Viral load care of HIV-1 infected children and adolescents: A longitudinal study in rural Zimbabwe

Maintaining virologic suppression of children and adolescents on ART in rural communities in sub-Saharan Africa is challenging. We explored switching drug regimens to protease inhibitor (PI) based treatment and reducing nevirapine and zidovudine use in a differentiated community service delivery mod...

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Veröffentlicht in:PloS one 2021-01, Vol.16 (1), p.e0245085
Hauptverfasser: Mapangisana, Tichaona, Machekano, Rhoderick, Kouamou, Vinie, Maposhere, Caroline, McCarty, Kathy, Mudzana, Marceline, Munyati, Shungu, Mutsvangwa, Junior, Manasa, Justen, Shamu, Tinei, Bogoshi, Mampedi, Israelski, Dennis, Katzenstein, David
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container_title PloS one
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creator Mapangisana, Tichaona
Machekano, Rhoderick
Kouamou, Vinie
Maposhere, Caroline
McCarty, Kathy
Mudzana, Marceline
Munyati, Shungu
Mutsvangwa, Junior
Manasa, Justen
Shamu, Tinei
Bogoshi, Mampedi
Israelski, Dennis
Katzenstein, David
description Maintaining virologic suppression of children and adolescents on ART in rural communities in sub-Saharan Africa is challenging. We explored switching drug regimens to protease inhibitor (PI) based treatment and reducing nevirapine and zidovudine use in a differentiated community service delivery model in rural Zimbabwe. From 2016 through 2018, we followed 306 children and adolescents on ART in Hurungwe, Zimbabwe at Chidamoyo Christian Hospital, which provides compact ART regimens at 8 dispersed rural community outreach sites. Viral load testing was performed (2016) by Roche and at follow-up (2018) by a point of care viral load assay. Virologic failure was defined as viral load ≥1,000 copies/ml. A logistic regression model which included demographics, treatment regimens and caregiver's characteristics was used to assess risks for virologic failure and loss to follow-up (LTFU). At baseline in 2016, 296 of 306 children and adolescents (97%) were on first-line ART, and only 10 were receiving a PI-based regimen. The median age was 12 years (IQR 8-15) and 55% were female. Two hundred and nine (68%) had viral load suppression (
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We explored switching drug regimens to protease inhibitor (PI) based treatment and reducing nevirapine and zidovudine use in a differentiated community service delivery model in rural Zimbabwe. From 2016 through 2018, we followed 306 children and adolescents on ART in Hurungwe, Zimbabwe at Chidamoyo Christian Hospital, which provides compact ART regimens at 8 dispersed rural community outreach sites. Viral load testing was performed (2016) by Roche and at follow-up (2018) by a point of care viral load assay. Virologic failure was defined as viral load ≥1,000 copies/ml. A logistic regression model which included demographics, treatment regimens and caregiver's characteristics was used to assess risks for virologic failure and loss to follow-up (LTFU). At baseline in 2016, 296 of 306 children and adolescents (97%) were on first-line ART, and only 10 were receiving a PI-based regimen. The median age was 12 years (IQR 8-15) and 55% were female. Two hundred and nine (68%) had viral load suppression (&lt;1,000 copies/ml) and 97(32%) were unsuppressed (viral load ≥1000). At follow-up in 2018, 42/306 (14%) were either transferred 23 (7%) or LTFU 17 (6%) and 2 had died. In 2018, of the 264 retained in care, 107/264 (41%), had been switched to second-line, ritonavir-boosted PI with abacavir as a new nucleotide analog reverse transcriptase inhibitor (NRTI). Overall viral load suppression increased from 68% in 2016 to 81% in 2018 (P&lt;0.001). Viral load testing, and switching to second-line, ritonavir-boosted PI with abacavir significantly increased virologic suppression among HIV-infected children and adolescents in rural Zimbabwe.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0245085</identifier><identifier>PMID: 33444325</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Adolescent ; Adolescents ; Age ; Anti-Retroviral Agents - administration &amp; dosage ; Antiretroviral agents ; Antiretroviral therapy ; Biology and Life Sciences ; Biomedical research ; Caregivers ; Child ; Children ; Children &amp; youth ; Computer programs ; Correlation analysis ; Data analysis ; Diagnosis ; Disease transmission ; Drafting software ; Drug resistance ; Drug therapy ; Editing ; Efavirenz ; Electronic mail ; Epidemiology ; Female ; Follow-Up Studies ; Funding ; Health care ; Health sciences ; HIV ; HIV infection in children ; HIV Infections - blood ; HIV Infections - drug therapy ; HIV-1 - metabolism ; Hospitals ; Human immunodeficiency virus ; Humans ; Lamivudine ; Longitudinal Studies ; Male ; Measurement ; Medical personnel ; Medicine ; Medicine and Health Sciences ; Microbiology ; Non-nucleoside reverse transcriptase inhibitors ; Nucleoside reverse transcriptase inhibitors ; Nucleotides ; Pediatric research ; Pediatrics ; People and Places ; Pharmacy ; Preventive medicine ; Public health ; RNA-directed DNA polymerase ; Rural areas ; Rural health ; Rural Population ; Software ; Teenagers ; Tenofovir ; Training ; Viral Load ; Viremia ; Zimbabwe</subject><ispartof>PloS one, 2021-01, Vol.16 (1), p.e0245085</ispartof><rights>COPYRIGHT 2021 Public Library of Science</rights><rights>2021 Mapangisana et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mapangisana, Tichaona</au><au>Machekano, Rhoderick</au><au>Kouamou, Vinie</au><au>Maposhere, Caroline</au><au>McCarty, Kathy</au><au>Mudzana, Marceline</au><au>Munyati, Shungu</au><au>Mutsvangwa, Junior</au><au>Manasa, Justen</au><au>Shamu, Tinei</au><au>Bogoshi, Mampedi</au><au>Israelski, Dennis</au><au>Katzenstein, David</au><au>Fokam, Joseph</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Viral load care of HIV-1 infected children and adolescents: A longitudinal study in rural Zimbabwe</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2021-01-14</date><risdate>2021</risdate><volume>16</volume><issue>1</issue><spage>e0245085</spage><pages>e0245085-</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Maintaining virologic suppression of children and adolescents on ART in rural communities in sub-Saharan Africa is challenging. We explored switching drug regimens to protease inhibitor (PI) based treatment and reducing nevirapine and zidovudine use in a differentiated community service delivery model in rural Zimbabwe. From 2016 through 2018, we followed 306 children and adolescents on ART in Hurungwe, Zimbabwe at Chidamoyo Christian Hospital, which provides compact ART regimens at 8 dispersed rural community outreach sites. Viral load testing was performed (2016) by Roche and at follow-up (2018) by a point of care viral load assay. Virologic failure was defined as viral load ≥1,000 copies/ml. A logistic regression model which included demographics, treatment regimens and caregiver's characteristics was used to assess risks for virologic failure and loss to follow-up (LTFU). At baseline in 2016, 296 of 306 children and adolescents (97%) were on first-line ART, and only 10 were receiving a PI-based regimen. The median age was 12 years (IQR 8-15) and 55% were female. Two hundred and nine (68%) had viral load suppression (&lt;1,000 copies/ml) and 97(32%) were unsuppressed (viral load ≥1000). At follow-up in 2018, 42/306 (14%) were either transferred 23 (7%) or LTFU 17 (6%) and 2 had died. In 2018, of the 264 retained in care, 107/264 (41%), had been switched to second-line, ritonavir-boosted PI with abacavir as a new nucleotide analog reverse transcriptase inhibitor (NRTI). Overall viral load suppression increased from 68% in 2016 to 81% in 2018 (P&lt;0.001). Viral load testing, and switching to second-line, ritonavir-boosted PI with abacavir significantly increased virologic suppression among HIV-infected children and adolescents in rural Zimbabwe.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>33444325</pmid><doi>10.1371/journal.pone.0245085</doi><tpages>e0245085</tpages><orcidid>https://orcid.org/0000-0001-8931-4484</orcidid><orcidid>https://orcid.org/0000-0003-4027-6901</orcidid><oa>free_for_read</oa></addata></record>
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identifier ISSN: 1932-6203
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issn 1932-6203
1932-6203
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subjects Adolescent
Adolescents
Age
Anti-Retroviral Agents - administration & dosage
Antiretroviral agents
Antiretroviral therapy
Biology and Life Sciences
Biomedical research
Caregivers
Child
Children
Children & youth
Computer programs
Correlation analysis
Data analysis
Diagnosis
Disease transmission
Drafting software
Drug resistance
Drug therapy
Editing
Efavirenz
Electronic mail
Epidemiology
Female
Follow-Up Studies
Funding
Health care
Health sciences
HIV
HIV infection in children
HIV Infections - blood
HIV Infections - drug therapy
HIV-1 - metabolism
Hospitals
Human immunodeficiency virus
Humans
Lamivudine
Longitudinal Studies
Male
Measurement
Medical personnel
Medicine
Medicine and Health Sciences
Microbiology
Non-nucleoside reverse transcriptase inhibitors
Nucleoside reverse transcriptase inhibitors
Nucleotides
Pediatric research
Pediatrics
People and Places
Pharmacy
Preventive medicine
Public health
RNA-directed DNA polymerase
Rural areas
Rural health
Rural Population
Software
Teenagers
Tenofovir
Training
Viral Load
Viremia
Zimbabwe
title Viral load care of HIV-1 infected children and adolescents: A longitudinal study in rural Zimbabwe
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