British Columbia Centre for Excellence in HIV/AIDS, St Paul's Hospital, Vancouver, British Columbia, Canada.
J Acquir Immune Defic Syndr. 2010 Dec;55(4):460-5. doi: 10.1097/QAI.0b013e3181f2ac87.
To model the effect of adherence and duration of viral suppression on the risk of viral rebound.
Viral rebound was defined as the first of at least two consecutive viral loads greater than 400 copies/mL after initial viral suppression. The main exposures were adherence, presence of antiretroviral class resistance before rebound or censoring date, and the percentage of follow-up time with viral suppression.
A total of 274 (N = 1305 [21%]) individuals experienced viral rebound. Median time of suppression before rebound was 2 years. Viral rebound was less likely to occur among those with longer duration of continuous viral suppression (odds ratio, 0.37; 95% confidence interval, 0.32 to 0.42). Among individuals with moderate levels of adherence (80% to less than 95%), the probability of virologic failure was 0.85 after being suppressed for 12 months and it was 0.08 after 72 months being suppressed (P < 0.01). Individuals with drug resistance were at a higher risk of viral rebound.
The risk of viral rebound decreased with longer duration of viral suppression within each of adherence strata studied. Although perfect adherence remains an important goal of therapy to prevent disease progression, individuals with long-term viral suppression may be able to miss more doses without experiencing viral rebound.
建立药物依从性和病毒抑制持续时间与病毒反弹风险的关系模型。
病毒反弹定义为初始病毒抑制后至少连续两次病毒载量大于 400 拷贝/ml 的首次发生。主要暴露因素包括药物依从性、反弹或截止日期前是否存在抗逆转录病毒药物耐药、以及病毒抑制的随访时间百分比。
共 274 名(N=1305[21%])患者发生病毒反弹。在发生病毒反弹前,病毒抑制的中位时间为 2 年。病毒持续抑制时间越长,病毒反弹的可能性越低(比值比,0.37;95%置信区间,0.32 至 0.42)。在药物依从性处于中等水平(80%至<95%)的患者中,抑制 12 个月后病毒失败的概率为 0.85,而抑制 72 个月后概率为 0.08(P<0.01)。耐药患者病毒反弹的风险更高。
在每个依从性分层中,病毒抑制持续时间越长,病毒反弹的风险越低。尽管完美的依从性仍然是预防疾病进展的治疗重要目标,但长期病毒抑制的患者可能能够错过更多剂量而不发生病毒反弹。