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A population-based study of concurrent prescriptions of opioid analgesic and selective serotonin reuptake inhibitor medications during pregnancy and risk for adverse birth outcomes
Department of Psychological & Brain Sciences, Indiana University-Bloomington, Bloomington, IN, USA.
Department of Psychological & Brain Sciences, Indiana University-Bloomington, Bloomington, IN, USA.
Department of Applied Health Science, School of Public Health, Indiana University-Bloomington, Bloomington, IN, USA.
Department of Epidemiology and Biostatistics, School of Public Health, Indiana University-Bloomington, Bloomington, IN, USA.
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2021 (engelsk)Inngår i: Paediatric and Perinatal Epidemiology, ISSN 0269-5022, E-ISSN 1365-3016, Vol. 35, nr 2, s. 184-193Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

BACKGROUND: Pregnant women with painful conditions often have mental health problems, including depression and anxiety. Co-morbid conditions may cause pregnant women to use multiple medications, although safety of such practice is poorly understood.

OBJECTIVES: We investigated the influence of combined prescriptions of opioid analgesics and selective serotonin reuptake inhibitors (SSRIs) during pregnancy on two adverse birth outcomes.

METHODS: We analysed Swedish population-based births (n = 688 914) between 2007 and 2013. Using national registers, we obtained data on filled medication prescriptions, birth outcomes, and a wide range of parental characteristics. We estimated preterm birth and small-for-gestational-age risk following independent or combined prescriptions of the two medications compared with no filled prescriptions for either medication. We adjusted for confounders using inverse probability of treatment weights.

RESULTS: After adjusting for confounders, preterm birth risk was higher among women with opioid analgesic prescriptions only (5.9%; risk ratio [RR] 1.27, 95% confidence interval [CI] 1.22, 1.33), SSRIs only (6.2%; RR 1.34, 95% CI 1.27, 1.42), and both medications (7.8%; RR 1.70, 95% CI 1.47, 1.96) compared with unexposed women (4.6%). The interaction between the medications on preterm birth was small (risk difference [RD] 0.4%, 95% CI -0.8%, 1.6%); relative excess risk due to interaction [RERI] 0.09, 95% CI -0.17, 0.34; RR 1.00, 95% CI 0.85, 1.17). For small for gestational age, risk was approximately 2% across all groups, and there was no interaction between the medications (RD 0.3%, 95% CI -0.4%, 1.1%); RERI 0.15, 95% CI -0.16, 0.47; RR 1.15, 95% CI 0.87, 1.52).

CONCLUSIONS: Compared with unexposed pregnancies, those with either medication alone had a small increased risk for preterm birth but no increased risk for small for gestational age. The magnitude of associations with combined exposure to both medications were not greater than the sum of the associations with each medication considered individually.

sted, utgiver, år, opplag, sider
Blackwell Science Ltd. , 2021. Vol. 35, nr 2, s. 184-193
Emneord [en]
Antidepressant drugs, opioid analgesic, polypharmacy, prenatal care, preterm birth, small-for-gestational-age infant
HSV kategori
Identifikatorer
URN: urn:nbn:se:oru:diva-88425DOI: 10.1111/ppe.12721ISI: 000600684400001PubMedID: 33350491Scopus ID: 2-s2.0-85097866155OAI: oai:DiVA.org:oru-88425DiVA, id: diva2:1516400
Forskningsfinansiär
Swedish Research Council, 2014-38313831 2018-02679Forte, Swedish Research Council for Health, Working Life and Welfare, 50623213
Merknad

Funding Agencies:

National Science Foundation (NSF)1342962

United States Department of Health & Human Services

National Institutes of Health (NIH) - USA

NIH National Institute on Drug Abuse (NIDA) R00DA040727 R01DA048042

Swedish Initiative for Research on Microdata in the Social and Medical Sciences 340-20135867

Tilgjengelig fra: 2021-01-12 Laget: 2021-01-12 Sist oppdatert: 2025-02-11bibliografisk kontrollert

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