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. Author manuscript; available in PMC: 2023 Jul 24.
Published in final edited form as: Drug Saf. 2023 Jan 16;46(3):257–271. doi: 10.1007/s40264-022-01267-z

Table 4.

Crude and adjusted (IP-weighted) odds ratios of adverse neonatal and pregnancy outcomes associated with prenatal exposure to methadone both early and late in pregnancy compared with buprenorphine both early and late in pregnancy.

Exposure to OATs in both early and late pregnancya,b
Neonatal outcomes Cases, n (%) Crude OR (95% CI) Weighted OR (95% CI)
Preterm birth (<37 weeks)
 Buprenorphine <11 Ref. Ref.
 Methadone 31 (24.8) 7.77 (2.14, 28.18) 14.49 (3.20, 65.57)
Low birthweight (<2500 g)
 Buprenorphine <11 Ref. Ref.
 Methadone 35 (28) 6.75 (2.32, 19.66) 7.36 (2.18, 24.87)
Neonatal Intensive Care Unit Admission (NICUa)
 Buprenorphine 18 (27.69) Ref. Ref.
 Methadone 69 (55.2) 3.23 (1.71, 6.06) 2.83 (1.23, 6.48)
Neonatal abstinence syndrome (NAS)
 Buprenorphine 37 (56.92) Ref. Ref.
 Methadone 75 (60) 1.27 (0.70, 2.30) 1.11 (0.54, 2.28)
Respiratory symptoms
 Buprenorphine 11 (16.92) Ref. Ref.
 Methadone 29 (23.2) 1.58 (0.75, 3.34) 1.51 (0.55, 4.12)
Feeding difficulties
 Buprenorphine 18 (27.69) Ref. Ref.
 Methadone 16 (12.8) 0.40 (0.20, 0.83) 0.37 (0.15, 0.92)
Small for gestational age
 Buprenorphine <11 Ref. Ref.
 Methadone 19 (15.2) 1.08 (0.46, 2.53) 1.12 (0.43, 2.96)
Maternal and obstetrical complications
Length of maternal hospital stay (>7 days)c
 Buprenorphine 28 (43.08) Ref. Ref.
 Methadone 91 (72.8) 3.46 (1.86, 6.42) 3.77 (1.80, 7.90)
Caesarean delivery
 Buprenorphine 23 (35.38) Ref. Ref.
 Methadone 34 (27.2) 0.57 (0.31, 1.07) 0.74 (0.35, 1.57)
Preeclampsia
 Buprenorphine <11 Ref. Ref.
 Methadone <11 1.86 (0.33, 10.60) 2.56 (0.45, 14.43)
Postpartum hemorrhage
 Buprenorphine <11 Ref. Ref.
 Methadone <11 0.29 (0.06, 1.37) 0.43 (0.07, 2.45)

Abbreviations: IP = inverse probability; OR = odds ratios; CI = confidence intervals.

a

Small cell count <11 was suppressed.

b

Stabilized inverse-probability treatment weights (IPTWs) of early and late exposure were computed with the numerator model adjusting for baseline covariates (i.e., maternal age, race, year of birth, multiple gestation, pre-existing comorbid conditions, and healthcare resource utilization at baseline), and the denominator model adjusting for additional time-varying comedication use, substances use, and markers of OUD severity. Previous exposure history was included in the models for late exposure. Infant sex was included for adverse neonatal outcomes. A product of stabilized IPTWs for early and late exposure was used in outcome models.

c

Missing values were ≤0.5% and only complete cases were analyzed.