宏基因组二代测序技术诊断非HIV感染的耶氏肺孢子菌重症肺炎的临床价值

Value of mNGS in clinical diagnosis of Pneumocystis jirovecii-induced severe pneumonia in non-HIV infection patients

  • 摘要:
    目的 探讨宏基因组二代测序技术(mNGS)在非人类免疫缺陷病毒(HIV)感染的耶氏肺孢子菌重症肺炎患者诊断及预后中的应用价值。
    方法 对2023年1月-2024年7月期间, 于北京电力医院重症监护病房住院、经mNGS确诊的17例非HIV感染耶氏肺孢子菌重症肺炎患者开展回顾性分析, 详细收集患者基本信息及转归资料。依据患者入住重症监护病房(ICU)后28 d生存状况划分为死亡组与存活组, 分析影响非HIV耶氏肺孢子菌重症肺炎预后的相关因素。
    结果 共纳入17例非HIV感染的耶氏肺孢子菌重症肺炎患者, 其中男性10例, 平均年龄(70.65±12.67)岁。12例患者合并免疫功能低下疾病, 从发病到确诊耶氏肺孢子菌重症肺炎的平均时间为6 d。除1例仅检出耶氏肺孢子菌外, 余患者为混合感染。经治疗后, 9例患者死亡(52.94%)。相比于存活组, 死亡组患者年龄更大(P=0.082), 高血压病比例更高(P=0.050), 发病至确诊时间更长(P=0.010), 需要机械通气的患者例数更多(P=0.057)。
    结论 非HIV感染的耶氏肺孢子菌重症肺炎患者多合并免疫功能低下疾病, 以混合感染为主, 病死率较高, mNGS能够快速为该类患者提供病原学依据。既往高血压病史、较长的发病至确诊时间是非HIV感染的耶氏肺孢子菌重症肺炎患者预后不良的危险因素。

     

    Abstract:
    OBJECTIVE To explore the application value of metagenomic next-generation sequencing (mNGS) in the diagnosis and prognosis of patients with non-human immunodeficiency virus (HIV)-infected severe Pneumocystis jirovecii pneumonia (PJP).
    METHODS A retrospective analysis was conducted on 17 patients with non-HIV-infected severe PJP diagnosed by mNGS who were admitted to the intensive care unit (ICU) of Beijing Electric Power Hospital from Jan. 2023 to Jul. 2024. Detailed data on the patients′ basic information and outcomes was collected. Patients were divided into the death group and the survival group based on their 28-day survival status after admission to the ICU, and relevant factors affecting the prognosis of non-HIV-infected severe PJP were analyzed.
    RESULTS A total of 17 patients with non-HIV-infected severe PJP were enrolled, including 10 males, with an average age of (70.65±12.67) years. Twelve patients were complicated with immunocompromised diseases, and the average time from onset to diagnosis of severe pneumonia caused by P. jirovecii was 6 days. Except for 1 patient who was only infected with P. jirovecii, the remaining patients had mixed infections. After treatment, 9 patients died (52.94%). Compared with the survival group, patients in the death group were older (P=0.082), had high proportion with hypertension (P=0.050), had a long time from onset to diagnosis (P=0.010) and had more patients requiring mechanical ventilation (P=0.057).
    CONCLUSIONS Patients with non-HIV-infected severe PJP often have comorbidities that compromise their immune function, primarily presenting with mixed infections and a higher mortality rate. mNGS can rapidly provide etiological basis for such patients. A previous history of hypertension and a longer time from onset and diagnosis are risk factors for poor prognosis in patients with non-HIV-infected severe PJP.

     

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