The impact of epilepsy and antiseizure medications on pregnancy and neonatal outcomes: A nationwide cohort study

Abstract Purpose Our objective was to assess the adverse outcomes during pregnancy, as well as for the fetus and neonates, in women with epilepsy, both with and without the use of antiseizure medications (ASMs). Methods A cohort of singleton pregnancies between January 1, 2004 and December 31, 2014...

Full description

Bibliographic Details
Main Authors: Cheng‐Yen Kuo, Chang‐Fu Kuo, Lai‐Chu See, Meng‐Jiung Chiou, Po‐Cheng Hung, Jainn‐Jim Lin, Kuang‐Lin Lin, Huei‐Shyong Wang, I‐Jun Chou
Format: Article
Language:English
Published: Wiley 2023-12-01
Series:Brain and Behavior
Subjects:
Online Access:https://doi.org/10.1002/brb3.3287
_version_ 1827366567736770560
author Cheng‐Yen Kuo
Chang‐Fu Kuo
Lai‐Chu See
Meng‐Jiung Chiou
Po‐Cheng Hung
Jainn‐Jim Lin
Kuang‐Lin Lin
Huei‐Shyong Wang
I‐Jun Chou
author_facet Cheng‐Yen Kuo
Chang‐Fu Kuo
Lai‐Chu See
Meng‐Jiung Chiou
Po‐Cheng Hung
Jainn‐Jim Lin
Kuang‐Lin Lin
Huei‐Shyong Wang
I‐Jun Chou
author_sort Cheng‐Yen Kuo
collection DOAJ
description Abstract Purpose Our objective was to assess the adverse outcomes during pregnancy, as well as for the fetus and neonates, in women with epilepsy, both with and without the use of antiseizure medications (ASMs). Methods A cohort of singleton pregnancies between January 1, 2004 and December 31, 2014 was identified using the Taiwan National Health Database. The pregnancies were categorized into ASM exposure, ASM nonexposure, and control (consisting of women without an epilepsy diagnosis) groups. We recorded adverse outcomes in neonates and documented pregnancy complications. The generalized estimating equation with logit link was used to estimate adjusted odds ratios. Results There were 629 singleton pregnancies in the group exposed to ASMs, 771 in the epilepsy group without ASM exposure, and 2,004,479 in the control group. Women with epilepsy had a significantly higher risk of puerperal cerebrovascular diseases (adjusted odds ratios in the exposure and nonexposure groups = 54.46 and 20.37, respectively), respiratory distress syndrome (5.1 and 2.99), mortality (3.15 and 3.22), sepsis (2.67 and 2.54), pregnancy‐related hypertension (1.71 and 1.8), preeclampsia (1.87 and 1.79), cesarean delivery (1.72 and 2.15), and preterm labor (1.38 and 1.56). The use of ASMs may increase the risk of eclampsia (adjusted odds ratio = 12.27). Compared to controls, fetuses/neonates born to women with epilepsy had a higher risk of unexplained stillbirth (adjusted odds ratios in the exposure and nonexposure groups = 2.51 and 2.37, respectively), congenital anomaly (1.37 and 1.33), central nervous system malformation (3.57 and 2.25), low birth weight (1.90 and 1.97), and a low Apgar score at 5 min (2.63 and 1.3). The use of ASMs may introduce an additional risk of small for gestational age; the adjusted odds ratio was 1.51. Conclusion Women with epilepsy, irrespective of their exposure to ASMs, had a slightly elevated risk of pregnancy and perinatal complications. Puerperal cerebrovascular diseases may be a hidden risk for women with epilepsy.
first_indexed 2024-03-08T08:53:25Z
format Article
id doaj.art-72f7da08bc8d44e0b534ca1438581d1c
institution Directory Open Access Journal
issn 2162-3279
language English
last_indexed 2024-03-08T08:53:25Z
publishDate 2023-12-01
publisher Wiley
record_format Article
series Brain and Behavior
spelling doaj.art-72f7da08bc8d44e0b534ca1438581d1c2024-02-01T07:45:36ZengWileyBrain and Behavior2162-32792023-12-011312n/an/a10.1002/brb3.3287The impact of epilepsy and antiseizure medications on pregnancy and neonatal outcomes: A nationwide cohort studyCheng‐Yen Kuo0Chang‐Fu Kuo1Lai‐Chu See2Meng‐Jiung Chiou3Po‐Cheng Hung4Jainn‐Jim Lin5Kuang‐Lin Lin6Huei‐Shyong Wang7I‐Jun Chou8Division of Pediatric Neurology Chang Gung Memorial Hospital Taoyuan TaiwanDivision of Rheumatology, Allergy and Immunology Chang Gung Memorial Hospital Taoyuan TaiwanDivision of Rheumatology, Allergy and Immunology Chang Gung Memorial Hospital Taoyuan TaiwanCenter for Artificial Intelligence in Medicine Chang Gung Memorial Hospital Taoyuan TaiwanDivision of Pediatric Neurology Chang Gung Memorial Hospital Taoyuan TaiwanDivision of Pediatric Neurology Chang Gung Memorial Hospital Taoyuan TaiwanDivision of Pediatric Neurology Chang Gung Memorial Hospital Taoyuan TaiwanDivision of Pediatric Neurology Chang Gung Memorial Hospital Taoyuan TaiwanDivision of Pediatric Neurology Chang Gung Memorial Hospital Taoyuan TaiwanAbstract Purpose Our objective was to assess the adverse outcomes during pregnancy, as well as for the fetus and neonates, in women with epilepsy, both with and without the use of antiseizure medications (ASMs). Methods A cohort of singleton pregnancies between January 1, 2004 and December 31, 2014 was identified using the Taiwan National Health Database. The pregnancies were categorized into ASM exposure, ASM nonexposure, and control (consisting of women without an epilepsy diagnosis) groups. We recorded adverse outcomes in neonates and documented pregnancy complications. The generalized estimating equation with logit link was used to estimate adjusted odds ratios. Results There were 629 singleton pregnancies in the group exposed to ASMs, 771 in the epilepsy group without ASM exposure, and 2,004,479 in the control group. Women with epilepsy had a significantly higher risk of puerperal cerebrovascular diseases (adjusted odds ratios in the exposure and nonexposure groups = 54.46 and 20.37, respectively), respiratory distress syndrome (5.1 and 2.99), mortality (3.15 and 3.22), sepsis (2.67 and 2.54), pregnancy‐related hypertension (1.71 and 1.8), preeclampsia (1.87 and 1.79), cesarean delivery (1.72 and 2.15), and preterm labor (1.38 and 1.56). The use of ASMs may increase the risk of eclampsia (adjusted odds ratio = 12.27). Compared to controls, fetuses/neonates born to women with epilepsy had a higher risk of unexplained stillbirth (adjusted odds ratios in the exposure and nonexposure groups = 2.51 and 2.37, respectively), congenital anomaly (1.37 and 1.33), central nervous system malformation (3.57 and 2.25), low birth weight (1.90 and 1.97), and a low Apgar score at 5 min (2.63 and 1.3). The use of ASMs may introduce an additional risk of small for gestational age; the adjusted odds ratio was 1.51. Conclusion Women with epilepsy, irrespective of their exposure to ASMs, had a slightly elevated risk of pregnancy and perinatal complications. Puerperal cerebrovascular diseases may be a hidden risk for women with epilepsy.https://doi.org/10.1002/brb3.3287antiseizure medications (ASMs)epilepsyoutcomepregnancywomen with epilepsy
spellingShingle Cheng‐Yen Kuo
Chang‐Fu Kuo
Lai‐Chu See
Meng‐Jiung Chiou
Po‐Cheng Hung
Jainn‐Jim Lin
Kuang‐Lin Lin
Huei‐Shyong Wang
I‐Jun Chou
The impact of epilepsy and antiseizure medications on pregnancy and neonatal outcomes: A nationwide cohort study
Brain and Behavior
antiseizure medications (ASMs)
epilepsy
outcome
pregnancy
women with epilepsy
title The impact of epilepsy and antiseizure medications on pregnancy and neonatal outcomes: A nationwide cohort study
title_full The impact of epilepsy and antiseizure medications on pregnancy and neonatal outcomes: A nationwide cohort study
title_fullStr The impact of epilepsy and antiseizure medications on pregnancy and neonatal outcomes: A nationwide cohort study
title_full_unstemmed The impact of epilepsy and antiseizure medications on pregnancy and neonatal outcomes: A nationwide cohort study
title_short The impact of epilepsy and antiseizure medications on pregnancy and neonatal outcomes: A nationwide cohort study
title_sort impact of epilepsy and antiseizure medications on pregnancy and neonatal outcomes a nationwide cohort study
topic antiseizure medications (ASMs)
epilepsy
outcome
pregnancy
women with epilepsy
url https://doi.org/10.1002/brb3.3287
work_keys_str_mv AT chengyenkuo theimpactofepilepsyandantiseizuremedicationsonpregnancyandneonataloutcomesanationwidecohortstudy
AT changfukuo theimpactofepilepsyandantiseizuremedicationsonpregnancyandneonataloutcomesanationwidecohortstudy
AT laichusee theimpactofepilepsyandantiseizuremedicationsonpregnancyandneonataloutcomesanationwidecohortstudy
AT mengjiungchiou theimpactofepilepsyandantiseizuremedicationsonpregnancyandneonataloutcomesanationwidecohortstudy
AT pochenghung theimpactofepilepsyandantiseizuremedicationsonpregnancyandneonataloutcomesanationwidecohortstudy
AT jainnjimlin theimpactofepilepsyandantiseizuremedicationsonpregnancyandneonataloutcomesanationwidecohortstudy
AT kuanglinlin theimpactofepilepsyandantiseizuremedicationsonpregnancyandneonataloutcomesanationwidecohortstudy
AT hueishyongwang theimpactofepilepsyandantiseizuremedicationsonpregnancyandneonataloutcomesanationwidecohortstudy
AT ijunchou theimpactofepilepsyandantiseizuremedicationsonpregnancyandneonataloutcomesanationwidecohortstudy
AT chengyenkuo impactofepilepsyandantiseizuremedicationsonpregnancyandneonataloutcomesanationwidecohortstudy
AT changfukuo impactofepilepsyandantiseizuremedicationsonpregnancyandneonataloutcomesanationwidecohortstudy
AT laichusee impactofepilepsyandantiseizuremedicationsonpregnancyandneonataloutcomesanationwidecohortstudy
AT mengjiungchiou impactofepilepsyandantiseizuremedicationsonpregnancyandneonataloutcomesanationwidecohortstudy
AT pochenghung impactofepilepsyandantiseizuremedicationsonpregnancyandneonataloutcomesanationwidecohortstudy
AT jainnjimlin impactofepilepsyandantiseizuremedicationsonpregnancyandneonataloutcomesanationwidecohortstudy
AT kuanglinlin impactofepilepsyandantiseizuremedicationsonpregnancyandneonataloutcomesanationwidecohortstudy
AT hueishyongwang impactofepilepsyandantiseizuremedicationsonpregnancyandneonataloutcomesanationwidecohortstudy
AT ijunchou impactofepilepsyandantiseizuremedicationsonpregnancyandneonataloutcomesanationwidecohortstudy