2014
DOI: 10.1016/j.jhep.2014.04.038
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Efficacy and safety of tenofovir disoproxil fumarate in pregnancy to prevent perinatal transmission of hepatitis B virus

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Cited by 156 publications
(208 citation statements)
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“…Perinatal transmission was reduced to 0 and 2% in the lamivudine and tenofovir cohorts, respectively, compared with 20% in the untreated groups. No diff erences were noted in obstetric or infant safety outcomes ( 110 ). Although some studies have suggested a favorable safety profi le for antiviral therapy even in the fi rst and second trimesters of pregnancy, when utilized purely for purposes of reducing MTCT, antiviral therapy should be initiated in the third trimester (thus minimizing the risk associated with fetal exposure to these medications).…”
Section: Hepatitis C (Hcv)mentioning
confidence: 99%
“…Perinatal transmission was reduced to 0 and 2% in the lamivudine and tenofovir cohorts, respectively, compared with 20% in the untreated groups. No diff erences were noted in obstetric or infant safety outcomes ( 110 ). Although some studies have suggested a favorable safety profi le for antiviral therapy even in the fi rst and second trimesters of pregnancy, when utilized purely for purposes of reducing MTCT, antiviral therapy should be initiated in the third trimester (thus minimizing the risk associated with fetal exposure to these medications).…”
Section: Hepatitis C (Hcv)mentioning
confidence: 99%
“…1 Among the last two agents, TDF should be preferred, because it has a better resistance profile and more extensive safety data in pregnant HBV positive women. 1,[196][197][198] In a woman of childbearing age without advanced fibrosis who plans a pregnancy in the near future, it may be prudent to delay therapy until the child is born. In a woman of childbearing age with advanced fibrosis or cirrhosis who agrees for a ''planned pregnancy'' in the future, PegIFNa therapy may be tried as it is given for a finite duration.…”
Section: Pregnancy Recommendationsmentioning
confidence: 99%
“…First, pregnant women with high (>10 6-7 IU/mL) HBV DNA levels have an increased (>10 %) risk of vertical HBV transmission despite HBV immunoglobulin administration and vaccination [13][14][15]. Thus, it is recommended that they receive oral antiviral therapy during the last trimester of their pregnancy [1••].…”
Section: Hbeag-positive Patients In the Immunotolerant Phasementioning
confidence: 99%
“…Thus, it is recommended that they receive oral antiviral therapy during the last trimester of their pregnancy [1••]. In such patients, treatment with LAM, TBV, or TDF during this period, alongside passive and active immunization of the newborn, has been shown to be safe and to reduce the probability of intrauterine and perinatal HBV transmission [13][14][15]. If NA therapy is given only for the prevention of perinatal transmission, it is usually discontinued within the first 3 months after delivery [1••], but close follow-up of the mothers should continue, in order to detect possible postpartum flares [16].…”
Section: Hbeag-positive Patients In the Immunotolerant Phasementioning
confidence: 99%