Manosuthi W, Thongyen S, Chumpathat N, Muangchana K, Sungkanuparph S
Bamrasnaradura Infectious Diseases Institute, Ministry of Public Health, Nonthaburi, Thailand.
HIV Med. 2006 Sep;7(6):378-82. doi: 10.1111/j.1468-1293.2006.00396.x.
To determine the incidence and risk factors of rash associated with efavirenz in HIV-infected patients with preceding nevirapine-associated rash.
A retrospective cohort study was conducted in HIV-infected patients diagnosed with nevirapine-associated rash who subsequently received efavirenz between July 2003 and January 2005. Patients were followed up for 3 months after receiving efavirenz. Possible risk factors, including demographics, previous opportunistic infections, CD4 cell count, viral load, severity of nevirapine-associated rash and concurrent drugs, were studied and compared between those who had (group A) and did not have (group B) rash associated with efavirenz.
A total of 122 patients (52.5% male) were included in the study, with a mean age of 38.2 years. Median (and interquartile range) CD4 cell count and viral load were 55 (20-167) cells/microL and 86,150 (35,321-700,750) HIV-1 RNA copies/mL, respectively. Of the 122 patients, 10 (8.2%) developed rash associated with efavirenz and all required discontinuation of efavirenz. The baseline characteristics of group A (10 patients) and group B (112 patients) were similar. Median (and interquartile range) time from nevirapine discontinuation to efavirenz initiation was 12 (9-21) days in group A and 11 (7-21) days in group B (P=0.765). None of the risk factors investigated was associated with developing rash associated with efavirenz. The preceding development of severe nevirapine-associated rash had a trend towards a higher rate in group A than in group B (20.0% vs 10.7%; odds ratio=2.08; 95% confidence interval 0.39-10.97; P=0.322).
The majority (>90%) of HIV-infected patients with CD4 counts <200 cells/muL who had preceding nevirapine-associated rash could tolerate efavirenz well. Efavirenz may be an option for subsequent use in these patients, particularly in those who had preceding nevirapine-associated rash.
确定在先前出现过奈韦拉平相关皮疹的HIV感染患者中,依非韦伦相关皮疹的发生率及危险因素。
对2003年7月至2005年1月期间诊断为奈韦拉平相关皮疹且随后接受依非韦伦治疗的HIV感染患者进行一项回顾性队列研究。患者在接受依非韦伦治疗后随访3个月。研究并比较了可能的危险因素,包括人口统计学特征、既往机会性感染、CD4细胞计数、病毒载量、奈韦拉平相关皮疹的严重程度及同时使用的药物,将出现(A组)和未出现(B组)依非韦伦相关皮疹的患者进行对比。
共纳入122例患者(52.5%为男性),平均年龄38.2岁。CD4细胞计数中位数(及四分位间距)和病毒载量分别为55(20 - 167)个/微升和86,150(35,321 - 700,750)拷贝/mL的HIV-1 RNA。122例患者中,10例(8.2%)出现依非韦伦相关皮疹,均需停用依非韦伦。A组(10例患者)和B组(112例患者)的基线特征相似。A组从停用奈韦拉平到开始使用依非韦伦的时间中位数(及四分位间距)为12(9 - 21)天,B组为11(7 - 21)天(P = 0.765)。所调查的危险因素均与出现依非韦伦相关皮疹无关。A组中先前出现严重奈韦拉平相关皮疹的比例有高于B组的趋势(20.0%对10.7%;比值比 = 2.08;95%置信区间0.39 - 1,0.97;P = 0.322)。
大多数(> = 90%)CD4计数<200个/微升且先前出现过奈韦拉平相关皮疹的HIV感染患者能够很好地耐受依非韦伦。依非韦伦可能是这些患者后续治疗的一个选择,尤其是那些先前出现过奈韦拉平相关皮疹的患者。