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. Author manuscript; available in PMC: 2018 Jan 1.
Published in final edited form as: Am J Obstet Gynecol. 2016 Sep 26;216(1):64.e1–64.e7. doi: 10.1016/j.ajog.2016.09.095

Revised Table 2.

Buprenorphine pharmacokinetic parameters

Parameter (untransformed raw data, Mean ± SD) PK-2 (2nd Trimester)
N = 7
PK-3 (3nd Trimester)
N = 11
PK-P (Postpartum)
N = 10
p valuei (PK-2:PK-3) p valueii (½PK-2+½PK-3:PK-P)
Dose, mg 8.0 ± 3.1 10.0 ± 3.7 8.0 ± 0.0 0.3333 0.0276
Tmax, h 1.6 ± 2.8 1.0 ± 1.1 1.9 ± 3.6 0.9661 0.8411
Dose-normalized Cmax, ng/ml 0.5 ± 0.1 0.5 ± 0.2 0.7 ± 0.3 0.9964 0.0365
Dose-normalized C0, ng/ml 0.1 ± 0.0 0.2 ± 0.2 0.3 ± 0.3 0.8959 0.0032
Dose-normalized C12, ng/ml 0.1 ± 0.0 0.1 ± 0.1 0.3 ± 0.3 0.1260 0.0001
Dose-normalized Cavg, ng/ml 0.2 ± 0.1 0.2 ± 0.1 0.3 ± 0.2 0.7965 0.0068
Dose-normalized AUC, ng* h/mL 1.9 ± 1.4 2.2 ± 1.2 4.0 ± 2.5 0.7953 0.0068

Tmax, time to maximum concentration; Dose-norm, Dose-normalized or plasma concentration/dose; Cmax, maximum plasma concentration; C0, time zero trough plasma concentration; C12, twelve-hour plasma concentration; Cavg, average plasma concentration from time zero to twelve-hours; AUC0→12, area under the plasma concentration-time curve from time zero to twelve-hours

*

Data presented as mean ± sd (raw and untransformed)

P-value columns represent comparisons between:

i

2nd vs 3rd trimester: PK-2 vs PK-3

ii

Pregnancy vs Postpartum: the average of PK-2 & PK-3 vs PK-P