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类风湿关节炎患者接受甲氨蝶呤治疗后发生肺孢子菌肺炎的相关因素:一项单中心回顾性研究。

Factors Associated with Pneumocystis jirovecii Pneumonia in Patients with Rheumatoid Arthritis Receiving Methotrexate: A Single-center Retrospective Study.

机构信息

Department of Rheumatology, Seirei Hamamatsu General Hospital, Japan.

Department of General Internal Medicine, Seirei Hamamatsu General Hospital, Japan.

出版信息

Intern Med. 2022 Apr 1;61(7):997-1006. doi: 10.2169/internalmedicine.8205-21. Epub 2021 Sep 11.

Abstract

Objective To investigate the risk factors for the development of Pneumocystis jirovecii pneumonia (PCP) in patients with rheumatoid arthritis (RA) undergoing methotrexate (MTX) therapy. Methods This single-center retrospective cohort study included consecutive patients with RA who received MTX for at least one year. The study population was divided into PCP and non-PCP groups, depending on the development of PCP, and their characteristics were compared. We excluded patients who received biologic disease-modifying anti-rheumatic drugs (DMARDs), Janus kinase inhibitors, and anti-PCP drugs for prophylaxis. Results Thirteen patients developed PCP, and 333 did not develop PCP. At the initiation of MTX therapy, the PCP group had lower serum albumin levels, a higher frequency of pulmonary disease and administration of DMARDs, and received a higher dosage of prednisolone (PSL) than the non-PCP group. A multivariate Cox regression analysis revealed that the concomitant use of PSL [hazard ratio (HR) 5.50, p=0.003], other DMARDs (HR 5.98, p=0.002), and serum albumin <3.5 mg/dL (HR 4.30, p=0.01) were risk factors for the development of PCP during MTX therapy. Patients with these risk factors had a significantly higher cumulative probability of developing PCP than patients who lacked these risk factors. Conclusion Clinicians should pay close attention to patients with RA who possess risk factors for the development of PCP during MTX therapy.

摘要

目的

探讨接受甲氨蝶呤(MTX)治疗的类风湿关节炎(RA)患者发生肺孢子菌肺炎(PCP)的危险因素。

方法

本单中心回顾性队列研究纳入了接受 MTX 治疗至少 1 年的连续 RA 患者。根据是否发生 PCP,将研究人群分为 PCP 组和非 PCP 组,并比较两组患者的特征。我们排除了接受生物 DMARDs、Janus 激酶抑制剂和抗 PCP 药物预防的患者。

结果

13 例患者发生了 PCP,333 例患者未发生 PCP。在开始 MTX 治疗时,PCP 组的血清白蛋白水平较低,肺病和 DMARD 治疗的频率较高,并且接受的泼尼松龙(PSL)剂量较高。多变量 Cox 回归分析显示,PSL 联合使用(风险比 [HR] 5.50,p=0.003)、其他 DMARDs(HR 5.98,p=0.002)和血清白蛋白<3.5mg/dL(HR 4.30,p=0.01)是 MTX 治疗期间发生 PCP 的危险因素。有这些危险因素的患者发生 PCP 的累积概率明显高于没有这些危险因素的患者。

结论

临床医生应密切关注接受 MTX 治疗的 RA 患者,警惕其发生 PCP 的风险因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c5f/9038457/85682dcb9ce3/1349-7235-61-0997-g001.jpg

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