Abstract

Many drugs commonly prescribed during pregnancy lack a fetal safety recommendation – called FDA ‘category C’ drugs. This study aims to classify these drugs into harmful and safe categories using knowledge gained from chemoinformatics (i.e., pharmacological similarity with drugs of known fetal effect) and empirical data (i.e., derived from Electronic Health Records). Our fetal loss cohort contains 14,922 affected and 33,043 unaffected pregnancies and our congenital anomalies cohort contains 5,658 affected and 31,240 unaffected infants. We trained a random forest to classify drugs of unknown pregnancy class into harmful or safe categories, focusing on two distinct outcomes: fetal loss and congenital anomalies. Our models achieved an out-of-bag accuracy of 91% for fetal loss and 87% for congenital anomalies outperforming null models. Fifty-seven ‘category C’ medications were classified as harmful for fetal loss and eleven for congenital anomalies. This includes medications with documented harmful effects, including naproxen, ibuprofen and rubella live vaccine. We also identified several novel drugs, e.g., haloperidol, that increased the risk of fetal loss. Our approach provides important information on the harmfulness of ‘category C’ drugs. This is needed, as no FDA recommendation exists for these drugs’ fetal safety.

Highlights

  • Over the years the number of medications taken by pregnant women has grown

  • We extracted females with live-born births at Columbia University Medical Center (CUMC) - New York Presbyterian Hospital (NYPH) or CUMC-NYPH where data on maternal drug exposure was captured in the Electronic Health Record (EHR) system

  • This means that the female had at least one prescription recorded in the EHR within a 1.3-year period prior to the child’s birthdate

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Summary

Introduction

Over the years the number of medications taken by pregnant women has grown. Concern over this ‘epidemic of prescribing’ among pregnant women began in the 1970 s4. An estimated 37.8% of pregnant women on medications received at least one FDA category C drug[7] without having clear guidance over the potential fetal risks these medications incur. An EHR system containing linked maternal and fetal information would be the ideal dataset for an algorithm that classifies FDA category C (i.e., drugs with unknown fetal effect) into harmful and safe bins. This study aims to systematically investigate fetal outcomes, both fetal loss and congenital anomalies, following pharmacological exposure to category C drugs. This will provide both pharmacologists and physicians with a much-needed initial classification of these ‘unknown fetal effect’ drugs. Because fetal loss and congenital anomalies are two distinct outcomes, we perform two separate retrospective cohort studies

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