Acceptability and feasibility of a screen-and-treat programme for hepatitis B virus infection in The Gambia: the Prevention of Liver Fibrosis and Cancer in Africa (PROLIFICA) study
Despite the introduction of immunisation for hepatitis B virus (HBV) in the 1990s, HBV-related morbidity and mortality remain high in sub-Saharan Africa. Identification and treatment of asymptomatic people with chronic HBV infection should reduce the disease burden. We therefore assessed the feasibi...
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Published in | The Lancet global health Vol. 4; no. 8; pp. e559 - e567 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Elsevier Ltd
01.08.2016
Elsevier |
Subjects | |
Online Access | Get full text |
ISSN | 2214-109X 2572-116X 2214-109X |
DOI | 10.1016/S2214-109X(16)30130-9 |
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Abstract | Despite the introduction of immunisation for hepatitis B virus (HBV) in the 1990s, HBV-related morbidity and mortality remain high in sub-Saharan Africa. Identification and treatment of asymptomatic people with chronic HBV infection should reduce the disease burden. We therefore assessed the feasibility of a screen-and-treat programme for HBV infection in The Gambia, west Africa, and estimated the proportion of HBV-infected people who had significant liver disease in need of treatment.
Between Dec 7, 2011, and Jan 24, 2014, individuals living in randomly selected communities in western Gambia were offered hepatitis B surface antigen (HBsAg) screening via a point-of-care test. The test was also offered to potential blood donors attending the central hospital in the capital, Banjul. HBsAg-positive individuals were invited for a comprehensive liver assessment and were offered treatment according to international guidelines. We defined linkage to care as visiting the liver clinic at least once. Eligibility for treatment was judged in accordance with the 2012 European Association for the Study of the Liver guidelines.
HBsAg screening was accepted by 5980 (weighted estimate 68·9%, 95% CI 65·0–72·4) of 8170 adults from 27 rural and 27 urban communities and 5559 (81·4%, 80·4–82·3) of 6832 blood donors. HBsAg was detected in 495 (8·8%, 7·9–9·7) individuals in communities and 721 (13·0%, 12·1–13·9) blood donors. Prevalence was higher in men (239 [10·5%, 8·9–12·1] of 2328 men vs 256 [7·6%, 6·5–8·7] of 3652 women; p=0·004) and middle-aged participants. Linkage to care was high in the communities, with 402 (81·3%) of 495 HBsAg-positive individuals attending the clinic. However, only 300 (41·6%) of 721 HBsAg-positive people screened at the blood bank linked into care. Of those who attended the clinic, 18 (4·4%, 2·5–7·7) patients from the communities and 29 (9·7%, 6·8–13·6) from the blood bank were eligible for treatment. Male sex was strongly associated with treatment eligibility (odds ratio 4·35, 1·50–12·58; p=0·007).
HBV infection remains highly prevalent in The Gambia. The high coverage of community-based screening, good linkage into care, and the small proportion of HBsAg carriers who need treatment suggest that large-scale screening and treatment programmes are feasible in sub-Saharan Africa.
European Commission (FP7). |
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AbstractList | Despite the introduction of immunisation for hepatitis B virus (HBV) in the 1990s, HBV-related morbidity and mortality remain high in sub-Saharan Africa. Identification and treatment of asymptomatic people with chronic HBV infection should reduce the disease burden. We therefore assessed the feasibility of a screen-and-treat programme for HBV infection in The Gambia, west Africa, and estimated the proportion of HBV-infected people who had significant liver disease in need of treatment.
Between Dec 7, 2011, and Jan 24, 2014, individuals living in randomly selected communities in western Gambia were offered hepatitis B surface antigen (HBsAg) screening via a point-of-care test. The test was also offered to potential blood donors attending the central hospital in the capital, Banjul. HBsAg-positive individuals were invited for a comprehensive liver assessment and were offered treatment according to international guidelines. We defined linkage to care as visiting the liver clinic at least once. Eligibility for treatment was judged in accordance with the 2012 European Association for the Study of the Liver guidelines.
HBsAg screening was accepted by 5980 (weighted estimate 68·9%, 95% CI 65·0–72·4) of 8170 adults from 27 rural and 27 urban communities and 5559 (81·4%, 80·4–82·3) of 6832 blood donors. HBsAg was detected in 495 (8·8%, 7·9–9·7) individuals in communities and 721 (13·0%, 12·1–13·9) blood donors. Prevalence was higher in men (239 [10·5%, 8·9–12·1] of 2328 men vs 256 [7·6%, 6·5–8·7] of 3652 women; p=0·004) and middle-aged participants. Linkage to care was high in the communities, with 402 (81·3%) of 495 HBsAg-positive individuals attending the clinic. However, only 300 (41·6%) of 721 HBsAg-positive people screened at the blood bank linked into care. Of those who attended the clinic, 18 (4·4%, 2·5–7·7) patients from the communities and 29 (9·7%, 6·8–13·6) from the blood bank were eligible for treatment. Male sex was strongly associated with treatment eligibility (odds ratio 4·35, 1·50–12·58; p=0·007).
HBV infection remains highly prevalent in The Gambia. The high coverage of community-based screening, good linkage into care, and the small proportion of HBsAg carriers who need treatment suggest that large-scale screening and treatment programmes are feasible in sub-Saharan Africa.
European Commission (FP7). Summary Background Despite the introduction of immunisation for hepatitis B virus (HBV) in the 1990s, HBV-related morbidity and mortality remain high in sub-Saharan Africa. Identification and treatment of asymptomatic people with chronic HBV infection should reduce the disease burden. We therefore assessed the feasibility of a screen-and-treat programme for HBV infection in The Gambia, west Africa, and estimated the proportion of HBV-infected people who had significant liver disease in need of treatment. Methods Between Dec 7, 2011, and Jan 24, 2014, individuals living in randomly selected communities in western Gambia were offered hepatitis B surface antigen (HBsAg) screening via a point-of-care test. The test was also offered to potential blood donors attending the central hospital in the capital, Banjul. HBsAg-positive individuals were invited for a comprehensive liver assessment and were offered treatment according to international guidelines. We defined linkage to care as visiting the liver clinic at least once. Eligibility for treatment was judged in accordance with the 2012 European Association for the Study of the Liver guidelines. Findings HBsAg screening was accepted by 5980 (weighted estimate 68·9%, 95% CI 65·0–72·4) of 8170 adults from 27 rural and 27 urban communities and 5559 (81·4%, 80·4–82·3) of 6832 blood donors. HBsAg was detected in 495 (8·8%, 7·9–9·7) individuals in communities and 721 (13·0%, 12·1–13·9) blood donors. Prevalence was higher in men (239 [10·5%, 8·9–12·1] of 2328 men vs 256 [7·6%, 6·5–8·7] of 3652 women; p=0·004) and middle-aged participants. Linkage to care was high in the communities, with 402 (81·3%) of 495 HBsAg-positive individuals attending the clinic. However, only 300 (41·6%) of 721 HBsAg-positive people screened at the blood bank linked into care. Of those who attended the clinic, 18 (4·4%, 2·5–7·7) patients from the communities and 29 (9·7%, 6·8–13·6) from the blood bank were eligible for treatment. Male sex was strongly associated with treatment eligibility (odds ratio 4·35, 1·50–12·58; p=0·007). Interpretation HBV infection remains highly prevalent in The Gambia. The high coverage of community-based screening, good linkage into care, and the small proportion of HBsAg carriers who need treatment suggest that large-scale screening and treatment programmes are feasible in sub-Saharan Africa. Funding European Commission (FP7). Background: Despite the introduction of immunisation for hepatitis B virus (HBV) in the 1990s, HBV-related morbidity and mortality remain high in sub-Saharan Africa. Identification and treatment of asymptomatic people with chronic HBV infection should reduce the disease burden. We therefore assessed the feasibility of a screen-and-treat programme for HBV infection in The Gambia, west Africa, and estimated the proportion of HBV-infected people who had significant liver disease in need of treatment.Methods: Between Dec 7, 2011, and Jan 24, 2014, individuals living in randomly selected communities in western Gambia were offered hepatitis B surface antigen (HBsAg) screening via a point-of-care test. The test was also offered to potential blood donors attending the central hospital in the capital, Banjul. HBsAg-positive individuals were invited for a comprehensive liver assessment and were offered treatment according to international guidelines. We defined linkage to care as visiting the liver clinic at least once. Eligibility for treatment was judged in accordance with the 2012 European Association for the Study of the Liver guidelines.Findings: HBsAg screening was accepted by 5980 (weighted estimate 68·9%, 95% CI 65·0-72·4) of 8170 adults from 27 rural and 27 urban communities and 5559 (81·4%, 80·4-82·3) of 6832 blood donors. HBsAg was detected in 495 (8·8%, 7·9-9·7) individuals in communities and 721 (13·0%, 12·1-13·9) blood donors. Prevalence was higher in men (239 [10·5%, 8·9-12·1] of 2328 men vs 256 [7·6%, 6·5-8·7] of 3652 women; p=0·004) and middle-aged participants. Linkage to care was high in the communities, with 402 (81·3%) of 495 HBsAg-positive individuals attending the clinic. However, only 300 (41·6%) of 721 HBsAg-positive people screened at the blood bank linked into care. Of those who attended the clinic, 18 (4·4%, 2·5-7·7) patients from the communities and 29 (9·7%, 6·8-13·6) from the blood bank were eligible for treatment. Male sex was strongly associated with treatment eligibility (odds ratio 4·35, 1·50-12·58; p=0·007).Interpretation: HBV infection remains highly prevalent in The Gambia. The high coverage of community-based screening, good linkage into care, and the small proportion of HBsAg carriers who need treatment suggest that large-scale screening and treatment programmes are feasible in sub-Saharan Africa.Funding: European Commission (FP7). Despite the introduction of immunisation for hepatitis B virus (HBV) in the 1990s, HBV-related morbidity and mortality remain high in sub-Saharan Africa. Identification and treatment of asymptomatic people with chronic HBV infection should reduce the disease burden. We therefore assessed the feasibility of a screen-and-treat programme for HBV infection in The Gambia, west Africa, and estimated the proportion of HBV-infected people who had significant liver disease in need of treatment.BACKGROUNDDespite the introduction of immunisation for hepatitis B virus (HBV) in the 1990s, HBV-related morbidity and mortality remain high in sub-Saharan Africa. Identification and treatment of asymptomatic people with chronic HBV infection should reduce the disease burden. We therefore assessed the feasibility of a screen-and-treat programme for HBV infection in The Gambia, west Africa, and estimated the proportion of HBV-infected people who had significant liver disease in need of treatment.Between Dec 7, 2011, and Jan 24, 2014, individuals living in randomly selected communities in western Gambia were offered hepatitis B surface antigen (HBsAg) screening via a point-of-care test. The test was also offered to potential blood donors attending the central hospital in the capital, Banjul. HBsAg-positive individuals were invited for a comprehensive liver assessment and were offered treatment according to international guidelines. We defined linkage to care as visiting the liver clinic at least once. Eligibility for treatment was judged in accordance with the 2012 European Association for the Study of the Liver guidelines.METHODSBetween Dec 7, 2011, and Jan 24, 2014, individuals living in randomly selected communities in western Gambia were offered hepatitis B surface antigen (HBsAg) screening via a point-of-care test. The test was also offered to potential blood donors attending the central hospital in the capital, Banjul. HBsAg-positive individuals were invited for a comprehensive liver assessment and were offered treatment according to international guidelines. We defined linkage to care as visiting the liver clinic at least once. Eligibility for treatment was judged in accordance with the 2012 European Association for the Study of the Liver guidelines.HBsAg screening was accepted by 5980 (weighted estimate 68·9%, 95% CI 65·0-72·4) of 8170 adults from 27 rural and 27 urban communities and 5559 (81·4%, 80·4-82·3) of 6832 blood donors. HBsAg was detected in 495 (8·8%, 7·9-9·7) individuals in communities and 721 (13·0%, 12·1-13·9) blood donors. Prevalence was higher in men (239 [10·5%, 8·9-12·1] of 2328 men vs 256 [7·6%, 6·5-8·7] of 3652 women; p=0·004) and middle-aged participants. Linkage to care was high in the communities, with 402 (81·3%) of 495 HBsAg-positive individuals attending the clinic. However, only 300 (41·6%) of 721 HBsAg-positive people screened at the blood bank linked into care. Of those who attended the clinic, 18 (4·4%, 2·5-7·7) patients from the communities and 29 (9·7%, 6·8-13·6) from the blood bank were eligible for treatment. Male sex was strongly associated with treatment eligibility (odds ratio 4·35, 1·50-12·58; p=0·007).FINDINGSHBsAg screening was accepted by 5980 (weighted estimate 68·9%, 95% CI 65·0-72·4) of 8170 adults from 27 rural and 27 urban communities and 5559 (81·4%, 80·4-82·3) of 6832 blood donors. HBsAg was detected in 495 (8·8%, 7·9-9·7) individuals in communities and 721 (13·0%, 12·1-13·9) blood donors. Prevalence was higher in men (239 [10·5%, 8·9-12·1] of 2328 men vs 256 [7·6%, 6·5-8·7] of 3652 women; p=0·004) and middle-aged participants. Linkage to care was high in the communities, with 402 (81·3%) of 495 HBsAg-positive individuals attending the clinic. However, only 300 (41·6%) of 721 HBsAg-positive people screened at the blood bank linked into care. Of those who attended the clinic, 18 (4·4%, 2·5-7·7) patients from the communities and 29 (9·7%, 6·8-13·6) from the blood bank were eligible for treatment. Male sex was strongly associated with treatment eligibility (odds ratio 4·35, 1·50-12·58; p=0·007).HBV infection remains highly prevalent in The Gambia. The high coverage of community-based screening, good linkage into care, and the small proportion of HBsAg carriers who need treatment suggest that large-scale screening and treatment programmes are feasible in sub-Saharan Africa.INTERPRETATIONHBV infection remains highly prevalent in The Gambia. The high coverage of community-based screening, good linkage into care, and the small proportion of HBsAg carriers who need treatment suggest that large-scale screening and treatment programmes are feasible in sub-Saharan Africa.European Commission (FP7).FUNDINGEuropean Commission (FP7). |
Author | Mendy, Maimuna Taal, Makie Sarr, Louise Kambi, Aboubacar Howell, Jessica Ghosh, Sumantra Ndow, Gibril Shimakawa, Yusuke Mpabanzi, Liliane Jatta, Abdullah Whittle, Hilton Sow, Amina Jeng, Adam Stanger, William Lemoine, Maud Njie, Ramou Mboup, Souleymane Tamba, Saydiba Njai, Harr F D'Alessandro, Umberto Taylor-Robinson, Simon D Corrah, Tumani Toure-Kane, Coumba Chemin, Isabelle Nayagam, Shevanthi Thursz, Mark R Nyan, Ousman Suso, Penda |
Author_xml | – sequence: 1 givenname: Maud surname: Lemoine fullname: Lemoine, Maud organization: Medical Research Council Laboratories, The Gambia Unit, Fajara, The Gambia – sequence: 2 givenname: Yusuke surname: Shimakawa fullname: Shimakawa, Yusuke organization: Medical Research Council Laboratories, The Gambia Unit, Fajara, The Gambia – sequence: 3 givenname: Ramou surname: Njie fullname: Njie, Ramou organization: International Agency for Research on Cancer (IARC), Lyon, France – sequence: 4 givenname: Makie surname: Taal fullname: Taal, Makie organization: Ministry of Health and Social Welfare, Banjul, The Gambia – sequence: 5 givenname: Gibril surname: Ndow fullname: Ndow, Gibril organization: Medical Research Council Laboratories, The Gambia Unit, Fajara, The Gambia – sequence: 6 givenname: Isabelle surname: Chemin fullname: Chemin, Isabelle organization: INSERM U1052, CNRS UMR5286, Centre de Recherche en Cancérologie, Université Claude Bernard, Lyon, France – sequence: 7 givenname: Sumantra surname: Ghosh fullname: Ghosh, Sumantra organization: INSERM U1052, CNRS UMR5286, Centre de Recherche en Cancérologie, Université Claude Bernard, Lyon, France – sequence: 8 givenname: Harr F surname: Njai fullname: Njai, Harr F organization: Medical Research Council Laboratories, The Gambia Unit, Fajara, The Gambia – sequence: 9 givenname: Adam surname: Jeng fullname: Jeng, Adam organization: Medical Research Council Laboratories, The Gambia Unit, Fajara, The Gambia – sequence: 10 givenname: Amina surname: Sow fullname: Sow, Amina organization: Department of bacteriology and Virology, CHU Le Dantec, Dakar, Senegal – sequence: 11 givenname: Coumba surname: Toure-Kane fullname: Toure-Kane, Coumba organization: Department of bacteriology and Virology, CHU Le Dantec, Dakar, Senegal – sequence: 12 givenname: Souleymane surname: Mboup fullname: Mboup, Souleymane organization: Department of bacteriology and Virology, CHU Le Dantec, Dakar, Senegal – sequence: 13 givenname: Penda surname: Suso fullname: Suso, Penda organization: Medical Research Council Laboratories, The Gambia Unit, Fajara, The Gambia – sequence: 14 givenname: Saydiba surname: Tamba fullname: Tamba, Saydiba organization: Medical Research Council Laboratories, The Gambia Unit, Fajara, The Gambia – sequence: 15 givenname: Abdullah surname: Jatta fullname: Jatta, Abdullah organization: Medical Research Council Laboratories, The Gambia Unit, Fajara, The Gambia – sequence: 16 givenname: Louise surname: Sarr fullname: Sarr, Louise organization: Medical Research Council Laboratories, The Gambia Unit, Fajara, The Gambia – sequence: 17 givenname: Aboubacar surname: Kambi fullname: Kambi, Aboubacar organization: Medical Research Council Laboratories, The Gambia Unit, Fajara, The Gambia – sequence: 18 givenname: William surname: Stanger fullname: Stanger, William organization: Division of Digestive Diseases, St Mary's Hospital, Imperial College London, London, UK – sequence: 19 givenname: Shevanthi surname: Nayagam fullname: Nayagam, Shevanthi organization: Division of Digestive Diseases, St Mary's Hospital, Imperial College London, London, UK – sequence: 20 givenname: Jessica surname: Howell fullname: Howell, Jessica organization: Division of Digestive Diseases, St Mary's Hospital, Imperial College London, London, UK – sequence: 21 givenname: Liliane surname: Mpabanzi fullname: Mpabanzi, Liliane organization: Department of Surgery, Maastricht University Medical Centre, Maastricht University, Netherlands – sequence: 22 givenname: Ousman surname: Nyan fullname: Nyan, Ousman organization: Edward Francis Small Teaching Hospital (EFSTH), Banjul, The Gambia – sequence: 23 givenname: Tumani surname: Corrah fullname: Corrah, Tumani organization: Medical Research Council Laboratories, The Gambia Unit, Fajara, The Gambia – sequence: 24 givenname: Hilton surname: Whittle fullname: Whittle, Hilton organization: Faculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, London, UK – sequence: 25 givenname: Simon D surname: Taylor-Robinson fullname: Taylor-Robinson, Simon D organization: Division of Digestive Diseases, St Mary's Hospital, Imperial College London, London, UK – sequence: 26 givenname: Umberto surname: D'Alessandro fullname: D'Alessandro, Umberto organization: Medical Research Council Laboratories, The Gambia Unit, Fajara, The Gambia – sequence: 27 givenname: Maimuna surname: Mendy fullname: Mendy, Maimuna organization: International Agency for Research on Cancer (IARC), Lyon, France – sequence: 28 givenname: Mark R surname: Thursz fullname: Thursz, Mark R email: m.thursz@imperial.ac.uk organization: Division of Digestive Diseases, St Mary's Hospital, Imperial College London, London, UK |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/27443781$$D View this record in MEDLINE/PubMed https://pasteur.hal.science/pasteur-02875279$$DView record in HAL |
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Snippet | Despite the introduction of immunisation for hepatitis B virus (HBV) in the 1990s, HBV-related morbidity and mortality remain high in sub-Saharan Africa.... Summary Background Despite the introduction of immunisation for hepatitis B virus (HBV) in the 1990s, HBV-related morbidity and mortality remain high in... Background: Despite the introduction of immunisation for hepatitis B virus (HBV) in the 1990s, HBV-related morbidity and mortality remain high in sub-Saharan... |
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SubjectTerms | Adult Age Factors Antiviral Agents Blood Donors Communicable Diseases Feasibility Studies Female Gambia - epidemiology Hepatitis B - diagnosis Hepatitis B - epidemiology Hepatitis B Surface Antigens - blood Hepatitis B virus - immunology Humans Internal Medicine Life Sciences Liver Cirrhosis - diagnosis Liver Cirrhosis - therapy Male Mass Screening - methods Middle Aged Point-of-Care Systems Prevalence Santé publique et épidémiologie Sex Factors |
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Title | Acceptability and feasibility of a screen-and-treat programme for hepatitis B virus infection in The Gambia: the Prevention of Liver Fibrosis and Cancer in Africa (PROLIFICA) study |
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