Wester C William, Kim Soyeon, Bussmann Hermann, Avalos Ava, Ndwapi Ndwapi, Peter Trevor F, Gaolathe Tendani, Mujugira Andrew, Busang Lesego, Vanderwarker Chris, Cardiello Peter, Johnson Onalethata, Thior Ibou, Mazonde Patson, Moffat Howard, Essex Max, Marlink Richard
Botswana-Harvard School of Public Health AIDS Initiative Partnership for Research and Education, Gaborone, Botswana.
J Acquir Immune Defic Syndr. 2005 Nov 1;40(3):336-43. doi: 10.1097/01.qai.0000159668.80207.5b.
To describe the response to highly active antiretroviral treatment (HAART) in a public sector pilot antiretroviral (ARV) treatment program in Botswana.
The response to HAART is described in adult HIV-infected ARV-naive patients initiating treatment from April 2001 to January 2002 at Princess Marina Hospital in Gaborone, Botswana. Patients had medical and laboratory evaluations before initiating ARV treatment and were followed longitudinally. For analysis, data were collected from charts and patient management records.
One hundred fifty-three ARV-naive patients initiated HAART. Most received didanosine plus stavudine (ddI + d4T) with efavirenz or nevirapine. The mean CD4 cell count increase was 149 cells/mm at 24 weeks and 204 cells/mm at 48 weeks. The percentage of patients with an HIV-1 RNA level < or =400 copies/mL was 87.0% at 24 weeks and 78.8% at 48 weeks. The Kaplan-Meier 1-year survival estimate was 84.7% (79.0%, 90.8%), with a 3.2-fold increased risk (P = 0.004) of mortality among patients with a CD4 cell count <50 cells/mm. The 1-year Kaplan-Meier estimate of toxicity-related drug switches was 32.2% (20.3%, 40.4%). The most common toxicity was peripheral neuropathy, occurring more frequently in patients with a preexisting diagnosis of peripheral neuropathy and among those placed on ddI + d4T-containing regimens.
An excellent response to HAART was observed among HIV-1C-infected patients, paralleling those seen elsewhere. Despite excellent responses, high rates of toxicity were observed for ddI + d4T-containing regimens.
描述博茨瓦纳公共部门抗逆转录病毒治疗(ARV)试点项目中对高效抗逆转录病毒治疗(HAART)的反应。
描述了2001年4月至2002年1月在博茨瓦纳哈博罗内的玛丽娜公主医院开始接受治疗的成年初治HIV感染患者对HAART的反应。患者在开始抗逆转录病毒治疗前进行了医学和实验室评估,并进行了纵向随访。为进行分析,从病历和患者管理记录中收集数据。
153例初治患者开始接受HAART。大多数患者接受去羟肌苷加司他夫定(ddI + d4T)联合依非韦伦或奈韦拉平治疗。24周时CD4细胞计数平均增加149个细胞/mm,48周时增加204个细胞/mm。HIV-1 RNA水平≤400拷贝/mL的患者比例在24周时为87.0%,48周时为78.8%。Kaplan-Meier法估计的1年生存率为84.7%(79.0%,90.8%),CD4细胞计数<50个细胞/mm的患者死亡风险增加3.2倍(P = 0.004)。与毒性相关的药物换药的1年Kaplan-Meier估计值为32.2%(20.3%,40.4%)。最常见的毒性是周围神经病变,在既往诊断为周围神经病变的患者以及接受含ddI + d4T方案治疗的患者中更频繁出现。
在HIV-1C感染患者中观察到对HAART的良好反应,与其他地方观察到的情况相似。尽管反应良好,但含ddI + d4T方案的毒性发生率较高。