自然史研究和监测中CD4细胞计数为200 × 10(6)/1或以下:一个足够还是两个更好?

P J Easterbrook, L M Yu, K McLean, D Hawkins, B Gazzard
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引用次数: 0

摘要

进行了一项回顾性队列研究,以检查与使用当前美国艾滋病病例定义类别(初始CD4计数<或= 200细胞× 10(6)/l(<或= 200)相比,需要连续两次计数低于该水平的定义的错误分类的程度和临床意义。检查的主要结果是随后CD4计数> 200 × 10(6)/l(> 200)的概率和进展到艾滋病和死亡的时间。在参加两家医院艾滋病毒诊所的、初始CD4细胞计数<或= 200的2025名男性同性恋艾滋病毒阳性患者中,1524名(75%)随后连续计数<或= 200,但只有一半在下一次CD4计数时连续计数<或= 200。10%没有进一步计数或只有非连续计数<或= 200,15%只有一个CD4计数可用于分析。首次计数<或= 200后一年内CD4计数> 200的患者累积比例约为连续两次计数<或= 200的亚组(19%)的两倍(39%)。在连续两次或两次以上计数<或= 200的亚组中,从最初计数<或= 200到艾滋病和死亡的时间也分别缩短了6个月和2个月。如果单个CD4计数低于该水平被接受,那么很大一部分患者将过早地被分类为CD4细胞计数<或= 200。在自然史研究和临床试验中,应优先采用两次连续计数<或= 200的定义,而不是单次计数<或= 200,在这些研究中,精确估计到达或离开定义的CD4阈值的时间是很重要的。然而,在监测规划中,这种方法可能不切实际,因为缺少或不经常进行连续CD4计数,尽管可以根据这些过早错误分类的估计进行调整。
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CD4 cell counts of 200 x 10(6)/1 or below in natural history studies and surveillance: is one enough or are two better?

A retrospective cohort study was performed to examine the extent and clinical significance of misclassification associated with using the current United States AIDS case defining category of an initial CD4 count < or = 200 cells x 10(6)/l (< or = 200) compared with a definition requiring two consecutive counts below this level. The main outcomes examined were the probability of subsequent CD4 counts > 200 x 10(6)/l (> 200) and progression times to AIDS and death. Of the 2025 predominantly male homosexual HIV-positive patients attending two hospital based HIV clinics with initial CD4 cell counts < or = 200, 1524 (75%) subsequently had consecutive counts < or = 200, but only half did so at the next CD4 count. Ten per cent had either no further or only non-consecutive counts < or = 200, and 15% had only one CD4 count available for analysis. The cumulative proportion of patients with a CD4 count > 200 at one year after a first count of < or = 200 was about twice (39%) that observed among the subgroup with at least two consecutive counts < or = 200 (19%). The times from the initial counts of < or = 200 to AIDS and death were also shorter by six months and two months, respectively, in the subgroup with two or more consecutive counts < or = 200. A significant proportion of patients will be prematurely classified as having a CD4 cell count < or = 200 if a single CD4 count below this level is accepted. A definition of two consecutive counts < or = 200 should be adopted in preference to a single count < or = 200 for natural history studies and clinical trials, in which precise estimates of the time to or from a defined CD4 threshold are important. In surveillance programmes, however, such an approach may be impractical because of missing or infrequent serial CD4 counts, although adjustments can be made based on these estimates of premature misclassification.

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