Abstract
Measuring adherence has been a priority for researchers to help inform effective care for patients regularly consuming medications for chronic conditions. As a widely accepted “gold standard” adherence measure or operational definition does not exist, studies measure adherence using different modalities, which may lead to different conclusions about adherence patterns. The purpose of the scoping review was to identify modalities used to measure adherence to HIV medication, diabetes medication, and nutritional supplementation and explore the variation in adherence definitions, measurement modalities, and psychometric properties being reported across studies. Comprehensive searches were performed in PubMed, Scopus, and PsycINFO from January 2012 to January 2022. We included studies reporting psychometric properties of adherence/compliance to HIV medication, diabetes medication, or nutritional supplements. In total, we included 88 studies in the review. The 8-item Morisky Medication Adherence Scale (MMAS-8) was the most frequently used self-reported measure. We found almost no relationship between country income level and triangulation levels. The operational definition of adherence fell into four categories: numerical, dichotomous, ranked ordinal, and undefined. The amount of variation in an adherence definition category within a modality depended on whether the measures within the modality could be assessed numerically and whether widely accepted cutoffs existed for the measure. Across studies, 46 (52%) reported both validity and reliability, 28 (31%) reported validity only, and 14 (16%) reported reliability only. Fourteen types of validity and six types of reliability were identified across the studies. Measuring adherence accurately and reliably continues to be a challenge for research in HIV, diabetes, and nutritional supplementations. When reporting adherence measurements, we suggest including adherence results from multiple measures and modalities, presenting adherence results numerically, and reporting multiple types of validity and reliability.
Keywords: validity, reliability, medication adherence
Background
Suboptimal adherence to medications often hinders effective care for patients who regularly consume medications over prolonged periods.1 High levels of suboptimal adherence and nonadherence can lead to increased morbidity and mortality across illnesses.2 Diabetes, HIV, and micronutrient deficiencies are three chronic public health conditions that can be managed or ameliorated by adhering to medication treatments. We explored HIV and diabetes due to the large body of literature on adherence within the health topics. We included nutrition because this paper is part of a larger project on adherence to nutritional supplements.
Current estimates indicate that adherence to treatment remains low for all three conditions. While 38.4 million people worldwide lived with HIV in 2021, on average, only about 60% adhered to antiretroviral therapy guidelines.3–7 Adherence can prevent viral drug resistance, slow HIV progression, and reduce the risk of HIV transmission.8 Worldwide, 537 million adults lived with diabetes in 2021, and treatment adherence ranged from 38.5 to 93.1%.9,10 Adherence to diabetes treatments such as insulin or oral hypoglycemic medication can help control hyperglycemia and prevent vision loss, limb amputations, and myocardial infarction.11 Finally, one in three people around the world is estimated to have a micronutrient deficiency.12 Data on adherence to micronutrient supplements largely focuses on adherence to iron supplements in women of reproductive age, especially pregnant women. A study exploring iron folic acid adherence for pregnant women in 22 countries with high burdens of undernutrition found that only 8% of pregnant women adhered to the ideal iron folic acid supplementation schedule.13 While the effects of micronutrient deficiencies depend on the micronutrient, they can cause weakness, brain damage, and increase the risk of severe infections.14–17
The World Health Organization defines adherence as “the extent to which a person’s behavior (including medication-taking) corresponds with agreed recommendations from a health care provider”.2 Most researchers agree on the conceptual definition of adherence, but there is no consensus on its operational definition, mostly because a widely accepted “gold standard” adherence measure or operational definition does not exist. Studies measure adherence using different modalities (including self-reports and blood samples), which may lead to different conclusions about adherence patterns.
We define modalities of adherence measurement as channels used to assess adherence or the way that adherence information is collected. We define measures as the means of data collection that can fall within a modality. For example, questionnaires, pill counts (self-reported), in-person interviews, and telephone interviews are measures under the self-report modality. Adherence measures also fall under two categories: direct and indirect measures. Direct measures assess the concentration of a medicine in the body. Indirect measures do not assess the amount of the medication in the body but measure something approximating the amount of the medication ingested. For example, self-reported questionnaires may ask about medication-taking habits to approximate the concentration of medications in participants.
Multiple operational definitions and measurement modalities of adherence can pose research challenges such as inconsistent results and conclusions. When different adherence measurement methods are used, comparing results across studies and identifying erroneous results can be more difficult. However, because there is not a commonly agreed upon gold standard to assess adherence, triangulation may be the most viable strategy for assessing and reporting adherence. Triangulation (ie, relying on multiple measures or modalities) can increase the rigor of research findings by limiting the impact of bias or error associated with any one method and demonstrating similar findings across different adherence measurement methods.18
The purpose of this scoping review is to identify methods and modalities used to measure adherence. We focus specifically on HIV medication, diabetes medication, and nutritional supplementation and explore the variation in adherence definitions, measurement modalities, and psychometric property reporting across studies.
Methods
We conducted this scoping review largely following the methodology published by Peters et al.19 The Preferred Reporting Items for Systematic Reviews and Meta-Analyses extension for scoping review (PRISMA-ScR) reporting guideline was used (Supplementary Material 1 PRISMA-ScR Checklist).20
We searched three databases for studies on psychometric properties of adherence measurements: PubMed, PsycINFO, and Scopus. The search strategy included three sections: treatment adherence/compliance terms, study area terms (ie, HIV, diabetes, or nutritional supplementation terms), and psychometric terms (Supplementary Material 2 Search Strategy). The PubMed search included both MeSH and text word search field tabs. The PsycINFO and Scopus searches included title, abstract, and keyword search field tabs. We included both “adherence” and “compliance” as search terms in our strategy because the terms are often used interchangeably.21–23 The search ran in May 2022, and we uploaded all papers resulting from our search strategy onto Covidence.
Inclusion and Exclusion Criteria
We included only peer-reviewed, primary research studies written in English. We limited our review to studies published between January 1, 2012, to January 1, 2022, those that reported psychometric properties of adherence/compliance (ie, validity, reliability) and had adherence or compliance to HIV or diabetes medications or nutritional supplements as a behavioral outcome. However, we included glucose monitor articles if they met all other inclusion criteria except having an adherence/compliance behavioral outcome. Many anti-diabetic drugs influence glucose levels, so we included glucose monitors as they have been used as proxies for adherence.
We excluded studies that explored adherence or compliance but did not present data on the psychometric properties of adherence or compliance measures. For example, some studies reported the level of nutritional supplementation adherence in a community and identified individual- and community-level factors that were associated with nutritional supplementation adherence such as education or income. However, we excluded these studies because they did not report any psychometric data on their adherence data.
Selection Process
All studies from the database searches were uploaded into Covidence, which automatically deleted duplicate studies. One reviewer then manually screened the studies in Covidence for duplicates. Two reviewers then performed initial screenings on ten articles based on an article’s title, abstract, and keywords. The reviewers had 90% agreement. After resolving the disagreement through consensus, one reviewer completed the title, abstract, keyword, and full-text screening for the rest of the articles. Occasionally, the second reviewer assisted in article screening when the first reviewer was unsure if the article should be included.
Data Charting Process
We developed an extraction form in Covidence to facilitate the extraction process. Two members of the research team piloted the form on five articles to ensure information was captured consistently and completely. We did not revise the extraction table. The rest of the data were single-extracted, and two research team members reviewed the completed extraction table.
Data Items
The extracted variables included: general article information (title, authors, year of publication, funding, possible conflicts of interest), study characteristics (aims, study topic area, eligibility criteria, country, country income level), intervention characteristics (adherence measure type, adherence measure name, adherence definitions, validity calculations, reliability calculations), population characteristics (sample size, age, sex), study findings and conclusions.
Synthesis of Results
We explored the frequency and type of modality and measure used by health topic (ie, HIV, diabetes, and nutrition). In each study, the researchers only looked at the psychometric properties of adherence for one health topic. We examined differences in adherence definition categories by measures and modalities. We analyzed triangulation of adherence modalities and measures by country income group. Finally, we looked at the distribution of validity and reliability data by health topic.
Results
The review identified 591 articles across PubMed, PsycINFO, and Scopus that met the inclusion criteria. After removing duplicates, we screened titles, abstracts, and keywords for 494 articles and excluded 354 articles, mainly because they did not focus on adherence or compliance to HIV or diabetes medications or nutritional supplements. After a full-text screening of 140 articles, we excluded 62 more articles. In total, we included 78 articles in the review, which corresponded to 88 studies as some articles contained multiple studies (Table 1). The PRISMA-ScR flowchart (Figure 1) shows the screening process.
Table 1.
Overview of Study Characteristics
| Study | Health Topic | Country | Modalities | Measures | Adherence Definition Category | Validity/Reliability Types |
|---|---|---|---|---|---|---|
| Teshome et al 201824 | Nutrition | Kenya | (1) Blood sample (2) Electronic record (3) Pill count (non-self-reported) (4) Self-reports |
(1) Hemoglobin concentration (2) Medication event monitoring system (3) Sachet count (4) Self-reporting sheet |
(1) N/A (2) Dichotomous (3) Dichotomous (4) Dichotomous |
Uncategorized Validity, Uncategorized Reliability |
| Agala et al 202025 | HIV | Ethiopia | (1) Self-reports | (1) Simplified Medication Adherence Questionnaire | (1) Dichotomous | Internal Consistency Reliability, Concurrent Validity |
| Agot et al 201526 | HIV | Kenya, South Africa, and Tanzania | (1) Blood sample (2) Self-reports (3) Pill count (non-self-reported) |
(1) Plasma and intracellular drug concentration (2) In-person interview (3) Pill count |
(1) Ranked ordinal (2) Ranked ordinal (3) Dichotomous |
Positive Predictive Value |
| Amico et al 201427 | HIV | Peru, Brazil, Ecuador, the United States, Thailand, and South Africa | (1) Blood sample (2) Pill count (non-self-reported) (3) Self-reports (4) Pharmacy record (5) Self-report |
(1) TFV-DP concentration (2) In-clinic pill count (3) In-person interview (4) Medication possession ratio (5) Computer-assisted self-interview |
(1) Dichotomous (2) Ranked ordinal (3) Ranked ordinal (4) Ranked ordinal (5) Ranked ordinal |
Criterion Validity |
| Berg et al 201228 | HIV | United States | (1) Blood sample (2) Self-reports (3) Self-reports (4) Self-reports (5) Self-reports (6) Self-reports |
(1) Viral load (2) Rating questionnaire (3) Frequency questionnaire (4) Percent questionnaire (5) Visual analog scale (6) Community Programs for Clinical Research on AIDS |
(1) N/A (2) Dichotomous (3) Dichotomous (4) Dichotomous (5) Dichotomous (6) Dichotomous |
Construct Validity, Inter-Instrument Reliability |
| Bucek et al 202029 | HIV | United States | (1) Blood sample (2) Self-reports |
(1) Viral load (2) Pill count |
(1) Dichotomous (2) Numerical |
Uncategorized Reliability |
| Bulgiba et al 201330 | HIV | Malaysia | (1) Blood sample (2) Self-reports |
(1) Therapeutic drug monitoring (2) Adult AIDS Clinical Trials Group Adherence questionnaire |
(1) Numerical (2) Numerical |
Sensitivity, Specificity, Negative Predictive Value, Positive Predictive Value |
| Castillo-Mancilla et al 201531 | HIV | United States | (1) Pharmacy record (2) Blood sample (3) Blood sample |
(1) Average days between pharmacy refills (2) Dried blood spots (3) Peripheral blood mononuclear cells |
(1) Numerical (2) Dichotomous (3) Dichotomous |
Uncategorized Reliability |
| Chai et al 202232 | HIV | United States | (1) Pill count (non-self-reported) (2) Blood sample (3) Electronic record |
(1) Pill count (2) Dried blood spot (3) Digital pill system |
(1) Numerical (2) Dichotomous (3) Numerical |
Uncategorized Reliability |
| Da et al 201833 | HIV | China | (1) Blood sample (2) Self-reports (3) Self-reports (4) Self-reports (5) Self-reports |
(1) Viral load (2) One-month days missed adherence questionnaire (3) One-month days taken adherence questionnaire (4) 3-day adherence questionnaire (5) Weekend adherence questionnaire |
(1) Dichotomous (2) Dichotomous (3) Dichotomous (4) Dichotomous (5) Dichotomous |
Sensitivity, Specificity, Inter-Instrument Reliability, Criterion Validity |
| Desmond et al 201534 | HIV | South Africa | (1) Blood sample (2) Self-reports (3) Pharmacy record |
(1) Plasma concentration (2) Maternal verbal reports (3) Pharmacy returns |
(1) Dichotomous (2) Dichotomous (3) Numerical |
Specificity, Sensitivity, Negative Predictive Value, Positive Predictive Value |
| Dima et al 201335 | HIV | Romania | (1) Pill count (non-self-report) (2) Blood sample (3) Medical record (4) Self-reports |
(1) Unannounced pill counts (2) Viral load (3) Doctor’s assessment (4) Cuestionario para la Evaluacion de la Adhesion al Tratamiento Antirretroviral en Personas con Infeccion por VIH y Sida |
(1) Ranked ordinal (2) Dichotomous (3) Ranked ordinal (4) Dichotomous |
External Criterion Validity, Internal Consistency Reliability |
| Dowshen et al 201336 | HIV | United States | (1) Self-reports (2) Self-report |
(1) Visual analog scale (2) Interactive text message response |
(1) Numerical (2) Numerical |
Uncategorized Validity |
| Fredericksen et al 201437 | HIV | United States | (1) Pill count (non-self-reported) (2) Self-reports |
(1) Unannounced home-based pill counts (2) Unannounced phone-based pill counts |
(1) Numerical (2) Numerical |
Inter-Instrument Reliability |
| Haberer et al 201238 | HIV | United States | (1) Blood sample (2) Pill count (non-self-reported) (3) Electronic record |
(1) CD4 count (2) Unannounced pill count (3) Med-eMonitor |
(1) Dichotomous (2) Numerical (3) Numerical |
Uncategorized Validity |
| Hettema, Hosseinbor, and Ingersoll 201239 | HIV | United States | (1) Electronic record (2) Self-reports |
(1) Interactive voice response system (2) Timeline follow back |
(1) Dichotomous (2) Dichotomous |
Inter-Instrument Reliability |
| Holstad et al 201940 | HIV | United States | (1) Self-reports (2) Electronic record |
(1) Pill count participant survey (2) Picture Pill Count Scoring Instrument |
(1) N/A (2) N/A |
Uncategorized Validity, Internal Consistency Reliability, test-retest reliability |
| Johnston et al 201941 | HIV | South Africa | (1) Electronic record (2) Hair sample (3) Blood sample |
(1) Electronic adherence monitoring device (2) Hair efavirenz concentrations (3) Blood efavirenz concentrations |
(1) N/A (2) N/A (3) N/A |
Uncategorized Reliability |
| Kagee and Nel 201242 | HIV | South Africa | (1) Blood sample (2) Self-reports |
(1) Viral load (2) Study questionnaire |
(1) Dichotomous (2) Numerical |
Internal Consistency Reliability, Uncategorized Reliability |
| Kelly et al 201343 | HIV | Sierra Leone | (1) Pill count (non-self-report) (2) Self-reports (3) Self-reports (4) Self-reports |
(1) Unannounced pill counts (2) Visual analog scale (3) Adult AIDS Trial Group questionnaire (4) 7-day adherence measure questionnaire |
(1) Numerical (2) Numerical (3) Numerical (4) Numerical |
Criterion Validity, Uncategorized Reliability |
| Kerr et al 201244 | HIV | Thailand | (1) Blood sample (2) Self-reports (3) Self-reports |
(1) Viral load (2) Visual analog scale (3) Center for Adherence Support Evaluation adherence index |
(1) Dichotomous (2) Dichotomous (3) Dichotomous |
Specificity, Sensitivity |
| Mariani et al 202045 | HIV | Brazil | (1) Blood sample (2) Blood sample |
(1) Abbott RealTime HIV-1 viral load assay (2) The mPIMA HIV-1/2 viral load plasma test |
(1) N/A (2) N/A |
Sensitivity, Specificity, Uncategorized Reliability |
| Mugisha 201246 | HIV | Brazil, UK, Ireland, Spain, Italy, Australia, Uganda, South Africa | (1) Self-reports (2) Blood sample (3) Blood sample |
(1) Study-specific questionnaire (2) Viral load (3) Mean corpuscular volume |
(1) N/A (2) Dichotomous (3) N/A |
Negative Predictive Value, Positive Predictive Value |
| Pellowski, Kalichman, and Finitsis 201547 | HIV | United States | (1) Pill count (non-self-report) (2) Blood sample (3) Self-reports (4) Self-reports |
(1) Unannounced pill counts (2) Viral load (3) Computerized single item rating scale (4) Single item rating scale telephone interview |
(1) Numerical (2) Dichotomous (3) Numerical (4) Numerical |
Concurrent Validity, Criterion Validity, Predictive Validity, Test-Retest Reliability |
| Rekić et al 201348 | HIV | Italy, Norway, France | (1) Other | (1) Bilirubin–atazanavir nomogram | (1) Dichotomous | Negative Predictive Value, Positive Predictive Value, Sensitivity, Specificity |
| Simoni et al 201449 | HIV | United States | (1) Electronic record (2) Blood sample (3) Self-reports |
(1) Electronic drug monitor (2) Viral load (3) Self-reported 3-day antiretroviral therapy adherence questionnaire |
(1) Numerical (2) Dichotomous (3) Numerical |
Uncategorized Reliability |
| Smith et al 201650 | HIV | South Africa | (1) Blood sample (2) Pill count (non-self-reported) |
(1) Viral load (2) In-clinic pill count |
(1) Dichotomous (2) Dichotomous |
Sensitivity, Specificity |
| Stalter et al 202151 | HIV | Uganda, Kenya | (1) Blood sample (2) Urine sample |
(1) Liquid chromatography-mass spectrometry assay (2) Enzyme-linked immunosorbent assay |
(1) Dichotomous (2) Dichotomous |
Sensitivity, Specificity, Uncategorized Reliability |
| Sun et al 201752 | HIV | China | (1) Self-reports (2) Self-reports (3) Self-reports (4) Self-reports (5) Self-reports |
(1) Community Programs for Clinical Research on AIDS Antiretroviral Medication Self-Report (2) Social Support Raring Scale (3) 4-item Morisky Scale (4) Chinese HIV Treatment Adherence Self-Efficacy Scale (5) Visual analog scale |
(1) Numerical (2) N/A (3) N/A (4) Numerical (5) Numerical |
Content Validity, Convergent Validity, Internal Consistency Reliability, Test-Retest Reliability |
| Tolley et al 201853 | HIV | South Africa | (1) Self-reports | (1) Development of Measures of Adherence | (1) N/A | Content Validity, Internal Consistency Reliability |
| Usitalo et al 201454 | HIV | United States | (1) Blood sample (2) Self-reports |
(1) Viral load (2) Study questionnaire |
(1) Dichotomous (2) Dichotomous |
Inter-Instrument Reliability, within-rater reliability |
| Vreeman et al 201955 | HIV | Kenya, South Africa, Thailand | (1) Electronic record (2) Self-reports |
(1) MEMS (2) Self-reported questionnaire |
(1) Dichotomous (2) Dichotomous |
Sensitivity |
| Wickersham et al 201856 (Study 1) | HIV | United States | (1) Electronic record (2) Self-reports |
(1) Electronic event monitoring (2) 9-item Morisky Medication Adherence Scale |
(1) Numerical (2) Numerical |
Convergent Validity, Concurrent Validity, Content Validity, Test-Retest Reliability, Internal Consistency Reliability |
| Wickersham et al 201856 (Study 2) | HIV | United States | (1) Electronic record (2) Self-reports |
(1) Electronic event monitoring (2) 9-item Morisky Medication Adherence Scale |
(1) Numerical (2) Numerical |
Convergent Validity, Concurrent Validity, Content Validity, Test-Retest Reliability, Internal Consistency Reliability |
| Wilson et al 201657 | HIV | United States | (1) Electronic record (2) Self-reports |
(1) Medication event monitoring system (2) Study questionnaire |
(1) Numerical (2) Numerical |
Internal Consistency Reliability |
| Zhang et al 202058 | HIV | China | (1) Hair sample (2) Self-reports (3) Self-reports (4) Self-reports (5) Self-reports |
(1) Hair tenofovir (2) Frequency of adherence behavior questionnaire (3) Percent of days of adherence questionnaire (4) Visual analog scale (5) Composite adherence scores |
(1) Dichotomous (2) Ranked ordinal (3) Numerical (4) Numerical (5) Dichotomous |
Internal-instrument reliability |
| Zissette et al 202159 | HIV | South Africa, Kenya | (1) Self-reports | (1) Monitoring tool | (1) N/A | Content Validity, Internal Consistency Reliability |
| Alhazzani et al 202160 | Diabetes | Saudi Arabia | (1) Self-reports (2) Self-reports |
(1) English Self-Efficacy for Appropriate Medication Use Scale (2) Arabic Self-Efficacy for Appropriate Medication Use Scale |
(1) Numerical (2) Numerical |
Discriminant Validity, Construct Validity, Test-Retest Reliability, Internal Consistency Reliability |
| Anuradha, Prabhu, and Kalra 202261 | Diabetes | India | (1) Self-reports | (1) Self-reported questionnaire | (1) N/A | Internal Consistency Reliability, Inter-Item Reliability |
| Ashur et al 201562 | Diabetes | Libya | (1) Blood sample (2) Self-reports (3) Self-reports |
(1) HbA1c (2) English 8-item Morisky Medication Adherence Scale questionnaire (3) Arabic 8-item Morisky Medication Adherence Scale questionnaire |
(1) Dichotomous (2) Ranked ordinal (3) Ranked ordinal |
Internal Consistency Reliability, Split-Half Reliability, Positive Predictive Value, Negative Predictive Value, Specificity, Sensitivity |
| Athavale et al 201963 | Diabetes | United States | (1) Pharmacy record (2) Self-reports (3) Self-reports (4) Self-reports |
(1) Proportion of days covered (2) 5-point 1986 Morisky scale (3) Medication Adherence Reasons Scale (4) Medication adherence Estimation and Differentiation Scale |
(1) Numerical (2) Numerical (3) Numerical (4) Numerical |
Convergent Validity, Discriminant Validity, Internal Consistency Reliability |
| Ayoub et al 201964 | Diabetes | Lebanon | (1) Self-reports (2) Self-reports |
(1) Lebanese Medication Adherence Scale (2) Diabetes Medication Adherence Scale |
(1) Dichotomous (2) Dichotomous |
Convergent Validity, Positive Predictive Value, Negative Predictive Value, Specificity, Sensitivity, Internal Consistency Reliability, Inter-Instrument Reliability |
| Bailey et al 201465 | Diabetes | United States | (1) Electronic record (2) Electronic record |
(1) YSI 2300 STAT Plus glucose and lactate analyzer (2) Enlite Numerical glucose monitoring |
(1) Dichotomous(2) Dichotomous | Uncategorized Validity |
| Barola et al 202166 | Diabetes | India | (1) Blood sample (2) Self-reports |
(1) HbA1c (2) Hindi Diabetes Self-Management Profile Self Report |
(1) Dichotomous (2) Numerical |
Structural Validity, Internal Consistency Reliability, Predictive Validity |
| Boettcher et al 201567 | Diabetes | Austria, Germany | (1) Blood sample (2) Electronic record |
(1) HbA1c (2) Self-monitoring blood glucose meters |
(1) Dichotomous (2) N/A |
Uncategorized Validity |
| Borot et al 201468 (Study 1) | Diabetes | France | (1) Electronic record | (1) JewelPUMP | (1) N/A | Uncategorized Validity |
| Borot et al 201468 (Study 2) | Diabetes | France | (1) Electronic record | (1) Animas Vibe | (1) N/A | Uncategorized Validity |
| Borot et al 201468 (Study 3) | Diabetes | France | (1) Electronic record | (1) Accu-Chek Combo | (1) N/A | Uncategorized Validity |
| Borot et al 201468 (Study 4) | Diabetes | France | (1) Electronic record | (1) MiniMed Paradigm 712 | (1) N/A | Uncategorized Validity |
| Borot et al 201468 (Study 5) | Diabetes | France | (1) Electronic record | (1) OmniPod | (1) N/A | Uncategorized Validity |
| Chan et al 202069 | Diabetes | UK | (1) Self-reports (2) Self-reports |
(1) Beliefs about Medicines Questionnaire (2) Medication Adherence Report Scale |
(1) Numerical (2) Numerical |
Internal Consistency Reliability, Construct Validity |
| Chung et al 201570 (Study 1) | Diabetes | Malaysia | (1) Blood sample (2) Self-reports |
(1) HbA1c (2) Malaysian Medication Adherence Scale |
(1) Dichotomous (2) Ranked ordinal |
Sensitivity, Specificity, Negative Predictive Value, Positive Predictive Value, Concurrent Validity |
| Chung et al 201570 (Study 2) | Diabetes | Malaysia | (1) Self-reports (2) Self-reports |
(1) 8-item Morisky Medication Adherence Scale (2) Malaysian Medication Adherence Scale |
(1) Ranked ordinal (2) Ranked ordinal |
Internal Consistency Reliability, Test-Retest Reliability |
| Dibonaventura et al 201471 | Diabetes | United States | (1) Blood sample (2) Self-reports |
(1) HbA1c (2) 8-item Morisky Medication Adherence Scale questionnaire |
(1) Dichotomous (2) Ranked ordinal |
Construct Validity, Internal Consistency Reliability |
| Edge et al 201772 | Diabetes | UK | (1) Blood sample (2) Electronic record |
(1) Capillary blood glucose (2) Freestyle Libre sensor |
(1) Dichotomous (2) N/A |
Uncategorized Validity |
| Goh et al 202073 (Study 1) | Diabetes | Malaysia | (1) Blood sample (2) Self-reports |
(1) HbA1c (2) Patient Medication Adherence Instrument |
(1) Dichotomous (2) Dichotomous |
Construct Validity, Positive Predictive Value, Negative Predictive Value, Sensitivity, Specificity, Concurrent Validity, Internal Consistency Reliability |
| Goh et al 202073 (Study 2) | Diabetes | Malaysia | (1) Blood sample (2) Self-reports |
(1) HbA1c (2) Healthcare Professional Medication Adherence Instrument |
(1) Dichotomous (2) Dichotomous |
Construct Validity, Positive Predictive Value, Negative Predictive Value, Sensitivity, Specificity, Concurrent Validity, Internal Consistency Reliability |
| Gomes-Villas Boas, de Lima, and Pace 201474 | Diabetes | Brazil | (1) Self-reports (2) Self-reports |
(1) Measurement of Adherence to Treatment - Oral Antidiabetics (2) Measurement of Adherence to Treatment - Insulin |
(1) Numerical (2) Numerical |
Face Validity, Criterion Validity, Sensitivity, Specificity, Internal Consistency Reliability, Uncategorized Reliability |
| Gonzalez et al 201375 | Diabetes | United States | (1) Blood sample (2) Electronic record (3) Self-reports |
(1) HbA1c (2) MEMS (3) Self-reported questionnaire |
(1) Dichotomous (2) Numerical (3) Numerical |
Uncategorized Validity |
| Jansà et al 201376 | Diabetes | Spain | (1) Blood sample (2) Self-reports |
(1) HbA1c (2) Diabetes Self-Care Inventory-Revised Version |
(1) Dichotomous (2) Numerical |
Internal Consistency Reliability, Test-Retest Reliability, Structural Validity |
| Kim et al 201677 | Diabetes | South Korea | (1) Blood sample (2) Self-reports (3) Self-reports (4) Self-reports |
(1) HbA1c (2) Adherence to Refills and Medication Scale (3) Korean 8-item Morisky Medication Adherence Scale (4) Korean Adherence to Refills and Medication Scale |
(1) Dichotomous (2) Dichotomous (3) Ranked ordinal (4) Dichotomous |
Construct Validity, Convergent Validity, Known-Groups Validity, Internal Consistency Reliability |
| Kristina et al 201978 | Diabetes | Indonesia | (1) Blood sample (2) Self-reports (3) Self-reports |
(1) Fasting blood glucose level (2) Medication Adherence Reasons Scale (3) Morisky Green Levine Medication Adherence Scale |
(1) Dichotomous (2) Ranked ordinal (3) Ranked ordinal |
Convergent Validity, Sensitivity, Specificity, Positive Predictive Value, Negative Predictive Value, Internal Consistency Reliability, Test-Retest Reliability |
| Laghousi et al 202179 | Diabetes | Iran | (1) Self-reports | (1) Persian 8-item Morisky Medication Adherence Scale questionnaire | (1) Ranked ordinal | Content Validity, Construct Validity, Internal Consistency Reliability, Test-Retest Reliability |
| Lai, Sellappans, and Chua 202080 | Diabetes | Malaysia | (1) Self-reports (2) Self-reports |
(1) English Malaysian Medication Adherence Scale (2) Malay Malaysian Medication Adherence Scale |
(1) Ranked ordinal (2) Dichotomous |
Sensitivity, Specificity, Negative Predictive Value, Positive Predictive Value, Convergent Validity, Internal Consistency Reliability |
| Lee et al 201381 | Diabetes | Korea | (1) Blood sample (2) Self-reports (3) Self-reports |
(1) HbA1c (2) 4-item Morisky Medication Adherence Scale questionnaire (3) Korean 4-item Morisky Medication Adherence Scale questionnaire |
(1) Dichotomous (2) N/A (3) Ranked ordinal |
Convergent Validity, Construct Validity, Sensitivity, Specificity, Negative Predictive Value, Positive Predictive Value, Test-Retest Reliability, Internal Consistency Reliability |
| Mallah et al 201982 | Diabetes | Lebanon | (1) Blood sample (2) Self-reports (3) Self-reports |
(1) HbA1c (2) Lebanese Medication Adherence Scale (3) Diabetes Medication Adherence Scale |
(1) Dichotomous (2) N/A (3) Dichotomous |
Convergent Validity, Specificity, Sensitivity, Internal Consistency Reliability |
| Matsumoto et al 202183 | Diabetes | Japan | (1) Medical record (2) Pharmacy record (3) Self-reports |
(1) Medical health insurance claims (2) Pharmacy insurance claims (3) Self-reported questionnaire |
(1) N/A (2) N/A (3) N/A |
Sensitivity, Specificity, Inter-Instrument Reliability |
| Matuleviciene et al 201484 | Diabetes | Sweden | (1) Electronic record (2) Electronic record |
(1) DexcomG4 Sensor (2) Enlite Sensor |
(1) Dichotomous (2) Dichotomous |
Uncategorized Validity |
| Mayberry et al 201385 | Diabetes | United States | (1) Blood sample (2) Self-reports (3) Self-reports (4) Self-reports |
(1) HbA1c (2) Summary of Diabetes Self-Care Activities medications subscale (3) Diabetes treatment satisfaction questionnaire (4) Adherence to Refills and Medications Scale (diabetes) |
(1) Dichotomous (2) Numerical (3) Numerical (4) Numerical |
Convergent Validity, Construct Validity, Internal Consistency Reliability, Predictive Validity |
| Mehta et al 201586 | Diabetes | United States | (1) Blood sample (2) Electronic record (3) Self-reports |
(1) HbA1c (2) Blood glucose monitor (3) Diabetes Medication Questionnaire |
(1) Dichotomous (2) N/A (3) Numerical |
Convergent Validity, Criterion Validity, Internal Consistency Reliability, Test-Retest Reliability |
| Mikhael et al 201987 (Study 1) | Diabetes | Iraq | (1) Blood sample (2) Self-reports (3) Self-reports |
(1) HbA1c (2) Medication Adherence Questionnaire (3) Iraqi Anti-Diabetic Medication Adherence Scale |
(1) Dichotomous (2) N/A (3) Ranked ordinal |
Negative Predictive Value, Positive Predictive Value, Sensitivity, Specificity, Convergent Validity, Concurrent Validity, Internal Consistency Reliability, Test-Retest Reliability |
| Mikhael et al 201987 (Study 2) | Diabetes | Iraq | (1) Blood sample (2) Self-reports |
(1) HbA1c (2) Medication Adherence Questionnaire |
(1) Dichotomous (2) N/A |
Negative Predictive Value, Positive Predictive Value, Sensitivity, Specificity, Internal Consistency Reliability |
| Oliveira et al 202288 | Diabetes | Brazil | (1) Self-reports | (1) Self-reported questionnaire | (1) N/A | Content Validity, Inter-Instrument Reliability |
| Osborn and Gonzalez 201689 (Study 1) | Diabetes | United States | (1) Self-reports (2) Self-reports |
(1) Adherence to Refills and Medication Scale for Diabetes (2) Adapted Morisky Medication Adherence Scale for insulin adherence |
(1) Dichotomous (2) Dichotomous |
Convergent Validity, Criterion Validity, Internal Consistency Reliability |
| Osborn and Gonzalez 201689 (Study 2) | Diabetes | United States | (1) Self-reports (2) Self-reports |
(1) Summary of Diabetes Self-Care Activities medications subscale (2) Adapted Morisky Medication Adherence Scale for insulin adherence |
(1) Dichotomous (2) Numerical |
Convergent Validity |
| Osborn and Gonzalez 201689 (Study 3) | Diabetes | United States | (1) Self-reports (2) Self-reports |
(1) Summary of Diabetes Self-Care Activities insulin specific subscale (2) Adapted Morisky Medication Adherence Scale for insulin adherence |
(1) Dichotomous (2) Numerical |
Convergent Validity |
| Patton et al 201390 | Diabetes | United States | (1) Blood sample (2) Electronic record (3) Electronic record |
(1) HbA1c (2) Blood glucose monitor (3) Bolus |
(1) N/A (2) N/A (3) N/A |
Inter-Instrument Reliability, Uncategorized Reliability |
| Ranasinghe et al 201891 | Diabetes | Sri Lanka | (1) Blood sample (2) Self-reports |
(1) HbA1c (2) Brief medication questionnaire |
(1) Dichotomous (2) Ranked ordinal |
Criterion Validity, Specificity, Sensitivity, Test-Retest Reliability, Internal Consistency Reliability |
| Ratanawongsa et al 201592 | Diabetes | United States | (1) Blood sample (2) Blood sample (3) Blood sample (4) Blood sample (5) Pharmacy record |
(1) HbA1c (2) Systolic blood pressure (3) diastolic blood pressure (4) Low-density lipoprotein (5) Numerical medication gap |
(1) Dichotomous (2) Dichotomous (3) Dichotomous (4) Dichotomous (5) Dichotomous |
Uncategorized Validity |
| Shi et al 202193 | Diabetes | China | (1) Self-reports (2) Self-reports (3) Self-reports |
(1) 8-item Morisky Medication Adherence Scale questionnaire (2) General Adherence Scale (3) Chinese General Adherence Scale |
(1) Ranked ordinal (2) N/A (3) N/A |
Construct Validity, Content Validity, Criterion Validity, Internal Consistency Reliability, Split-Half Reliability, Test-Retest Reliability |
| Surekha et al 201694 | Diabetes | India | (1) Pill count (non-self-reported) (2) Self-reports |
(1) In-clinic pill count (2) 8-item Morisky Medication Adherence Scale questionnaire |
(1) Numerical (2) Ranked ordinal |
Sensitivity, Specificity, Negative Predictive Value, Positive Predictive Value, Internal Consistency Reliability |
| Tandon et al 201595 | Diabetes | Togo | (1) Self-reports (2) Blood sample (3) Self-reports |
(1) 4-item Morisky Medication Adherence Scale questionnaire (2) Fasting blood glucose level (3) 8-item Morisky Medication Adherence Scale questionnaire |
(1) Ranked ordinal (2) Dichotomous (3) Ranked ordinal |
Convergent Validity, Known-Groups Validity, Sensitivity, Specificity, Positive Predictive Value, Negative Predictive Value, Internal Consistency Reliability |
| Vincze, Losonczi, and Stauder 202096 | Diabetes | Hungary | (1) Blood sample (2) Self-reports (3) Self-reports |
(1) HbA1c (2) 8-item Morisky Medication Adherence Scale questionnaire (3) Hungarian Diabetes Self-Management Questionnaire |
(1) Dichotomous (2) Ranked ordinal (3) Numerical |
Construct Validity, known-group validity |
| Wang et al 201297 | Diabetes | Singapore | (1) Self-reports | (1) Modified Morisky, Green, Levine Adherence Scale | (1) Numerical | Content Validity, Internal Consistency Reliability |
| Zongo et al 201698 | Diabetes | Canada | (1) Blood sample (2) Self-reports (3) Self-reports (4) Self-reports (5) Self-reports |
(1) HbA1c (2) Self-report with 4 items (3) 8-item Morisky Medication Adherence Scale questionnaire (4) Proportion of missed pills (5) Single-item scale |
(1) Dichotomous (2) Ranked ordinal (3) Ranked ordinal (4) N/A (5) N/A |
Content Validity |
| Zongo et al 201699 | Diabetes | Canada | (1) Self-reports (2) Self-reports |
(1) English 8-item Morisky Medication Adherence Scale questionnaire (2) French 8-item Morisky Medication Adherence Scale questionnaire |
(1) Ranked ordinal (2) Ranked ordinal |
Content Validity, Internal Consistency Reliability |
| Zongo et al 201926 | Diabetes | Canada | (1) Medical record (2) Pharmacy record (3) Pharmacy record |
(1) Hospitalization records (2) Proportion of days covered (3) Daily polypharmacy possession ratio |
(1) Dichotomous (2) Numerical (3) Numerical |
Content Validity |
Figure 1.
PRISMA ScR Flowchart..
Notes: PRISMA figure adapted from Liberati A, Altman D, Tetzlaff J, et al. The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate health care interventions: explanation and elaboration. Journal of clinical epidemiology. 2009;62(10). Creative Commons.100
Overall, 36 studies addressed adherence to HIV medications, 51 studies examined adherence to diabetes medications, and one study explored adherence to nutritional supplements. The highest percentage of studies focused on North America (32%) followed by East Asia and Pacific (20%), and Sub-Saharan Africa (16%). Most studies (73%) explored the psychometric properties of adherence as a primary aim, while 27% investigated the psychometric properties of adherence as a secondary aim.
Measurement Modalities and Measures
We identified 9 modalities, 221 total measures, and 143 unique measures across all studies. The nine modalities included blood samples, hair samples, urine samples, electronic records, pharmacy records, medical records, pill counts (non-self-reported), self-reports (including questionnaires and pill counts), and other. Overall and within the HIV and diabetes studies, the three most common modalities were self-reports, blood samples, and electronic records, in that order (Table 2). Within the self-report modality, 97% of measures were questionnaires. The 8-item Morisky Medication Adherence Scale (MMAS-8) was the most frequently used self-reported measure, with 14 instances of use. Among the blood sample measures, 40% tested HbA1c levels and 25% examined viral loads.
Table 2.
Distribution of Measures and Modalities by Health Area
| Modality Category | Modality | Number of Measures | |||
|---|---|---|---|---|---|
| HIV | Diabetes | Nutrition | All | ||
| Self-reports | 48 (48.5%) | 67 (56.8%) | 1 (25%) | 116 (52.5%) | |
| Pill Count (non-self-reported) | 9 (9.1%) | 1 (0.8%) | 1 (25%) | 11 (5.0%) | |
| Other | 1 (1.0%) | 0 (0.0%) | 0 (0.0%) | 1 (0.4%) | |
| Biometric Samples | Blood Sample | 24 (24.2%) | 28 (23.7%) | 1 (25%) | 53 (24.0%) |
| Hair Sample | 2 (2.0%) | 0 (0.0%) | 0 (0.0%) | 2 (0.9%) | |
| Urine Sample | 1 (1.0%) | 0 (0.0%) | 0 (0.0%) | 1 (0.4%) | |
| Written Records | Electronic Record | 10 (10.1%) | 15 (12.7%) | 1 (25%) | 26 (11.8%) |
| Pharmacy Record | 3 (3.0%) | 5 (4.2%) | 0 (0.0%) | 8 (3.6%) | |
| Medical Record | 1 (1.0%) | 2 (1.7%) | 0 (0.0%) | 3 (1.4%) | |
| TOTAL | 99 (100%) | 118 (100%) | 4 (100%) | 221 (100%) | |
By country income groups, 49 studies were conducted in high-income countries (HICs), 27 studies in upper-middle-income countries (UMICs), 14 studies in lower-middle-income countries (LMICs), and 5 studies in low-income countries (LICs). (Seven studies in multiple country income groups were double counted). The use of triangulation was similar across country income groups. In each group, more than half the studies included at least two types of data collection methods and two different measures (Figure 2). The mean number of modalities in each study was 1.84 (SD = 0.73) overall, 1.90 (SD = 1.17) for HICs, 1.85 (SD = 1.18) for UMICs, 1.86 (SD = 0.86) for LMICs, and 1.8 (SD = 1.14) for LICs. In HICs, UMICs, and LICs, studies with more than two modalities and more than two measures were most common, whereas in LMICs, studies with exactly two modalities and two measures were most common. Almost no relationship exists between country income level and triangulation.
Figure 2.
Modalities And Measures, By Country Income Group.
Adherence Definitions
The operational definition of adherence fell into four categories: numerical, dichotomous, ranked ordinal, and undefined. Numerical definitions define adherence discretely (eg, scale scores) or continuously (eg, percentages). Examples of numerically defined adherence include percentages of pills taken in a certain time frame or adherence levels on visual analog scales in self-reported questionnaires. For example, Zhang et al asked participants how many days they took their medications as prescribed in the last month.58 From the responses, the authors calculated the percentage of days the participants were adherent in the past 30 days.58
Dichotomous definitions describe adherence in two states, such as adherent/non-adherent, good glycemic control/poor glycemic control, or undetectable viral load/detectable viral load. Cutoff points to dichotomize adherence across studies were the same for some measures such as HbA1c where good glycemic control was defined as HbA1c <7%. The threshold for adherence varied across studies for other measures such as viral load, where participants could be classified as “adherent” if their viral load was ≤20 copies/mL or ≤400 copies/mL depending on the study.
Finally, ranked ordinal definitions describe adherence as having multiple levels. Most measures (65%) defining adherence with a ranked ordinal scale used MMAS, which categorized adherence into high/medium/low.62,70,71,77–81,93–96,98,99 Based on the total score of the scale, high adherence was defined as a score of eight, medium as a score of six or seven, and low as a score less than six.62,70,71,77–81,93–96,98,99
Adherence was not defined for 40 (18%) measures. Approximately 14% of HIV measures, 21% of diabetes measures, and 25% of nutritional supplement measures did not define adherence. Many of the studies that did not define adherence aimed to create a new measure or to translate an existing measure. Some reasons why studies did not define adherence included having study aims testing the correlation between adherence measures,24,28,41,45,46,67,81–83,90,101 testing the internal reliability of a new measure,53,59,61 testing the content validity of a new measure,53,61,88 and testing the construct validity of a new measure.53,59
Overall, dichotomously defined measures were the most popular (89 of 221 measures or 40%) followed by numerical (27%) and ranked ordinal (14%). Dichotomous measures were also the most popular way to define adherence across health topics, country income levels, and measure types (direct/indirect). However, the most common type of adherence definition fluctuated across modalities because of the measures within the modality. For example, the dichotomous adherence definition type was most common within the blood sample modality because viral load and HbA1c measures define adherence dichotomously and comprise 64% of the blood samples in the review. Similarly, the majority of adherence definitions in the pharmacy modality were numerical because adherence was often expressed as a rate, such as the proportion of days covered or medication possession ratio.27,31,34,63,102
The amount of variation in an adherence definition category within a modality depended on 1) whether the measures within the modality could be assessed numerically and 2) whether widely accepted cutoffs existed for the measure. There was more variation in adherence definition types within modalities if measures could initially be measured numerically. This is because the researchers decided how they wanted to categorize adherence after collecting numeric data. For example, pill count measures were initially measured numerically. Some studies reported pill count as a discrete number or a percentage of remaining pills given the original number of pills dispensed.24,26,27,29,32,35,37,38,43,47,50,94 Other studies reported pill count in a dichotomous or ranked ordinal manner. For example, Teshome et al defined “high adherence” as the healthcare worker not seeing ≥80% of pills dispensed for the past 30 days.24
For self-reported measures, the wide variety of scales used across studies and the originally continuous nature of most scales resulted in a wide variation of adherence definitions within the modality. For example, Ayoub et al and Mallah et al were the only studies in the review to measure adherence using the Lebanese Medication Adherence Scale (LMAS-14), which initially measured adherence numerically on a scale from 0 to 42.64,82 Ayoub et al defined adherence on LMAS-14 dichotomously by classifying patients as adherent or non-adherent using a cut-off point of 38.64 Meanwhile, Mallah et al did not define adherence for LMAS-14 as the scale was a reference measure a new scale.82 Finally, there was less variation in adherence definition types within modalities if measures had widely accepted cutoffs, even if the measures could initially be defined numerically. For example, all measures for HbA1c in the review were originally measured numerically. However, adherence was reported dichotomously across studies, with good glycemic control as HbA1c <7%.62,66,67,70,71,73,75–77,81,82,85–87,91,92,96,98
Reporting Validity/ Reliability
Among the studies in the review, 46 (52%) reported both validity and reliability, 28 studies (31%) only reported validity, and 14 studies (16%) only reported reliability. Fourteen types of validity and six types of reliability appeared across the studies (Table 3). Almost half of all studies measured internal consistency reliability (through Cronbach’s alpha), and more than a quarter of studies tested sensitivity and specificity. Scores for the five most common validity types and three most common reliability types had overall distributions of at least 0.5 across all studies. Overall, Cronbach’s alpha had the lowest score range of 0.5 (0.97 to 0.47) with a mean score of 0.76 (Figure 3). The next most common type of reliability measured in the review (test-retest reliability) had a mean score of 0.55 with a range from 0.376 to 0.975. Finally, the Kappa coefficient for inter-instrument reliability had a mean score of 0.49 with a range from 0.107 to 0.995. Of the five most common validity measures, the negative predictive value had the highest mean score (0.76, range: 0.311–1), followed by sensitivity (0.66, range: 0.049–1), specificity (0.60, range: 0.177–0.98), positive predictive value (0.55, range: 0.237–0.948), and convergent validity (0.53, range: 0.36–0.88).
Table 3.
Types of Validity and Reliability
| Validity | Reliability | ||
|---|---|---|---|
| Validity Type | Number of studies (%) | Reliability Type | Number of studies (%) |
| Sensitivity | 26 (29.5%) | Internal Consistency Reliability | 41 (46.6%) |
| Specificity | 25 (28.4%) | ||
| Positive Predictive Value | 17 (19.3%) | ||
| Convergent Validity | 17 (19.3%) | Test-retest Reliability | 14 (15.9%) |
| Negative Predictive Value | 16 (18.2%) | ||
| Content Validity | 12 (13.6%) | Inter-instrument Reliability | 8 (9.09%) |
| Construct Validity | 12 (13.6%) | ||
| Criterion Validity | 10 (11.4%) | Split-half Reliability | 2 (2.3%) |
| Concurrent Validity | 8 (9.1%) | ||
| Predictive Validity | 4 (4.5%) | Inter-item Reliability | 1 (1.1%) |
| Known-groups Validity | 2 (2.3%) | ||
| Discriminant Validity | 2 (2.3%) | Within-rater Reliability | 1 (1.1%) |
| Structural Validity | 2 (2.3%) | ||
| Face Validity | 1 (1.1%) | Uncategorized Reliability | 12 (13.6%) |
| External Criterion Validity | 1 (1.1%) | ||
| Uncategorized Validity | 15 (17.0%) | ||
Figure 3.
Distribution Of Select Validity and Reliability Scores, By Health Topic.
Within each type of validity and reliability, the distribution of scores varied greatly between HIV and diabetes studies, except for internal consistency (Figure 3). (Nutritional supplementation was excluded from Figure 3 because there was only one study included in the review). The range of validity/reliability scores for diabetes studies was the same or similar to the overall score ranges, except for sensitivity and inter-instrument reliability. The sensitivity range for diabetes studies is about half (0.4) of the overall range because the overall sensitivity includes outliers from HIV studies. The range of inter-instrument reliability scores was also smaller (0.105) for diabetes than for the overall range. Diabetes studies reported a greater number of psychometric scores across the most common validity/reliability categories in Figure 3, except for inter-instrument reliability. Only two inter-instrument reliability scores were reported across diabetes studies.
In HIV studies, the median scores for specificity, positive predictive values, and negative predictive values were higher compared to diabetes studies, whereas in diabetes studies, the median scores for sensitivity and convergent validity were higher compared to HIV studies. Additionally, across the three most common types of reliability, median scores were higher for diabetes studies compared to HIV studies, except for internal consistency.
Among HIV studies, about 30% explored only validity or reliability, and 39% explored both validity and reliability. Most (61%) diabetes studies examined both validity and reliability, and the nutritional supplement study examined both psychometric properties as well. For UMICs, LMICs, and LICs, studies reporting both validity and reliability were most common. Studies only investigating validity were most common for HICs. Additionally, most studies explored both validity and reliability in all regions except Europe (where studies exploring only validity were most common).
True Effect Sizes
Of the 46 studies that reported validity and reliability, 26 shared a Pearson’s correlation coefficient, indicating the strength of the linear relationship between the test and reference measures used to measure adherence in each study. Studies that reported these results were nearly evenly divided between diabetes and HIV studies (57% and 43%, respectively). Pearson r values, which in these studies were calculated to show the correlation between test and reference measures, ranged from 0.09–0.93. From those values, we grouped studies into “low” (0.09–0.36), “medium” (0.37–0.65), or “high” (0.66–0.03) effect size. Some studies reported multiple effect sizes, using different reference and test measures, so those effect sizes have been included to reach a total of 28 reported effect sizes. Overall, we found that seven studies fell into the “low” range, 11 in the “medium” range, and 13 in the “high” effect size range. There was no significant difference found in whether these studies were reporting on adherence to diabetes or HIV medication; whether they were conducted in high-, middle-, or low-income settings; or based on population size.
Discussion
In this review, we summarized the methods and modalities used to measure adherence to HIV medication, diabetes medication, and nutritional supplements. We also analyzed variations in adherence definitions and how the psychometric properties are measured and reported.
Across 88 studies in the review, there were 9 modalities, 221 total measures, and 143 unique measures. All modalities and measures have strengths and limitations related to their acceptability, feasibility, reliability, and validity. Through triangulation, researchers can compare modalities and measures to choose those that best suit their study needs. In practice, triangulating modalities or measures lead to more flexibility in the field. Instead of relying on one measure, such as a medication event monitoring system, which requires specific equipment and training, having multiple acceptable adherence measures or modalities grants more feasibility for adherence research in a variety of contexts, especially in low-resource settings. Some measures may also overestimate or underestimate adherence systematically, while others may do so randomly. If the same measure is used in all studies, researchers would replicate the same limitation associated with the measure or modality across studies. Researchers can better balance measurement errors across adherence measures by using some that are more likely to overestimate and underestimate adherence to more accurately measure adherence behavior. Therefore, since no gold standard adherence measure exists, we recommend researchers include multiple measures and modalities in their studies and use triangulation to balance individual measurement errors and leveraging the diverse strengths of various measures and modalities.
In the review, we also identified three types of operational definitions for adherence: numerical, dichotomous, and ranked ordinal. While categorizing patients into levels of adherence can help clinicians or researchers divide patients for treatment interventions, follow-up, or other actions, the scientific significance of a cutoff is often marginal. Someone who is 94% adherent or 96% adherence on the scale may not have different health outcomes even if they are categorized as having poor adherence and good adherence respectively. Similarly, many studies measuring viral load defined dichotomous adherence cutoffs based on the test’s sensitivity or limit of detection rather than differences in clinical outcomes.29,33,35,42,44,46,47,49,50,54 This is why in some studies using sensitive instruments to measure viral load, undetectable viral load/adherence is classified as ≤20 copies/mL whereas in other studies using less sensitive instruments, undetectable viral load/adherence is classified as ≤400 copies/mL. One solution to these cutoffs is to conceptualize adherence as a spectrum and report adherence numerically.
Finally, the limited number of statistics for one type of validity or reliability in the review restricted our results to be largely qualitative and hindered our ability to compare statistical values. To allow for future quantitative reviews of the psychometric properties of validity and reliability, researchers could report a core group of statistics across studies. Future research and discussions are needed to determine which measures would be most meaningful and feasible to include in the core statistics group.
The distribution of scores within one type of validity or reliability measure differed greatly between HIV and diabetes, except for internal consistency. One reason for this difference among validity measures could be the nature of the diseases. HIV is an infectious disease, while diabetes is a non-communicable disease. The median scores and ranges for negative predictive value and specificity were higher than positive predictive value and sensitivity. This indicates that when choosing adherence measures for HIV, researchers prioritize minimizing false positives and maximizing true negatives over minimizing false negatives and maximizing true positives. In other words, it is more important to correctly identify people who are non-adherent than people who are adherent for HIV. This could be because people who are not virally suppressed may transmit the disease to others and are more susceptible to other diseases.
Finally, when calculating true effect sizes between the reference and test adherence measures, we found that 7 studies fell into the “low” range, 11 in the “medium” range, and 13 in the “high” effect size range. The higher effect size suggests more agreement between the reference adherence measure and the measure being tested. The variability in effect size among studies in our review shows a lack of consistency in the strength of the relationships between reference and test adherence measurements. Therefore, we are likely still far from finding a “gold standard” approach to adherence measurement.
Limitations
One limitation is the exclusion of non-English language studies, which would have provided more insights into the psychometric properties of adherence measures. Additionally, restricting the search to peer-reviewed primary research studies published within a ten-year period might have overlooked relevant literature published before or after this timeframe, potentially leading to gaps in the understanding of adherence. Expanding the timeframe searched would have improved our ability to present an unbiased summary of the psychometric properties of adherence within the HIV, diabetes, and nutritional supplementation literature. Finally, only one reviewer looked at all potential studies and analyzed the data, which limited the robustness of the review by constraining the diversity of perspectives in the analysis.
Conclusion
Measuring adherence accurately and reliably continues to be a challenge for research in HIV, diabetes, and nutritional supplementation. The ability to accurately measure adherence is imperative to assessing and monitoring the health of people with chronic diseases and reducing their morbidity and mortality. Currently, there is no standard operational definition for adherence or a widely accepted adherence measure for HIV, diabetes, or nutritional supplementation. Instead of searching for a standard measure, a rigorous way to measure adherence could be through multiple modalities and measures that all triangulate to a common conclusion.
Recommendations for Reporting
Based on the findings in our review, we offer three key recommendations for reporting adherence measurements. First, researchers should report adherence results from multiple measures and modalities. Each measurement and modality type has different strengths and limitations, which triangulation can help balance. In the absence of a gold standard measure, using multiple measures and cross-checking results can help enhance the validity of research findings and mitigate bias and provide a practical and nuanced solution to measuring adherence. Second, adherence results should be reported numerically. While categorizing patients into different adherence categories may be helpful in clinical settings, the cutoffs for categorization can differ based on a test’s precision and may not reflect differences in clinical outcomes. If researchers feel that categorization is appropriate, we still recommend reporting numeric results in case cutoffs change in the future. Finally, researchers investigating the validity and reliability of adherence measures should report multiple types of validity and reliability in their studies (including Cronbach’s alpha) to improve statistical comparisons across adherence measures.
Acknowledgments
We thank Alicia Paul for her help creating the search strategy and screening articles for inclusion and Jordyn Britton supporting the data extraction. We also thank Bee-Ah Kang, Aditi Luitel, Olajumoke Olarewaju, and Manvi Poddar for their thoughtful comments on the protocol and throughout the manuscript writing process.
Funding Statement
This research was funded by a grant from the Bill and Melinda Gates Foundation to Johns Hopkins University (INV-035431, Rajiv N. Rimal, Principal Investigator). The authors, not the funder, are responsible for the content of this article.
Ethics Approval
Ethical approval was not required for this scoping review, since all data came from information freely available in the public domain. This study does not involve human participants.
Author Contributions
All authors made a significant contribution to the work reported, whether that is in the conception, study design, execution, acquisition of data, analysis and interpretation, or in all these areas; took part in drafting, revising or critically reviewing the article; gave final approval of the version to be published; have agreed on the journal to which the article has been submitted; and agree to be accountable for all aspects of the work.
Disclosure
The authors report no conflicts of interest in this work.
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