Does Changing Antiretroviral Therapy in the First Trimester of Pregnancy for Safety Concerns Have an Impact on Viral Suppression?


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:
15 04 2019
Historique:
pubmed: 17 1 2019
medline: 19 12 2019
entrez: 17 1 2019
Statut: ppublish

Résumé

To determine whether changing antiretroviral therapy (ART) during pregnancy because of concern about fetal risks led to poorer virological outcomes. All pregnancies in women with HIV-1 infection enrolled in the national multicenter prospective French Perinatal cohort at 14 week gestation or more were included between January 2005 and December 2015, if the mother was on ART at conception with a plasma viral load <50 copies/mL. The reasons for a change in the ART were analyzed according to treatment guidelines at the time of the pregnancy and defined as for safety concerns in the absence of reported maternal intolerance. Virological and pregnancy outcomes were studied by survival analysis and logistic regression adjusted for a propensity score established for each patient according to baseline characteristics. Of 7079 pregnancies in the overall cohort, 1797 had ART at conception with a viral load <50 copies/mL before 14 week gestation. Of these, 22 changed regimens in the first trimester for intolerance, and 411 of the remaining 1775 (23%) solely for safety concerns. The proportion of change was higher when the initial treatment was not recommended in the national guidelines (OR adjusted: 23.1 [14.0-38.2]), than when it was an alternative option (ORa: 2.2 [1.3-3.7]), as compared to recommended first-line regimens. Treatment changes for safety concerns did not lead to poorer virological control, compared with pregnancies without such changes (19.3% vs. 15.6%, HRa: 1.0 [0.7-1.4]). Changing ART early in pregnancy to regimens considered safer for pregnancy, and neonatal health did not have a destabilizing effect on viral suppression.

Identifiants

pubmed: 30649033
doi: 10.1097/QAI.0000000000001954
doi:

Substances chimiques

Anti-HIV Agents 0

Types de publication

Journal Article Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

574-584

Auteurs

Violaine Peyronnet (V)

CESP INSERM U1018, AP-HP Hopital Bicètre, le Kremlin Bicètre, France.
AP-HP Hôpital L. Mourier, Colombes.

Josiane Warszawski (J)

CESP INSERM U1018, AP-HP Hopital Bicètre, le Kremlin Bicètre, France.
Univ Paris Sud, Le Kremlin-Bicêtre, France.
AP-HP Hôpital Bicêtre, le Kremlin-Bicêtre, France.

Jeanne Sibiude (J)

CESP INSERM U1018, AP-HP Hopital Bicètre, le Kremlin Bicètre, France.
AP-HP Hôpital L. Mourier, Colombes.
Univ Paris-Diderot, Paris, France.

Olivia Dialla (O)

CESP INSERM U1018, AP-HP Hopital Bicètre, le Kremlin Bicètre, France.

Agnès Bourgeois-Moine (A)

AP-HP Hôpital Bichat, Paris, France.

Eida Bui (E)

AP-HP Hôpital Trousseau, Paris, France.

Caroline Simon Toulza (CS)

CHU de Toulouse, Toulouse, France.

Delphine Peretti (D)

AP-HP Hôpital Bicêtre, le Kremlin-Bicêtre, France.

Cécile Brunet-Cartier (C)

CHU de Nantes, Nantes, France.

Véronique Avettand-Fenoel (V)

AP-HP Hôpital Necker-Enfants Malades, Paris, France.
Univ Paris-Descartes, Paris, France.

Jérôme L Chenadec (JL)

CESP INSERM U1018, AP-HP Hopital Bicètre, le Kremlin Bicètre, France.

Albert Faye (A)

Univ Paris-Diderot, Paris, France.
AP-HP Hôpital R. Debré, Paris, France.

Roland Tubiana (R)

AP-HP Hôpital Pitié Salpétrière, Paris, France.

Laurent Mandelbrot (L)

CESP INSERM U1018, AP-HP Hopital Bicètre, le Kremlin Bicètre, France.
AP-HP Hôpital L. Mourier, Colombes.
Univ Paris-Diderot, Paris, France.

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