Etonogestrel concentrations among contraceptive implant users in Botswana using and not using dolutegravir-based antiretroviral therapy.


Journal

Contraception
ISSN: 1879-0518
Titre abrégé: Contraception
Pays: United States
ID NLM: 0234361

Informations de publication

Date de publication:
09 2020
Historique:
received: 31 03 2020
revised: 27 04 2020
accepted: 28 04 2020
pubmed: 11 5 2020
medline: 16 10 2021
entrez: 11 5 2020
Statut: ppublish

Résumé

To evaluate whether etonogestrel concentrations are reduced to a level that could potentially reduce contraceptive efficacy when the etonogestrel contraceptive implant is used concomitantly with dolutegravir-based antiretroviral therapy (ART). We conducted a non-randomized, open-label, cross-sectional pharmacokinetic study among women using single-rod etonogestrel contraceptive implants in Botswana. We compared plasma etonogestrel concentrations, sampled at a single time-point between 3 and 12 months from implant insertion, among implant users living with HIV and receiving dolutegravir-based ART with HIV-negative implant users. We also assessed concentrations among implant users living with HIV and receiving efavirenz-based ART. We compared geometric mean etonogestrel concentrations analyzing data from 142 participants: 97 HIV-negative, 30 using dolutegravir, and 15 using efavirenz. The groups were similar. Duration of implant use was between 3 and 12 months (median = 5). Geometric mean etonogestrel plasma concentrations and 90% confidence intervals of the mean were 227.5(212.4-243.8), 289.6(251.8-333.0) and 76.4(63.9-91.4) pg/mL among the HIV-negative, dolutegravir- and efavirenz-based ART groups, respectively. All women in the HIV-negative and dolutegravir-based ART groups had etonogestrel concentrations above 90 pg/mL; 9/15 women (60%) using efavirenz-based ART had concentrations below 90 pg/mL. On average, etonogestrel levels were lower among individuals who had implants inserted for longer durations. Implant users receiving dolutegravir-based ART had a higher mean etonogestrel concentration compared to HIV-negative women, and none had etonogestrel concentrations below the posited threshold for ovulation suppression. In contrast, women in the efavirenz-group had much lower etonogestrel concentrations. Overall, these data provide evidence that the etonogestrel implant may be effectively combined with dolutegravir-based ART regimens. The etonogestrel implant remains a highly effective contraceptive option for women living with HIV who use dolutegravir-based ART.

Identifiants

pubmed: 32387328
pii: S0010-7824(20)30134-7
doi: 10.1016/j.contraception.2020.04.019
pii:
doi:

Substances chimiques

Contraceptive Agents 0
Contraceptive Agents, Female 0
Heterocyclic Compounds, 3-Ring 0
Oxazines 0
Piperazines 0
Pyridones 0
etonogestrel 304GTH6RNH
Desogestrel 81K9V7M3A3
dolutegravir DKO1W9H7M1

Types de publication

Clinical Study Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

174-179

Subventions

Organisme : NCATS NIH HHS
ID : UL1 TR000040
Pays : United States

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Auteurs

Ian J Bishop (IJ)

Columbia University Medical Center, 622 West 168th Street, New York, NY 10032, United States.

Alida M Gertz (AM)

Botswana-University of Pennsylvania Partnership, University of Botswana Main Campus 244G - Room 103, Gaborone, Botswana; Botswana Harvard Partnership, Private Bag BO 320, Gaborone, Botswana.

Boikhutso Simon (B)

Botswana Harvard Partnership, Private Bag BO 320, Gaborone, Botswana.

Leabaneng Tawe (L)

Botswana-University of Pennsylvania Partnership, University of Botswana Main Campus 244G - Room 103, Gaborone, Botswana.

Kwana Lechiile (K)

Botswana-University of Pennsylvania Partnership, University of Botswana Main Campus 244G - Room 103, Gaborone, Botswana.

Serena Liu (S)

Columbia University Medical Center, 622 West 168th Street, New York, NY 10032, United States.

Nicholas Teodoro (N)

Columbia University Medical Center, 622 West 168th Street, New York, NY 10032, United States.

Aamirah Mussa (A)

Botswana Harvard Partnership, Private Bag BO 320, Gaborone, Botswana.

Ava Avalos (A)

Botswana Harvard Partnership, Private Bag BO 320, Gaborone, Botswana.

Sifelani Malima (S)

Botswana Ministry of Health and Wellness, Nelson Mandela Drive, Gaborone, Botswana.

Tshego Maotwe (T)

Botswana Ministry of Health and Wellness, Nelson Mandela Drive, Gaborone, Botswana; Afya Bora Consortium Fellowship Program, Botswana.

Lesego Mokganya (L)

Botswana Ministry of Health and Wellness, Nelson Mandela Drive, Gaborone, Botswana.

Carolyn L Westhoff (CL)

Columbia University Medical Center, 622 West 168th Street, New York, NY 10032, United States.

Chelsea Morroni (C)

Botswana-University of Pennsylvania Partnership, University of Botswana Main Campus 244G - Room 103, Gaborone, Botswana; Botswana Harvard Partnership, Private Bag BO 320, Gaborone, Botswana; Liverpool School of Tropical Medicine, Pembroke Pl, Liverpool L3 5QA, United Kingdom. Electronic address: chelsea.morroni@lstmed.ac.uk.

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Classifications MeSH