Mirochnick M, Clarke D F, Dorenbaum A
Boston University School of Medicine, Massachusetts 02118, USA.
Clin Pharmacokinet. 2000 Oct;39(4):281-93. doi: 10.2165/00003088-200039040-00004.
Nevirapine is a potent non-nucleoside inhibitor of HIV-1 reverse transcriptase. It is effective when used as part of combination therapy to treat HIV-1-infected individuals and as monotherapy for prevention of mother-to-child HIV-1 transmission. Nevirapine pharmacokinetics are characterised by rapid absorption and distribution, followed by prolonged elimination. Nevirapine is generally well tolerated. The most common toxicity is rash, which is usually mild and self-limiting. The primary route of nevirapine elimination is through metabolism by the cytochrome P450 enzyme system. Nevirapine elimination accelerates during long term administration because of autoinduction of the enzymes involved in its elimination pathway. The recommended regimen for adults is nevirapine 200mg once daily for 2 weeks, followed by 200mg twice daily. Nevirapine elimination is prolonged in pregnant women during labour and in newborns. A regimen of a single 200mg oral dose administered to the mother during labour and a single 2 mg/kg dose administered to the newborn at 48 to 72 hours after birth maintains serum nevirapine concentrations above 100 microg/L (10 times the in vitro 50% inhibitory concentration against wild-type HIV-1) throughout the first week of life. This limited regimen has been shown to be extremely well tolerated and to reduce mother-to-child transmission by nearly 50% in mothers and infants receiving no other antiretrovirals. There are few data describing the safety and pharmacokinetics of nevirapine during long term use in pregnancy. In children, nevirapine elimination accelerates during the first years of life, reaching a maximum at around 2 years of age, followed by a gradual decline during the rest of childhood. Children should receive 4 mg/kg once daily for the first 2 weeks of therapy, followed by 7 mg/kg doses twice daily if below the age of 8 years or 4 mg/kg twice daily if older than 8 years. Alternatively, children may receive 150 mg/m2 across all ages, once daily for the first 2 weeks of therapy followed by the same dose twice daily.
奈韦拉平是一种强效的非核苷类HIV-1逆转录酶抑制剂。作为联合治疗的一部分用于治疗HIV-1感染个体以及作为预防母婴HIV-1传播的单一疗法时,它是有效的。奈韦拉平的药代动力学特点是吸收和分布迅速,随后消除时间延长。奈韦拉平一般耐受性良好。最常见的毒性是皮疹,通常较轻且为自限性。奈韦拉平消除的主要途径是通过细胞色素P450酶系统进行代谢。由于参与其消除途径的酶的自身诱导作用,长期给药期间奈韦拉平的消除加速。成人推荐方案是奈韦拉平200mg每日一次,连用2周,之后200mg每日两次。分娩期间孕妇及新生儿的奈韦拉平消除时间延长。分娩时给母亲口服单次200mg剂量,出生后48至72小时给新生儿单次2mg/kg剂量,可使出生后第一周内血清奈韦拉平浓度维持在100μg/L以上(是体外对野生型HIV-1 50%抑制浓度的10倍)。在未接受其他抗逆转录病毒药物治疗的母婴中,这种有限的方案已显示出耐受性极佳,并可将母婴传播减少近50%。关于奈韦拉平在孕期长期使用时的安全性和药代动力学的数据很少。在儿童中,奈韦拉平的消除在生命的最初几年加速,在2岁左右达到最大值,随后在儿童期其余时间逐渐下降。治疗的前2周儿童应每日一次接受4mg/kg剂量,8岁以下儿童之后应每日两次接受7mg/kg剂量,8岁以上儿童则每日两次接受4mg/kg剂量。或者,各年龄段儿童均可接受150mg/m²,治疗的前2周每日一次,之后每日两次接受相同剂量。