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mTOR 抑制剂与实体器官移植后肺囊虫肺炎的风险:系统评价和荟萃分析。

m-TOR inhibitors and risk of Pneumocystis pneumonia after solid organ transplantation: a systematic review and meta-analysis.

机构信息

Department of Clinical Pharmacy, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.

Liver Transplantation Research Center, Imam Khomeini Hospital Complex, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Eur J Clin Pharmacol. 2019 Nov;75(11):1471-1480. doi: 10.1007/s00228-019-02730-0. Epub 2019 Aug 3.

Abstract

PURPOSE

Although there is controversy, some evidences proposed increased risk of post-transplant Pneumocystis carinii pneumonia (PCP) in patients receiving mammalian target of rapamycin (mTOR) inhibitors. This study aimed to examine the association between m-TOR inhibitors and the risk of developing PCP in solid organ transplant (SOT) recipients.

METHODS

A comprehensive search was performed to find the eligible studies that investigated the incidence of PCP in patients treated with mTOR inhibitors after SOT. Random effect model was applied for meta-analysis.

RESULTS

Combination of 15 effect sizes showed a significant positive association between mTOR inhibitor administration and the risk of PCP (OR = 1.90, 95%CIs = 1.44, 2.75). There was no heterogeneity between studies (I = 3.5%). Subgroup analysis revealed increased risk of PCP after the first year of transplantation (P < 0.001).

CONCLUSION

In conclusion, administration of mTOR inhibitors is a potential risk factor for late-onset PCP after SOT. Targeted PCP prophylaxis based on recipients' risk factors rather universal prophylaxis may lessen the risk.

摘要

目的

尽管存在争议,但一些证据表明,接受雷帕霉素靶蛋白(mTOR)抑制剂治疗的患者发生移植后卡氏肺孢子虫肺炎(PCP)的风险增加。本研究旨在探讨 mTOR 抑制剂与实体器官移植(SOT)受者发生 PCP 的风险之间的关系。

方法

进行了全面检索,以寻找调查 SOT 后接受 mTOR 抑制剂治疗的患者发生 PCP 发生率的合格研究。应用随机效应模型进行荟萃分析。

结果

15 项效应量的组合表明,mTOR 抑制剂的使用与 PCP 的风险之间存在显著的正相关(OR=1.90,95%CI=1.44,2.75)。研究之间没有异质性(I=3.5%)。亚组分析显示,移植后第一年发生 PCP 的风险增加(P<0.001)。

结论

总之,mTOR 抑制剂的使用是 SOT 后迟发性 PCP 的潜在危险因素。基于受者危险因素的靶向 PCP 预防而非普遍预防可能会降低风险。

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