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在病毒学抑制的人类免疫缺陷病毒患者中不预防原发性卡氏肺孢子虫肺炎:COHERE 中一项实用试验的模拟。

Withholding Primary Pneumocystis Pneumonia Prophylaxis in Virologically Suppressed Patients With Human Immunodeficiency Virus: An Emulation of a Pragmatic Trial in COHERE.

机构信息

Department of Infectious Diseases, Bern University Hospital, Inselspital, University of Bern, Bern, Switzerland.

Department of Medical Statistics, London School of Hygiene and Tropical Medicine, London, United Kingdom.

出版信息

Clin Infect Dis. 2021 Jul 15;73(2):195-202. doi: 10.1093/cid/ciaa615.

DOI:10.1093/cid/ciaa615
PMID:32448894
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8516510/
Abstract

BACKGROUND

Using data from the COHERE collaboration, we investigated whether primary prophylaxis for pneumocystis pneumonia (PcP) might be withheld in all patients on antiretroviral therapy (ART) with suppressed plasma human immunodeficiency virus (HIV) RNA (≤400 copies/mL), irrespective of CD4 count.

METHODS

We implemented an established causal inference approach whereby observational data are used to emulate a randomized trial. Patients taking PcP prophylaxis were eligible for the emulated trial if their CD4 count was ≤200 cells/µL in line with existing recommendations. We compared the following 2 strategies for stopping prophylaxis: (1) when CD4 count was >200 cells/µL for >3 months or (2) when the patient was virologically suppressed (2 consecutive HIV RNA ≤400 copies/mL). Patients were artificially censored if they did not comply with these stopping rules. We estimated the risk of primary PcP in patients on ART, using the hazard ratio (HR) to compare the stopping strategies by fitting a pooled logistic model, including inverse probability weights to adjust for the selection bias introduced by the artificial censoring.

RESULTS

A total of 4813 patients (10 324 person-years) complied with eligibility conditions for the emulated trial. With primary PcP diagnosis as an endpoint, the adjusted HR (aHR) indicated a slightly lower, but not statistically significant, different risk for the strategy based on viral suppression alone compared with the existing guidelines (aHR, .8; 95% confidence interval, .6-1.1; P = .2).

CONCLUSIONS

This study suggests that primary PcP prophylaxis might be safely withheld in confirmed virologically suppressed patients on ART, regardless of their CD4 count.

摘要

背景

利用来自 COHERE 合作组织的数据,我们研究了是否可以对所有接受抗逆转录病毒治疗(ART)且血浆人类免疫缺陷病毒(HIV)RNA 得到抑制(≤400 拷贝/mL)的患者停止预防性治疗卡氏肺孢子虫肺炎(PcP),而不考虑 CD4 计数。

方法

我们实施了一种既定的因果推理方法,即利用观察性数据模拟随机试验。如果患者的 CD4 计数符合现有建议,即≤200 个细胞/µL,则接受 PcP 预防治疗的患者有资格参加模拟试验。我们比较了以下两种停止预防策略:(1)当 CD4 计数>200 个细胞/µL 持续>3 个月时;或(2)当患者病毒学抑制(连续 2 次 HIV RNA ≤400 拷贝/mL)时。如果患者不遵守这些停止规则,则将其人工截尾。我们使用风险比(HR)来比较停止策略,通过拟合汇总逻辑模型来估计接受 ART 的患者发生原发性 PcP 的风险,包括逆概率权重来调整因人工截尾引入的选择偏差。

结果

共有 4813 名患者(10324 人年)符合模拟试验的入选条件。以原发性 PcP 诊断为终点,调整后的 HR(aHR)表明,仅基于病毒抑制的策略风险略低,但无统计学意义(aHR,.8;95%置信区间,.6-1.1;P=0.2)。

结论

本研究表明,在已确诊的病毒学抑制的接受 ART 的患者中,无论其 CD4 计数如何,都可以安全地停止预防性治疗卡氏肺孢子虫肺炎。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcdc/8516510/1ba28cf67085/ciaa615_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcdc/8516510/1ba28cf67085/ciaa615_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bcdc/8516510/1ba28cf67085/ciaa615_fig1.jpg

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