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Prevalence and associated factors of HIV testing among reproductive-age women in eastern Africa: multilevel analysis of demographic and health surveys

Abstract

Background

Despite efforts made to reduce the spread of the human immune-deficiency virus (HIV), its testing coverage remains low in low and middle-income countries (LMIC). Besides, information on factors associated with HIV counseling and testing among reproductive-age women is not sufficiently available. Therefore, this study was aimed to determine the pooled prevalence and factors associated with HIV testing among reproductive-age women in eastern Africa.

Methods

Secondary data analysis was conducted based on the Demographic and Health Surveys (DHS) data conducted in East African countries. We pooled the most recent DHS surveys done in 11 East African countries. A total weighted sample of 183,411 reproductive-age women was included for this study. Both bivariable and multivariable multilevel logistic regression models were fitted. Variables with a p-value ≤0.2 in the bivariable analysis were selected for multivariable analysis. Finally, in the multivariable analysis, variables with a p-value ≤0.05 were considered as significant factors affecting HIV testing.

Results

The pooled prevalence of HIV testing in eastern Africa was 66.92% (95%CI: 66.70, 67.13%). In the multivariable multilevel analysis factors such as the age of respondent, marital status, educational level, HIV knowledge, HIV stigma indicator, risky sexual behavior and women who visit a health facility were positively associated with HIV testing coverage among reproductive-age women. While women from rich and richest households, having multiple sexual partners, being from rural dwellers, late initiation of sex and higher community illiteracy level had a lower chance of being tested for HIV.

Conclusion

The pooled prevalence of HIV testing in eastern Africa was higher than most previous studies. Age of respondent, residence, wealth index, marital status, educational level, HIV knowledge, stigma indicator, risky sexual behavior, women who visit a health facility, multiple sexual partnerships, early initiation of sex and community illiteracy level were significantly associated with HIV testing. There should be an integrated strategic plan to give education about methods of HIV transmission and the implication of HIV testing and counseling. So all the stakeholders should have an integrated approach by giving special attention to the factors that hinder HIV testing to increase awareness regarding the benefit of HIV testing and counseling to control the spread of HIV/AIDS.

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Background

Human immune deficiency virus (HIV) testing and counseling is a public health program concerned with diagnosing and minimizing the transmission of HIV/AIDS [1]. Currently, about 38 million people are living with HIV, nearly 36.2 million of them are adults and 1.8 million children [2]. Globally, 81% of all people living with HIV know their status and about 19 million remained unaware of their HIV status, which reduced to 7.1 million in 2019 [1]. The number of people who are newly infected with HIV declined from 3.4 million in 2011 to 2.1 million in 2013 [1]. Despite this progress, HIV/AIDS remains a major public health problem [3]. African countries, particularly eastern and southern regions are greatly affected by HIV/AIDS, which accounts for two-thirds of total new infections [4, 5].

Voluntary counseling and testing are considered as an initial step to detect, treat and prevent HIV/AIDS [6, 7]. The World Health Organization recommends HIV testing and counseling for all patients showing signs and symptoms of the disease [1, 8]. In Africa HIV testing coverage ranges from 33.5 to 82.3% [9,10,11,12].

According to studies conducted in different parts of the world age of the respondent, having multiple sexual partnerships, early initiation of sex, level of education, marital status and socio-economic status are some of the factors that are significantly associated with HIV testing [7, 10, 13, 14]. Besides, stigmatized attitudes, levels of knowledge about HIV/AIDS and risky sexual behavior have an association with HIV testing and counseling [7, 12, 13, 15,16,17,18,19].

Even though HIV testing is very crucial for all strategies related to care, prevention and treatment of HIV/AIDS, it is less practiced among reproductive-age women, particularly in developing countries [6, 16]. Every individual needs to know their HIV status for the benefit of themselves and others [1, 20, 21]. Although global efforts had made to reduce the spread of HIV/AIDS, its testing coverage remains low in developing countries [2]. The assessment and identification of factors that affect the utilization of HIV counseling and testing help policymakers to design effective strategies towards preventing and controlling HIV/ADIS. Besides, previous studies were conducted at a country level, most of them did not assess the community-level factors, which might be related to HIV testing coverage. Therefore, this study aimed to assess the pooled prevalence and factors associated with HIV testing among reproductive-age women in eastern Africa.

Methods

Data sources

This study was a secondary data analysis based on datasets from the most recent Demographic and Health Surveys (DHS) conducted in east Africa (Burundi, Ethiopia, Comoros, Uganda, Rwanda, Mozambique, Madagascar, Zimbabwe, Kenya, Zambia, and Malawi). The DHS is a nationally representative survey that collects data on basic health indicators like mortality, morbidity, family planning service utilization, fertility, maternal and child health. Each survey used a two-stage stratified sampling technique to select the study participants. We pooled the most recent DHS data done in 11 East African countries and a total weighted sample of 183,411 reproductive-age women was included for this study. The survey year and total weighted sample included for this study were presented in Table 1.

Table 1 Showing the survey year and total weighted sample for each country

Variables

The outcome variable of this study was “ever been tested for HIV” which was coded as “0” for no and “1” for yes.

The independent variables included in this study were categorized as individual and community-level factors. The individual-level factors included were: age of respondent, marital status, age at 1st sex, stigmatized attitude, educational level, household wealth status, HIV knowledge, risky sexual behavior, visiting of health facility and multiple sexual partnerships. The community-level factors were community illiteracy level and residence. The community illiteracy level of women was generated by aggregating the individual level factor women’s educational level by considering the proportion of women in the community that did not have formal education and by categorized this proportion as high and low based on the national median value.

Operational definition

HIV knowledge

It was generated based on three questions related to HIV prevention and three questions related to the modes of HIV transmission and graded as low (if a woman answered ≤3 questions correctly), high (if a woman answered 4–5 questions correctly) or comprehensive (if a woman answered all the 6 questions correctly) [22].

Risky sexual behaviors

Assessed based on the five questions; having had STI in last 12 months, genital sore/ulcer in last 12 months, genital discharge in last 12 months, having at least one sexual partner other than the husband in the last 12 months, and multiple lifetimes sexual partnership. These were combined into an index of risky sexual behavior with three categories: “No risk” (if the response is no for all questions), “Some risk” (if the response is yes for one of the five questions) and “High risk” (if the response is yes to at least two questions) [22].

HIV stigma indicator

Six questions, which indicate negative attitudes towards people living with HIV / AIDS were used to this variable. This was categorized as “No stigma” (if we got a score of 6), “Low stigma” (if we got a score of 4–5), “Moderate stigma” (if we got a score of 2–3), and “High stigma” (if we got only score 1) [22].

Data management and analysis

Data extraction, recoding and analysis were done using STATA version 14 software. Both descriptive and analytical analyses were conducted. The data were weighted before doing statistical analysis to restore the representativeness of the data and to get a reliable estimate and standard error. Because of the hierarchical structure of the DHS data, a multilevel binary logistic regression analysis was used. The Interclass Correlation Coefficient (ICC), Proportional Change in Variance (PCV) and Median Odds Ratio (MOR) were calculated to assess whether there was clustering or not. In this study, four models have fitted; the null model- a model without explanatory variables, model I- a model with individual-level factors, model II- a model with community-level factors and model III- a model with both individual and community-level factors. Model comparison was done based on deviance. Both bivariable and multivariable multi-level logistic regression were done. At the bivariable analysis variables with a p-value ≤0.2 were considered for multivariable analysis. Finally, variables with a P-value of ≤0.05 in the multivariable analysis were considered as a significant factor associated with HIV testing among reproductive-age women.

Results

Socio-demographic characteristics of study participants

A total weighted sample of 183, 411 reproductive-age women were included. About 21.54% of women were in the age group of 19 years and below. The majority (92.13%) of women initiated sex at an earlier age and more than half (56.82%) of them had visited health facilities in the last 12 months. Nearly, half (48.65%) of the study participants attained primary education. Regarding HIV knowledge, about 47.81% of respondents had comprehensive knowledge about HIV/AIDS and most (60.49%) of them had multiple sexual partnerships. Concerning risky sexual behavior, the majority (81.70%) of the participant had no risky sexual behavior and 71.96% of the participants were rural dwellers (Table 2).

Table 2 Sociodemographic characteristics of the respondents in eastern Africa (N = 183, 411)

Prevalence of HIV testing in eastern Africa

The pooled prevalence of HIV testing in eastern Africa was 66.92% (95%CI: 66.70, 67.13%) ranged from 7.56% in Madagascar to 85.74% in Rwanda (Fig. 1).

Fig. 1
figure 1

Showing the prevalence of HIV testing across different countries

Random effect model and model fitness

As shown in Table 2, the ICC value in the null model was 0.10, which indicates that about 10% of the total variation in HIV testing coverage was attributable to cluster variability. Besides, the MOR value in the null model was 1.77, which indicates that there was a significant clustering of HIV testing among reproductive-age women. Furthermore, the PCV (0.36) in the final model (model III) indicated that about 36% of the variation in HIV testing was explained by both individual and community-level factors. The final model (Model III) was the best-fitted model since it had the lowest deviance (Table 3). The model predictive ability was assessed using the Area Under the Curve (AUC) and Receiver Operating Curve (ROC). These are plotted based on the probability of sensitivity and 1 – specificity. Accordingly, the AUC of the final model was 84.5% and indicated that the model’s ability to predict HIV testing was good (Fig. 2).

Table 3 Random effect model and model fitness for the assessment of HIV testing among reproductive-age women in eastern Africa
Fig. 2
figure 2

Showing the area under the ROC curve

Factors associated with HIV testing

For assessing factors associated with HIV testing, we consider the final model since it had the lowest deviance. In the multivariable multilevel analysis factors such as the age of respondent, marital status, educational level, HIV knowledge, HIV stigma indicator, risky sexual behavior and women who visit a health facility were positively associated with HIV testing coverage among reproductive-age women. While women from rich and richest households, having multiple sexual partners, being from rural dwellers, late initiation of sex and higher community illiteracy level had a lower chance of being tested for HIV. Women aged 20 years and above had higher odds of being tested for HIV compared with women of 15–19 years old. The odds of testing for HIV was 2.67 (AOR = 2.67: 95%CI; 2.60, 2.74) times higher for women visiting health centers in the last 12 months compared with their counterparts. Regarding educational level, the odds of testing for HIV was 2.30 (AOR = 2.30: 95%CI; 2.22, 2.38), 2.39 (AOR = 2.39: 95%CI; 2.29, 2.50) and 3.13 (AOR = 3.13: 95%CI; 2.89, 3.39) times higher for women with primary, secondary and higher educational level, respectively, compared to women with no formal education. Being from rich (AOR = 0.93: 95%CI; 0.89, 0.97) and richest (AOR = 0.80: 95%CI; 0.76, 0.84) households had lower odds of being tested for HIV. Being married had 1.32 (AOR = 1.32: 95%CI; 1.28, 1.36) times more likely to be tested for HIV compared with their counterpart. Individuals who initiate sex after 20 years of age had 33% (AOR = 0.67: 95%CI; 0.65, 0.69) lower odds of being tested for HIV compared to those who initiate sex early. Regarding stigma, women with higher, moderate and low stigma scores had 1.56 (AOR = 1.56: 95%CI; 1.46, 1.66), 2.24 (AOR = 2.24: 95%CI; 2.16, 2.32), and 2.27 (AOR = 2.27: 95%CI; 2.19, 2.35) times higher odds of being tested for HIV compared to those with no stigma. Women with higher (AOR = 6.44: 95%CI: 6.21, 6.68) and comprehensive knowledge (AOR = 10.7: 95%CI; 10.29, 11.12) about HIV/AIDS had higher odds of being tested for HIV compared with women with low knowledge. Women having high (AOR = 1.78: 95%CI; 1.67, 1.90) and some risky sexual behavior (AOR = 1.59: 955CI; 1.53, 1.66) had higher odds of being tested for HIV compared to women with no risky sexual behavior. Women with multiple sexual partners had a 36% lower chance of being tested for HIV (AOR = 0.64: 95%CI; 0.62, 0.66) as compared to their counterparts. Women from the rural areas had 31% (AOR = 0.69: 95%CI; 0.67, 0.72) lower odds of being tested for HIV compared with their counterparts. Being from communities with higher community illiteracy levels had 27% (AOR = 0.73: 95%CI; 0.68, 0.78) lower odds of being tested for HIV compared with women from communities with lower community illiteracy levels (Table 4).

Table 4 The bivariable and multivariable multilevel binary logistic regression analysis of factors associated with HIV testing in East Africa in the final model

Discussion

The pooled prevalence of HIV testing in east Africa was 66.9% (95%CI; 66.70, 67.13%), which varies greatly from region to region. The regional variations in quality and access to HIV testing facilities as well as knowledge related to HIV / AIDS may be the reasons for the reported regional variations of HIV testing in eastern Africa [9, 14]. The prevalence reported in this study was in line with the report in Kenya [12]. The finding in this study was greater than the study conducted elsewhere [3, 16, 23] and it was smaller than reports from different studies [9, 10]. The observed variations in the prevalence of HIV testing might be explained by cultural beliefs and lifestyle differences across regions [14]. Besides, the discrepancy might be due to the difference in quality and accessibility of HIV testing facilities [9, 14, 24, 25].

In this study age of respondent, multiple sexual partnerships, marital status, visiting health facility, stigmatized attitude towards HIV/AIDS, HIV knowledge, risky sexual behavior, residence, educational level, wealth status, age at first sex, and community illiteracy level were significant factors associated with HIV testing.

The odds of HIV testing was higher among married women compared with their counterpart. This finding was in agreement with the study done in Ethiopia [22]. This might be due to compulsory counseling and testing promotion for couples intending to get married by different organizations including religious groups [22]. Women who visit health care facilities had higher odds of being tested for HIV, which was supported by another study [16]. This might be because health professionals initiate people who visited health facilities for HIV testing [16].

In this study women from higher socioeconomic status had lower odds of being tested for HIV, which is contrary to another study [7]. This is justified by being rich may be associated with a greater awareness of risks and with reduced financial barriers to testing [26]. Women with primary and above educational levels had a higher chance of being tested for HIV, which is supported by different studies [16, 27]. The reason for this discrepancy might be as education can improve HIV knowledge as well as empowers women to make decisions to visit the health facility and use health services [28].

Women who had multiple sexual partners had less chance of being tested for HIV compared with their counterparts. However, the finding of this study was in contrast to another study [16]. This difference might be associated with individuals with a history of multiple sexual partnerships who might be fear of having HIV and have no interest to know their status. The study at hand revealed that women with higher and comprehensive knowledge about HIV had higher odds of being tested for HIV. This is supported by a study conducted in South Africa [13]. Different studies reported people with higher HIV-associated stigma scores had less chance of being tested for HIV. This is explained as people could be hesitant to test because the disclosure of a positive HIV test result may lead to loss of friendship, family relations, jobs and housing and health care due to stigmatization [2, 18, 22]. However, in the present study people with stigmatized attitudes had a higher chance of being tested for HIV and this might be explained by the variation in the cultural and socioeconomic status of the population included in this study.

In this study, women with risky sexual behavior had higher odds of being tested for HIV. This is supported by another study [22]. Individuals with risky sexual behavior live under persistent fear and uncertainty about their serostatus and are usually suspicious and worried that they might have infected with HIV. This urges them to develop habits of seeking VCT service [17].

Individuals who initiated sex early had a higher chance of being tested for HIV and this is supported by the study conducted in Malawi [14]. This might be explained as early age at first sexual intercourse is associated with a higher risk of acquiring the different sexually transmitted disease and risky sexual behaviors that may lead to a higher risk for HIV infection, which in turn enforce them to know their HIV status [29].

Women from rural dwellers had lower odds of being tested for HIV, which was supported by the study conducted in Ethiopia [16]. This may be justified by the better availability and accessibility of HIV testing facilities in urban settings compared with rural [30, 31]. Women from communities with higher illiteracy levels had less chance of being tested for HIV. This finding was supported by studies conducted in Ethiopia and Zambia [10, 16]. This might be associated with educational attainment may increase uptake of testing through increased recognition of the importance of knowing one’s HIV status [20, 32].

Strength and limitation of the study

The study was based on weighted nationally representative data from 11 eastern African countries with a large sample size. Also, the analysis used the multilevel analysis to accommodate the hierarchical nature of the DHS data. Moreover, since it is based on the national survey data, the study has the potential to give insight for policy-makers and program planners to design appropriate intervention strategies both at the national and regional levels. However, this study had limitations in that the DHS survey was based on respondents’ self-report, this might have the possibility of recall bias. Besides, since this study was based on cross-sectional collected DHS data, we are unable to show the temporal relationship between HIV testing and independent variables.

Conclusion

The prevalence of HIV testing in this study was higher than the report from previous studies. Age of respondent, marital status, educational level, HIV knowledge, stigma indicator, risky sexual behavior, women who visit a health facility, early initiation of sex, wealth status, multiple sexual partnerships, residence and community illiteracy level were significantly associated with HIV testing among reproductive-age women. Therefore, there should be an integrated strategic plan to give education about methods of HIV transmission and the implication of HIV testing and counseling.

Also, it is instrumental to bringing behavioral change, reducing unprotected sex and helping to reduce early initiation of sex and avoidance of having multiple sexual partners. So all the stakeholders should have an integrated approach by giving special attention to the factors that hinder HIV testing to increase awareness regarding the benefit of HIV testing and counseling to control the spread of HIV/AIDS.

Availability of data and materials

Data is available online and you can access it from www.measuredhs.com.

Abbreviations

CI:

Confidence Interval

CSA:

Central Statistical Agency

DHS:

Demographic Health Survey

EA:

Enumeration Area

ICC:

Intraclass correlation coefficient

LLR:

likelihood Ratio

WHO:

World Health Organization

References

  1. UNAIDS W. Global AIDS response progress reporting 2015. Geneva: UNAIDS; 2015.

    Google Scholar 

  2. Paulin HN, Blevins M, Koethe JR, Hinton N, Vaz LME, Vergara AE, et al. HIV testing service awareness and service uptake among female heads of household in rural Mozambique: results from a province-wide survey. BMC Public Health. 2015;15(1):132. https://0-doi-org.brum.beds.ac.uk/10.1186/s12889-015-1388-z.

    Article  PubMed  PubMed Central  Google Scholar 

  3. Asaolu IO, Gunn JK, Center KE, Koss MP, Iwelunmor JI, Ehiri JE. Predictors of HIV testing among youth in sub-Saharan Africa: a cross-sectional study. PLoS One. 2016;11(10):e0164052. https://0-doi-org.brum.beds.ac.uk/10.1371/journal.pone.0164052.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  4. Webb D. HIV and AIDS in Africa: Pluto Press; 1997.

  5. Avert. HIV and AIDS in East and Southern Africa regional overview. 2017.

    Google Scholar 

  6. Global H. AIDS statistics–2019 fact sheet (2019). 2020.

    Google Scholar 

  7. Leta T, Sandøy I, Fylkesnes K. Factors affecting voluntary HIV counselling and testing among men in Ethiopia: a cross-sectional survey. BMC Public Health. 2012;12(1):438. https://0-doi-org.brum.beds.ac.uk/10.1186/1471-2458-12-438.

    Article  PubMed  PubMed Central  Google Scholar 

  8. World Health O. HIV testing and counselling : the gateway to treatment, care and support. Geneva: World Health Organization; 2003.

    Google Scholar 

  9. Salima N, Leah E, Stephen L. HIV testing among women of reproductive age exposed to intimate partner violence in Uganda. Open Public Health J. 2018;11(1):275-87.

  10. Muyunda B, Mee P, Todd J, Musonda P, Michelo C. Estimating levels of HIV testing coverage and use in prevention of mother-to-child transmission among women of reproductive age in Zambia. Arch Public Health. 2018;76(1):80. https://0-doi-org.brum.beds.ac.uk/10.1186/s13690-018-0325-x.

    Article  PubMed  PubMed Central  Google Scholar 

  11. Muyunda B, Musonda P, Mee P, Todd J, Michelo C. Educational attainment as a predictor of HIV testing uptake among women of child-bearing age: analysis of 2014 demographic and health survey in Zambia. Front Public Health. 2018;6:192.

    Article  Google Scholar 

  12. Nall A, Chenneville T, Rodriguez LM, O'Brien JL. Factors affecting HIV testing among youth in Kenya. Int J Environ Res Public Health. 2019;16(8):1450. https://0-doi-org.brum.beds.ac.uk/10.3390/ijerph16081450.

    Article  PubMed Central  Google Scholar 

  13. Peltzer K, Matseke G. Determinants of HIV testing among young people aged 18–24 years in South Africa. Afr Health Sci. 2013;13(4):1012–20. https://0-doi-org.brum.beds.ac.uk/10.4314/ahs.v13i4.22.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  14. Mandiwa C, Namondwe B. Uptake and correlates of HIV testing among men in Malawi: evidence from a national population-based household survey. BMC Health Serv Res. 2019;19(1):203.

    Article  Google Scholar 

  15. Kaai S, Bullock S, Burchell AN, Major C. Factors that affect HIV testing and counseling services among heterosexuals in Canada and the United Kingdom: an integrated review. Patient Educ Couns. 2012;88(1):4–15. https://0-doi-org.brum.beds.ac.uk/10.1016/j.pec.2011.11.011.

    Article  PubMed  Google Scholar 

  16. Bekele YA, Fekadu GA. Factors associated with HIV testing among young females; further analysis of the 2016 Ethiopian demographic and health survey data. PLoS One. 2020;15(2):e0228783. https://0-doi-org.brum.beds.ac.uk/10.1371/journal.pone.0228783.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  17. Khamisa N, Mokgobi M. Risky sexual behaviour and human immunodeficiency virus (HIV) and acquired immune deficiency syndrome (AIDS) among healthcare workers. South Afr J HIV Med. 2018;19(1):744.

    Article  Google Scholar 

  18. Young SD, Bendavid E. The relationship between HIV testing, stigma, and health service usage. AIDS Care. 2010;22(3):373–80. https://0-doi-org.brum.beds.ac.uk/10.1080/09540120903193666.

    Article  PubMed  PubMed Central  Google Scholar 

  19. Kautako-Kiambi M, Ekila MB, Kama-Lemba S, Wumba R, Aloni MN. Voluntary counseling and testing for HIV in rural area of Democratic Republic of the Congo: knowledge, attitude, and practice survey among service users. J Trop Med. 2015;2015:281093.

    Article  Google Scholar 

  20. Martell AN. Association of HIV testing, educational attainment, and age among black and non-black men; 2014.

    Google Scholar 

  21. Mugabe D, Bhatt N, Carlucci JG, Gudo ES, Gong W, Sidat M, et al. Self-reported non-receipt of HIV test results: a silent barrier to HIV epidemic control in Mozambique. PLoS One. 2019;14(10):e0224102. https://0-doi-org.brum.beds.ac.uk/10.1371/journal.pone.0224102.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  22. Erena AN, Shen G, Lei P. Factors affecting HIV counselling and testing among Ethiopian women aged 15–49. BMC Infect Dis. 2019;19(1):1076. https://0-doi-org.brum.beds.ac.uk/10.1186/s12879-019-4701-0.

    Article  PubMed  PubMed Central  Google Scholar 

  23. Fikadie G, Bedimo M, Alamrew Z. Prevalence of voluntary counseling and testing utilization and its associated factors among Bahirdar University students. Adv Prev Med. 2014;2014:906107.

    Article  Google Scholar 

  24. Control CfD, Prevention. Advancing HIV prevention: new strategies for a changing epidemic--United States, 2003. MMWR Morb Mortal Wkly Rep. 2003;52(15):329.

    Google Scholar 

  25. Adler NE, Newman K. Socioeconomic disparities in health: pathways and policies. Health Aff. 2002;21(2):60–76. https://0-doi-org.brum.beds.ac.uk/10.1377/hlthaff.21.2.60.

    Article  Google Scholar 

  26. Obermeyer CM, Neuman M, Hardon A, Desclaux A, Wanyenze R, Ky-Zerbo O, et al. Socio-economic determinants of HIV testing and counselling: a comparative study in four a frican countries. Tropical Med Int Health. 2013;18(9):1110–8. https://0-doi-org.brum.beds.ac.uk/10.1111/tmi.12155.

    Article  Google Scholar 

  27. Ssebunya RN, Wanyenze RK, Namale L, Lukolyo H, Kisitu GP, Nahirya-Ntege P, et al. Prevalence and correlates of HIV testing among adolescents 10–19 years in a post-conflict pastoralist community of Karamoja region, Uganda. BMC Public Health. 2018;18(1):612. https://0-doi-org.brum.beds.ac.uk/10.1186/s12889-018-5544-0.

    Article  PubMed  PubMed Central  Google Scholar 

  28. Jamison EA, Jamison DT, Hanushek EA. The effects of education quality on income growth and mortality decline. Econ Educ Rev. 2007;26(6):771–88. https://0-doi-org.brum.beds.ac.uk/10.1016/j.econedurev.2007.07.001.

    Article  Google Scholar 

  29. Ghebremichael M, Larsen U, Paintsil E. Association of age at first sex with HIV-1, HSV-2, and other sexual transmitted infections among women in northern Tanzania. Sex Transm Dis. 2009;36(9):570–6. https://0-doi-org.brum.beds.ac.uk/10.1097/OLQ.0b013e3181a866b8.

    Article  PubMed  PubMed Central  Google Scholar 

  30. Spasojevic N, Vasilj I, Hrabac B, Celik D. Rural - Urban differences in health care quality assessment. Mater Soc. 2015;27(6):409–11. https://0-doi-org.brum.beds.ac.uk/10.5455/msm.2015.27.409-411.

    Article  Google Scholar 

  31. Swann M. Economic strengthening for HIV prevention and risk reduction: a review of the evidence. AIDS Care. 2018;30(sup3):37–84.

    Article  Google Scholar 

  32. Teklehaimanot HD, Teklehaimanot A, Yohannes M, Biratu D. Factors influencing the uptake of voluntary HIV counseling and testing in rural Ethiopia: a cross sectional study. BMC Public Health. 2016;16(1):239. https://0-doi-org.brum.beds.ac.uk/10.1186/s12889-016-2918-z.

    Article  PubMed  PubMed Central  Google Scholar 

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Acknowledgments

We greatly acknowledge MEASURE DHS for granting access to the Demographic and Health Surveys data.

Funding

No funding was obtained for this study.

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Contributions

GAT, MGW, ABT conceived the study. GAT, MGW, ABT analyzed the data. GAT, MGW, ABT, drafted the manuscript and reviewed the article. GAT, MGW, ABT extensively reviewed the article. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Misganaw Gebrie Worku.

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Since the study was a secondary data analysis of publically available survey data from the MEASURE DHS program, ethical approval and participant consent were not necessary for this particular study. We requested DHS Program and permission was granted to download and use the data for this study from http://www.dhsprogram.com. The Institution Review Board approved procedures for DHS public-use datasets do not in any way allow respondents, households, or sample communities to be identified. There are no names of individuals or household addresses in the data files.

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Not applicable since the study was a secondary data analysis already collected by CSA.

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Worku, M.G., Tesema, G.A. & Teshale, A.B. Prevalence and associated factors of HIV testing among reproductive-age women in eastern Africa: multilevel analysis of demographic and health surveys. BMC Public Health 21, 1262 (2021). https://0-doi-org.brum.beds.ac.uk/10.1186/s12889-021-11292-9

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