Tenofovir Exposure during Pregnancy and Postpartum in Women Receiving Tenofovir Disoproxil Fumarate for the Prevention of Mother-to-Child Transmission of Hepatitis B Virus

被引:3
|
作者
Cressey, Tim R. [1 ,2 ,3 ]
Harrison, Linda [4 ]
Achalapong, Jullapong [5 ]
Kanjanavikai, Prateep [6 ]
Ayudhaya, Orada Patamasingh Na [7 ]
Liampongsabuddhi, Prateung [8 ]
Siriwachirachai, Thitiporn [9 ]
Putiyanun, Chaiwat [10 ]
Suriyachai, Pornnapa
Tierney, Camlin [4 ]
Salvadori, Nicolas [1 ]
Chinwong, Dujrudee [11 ]
Decker, Luc [12 ]
Tawon, Yardpiroon [1 ]
Murphy, Trudy V. [13 ]
Ngo-Giang-Huong, Nicole [1 ,2 ,12 ]
Siberry, George K. [14 ]
Jourdain, Gonzague [1 ,2 ,11 ]
机构
[1] Chiang Mai Univ, Fac Associated Med Sci, Dept Med Technol, PHPT IRD, Chiang Mai, Thailand
[2] Harvard TH Chan Sch Publ Hlth, Dept Immunol & Infect Dis, Boston, MA 02115 USA
[3] Univ Liverpool, Dept Mol & Clin Pharmacol, Liverpool, Merseyside, England
[4] Harvard TH Chan Sch Publ Hlth, CBAR, Boston, MA USA
[5] Chiangrai Prachanukroh Hosp, Chiang Rai, Thailand
[6] Banglamung Hosp, Chon Buri, Thailand
[7] Nopparat Rajathanee Hosp, Bangkok, Thailand
[8] Lampang Hosp, Lampang, Thailand
[9] Khon Kaen Hosp, Khon Kaen, Thailand
[10] Chiang Kham Hosp, Phayao, Thailand
[11] Chiang Mai Univ, Fac Pharm, Dept Pharmaceut Care, Chiang Mai, Thailand
[12] IRD, Unite Mixte Int PHPT 174, Chiang Mai, Thailand
[13] Ctr Dis Control & Prevent, Atlanta, GA USA
[14] Eunice Kennedy Shriver Natl Inst Child Hlth & Hum, NIH, Bethesda, MD USA
关键词
pregnancy; tenofovir; hepatitis B virus; pharmacokinetics; CLINICAL-PHARMACOLOGY; PHARMACOKINETICS; HIV;
D O I
10.1128/AAC.01686-18
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We assessed tenofovir exposure during pregnancy and postpartum in hepatitis B virus (HBV)-infected HIV-uninfected women receiving tenofovir disoproxil fumarate (TDF) to prevent mother-to-child transmission of HBV. Data from 154 women who received TDF within a randomized controlled trial were included. Individual plasma tenofovir exposures (area under the concentration-time curve from 0 to 24 h [AUC0-24]) were estimated using a population pharmacokinetic approach. The estimated geometric mean tenofovir AUC(0-24) was 20% (95% confidence interval [95% CI], 19 to 21%) lower during pregnancy than during postpartum; this modest reduction in the absence of HBV transmission suggests that no dose adjustment is needed.
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页数:5
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