首页|特发性炎性肌病合并肺孢子菌肺炎患者的临床特征及预后分析

特发性炎性肌病合并肺孢子菌肺炎患者的临床特征及预后分析

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目的 分析特发性炎性肌病(IIM)合并肺孢子菌肺炎(PJP)患者的临床特征并探究其预后相关因素.方法 回顾性分析2014年1月至2022年12月在北京协和医院住院接受诊疗的IIM合并PJP患者临床资料.共纳入IIM合并PJP患者58例,其中男性19例(32.9%)、女性39例(67.1%),年龄26~79(56.3±12.1)岁.根据临床结局将研究对象分为存活组(21例)及死亡组(37例),通过Cox回归模型分析IIM合并PJP患者的预后相关因素.结果 死亡组抗黑色素瘤分化相关基因-5(MDA5)抗体阳性、呼吸衰竭、合并院内获得性肺炎、采用二线PJP治疗、卡泊芬净治疗的患者多于存活组(均P<0.05);死亡组患者的原发病起病至感染起病时间、糖皮质激素治疗至感染起病时间、免疫抑制剂治疗至感染起病时间均显著短于存活组(均P<0.05);死亡组患者外周血中性粒细胞比例及肌酸激酶高于存活组(均P<0.05),淋巴细胞计数及比例、血小板、最低白蛋白、NK细胞计数、T细胞计数、CD8+T细胞计数低于存活组(均P<0.05).多因素分析后发现,仅抗MDA5抗体阳性(HR=3.54,P<0.05,95%CI:1.27~9.89),合并口腔念珠菌感染(HR=2.62,P<0.05,95%CI:1.07~6.43)和血小板降低(HR=5.00,P<0.01,95%CI:1.88~13.32)是IIM合并PJP患者生存的独立危险因素.结论 本组IIM患者合并PJP以中年女性为主,病死率高达63.8%.抗MDA5抗体阳性、口腔念珠菌感染、血小板降低可能是IIM合并PJP患者预后的独立危险因素.
Clinical characteristics and prognostic analysis of concurrent Pneumocystis jirovecii pneumonia in patients with idiopathic inflammatory myopathy
Objective To describe the clinical characteristics and to explore the prognostic factors of concurrent pneumocystis jirovecii pneumonia(PJP)in patients with idiopathic inflammatory myopathy(IIM).Methods We retrospectively enrolled consecutive IIM patients diagnosed with PJP at our center between January 2014 and December 2022.Fifty-eight IIM-PJP patients were enrolled in our study,with the age of 26-79(56.3±12.1)years.There were 19 males(32.9%)and 39 females(67.1%).The participants were classified into survival group(21 patients)and non-survival group(37 patients)according to the clinical outcome.Cox regression models were used to analyze the prognostic factors.Results Compared with the survival group,there were more patients with anti-melanoma differentiation-associated gene(MDA5)positive,respiratory failure,hospital-acquired pneumonia,second-line PJP treatment,and caspofungin treatment in non-survival group(P<0.05).Meanwhile,the time from onset of IIM,corticosteroid therapy,and immunosuppressant medication to diagnosis of PJP was significantly shorter in non-survival patients than survival patients(P<0.05).Additionally,non-survival patients had higher neutrophil percentage and creatine kinase(P<0.05),and lower lymphocyte count and percentage,platelets,minimal albumin,NK cell count,T cell count,and CD8+T cell count(P<0.05).Multivariate analysis showed that anti-MDA5 positive(HR=3.54,P<0.05,95%CI:1.27-9.89),oral candidiasis infection(HR=2.62,P<0.05,95%CI:1.07-6.43)and thrombocytopenia(HR=5.00,P<0.01,95%CI:1.88-13.32)were independent risk factors for IIM-PJP patients.Conclusions Middle-aged females were the main IIM-PJP in our group,and the mortality rate was 63.8%.Anti-MDA5 antibody positive,oral candidiasis infection,and thrombocytopenia were independent survival risk factors for them.

Pneumonia,PneumocystisPrognosisIdiopathic inflammatory myopathy

石钰洁、陈茹萱、徐凯、邵池、黄慧

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中国医学科学院北京协和医学院北京协和医院呼吸与危重症医学科,北京 100730

中国医学科学院北京协和医学院北京协和医院放射科,北京 100730

肺炎,肺囊虫性 预后 肌炎

2025

中华结核和呼吸杂志
中华医学会

中华结核和呼吸杂志

北大核心
影响因子:2.692
ISSN:1001-0939
年,卷(期):2025.48(1)