Methylphenidate in Pregnancy
Autor: | Irena Nulman, Rebecka Wajnberg, Judy Arnon, Svetlana Shechtman, Pina Bozzo, Jonathan Luke Richardson, Evelin Beck, Asher Ornoy, Orna Diav-Citrin, Cornelia Borisch |
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Rok vydání: | 2016 |
Předmět: |
Risk
Pediatrics medicine.medical_specialty Cardiovascular Abnormalities Abortion Miscarriage 03 medical and health sciences 0302 clinical medicine Pregnancy medicine Humans 030219 obstetrics & reproductive medicine Methylphenidate business.industry Proportional hazards model Hazard ratio Abnormalities Drug-Induced Gestational age Abortion Induced medicine.disease Teratology Abortion Spontaneous Pregnancy Complications Psychiatry and Mental health Central Nervous System Stimulants Female business 030217 neurology & neurosurgery Follow-Up Studies medicine.drug |
Zdroj: | The Journal of Clinical Psychiatry. 77:1176-1181 |
ISSN: | 0160-6689 |
Popis: | INTRODUCTION Methylphenidate is a central nervous system stimulant medicinally used in the treatment of attention-deficit disorder with or without hyperactivity (ADD/ADHD). Data on its use in human pregnancy are limited. The primary objective of the study was to evaluate the risk of major congenital anomalies after pregnancy exposure to methylphenidate for medical indications. METHODS In a prospective, comparative, multicenter observational study performed in 4 participating Teratology Information Services (in Jerusalem, Berlin, Newcastle upon Tyne, and Toronto) between 1996 and 2013, methylphenidate-exposed pregnancies were compared with pregnancies counseled for nonteratogenic exposure (NTE) after matching by maternal age, gestational age, and year at initial contact. RESULTS 382 methylphenidate-exposed pregnancies (89.5% in the first trimester) were followed up. The overall rate of major congenital anomalies was similar between the groups (10/309 = 3.2% [methylphenidate] vs 13/358 = 3.6% [NTE], P = .780). The rates of major congenital anomalies (6/247 = 2.4% [methylphenidate] vs 12/358 = 3.4% [NTE], P = .511) and cardiovascular anomalies (2/247 = 0.8% [methylphenidate] vs 3/358 = 0.8% [NTE], P = .970) were also similar after exclusion of genetic or cytogenetic anomalies and limiting methylphenidate exposure to the period of organogenesis (weeks 4-13 after the last menstrual period). There was a higher rate of miscarriages and elective terminations of pregnancy in the methylphenidate group. Significant predictors for the miscarriages using Cox proportional hazards model were methylphenidate exposure (adjusted hazard ratio [HR] = 1.98; 95% CI, 1.23-3.20; P = .005) and past miscarriage (adjusted HR = 1.35; 95% CI, 1.18-1.55; P < .001). CONCLUSIONS The present study suggests that methylphenidate does not seem to increase the risk for major malformations. Further studies are required to establish its pregnancy safety and its possible association with miscarriages. |
Databáze: | OpenAIRE |
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