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风湿性疾病患者接受高危免疫抑制剂治疗时,肺孢子菌肺炎(PJP)的预防模式。

Pneumocystis jirovecii pneumonia (PJP) prophylaxis patterns among patients with rheumatic diseases receiving high-risk immunosuppressant drugs.

机构信息

Division of Rheumatology, University of California San Francisco, United States; Veterans Affairs Medical Center, 4150 Clement St., Mailstop 111R, San Francisco, CA 94121 United States; Center for Healthcare Value, Philip R. Lee Institute for Health Policy Studies, University of California, San Francisco, United States.

Division of Rheumatology, University of California San Francisco, United States.

出版信息

Semin Arthritis Rheum. 2019 Jun;48(6):1087-1092. doi: 10.1016/j.semarthrit.2018.10.018. Epub 2018 Nov 3.

Abstract

INTRODUCTION/OBJECTIVES: Pneumocystis jirovecii pneumonia (PJP) is a rare but potentially fatal opportunistic infection; however, consensus varies around which conditions or medications confer a level of risk sufficient to justify antibiotic prophylaxis for PJP. We used electronic health record (EHR) data to assess the current patterns of PJP prophylaxis, PJP outcomes, and prophylaxis-related adverse events among patients with rheumatic diseases who were receiving high-risk immunosuppressant drugs.

METHODS

Data derive from the EHR of a large health system. We included new immunosuppressant users with diagnoses of vasculitis, myositis, or systemic lupus erythematosus. We calculated the proportion of patients who received PJP prophylaxis for each diagnosis and drug combination. We also calculated the number of PJP infections and the number of antibiotic adverse drug events (ADEs) per patient-year of exposure.

RESULTS

We followed 316 patients for 23.2 + /- 14.2 months. Overall, 124 (39%) of patients received prophylactic antibiotics for PJP. At least 25% of patients with the highest risk conditions (e.g. vasculitis) or highest risk immunosuppressants (e.g. cyclophosphamide) did not receive PJP prophylaxis. We found no cases of PJP infection over 640 patient-years of follow up, including among those not receiving prophylaxis, and an overall incidence rate of ADEs of 2.2% per patient-year.

CONCLUSIONS

PJP prophylaxis for patients with rheumatic conditions is inconsistent, with one quarter of patients who have high risk conditions or high risk immunosuppressants not receiving prophylaxis. However, given extremely low rates of PJP infection, but detectable ADEs to prophylactic antibiotics, our findings suggest that evidence to guide more personalized risk assessments are needed to inform PJP prophylaxis.

摘要

简介/目的:卡氏肺孢子虫肺炎(PJP)是一种罕见但具有潜在致命性的机会性感染;然而,对于哪些疾病或药物会导致足够的风险水平,需要用抗生素预防 PJP,目前尚无共识。我们使用电子健康记录(EHR)数据评估正在接受高风险免疫抑制剂药物治疗的风湿性疾病患者中,目前预防卡氏肺孢子虫肺炎(PJP)的模式、PJP 结果和与预防相关的不良事件。

方法

数据来源于大型医疗系统的电子健康记录。我们纳入了新使用免疫抑制剂且患有血管炎、肌炎或系统性红斑狼疮的患者。我们计算了每种诊断和药物组合中接受 PJP 预防的患者比例。我们还计算了每位患者接受暴露于免疫抑制剂药物治疗的 PJP 感染人数和抗生素不良药物事件(ADE)人数。

结果

我们对 316 名患者进行了 23.2±14.2 个月的随访。总体而言,124 名(39%)患者接受了 PJP 预防抗生素治疗。有最高风险疾病(如血管炎)或最高风险免疫抑制剂(如环磷酰胺)的患者中,至少有 25%的患者未接受 PJP 预防。在 640 多患者年的随访中,我们未发现 PJP 感染病例,包括未接受预防的患者,且 ADE 的总发生率为每年每患者 2.2%。

结论

风湿性疾病患者的 PJP 预防不一致,有四分之一的高风险疾病或高风险免疫抑制剂的患者未接受预防。然而,鉴于 PJP 感染率极低,但可检测到预防性抗生素的 ADE,我们的研究结果表明,需要有证据来指导更个性化的风险评估,以确定 PJP 的预防策略。

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