Safety of prenatal opioid analgesics: Do results differ between public health insurance beneficiary and population‐based cohorts?

Author:

Brogly Susan B.12,Bowie Alexa C.3,Li Wenbin2,Camden Andi245,Velez Maria P.26,Guttmann Astrid245,Werler Martha M.7

Affiliation:

1. Department of Surgery Queen's University Kingston Canada

2. ICES Toronto Canada

3. Department of Public Health Sciences Queen's University Kingston Canada

4. Dalla Lana School of Public Health University of Toronto Toronto Canada

5. The Hospital for Sick Children Toronto Canada

6. Department of Obstetrics and Gynaecology Queen's University Kingston Canada

7. Department of Epidemiology Boston University School of Public Health Boston Massachusetts USA

Abstract

AbstractBackgroundPregnant patients with particular types of health insurance may have distinct demographic and medical characteristics that have a biologic effect on associations between opioid analgesics and congenital anomalies (CA).MethodsWe followed 199,884 pregnant prescription beneficiaries in Ontario, Canada (1996–2018). Opioid analgesics dispensed in the first trimester and CA were identified from universal‐access administrative health records. We estimated propensity score adjusted risk ratios (RR) between first trimester exposure and CA (any, major, minor, specific). RRs were compared to those published from an Ontario population‐based cohort (N = 599,579, 2013–2018).Results15,724 (7.9%) were exposed to first trimester opioid analgesics, mainly codeine (58.1%) or oxycodone (21.3%); CA prevalence in exposed was 3.1%. RRs in the beneficiary cohort appeared higher than the population‐based cohort for any CA with hydromorphone (RR = 2.34, 95% CI: 1.65, 3.30) and oxycodone (RR = 1.73, 95% CI: 1.46, 2.05) and major CA with hydromorphone (RR = 2.74, 95% CI: 1.91, 3.94) and oxycodone (RR = 1.72, 95% CI: 1.42, 2.08). Other RRs that appeared higher in the beneficiary cohort included cardiovascular (codeine, oxycodone), gastrointestinal (oxycodone), musculoskeletal (any, hydromorphone, oxycodone), CNS (oxycodone), chromosomal (codeine), and neoplasm and tumor (oxycodone) anomalies. The beneficiary cohort had higher opioid doses, was younger, had lower socioeconomic status, and greater comorbidities.ConclusionsIncreased risks of CA after first trimester opioid analgesics were observed in low‐income prescription beneficiaries, and some estimates were higher than a population‐based cohort from the same setting. Biological differences associated with younger age, lower socioeconomic status and greater comorbidity may affect generalizability of results from pregnant low‐income beneficiaries.

Funder

Eunice Kennedy Shriver National Institute of Child Health and Human Development

Institute for Clinical Evaluative Sciences

Ministry of Health

Publisher

Wiley

Subject

Health, Toxicology and Mutagenesis,Developmental Biology,Toxicology,Embryology,Pediatrics, Perinatology and Child Health

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