Your browser doesn't support javascript.
loading
Integrase inhibitor drugs during pregnancy and congenital anomalies: A case/non-case study from the global pharmacovigilance database VigiBase®.
Saint-Lary, Laura; Lacroix, Isabelle; Leroy, Valériane; Sommet, Agnès.
Afiliación
  • Saint-Lary L; CERPOP, Inserm, Université de Toulouse, Université Paul Sabatier III, Toulouse, France.
  • Lacroix I; CERPOP, Inserm, Université de Toulouse, Université Paul Sabatier III, Toulouse, France.
  • Leroy V; Service de Pharmacologie Clinique, CHU de Toulouse, Université Toulouse 3, Toulouse, France.
  • Sommet A; CERPOP, Inserm, Université de Toulouse, Université Paul Sabatier III, Toulouse, France.
Pharmacol Res Perspect ; 12(4): e1247, 2024 Aug.
Article en En | MEDLINE | ID: mdl-39086081
ABSTRACT
In 2018, a significant neural tube defects (NTD) signal was reported after pre-conceptional exposure to dolutegravir, but was not confirmed in further analysis. Since 2019, dolutegravir-based regimen, an integrase inhibitor (INI), is recommended by WHO as the most-effective first-line therapy in all patients living with HIV. To explore the potential INI-related teratogenic effect, we searched disproportionate signals between exposure to INI-class drugs and congenital anomalies, compared to non-INI drugs, using the international pharmacovigilance database, VigiBase®. We selected all the reports registered in VigiBase® between 01/01/2007 and 30/03/2021 on any antiretroviral drug-related fetal or neonatal adverse drug reactions, declared either in children (<2 years) exposed in utero or in pregnant women (12-50 years). A case/non-case study was conducted to detected signals between congenital anomalies and prenatal exposure to any INI-class drug, compared to non-INI drugs, by estimating adjusted reporting odds ratios (aROR) with 95% confidence intervals (95%CI). We identified 2521 unique reports, among which 664 (26.3%) were related to INI-class use. Overall, 520 congenital anomalies were cited from 327 unique reports, of whom 31.0% were INI-related. Compared to non-INI drugs, no significant disproportionate reporting signal between prenatal exposure to INI-class drugs and congenital anomalies was found (aROR 1.13; 95% CI0.85-1.51). However, specific significant signals were reported for raltegravir/elvitegravir/dolutegravir drug exposure and urinary malformations (aROR 2.43; 95%CI1.08-5.43), digestive malformations (aROR 3.09; 95%CI1.22-7.84), and NTDs (aROR 3.02; 95%CI1.09-8.37). Although specific congenital anomalies signals associated with raltegravir/elvitegravir/dolutegravir exposure were notified, causal relationship needs to be further investigated in prospective studies.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Piridonas / Anomalías Inducidas por Medicamentos / Bases de Datos Factuales / Farmacovigilancia / Compuestos Heterocíclicos con 3 Anillos Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Middle aged / Newborn / Pregnancy Idioma: En Revista: Pharmacol Res Perspect Año: 2024 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Piridonas / Anomalías Inducidas por Medicamentos / Bases de Datos Factuales / Farmacovigilancia / Compuestos Heterocíclicos con 3 Anillos Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Middle aged / Newborn / Pregnancy Idioma: En Revista: Pharmacol Res Perspect Año: 2024 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Estados Unidos