Interactions between etonogestrel-releasing contraceptive implant and 3 antiretroviral regimens.


Journal

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

Informations de publication

Date de publication:
01 2022
Historique:
received: 23 11 2020
revised: 05 08 2021
accepted: 09 08 2021
pubmed: 19 8 2021
medline: 28 1 2022
entrez: 18 8 2021
Statut: ppublish

Résumé

Long-acting reversible contraceptives are effective contraceptives for women with HIV, but there are limited data on etonogestrel implant and antiretroviral therapy pharmacokinetic drug-drug interactions. We evaluated etonogestrel/antiretroviral therapy drug-drug interactions, and the effects of etonogestrel on ritonavir-boosted-atazanavir, ritonavir-boosted-lopinavir, and efavirenz pharmacokinetics. We enrolled postpartum women using etonogestrel implants and receiving ritonavir-boosted-atazanavir, ritonavir-boosted-lopinavir, or efavirenz-based regimens between 2012 and 2015. Etonogestrel implants were inserted 2 to 12 weeks postpartum. We performed pharmacokinetic sampling pre-etonogestrel insertion and 6 to 7 weeks postinsertion. We measured antiretroviral concentrations pre and postetonogestrel insertion, and compared etonogestrel concentrations between antiretroviral regimens. We considered a minimum serum etonogestrel concentration of 90 pg/mL adequate for ovulation suppression. We collected pharmacokinetic data for 74 postpartum women, 22 on ritonavir-boosted-atazanavir, 26 on ritonavir-boosted-lopinavir, and 26 on efavirenz. The median serum concentrations of etonogestrel when co-administered were highest with etonogestrel/ritonavir-boosted-atazanavir (604 pg/mL) and etonogestrel/ritonavir-boosted-lopinavir (428 pg/mL), and lowest with etonogestrel/efavirenz (125 pg/mL); p < 0.001. Minimum concentration (C Unlike efavirenz, ritonavir-boosted-atazanavir and ritonavir-boosted-lopinavir were not associated with significant decreases in etonogestrel concentrations. Efavirenz was associated with a significant decrease in etonogestrel concentrations. The findings demonstrate no interactions between etonogestrel and ritonavir-boosted-lopinavir or ritonavir-boosted-atazanavir, but confirm the decreased efficacy of etonogestrel with efavirenz-based antiretrovirals. This information should be used to counsel women with HIV who desire long-acting reversible contraceptives.

Identifiants

pubmed: 34407424
pii: S0010-7824(21)00350-4
doi: 10.1016/j.contraception.2021.08.006
pmc: PMC8678338
mid: NIHMS1752166
pii:
doi:

Substances chimiques

Anti-HIV Agents 0
Contraceptive Agents 0
Drug Combinations 0
HIV Protease Inhibitors 0
atazanavir, ritonavir drug combination 0
etonogestrel 304GTH6RNH
Atazanavir Sulfate 4MT4VIE29P
Desogestrel 81K9V7M3A3
Ritonavir O3J8G9O825

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

67-74

Subventions

Organisme : NICHD NIH HHS
ID : K23 HD104517
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI068616
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI068632
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI106716
Pays : United States

Informations de copyright

Copyright © 2021. Published by Elsevier Inc.

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Auteurs

Regis Kreitchmann (R)

Irmandade da Santa Casa de Misericordia de Porto Alegre, Porto Alegre, Brazil; Federal University of Health Sciences of Porto Alegre, Brazil. Electronic address: regis.kr@terra.com.br.

Alice Stek (A)

University of Southern California School of Medicine, Los Angeles, CA, United States.

Brookie M Best (BM)

University of California San Diego, San Diego, CA, United States.

Edmund Capparelli (E)

University of California San Diego, San Diego, CA, United States.

JiaJia Wang (J)

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

David Shapiro (D)

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

Nahida Chakhtoura (N)

Maternal and Pediatric Infectious Diseases Branch, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), Bethesda, MD, United States.

Mark Mirochnick (M)

Boston University School of Medicine, Boston, MA, United States.

Ahizechukwu C Eke (AC)

Johns Hopkins University School of Medicine, Baltimore, MD, United States.

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Classifications MeSH