Predictors of Viremia in Postpartum Women on Antiretroviral Therapy.


Journal

Journal of acquired immune deficiency syndromes (1999)
ISSN: 1944-7884
Titre abrégé: J Acquir Immune Defic Syndr
Pays: United States
ID NLM: 100892005

Informations de publication

Date de publication:
01 01 2020
Historique:
pubmed: 28 10 2019
medline: 7 7 2020
entrez: 26 10 2019
Statut: ppublish

Résumé

HIV-infected, postpartum women on antiretroviral therapy (ART) have high rates of viremia. We examined predictors of postpartum viremia in the PROMISE study. Women with pre-ART CD4 T-cell counts ≥400 cells/mm who started ART during pregnancy were randomized postpartum to continue ART (CTART) or discontinue ART (DCART). Viral load and self-reported adherence were collected every 12 weeks, up to 144 weeks. Women in DCART reinitiated therapy when clinically indicated. Viremia was defined as 2 consecutive viral loads >1000 copies/mL after 24 weeks on ART. Adherence was dichotomized as missing versus not missing ART doses in the past 4 weeks. Predictors of viremia were examined using Cox proportional hazards regression with adherence as a time-varying covariate. Among 802 women in the CTART arm, median age at entry was 27 years and median CD4 T-cell count 696 cells/mm. Of 175 women in CTART with viremia (22%), 141 had resistance data, and 12% had resistance to their current regimen. There was an estimated 0.12 probability of viremia by week 48 and 0.25 by week 144. Predictors of viremia included missed ART doses within the past 4 weeks, younger age, shorter duration of pre-entry ART, and being from the South American/Caribbean region. Of 137 women in DCART who reinitiated therapy, probability of viremia was similar to CTART (0.24 by week 96; 0.27 by week 144). Rates of postpartum viremia are high and viremia is more likely in younger postpartum women who start ART later in pregnancy. Interventions should target these higher-risk women.

Sections du résumé

BACKGROUND
HIV-infected, postpartum women on antiretroviral therapy (ART) have high rates of viremia. We examined predictors of postpartum viremia in the PROMISE study.
METHODS
Women with pre-ART CD4 T-cell counts ≥400 cells/mm who started ART during pregnancy were randomized postpartum to continue ART (CTART) or discontinue ART (DCART). Viral load and self-reported adherence were collected every 12 weeks, up to 144 weeks. Women in DCART reinitiated therapy when clinically indicated. Viremia was defined as 2 consecutive viral loads >1000 copies/mL after 24 weeks on ART. Adherence was dichotomized as missing versus not missing ART doses in the past 4 weeks. Predictors of viremia were examined using Cox proportional hazards regression with adherence as a time-varying covariate.
RESULTS
Among 802 women in the CTART arm, median age at entry was 27 years and median CD4 T-cell count 696 cells/mm. Of 175 women in CTART with viremia (22%), 141 had resistance data, and 12% had resistance to their current regimen. There was an estimated 0.12 probability of viremia by week 48 and 0.25 by week 144. Predictors of viremia included missed ART doses within the past 4 weeks, younger age, shorter duration of pre-entry ART, and being from the South American/Caribbean region. Of 137 women in DCART who reinitiated therapy, probability of viremia was similar to CTART (0.24 by week 96; 0.27 by week 144).
CONCLUSIONS
Rates of postpartum viremia are high and viremia is more likely in younger postpartum women who start ART later in pregnancy. Interventions should target these higher-risk women.

Identifiants

pubmed: 31651545
doi: 10.1097/QAI.0000000000002228
pmc: PMC6898779
mid: NIHMS1540913
pii: 00126334-202001010-00010
doi:

Substances chimiques

Anti-HIV Agents 0

Types de publication

Journal Article Randomized Controlled Trial Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

72-80

Subventions

Organisme : NIAID NIH HHS
ID : UM1 AI069424
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI069456
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI068632
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI069530
Pays : United States
Organisme : NIAID NIH HHS
ID : U01 AI068616
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI068616
Pays : United States
Organisme : NIAID NIH HHS
ID : U01 AI069424
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI106716
Pays : United States
Organisme : NIAID NIH HHS
ID : U01 AI068632
Pays : United States
Organisme : NICHD NIH HHS
ID : HHSN275201800001C
Pays : United States
Organisme : NICHD NIH HHS
ID : HHSN275201800001I
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI068636
Pays : United States
Organisme : NIAID NIH HHS
ID : U01 AI025868
Pays : United States

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Auteurs

Risa M Hoffman (RM)

Division of Infectious Diseases, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA.

Meredith G Warshaw (MG)

Center for Biostatistics in AIDS Research, Harvard T.H. Chan School of Public Health, Boston, MA.

K Rivet Amico (KR)

Health Behavior & Health Education, School of Public Health, University of Michigan, Ann Arbor, MI.

Jose Pilotto (J)

JP, Fundação Oswaldo Cruz/IOC Laboratório de AIDS e Imunologia Molecular, Rio de Janeiro, Brazil.

Gaerolwe Masheto (G)

Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.

Jullapong Achalapong (J)

Chiang Rai Prachanukroh Hospital, Chiang Rai, Thailand.

Elizabeth Machado (E)

Instituto de Puericultura e Pediatria Martagão Gesteira, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.

Kulkanya Chokephaibulkit (K)

Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.

Geraldo Duarte (G)

Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.

Esau João (E)

Infectious Diseases Department, Hospital Federal dos Servidores do Estado, Rio de Janeiro, RJ, Brazil.

Kathleen K Graham (KK)

Children's Diagnostic and Treatment Center, Fort Lauderdale, FL.

Katherine M Knapp (KM)

Infectious Diseases Department, St Jude Children's Research Hospital, Memphis, TN.

Alice M Stek (AM)

Department of Obstetrics and Gynecology, School of Medicine, University of Southern CaliforniaLos Angeles, CA.

Gwendolyn B Scott (GB)

School of Medicine, University of Miami Miller, Miami, FL.

Anne Coletti (A)

FHI 360, Durham, NC.

Amy J Loftis (AJ)

Institute for Global Health and Infectious Diseases, University of North Carolina, Chapel Hill, NC; and.

Nahida Chakhtoura (N)

Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), NIH, Bethesda, MD.

Judith S Currier (JS)

Division of Infectious Diseases, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA.

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