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Predictors of non-adherence to antiretroviral therapy among HIV infected patients in northern Tanzania

  • Seleman Khamis Semvua ,

    Roles Conceptualization, Data curation, Formal analysis, Funding acquisition, Investigation, Methodology, Project administration, Resources, Software, Supervision, Validation, Visualization, Writing – original draft

    semvua006@yahoo.co.uk

    Affiliations Kilimanjaro Christian Medical Centre-Duke Research Collaboration, Moshi, Tanzania, Desmond Tutu HIV Centre, University Of Cape Town, Cape Town, South Africa, Kilimanjaro Christian Medical University College, Moshi, Tanzania

  • Catherine Orrell,

    Roles Conceptualization, Formal analysis, Investigation, Methodology, Supervision, Visualization, Writing – original draft, Writing – review & editing

    Affiliation Desmond Tutu HIV Centre, University Of Cape Town, Cape Town, South Africa

  • Blandina Theophil Mmbaga,

    Roles Conceptualization, Funding acquisition, Methodology, Project administration, Resources, Supervision, Writing – original draft, Writing – review & editing

    Affiliations Kilimanjaro Christian Medical Centre-Duke Research Collaboration, Moshi, Tanzania, Kilimanjaro Christian Medical University College, Moshi, Tanzania, Duke Global Health Institute, Durham, North Carolina, United States of America, Kilimanjaro Clinical Research Institute-Kilimanjaro Christian Medical Centre, Moshi, Tanzania

  • Hadija Hamis Semvua,

    Roles Conceptualization, Investigation, Methodology, Resources, Writing – original draft, Writing – review & editing

    Affiliations Kilimanjaro Christian Medical University College, Moshi, Tanzania, Kilimanjaro Clinical Research Institute-Kilimanjaro Christian Medical Centre, Moshi, Tanzania

  • John A. Bartlett,

    Roles Conceptualization, Formal analysis, Funding acquisition, Investigation, Methodology, Project administration, Resources, Validation, Writing – original draft, Writing – review & editing

    Affiliations Kilimanjaro Christian Medical University College, Moshi, Tanzania, Duke Global Health Institute, Durham, North Carolina, United States of America

  • Andrew A. Boulle

    Roles Conceptualization, Data curation, Formal analysis, Investigation, Methodology, Supervision, Validation, Writing – original draft, Writing – review & editing

    Affiliation Desmond Tutu HIV Centre, University Of Cape Town, Cape Town, South Africa

Abstract

Background

Antiretroviral therapy (ART) has been shown to reduce HIV-related morbidity and mortality amongst those living with HIV and reduce transmission of the virus to those who are yet to be infected. However, these outcomes depend on maximum ART adherence, and HIV programs around the world make efforts to ensure optimal adherence. Predictors of ART non-adherence vary considerably across populations and settings with respect to demographic, psychological, behavioral and economic factors. The objective of this study is to investigate risk factors that predict non-adherence to antiretroviral treatment among HIV-infected individuals in northern Tanzania.

Methods

At Kilimanjaro Christian Medical Centre (KCMC), a tertiary and referral hospital in northern Tanzania, we used an existing ART database to randomly select HIV-infected patients above 18 years of age who have been on triple ART for at least two years. We used interviewer administered structured questionnaires to cross-sectionally determine predictors of ART non-adherence. We determined non-adherence through retrospective review of pharmacy drug refill (PDR) records of the interviewed participants using a pharmacy database.

Results

Non-adherence was defined as collecting less than 95% of expected monthly refills in the previous 2 years. Multivariable logistic regression model was used to determine the predictors of non-adherence. Of the 256 patients enrolled mean age was 44 years (SD ± 11) and median CD4 count was 499 cells per microliter (IQR 332–690). Median PDR adherence was 71% (IQR 58%–75%). Non-adherence was associated with younger age and unemployment.

Conclusion

In this setting, adherence strategies could be adapted to address issues facing young adults, and those with household challenges such as unemployment. Further research is required to better understand the potential roles of these factors in suboptimal adherence.

Introduction

The use of antiretroviral therapy (ART) has been shown to prolong and improve the quality of life of people living with HIV/AIDS[1] and reduce transmission of the virus to those who are yet to be infected[2] In the past decades the World Health Organization (WHO) has been focusing on scaling up ART coverage[3, 4] and as of 2015, 17 million people living with HIV globally were on antiretroviral medication[5] In Tanzania 1.4 million people were living with HIV and 53% of them were already on antiretroviral treatment by 2015[6]after the government’s efforts to strengthen and scale up free and comprehensive care and treatment services in public and private facilities[7]

Successful antiretroviral therapy results in viral suppression, immunologic improvement, and reduced viral transmission as well as reduced drug resistance. These outcomes depend substantially on consistent adherence to treatment[8, 9]. Data from prospective studies associate suboptimal adherence with drug resistance[9], reduced viral suppression and immunologic failure[8] as well as progression to AIDS[10]. However maintaining optimal adherence and retention of patients in care and treatment programs has been a major challenge[1], and therefore increased efforts to promote adherence are important for successful antiretroviral therapy.

Non-adherence to antiretroviral therapy has been associated with a range of factors including sociodemographic, psychological, socioeconomic, sociobehavioral and contextual factors[1113]. Although ART non-adherence is influenced by these factors, a systematic review of studies done in developed and developing nations suggest that the barriers to adherence are consistent across settings and countries[14]. Another systematic review and meta-analysis of studies done in low, middle and high income countries shows a higher proportion of people living with HIV (PLHIV) in low income countries who achieve good adherence as compared to PLHIV in high income countries[15]. Studies suggest that most of the barriers to optimal adherence are consistent in both developed and developing settings, although there are contextual barriers such as issues of access which are more common in developing countries[14]. Nevertheless, optimal levels of ART adherence can be achieved in sub Saharan African settings if barriers to optimal adherence are addressed[16, 17].

Since the gold standard approach for assessing ART adherence has not been established [18, 19] many researchers use patient self-reporting because of its low cost and simplicity[20], although this measure has led to underestimation of non-adherence[21]. Pharmacy adherence measures (PAM) are also relatively simple to administer and have provided more clinically relevant results compared to self-reports[2224].

Adherence is a dynamic process that changes over time[25] and predictors of non-adherence vary considerably and therefore no single factor has been consistently associated with non-adherence across all studies[26, 27]. This underscores the need to conduct studies to determine potential predictors of non-adherence in different contexts. Whereas cross sectional and qualitative studies suggest a number of potential predictors of ART non-adherence in northern Tanzania after initiation of free HIV care and treatment, and suggest programs to improve adherence[28, 29], the current prevalence of these predictors has not been quantified. In this study we sought to quantify non-adherence among northern Tanzanian HIV-infected patients on ART for at least two years, measure the potential predictors of non-adherence and explore associations with available adherence measures. The findings of this study will inform contextually tailored adherence interventions.

Materials and methods

Study setting

This study was conducted at Kilimanjaro Christian Medical Center (KCMC) in the northern part of Tanzania. The hospital is a non-profit organization under the Good Samaritan Foundation (GSF) of the ELCT, working in memorandum of understanding with the Tanzania government. It is a tertiary referral hospital which serves in-patient and out-patients referred or directly received from four regions (Kilimanjaro, Arusha, Tanga and Manyara) which form the northern part of Tanzania. The hospital HIV care and treatment department registers admitted patients diagnosed with HIV infection in the wards and out-patients diagnosed in the HIV counseling and testing unit. The HIV care and treatment department is divided into two parts, (a) HIV care and treatment clinic (CTC) which takes care of HIV infected adult individuals (b) child centered and family care clinic (CCFCC) which takes care of children and their families.

Based on the current (2012) local HIV care guidelines[30], HIV-infected patients with CD4 counts below 350 cells/mm3 regardless of the WHO clinical stage or with WHO stage 3 or 4 regardless of CD4 counts are eligible for antiretroviral therapy. Counseling for HIV-infected patients is done by trained nurses before and after treatment initiation. Based on clinical status and baseline laboratory tests, clinic physicians initiate medications while clinic pharmacists are responsible for final counseling and dispensing. Continued drug refill visits are scheduled every one or two months depending on patient’s clinical status and hospital ART stock status. The hospital HIV care and treatment team is responsible for assessing patient progress as they visit for drug refills. The clinic pharmacy also stocks drugs for opportunistic infections for when these are prescribed.

Inclusion and exclusion

The study included HIV-infected patients ≥18 years of age, who had been on triple antiretroviral drugs as part of their HIV lifelong care for at least two years and who could provide informed consent. The study excluded patients with impaired recall capacity based on interviewer assessment, and those who are in the KCMC ART database as occasional visitors but not primarily enrolled as KCMC HIV care and treatment clinic patients.

Study design, sampling and recruitment

A cross-sectional survey design was used. The target sample size was 214 eligible HIV infected patients calculated to offer 80% power to detect a 14% non-adherence among men as compared to women, the two groups equally distributed in the study population[29, 31, 32]. A simple random sampling was done using the clinic database. A random sample of 257 (214 + 20% to account for losses) out of 2315 patient identification numbers was selected from the clinic database. Initial screening was done based on age and duration on ART. Eligible patient’s clinic visit dates were identified using the appointment register. These patients were contacted through mobile phone calls and/or physically by the interviewers on the day of their clinic visit. The interviewers requested private meetings (after completion of clinic visit) with patients and introduced the study. For patients who had enough time, the oral consenting process started immediately and written consent forms for further reading were provided. For those who did not have enough time on the day, a meeting on a different day was requested at the patient’s convenience. Once the patient was ready to provide written informed consent interviews were planned and conducted.

Measurements

Pharmacy drug refills (PDR) were reviewed for the two years preceding the interview to enable a calculation of adherence based on retrospective PDR data. Adherence was measured based on the number of refills done out of 24 refills expected in the past two years. Less than 95% PDR was considered non-adherence as defined by Tanzania Ministry of Health. Participants were also asked to recall their pill-taking history over the preceding four days for a second measure of adherence. Predictors of and reasons for ART non-adherence were elicited using closed and open-ended questions in a structured questionnaire that was adapted from ACTG validated questionnaire[33]. In addition to the study interest in longer term adherence, the inclusion of patients with at least two years of follow up facilitated the first adherence measure (Pharmacy Adherence Measure) used in this study. A total of four months (from mid-July to late November 2015) were used for data collection, three months of participant interviews and one month of reviewing PDR records.

Demographic information included age, gender, marital status, level of education, occupation and residence (rural versus urban). Recall non-adherence was assessed by calculating the proportion of doses missed in the previous four days as recalled by patients. The last time ART medication was missed was assessed and categorized as never, >3 months ago, 1–3 months ago, 2–4 weeks ago, 1–2 weeks ago and within the past week. The past 4-days adherence was also assessed by asking “During the past 4 days how many days have you missed taking all your doses?” Behavioral reasons for non-adherence were elicited by listing the predetermined factors and asking participants “How often do the following reasons make you miss your medication?” The response was never, sometimes or often. An open-ended question was formulated to enable participants list other factors not covered in the list. Patient satisfaction with the service offered to them by clinicians, nurses, pharmacists and laboratory personnel was assessed through a “yes” or “no" response to a question enquiring about their satisfaction. Participant awareness of the current line of treatment, baseline and current CD4 counts was measured by asking “What line of treatment are you currently on?” and “What was your baseline CD4 count/What is your current CD4 count?” The response was cross-checked with the treatment regimen and CD4 count information recorded on the participants’ CTC cards.

Non-adherence

In this study non-adherence was defined as less than 95% of the expected 24 monthly pharmacy drug refills (PDR) of two years past the pharmacy retrospective data review. A complementary threshold was used for sensitivity analysis to determine whether the same risk factors will be found based on 80% PDR. The 95% threshold is consistent with the Tanzania Ministry of Health and WHO recommendation for ART adherence[1, 34]. Patients 4-days self-recall was also used as a second measure to determine non-adherence at 95% threshold by calculating the percentage number of pills taken in the past 4 days.

Statistical analysis

For the descriptive analysis of the patient characteristics, mean and standard deviations (SD) were calculated for normally distributed variables whereas median and interquartile ranges (IQR) were calculated for skewed variables. An adherence threshold of 95% and a complementary threshold of 80% were used to report non-adherence based on both adherence measures. Adherence levels of interviewed participants (using the two thresholds) were compared based on the sociodemographic characteristics. Adherence levels were also compared across most recent CD4 count strata and by duration on ART. Chi-squared p-values were calculated for each comparison. Assessments of associations with ART non-adherence were done based on an a priori multivariable logistic regression model. This method was preferred since the interest was to test the risk factors to ART non-adherence as determine by prior studies. Age, sex, employment, education, marital status, residences, duration on ART and most recent CD4 count were considered to be the potential predictors of non-adherence based on literature. They were all included in the multivariable model and their association with non-adherence was ascertained. The reasons for non-adherence were assessed by calculating the proportion of patients who reported each reason among all included participants, and also by calculating this proportion among participants who were found to be non-adherent at the 80% threshold based on PDR measure. Measures of effect were interpreted based on the size of effect and p-value, without reliance on a dichotomous cut-off of significance which would have artificially differentiated findings with broadly similar statistical support.

ART program in Tanzania

The ART program changes with time as research reveals new HIV/AIDS related information and the WHO point out new recommendation regarding management of HIV/AIDS. At the period of this research the program was using the Tanzania ministry of Health guideline 2012. The PDR data collection and analysis was done immediately after the recruitment and interviews and no significant changes occurred in the program

Ethical clearances

Ethical clearance approvals were secured from the Kilimanjaro Christian Medical University College (KCMUCo) and University of Cape Town (UCT) ethics committees. Oral and written consent were obtained from each patient before enrollment into the study. Interviews were done in special clinic rooms, and patient ID numbers were used and names were kept anonymous.

Results

A total of 257 patients were recruited to participate in the study. One participant was excluded due to impaired recall capacity as a result of a mental health problem and 28 participants who were not different from the overall sample (Table 1) were excluded due to incomplete prescription refill information, and therefore a total of 228 patients were included in the regression analysis. Fig 1 shows numbers of patients included in each step of the study from recruitment for interview to analysis. Approximately two thirds (66.2%) of the participants were female. The mean age of the participants was 44 years (SD: ± 11) and the median duration on ART was 4.5 years (IQR: 3–6.8). Median PDR adherence was 71% (IQR 58%–75%). The median CD4 count at the point of ART initiation was 105 cells per microliter (IQR: 49–201) and the median CD4 count at the point of interview was 499 cells per microliter (IQR: 332–690). Just over half of participants were currently married (51.3%). 57.0% reported residing in a township and 21.5% were not employed (Table 2).

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Table 1. Demographic characteristics of the recruited and excluded patients.

https://doi.org/10.1371/journal.pone.0189460.t001

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Table 2. Demographic characteristics of the participants (N = 228).

https://doi.org/10.1371/journal.pone.0189460.t002

Participants’ non-adherence

Median adherence for PDR was 71% (IQR: 58%–75%) and for patient-recall was 100%. At 95% adherence threshold, 42% (95%CI: 36–49%) and 10% (95%CI: 5–11%) of the participants were non-adherent based on PDR and patient-recall measures, respectively. At the 80% adherence threshold, 25% (95%CI: 20–31%) and 7% (95%CI: 6–14%) of the participants were non-adherent based on PDR and patient-recall measures, respectively.

Pharmacy drug refill pattern of adherence based on participant characteristics

Table 3 shows that, 78% of participants older than 40 years of age and 68% of those ≤ 40 years of age were adherent at 80% adherence threshold (p = 0.076). The highest proportion of adherent participants based on education levels was amongst those with college/university education (91%) followed by those with primary education (73%) and those with secondary education (70%., p = 0.046). 78% of employed participants as well as those who are self-employed were adherent while only 61% of those who are unemployed were adherent at 80% threshold (p = 0.057). The same trend was observed when the threshold of 95% was used: 62% of employed and 63% of self-employed was adherent while only 39% of unemployed participants were adherent (p = 0.010). The proportion of adherent participants varied across CD4 groups with lowest adherence in those with current CD4 cell counts of 350 to 500 cells/ μL. Adherence was also lowest among patients with longest (> = 10 years) duration on ART.

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Table 3. Adherence of interviewed participants based on demographic characteristics.

https://doi.org/10.1371/journal.pone.0189460.t003

Multivariable analysis of the predictors of pharmacy drug defill non-adherence based on 95% adherence threshold

The final multivariable model (Table 4) suggested that, non-adherence to ART was associated with younger age, with an adjusted OR for every 10-year increase in age of 0.54 (95% CI: 0.36–0.80, p = 0.002), Non-adherence was also associated with unemployment, adjusted OR 2.89 (95% CI: 1.21–6.86, p = 0.016).

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Table 4. Unadjusted and adjusted odds ratios (OR) for predictors of non-adherence to antiretroviral therapy among HIV-infected north Tanzanians (95% adherence threshold).

https://doi.org/10.1371/journal.pone.0189460.t004

Multivariable analysis of the predictors of pharmacy drug refill non-adherence based on 80% adherence threshold

The final multivariable model (Table 5) suggested that, non-adherence to ART was associated with younger age, with an adjusted OR for every 10-year increase in age of 0.54 (95% CI: 0.36–0.80, p = 0.002), and marital status with adjusted OR for being previously married of 4.15 compared to never being married (95% CI: 1.29–13.29, p = 0.024 across all categories). Non-adherence was also associated with unemployment, adjusted OR 2.89 (95% CI: 1.21–6.86, p = 0.016), and staying in urban areas with an adjusted OR of 2.25 (95% CI: 1.02–4.98, p = 0.045). While there was statistical support for an association between higher most recent CD4 counts and non-adherence, this was not consistent across all levels of CD4 count when compared to those below 350 cells/μl. There was weaker statistical support for the association between ART non-adherence and education level with adjusted OR for primary education level compared to tertiary education of 4.03 (95% CI: 1.26–12.84, p = 0.116 across all categories, (Table 3), as well for male gender, with the OR for men being 2.07 (95% CI 0.86–4.99, p = 0.106)

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Table 5. Unadjusted and adjusted odds ratios (OR) for predictors of non-adherence to antiretroviral therapy among HIV-infected north Tanzanians using 80% adherence threshold.

https://doi.org/10.1371/journal.pone.0189460.t005

Prevalence of patient self-reported reasons for missing ART pills in three months preceding the interview

Table 6 describes the prevalence (in the overall sample and among those who were PDR non-adherent at 80% threshold) of different reasons that were attributing to missing ART pills in the three months preceding the interview. In the overall sample most prevalent factors were traveling away from home (21.5%), forgetfulness (34.2%), running out of pills (15.4%) and busy working for survival (15.8%). Other reasons which were reported in the overall sample by at least 5% of patients included avoiding side effects (6.6%), feeling healthy (7.0%), taking alcohol (6.6%), failing to meet dietary instructions (5.7%), transport problems to the clinic (6.1%), events perceived to be related to taking ART (5.3%), getting tired of too many pills (5.3%), fear of stigmatization by people outside family (7.5%), fear of stigmatization by family members (7.0%), waking up too early for work (11.4%) and financial constraints (8.3%). Reasons which were more prevalent in a subsample of participants who were PDR non-adherent included, avoiding side effect (10.3%) feeling healthy (12.1%), taking alcohol (12.1%), religious belief (10.3%), not fully understanding regimen (6.9%), travelling away (29.3%), having too many pills to take (6.9%) and being tired of taking too many pills (10.3%).

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Table 6. Patient self-reported reasons for missing ART pills three months preceding the interview.

https://doi.org/10.1371/journal.pone.0189460.t006

Discussion

Principal findings

In this setting, 42% of individuals on ART collected under 95% of their pharmacy drug refills in the two years prior to the interview, and 25% were considered non-adherent using collection of less than 80% of their PDR as the adherence threshold. Patient recall non-adherence was lower and poorly correlated with PDR non-adherence, 10% and 7% at <95% and <80% thresholds, respectively. Factors with some evidence of association with non-adherence were younger age and being unemployed in both adherence thresholds, while the use of a more lineant threshold of 80% showed additional association with marital partnership characteristics, low education level, higher CD4 counts, male gender and living in urban areas[35, 36].

Comparison with other studies

Previous studies done both in this setting[29, 37] and other resource-limited settings[38, 39], have demonstrated low levels of ART non-adherence consistent with the patient recall non-adherence data in this study. A meta-analysis of studies which used both of the approaches used in this study and measured non-adherence at different thresholds, reported overall non-adherence as high as 32% among African ART users[16]. This level of non-adherence, which is likely to have been underestimated as the majority of included studies used self-reported measures to estimate adherence, is consistent with the PDR non-adherence in our study.

Younger age has been associated with non-adherence among Tanzanian ART users[32, 40] as in other African studies[41, 42]. We saw a similar trend in our study. This is of concern as the majority of HIV infections occur in this age group[4346]. Some studies have suggested increased non-adherence among men[32, 35, 36, 47, 48]. While this was also the case in our study, the there was only modest statistical support for this association. There is varying data on the impact of relationship status with non-adherence. Some studies have not found an association between relationship status and non-adherence while others have found marriage to be risk factor[38] for poor adherence. In our setting there was an association between poor adherence and marriage ending either due to dissolution or death. There was also a positive association between education and adherence levels in our study similar to Yaya et al’s observation in Togo, a typical Sub-Saharan African context[49].

Review of literature suggests that, in low and high (but not middle) income countries, employment status of HIV-infected patients impacts ART adherence[41, 50]. Our study found that, ART non-adherence in the Tanzanian setting is associated with unemployment. Similar to other studies, for example, Muya et al[32], which associated non-adherence with increased CD4 count and duration on ART, this study found increased risk for ART non-adherence with higher CD4 counts, although the association was inconsistent across CD4 count strata and warrants further exploration. There was also an association between ART non-adherence and living in urban areas as it was observed in the study of veteran ART users in the United States[51].

Strengths and weaknesses of the study

This study adapted a validated questionnaire to elicit potential predictors of ART non-adherence and to determine 4-day adherence recall[33]. Unlike most other studies, we determined non-adherence using two measures (PDR and patient recall) to provide a dual assessment of adherence. Although the PDR method assumes complete and accurate data entry as well as complete swallowing of the collected pills, it still provides an effective and simple way of measuring non-adherence[22] and has been observed to offer clinically relevant information[23, 41]. Patient recall measures are well known for subjectivity, recall bias and underestimation of non-adherence[20, 21, 52, 53] nonetheless the correlation with viral load, affordability and simplicity [20, 54, 55] cannot be overlooked. We argue that, incomplete data entry which underestimates adherence may have attributed to profound difference in non-adherence-estimates of the two measures. The large difference in non-adherence estimates might also have been the result of the sampling approaches, one being cross-sectional and the other integrating data over a 2-year period. Since the two measures were poorly correlated in our study, we preferred using PDR over the patient recall measure in further analyses based on findings and recommendations from previous studies[2224], and therefore in addition to the strength of using two adherence measures, associations were assessed against the more robust measure. However, this study suffers the limitation of under-assessment of adherence due to possible incorrect and incomplete data entries. The study was also under-powered for testing many of the associations due to the limited sample size. The chosen approach is informative, although does not use longitudinal analysis techniques to analyze longitudinal data and therefore ignores the complex nature of dealing with complicated drug prescription data.

Implications of the study findings and future research

These results highlight that, in order to achieve minimal levels of non-adherence, the ART care and treatment team should focus adherence interventions in patients who are younger, those who were previously married and those with lower levels of education. Adherence intervention could also be focused on patients who are not employed, and possibly men, those with high CD4 counts and those who live in urban areas. Further, perhaps qualitative, research could be used to gain a better understanding of youth-specific ART concerns and to identify manageable issues for those who are unemployed or have lost the support of marital partners, to inform future interventions. Achieving high levels of adherence will improve virological, immunological and clinical outcomes and offer better quality and prolonged life.

Conclusion

The study has demonstrated that a substantial proportion of patients are sub-optimally adherent to ART, and that there are a number of identifiable associations with non-adherence which could guide future interventions to improve adherence support. Adherence promotion strategies could be adapted to address youth-specific factors, and household factors such as loss of support from a spouse and unemployment. Additional patient groups in whom further exploration of adherence issues is warranted include men, those in urban settings and potentially those with higher recent CD4 counts.

Supporting information

S1 Questionnaire. Questionnaire—Predictors of non-adherence.

https://doi.org/10.1371/journal.pone.0189460.s002

(DOCX)

Acknowledgments

I would like to express my sincere appreciation to the Sociobehavioral Sciences Training and Research (SBS)—grant number D43TW009595 for funding my MPH studies at UCT and also supporting this research as part of MPH dissertation.

Special appreciation to the SBS project team; Prof. John A. Bartlett, Mr. Charles Muiruri, Mrs. Jessie Hardson, Mr. Frank M. Kimaro and Mr. Francis Karia for their timely follow up of my funding schedules.

I would like to express the data collection team, Mrs Adelina Lymo, Miss Elizabeth Amos Kazungu, Mrs Lilian Beatus and Mrs Editha Mushi for the hard work through successful data collection.

References

  1. 1. WHO/UNAIDS. GLOBAL AIDS RESPONSE PROGRESS REPORTING 2014; Construction of Core Indicators for monitoring the 2011 United Nations Political Declaration on HIV and AIDS. 2014.
  2. 2. Fang C-T, Hsu H-M, Twu S-J, Chen M-Y, Chang Y-Y, Hwang J-S, et al. Decreased HIV transmission after a policy of providing free access to highly active antiretroviral therapy in Taiwan. Journal of Infectious Diseases. 2004;190(5):879–85. pmid:15295691
  3. 3. WHO. Scaling up antiretroviral therapy in resource-limited settings: treatment guidelines for a public health approach—2006. 2006.
  4. 4. Vitoria M, Vella S, Ford N. Scaling up antiretroviral therapy in resource-limited settings: adapting guidance to meet the challenges. Current Opinion in HIV and AIDS. 2013;8(1):12–8. pmid:23188179
  5. 5. HIV/AIDS JUNPo. Global AIDS update 2016. Geneva: UNAIDS. 2016.
  6. 6. AVERT. HIV AND AIDS IN TANZANIA 2015.
  7. 7. UR T. GLOBAL AIDS RESPONSE COUNTRY PROGRESS REPORT 2014.
  8. 8. 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. pmid:11915001
  9. 9. Sethi AK, Celentano DD, Gange SJ, Moore RD, Gallant JE. Association between adherence to antiretroviral therapy and human immunodeficiency virus drug resistance. Clinical Infectious Diseases. 2003;37(8):1112–8. pmid:14523777
  10. 10. 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. Aids. 2001;15(9):1181–3. pmid:11416722
  11. 11. Peltzer K, Pengpid S. Socioeconomic factors in adherence to HIV therapy in low-and middle-income countries. Journal of health, population, and nutrition. 2013;31(2):150. pmid:23930333
  12. 12. Falagas ME, Zarkadoulia EA, Pliatsika PA, Panos G. Socioeconomic status (SES) as a determinant of adherence to treatment in HIV infected patients: a systematic review of the literature. Retrovirology. 2008;5(1):13.
  13. 13. Hodgson I, Plummer ML, Konopka SN, Colvin CJ, Jonas E, Albertini J, et al. A systematic review of individual and contextual factors affecting ART initiation, adherence, and retention for HIV-infected pregnant and postpartum women. PLoS One. 2014;9(11):e111421. pmid:25372479
  14. 14. Mills EJ, Nachega JB, Bangsberg DR, Singh S, Rachlis B, Wu P, et al. Adherence to HAART: a systematic review of developed and developing nation patient-reported barriers and facilitators. PLoS medicine. 2006;3(11):e438. pmid:17121449
  15. 15. Uthman OA, Magidson JF, Safren SA, Nachega JB. Depression and adherence to antiretroviral therapy in low-, middle-and high-income countries: a systematic review and meta-analysis. Current HIV/AIDS Reports. 2014;11(3):291–307. pmid:25038748
  16. 16. Mills EJ, Nachega JB, Buchan I, Orbinski J, Attaran A, Singh S, et al. Adherence to antiretroviral therapy in sub-Saharan Africa and North America: a meta-analysis. Jama. 2006;296(6):679–90. pmid:16896111
  17. 17. Nachega JB, Stein D, Lehman D, Hlatshwayo D, Mothopeng R, Chaisson R, et al. Adherence to antiretroviral therapy in HIV-infected adults in Soweto, South Africa. AIDS Research & Human Retroviruses. 2004;20(10):1053–6.
  18. 18. Chalker J, Wagner A, Tomson G, Laing R, Johnson K, Wahlström R, et al. Urgent need for coordination in adopting standardized antiretroviral adherence performance indicators. JAIDS Journal of Acquired Immune Deficiency Syndromes. 2010;53(2):159–61. pmid:19861899
  19. 19. Chesney MA. The elusive gold standard: future perspectives for HIV adherence assessment and intervention. JAIDS Journal of Acquired Immune Deficiency Syndromes. 2006;43:S149–S55. pmid:17133199
  20. 20. Berg KM, Arnsten JH. Practical and conceptual challenges in measuring antiretroviral adherence. Journal of acquired immune deficiency syndromes (1999). 2006;43(Suppl 1):S79.
  21. 21. Gao X, Nau DP. Congruence of three self-report measures of medication adherence among HIV patients. Annals of Pharmacotherapy. 2000;34(10):1117–22. pmid:11054976
  22. 22. Nachega JB, Hislop M, Dowdy DW, Lo M, Omer SB, Regensberg L, et al. Adherence to highly active antiretroviral therapy assessed by pharmacy claims predicts survival in HIV-infected South African adults. JAIDS Journal of Acquired Immune Deficiency Syndromes. 2006;43(1):78–84. pmid:16878045
  23. 23. Grossberg R, Zhang Y, Gross R. A time-to-prescription-refill measure of antiretroviral adherence predicted changes in viral load in HIV. Journal of clinical epidemiology. 2004;57(10):1107–10. pmid:15528063
  24. 24. Goldman JD, Cantrell RA, Mulenga LB, Tambatamba BC, Reid SE, Levy JW, et al. Simple adherence assessments to predict virologic failure among HIV-infected adults with discordant immunologic and clinical responses to antiretroviral therapy. AIDS research and human retroviruses. 2008;24(8):1031–5. pmid:18724803
  25. 25. Carrieri P, Cailleton V, Le Moing V, Spire B, Dellamonica P, Bouvet E, et al. The dynamic of adherence to highly active antiretroviral therapy: results from the French National APROCO cohort. JAIDS Journal of Acquired Immune Deficiency Syndromes. 2001;28(3):232–9. pmid:11694829
  26. 26. Chesney MA. Factors affecting adherence to antiretroviral therapy. Clinical Infectious Diseases. 2000;30(Supplement_2):S171–S6.
  27. 27. Sabaté E. Adherence to long-term therapies: evidence for action: World Health Organization; 2003.
  28. 28. Lyimo RA, de Bruin M, van den Boogaard J, Hospers HJ, van der Ven A, Mushi D. Determinants of antiretroviral therapy adherence in northern Tanzania: a comprehensive picture from the patient perspective. BMC public health. 2012;12(1):716.
  29. 29. Watt MH, Maman S, Golin CE, Earp JA, Eng E, Bangdiwala SI, et al. Factors associated with self-reported adherence to antiretroviral therapy in a Tanzanian setting. AIDS care. 2010;22(3):381–9. pmid:20390519
  30. 30. Health TMo. NATIONAL GUIDELINES FOR THE MANAGEMENT OF HIV AND AIDS. 2012.
  31. 31. Hsieh FY, Bloch DA, Larsen MD. A simple method of sample size calculation for linear and logistic regression. Statistics in medicine. 1998;17(14):1623–34. pmid:9699234
  32. 32. Muya AN, Geldsetzer P, Hertzmark E, Ezeamama AE, Kawawa H, Hawkins C, et al. Predictors of nonadherence to antiretroviral therapy among HIV-infected adults in Dar es Salaam, Tanzania. Journal of the International Association of Providers of AIDS Care (JIAPAC). 2015;14(2):163–71.
  33. 33. Reynolds NR, Sun J, Nagaraja HN, Gifford AL, Wu AW, Chesney MA. Optimizing measurement of self-reported adherence with the ACTG Adherence Questionnaire: a cross-protocol analysis. JAIDS Journal of Acquired Immune Deficiency Syndromes. 2007;46(4):402–9. pmid:18077832
  34. 34. Health TMo. National Guidelines for the Management of HIV and AIDS. 2015.
  35. 35. Bam K, Rajbhandari RM, Karmacharya DB, Dixit SM. Strengthening adherence to Anti Retroviral Therapy (ART) monitoring and support: operation research to identify barriers and facilitators in Nepal. BMC health services research. 2015;15(1):188.
  36. 36. Li L, Lee SJ, Wen Y, Lin C, Wan D, Jiraphongsa C. Antiretroviral therapy adherence among patients living with HIV/AIDS in Thailand. Nursing & health sciences. 2010;12(2):212–20.
  37. 37. Ramadhani HO, Thielman NM, Landman KZ, Ndosi EM, Gao F, Kirchherr JL, et al. Predictors of incomplete adherence, virologic failure, and antiviral drug resistance among HIV-infected adults receiving antiretroviral therapy in Tanzania. Clinical Infectious Diseases. 2007;45(11):1492–8. pmid:17990233
  38. 38. 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.
  39. 39. Shigdel R, Klouman E, Bhandari A, Ahmed LA. Factors associated with adherence to antiretroviral therapy in HIV-infected patients in Kathmandu District, Nepal. HIV/AIDS (Auckland, NZ). 2014;6:109.
  40. 40. Watt MH, Maman S, Earp JA, Eng E, Setel PW, Golin CE, et al. “It's all the time in my mind”: Facilitators of adherence to antiretroviral therapy in a Tanzanian setting. Social science & medicine. 2009;68(10):1793–800.
  41. 41. Govindasamy D, Ford N, Kranzer K. Risk factors, barriers and facilitators for linkage to antiretroviral therapy care: a systematic review. Aids. 2012;26(16):2059–67. pmid:22781227
  42. 42. Nachega JB, Hislop M, Nguyen H, Dowdy DW, Chaisson RE, Regensberg L, et al. Antiretroviral therapy adherence, virologic and immunologic outcomes in adolescents compared with adults in southern Africa. Journal of acquired immune deficiency syndromes (1999). 2009;51(1):65.
  43. 43. Hall HI, Song R, Rhodes P, Prejean J, An Q, Lee LM, et al. Estimation of HIV incidence in the United States. Jama. 2008;300(5):520–9. pmid:18677024
  44. 44. Kapiga SH, Lyamuya EF, Lwihula GK, Hunter DJ. The incidence of HIV infection among women using family planning methods in Dar es Salaam, Tanzania. Aids. 1998;12(1):75–84. pmid:9456257
  45. 45. Mwita W, Urassa M, Isingo R, Ndege M, Marston M, Slaymaker E, et al. HIV prevalence and incidence in rural Tanzania: results from 10 years of follow-up in an open cohort study. Journal of acquired immune deficiency syndromes (1999). 2007;46(5):616.
  46. 46. Rehle T, Shisana O, Pillay V, Zuma K, Puren A, Parker W. National HIV incidence measures-new insights into the South African epidemic. South African Medical Journal. 2007;97(3):194–9. pmid:17440667
  47. 47. Talam N, Gatongi P, Rotich J, Kimaiyo S. Factors affecting antiretroviral drug adherence among HIV/AIDS adult patients attending HIV/AIDS clinic at Moi Teaching and Referral Hospital, Eldoret, Kenya. 2008.
  48. 48. Venkatesh KK, Srikrishnan A, Mayer KH, Kumarasamy N, Raminani S, Thamburaj E, et al. Predictors of nonadherence to highly active antiretroviral therapy among HIV-infected South Indians in clinical care: implications for developing adherence interventions in resource-limited settings. AIDS patient care and STDs. 2010;24(12):795–803. pmid:21091232
  49. 49. Yaya I, Landoh DE, Saka B, Wasswa P, Aboubakari A-s, N’Dri MK, et al. Predictors of adherence to antiretroviral therapy among people living with HIV and AIDS at the regional hospital of Sokodé, Togo. BMC public health. 2014;14(1):1308.
  50. 50. Nachega JB, Uthman OA, Peltzer K, Richardson LA, Mills EJ, Amekudzi K, et al. Association between antiretroviral therapy adherence and employment status: systematic review and meta-analysis. Bulletin of the World Health Organization. 2015;93(1):29–41. pmid:25558105
  51. 51. Ohl ME, Perencevich E, McInnes DK, Kim N, Rimland D, Akgun K, et al. Antiretroviral adherence among rural compared to urban veterans with HIV infection in the United States. AIDS and Behavior. 2013;17(1):174–80. pmid:23080359
  52. 52. 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. pmid:11550118
  53. 53. Chesney MA, Ickovics J, Chambers D, Gifford A, Neidig J, Zwickl B, et al. Self-reported adherence to antiretroviral medications among participants in HIV clinical trials: the AACTG adherence instruments. AIDS care. 2000;12(3):255–66. pmid:10928201
  54. 54. Haubrich RH, Little SJ, Currier JS, Forthal DN, Kemper CA, Beall GN, et al. The value of patient-reported adherence to antiretroviral therapy in predicting virologic and immunologic response. Aids. 1999;13(9):1099–107. pmid:10397541
  55. 55. Simoni JM, Pearson CR, Pantalone DW, Marks G, Crepaz N. Efficacy of interventions in improving highly active antiretroviral therapy adherence and HIV-1 RNA viral load: a meta-analytic review of randomized controlled trials. Journal of acquired immune deficiency syndromes (1999). 2006;43(0 1):S23.