TY - JOUR
T1 - First-trimester use of antiseizure medications and the risk of miscarriage
T2 - a population-based cohort study
AU - Forbes, Harriet
AU - Madley-Dowd, Paul
AU - Ahlqvist, Viktor
AU - Campbell, Jennifer
AU - Davies, Neil M.
AU - Liebling, Rachel
AU - Lyall, Kristen
AU - Newschaffer, Craig
AU - Rast, Jessica
AU - Tomson, Torbjörn
AU - Zhong, Caichen
AU - Magnusson, Cecilia
AU - Rai, Dheeraj
AU - Lee, Brian K.
N1 - Publisher Copyright:
© Author(s) (or their employer(s)) 2024.
PY - 2024/7/15
Y1 - 2024/7/15
N2 - Background Antiseizure medications (ASMs) during the first trimester of pregnancy have been associated with an increased risk of miscarriage. Methods We carried out a population-based cohort study using routinely collected healthcare data from the UK, 1995-2018. Pregnancies were identified in the Clinical Practice Research Datalink and we estimated the HR of miscarriage associated with prescriptions of ASMs during the first trimester of pregnancy, using Cox regression, adjusting for potential confounders, including ASM indications. Results ASMs were prescribed during the first trimester in 7832 (0.8%) of 1 023 787 included pregnancies. 14.5% of pregnancies with first-trimester exposure to ASMs ended in miscarriage, while 12.2% without ASM exposure in the first trimester ended in miscarriage; after adjustment, there was a 1.06-fold relative hazard of miscarriage (95% CI 1.00 to 1.13) in women with first-trimester ASM use. After restricting to women with specific ASM indications, this association was not evident in women with epilepsy (adjusted HR 0.98, 95% CI 0.89 to 1.08), but was observed in women with bipolar or other psychiatric conditions (1.08, 95% CI 1.00 to 1.16) although CIs overlapped. Compared with discontinuation of ASMs prior to pregnancy, there was no evidence of increased risk of miscarriage for first-trimester ASM use in women with bipolar or other psychiatric conditions (1.02, 95% CI 0.87 to 1.20). Conclusion We found no clear evidence to suggest that first-trimester ASM use increased the risk of miscarriage. Taken together, our analyses suggest that apparent associations between first-trimester ASM use and miscarriage may be the result of confounding by the presence of a bipolar disorder or associated unmeasured variables.
AB - Background Antiseizure medications (ASMs) during the first trimester of pregnancy have been associated with an increased risk of miscarriage. Methods We carried out a population-based cohort study using routinely collected healthcare data from the UK, 1995-2018. Pregnancies were identified in the Clinical Practice Research Datalink and we estimated the HR of miscarriage associated with prescriptions of ASMs during the first trimester of pregnancy, using Cox regression, adjusting for potential confounders, including ASM indications. Results ASMs were prescribed during the first trimester in 7832 (0.8%) of 1 023 787 included pregnancies. 14.5% of pregnancies with first-trimester exposure to ASMs ended in miscarriage, while 12.2% without ASM exposure in the first trimester ended in miscarriage; after adjustment, there was a 1.06-fold relative hazard of miscarriage (95% CI 1.00 to 1.13) in women with first-trimester ASM use. After restricting to women with specific ASM indications, this association was not evident in women with epilepsy (adjusted HR 0.98, 95% CI 0.89 to 1.08), but was observed in women with bipolar or other psychiatric conditions (1.08, 95% CI 1.00 to 1.16) although CIs overlapped. Compared with discontinuation of ASMs prior to pregnancy, there was no evidence of increased risk of miscarriage for first-trimester ASM use in women with bipolar or other psychiatric conditions (1.02, 95% CI 0.87 to 1.20). Conclusion We found no clear evidence to suggest that first-trimester ASM use increased the risk of miscarriage. Taken together, our analyses suggest that apparent associations between first-trimester ASM use and miscarriage may be the result of confounding by the presence of a bipolar disorder or associated unmeasured variables.
UR - https://www.scopus.com/pages/publications/85199125588
UR - https://www.scopus.com/pages/publications/85199125588#tab=citedBy
U2 - 10.1136/jnnp-2023-333149
DO - 10.1136/jnnp-2023-333149
M3 - Article
C2 - 38777577
AN - SCOPUS:85199125588
SN - 0022-3050
VL - 95
SP - 693
EP - 703
JO - Journal of Neurology, Neurosurgery and Psychiatry
JF - Journal of Neurology, Neurosurgery and Psychiatry
IS - 8
ER -