TY - JOUR
T1 - Association between methylphenidate and amphetamine use in pregnancy and risk of congenital malformations
T2 - A cohort study from the international pregnancy safety study consortium
AU - Huybrechts, Krista F.
AU - Bröms, Gabriella
AU - Christensen, Lotte Brix
AU - Einarsdóttir, Kristjana
AU - Engeland, Anders
AU - Furu, Kari
AU - Gissler, Mika
AU - Hernandez-Diaz, Sonia
AU - Karlsson, Pär
AU - Karlstad, Øystein
AU - Kieler, Helle
AU - Lahesmaa-Korpinen, Anna Maria
AU - Mogun, Helen
AU - Nørgaard, Mette
AU - Reutfors, Johan
AU - Sørensen, Henrik Toft
AU - Zoega, Helga
AU - Bateman, Brian T.
N1 - Publisher Copyright:
© 2018 American Medical Association. All rights reserved.
PY - 2018/2
Y1 - 2018/2
N2 - Importance: Given the rapidly increasing use of stimulant medications during pregnancy and among women of reproductive age who may become pregnant inadvertently, there is a need to better understand their safety. Objective: To examine the risk of congenital malformations associated with intrauterine exposure to stimulants. Design, Setting, and Participants: Cohort study of the Medicaid-insured population in the United States nested in the 2000-2013 US Medicaid Analytic eXtract, with follow-up of safety signals detected in the Medicaid Analytic eXtract data using the Nordic Health registries (2003-2013) (Denmark, Finland, Iceland, Norway, and Sweden). A total of 1 813 894 publicly insured pregnancies in the United States and 2 560 069 singleton pregnancies in the 5 Nordic countries ending in live births were included. Relative risks were estimated accounting for underlying psychiatric disorders and other potential confounders. Relative risk estimates for the US and Nordic data were pooled using a fixed-effects meta-analytic approach. The study was conducted from July 1, 2015, to March 31, 2017. Exposures: Methylphenidate and amphetamines dispensed during the first trimester. Main Outcomes and Measures: Major congenital malformations and subgroup of cardiac malformations. Results: In the US data, of the 1 813 894 pregnancies evaluated, 35.0per 1000 infants not exposed to stimulantswere diagnosed as having congenital malformations, compared with 45.9 per 1000 infants formethylphenidate and 45.4 for amphetamines. For cardiac malformations, the riskswere 12.7 (95%CI, 12.6-12.9), 18.8 (95%CI, 13.8-25.6), and 15.4 (95%CI, 12.5-19.0) per 1000 infants, respectively. The adjusted relative risks formethylphenidatewere 1.11 (95%CI, 0.91-1.35) for any malformation and 1.28 (95%CI,0.94-1.74) for cardiac malformations. No increased riskswere observed for amphetamines: 1.05 (95%CI,0.93-1.19) for any malformations and 0.96 (95%CI,0.78-1.19) for cardiac malformations. Findingswere confirmed in sensitivity analyses accounting for proxies of unmeasured confounders and increasing the specificity of the exposure and outcome definitions. Replication of the analyses formethylphenidate using the Nordic data including 2 560069 pregnancies yielded a relative risk of 1.28 (95%CI,0.83-1.97) for cardiac malformations, resulting in a pooled estimate of 1.28 (95%CI, 1.00-1.64). Conclusions and Relevance: These findings suggest a small increase in the risk of cardiac malformations associated with intrauterine exposure to methylphenidate but not to amphetamines. This information is important when weighing the risks and benefits of alternative treatment strategies for attention-deficit/hyperactivity disorder in women of reproductive age and during early pregnancy.
AB - Importance: Given the rapidly increasing use of stimulant medications during pregnancy and among women of reproductive age who may become pregnant inadvertently, there is a need to better understand their safety. Objective: To examine the risk of congenital malformations associated with intrauterine exposure to stimulants. Design, Setting, and Participants: Cohort study of the Medicaid-insured population in the United States nested in the 2000-2013 US Medicaid Analytic eXtract, with follow-up of safety signals detected in the Medicaid Analytic eXtract data using the Nordic Health registries (2003-2013) (Denmark, Finland, Iceland, Norway, and Sweden). A total of 1 813 894 publicly insured pregnancies in the United States and 2 560 069 singleton pregnancies in the 5 Nordic countries ending in live births were included. Relative risks were estimated accounting for underlying psychiatric disorders and other potential confounders. Relative risk estimates for the US and Nordic data were pooled using a fixed-effects meta-analytic approach. The study was conducted from July 1, 2015, to March 31, 2017. Exposures: Methylphenidate and amphetamines dispensed during the first trimester. Main Outcomes and Measures: Major congenital malformations and subgroup of cardiac malformations. Results: In the US data, of the 1 813 894 pregnancies evaluated, 35.0per 1000 infants not exposed to stimulantswere diagnosed as having congenital malformations, compared with 45.9 per 1000 infants formethylphenidate and 45.4 for amphetamines. For cardiac malformations, the riskswere 12.7 (95%CI, 12.6-12.9), 18.8 (95%CI, 13.8-25.6), and 15.4 (95%CI, 12.5-19.0) per 1000 infants, respectively. The adjusted relative risks formethylphenidatewere 1.11 (95%CI, 0.91-1.35) for any malformation and 1.28 (95%CI,0.94-1.74) for cardiac malformations. No increased riskswere observed for amphetamines: 1.05 (95%CI,0.93-1.19) for any malformations and 0.96 (95%CI,0.78-1.19) for cardiac malformations. Findingswere confirmed in sensitivity analyses accounting for proxies of unmeasured confounders and increasing the specificity of the exposure and outcome definitions. Replication of the analyses formethylphenidate using the Nordic data including 2 560069 pregnancies yielded a relative risk of 1.28 (95%CI,0.83-1.97) for cardiac malformations, resulting in a pooled estimate of 1.28 (95%CI, 1.00-1.64). Conclusions and Relevance: These findings suggest a small increase in the risk of cardiac malformations associated with intrauterine exposure to methylphenidate but not to amphetamines. This information is important when weighing the risks and benefits of alternative treatment strategies for attention-deficit/hyperactivity disorder in women of reproductive age and during early pregnancy.
UR - http://www.scopus.com/inward/record.url?scp=85041123981&partnerID=8YFLogxK
U2 - 10.1001/jamapsychiatry.2017.3644
DO - 10.1001/jamapsychiatry.2017.3644
M3 - Article
C2 - 29238795
AN - SCOPUS:85041123981
SN - 2168-622X
VL - 75
SP - 167
EP - 175
JO - JAMA Psychiatry
JF - JAMA Psychiatry
IS - 2
ER -