儿童腺病毒与肺炎支原体共感染重症肺炎早期预测因素的病例对照研究OA
Early predictors of severe pneumonia in children with adenovirus and mycoplasma pneumoniae coinfection:a case-control study
背景 人腺病毒(human adenovirus,HAdV)和肺炎支原体(Mycoplasma pneumoniae,MP)是儿童社区获得性肺炎(community-acquired pneumonia,CAP)的常见病原体.两者共感染可显著增加重症肺炎的发生风险,重症常导致不良的临床结局.目的 分析儿童HAdV与MP共感染肺炎的临床特征,并筛选重症的早期预测因素.设计 病例对照研究.方法 纳入2018年9月1日至2024年5月1日在天津市儿童医院住院、年龄在29 d至18岁、存在HAdV和MP共感染的CAP患儿,排除合并其他明确病原体感染、存在慢性气道疾病或严重基础疾病以及入院后24 h内已符合重症肺炎诊断标准的患儿.将研究对象分为重症组(入院后≥24 h诊断为重症肺炎)和普通组.将入院24 h内的症状、体征、实验室及影像学指标中单因素分析P<0.05的变量纳入多因素Logistic回归分析,筛选HAdV和MP共感染重症肺炎的独立早期预测因素,并采用受试者工作特征(ROC)曲线、校准曲线及Hosmer-Lemeshow检验评价联合预测效能.主要结局指标 儿童HAdV和MP共感染重症肺炎的早期预测指标.结果 225例HAdV和MP共感染肺炎患儿的中位发病年龄为7.0(5.0,9.0)岁,其中男童121例(53.8%).普通组80例(35.6%)、重症组145例(64.4%).与普通组相比,重症组热峰、塑形性支气管炎发生率、湿啰音及呼吸音减低比例均更高,热程延长;重症组中性粒细胞与淋巴细胞比值(neutrophil-lymphocyte ratio,NLR)、系统免疫炎症指数(systemic immune-inflammation index,SII)、CRP、ESR、IL-6、乳酸脱氢酶(lactate dehydrogenase,LDH)、ALT、D-二聚体水平均高于普通组;重症组影像学显示肺不张、大片肺实变发生率均高于普通组;P均<0.05.多因素Logistic回归分析结果显示,肺不张、大片肺实变、热峰(连续变量)、ESR>40 mm·h-1及LDH>400 U·L-1均为HAdV和MP共感染患儿发生重症肺炎的独立危险因素(P均<0.05).ROC曲线分析结果显示对重症患儿具有良好的区分能力,曲线下面积(area under the curve,AUC)为0.801(95%CI:0.741~0.861),校准曲线显示模型预测风险与实际观察风险总体一致,Hosmer-Lemeshow拟合优度检验显示模型拟合良好(χ²=10.19,P=0.252),提示模型具有较好的校准度.结论 肺不张、大片肺实变、热峰升高、ESR>40 mm·h⁻¹及LDH>400 U·L⁻¹是HAdV和MP共感染儿童发生重症肺炎的独立早期预测因素.ROC曲线分析显示热峰39.9℃为预测重症肺炎的参考截断值.上述因素均可于患儿入院24 h内获得,有助于住院早期识别重症高危患儿,为临床及时干预提供参考依据.
Background Human adenovirus(HAdV)and Mycoplasma pneumoniae(MP)are common pathogens of community-acquired pneumonia(CAP)in children.HAdV-MP coinfection may substantially increase the risk of severe pneumonia,which is often associated with adverse clinical outcomes.Objective To characterize the clinical features of children with pneumonia and HAdV-MP coinfection,and identify early predictors of severe pneumonia.Design Case-control study.Methods Children aged 29 days to 18 years with CAP and HAdV-MP coinfection who were hospitalized at Tianjin Children's Hospital between September 1,2018,and May 1,2024,were enrolled.Patients with confirmed coinfection with other pathogens,chronic airway diseases or severe underlying conditions,or those who met the diagnostic criteria for severe pneumonia within 24 h of admission were excluded.Patients were classified into the severe group(diagnosed with severe pneumonia≥24 h after admission)and the non-severe group.Variables with P<0.05 in univariable analyses,including symptoms,signs,laboratory findings,and imaging findings obtained within 24 h of admission,were entered into a multivariable logistic regression model to identify independent early predictors of severe pneumonia.The predictive performance of the combined model was evaluated using receiver operating characteristic(ROC)curve analysis,calibration curves,and the Hosmer-Lemeshow goodness-of-fit test.Main Outcome Measures Early predictors of severe pneumonia in children with HAdV-MP coinfection.Results A total of 225 children with HAdV-MP coinfection were included,with a median age at disease onset of 7.0(5.0,9.0)years;121(53.8%)were boys.Eighty patients(35.6%)were classified into the non-severe group and 145(64.4%)into the severe group.Compared with the non-severe group,the severe group had a higher peak body temperature,a higher incidence of plastic bronchitis,higher proportions of patients with moist rales and decreased breath sounds,and a longer duration of fever.The severe group also had higher neutrophil-to-lymphocyte ratio(NLR),systemic immune-inflammation index(SII),C-reactive protein(CRP),erythrocyte sedimentation rate(ESR),interleukin-6(IL-6),lactate dehydrogenase(LDH),alanine aminotransferase(ALT),and D-dimer levels.On imaging,atelectasis and large-area pulmonary consolidation were more common in the severe group than in the non-severe group(all P<0.05).Multivariable logistic regression analysis identified atelectasis,large-area pulmonary consolidation,peak body temperature(continuous variable),ESR>40 mm·h-1,and LDH>400 U·L-1 as independent risk factors for severe pneumonia in children with HAdV-MP coinfection(all P<0.05).ROC curve analysis demonstrated good discrimination,with an area under the curve(AUC)of 0.801(95%CI:0.741-0.861).The calibration curve showed good agreement between predicted and observed risks,and the Hosmer-Lemeshow goodness-of-fit test indicated good model fit(χ²=10.19,P=0.252),suggesting good calibration.Conclusion Atelectasis,large-area pulmonary consolidation,higher peak body temperature,ESR>40 mm·h-1,and LDH>400 U·L-1 are independent early predictors of severe pneumonia in children with HAdV-MP coinfection.ROC analysis identified a peak temperature of 39.9℃ as the optimal cutoff value for predicting severe pneumonia.These variables can all be obtained within 24 hours of hospital admission,facilitating early identification of children at high risk for severe pneumonia and providing a basis for timely clinical intervention.
王雪琳;贠亚男;张秀青;毕莹;邹映雪
天津大学儿童医院/天津市儿童医院马场院区呼吸科 天津市儿童出生缺陷防治重点实验室 天津,300074天津大学儿童医院/天津市儿童医院马场院区呼吸科 天津市儿童出生缺陷防治重点实验室 天津,300074天津大学儿童医院/天津市儿童医院马场院区呼吸科 天津市儿童出生缺陷防治重点实验室 天津,300074天津大学儿童医院/天津市儿童医院马场院区呼吸科 天津市儿童出生缺陷防治重点实验室 天津,300074天津大学儿童医院/天津市儿童医院马场院区呼吸科 天津市儿童出生缺陷防治重点实验室 天津,300074
儿童腺病毒肺炎支原体共感染重症肺炎早期预测因素
ChildrenHuman adenovirusMycoplasma pneumoniaeCoinfectionSevere pneumoniaEarly predictors
《中国循证儿科杂志》 2026 (4)
260-265,6
天津市医学重点学科建设资助项目:TJYXZDXK-3-016B
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