Interpersonal therapy versus antidepressant medication for treatment of postpartum depression and anxiety among women with HIV in Zambia: a randomized feasibility trial.


Journal

Journal of the International AIDS Society
ISSN: 1758-2652
Titre abrégé: J Int AIDS Soc
Pays: Switzerland
ID NLM: 101478566

Informations de publication

Date de publication:
07 2022
Historique:
received: 18 10 2021
accepted: 14 06 2022
entrez: 8 7 2022
pubmed: 9 7 2022
medline: 14 7 2022
Statut: ppublish

Résumé

Postpartum depression (PPD) is a prevalent and debilitating disease that may affect medication adherence and thus maternal health and vertical transmission among women with HIV. We assessed the feasibility of a trial of interpersonal psychotherapy (IPT) versus antidepressant medication (ADM) to treat PPD and/or anxiety among postpartum women with HIV in Lusaka, Zambia. Between 29 October 2019 and 8 September 2020, we pre-screened women 6-8 weeks after delivery with the Edinburgh Postnatal Depression Scale (EPDS) and diagnosed PPD or anxiety with the Mini International Neuropsychiatric Interview. Consenting participants were randomized 1:1 to up to 11 sessions of IPT or daily self-administered sertraline and followed for 24 weeks. We assessed EPDS score, Clinical Global Impression-Severity of Illness (CGI-S) and medication side effects at each visit and measured maternal HIV viral load at baseline and final study visit. Retention, visit adherence, change in EPDS, CGI-S and log viral load were compared between groups with t-tests and Wilcoxon signed rank tests; we report mean differences, relative risks and 95% confidence intervals. A participant satisfaction survey assessed trial acceptability. 78/80 (98%) participants were retained at the final study visit. In the context of the COVID-19 pandemic, visit adherence was greater among women allocated to ADM (9.9 visits, SD 2.2) versus IPT (8.9 visits, SD 2.4; p = 0.06). EPDS scores decreased from baseline to final visit overall, though mean change was greater in the IPT group (-13.8 points, SD 4.7) compared to the ADM group (-11.4 points, SD 5.5; p = 0.04). Both groups showed similar changes in mean log viral load from baseline to final study visit (mean difference -0.43, 95% CI -0.32, 1.18; p = 0.48). In the IPT group, viral load decreased significantly from baseline (0.9 log copies/ml, SD 1.7) to final visit (0.2 log copies/ml, SD 0.9; p = 0.01). This pilot study demonstrates that a trial of two forms of PPD treatment is feasible and acceptable among women with HIV in Zambia. IPT and ADM both improved measures of depression severity; however, a full-scale trial is required to determine whether treatment of PPD and anxiety improves maternal-infant HIV outcomes.

Identifiants

pubmed: 35803896
doi: 10.1002/jia2.25959
pmc: PMC9270230
doi:

Substances chimiques

Antidepressive Agents 0

Banques de données

ClinicalTrials.gov
['NCT04094870']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e25959

Subventions

Organisme : FIC NIH HHS
ID : K01 TW010857
Pays : United States
Organisme : NIH HHS
ID : UL1TR002489
Pays : United States
Organisme : NIMH NIH HHS
ID : R21 MH115806
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR002489
Pays : United States
Organisme : NIMH NIH HHS
ID : 1R21MH115806
Pays : United States
Organisme : NICHD NIH HHS
ID : T32 HD075731
Pays : United States
Organisme : FIC NIH HHS
ID : D43 TW009340
Pays : United States

Informations de copyright

© 2022 The Authors. Journal of the International AIDS Society published by John Wiley & Sons Ltd on behalf of the International AIDS Society.

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Auteurs

M Bridget Spelke (MB)

Department of Obstetrics and Gynecology, University of North Carolina School of Medicine, Chapel Hill, North Carolina, USA.
University of North Carolina - Global Projects Zambia, Lusaka, Zambia.

Ravi Paul (R)

Department of Psychiatry, University of Zambia School of Medicine, Lusaka, Zambia.

Bryan S Blette (BS)

Department of Biostatistics, University of North Carolina Gillings School of Global Public Health, Chapel Hill, North Carolina, USA.

Samantha Meltzer-Brody (S)

Department of Psychiatry, University of North Carolina School of Medicine, Chapel Hill, North Carolina, USA.

Crystal E Schiller (CE)

Department of Psychiatry, University of North Carolina School of Medicine, Chapel Hill, North Carolina, USA.

J M Ncheka (JM)

Department of Psychiatry, University of Zambia School of Medicine, Lusaka, Zambia.

Margaret P Kasaro (MP)

University of North Carolina - Global Projects Zambia, Lusaka, Zambia.

Joan T Price (JT)

Department of Obstetrics and Gynecology, University of North Carolina School of Medicine, Chapel Hill, North Carolina, USA.
University of North Carolina - Global Projects Zambia, Lusaka, Zambia.

Jeffrey S A Stringer (JSA)

Department of Obstetrics and Gynecology, University of North Carolina School of Medicine, Chapel Hill, North Carolina, USA.
University of North Carolina - Global Projects Zambia, Lusaka, Zambia.

Elizabeth M Stringer (EM)

Department of Obstetrics and Gynecology, University of North Carolina School of Medicine, Chapel Hill, North Carolina, USA.
University of North Carolina - Global Projects Zambia, Lusaka, Zambia.

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