- Open Access
Trends in hepatitis B virus testing practices and management in HIV clinics across sub-Saharan Africa
- Patrick A. Coffie†1, 2Email author,
- Matthias Egger3, 4,
- Michael J. Vinikoor5, 6,
- Marcel Zannou7,
- Lameck Diero8,
- Akouda Patassi9,
- Mark H. Kuniholm10,
- Moussa Seydi11,
- Guillaume Bado12,
- Ponsiano Ocama13,
- Monique I. Andersson14,
- Eugène Messou2, 15,
- Albert Minga16,
- Philippa Easterbrook17, 18,
- Kathryn Anastos19,
- François Dabis20, 21,
- Gilles Wandeler†3, 11, 22Email author and
- for the IeDEA collaboration
© The Author(s). 2017
Published: 1 November 2017
Approximately 8% of HIV-infected individuals are co-infected with hepatitis B virus (HBV) in sub-Saharan Africa (SSA). Knowledge of HBV status is important to guide optimal selection of antiretroviral therapy (ART) and monitor/prevent liver-related complications. We describe changes in testing practices and management of HBV infection over a 3-year period in HIV clinics across SSA.
A medical chart review was conducted in large urban HIV treatment centers in Côte d’Ivoire (3 sites), Benin, Burkina Faso, Cameroon, Kenya, Senegal, South Africa, Togo, Uganda and Zambia (1 site each). Of the patients who started ART between 2010 and 2012, 100 per year were randomly selected from each clinic. Demographic, clinical and laboratory information as well as individual treatment histories were collected using a standardized questionnaire. We examined changes over time in the proportion of patients screened for HBV infection (HBV surface antigen [HBsAg]-positivity), identified predictors of HBV testing using logistic regression, and assessed the proportion of patients initiating a tenofovir (TDF)-containing ART regimen.
Overall, 3579 charts of patients initiating ART (64.4% female, median age 37 years) were reviewed in 12 clinics. The proportion of patients screened for HBsAg increased from 17.8% in 2010 to 24.4% in 2012 overall, and ranged from 0.7% in Kenya to 96% in South Africa. In multivariable analyses, age and region were associated with HBsAg screening. Among 759 individuals tested, 88 (11.6%; 95% confidence interval [CI] 9.4–14.1) were HBV-infected, of whom 71 (80.7%) received a TDF-containing ART regimen. HBsAg-positive individuals were twice as likely to receive a TDF-containing first-line ART regimen compared to HBsAg-negative patients (80.7% vs. 40.3%, p < 0.001). The proportion of patients on TDF-containing ART increased from 57.9% in 2010 to 90.2% in 2012 in HIV/HBV-co-infected patients (Chi-2 test for trend: p = 0.01). Only 114 (5.0%) patients were screened for anti-HCV antibodies and one of them (0.9%, 95% CI 0.02–4.79) had a confirmed HCV infection.
The systematic screening for HBV infection in HIV-positive patients before ART initiation was limited in most African countries and its uptake varied widely across clinics. Overall, the prescription of TDF increased over time, with 90% of HIV/HBV-coinfected patients receiving this drug in 2012.
In sub-Saharan Africa (SSA), approximately 8% of HIV-infected individuals are hepatitis B surface antigen (HBsAg)-positive . In SSA, most hepatitis B virus (HBV) infections occur before the age of 5 years through household contacts  and HBV is the single most important cause of liver disease with attributable fractions of cirrhosis and hepatocellular carcinoma reaching 34% and 47%, respectively . However, in the absence of routine screening in the general population, the majority of infected people do not know their HBV status.
HIV/HBV-coinfected patients are at higher risk of impaired immunological recovery and hepatotoxicity during antiretroviral therapy (ART) compared to HBV-uninfected ones, and overall mortality tends to be higher in the presence of HBV infection [4–6]. Knowledge of HBV status at ART start is important for clinical monitoring and to guide the selection of the initial ART regimen, as tenofovir disoproxil fumarate (TDF) should be combined with lamivudine (3TC) or emtricitabine (FTC) and a non-nucleoside reverse transcriptase inhibitor (NNRTI) in the presence of HBV infection [7, 8]. Knowledge of HBV status has other benefits: it helps to guide the choice of second-line treatment in case of failure of initial ART or drug toxicity; enables HBV vaccination in those non-immune; and in pregnant women allows optimization of prevention of mother-to-child transmission through use of immunoglobulins and antivirals in addition to birth dose of hepatitis B vaccine and infant vaccination.
Although most international and national ART guidelines recommend screening for HBV infection prior to ART initiation, HBV testing uptake has been poor in most resource-limited settings (RLS). In a recent analysis of over 60,000 patients initiating ART in Lusaka, Zambia, the proportion of patients tested for HBV co-infection increased steadily between 2010 and 2012 but remained below 50% overall and screening uptake varied widely across clinics . Taking advantage of a large, international HIV cohort collaboration in SSA, we aimed to describe changes in testing practices related to viral hepatitis over a 3-year period in HIV clinics from ten countries across SSA. Our main objective was to measure HBV and hepatitis C virus (HCV) testing uptake in routine clinical settings. In addition, through standardized chart extractions we investigated the impact of HBV infection on the choice of initial ART regimen in these settings. A further objective was to provide insight into current viral hepatitis testing practices and feasibility challenges in HIV clinics across SSA to inform international guidelines .
Study population and data collection
Among the total number of patients who started ART between 2010 and 2012, we randomly selected a sample of 100 adults (>18 years) initiating ART per year at each clinic, i.e. up to 300 patients per clinic in total. If the number of patients starting ART was smaller than 100 for a given year, all patients were selected for that year. All demographic and HIV-related clinical data were entered into a local database for clinical care, evaluation and reporting purposes, within the IeDEA framework. As information on viral hepatitis screening, monitoring and treatment were not routinely available in the data collected by IeDEA, we performed a chart review using a standardized data collection protocol in all study sites. In addition to data on screening for HBsAg, anti-HCV antibody and any other available HBV and HCV serological and virological tests, we collected information related to ART history, routinely performed laboratory tests and HCV treatment.
Patient characteristics were presented as medians with interquartile range (IQR) for continuous variables and absolute numbers and percentages for categorical ones. The proportion of people tested and the prevalence of HBV infection were reported with 95% confidence intervals (CI) overall and by year of ART initiation and country. The proportion of individuals receiving TDF as part of their initial ART regimen was evaluated by HBsAg status. Differences in proportions of HBsAg-positivity between countries were assessed using Chi-square and Fisher’s exact tests. Changes in screening uptake over time were evaluated with a Chi-square test for trend. We investigated associations between HBsAg testing and sex, age and region (Central Africa, East Africa, West Africa and Southern Africa) using logistic regression. Variables associated with HBsAg screening in univariable regression (p < 0.20) were included in multivariable models. All statistical analyses were performed using Stata 9.0 (StataCorp, College Station, TX, USA).
Characteristics of clinical sites and patients
Characteristics of HIV-infected patients at initiation of antiretroviral therapy in ten African countries, 2010–2012 (N = 3579)
Number of sites
Type of care
Primary / Tertiary
Number of patients included (proportion of total population followed)
Median age in years (IQR)
Female sex (%)
Type of ART (%)
2 NRTI +1 NNRTI
2 NRTI +1 PI
Viral hepatitis screening practices
Factors associated with hepatitis B screening among HIV-infected patients in ten African countries, 2010–2012 (N = 3579)
n / N (%)
Age in years (%)
469 / 2270 (20.7)
302 / 1309 (23.1)
489 / 2303 (21.2)
282 / 1276 (22.1)
African region (%)
12 / 298 (4.0)
313 / 2097 (14.9)
98 / 584 (16.8)
348 / 600 (58.0)
Information on HCV testing was available in the files for 2271 individuals (63.4% of the total study sample). Overall, only 114 (5.0%) of these patients were tested for the presence of anti-HCV antibodies. The sites in Kenya, Zambia and Cameroon did not perform any HCV testing and only sites in Côte d’Ivoire (11 patients, 8.9%), Burkina Faso (21 patients, 7.0%), Senegal (19 patients, 6.4%) and South Africa (45 patients, 15.0%) tested more than 10 patients. Only two patients had a positive anti-HCV result, and one of them was a confirmed HCV infection by nucleic acid amplification. Among 114 patients tested for anti-HCV, 110 were also screened for HBsAg. No patients tested positive for both HBsAg and anti-HCV.
Prevalence of HBsAg and initial treatment
Among 771 patients screened for HBsAg, 12 results were not available in the patient charts (2 in Uganda, 1 in Zambia and 9 in South Africa). Of 759 individuals with HBsAg results, 88 (11.6%; 95% CI 9.4–14.1) had a positive test. The prevalence of HIV/HBV-co-infection was 0% in Kenya, 4.3% in Uganda, 4.7% in South Africa, 11.9% in Zambia, 14.3% in Benin, 16.7% in Cameroon, 18.5% in Senegal, 20.0% in Togo, 21.1% in Burkina Faso and 27.0% in Côte d’Ivoire (p < 0.001).
Despite the consistent recommendation in national and international HIV guidelines to test all HIV-infected patients for HBV-coinfection before ART initiation, screening uptake was generally poor in this study of 12 large urban tertiary hospitals in SSA. Of over 3500 HIV-infected individuals from ten African countries, less than one-quarter was tested for the presence of HBV infection. In most sites, HBsAg testing uptake increased only minimally between 2010 and 2012, with large differences in the proportion of patients tested across clinics and countries. None of the 88 HIV/HBV-co-infected patients in this sample had an HBV viral load test performed after a positive HBsAg test. However, the majority of HIV/HBV-co-infected patients initiated a standard-of-care TDF-containing ART regimen.
The implementation of HBV testing practices for HIV-infected patients was sub-optimal in the majority of the clinical sites assessed. The South African clinic was the only one to achieve near-complete HBV testing rates throughout the study period, reflecting a local policy of routine HBsAg testing at diagnosis, and a clear improvement in testing uptake over time was only seen in the sites in Burkina Faso, Senegal and Zambia. The limited availability of HBsAg and anti-HCV screening shown in our study reflects a missed opportunity as the population studied is already engaged in HIV care and testing would likely be acceptable to most patients. There are several potential barriers to more widespread adoption of testing for viral hepatitis in SSA, including financial reasons (the costs of rapid tests and nucleic acid testing are rarely covered by national HIV programs or donor agencies); logistical reasons (poor availability of quality-assured rapid tests in most clinics), and lack of clear national guidance on testing strategies . There is also an emerging view that with the increasing use of TDF-based ART as the preferred first-line regimen, the majority of HBV-coinfected patients will receive effective suppressive treatment and HBsAg testing is no longer required. However, knowledge of HBsAg status is particularly important when switching to second-line ART for treatment failure or drug toxicity to ensure that the new regimen continues to be effective against HBV and avoid the risk of flare . Whereas health disparities in access to care for liver diseases in SSA are well documented , similar system-related barriers to viral hepatitis testing have been underlined in a recent report for Europe . Thus, there is an urgent need to improve access to simple and cheap diagnostic tests for HBV and HCV infection globally, a goal that can only be achieved by translating international guidelines into national strategies and increased political will and resources . Improvements in blood safety in SSA illustrate that with adequate funding mechanisms and a well-defined global policy high success rates are achievable: the proportion of countries testing at least 95% of blood donations for HBsAg increased from 76% to 94% in the last decade .
As expected in settings where HBsAg testing was limited, additional hepatitis diagnostic testing was uncommon. Indeed, due to high cost and limited laboratory capacities in most sites, HBV DNA measurement was unavailable. The use of dried blood spots for HBV viral load measurements , and less expensive nucleic acid amplification techniques should improve uptake of confirmatory HBV viral load testing in the future. HCV screening was unavailable in most settings and only performed in highly selected groups of patients. More than 75% of HCV test results came from the cohorts in South Africa, Senegal and Burkina Faso, where access to HCV testing was improved by the presence of specifically trained laboratory personnel. Overall only two patients had a positive anti-HCV test, in line with recent data from Zambia and Mozambique which highlighted the low prevalence of HCV infection in southern Africa . However, as the burden of HCV infection in HIV-positive people varies widely across African sub-regions , HCV testing strategies should be tailored to the local epidemiological context, including routine testing in high prevalence settings and focused testing in HIV-infected high-risk groups such as persons who inject drugs, men who have sex with men, sex workers and prisoners, as well as children of HIV/HCV-co-infected women.
The prevalence of HBV-infection (11.6%) in our study probably overestimated the true population prevalence among people living with HIV: several clinics had more than 20% of patients with a positive HBsAg test, most likely because patients with clinical features of liver disease were more likely to be tested than asymptomatic patients. This is also reflected by the lower HBV-prevalence found in South Africa, where systematic screening was performed. Importantly, the proportion of HIV/HBV-co-infected individuals who received a standard-of-care TDF-containing regimen increased over time. Considering that over two-thirds of HBV infections were diagnosed in West African sites where TDF was not part of the preferred first-line ART regimens during the study period, it is encouraging to note that by 2012, 90% of HBV-infected patients had TDF included in their initial ART regimen, irrespective of clinic or country. Conversely, HBsAg-negative patients were less likely to receive TDF, reflecting the national treatment guidelines during the study period. By 2012, 80% of low-and middle-income countries globally had adopted the 2010 World Health Organization (WHO) guidelines and began the transition away from stavudine to TDF or zidovudine (AZT) for all new ART initiations . However, progress in the uptake of TDF as part of the preferred first-line ART has been variable across countries: whereas Zambia started to include TDF in first-line ART in 2007, many West African countries were still using AZT in first-line ART at the end of 2012. In fact, most countries in West Africa only started the implementation of TDF in first-line ART in 2015.
This is the largest study to date assessing HBV and HCV screening practices in routine clinical HIV care settings in SSA. It was nested within an established observational data collection platform (the IeDEA network) and utilized standardized data collection instruments at all sites for chart review. Unfortunately, we could not obtain more detailed information on demographic factors such as education level or employment, as these data were not reported identically in the charts of most clinics. Socioeconomic factors could well have played a role in access to HBV and HCV screening in our study, especially in settings where no systematic testing was performed. A further limitation of our study was the absence of data on the reasons for HBV testing for the majority of patients, except for the South African clinic which had a documented policy of screening all patients during the study period. As a consequence, we could not determine the proportion of patients who were tested due to clinical signs of liver disease, which potentially led to an over-estimation of HBsAg prevalence. In addition, we may have under-estimated the proportion of HBV-coinfected patients in our study as we would not have diagnosed patients with occult HBV infection, which is expected to be present in 10%–15% of HIV-infected individuals in SSA [22, 23]. Finally, as only large urban clinics were selected for this study, our results may not be generalizable to rural areas. Indeed, HBV and HCV testing is likely to be even more limited in rural settings.
In summary, our results highlight the heterogeneity in HBsAg testing and the near-absence of HCV testing for HIV-infected individuals in SSA. As the availability of TDF for long-term treatment of HBV infection and direct-acting antivirals for HCV infection is increasing globally, early diagnosis of HBV and, in specific risk groups, of HCV infections is of utmost importance. The WHO hepatitis testing guidelines recommend focused testing for HBV and HCV in most affected populations that include HIV-infected persons . They also recommend that hepatitis testing should make use of existing opportunities and infrastructure for testing that include health facility and community-based testing for HIV. The availability of polyvalent platforms will allow increasingly for multiplex testing for HBV, HCV, HIV and syphilis. HIV programs should consider adopting HBsAg testing uptake as a metric for program evaluation and surveys similar to this one should be repeated regularly to monitor progress, including in rural areas. Finally, in order to improve current testing practices, more efforts are needed to understand the main reasons for the limited uptake of HBV and HCV diagnostic practices in many low-income settings.
We thank all study participants and staff of all participating sites.
This study was supported by the National Institute of Allergy and Infectious Diseases (NIAID), the National Institute of Child Health and Human Development (NICHD), the National Cancer Institute (NCI) under award numbers U01AI069924 for IeDEA-Southern Africa, U01AI096299 for IeDEA-Central Africa, U01 AI069911 for IeDEA-East Africa and U01AI069919 for IeDEA-West Africa. GW was supported by an Ambizione-PROSPER fellowship from the Swiss National Science Foundation (PZ00P3_154730). M.J.V. was supported by the NIH Fogarty International Center (K01TW009998).
Publication of this article was funded by the World Health Organization.
Availability of data and materials
The datasets supporting the conclusions of this article are available upon request to the corresponding author.
About this supplement
This article has been published as part of BMC Infectious Diseases Volume 17 Supplement 1, 2017: Testing for chronic hepatitis B and C – a global perspective. The full contents of the supplement are available online at https://bmcinfectdis.biomedcentral.com/articles/supplements/volume-17-supplement-1.
PAC and GW designed the study, performed statistical analysis and drafted the initial manuscript. MJV, MZ, LD, AP, MHK, MS, GB, PO, MIA, EM, AM, and DM supervised the data collection. ME, PE, FD helped with data interpretation and the draft of initial manuscript. All the authors read and approved the final manuscript.
Ethics approval and consent to participate
Ethical permission for participation in IeDEAwas given by the national ethics committee of each participating country and all patients were informed and had to give their written consent before being included.
Specific ethics approval for this study was sought from the following institutions:
“Comité d’Ethique pour la Recherche en Santé au Bénin (CNERB)” in Benin, “Comité d’Ethique pour la Recherche en Santé au Burkina Faso” (CERS_BF) in Burkina-Faso, “Comité National d’Ethique et la Recherche en Santé” (CNER_CI) in Côte d’Ivoire, the “Comité de Bioéthique pour la Recherche en Santé (CBRS)” in Togo, “Comité National d’Ethique pour la Recherche en Santé au Senegal” (CNERS) Senegal, « Health Research Ethics Committee » of Stellenbosch University, South Africa.
Consent for publication
The Authors declare that they have no competing interests.
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