Sklar Peter A, Ward Douglas J, Baker Rose K, Wood Kathleen C, Gafoor Zarina, Alzola Carlos F, Moorman Anne C, Holmberg Scott D
Division of Infectious Dieseases, George Washington university and Dupont Circle Physicians Group, Washington, DC, USA.
AIDS. 2002 Oct 18;16(15):2035-41. doi: 10.1097/00002030-200210180-00008.
To examine the prevalence and clinical correlates of subsequently measurable viremia in HIV-infected patients who have achieved viral suppression below the limits of quantification (< 50 copies/ml).
Non-randomized dynamic cohort study of ambulatory HIV patients in nine HIV clinics in eight cities.
Patients had two consecutive HIV-1 RNA levels < 50 copies/ml (minimum, 2 months apart) that were followed by at least two more viral level determinations while remaining on the same antiretroviral therapy (ART) between January 1997 and June 2000 (median 485 days). Transiently viremic patients were defined having a subsequently measurable viremia but again achieved suppression < 50 copies/ml.
Of the 448 patients, 122 (27.2%) had transient viremia, 19 (4.2%) had lasting low-level viremia and 33 (7.4%) had lasting high-level viremia (defined as 50-400 and > 400 copies/ml, respectively). Only 16 (13.1%) of those who had transient viremia later had persistent viremia > 50 copies/ml. The occurrence of transient viremia did not vary with whether the patient was ART-naive or experienced (P = 0.31), or currently taking protease inhibitors or not (P = 0.08). On consistent ART, the median percentage increase in CD4 cell count was statistically different between subgroups of our cohort (Kruskal-Wallis, P = 0.002).
Transiently detectable viremia, usually 50-400 copies/ml, was frequent among patients who had two consecutive HIV-1 RNA levels below the limits of quantification. In this analysis, such viremia did not appear to affect the risk of developing lasting viremia. Caution is warranted before considering a regimen as 'failing' and changing medications.
研究在已实现病毒载量抑制至低于定量检测下限(<50拷贝/毫升)的HIV感染患者中,后续可检测到病毒血症的患病率及其临床相关因素。
对八个城市的九家HIV诊所的门诊HIV患者进行非随机动态队列研究。
患者连续两次HIV-1 RNA水平<50拷贝/毫升(间隔至少2个月),随后在1997年1月至2000年6月期间(中位时间485天)继续接受相同的抗逆转录病毒治疗(ART)时至少又进行了两次病毒水平检测。短暂病毒血症患者定义为随后可检测到病毒血症,但再次实现抑制至<50拷贝/毫升。
448例患者中,122例(27.2%)有短暂病毒血症,19例(4.2%)有持续性低水平病毒血症,33例(7.4%)有持续性高水平病毒血症(分别定义为50 - 400拷贝/毫升和>400拷贝/毫升)。短暂病毒血症患者中只有16例(13.1%)后来出现持续性病毒血症>50拷贝/毫升。短暂病毒血症的发生与患者是否初治或经治(P = 0.31),或当前是否服用蛋白酶抑制剂无关(P = 0.08)。在持续接受ART治疗的情况下,我们队列亚组间CD4细胞计数的中位百分比增加有统计学差异(Kruskal-Wallis检验,P = 0.002)。
在连续两次HIV-1 RNA水平低于定量检测下限的患者中,短暂可检测到的病毒血症(通常为50 - 400拷贝/毫升)很常见。在本分析中,这种病毒血症似乎并未影响发生持续性病毒血症的风险。在将一种治疗方案视为“失败”并更换药物之前,应谨慎行事。