Please note that Supporting Information files do not need this step.

Attachment

Submitted filename: PLOS Review Alcohol consumption increases non.docx

PLoS One. 2020 Nov 24;15(11):e0242801. doi: 10.1371/journal.pone.0242801.r002

Author response to Decision Letter 0


15 Oct 2020

Reviewer #1:

1. I found the authors digressing away from their research questions in the discussion and taking away more value from the study. The discussion should have focused on the effects of alcohol consumption on adherence.

Author’s response: Thank you for this comment. We have revised the discussion and have focused on effects of alcohol consumption on adherence to ART. We have deleted the earlier discussions on non-significant finings.

2. Assumptions made in the determination of the sample size are unclear.

Yes

Authors’ response: We have revised the description of sample size estimation and it reads: “Using Yamane’s formula shown below, we estimated that 381 participants were needed for this study based on the following assumptions: 95% confidence limit, 5% precision (sampling error), and an estimated 8,000 PLHIV enrolled to the community-based ART delivery model. Sample size (n) = N/1+N(e)2, where N is the total number of PLHIV enrolled to the community-based ART delivery model = 8,000 PLHIV and e is the maximum allowable error = 5% or 0.05. Accordingly, n = 8000/1+8000(0.05)2 = 380.9 ≈ 381.”

4. There are a lot of grammatical areas in the manuscript.

Authors’ response: We have checked the entire manuscript and have addressed all the typos/grammatical errors.

Reviewer #2:

1. Could you check out the entire manuscript for typos and missing words e.g. line 85?

Authors’ response: We have critically checked the manuscript for typos and missing words. The revised manuscript now has no missing words and typos.

Introduction

1. The second sentence of the introduction grossly misrepresents facts on the population in the east and Southern Africa.

Authors’ response: We have updated the data on people living with HIV in east and southern Africa using the updated data from the Centers for Disease Control and Prevention. Please refer to reference # 2.

2. Literature about factors associated with ART non adherence seem to be readily available. The value of this paper could be on how the community based ART delivery model helps to improve adherence to ART or why this model fails to address alcohol as a barrier to ART adherence. This is because previous studies have reported being single/never married, poverty/less income, fatigue/side effects as reasons/factors associated with non-adherence to ART. Health education and disclosure as facilitators of ART. Your study maintains disclosure and health education as being associated with ART adherence in addition to turning previously reported barriers of being single/never married, side effects and less income to not being associated with non-adherence. Could the previously reported barriers now turned into being not associated with non-adherence be attributed to community ART delivery model?

Authors’ response: Thank you for this comment. We have revised the discussion section and have now focused on alcohol consumption and non-adherence to ART. In the earlier submission, we had discussed both significant and non-significant results. Now, the latter discussions have been deleted to avoid deviation/or digression.

3. The authors term this study as cross sectional though on further reflection, one wonders whether this was really the right study design. The fact that the authors refer to a drug refill prior to data collection and that at the point of data collection when non adherence was determined, leave one wondering whether this was not a cohort study with a retrospective /prospective start. With cross sectional design, the exposure and outcome happen at the same time. For the current study, the exposure which were the drugs were given earlier and the outcome which was non adherence was determined later. This is typical of cohort. Alternatively, this could be a case control study design. Participants were recruited by virtual of being cases/non adherent and worked backwards to determine what could have been the exposure. Considering the above, the manuscript will require reanalysis.

Authors’ response: We are grateful for this comment. We did not follow-up a group of individuals initiated on ART, either prospectively or retrospectively. We assessed adherence to ART through pill counts and collected data on factors associated with non-adherence at same point in time. Since both the outcome and exposures were assessed at same point in time, we thought this fits a cross-sectional study design. We have made slight revision in the description of the study design for clarity and it reads: “We used an analytic cross-sectional study design since the outcome (non-adherence to ART) and the associated factors (exposures) were assessed at the same point in time.” We hope this is acceptable now.

4. Abbreviations like CDPPS ought to be written out prior to their use see line 120

Authors’ response: Thank you. We have fully defined this abbreviation and have revised the sentence for clarity and it reads: “For TASO Gulu, there are about 80 community drug distribution points (sites for delivery of community-based ART) spread across the 6 districts of Gulu, Nwoya, Amuru, Pader, Oyam, and Omoro, all in northern Uganda.”

5. Prior description of TASO Gulu need to be referenced too.

Author’s response: We have provided a reference now. Please refer to reference #9.

6. It is not clear why authors did not use non adherence to ART in earlier studies in sample size estimation when the subject is heavily researched.

Authors’ response: Thank you for this comment. We agree that adherence to ART has been researched in some parts of Uganda, predominantly in urban settings. We deemed that estimates in prior studies might not accurately estimate the sample size for our setting. This is because our setting is predominantly rural, post-conflict, and most of the people are socio-economically poor. It was these differences alongside the assumptions that we have described that made us to calculate a sample size specific to our context. We propose to maintain the estimate. Thank you.

7. How did the 99 participants with zero education give a written informed consent?

Author’s response: We presume the 99 participants referred to here are those participants without formal education as shown in Table 1. For such participants, informed consent was obtained through thumb prints. We have made a slight revision in the ethical issues section to this effect and it reads: “However, for participants who cannot read and write (those with no formal education), informed consent was obtained through thumb print.”

8. Isn't low prevalence of none adherence in this study a reflection of the eligibility criteria to start accessing ART through the community based ART delivery model? This brings in focus the study having been carried out among participants that are likely to be adherent to ART. Also this should have been discussed in the discussion section.

Authors’ response: We have discussed the implication of the eligibility criteria now. The new sentence reads in part: “However, there is also the possibility that the low prevalence of non-adherence to ART is a reflection of enrolling participants who were likely to be adherent to ART. This further implies that non-adherence to ART cannot be ignored even amongst PLHIV who have proven record of good adherence to ART.”

9. The discussion section ought to be structured in such a way that reflects how the community based ART delivery model helps to overcome non adherence to ART than the current format that reproduces what we already know.

Authors’ response: We are grateful for this comment. We have now focused the discussion on the role of community-based ART in overcoming barriers to adherence. We have removed redundant discussions.

We have include a new sentence that reads: “The community-based ART delivery model therefore appears to have overcome most of the barriers to ART adherence due to improved access to HIV care to ≤5 km radius to one’s homestead. The model has made ART delivery more efficient and effective for both the health system and PLHIV. Besides this, the model provides appropriate support to PLHIV that promotes their long-term retention.”

10. The conclusion too should reflect to what extent does the community based ART delivery model overcomes barriers to ART non adherence.

Authors’ response: We have incorporated this change in the revised manuscript. The revised conclusion reads:

“In conclusion, our data shows that a small proportion of PLHIV enrolled to the community-based ART delivery model in northern Uganda are non-adherent to ART, suggesting the model has lessened most of the barriers to perfect ART adherence. However, alcohol consumption increases non-adherence to ART so ongoing psychosocial support is critical. These findings strengthens the evidence base for scaling up community-based ART delivery model in similar settings across developing countries.”

Decision Letter 1

Tim Mathes

23 Oct 2020

PONE-D-20-22867R1

Alcohol consumption increases non-adherence to ART among people living with HIV enrolled to the community-based care model in rural northern Uganda

PLOS ONE

Dear Dr. Izudi,

Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that consideres the previously raised additional editor comments: 

- STROBE is just a reporting guideline. So you cannot follow STROBE in “the design, conduct, and analysis of this study” (line 194). Please report all results according STROBE and ESPACOMP (https://www.equator-network.org/reporting-guidelines/espacomp-medication-adherence-reporting-guideline-emerge/).

- It should be described more clearly which predictors you included in the multivariate regression.

The original revision should be supplemented by these suggestions. 

Please submit your revised manuscript by 29.10.2020. If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at plosone@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pone/ and select the 'Submissions Needing Revision' folder to locate your manuscript file.

Please include the following items when submitting your revised manuscript:

  • A rebuttal letter that responds to each point raised by the academic editor and reviewer(s). You should upload this letter as a separate file labeled 'Response to Reviewers'.

  • A marked-up copy of your manuscript that highlights changes made to the original version. You should upload this as a separate file labeled 'Revised Manuscript with Track Changes'.

  • An unmarked version of your revised paper without tracked changes. You should upload this as a separate file labeled 'Manuscript'.

If you would like to make changes to your financial disclosure, please include your updated statement in your cover letter. Guidelines for resubmitting your figure files are available below the reviewer comments at the end of this letter.

If applicable, we recommend that you deposit your laboratory protocols in protocols.io to enhance the reproducibility of your results. Protocols.io assigns your protocol its own identifier (DOI) so that it can be cited independently in the future. For instructions see: http://journals.plos.org/plosone/s/submission-guidelines#loc-laboratory-protocols

We look forward to receiving your revised manuscript.

Kind regards,

Tim Mathes

Academic Editor

PLOS ONE

[Note: HTML markup is below. Please do not edit.]

[NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files.]

While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Registration is free. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email PLOS at figures@plos.org. Please note that Supporting Information files do not need this step.

PLoS One. 2020 Nov 24;15(11):e0242801. doi: 10.1371/journal.pone.0242801.r004

Author response to Decision Letter 1


23 Oct 2020

Editor comments:

1. STROBE is just a reporting guideline. So you cannot follow STROBE in “the design, conduct, and analysis of this study” (line 194). Please report all results according STROBE and ESPACOMP (https://www.equator-network.org/reporting-guidelines/espacomp-medication-adherence-reporting-guideline-emerge/).

Authors’ responses: Thank you. We have revised the sentence and it now reads: “We followed the Strengthening of the Reporting of Observational Studies in Epidemiology (STROBE) guidelines and the ESPACOMP Medication Adherence Reporting Guidelines (EMERGE) to report the study findings.”

2. It should be described more clearly which predictors you included in the multivariate regression.

Authors’ responses: We have described the predictors in the multivariate regression analysis. The new sentence reads: “In the multivariate regression analysis, we included tribe, marital status, level of income, current alcohol consumption, duration on ART, health education on ART related side effects, and HIV status disclosure.”

3. The original revision should be supplemented by these suggestions.

Authors’ responses: Thank you. We have supplemented the original version of the manuscript with the aforementioned suggestions.

Decision Letter 2

Tim Mathes

10 Nov 2020

Alcohol consumption increases non-adherence to ART among people living with HIV enrolled to the community-based care model in rural northern Uganda

PONE-D-20-22867R2

Dear Dr. Izudi,

We’re pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it meets all outstanding technical requirements.

Within one week, you’ll receive an e-mail detailing the required amendments. When these have been addressed, you’ll receive a formal acceptance letter and your manuscript will be scheduled for publication.

An invoice for payment will follow shortly after the formal acceptance. To ensure an efficient process, please log into Editorial Manager at http://www.editorialmanager.com/pone/, click the 'Update My Information' link at the top of the page, and double check that your user information is up-to-date. If you have any billing related questions, please contact our Author Billing department directly at authorbilling@plos.org.

If your institution or institutions have a press office, please notify them about your upcoming paper to help maximize its impact. If they’ll be preparing press materials, please inform our press team as soon as possible -- no later than 48 hours after receiving the formal acceptance. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information, please contact onepress@plos.org.

Kind regards,

Tim Mathes

Academic Editor

PLOS ONE

Additional Editor Comments (optional):

Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. If the authors have adequately addressed your comments raised in a previous round of review and you feel that this manuscript is now acceptable for publication, you may indicate that here to bypass the “Comments to the Author” section, enter your conflict of interest statement in the “Confidential to Editor” section, and submit your "Accept" recommendation.

Reviewer #1: All comments have been addressed

Reviewer #2: All comments have been addressed

**********

2. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: Yes

Reviewer #2: Yes

**********

3. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: Yes

Reviewer #2: Yes

**********

4. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

Reviewer #2: Yes

**********

5. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: Yes

Reviewer #2: Yes

**********

6. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: Dear Editor

The authors have attended to all my concerns. Well done This will contribute significantly to the improvement in HIV treatment outcomes. I do give them a go ahead.

Reviewer #2: 1. Introduction section; the second sentence (line 61-62) should be revised for better clarity.

2. Ethical issues under the methods section, was the informed consent witnessed in both situations of participants who could and could not write/read?

**********

7. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

If you choose “no”, your identity will remain anonymous but your review may still be made public.

Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #1: Yes: Dr M Madhombiro

Reviewer #2: Yes: Dominic Bukenya

Acceptance letter

Tim Mathes

13 Nov 2020

PONE-D-20-22867R2

Alcohol consumption increases non-adherence to ART among people living with HIV enrolled to the community-based care model in rural northern Uganda

Dear Dr. Izudi:

I'm pleased to inform you that your manuscript has been deemed suitable for publication in PLOS ONE. Congratulations! Your manuscript is now with our production department.

If your institution or institutions have a press office, please let them know about your upcoming paper now to help maximize its impact. If they'll be preparing press materials, please inform our press team within the next 48 hours. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information please contact onepress@plos.org.

If we can help with anything else, please email us at plosone@plos.org.

Thank you for submitting your work to PLOS ONE and supporting open access.

Kind regards,

PLOS ONE Editorial Office Staff

on behalf of

Dr. Tim Mathes

Academic Editor

PLOS ONE

Associated Data

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

    Supplementary Materials

    S1 File. Dataset.

    (DTA)

    Attachment

    Submitted filename: PLOS Review Alcohol consumption increases non.docx

    Data Availability Statement

    All relevant data are within the manuscript and its Supporting Information files.


    Articles from PLoS ONE are provided here courtesy of PLOS

    RESOURCES