Where are the data to assess the safety of paternal drug exposure? A systematic review of secondary databases: A contribution from IMI concePTION

Author:

Gaitonde Sneha123,Moride Yola2,Suarez Elizabeth24,Lopez‐Leon Sandra12ORCID

Affiliation:

1. Quantitative Safety & Epidemiology Novartis Pharmaceuticals East Hanover New Jersey USA

2. Rutgers Center for Pharmacoepidemiology and Treatment Science Rutgers University New Brunswick New Jersey USA

3. Rutgers University Ernest Mario School of Pharmacy Piscataway New Jersey USA

4. Department of Biostatistics and Epidemiology Rutgers School of Public Health Piscataway New Jersey USA

Abstract

AbstractBackgroundMost studies assessing the safety of parental drug exposures during pregnancy and around the time of conception describe the effects of maternal exposure. Recent publications have raised awareness of the need for additional research regarding the safety of paternal drug exposures on pregnancy outcomes.ObjectivesTo identify and describe studies that use secondary databases in paternal drug safety studies and to describe the secondary databases that were used.MethodsA systematic review of studies assessing paternal medication exposure and pregnancy and infant outcomes using secondary databases was performed. In addition, the secondary databases used for these studies was described. Literature search was conducted using Embase, Web of Science, and PubMed, over the period January 1, 2012 to April 30, 2023. For each eligible study, paternal drug exposure, outcome, and data source characteristics were extracted in a data extraction form.ResultsAfter reviewing the literature, 17 studies met inclusion criteria. The medications assessed for paternal safety were anti‐rheumatic drugs (n = 10), anti‐depressants (n = 3), anticonvulsants (n = 2), and anti‐diabetes medications (n = 2). Pregnancy safety outcomes included congenital malformations, birth weight, and developmental disorders. The studies used five different databases across Europe and North America. The included studies used databases from Denmark (n = 12), Norway (n = 2), Sweden (n = 1), Canada (n = 1), and the United States (n = 1). The European studies utilized national patient registers that linked fathers to births and prescription histories. The North American databases used included insurance claims and electronic health records.ConclusionsOur review shows that few studies have been completed on paternal medication exposures and pregnancy outcomes, despite the availability of secondary databases that contain data necessary to link fathers to infants. More research on the potential adverse impacts of paternal medication exposures is needed.

Funder

Novartis Pharmaceuticals Corporation

Publisher

Wiley

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