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基于mNGS检测的重症肺炎病原学特征与危险因素分析

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目的 分析重症肺炎患者肺泡灌洗液宏基因组二代测序(mNGS)下重症肺炎的病原学特征与预测价值.方法 将159例肺炎患者根据重症肺炎的诊断标准分为重症组(55例)与非重症组(104例),收集患者入院后的一般临床资料、血液检验数据及肺泡灌洗液mNGS、痰培养结果,对比两组患者感染的病原学特征;单因素分析筛选出两组患者比较差异有统计学意义的指标,再进行Logistic回归分析筛选重症肺炎的危险因素,绘制受试者工作特征曲线(ROC)和曲线下面积(AUC),以评价各指标对重症肺炎的预测价值.结果 与痰培养比较,mNGS在两组患者的病原体检出率均显著增高(P<0.000 1),肺泡灌洗液mNGS的总检出率高于痰培养(x2=318.001,P<0.000 1);mNGS可检出鹦鹉热衣原体、钩端螺旋体、恙虫病东方体等非典型病原体;重症肺炎组所有检出病原体中混合感染占(60%),非重症肺炎组所有检出病原体中混合感染占(29%);单因素分析显示,重症组与非重症组性别、年龄、吸烟、病原体类型、血红蛋白、淋巴细胞百分比、中性粒细胞百分比、红细胞分布宽度(RDW)、降钙素原(PCT)、C-反应蛋白、白蛋白、D-二聚体比较,差异具有统计学意义(P<0.05);多因素logistic回归分析提示,病原体类型、RDW与PCT是重症肺炎独立危险因素(P<0.05);单一指标预测时,PCT的AUC最大,为0.856,灵敏度87.27%、特异性66.35%;联合预测时,PCT与RDW联合AUC为0.818,灵敏度76.36%、特异性为76.92%.结论 mNGS技术检测病原体阳性率较高,对于非典型病原体检测具有特殊价值,重症肺炎组更容易患混合类病原体感染,PCT单独或与RDW联合检测是预测重症肺炎较好的指标.
Etiological characteristics of severe pneumonia based on mNGS detection and its risk factors analysis
Objective To analyze etiological characteristics of severe pneumonia based on metagenomic next-generation sequencing(mNGS)of pulmonary alveolar lavage fluid of patients with severe pneumonia and predictive value.Methods A total of 159 patients with pneumonia were divided into severe group(55 cases)and non-severe group(104 cases)according to the diagnostic criteria of severe pneumonia.General clinical data,blood test data,mNGS detection of alveolar lavage fluid and sputum culture results of patients were collected after admission.Etiological characteristics were compared between two groups.Univariate analysis was used to screen the indicators with statistically significant differences between two groups of the patients.logistic regression analysis was performed to screen risk factors for severe pneumonia.Receiver operating characteristic(ROC)curve and area under the curve(AUC)were used to evaluate the predictive value of each indicator for severe pneumonia.Results When compared to sputum culture,pathogen detection rates of mNGS in both groups were significantly increased(P<0.000 1).The total detection rate of mNGS in alveolar lavage fluid was higher in two groups than that in sputum culture(x2=318.001,P<0.000 1).mNGS could detect chlamydia ptactaci,leptospirosis,Orientia tsutsugamushi and other atypical pathogens.In severe pneumonia group,mixed infections accounted for 60%of all detected pathogens,while mixed infections accounted for 29%of all detected pathogens in non-severe pneumonia group.Univariate analysis showed that there were statistically significant differences in gender,age,smoking,pathogen type,hemoglobin,lymphocyte percentage,neutrophil percentage,red blood cell distribution width(RDW),procalcitonin(PCT),C-reactive protein,albumin,and D-dimer between severe and non-severe groups(P<0.05).Multivariate logistic regression analysis showed that pathogen type,RDW,and PCT were independent risk factors for severe pneumonia(P<0.05).When predicting with a single indicator,PCT had the highest AUC of 0.856,with a sensitivity of 87.27%and specificity of 66.35%.When predicting with the combination,the AUC of combined PCT and RDW was 0.818,with a sensitivity of 76.36%and specificity of 76.92%.Conclusion mNGS technology has a high positive rate for pathogen detection and a special value for atypical pathogen detection.Severe pneumonia group is more prone to mixed pathogen infections.PCT alone or in combination with RDW detection is a good indicator for predicting severe pneumonia.

severe pneumoniametagenomic next-generation sequencingetiologyerythrocyte widthprocalcitonintype of infection

王坤利、罗璐灵、刘刚、廖婷婷、王美娟、杨然、胡系伟

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贵州医科大学附属医院全科医学科,贵州贵阳 550004

贵州医科大学研究生院,贵州贵阳 550004

贵州医科大学附属医院呼吸与危重症医学科,贵州贵阳 550004

重症肺炎 mNGS 病原学 红细胞宽度 降钙素原 感染类型

2024

贵州医科大学学报
贵阳医学院

贵州医科大学学报

CSTPCD
影响因子:0.827
ISSN:2096-8388
年,卷(期):2024.49(11)