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Second-generation antipsychotics and pregnancy complications.
Ellfolk, Maria; Leinonen, Maarit K; Gissler, Mika; Lahesmaa-Korpinen, Anna-Maria; Saastamoinen, Leena; Nurminen, Marja-Leena; Malm, Heli.
Afiliação
  • Ellfolk M; Teratology Information, Department of Emergency Medicine Services, Helsinki University and Helsinki University Hospital, Tukholmankatu 17, 00029, Helsinki, Finland.
  • Leinonen MK; Information Services Department, Unit of Statistics and Registers, National Institute for Health and Welfare, PL 30, 00271, Helsinki, Finland.
  • Gissler M; Information Services Department, Unit of Statistics and Registers, National Institute for Health and Welfare, PL 30, 00271, Helsinki, Finland.
  • Lahesmaa-Korpinen AM; Research Centre for Child Psychiatry, University of Turku, Itäinen Pitkäkatu 1, 20520, Turku, Finland.
  • Saastamoinen L; Department of Neurobiology, Care Sciences and Society, Karolinska Institute, SE-141 83, Huddinge, Sweden.
  • Nurminen ML; Hospital & Health Care, Terveystalo, Jaakonkatu 3 B, 00100, Helsinki, Finland.
  • Malm H; Research Unit, The Social Insurance Institution, Nordenskiöldinkatu 12, 00250, Helsinki, Finland.
Eur J Clin Pharmacol ; 76(1): 107-115, 2020 Jan.
Article em En | MEDLINE | ID: mdl-31680189
PURPOSE: To study if second-generation antipsychotic (S-GA) use during pregnancy is associated with an increased risk of pregnancy and neonatal complications. METHODS: A population-based birth cohort study using national register data extracted from the "Drugs and Pregnancy" database in Finland, years 1996-2016. The sampling frame included 1,181,090 pregnant women and their singleton births. Women were categorized into three groups: exposed to S-GAs during pregnancy (n = 4225), exposed to first-generation antipsychotics (F-GAs) during pregnancy (n = 1576), and unexposed (no purchases of S-GAs or F-GAs during pregnancy, n = 21,125). Pregnancy outcomes in S-GA users were compared with those in the two comparison groups using multiple logistic regression models. RESULTS: Comparing S-GA users with unexposed ones, the risk was increased for gestational diabetes (adjusted odds ratio, OR 1.43; 95% CI 1.25-1.65), cesarean section (OR 1.35; 95% CI 1.18-1.53), being born large for gestational age (LGA) (OR 1.57; 95% CI 1.14-2.16), and preterm birth (OR 1.29; 95% CI 1.03-1.62). The risk for these outcomes increased further with continuous S-GA use. Infants in the S-GA group were also more likely to suffer from neonatal complications. Comparing S-GA users with the F-GA group, the risk of cesarean section and LGA was higher (OR 1.25, 95% CI 1.03-1.51; and OR 1.89, 95% CI 1.20-2.99, respectively). Neonatal complications did not differ between the S-GA and F-GA groups. CONCLUSIONS: Prenatal exposure to S-GAs is associated with an increased risk of pregnancy complications related to impaired glucose metabolism. Neonatal problems are common and occur similarly in S-GA and F-GA users.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Complicações na Gravidez / Antipsicóticos Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Newborn / Pregnancy País/Região como assunto: Europa Idioma: En Revista: Eur J Clin Pharmacol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Finlândia

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Complicações na Gravidez / Antipsicóticos Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Newborn / Pregnancy País/Região como assunto: Europa Idioma: En Revista: Eur J Clin Pharmacol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Finlândia