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DOI 10.1097/qai.0b013e31823ff052

Медицинская библиотека · Journal of acquired immune deficiency syndromes (1999) · 2012

Efavirenz pharmacokinetics during the third trimester of pregnancy and postpartum.

Cressey Tim R, Stek Alice, Capparelli Edmund, Bowonwatanuwong Chureeratana, Prommas Sinart, Sirivatanapa Pannee, Yuthavisuthi Prapap, Neungton Chanon, Huo Yanling, Smith Elizabeth, Best Brookie M, Mirochnick Mark, IMPAACT P1026s Team

Клиническое исследованиеСтатьяМногоцентровое исследованиеПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

BACKGROUND

The impact of pregnancy on efavirenz (EFV) pharmacokinetics is unknown.

METHODS

International Maternal Pediatric Adolescent AIDS Clinical Trials P1026s is an on-going, prospective, nonblinded study of antiretroviral pharmacokinetics in HIV-infected pregnant women that included a cohort receiving 600 mg EFV once daily as part of combination antiretroviral therapy. Intensive steady-state 24-hour blood sampling was performed during the third trimester and at 6-12 weeks postpartum. Maternal and umbilical cord blood samples were drawn at delivery. Pharmacokinetics targets were the estimated 10th percentile EFV area under the curve (AUC) in nonpregnant historical controls (40.0 mcg·hr(-1)·mL(-1)) and a trough concentration of 1 mcg/mL.

RESULTS

Twenty-five women were enrolled during the third trimester: median (range) age was 29.3 (18.9-42.9) years, weight 69.0 (40-130) kg, and gestational age 32.9 (30.1-38.7) weeks. Median (range) EFV AUC(0-24), C(max), and C(24 hours) were 55.4 mcg·hr(-1)·mL(-1) (13.5-220.3), 5.4 mcg/mL (1.9-12.2), and 1.6 mcg/mL (0.23-8.13), respectively. EFV AUC and C(max) did not differ during pregnancy and postpartum but C(24 hours) was lower during the third trimester (1.6 vs. 2.1 mcg/mL, P = 0.01). During the third trimester, 5 of 25 (20%) women had an EFV AUC below the target and 3 of 25 (12%) had a trough concentration below 1 mcg/mL. EFV cord blood/maternal concentration ratio was 0.49 (0.37-0.74). All women had a HIV-1 RNA viral load less than 400 copies per milliliter at delivery and 19 (76%) had a viral load below 50 copies per milliliter. One child was perinatally HIV infected. Three women were exposed to EFV throughout the first 6 weeks of pregnancy. EFV was well tolerated, and among the 25 infants, no congenital anomalies or newborn complications were reported.

CONCLUSIONS

Changes in EFV pharmacokinetics during pregnancy compared with postpartum are not sufficiently large enough to warrant a dose adjustment during pregnancy.

Для цитирования: Cressey Tim R, Stek Alice, Capparelli Edmund, Bowonwatanuwong Chureeratana, Prommas Sinart, Sirivatanapa Pannee, Yuthavisuthi Prapap, Neungton Chanon, Huo Yanling, Smith Elizabeth, Best Brookie M, Mirochnick Mark, IMPAACT P1026s Team. Efavirenz pharmacokinetics during the third trimester of pregnancy and postpartum.. Journal of acquired immune deficiency syndromes (1999). 2012. DOI: 10.1097/qai.0b013e31823ff052.

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