Ampicillin Pharmacokinetics in Peripartum and Laboring Women.


Journal

American journal of perinatology
ISSN: 1098-8785
Titre abrégé: Am J Perinatol
Pays: United States
ID NLM: 8405212

Informations de publication

Date de publication:
02 Dec 2021
Historique:
pubmed: 21 10 2021
medline: 21 10 2021
entrez: 20 10 2021
Statut: aheadofprint

Résumé

 Ampicillin is used for multiple peripartum indications including prevention of neonatal group B streptococcus (GBS) and treatment of chorioamnionitis. Despite its widespread use in obstetrics, existing pharmacokinetic data for ampicillin do not address contemporary indications or dosing paradigms for this population. We sought to characterize the pharmacokinetic profile of ampicillin administered to laboring women.  Using whole blood dried blood spot sampling technique, maternal blood samples were collected at specified times from 31 women receiving intravenous (IV) ampicillin for peripartum indications. Women received either a 2-g loading dose with 1-g administered every 4 hours (GBS) or 2-g every 6 hours (chorioamnionitis). Pharmacokinetics were analyzed via a population approach with nonlinear mixed-effect modeling.  The data were best described by a two-compartment model with first-order elimination, with the following whole blood parameters: central volume of distribution (V  Although large variation in the pharmacokinetics of ampicillin in pregnant women exists, as predicted by our model, current standard dosing strategies achieve adequate exposure for GBS in nearly all patients. · IV ampicillin is widely used in obstetrics.. · Pharmacokinetic studies are lacking.. · Ampicillin pharmacokinetics were established.. · Ampicillin clearance and volume of distribution are high.. · Current ampicillin dosing strategies are sufficient..

Identifiants

pubmed: 34670320
doi: 10.1055/a-1674-6394
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Thieme. All rights reserved.

Déclaration de conflit d'intérêts

A.F. is a scientific consultant for Takeda Pharmaceuticals, none of the other authors declare any conflicts of interest.

Auteurs

Amy E Judy (AE)

Department of Obstetrics and Gynecology, Stanford University School of Medicine, Stanford, California.

Adam Frymoyer (A)

Department of Pediatrics, Stanford University School of Medicine, Stanford, California.

Jessica Ansari (J)

Department of Anesthesiology, Perioperative and Pain Medicine, Stanford University School of Medicine, Stanford, California.

David R Drover (DR)

Department of Anesthesiology, Perioperative and Pain Medicine, Stanford University School of Medicine, Stanford, California.

Brendan Carvalho (B)

Department of Anesthesiology, Perioperative and Pain Medicine, Stanford University School of Medicine, Stanford, California.

Classifications MeSH