The epidemiology of adolescents living with perinatally acquired HIV: A cross-region global cohort analysis

Bibliographic Details
Main Author: Slogrove, A.
Publication Date: 2018
Other Authors: Schomaker, M., Davies, M., Williams, P., Balkan, S., Ben-Farhat, J., Calles, N., Chokephaibulkit, K., Duff, C., Eboua, T., Kekitiinwa-Rukyalekere, A., Maxwell, N., Pinto, J., Seage, G., Teasdale, C., Wanless, S., Warszawski, J., Wools-Kaloustian, K., Yotebieng, M., Timmerman, V., Collins, I., Goodall, R., Smith, C., Patel, K., Paul, M., Gibb, D., Vreeman, R., Abrams, E., Hazra, R., Van Dyke, R., Bekker, L., Mofenson, L., Vicari, M., Essajee, S., Penazzato, M., Anabwani, G., Q Mohapi, E., N Kazembe, P., Hlatshwayo, M., Lumumba, M., Goetghebuer, T., Thorne, C., Galli, L., van Rossum, A., Giaquinto, C., Marczynska, M., Marques, L., Prata, F., Ene, L., Okhonskaia, L., Rojo, P., Fortuny, C., Naver, L., Rudin, C., Le Coeur, S., Volokha, A., Rouzier, V., Succi, R., Sohn, A., Kariminia, A., Edmonds, A., Lelo, P., Ayaya, S., Ongwen, P., Jefferys, L., Phiri, S., Mubiana-Mbewe, Mw., Sawry, S., Renner, L., Sylla, M., Abzug, M., Levin, M., Oleske, J., Chernoff, M., Traite, S., Purswani, M., Chadwick, E., Judd, A., Leroy, V.
Format: Article
Language: eng
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: http://hdl.handle.net/10400.16/2313
Summary: Background: Globally, the population of adolescents living with perinatally acquired HIV (APHs) continues to expand. In this study, we pooled data from observational pediatric HIV cohorts and cohort networks, allowing comparisons of adolescents with perinatally acquired HIV in "real-life" settings across multiple regions. We describe the geographic and temporal characteristics and mortality outcomes of APHs across multiple regions, including South America and the Caribbean, North America, Europe, sub-Saharan Africa, and South and Southeast Asia. Methods and findings: Through the Collaborative Initiative for Paediatric HIV Education and Research (CIPHER), individual retrospective longitudinal data from 12 cohort networks were pooled. All children infected with HIV who entered care before age 10 years, were not known to have horizontally acquired HIV, and were followed up beyond age 10 years were included in this analysis conducted from May 2016 to January 2017. Our primary analysis describes patient and treatment characteristics of APHs at key time points, including first HIV-associated clinic visit, antiretroviral therapy (ART) start, age 10 years, and last visit, and compares these characteristics by geographic region, country income group (CIG), and birth period. Our secondary analysis describes mortality, transfer out, and lost to follow-up (LTFU) as outcomes at age 15 years, using competing risk analysis. Among the 38,187 APHs included, 51% were female, 79% were from sub-Saharan Africa and 65% lived in low-income countries. APHs from 51 countries were included (Europe: 14 countries and 3,054 APHs; North America: 1 country and 1,032 APHs; South America and the Caribbean: 4 countries and 903 APHs; South and Southeast Asia: 7 countries and 2,902 APHs; sub-Saharan Africa, 25 countries and 30,296 APHs). Observation started as early as 1982 in Europe and 1996 in sub-Saharan Africa, and continued until at least 2014 in all regions. The median (interquartile range [IQR]) duration of adolescent follow-up was 3.1 (1.5-5.2) years for the total cohort and 6.4 (3.6-8.0) years in Europe, 3.7 (2.0-5.4) years in North America, 2.5 (1.2-4.4) years in South and Southeast Asia, 5.0 (2.7-7.5) years in South America and the Caribbean, and 2.1 (0.9-3.8) years in sub-Saharan Africa. Median (IQR) age at first visit differed substantially by region, ranging from 0.7 (0.3-2.1) years in North America to 7.1 (5.3-8.6) years in sub-Saharan Africa. The median age at ART start varied from 0.9 (0.4-2.6) years in North America to 7.9 (6.0-9.3) years in sub-Saharan Africa. The cumulative incidence estimates (95% confidence interval [CI]) at age 15 years for mortality, transfers out, and LTFU for all APHs were 2.6% (2.4%-2.8%), 15.6% (15.1%-16.0%), and 11.3% (10.9%-11.8%), respectively. Mortality was lowest in Europe (0.8% [0.5%-1.1%]) and highest in South America and the Caribbean (4.4% [3.1%-6.1%]). However, LTFU was lowest in South America and the Caribbean (4.8% [3.4%-6.7%]) and highest in sub-Saharan Africa (13.2% [12.6%-13.7%]). Study limitations include the high LTFU rate in sub-Saharan Africa, which could have affected the comparison of mortality across regions; inclusion of data only for APHs receiving ART from some countries; and unavailability of data from high-burden countries such as Nigeria. Conclusion: To our knowledge, our study represents the largest multiregional epidemiological analysis of APHs. Despite probable under-ascertained mortality, mortality in APHs remains substantially higher in sub-Saharan Africa, South and Southeast Asia, and South America and the Caribbean than in Europe. Collaborations such as CIPHER enable us to monitor current global temporal trends in outcomes over time to inform appropriate policy responses.
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spelling The epidemiology of adolescents living with perinatally acquired HIV: A cross-region global cohort analysisHIV InfectionsBackground: Globally, the population of adolescents living with perinatally acquired HIV (APHs) continues to expand. In this study, we pooled data from observational pediatric HIV cohorts and cohort networks, allowing comparisons of adolescents with perinatally acquired HIV in "real-life" settings across multiple regions. We describe the geographic and temporal characteristics and mortality outcomes of APHs across multiple regions, including South America and the Caribbean, North America, Europe, sub-Saharan Africa, and South and Southeast Asia. Methods and findings: Through the Collaborative Initiative for Paediatric HIV Education and Research (CIPHER), individual retrospective longitudinal data from 12 cohort networks were pooled. All children infected with HIV who entered care before age 10 years, were not known to have horizontally acquired HIV, and were followed up beyond age 10 years were included in this analysis conducted from May 2016 to January 2017. Our primary analysis describes patient and treatment characteristics of APHs at key time points, including first HIV-associated clinic visit, antiretroviral therapy (ART) start, age 10 years, and last visit, and compares these characteristics by geographic region, country income group (CIG), and birth period. Our secondary analysis describes mortality, transfer out, and lost to follow-up (LTFU) as outcomes at age 15 years, using competing risk analysis. Among the 38,187 APHs included, 51% were female, 79% were from sub-Saharan Africa and 65% lived in low-income countries. APHs from 51 countries were included (Europe: 14 countries and 3,054 APHs; North America: 1 country and 1,032 APHs; South America and the Caribbean: 4 countries and 903 APHs; South and Southeast Asia: 7 countries and 2,902 APHs; sub-Saharan Africa, 25 countries and 30,296 APHs). Observation started as early as 1982 in Europe and 1996 in sub-Saharan Africa, and continued until at least 2014 in all regions. The median (interquartile range [IQR]) duration of adolescent follow-up was 3.1 (1.5-5.2) years for the total cohort and 6.4 (3.6-8.0) years in Europe, 3.7 (2.0-5.4) years in North America, 2.5 (1.2-4.4) years in South and Southeast Asia, 5.0 (2.7-7.5) years in South America and the Caribbean, and 2.1 (0.9-3.8) years in sub-Saharan Africa. Median (IQR) age at first visit differed substantially by region, ranging from 0.7 (0.3-2.1) years in North America to 7.1 (5.3-8.6) years in sub-Saharan Africa. The median age at ART start varied from 0.9 (0.4-2.6) years in North America to 7.9 (6.0-9.3) years in sub-Saharan Africa. The cumulative incidence estimates (95% confidence interval [CI]) at age 15 years for mortality, transfers out, and LTFU for all APHs were 2.6% (2.4%-2.8%), 15.6% (15.1%-16.0%), and 11.3% (10.9%-11.8%), respectively. Mortality was lowest in Europe (0.8% [0.5%-1.1%]) and highest in South America and the Caribbean (4.4% [3.1%-6.1%]). However, LTFU was lowest in South America and the Caribbean (4.8% [3.4%-6.7%]) and highest in sub-Saharan Africa (13.2% [12.6%-13.7%]). Study limitations include the high LTFU rate in sub-Saharan Africa, which could have affected the comparison of mortality across regions; inclusion of data only for APHs receiving ART from some countries; and unavailability of data from high-burden countries such as Nigeria. Conclusion: To our knowledge, our study represents the largest multiregional epidemiological analysis of APHs. Despite probable under-ascertained mortality, mortality in APHs remains substantially higher in sub-Saharan Africa, South and Southeast Asia, and South America and the Caribbean than in Europe. Collaborations such as CIPHER enable us to monitor current global temporal trends in outcomes over time to inform appropriate policy responses.Public Library of ScienceRepositório Científico da Unidade Local de Saúde de Santo AntónioSlogrove, A.Schomaker, M.Davies, M.Williams, P.Balkan, S.Ben-Farhat, J.Calles, N.Chokephaibulkit, K.Duff, C.Eboua, T.Kekitiinwa-Rukyalekere, A.Maxwell, N.Pinto, J.Seage, G.Teasdale, C.Wanless, S.Warszawski, J.Wools-Kaloustian, K.Yotebieng, M.Timmerman, V.Collins, I.Goodall, R.Smith, C.Patel, K.Paul, M.Gibb, D.Vreeman, R.Abrams, E.Hazra, R.Van Dyke, R.Bekker, L.Mofenson, L.Vicari, M.Essajee, S.Penazzato, M.Anabwani, G.Q Mohapi, E.N Kazembe, P.Hlatshwayo, M.Lumumba, M.Goetghebuer, T.Thorne, C.Galli, L.van Rossum, A.Giaquinto, C.Marczynska, M.Marques, L.Prata, F.Ene, L.Okhonskaia, L.Rojo, P.Fortuny, C.Naver, L.Rudin, C.Le Coeur, S.Volokha, A.Rouzier, V.Succi, R.Sohn, A.Kariminia, A.Edmonds, A.Lelo, P.Ayaya, S.Ongwen, P.Jefferys, L.Phiri, S.Mubiana-Mbewe, Mw.Sawry, S.Renner, L.Sylla, M.Abzug, M.Levin, M.Oleske, J.Chernoff, M.Traite, S.Purswani, M.Chadwick, E.Judd, A.Leroy, V.2020-02-18T12:06:07Z2018-03-012018-03-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.16/2313eng1549-127710.1371/journal.pmed.1002514info:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2025-02-26T10:09:53Zoai:repositorio.chporto.pt:10400.16/2313Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T21:21:15.574081Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv The epidemiology of adolescents living with perinatally acquired HIV: A cross-region global cohort analysis
title The epidemiology of adolescents living with perinatally acquired HIV: A cross-region global cohort analysis
spellingShingle The epidemiology of adolescents living with perinatally acquired HIV: A cross-region global cohort analysis
Slogrove, A.
HIV Infections
title_short The epidemiology of adolescents living with perinatally acquired HIV: A cross-region global cohort analysis
title_full The epidemiology of adolescents living with perinatally acquired HIV: A cross-region global cohort analysis
title_fullStr The epidemiology of adolescents living with perinatally acquired HIV: A cross-region global cohort analysis
title_full_unstemmed The epidemiology of adolescents living with perinatally acquired HIV: A cross-region global cohort analysis
title_sort The epidemiology of adolescents living with perinatally acquired HIV: A cross-region global cohort analysis
author Slogrove, A.
author_facet Slogrove, A.
Schomaker, M.
Davies, M.
Williams, P.
Balkan, S.
Ben-Farhat, J.
Calles, N.
Chokephaibulkit, K.
Duff, C.
Eboua, T.
Kekitiinwa-Rukyalekere, A.
Maxwell, N.
Pinto, J.
Seage, G.
Teasdale, C.
Wanless, S.
Warszawski, J.
Wools-Kaloustian, K.
Yotebieng, M.
Timmerman, V.
Collins, I.
Goodall, R.
Smith, C.
Patel, K.
Paul, M.
Gibb, D.
Vreeman, R.
Abrams, E.
Hazra, R.
Van Dyke, R.
Bekker, L.
Mofenson, L.
Vicari, M.
Essajee, S.
Penazzato, M.
Anabwani, G.
Q Mohapi, E.
N Kazembe, P.
Hlatshwayo, M.
Lumumba, M.
Goetghebuer, T.
Thorne, C.
Galli, L.
van Rossum, A.
Giaquinto, C.
Marczynska, M.
Marques, L.
Prata, F.
Ene, L.
Okhonskaia, L.
Rojo, P.
Fortuny, C.
Naver, L.
Rudin, C.
Le Coeur, S.
Volokha, A.
Rouzier, V.
Succi, R.
Sohn, A.
Kariminia, A.
Edmonds, A.
Lelo, P.
Ayaya, S.
Ongwen, P.
Jefferys, L.
Phiri, S.
Mubiana-Mbewe, Mw.
Sawry, S.
Renner, L.
Sylla, M.
Abzug, M.
Levin, M.
Oleske, J.
Chernoff, M.
Traite, S.
Purswani, M.
Chadwick, E.
Judd, A.
Leroy, V.
author_role author
author2 Schomaker, M.
Davies, M.
Williams, P.
Balkan, S.
Ben-Farhat, J.
Calles, N.
Chokephaibulkit, K.
Duff, C.
Eboua, T.
Kekitiinwa-Rukyalekere, A.
Maxwell, N.
Pinto, J.
Seage, G.
Teasdale, C.
Wanless, S.
Warszawski, J.
Wools-Kaloustian, K.
Yotebieng, M.
Timmerman, V.
Collins, I.
Goodall, R.
Smith, C.
Patel, K.
Paul, M.
Gibb, D.
Vreeman, R.
Abrams, E.
Hazra, R.
Van Dyke, R.
Bekker, L.
Mofenson, L.
Vicari, M.
Essajee, S.
Penazzato, M.
Anabwani, G.
Q Mohapi, E.
N Kazembe, P.
Hlatshwayo, M.
Lumumba, M.
Goetghebuer, T.
Thorne, C.
Galli, L.
van Rossum, A.
Giaquinto, C.
Marczynska, M.
Marques, L.
Prata, F.
Ene, L.
Okhonskaia, L.
Rojo, P.
Fortuny, C.
Naver, L.
Rudin, C.
Le Coeur, S.
Volokha, A.
Rouzier, V.
Succi, R.
Sohn, A.
Kariminia, A.
Edmonds, A.
Lelo, P.
Ayaya, S.
Ongwen, P.
Jefferys, L.
Phiri, S.
Mubiana-Mbewe, Mw.
Sawry, S.
Renner, L.
Sylla, M.
Abzug, M.
Levin, M.
Oleske, J.
Chernoff, M.
Traite, S.
Purswani, M.
Chadwick, E.
Judd, A.
Leroy, V.
author2_role author
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dc.contributor.none.fl_str_mv Repositório Científico da Unidade Local de Saúde de Santo António
dc.contributor.author.fl_str_mv Slogrove, A.
Schomaker, M.
Davies, M.
Williams, P.
Balkan, S.
Ben-Farhat, J.
Calles, N.
Chokephaibulkit, K.
Duff, C.
Eboua, T.
Kekitiinwa-Rukyalekere, A.
Maxwell, N.
Pinto, J.
Seage, G.
Teasdale, C.
Wanless, S.
Warszawski, J.
Wools-Kaloustian, K.
Yotebieng, M.
Timmerman, V.
Collins, I.
Goodall, R.
Smith, C.
Patel, K.
Paul, M.
Gibb, D.
Vreeman, R.
Abrams, E.
Hazra, R.
Van Dyke, R.
Bekker, L.
Mofenson, L.
Vicari, M.
Essajee, S.
Penazzato, M.
Anabwani, G.
Q Mohapi, E.
N Kazembe, P.
Hlatshwayo, M.
Lumumba, M.
Goetghebuer, T.
Thorne, C.
Galli, L.
van Rossum, A.
Giaquinto, C.
Marczynska, M.
Marques, L.
Prata, F.
Ene, L.
Okhonskaia, L.
Rojo, P.
Fortuny, C.
Naver, L.
Rudin, C.
Le Coeur, S.
Volokha, A.
Rouzier, V.
Succi, R.
Sohn, A.
Kariminia, A.
Edmonds, A.
Lelo, P.
Ayaya, S.
Ongwen, P.
Jefferys, L.
Phiri, S.
Mubiana-Mbewe, Mw.
Sawry, S.
Renner, L.
Sylla, M.
Abzug, M.
Levin, M.
Oleske, J.
Chernoff, M.
Traite, S.
Purswani, M.
Chadwick, E.
Judd, A.
Leroy, V.
dc.subject.por.fl_str_mv HIV Infections
topic HIV Infections
description Background: Globally, the population of adolescents living with perinatally acquired HIV (APHs) continues to expand. In this study, we pooled data from observational pediatric HIV cohorts and cohort networks, allowing comparisons of adolescents with perinatally acquired HIV in "real-life" settings across multiple regions. We describe the geographic and temporal characteristics and mortality outcomes of APHs across multiple regions, including South America and the Caribbean, North America, Europe, sub-Saharan Africa, and South and Southeast Asia. Methods and findings: Through the Collaborative Initiative for Paediatric HIV Education and Research (CIPHER), individual retrospective longitudinal data from 12 cohort networks were pooled. All children infected with HIV who entered care before age 10 years, were not known to have horizontally acquired HIV, and were followed up beyond age 10 years were included in this analysis conducted from May 2016 to January 2017. Our primary analysis describes patient and treatment characteristics of APHs at key time points, including first HIV-associated clinic visit, antiretroviral therapy (ART) start, age 10 years, and last visit, and compares these characteristics by geographic region, country income group (CIG), and birth period. Our secondary analysis describes mortality, transfer out, and lost to follow-up (LTFU) as outcomes at age 15 years, using competing risk analysis. Among the 38,187 APHs included, 51% were female, 79% were from sub-Saharan Africa and 65% lived in low-income countries. APHs from 51 countries were included (Europe: 14 countries and 3,054 APHs; North America: 1 country and 1,032 APHs; South America and the Caribbean: 4 countries and 903 APHs; South and Southeast Asia: 7 countries and 2,902 APHs; sub-Saharan Africa, 25 countries and 30,296 APHs). Observation started as early as 1982 in Europe and 1996 in sub-Saharan Africa, and continued until at least 2014 in all regions. The median (interquartile range [IQR]) duration of adolescent follow-up was 3.1 (1.5-5.2) years for the total cohort and 6.4 (3.6-8.0) years in Europe, 3.7 (2.0-5.4) years in North America, 2.5 (1.2-4.4) years in South and Southeast Asia, 5.0 (2.7-7.5) years in South America and the Caribbean, and 2.1 (0.9-3.8) years in sub-Saharan Africa. Median (IQR) age at first visit differed substantially by region, ranging from 0.7 (0.3-2.1) years in North America to 7.1 (5.3-8.6) years in sub-Saharan Africa. The median age at ART start varied from 0.9 (0.4-2.6) years in North America to 7.9 (6.0-9.3) years in sub-Saharan Africa. The cumulative incidence estimates (95% confidence interval [CI]) at age 15 years for mortality, transfers out, and LTFU for all APHs were 2.6% (2.4%-2.8%), 15.6% (15.1%-16.0%), and 11.3% (10.9%-11.8%), respectively. Mortality was lowest in Europe (0.8% [0.5%-1.1%]) and highest in South America and the Caribbean (4.4% [3.1%-6.1%]). However, LTFU was lowest in South America and the Caribbean (4.8% [3.4%-6.7%]) and highest in sub-Saharan Africa (13.2% [12.6%-13.7%]). Study limitations include the high LTFU rate in sub-Saharan Africa, which could have affected the comparison of mortality across regions; inclusion of data only for APHs receiving ART from some countries; and unavailability of data from high-burden countries such as Nigeria. Conclusion: To our knowledge, our study represents the largest multiregional epidemiological analysis of APHs. Despite probable under-ascertained mortality, mortality in APHs remains substantially higher in sub-Saharan Africa, South and Southeast Asia, and South America and the Caribbean than in Europe. Collaborations such as CIPHER enable us to monitor current global temporal trends in outcomes over time to inform appropriate policy responses.
publishDate 2018
dc.date.none.fl_str_mv 2018-03-01
2018-03-01T00:00:00Z
2020-02-18T12:06:07Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.16/2313
url http://hdl.handle.net/10400.16/2313
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 1549-1277
10.1371/journal.pmed.1002514
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Public Library of Science
publisher.none.fl_str_mv Public Library of Science
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repository.name.fl_str_mv Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia
repository.mail.fl_str_mv info@rcaap.pt
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