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Multisite evaluation of a point-of-care instrument for CD4(+) T-cell enumeration using venous and finger-prick blood: the PIMA CD4.采用静脉血和指血对床边 CD4(+) T 细胞计数仪进行多中心评估:PIMA CD4。
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Development and validation of decision rules to guide frequency of monitoring CD4 cell count in HIV-1 infection before starting antiretroviral therapy.在开始抗逆转录病毒治疗之前,指导 HIV-1 感染中 CD4 细胞计数监测频率的决策规则的制定和验证。
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Accurate CD4 T-cell enumeration and antiretroviral drug toxicity monitoring in primary healthcare clinics using point-of-care testing.在基层医疗诊所使用即时检测进行准确的 CD4 T 细胞计数和抗逆转录病毒药物毒性监测。
AIDS. 2011 Mar 27;25(6):807-12. doi: 10.1097/QAD.0b013e328344f424.
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Assessing agreement in the timing of treatment initiation determined by repeated measurements of novel versus gold standard technologies with application to the monitoring of CD4 counts in HIV-infected patients.评估新型技术与金标准技术重复测量确定的治疗起始时间的一致性,并将其应用于 HIV 感染患者 CD4 计数的监测。
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Pretreatment CD4 cell slope and progression to AIDS or death in HIV-infected patients initiating antiretroviral therapy--the CASCADE collaboration: a collaboration of 23 cohort studies.开始抗逆转录病毒治疗的 HIV 感染者的预处理 CD4 细胞斜率与艾滋病或死亡的进展 - CASCADE 合作:23 项队列研究的合作。
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CD4(+) T cell count decreases by ethnicity among untreated patients with HIV infection in South Africa and Switzerland.在南非和瑞士,未接受治疗的HIV感染患者中,CD4(+) T细胞计数因种族而异。
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Comparison of early CD4 T-cell count in HIV-1 seroconverters in Côte d'Ivoire and France: the ANRS PRIMO-CI and SEROCO cohorts.比较科特迪瓦和法国 HIV-1 血清转换者的早期 CD4 T 细胞计数:ANRS PRIMO-CI 和 SEROCO 队列。
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基于 CD4 计数监测的影响抗逆转录病毒治疗开始时间的因素。

Factors affecting timing of antiretroviral treatment initiation based on monitoring CD4 counts.

机构信息

Center for Biostatistics in AIDS Research, Department of Biostatistics, Harvard School of Public Health, Boston, MA 20114, USA.

出版信息

J Acquir Immune Defic Syndr. 2012 Nov 1;61(3):326-33. doi: 10.1097/QAI.0b013e31826be75e.

DOI:10.1097/QAI.0b013e31826be75e
PMID:22878419
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3649850/
Abstract

OBJECTIVE

To evaluate factors affecting antiretroviral therapy (ART) start time when triggered by a CD4 count <350 cells/μL while monitoring counts over time. Measurement frequency, requirement for confirmatory counts, and precision and accuracy of CD4 enumeration technology were considered.

METHODS

Using a model of CD4 count trajectories among seroconverters in the Multicenter AIDS Cohort Study, sequences of counts were simulated for a large hypothetical population monitored for 5 years from seroconversion. Time of first count <350 cells/μL was defined as ART start time. The simulation was adapted to evaluate the effect of the above factors on these times. ART initiation was considered "very late" among patients whose underlying trajectory declined less than 200 cells/μL during the period simulated if no previous observed count was <350 cells/μL.

RESULTS

For 12-, 6-, 4-, and 3-monthly measurements, median start time was 48, 36, 32, and 30 months after seroconversion and proportion of patients starting ART very late was 11.5%, 1.6%, 0.2%, and 0.1%. For 6-monthly measurements, requiring confirmation increased the median to 49 months and proportion to 8.9%. Changes in standard deviation of short-term variability in counts of 25% and measurement bias for a novel technology of ±10% changed median time by ±6 months with modest change in the proportion very late (range, 0.5%-3.2%).

CONCLUSION

: 6-monthly measurements appear adequate in achieving low rates of very late ART whereas confirmation affects rates adversely. Studies comparing new versus standard measurement technologies should focus on ruling out modest bias, particularly proximal to important thresholds for treatment management.

摘要

目的

评估在监测 CD4 计数随时间变化的同时,当 CD4 计数<350 个/μL 时触发抗逆转录病毒治疗(ART)的开始时间所涉及的因素。考虑了测量频率、对确认性计数的要求以及 CD4 计数技术的精度和准确性。

方法

利用在 Multicenter AIDS Cohort Study 中发生血清转换的个体的 CD4 计数轨迹模型,对从血清转换开始监测 5 年的大型假设人群的计数序列进行了模拟。首次计数<350 个/μL 的时间被定义为 ART 开始时间。该模拟被用于评估上述因素对这些时间的影响。如果在模拟期间基础轨迹下降小于 200 个/μL,则在没有以前观察到的计数<350 个/μL 的情况下,将患者的 ART 起始视为“非常晚”。

结果

对于 12、6、4 和 3 个月的测量,中位数开始时间分别为血清转换后 48、36、32 和 30 个月,非常晚开始 ART 的患者比例分别为 11.5%、1.6%、0.2%和 0.1%。对于 6 个月的测量,确认要求将中位数增加到 49 个月,比例增加到 8.9%。计数短期变异性的标准差变化 25%和新型技术的测量偏差±10%会使中位数时间变化±6 个月,非常晚的比例变化较小(范围为 0.5%-3.2%)。

结论

6 个月的测量似乎足以实现非常晚的 ART 的低发生率,而确认会对发生率产生不利影响。比较新型和标准测量技术的研究应特别关注排除适度的偏差,尤其是在接近治疗管理的重要阈值时。