Use of antiseizure medications during pregnancy and adverse neonatal outcomes

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dc.contributor.authorLavu, Alekhya
dc.contributor.examiningcommitteeFalk, Jamison (Pharmacy)
dc.contributor.examiningcommitteeChelsea, Ruth (Pediatrics and Child Health)
dc.contributor.examiningcommitteeDe-Vera, Mary (University of British Columbia)
dc.contributor.supervisorEltonsy, Sherif
dc.contributor.supervisorAlessi-Severini, Silvia
dc.date.accessioned2024-04-24T13:38:37Z
dc.date.available2024-04-24T13:38:37Z
dc.date.issued2024-04-22
dc.date.submitted2024-04-22T17:55:14Zen_US
dc.degree.disciplinePharmacy
dc.degree.levelDoctor of Philosophy (Ph.D.)
dc.description.abstractBackground: Epilepsy during pregnancy can lead to various adverse health outcomes in both pregnant people and infants. Furthermore, in-utero exposure to antiseizure medications (ASMs), employed in the management of epilepsy, is also associated with an increased risk of adverse birth outcomes. With the exponential increase in the use of ASMs over the last few decades, it is crucial to understand the safety of in-utero exposure to ASMs. In this thesis we aimed to evaluate the safety of ASMs in all pregnant people, pregnant people with epilepsy (PPWE) and pregnant people without epilepsy (PPWOE), using both evidence synthesis methods and real-world data. Methods: First, we conducted a systematic review and meta-analysis to evaluate the risk of adverse birth weight outcomes due to in-utero exposure to ASMs in the published literature from inception to March 23rd, 2022. (Chapter 2: Protocol & Chapter 3: Report). Second, we conducted two population-based cohort studies utilizing the administrative databases in Manitoba to study the safety of in-utero exposure to ASMs and gabapentin in pregnancy. We included all pregnant people in Manitoba between 1998-2021. In study 1 (Chapter 4: ASMs) we evaluated the ASMs safety and in study 2 (Chapter 5: gabapentin) we evaluated gabapentin safety among all pregnant people, PPWE and PPWOE. Results: In the systematic review, we found a significant association between in-utero exposure to all ASMs in pregnant people and small for gestational age (SGA), with relative risk (RR) 1.33 (95% CI 1.18 to 1.50, I2 74%), low birth weight (LBW) RR 1.54 (95% CI 1.33 to 1.77, I2 67%), and decreased birth weight with a mean difference (MD) of -118.87 (95% CI -161.03 to -76.71, I2 42%) g compared to unexposed pregnant people. We found similar results among PPWE when compared to unexposed pregnant people, but they did not reach statistical significance. In our cohort study, among all pregnant people exposed to ASMs we found a significant increased risk of SGA (adjusted odds ratio [aOR] 1.16, 95% CI 1.04-1.30), LBW (aOR 1.66, 95% CI 1.47-1.88), preterm birth (aOR 1.56, 95% CI 1.41-1.73), neonatal intensive care unit (NICU) admissions (aOR 1.91, 95% CI 1.74-2.10), and length of hospital stay (LOS) infant (aOR 1.68, 95% CI 1.56-1.82) when compared with unexposed pregnant people. We found similar results among PPWOE when compared with unexposed PPWOE. For gabapentin exposure, among all pregnant people we found a significant increased risk of LBW (aOR 1.95, 95% CI 1.58-2.41), preterm birth (aOR 1.68, 95% CI 1.39-2.03), NICU admissions (aOR 2.04, 95% CI 1.71-2.42), pregnant peoples LOS (aOR 1.33, 95% CI 1.15-1.54), infant LOS (aOR 2.09, 95% CI 1.81-2.41) compared to unexposed pregnant people. We found similar results among exposed PPWOE when compared with unexposed PPWOE. Conclusions: Both the choice of ASM use and the underlying condition (epilepsy) contribute to an elevated adverse risk during pregnancy. With the increased risk of adverse neonatal outcomes associated with in-utero exposure to ASMs, including gabapentin, clinicians should carefully assess the risk-benefit ratio before prescribing these medications. Moreover, the use of gabapentin requires caution among pregnant people.
dc.description.noteOctober 2024
dc.description.sponsorshipHealth Sciences Centre Foundation :
dc.identifier.urihttp://hdl.handle.net/1993/38181
dc.language.isoeng
dc.rightsopen accessen_US
dc.subjectFetal safety
dc.subjectPharmacoepidemiology
dc.subjectEvidence generation
dc.subjectEvidence synthesis
dc.subjectMedications in pregnancy
dc.subjectAntiseizure medications
dc.subjectEpilepsy
dc.subjectSeizures
dc.subjectGabapentin
dc.subjectPregnancy safety
dc.subjectPharmacoepidemiology
dc.subjectNeurology
dc.titleUse of antiseizure medications during pregnancy and adverse neonatal outcomes
dc.typedoctoral thesisen_US
local.subject.manitobayes
oaire.awardTitleOperating grant
project.funder.nameManitoba Medical Service Foundation
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