University of Belgrade School of Medicine, Belgrade, Serbia.
J Clin Virol. 2010 Feb;47(2):131-5. doi: 10.1016/j.jcv.2009.11.017. Epub 2009 Dec 16.
With the introduction of highly active antiretroviral treatment (HAART) an impressive improvement in patient survival and quality of life has bee observed. However, the optimal timing of initial HAART is still under consideration.
To investigate the prognosis of HAART treated patients in Serbia, related to the timing of HAART initiation.
A series of 563 patients on HAART was retrospectively analyzed to investigate treatment response and survival.
After a mean of 6 years (range 1-14) of treatment with PI-based and/or NNRTI-based regimens, a favorable response was achieved in 72.4%, treatment failure occurred in 7.9%, while 19.7% had a dissociative immunological/virological response. If treatment was initiated during primary HIV infection it took a shorter time to achieve a favorable response than in patients who began HAART in chronic HIV infection (2.7+/-2.2 years vs. 6.9+/-2.7 years, P<0.01). A higher proportion of patients with primary HIV infection then those treated in the chronic phase achieved a favorable response to HAART (88.4% vs. 71.9%, P=0.045). Patients who initiated HAART when their CD4 cell counts were below 200 cells/microL needed longer treatment for favorable response (8 years vs. 6 years, log rank P<0.01). Forty-seven (8.3%) patients died. The overall estimated survival was 13 years. Patients older then 40 and IVDU were more likely to die during HAART (OR 2.6, 95% CI 1.1-5.9, P=0.016, and OR 2.0, 95% CI 1.0-3.7, P=0.02, respectively). However, reaching and maintaining undetectable viremia was an independent predictor of longer survival (OR 11.3, 95% CI 4.6-27.7, P<0.01).
Reaching and maintaining undetectable viremia during HAART predicted longer survival, even if sub-clinical immunodeficiency remained.
随着高效抗逆转录病毒治疗(HAART)的引入,患者的生存和生活质量得到了显著改善。然而,HAART 的最佳起始时间仍在讨论中。
研究塞尔维亚接受 HAART 治疗的患者的预后,与 HAART 起始时间有关。
对 563 例接受 HAART 的患者进行回顾性分析,以调查治疗反应和生存情况。
在接受基于 PI 和/或 NNRTI 的方案治疗平均 6 年后(范围 1-14 年),72.4%的患者获得了良好的反应,7.9%的患者发生了治疗失败,而 19.7%的患者出现了免疫/病毒学分离反应。如果在原发性 HIV 感染时开始治疗,与在慢性 HIV 感染时开始 HAART 的患者相比,达到良好反应所需的时间更短(2.7±2.2 年比 6.9±2.7 年,P<0.01)。在原发性 HIV 感染时开始治疗的患者中,有更高比例的患者对 HAART 有良好反应(88.4%比 71.9%,P=0.045)。在 CD4 细胞计数低于 200 个/μL 时开始 HAART 的患者需要更长时间才能达到良好反应(8 年比 6 年,对数秩 P<0.01)。47(8.3%)例患者死亡。总的估计生存率为 13 年。年龄大于 40 岁和静脉吸毒者在 HAART 期间更有可能死亡(OR 2.6,95%CI 1.1-5.9,P=0.016,和 OR 2.0,95%CI 1.0-3.7,P=0.02)。然而,达到并维持不可检测的病毒载量是生存时间延长的独立预测因素(OR 11.3,95%CI 4.6-27.7,P<0.01)。
即使亚临床免疫缺陷仍然存在,HAART 期间达到并维持不可检测的病毒载量可预测更长的生存时间。