Utilization of Topiramate During Pregnancy and Risk of Birth Defects
Methods.— Sourced from patients' pharmacy and medical claims from 2002 through 2010, this study identified infants born from mothers exposed to topiramate (n = 870) and other anti‐epileptic drugs (n = 3615) in the first trimester of pregnancy. First trimester exposure was based on prescription dispensing dates and days supplied relative to infant birth date, accounting for premature delivery. Infants born to women with migraine without epilepsy (n = 26,865), women with epilepsy (n = 2607), and women with diabetes mellitus (n = 13,062), as well as randomly sampled women (n = 99,761), were used for comparison. Topiramate use was excluded from all groups with the exception of the topiramate and random sample cohorts. Non‐anti‐epileptic drug teratogens were excluded from each cohort (except random sample). Unadjusted relative risks and 95% confidence intervals for topiramate vs each comparator were calculated. Risks >1 indicate a higher risk with topiramate vs comparator, whereas risks <1 indicate a lower risk with topiramate vs comparator.
Results.— The frequency of oral clefts was 0.23% for topiramate use, 0.17% for other anti‐epileptic drug use (topiramate vs comparator relative risk = 1.39 [95% confidence interval: 0.28‐6.85]), 0.16% for migraineurs (1.47 [0.36‐6.06]), 0.31% for epileptics (0.75 [0.16‐3.52]), 0.26% for diabetics (0.88 [0.21‐3.67]), and 0.16% for the random sample (1.44 [0.36‐5.81]). The frequency of major congenital malformations was 4.33% for topiramate use, 3.21% for other anti‐epileptic drugs (1.33 [0.92‐1.90]), 3.79% for migraineurs (1.12 [0.81‐1.55]), 4.33% for epileptics (0.98 [0.68‐1.41]), 6.58% for diabetics (0.65 [0.47‐0.89]), and 3.77% for the random sample (1.13 [0.82‐1.55]).
Conclusions.— This retrospective study quantified the association between topiramate exposure during pregnancy and the risk of oral cleft or major congenital malformations, and suggested little or no increase in risk in comparison with exposure to other anti‐epileptic drugs or to disease states, such as migraine, epilepsy, or diabetes. However, small numbers of events limit the strength of inferences.
Document Type: Research Article
Affiliations: 1: From the Mount Sinai School of Medicine, New York, NY, USA (M.W. Green); Brigham and Women's Hospital, Boston, MA, USA (J.D. Seeger); Vivus, Inc., Mountain View, CA, USA (C. Peterson); Wolters Kluwer Pharma Solutions, Yardley, PA, USA (A. Bhattacharyya). 2: From the Mount Sinai School of Medicine, New York, NY, USA (M.W. Green); Brigham and Women's Hospital, Boston, MA, USA (J.D. Seeger); Vivus, Inc., Mountain View, CA, USA (C. Peterson); Wolters Kluwer Pharma Solutions, Yardley, PA, USA (A. Bhattacharyya).
Publication date: July 1, 2012