支气管肺泡灌洗液宏基因二代测序检测肺部感染病原体的临床应用

Clinical application of metagenomic next-generation sequencing from bronchoalveolar in detection of pathogens causing pulmonary infections

  • 摘要:
    目的 探讨支气管肺泡灌洗液宏基因二代测序(mNGS)在肺部感染病原体检测中的应用。
    方法 回顾性分析2023年1月-2024年1月阜阳市第二人民医院收治的98例肺部感染患者的临床资料, BALF均行mNGS和传统病原学检测, 以临床综合判断(采用肺泡灌洗液、痰液、血液等结合评估)为金标准, 评估mNGS和传统病原学检测在肺部感染病原学诊断的差异, 并比较肺部感染合并肺部基础疾病、重症与非重症及感染类型中的病原体检出率, 分析对临床调整抗感染方案的影响。
    结果 mNGS检测肺部感染病原体阳性率为88.78%高于传统病原学(P<0.001), mNGS检测耗时为(16.57±2.64)h短于传统病原学(P<0.05);有、无基础疾病患者采用mNGS检测阳性率为93.02%、85.45%, 高于传统病原学检测(P<0.05);重症、非重症患者采用mNGS检测阳性率为91.43%、87.30%, 高于传统病原学检测(P<0.05)。87例mNGS检测阳性患者共检出122株病原菌, 未检测出EB病毒;54例传统病原学检测阳性患者共检出75株病原菌, 未检测出奈瑟菌、根霉菌属、细小病毒和鹦鹉热衣原体;mNGS对细菌检出率为58.20%高于传统病原学(P=0.034)。mNGS检测对单一型感染、混合感染的检出率为85.51%、93.10%高于传统病原学检测(P<0.05)。在肺部感染中, mNGS指导了53.06%的患者调整抗感染方案, 有基础肺病组的患者中有60.47%调整抗感染方案, 无基础肺病中有47.27%调整抗感染方案(P=0.194);重症者中有68.57%调整抗感染治疗方案, 非重症者中有44.44%调整抗感染方案(P=0.022)。
    结论 肺泡灌洗液mNGS可发现部分少见病原体, 提高肺部感染病原体检出率, 并可指导临床调整抗感染策略。

     

    Abstract:
    OBJECTIVE To investigate the application of metagenomic next-generation sequencing (mNGS) of bronchoalveolar lavage fluid (BALF) in the detection of pathogens of pulmonary infection.
    METHODS The clinical data of 98 patients with pulmonary infections admitted to NO. 2 People′s Hospital of Fuyang City from Jan. 2023 to Jan. 2024 were retrospectively analyzed, mNGS and traditional pathogenicity test were performed in BALF, and comprehensive clinical judgment (using a combination of alveolar lavage fluid, sputum, blood, etc. to assess) was used as the gold standard to evaluate the differences between mNGS and traditional pathogenicity tests in the pathogenic diagnosis of pulmonary infections, compare the pathogen detection rates in pulmonary infections complicated with underlying diseases, severe and non-severe illness and different infection types, and to analyze the impact on clinical adjustment of anti-infection regimens.
    RESULTS The positive detection rate of mNGS for pulmonary infection pathogens was 88.78%, higher than that of traditional pathogenology (P < 0.001). The time required for mNGS was (16.57±2.64) h, shorter than that of traditional pathogenology (P < 0.05). The positive detection rates of mNGS in patients with and without underlying diseases were 93.02% and 85.45%, respectively, higher than those of traditional pathogenology (P < 0.05). The positive detection rates of mNGS in severe and non-severe patients were 91.43% and 87.30%, respectively, higher than those of traditional pathogenology (P < 0.05). A total of 122 strains of pathogens were detected in 87 patients with positive mNGS tests, and EB virus was not detected. A total of 75 strains of pathogens were detected in 54 patients with positive traditional pathogenetic tests, and Neisseria, Rhizopus, parvovirus, and Chlamydia psittaci were not detected. The detection rate of bacteria by mNGS was 58.20%, higher than that by traditional pathogenetic tests (P=0.034). The detection rates of mNGS test for monotypic infection and mixed infection were 85.51% and 93.10%, respectively, higher than those by traditional pathogenetic test (P < 0.05). In pulmonary infections, mNGS guided adjustment of anti-infective treatment in 53.06% of patients, 60.47% of those in the group with underlying pulmonary disease, and 47.27% of those without underlying disease (P=0.194). Among severe cases, 68.57% had their anti-infective treatment plan adjusted, compared to 44.44% of non-severe patients (P=0.022).
    CONCLUSION The mNGS of BALF idenfies some rare pathogens, improves the detection rate of pathogens in pulmonary infections, and may guide the clinical adjustment of anti-infective strategies.

     

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