Major Congenital Malformations after First-Trimester Exposure to ACE Inhibitors
William O. Cooper, M.D., M.P.H., Sonia Hernandez-Diaz, M.D., Dr.P.H., Patrick G. Arbogast, Ph.D., Judith A. Dudley, B.S., Shannon Dyer, B.S., Patricia S. Gideon, R.N., Kathi Hall, B.S., and Wayne A. Ray, Ph.D.
Background Use of angiotensin-convertingenzyme (ACE)inhibitors during the second and third trimesters of pregnancyis contraindicated because of their association with an increasedrisk of fetopathy. In contrast, first-trimester use of ACE inhibitorshas not been linked to adverse fetal outcomes. We conducteda study to assess the association between exposure to ACE inhibitorsduring the first trimester of pregnancy only and the risk ofcongenital malformations.
Methods We studied a cohort of 29,507 infants enrolled in TennesseeMedicaid and born between 1985 and 2000 for whom there was noevidence of maternal diabetes. We identified 209 infants withexposure to ACE inhibitors in the first trimester alone, 202infants with exposure to other antihypertensive medicationsin the first trimester alone, and 29,096 infants with no exposureto antihypertensive drugs at any time during gestation. Majorcongenital malformations were identified from linked vital recordsand hospitalization claims during the first year of life andconfirmed by review of medical records.
Results Infants with only first-trimester exposure to ACE inhibitorshad an increased risk of major congenital malformations (riskratio, 2.71; 95 percent confidence interval, 1.72 to 4.27) ascompared with infants who had no exposure to antihypertensivemedications. In contrast, fetal exposure to other antihypertensivemedications during only the first trimester did not confer anincreased risk (risk ratio, 0.66; 95 percent confidence interval,0.25 to 1.75). Infants exposed to ACE inhibitors were at increasedrisk for malformations of the cardiovascular system (risk ratio,3.72; 95 percent confidence interval, 1.89 to 7.30) and thecentral nervous system (risk ratio, 4.39; 95 percent confidenceinterval, 1.37 to 14.02).
Conclusions Exposure to ACE inhibitors during the first trimestercannot be considered safe and should be avoided.
Source Information
From the Departments of Pediatrics (W.O.C., S.D.), Biostatistics (P.G.A.), and Preventive Medicine (J.A.D., P.S.G., K.H., W.A.R.), Vanderbilt University School of Medicine, Nashville; and the Slone Epidemiology Center, Boston University, Boston (S.H.-D.).
Address reprint requests to Dr. Cooper at the Department of Pediatrics, Vanderbilt University School of Medicine, AA-0216 MCN, Nashville, TN 37232, or at william.cooper{at}vanderbilt.edu.
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