Generic selectors
Exact matches only
Search in title
Search in content
Post Type Selectors
Filter by Categories
Case Report
Editorial
Original Article
Review Article
Generic selectors
Exact matches only
Search in title
Search in content
Post Type Selectors
Filter by Categories
Case Report
Editorial
Original Article
Review Article
View/Download PDF

Translate this page into:

Original Article
6 (
1
); 24-30
doi:
10.25259/CJHS_16_2019

A comparative study of the predictors of treatment adherence among patients on antiretroviral therapy at rural and urban centers in Cross River State, Nigeria

Department of Family Medicine, University of Calabar Teaching Hospital, Calabar, Cross River, Nigeria
Corresponding author: Felix Archibong, Department of Family Medicine, University of Calabar Teaching Hospital, Calabar, Cross River, Nigeria. dr.felixarchibong@yahoo.com
Licence
This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, transform, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.

How to cite this article: Archibong F, Ugbonna UK, Okoye I, Legogie A, Fadipe I, Nyong E, et al. A comparative study of the predictors of treatment adherence among patients on antiretroviral therapy at rural and urban centers in Cross River State, Nigeria. Calabar J Health Sci 2022;6:24-30.

Abstract

Objectives:

Adherence to antiretroviral therapy (ART) is an important factor required to suppress viral activities and its load in the human body. There are identified factors that determine adherence to ART and these factors have been noticed based on environments. This study compared predictors of ART adherence between the urban and rural centers within the same State in Nigeria.

Material and Methods:

The study was a cross-sectional analytic study involving 322 participants. Data were analyzed using Statistical Package for the Social Sciences version 20. Descriptive and inferential statistics were done with the data collected.

Results:

There were more adherent participants in the urban than the rural center in a ratio of 2.2:1. There was also significant difference in the predictors of adherence to ART in these two centers. The factors that were not present in both centers were: Stigma experience, family support, and sex.

Conclusion:

Predictors of treatment adherence vary between the urban and rural treatment centers even within the same senatorial district of a state. Therefore, it is advisable to always determine factors that predicts adherence to ART which would serve as a guide to proper treatment of the patient.

Keywords

Adherence
Antiretroviral therapy
Urban
Rural
Cross river state

INTRODUCTION

Human immunodeficiency virus infection/acquired immunodeficiency syndrome (HIV/AIDS) has remained a burden to most families in sub-Saharan Africa which harbors about 70% of the world’s HIV infected population.[1] The prevalence of HIV/AIDS in Nigeria based on the sentinel surveillance of 2019 was 1.4% and Cross River State had an estimated prevalence of 1.7% which was the 5th medium prevalence in Nigeria with a range of 8.2% (in the urban areas) to 1.8% (in the rural areas).[1]

In the absence of a cure for HIV/AIDS, antiretroviral therapy (ART) has remained the only available option that offers the possibility of reducing HIV/AIDS-related morbidity and mortality while improving the quality of life of the people living with HIV and AIDS (PLWHA).[2,3] However, ART has to be taken as a lifelong therapy and its success depends on continual adherence to the medication regimen.[4,5]

ART has improved the health of many HIV positive individuals who would have died due to this infection.[6,7] This evidence was shown in the annual number of HIV/ AIDS deaths which declined from 2.5 million in 2005 to 0.67 million in 2017.[8] In part, this decline in the death of PLWHA was likely a result of the substantial increase in access to HIV/AIDS treatment and adherence to ART.[8,9]

The World Health Organization defined adherence as the extent to which a person’s behavior: taking medication, following a diet, and/or executing lifestyle changes, corresponds with agreed recommendations from a healthcare provider.[10] and the Nigerian National Guidelines for HIV and AIDS Treatment and Care in Adolescents and Adults agree with this ≥ 95% cutoff for ART adherence, asserting that for a patient to be tagged as adherent to ART, he must not miss more than one dose in 10 days if on a twice daily regimen or one dose in 20 days if on a once daily regime.[11]

The identified factors that can influence medication adherence in PLWHA can be categorized into three groups: Patient-related, health system-related, and clinical factors.[12] Predictors of adherence to ART vary among patients, environments, and communities.

The health system-related factors includes: Drugs being out of stock, insufficient amount of time a clinician spends with the patient due to overtaxing of the healthcare system, lack of utilization of health information, lack of feedback from patient, and meeting different doctors at each consultation follow-up visits.

The patient-related factors that may lead to non-adherence are lack of patient’s understanding of the relationship between the disease, the required percentage of adherence and quality of life, lack of involvement in the treatment decision-making process, feelings of stigmatization, sharing drugs with spouse and other family members, feelings of wellness, undetectable level of virus in peripheral blood following long-term ART and faith in miraculous healing.[13,14]

The above listed factors can vary based on the environment such as urban and rural communities. This study aims to assess, identify, and compare the factors that predict treatment adherence among patients on ART in an urban and a rural clinic, to improve patients’ management outcome.

MATERIAL AND METHODS

This was a cross-sectional analytical study conducted within 4 months from March to June 2015. Using interviewer’s administered questionnaire of adapted Morisky 8-item medication adherence questionnaire,[15] Duke functional social questionnaire,[16] modified family support scale,[17] data for this study were collected at the Family Medicine Clinic of the University of Calabar Teaching Hospital (UCTH), Calabar and General Hospital (GH), Ikot Ene in Akpabuyo LGA, Cross River State, Nigeria. These intervention sites were established and funded by President’s Emergency Plan for AIDS Relief (PEPFAR) and had been operational since 2005.

A total of 322 participants (161 from each study sites) were recruited into the study after calculating sample size using formula for demonstrating significant difference in two independent groups.[18] and systematic sampling technique was utilized for selection criteria into the study. The inclusion criteria were PLWHA 18 years of age and above that were on ART for at least 6 months, who had consented to participate in the study. All critically ill patients were excluded from the study.

Data collected for this study was analyzed using the Statistical Package for the Social Sciences version 20 software, manufactured by International Business Machines Corporations, United State of Ameriaca. Descriptive and inferential statistics were done.

Ethical approved for this study was given by the Health Research and Ethics Committee of the UCTH with protocol number NHREC/07/2012/UCTH/HREC/33/250. There was no conflict of interest in any of the authors.

RESULTS

Comparing the socio-demographic characteristics of the study participants in the urban and rural centers [Table 1]. The trend in the tribe distribution had a statistically significant difference ranging from 1.9% to 10.5% as seen among the Ejagham and Ibibio ethic groups respectively. There was a significant difference of 12.4% in the distribution of religion between the urban and rural respondents. The ratio of females to males in both centers was 1.1:1.0, however, this difference was not statistically significant. The difference in the trend of age group and marital status in the respondents in the urban and rural centers ranged from 1.3–5.5% and 0–9.9%, respectively. These differences were not statistically significant.

Table 1: Comparing the socio-demographic characteristics of study participants in urban and rural centers.
Variable Urban (n=161) Frequency (%) Rural (n=161) Frequency (%) Total (n=322) Frequency (%) Chi-square P-value
Sex
Male 76 (47.2) 77 (47.8) 153 (47.5) 1.393 0.498
Female 85 (52.8) 84 (52.2) 169 (52.5)
Age group (years)
20–29 42 (26.2) 51 (31.7) 93 (28.9) 1.572 0.666
30–39 78 (48.4) 75 (46.6) 153 (47.5)
40–49 35 (21.7) 31 (19.3) 66 (20.5)
≥50 6 (3.7) 4 (2.4) 10 (3.1)
Mean age±SD 34.96±7.11 34.07±7.00 34.52±7.00 2.561** 0.320
Marital status
Never married 19 (11.8) 10 (6.2) 29 (9.0) 6.565 0.255
Married 104 (64.6) 120 (74.5) 224 (69.6)
Cohabiting 20 (12.4) 15 (9.3) 35 (10.9)
Previously married 18 (11.2) 16 (9.9) 34 (10.5)
Tribe
Efik 49 (30.4) 61 (37.9) 110 (34.2) 16.268 0.039*
Ejagham 23 (14.3) 20 (12.4) 43 (13.3)
Ibibio 34 (21.2) 51 (31.7) 85 (26.4)
Annang 15 (9.3) 10 (6.2) 25 (7.8)
***Others 40 (24.8) 19 (11.8) 59 (18.3)
Religion
Christianity 146 (90.7) 156 (96.9) 302 (93.8) 5.331 0.021*
Islam 15 (9.3) 5 (3.1) 20 (6.2)
Statistically significant. **t-test. ***Others include Hausa, Yakkur, Ijaw, Ibo, Yoruba

Table 2 compares the socio-economic characteristics of the study participants in the urban and rural centers. It was noticed that the trend in educational level had a differences ranging from 0.6% to 15.5%. The differences in the trend of the distribution of the employment of the respondents in both centers ranged from 0 to 8.6% with self-employment having the highest difference. Comparing the average monthly income and place of residence in both study centers, differences were 6.8% and 23.6%, respectively

Table 2: Comparing the socio-economic characteristics of study participants in urban and rural centers.
Variable Urban (n=161) Frequency (%) Rural (n=161) Frequency (%) Total (n=322) Frequency (%) Chi-square P-value
Educational level
None 10 (6.2) 13 (8.1) 23 (7.1) 21.898 <0.001*
Primary 14 (8.7) 16 (9.9) 30 (9.3)
Secondary 65 (40.4) 84 (52.2) 149 (46.3)
Post-secondary 43 (26.7) 44 (27.3) 87 (27.1)
University 29 (18.0) 4(2.5) 33 (10.2)
Employment
By Government 26 (16.1) 21 ( 13.0) 47 (14.6) 10.562 0.032*
By Private sector 48 (29.8) 48 (29.8) 96 (29.8)
Self employed 68 (42.3) 82 (50.9) 150 (46.6)
Unemployed 19 (11.8) 10 (6.3) 29 (9.0)
Monthly income (₦)
<19,000 23 (14.3) 12 (7.5) 35 (10.9) 5.610 0.061
≥19,000 138 (85.7) 149 (92.5) 287 (89.1)
Area of residence
Urban 110 (68.3) 148 (91.9) 258 (80.1) 16.884 0.184
Rural 51 (31.7) 13 (8.1) 64 (19.9)
Statistically significant

Table 3 presents the comparison of the patient-related factors that predicted adherence to ART at the two study centers.

Table 3: Comparing patient-related characteristics of study participants in urban and rural centers.
Variable Urban (n=161) Frequency (%) Rural (n=161) Frequency (%) Total (n=322) Frequency (%) Chi-square P-value
Art should be taken for life
Yes 153 (95.0) 160 (99.4) 313 (97.2) 6.354 0.012*
No 8 (5.0) 1 (0.6) 9 (2.8)
≥95% Adherence is required
Yes 96 (59.6) 91 (56.5) 187 (58.1) 0.319 0.572
No 65 (40.4) 70 (43.5) 135 (41.9)
Self-reporting adherence
Yes 107 (66.5) 95 (59.0) 202 (62.7) 1.68 0.715
No 54 (33.5) 66 (41.0) 120 (37.3)
Adherence on pharmacy records
Yes 106 (65.8) 80 (49.4) 186 (57.6) 1.85 0.001*
No 55 (34.2) 81 (50.6) 136 (42.4)
Clinical stage
Stage 1 25 (15.5) 9 (5.6) 34 (10.6) 13.229 0.004*
Stage 2 45 (28.0) 53 (32.9) 98 (30.4)
Stage 3 61 (37.9) 51 (31.7) 112 (34.8)
Stage 4 30 (18.6) 48 (29.8) 78 (24.2)
CD4
Class A (>500) 132 (82.0) 140 (87.0) 272 (84.5) 2.625 0.269
Class B (200–500) 28 (17.4) 21 (13.0) 49 (15.2)
Class C (<200) 1 (0.6) 0 (0.0) 1 (0.3)
BMI
Underweight (<18.5) 3 (1.9) 2 (1.2) 5 (1.6) 2.402 0.121
Normal (18.5–24.9) 59 (37.1) 54 (33.5) 113 (35.3)
Over-wt. (25–29.9) 65 (40.9) 58 (36.0) 123 (38.4)
Obese (≥30) 34 (20.1) 47 (29.2) 81 (24.7)
Statistical significant

The result showed more participants (4.4%) in the rural center were aware of the need to take ART for life and this difference was statistically significant (P = 0.012).

The adherence to ART on pharmacy records had a difference 16.4% between the urban and rural centers. The trend in the distribution of clinical stages of the respondents in both study centers ranged from 4.9 to 11.2%. The difference in the self-reported adherence and awareness of the need for optimal adherence to ART was 7.5% and 3.1%, respectively. The trend in the distributions of CD4 and BMI had differences that ranged from 0.6–5% and 0.7–9.1%, respectively.

Table 4 presents the predictors of adherence to ART among the study participants in the urban and rural centers. The two centers had the following predictors in common: awareness that ≥95% adherence was a requirement, adherence on pharmacy records, clinical stage, family support, and stigmatization experience. In addition to, these predictors the rural center had family support.

Table 4: Predictors of art adherence among study participants in urban and rural centres.
Variable Adherence to ARV therapy (on pharmacy records)
Urban Rural
High (n=107) Low (n=54) X2 (P-value) High (n=95) Low (n=66) X2 (P-value)
ARV drugs should be taken for life
Yes 103 (67.3) 50 (32.7) 0.969 (0.530) 94 (58.8) 66 (41.2) 1.059 (0.132)
No 4 (50.0) 4 (50.0) 1 (100.0)
≥ 95% adherence is required
Yes 88 (91.7) 8 (8.3) 67.780 (< 0.001*) 77 (84.6) 14 (15.4) 56.747 (<0.001*)
No 19 (29.2) 46 (70.8) 18 (15.4) 52 (84.6)
Adherence on pharmacy records
Yes 99 (93.4) 7 (6.6) 101.022 (<0.001*) 74 (93.7) 5 (6.3) 78.524 (< 0.001*)
No 8 (14.5) 47 (85.5) 21 (26.7) 61 (73.3)
Clinical stage
Stage 1 15 (60.0) 10 (40.0) 14.959 (0.002*) 4 (44.4) 5 (55.6) 33.680 (< 0.001*)
Stage 2 23 (51.1) 22 (48.9) 16 (30.2) 37 (69.8)
Stage 3 41 (67.2) 20 (32.8) 35(68.6) 16 (31.4)
Stage 4 28 (93.3) 2 (6.7) 40 (83.3) 8 (16.7)
Social support
Low 2 (66.7) 1 (33.3) 2.495 (0.287) 1 (33.3) 2 (66.7) 7.841 (0.020*)
Moderate 34 (58.6) 24 (41.4) 21 (43.8) 27 (56.2)
High 71 (71.0) 29 (29.0) 73 (66.4) 37 (33.6)
Family support
Low 42 (56.0) 33 (44.0) 13.967 (0.001*) 2 (10.0) 18 (90.0) 45.913 (<0.001*)
Moderate 40 (66.7) 20 (33.3) 48 (51.6) 45 (48.4)
High 25 (96.2) 1 (3.8) 45 (93.8) 3 (6.2)
Stigmatization experience
No 42 (93.2) 3 (6.8) 22.579 (< 0.001*) 40 (91.3) 5 (8.7) 43.195 (< 0.001*)
Yes 65(56.0) 51(44) 55 (47.4) 61(52.6)

*Statistically significant

The urban center had 7% more respondents that were aware of the need to take ≥ 95% of their ART. The pharmacy record in the rural center was 0.3% more relationship than the urban center. The differences between the trends in clinical stages of the respondents in the urban and rural centers range from 2.2–86.6% and 11.2–66.6%, respectively.

The trend in social support in the rural respondents ranged between 11.2 and 32.8%. The differences in the trend in family support between the urban and rural centers were in a range of 4.8–68%. About 8.6% of the participants in the urban center experienced high stigmatization than those in the rural center.

Table 5 shows binary logistic regression of predictors of antiretroviral treatment adherence among study participants in the urban and rural centers. The result revealed that the two centers had in common adherence on pharmacy records and awareness that ≥95% adherence was a requirement as the predictors of adherence to ART. In addition to these, sex was a predictor in the urban center while family support and stigmatization were noticed as predictors in the rural center.

Table 5: Binary logistic regression of predictors of antiretroviral treatment adherence among study participants in urban and rural centers.
Variable Urban Rural
Odds ratio 95% Confidence interval P-value Odds ratio 95% Confidence interval P-value
≥ 95% adherence is required
Yes 6.4 1.95–21.20 0.002* 4.17 1.37–12.72 0.012*
No 1 1
Adherence on pharmacy records
Yes 36.67 11.27–132.72 < 0.001* 16.97 4.91–58.56 <0.001*
No 1 1
Clinical stage
Stage 1 and 2 0.91 0.28–2.96 0.8790 0.511 0.161–1.622 0.254
Stage 3 and 4 1 1
Family support
Low / moderate 0.96 0.28–3.25 0.947 0.12 0.027–0.698 0.017*
High 1 1
Stigma experience
No 4.61 0.613–34.61 0.138 4.67 1.12–19.45 0.034*
Low / High 1 1
Sex
Male 0.4 0.20–0.96 0.039
Female 1
Social support
Low / moderate 0.9 0.45–20.05 0.972
High 1
Statistically significant

There were three times more respondents in the urban center that were aware that ≥95% adherence was required than in the rural center. The ratio of adherence on pharmacy records between the urban and rural centers was 2.2:1. In the rural center participants with no stigmatization experience were more than 4 times more likely to adhere to ART. In the urban center, males were < ½ times likely to adhere to ART.

DISCUSSION

In this study, 66.5% of urban respondents were adherent to ART based on self-reported method while 65.8% of them were adherent as shown on pharmacy record. The difference between the two methods used was not significant. The adherence to ART was lower in the rural respondents both in the self-reported method (59.0%) and pharmacy record (49.4%). This difference between the methods could be explained by the suggestion that the use of pharmacy records in assessing adherence to ART is superior to self-reporting method, though not up to the 10–20% proposed difference.[19]

The proportion of adherence among urban respondents in this study was similar to a study in Ibadan (2015) with 63% adherence level.[20] However, it was different from a study carried out in Ethiopia (2015) where 83.1% of the respondents were adherent to ART.[21]

In this study, the predictors of ART adherence were: Sex, body mass index, family/community support, awareness of the need for ≥ 95% adherence, stigma experience, and adherence as shown on pharmacy records.

The difference in the ART adherence proportion between the rural and urban respondents in this study may be due to some environmental factors such as community/social supports. A study carried out in a Teaching Hospital in Wolaita Soddo, Ethiopia by Alagaw et al. (2013), revealed that the predictors of ART adherence were: Sources of food for consumption, food scarcity, the person or people the client lives with and presence of depression in the patient.[20] This was different from a study in Northern Ethiopia by Demeke and Chanie (2014), which showed that duration of treatment, family disclosure, living condition, and taking other medications along with ART were the predictors.[22] Another study in South-East Ethiopia by Lencha et al. (2015), reported that history of drug abuse, relationship with clinician and keeping to regular follow-up were the determinants of ART adherence.[23]

This study is in agreement with the studies cited above that predictors of ART vary with geographic areas and it further portrays that even in the same districts there could be difference between the urban and rural area.

CONCLUSION

There was the possibility of response bias by participants who may have falsely reported to be adherent to medications in order to impress the interviewer. However, the study showed that there are similarities and differences in the predictors of ART adherence between the urban and rural centers. The identified predictors above may serve as a guide for developing interventions aimed at improving the proportion of patient on ART and sustain the adherence among these clients.

Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

References

  1. . Revised National HIV and AIDS Strategic Framework 2019-2021 Abuja: NACA; . p. :13.
    [Google Scholar]
  2. , , , . Prevalence and determinants of adherence to HAART amongst PLHIV in a tertiary health facility in South-South Nigeria. BMC Infect Dis. 2013;13:401-9.
    [CrossRef] [PubMed] [Google Scholar]
  3. , . Current strategies for improving access and adherence to antiretroviral therapies in resource-limited settings. HIV AIDS (Auckl). 2013;5:1-17.
    [CrossRef] [PubMed] [Google Scholar]
  4. , , , , . Adherence to antiretroviral therapy in Nigeria: An overview of research studies and implications for policy and practice. HIV AIDS (Auckl). 2010;2:69-76.
    [CrossRef] [PubMed] [Google Scholar]
  5. , , , , , , et al. Adherence to antiretroviral therapy in sub-Saharan Africa and North America. J Am Med Assoc. 2006;296:679-90.
    [CrossRef] [PubMed] [Google Scholar]
  6. , , , , . Barriers to access to antiretroviral treatment in developing countries: A review. Trop Med Int Health. 2008;13:904-13.
    [CrossRef] [PubMed] [Google Scholar]
  7. , , , , , , et al. Response to antiretroviral therapy in HIV-infected patients attending a public, urban clinic in Kampala, Uganda. Clin Infect Dis. 2006;42:252-9.
    [CrossRef] [PubMed] [Google Scholar]
  8. . Fact Sheet-World AIDS Day 2017 GLOBAL HIV STATISTICS. Fact Sheet. 2018:1-6.
    [Google Scholar]
  9. . FACT SHEET 2015. Switzerland: UNAIDS; . p. :1-8.
    [Google Scholar]
  10. . Guidance on Operation and Service Delivery: Adherence to ART Geneva: World Health Organisation; . p. :174-96.
    [Google Scholar]
  11. . National Guldelines for Implementation of HIV Preventive Programmes for Female Sex Workers in Nigeria Washington, DC, United States: NACA; . p. :5-45.
    [Google Scholar]
  12. , , , , , , et al. Medication adherence and risk factors for non-adherence among patients taking highly active antiretroviral therapy. West Afr J Pharm. 2011;22:19-26.
    [Google Scholar]
  13. , , . Interventions to reduce HIV/AIDS stigma: What have we learned? AIDS Educ Prev. 2003;15:49-69.
    [CrossRef] [PubMed] [Google Scholar]
  14. , , . Adherence to antiretroviral drugs among AIDS patients in Sagamu, Nigeria. Int J Biomed Health Sci. 2008;4:41-5.
    [Google Scholar]
  15. , , . Concurrent and predictive validity of a self-reported measure of medication adherence. Med Care. 1986;24:67-74.
    [CrossRef] [PubMed] [Google Scholar]
  16. , , , . Duke-UNC functional social support questionnaire. Measurement of social support in family medicine patients. Med Care. 1988;26:709-23.
    [CrossRef] [PubMed] [Google Scholar]
  17. , , . The 13 item family support scale: Reliability and validity of the Greek translation in a sample of Greek health care professionals. Asia Pac Fam Med. 2011;10:3.
    [CrossRef] [PubMed] [Google Scholar]
  18. , . Essential Medical Statistics Massachusetts, USA: Blackwell Science Limited; . p. :420.
    [Google Scholar]
  19. , , , , , , et al. Pharmacy adherence measures to assess adherence to antiretroviral therapy: Review of the literature and implications for treatment monitoring. Clin Infect Dis. 2011;52:493-506.
    [CrossRef] [PubMed] [Google Scholar]
  20. , . Alexandria University Faculty of Medicine Effects of Adherence to Antiretroviral Therapy on Body Mass Index, Immunological and Virological Status of Nigerians Living with HIV/AIDS. 2016:51-4.
    [CrossRef] [Google Scholar]
  21. , , . Assessment of factors affecting art adherence among people living with human immune virus in Bale Robe Hospital, South East Ethiopia. Am J Public Health Res. 2015;3:60-7.
    [Google Scholar]
  22. , . Adherence to antiretroviral therapy and associated factors among patients living with HIV/AIDS in Dessie referral hospital, Northern Ethiopia. Int J Pharm Sci Res. 2014;5:572-81.
    [Google Scholar]
  23. , , , , . Adherence to antiretroviral therapy and associated factors among people living with HIV/AIDS at Gobba Hospital, Southeast Ethiopia: An institutional based study. Qual Prim Care. 2015;23:336-41.
    [Google Scholar]
Show Sections