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肾移植受者侵袭性肺曲霉病的发生和死亡的危险因素。

Risk factors for development and mortality of invasive pulmonary Aspergillosis in kidney transplantation recipients.

机构信息

Division of Infectious Diseases, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, 81 Irwon-ro, Gangnam-gu, Seoul, 06531, Republic of Korea.

Division of Infectious Diseases, Department of Medicine, Korea University Ansan Hospital, Korea University Medicine, Ansan-si, Gyeonggi-do, Republic of Korea.

出版信息

Eur J Clin Microbiol Infect Dis. 2020 Aug;39(8):1543-1550. doi: 10.1007/s10096-020-03871-2. Epub 2020 Apr 11.

Abstract

Invasive pulmonary aspergillosis (IPA) is a high mortality opportunistic infection among kidney transplant recipients. This study assessed the risk factors and outcomes of IPA after KT. A retrospective study was conducted at a tertiary-care referral hospital in Korea. Electronic medical records of patients diagnosed with IPA after KT between February 1995 and March 2015 were reviewed. The control patients comprised two patients who received KT before and after each IPA case. Twenty-six cases were diagnosed with IPA among 1963 recipients at a median of 58 years old. The most common cause of end-stage renal disease was diabetic nephropathy. The median time to diagnosis was 161 days. Delayed graft function was associated with the development of IPA. The overall 12-week mortality rate of IPA was 57.5%. Serum GM level ≥ 2 and BAL GM level ≥ 5 were associated with 12-week mortality in the Kaplan-Meier survival analyses. Approximately half of IPA in KT recipients developed during the late posttransplant period (> 6 months), especially after treatment for acute rejection. Careful monitoring for IPA is required in patients with delayed graft function, DM, and who received rejection therapy. Higher serum and BAL GM were associated with 12-week mortality.

摘要

侵袭性肺曲霉病(IPA)是肾移植受者中死亡率较高的机会性感染。本研究评估了肾移植后 IPA 的危险因素和结局。在韩国的一家三级转诊医院进行了一项回顾性研究。对 1995 年 2 月至 2015 年 3 月期间诊断为肾移植后 IPA 的患者的电子病历进行了回顾。对照组由每位 IPA 病例前后接受肾移植的两名患者组成。在 1963 名受者中,有 26 例诊断为 IPA,中位年龄为 58 岁。导致终末期肾病的最常见病因是糖尿病肾病。中位诊断时间为 161 天。延迟移植物功能与 IPA 的发生有关。IPA 的总 12 周死亡率为 57.5%。在 Kaplan-Meier 生存分析中,血清 GM 水平≥2 和 BAL GM 水平≥5 与 12 周死亡率相关。大约一半的 IPA 在肾移植受者中发生在移植后晚期(>6 个月),尤其是在接受急性排斥反应治疗后。对于延迟移植物功能、DM 和接受排斥反应治疗的患者,需要仔细监测 IPA。较高的血清和 BAL GM 与 12 周死亡率相关。

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