J Acquir Immune Defic Syndr. 2007 Dec 15;46(5):607-15. doi: 10.1097/QAI.0b013e31815b7dba.
The extent to which the prognosis for AIDS and death of patients initiating highly active antiretroviral therapy (HAART) continues to be affected by their characteristics at the time of initiation (baseline) is unclear.
We analyzed data on 20,379 treatment-naive HIV-1-infected adults who started HAART in 1 of 12 cohort studies in Europe and North America (61,798 person-years of follow-up, 1844 AIDS events, and 1005 deaths).
Although baseline CD4 cell count became less prognostic with time, individuals with a baseline CD4 count <25 cells/microL had persistently higher progression rates than individuals with a baseline CD4 count >350 cells/microL (hazard ratio for AIDS = 2.3, 95% confidence interval [CI]: 1.0 to 2.3; mortality hazard ratio = 2.5, 95% CI: 1.2 to 5.5, 4 to 6 years after starting HAART). Rates of AIDS were persistently higher in individuals who had experienced an AIDS event before starting HAART. Individuals with presumed transmission by means of injection drug use experienced substantially higher rates of AIDS and death than other individuals throughout follow-up (AIDS hazard ratio = 1.6, 95% CI: 0.8 to 3.0; mortality hazard ratio = 3.5, 95% CI: 2.2 to 5.5, 4 to 6 years after starting HAART).
Compared with other patient groups, injection drug users and patients with advanced immunodeficiency at baseline experience substantially increased rates of AIDS and death up to 6 years after starting HAART.
开始高效抗逆转录病毒治疗(HAART)的艾滋病患者的预后及死亡情况在多大程度上仍受起始治疗时(基线)特征的影响尚不清楚。
我们分析了在欧洲和北美的12项队列研究之一中开始HAART的20379名未接受过治疗的HIV-1感染成人的数据(61798人年的随访,1844例艾滋病事件,1005例死亡)。
尽管随着时间推移基线CD4细胞计数的预后价值降低,但基线CD4计数<25个细胞/微升的个体的进展率持续高于基线CD4计数>350个细胞/微升的个体(艾滋病风险比=2.3,95%置信区间[CI]:1.0至2.3;死亡风险比=2.5,95%CI:1.2至5.5,开始HAART后4至6年)。在开始HAART前发生过艾滋病事件的个体中,艾滋病发生率持续较高。在整个随访期间,推测通过注射吸毒传播的个体的艾滋病和死亡率显著高于其他个体(艾滋病风险比=1.6,95%CI:0.8至3.0;死亡风险比=3.5,95%CI:2.2至5.5,开始HAART后4至6年)。
与其他患者组相比,注射吸毒者和基线时患有晚期免疫缺陷的患者在开始HAART后长达6年的时间里,艾滋病和死亡率显著增加。