无HIV、移植或癌症患者的乙氏肺囊虫肺炎:错过预防的机会。

IF 1.8
Gregory J Challener, Mohamad El Labban, Amjad N Kanj, Gabriel E Ortiz Jaimes, Sarah B Leung, Jay H Ryu, Misbah Baqir
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引用次数: 0

摘要

背景:耶氏肺囊虫肺炎(PJP)是危及生命的免疫功能低下的患者。对于没有HIV、移植或癌症的免疫抑制患者的PJP预防尚无共识。方法:我们回顾性地回顾了1990年至2020年在梅奥诊所诊断的成人免疫抑制PJP患者的电子健康记录。HIV、实体器官移植或癌症患者被排除在外。人口统计数据、治疗方法和结果手工提取。结果:免疫抑制最常见的适应症是类风湿关节炎(19.7%)、血管炎(18.1%)和与结缔组织病无关的间质性肺疾病(ILD)(17.6%)。尽管PJP风险较高,但86.0%的患者未接受PJP预防。皮质类固醇是最常用的免疫抑制剂(84.5%),64.4%的患者接受高剂量治疗。非生物疾病缓解类抗风湿药物使用率为49.7%,包括甲氨蝶呤(51.0%)、硫唑嘌呤(22.9%)和羟氯喹(11.5%)。生物制剂占25.4%,主要是利妥昔单抗(59.2%)和英夫利昔单抗(22.4%)。76.7%的患者住院;70.3%需要重症监护病房(ICU), 46.6%需要机械通气。住院死亡率总体为30.4%,通气患者为53.6%。死亡预测因子包括ILD[比值比(OR), 4.61;ICU住院(OR, 3.60; 95% CI, 1.19-11.08)和呼吸机使用(OR, 3.46; 95% CI, 1.30-9.79)。生物制剂使用与较低的死亡几率相关(OR, 0.34; 95% CI, 0.11-0.89)。结论:我们队列中的大多数患者没有接受PJP预防,结果很差,死亡率很高。需要标准化的风险分层和预防方案来改善结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pneumocystis jirovecii Pneumonia in Patients Without HIV, Transplant, or Cancer: Missed Opportunities for Prevention.

Background: Pneumocystis jirovecii pneumonia (PJP) is life-threatening for immunocompromised patients. No consensus exists on PJP prophylaxis for immunosuppressed patients without HIV, transplant, or cancer.

Methods: We retrospectively reviewed the electronic health records of adult immunosuppressed patients with PJP diagnosed between 1990 and 2020 at Mayo Clinic. Patients with HIV, solid organ transplants, or cancer were excluded. Demographic data, treatments, and outcomes were manually abstracted.

Results: The most common indications for immunosuppression were rheumatoid arthritis (19.7%), vasculitis (18.1%), and interstitial lung disease (ILD) not related to connective tissue disease (17.6%). Despite having high risk of PJP, 86.0% of patients did not receive PJP prophylaxis. Corticosteroids were the most common immunosuppressive agent used (84.5%), with 64.4% of patients receiving high-dose treatment. Nonbiologic disease-modifying antirheumatic drugs were used for 49.7%, including methotrexate (51.0%), azathioprine (22.9%), and hydroxychloroquine (11.5%). Biologics were prescribed for 25.4%, primarily rituximab (59.2%) and infliximab (22.4%). Hospitalization occurred for 76.7% of patients; 70.3% required intensive care unit (ICU) admission, and 46.6% received mechanical ventilation. The in-hospital mortality rate was 30.4% overall and 53.6% for patients on ventilation. Predictors of death included ILD [odds ratio (OR), 4.61; 95% CI, 1.75-13.00], ICU admission (OR, 3.60; 95% CI, 1.19-11.08), and ventilator use (OR, 3.46; 95% CI, 1.30-9.79). Biologic use was associated with lower odds of death (OR, 0.34; 95% CI, 0.11-0.89).

Conclusions: Most patients in our cohort did not receive PJP prophylaxis, and outcomes were poor with high mortality rates. Standardized risk stratification and prophylaxis protocols are needed to improve outcomes.

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