Garcia Tamara, Florin Todd A, Leonard Jan, Shah Samir S, Ruddy Richard M, Wallihan Rebecca, Desai Ankita P, Alter Sherman, El-Assal Osama, Marzec Sarah, Keaton Meghan, Yun Ki Wook, Leber Amy L, Mejias Asuncion, Cohen Daniel M, Ramilo Octavio, Ambroggio Lilliam
Department of Pediatrics, Children's Hospital Colorado and University of Colorado, Aurora, CO.
Department of Pediatrics, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL.
Pediatr Emerg Care. 2025 Apr 1;41(4):305-310. doi: 10.1097/PEC.0000000000003338. Epub 2025 Feb 17.
Mycoplasma pneumoniae (Mp) is the most detected bacterial pathogen in children with community-acquired pneumonia (CAP). Our primary objective was to compare the clinical presentation, clinical management, and outcomes of children with and without Mp CAP across 6 children's hospitals.
Eligible children were 2 months old or above and diagnosed with CAP in a prospective multicenter cohort study between October 1, 2015 and June 31, 2018. Children were excluded if they had complex chronic conditions. Children were tested for Mp via polymerase chain reaction assays. Clinical outcomes included hospitalization, and among hospitalized children length of stay, pediatric intensive care unit (PICU) admission, and rehospitalization within 8 weeks of discharge. Negative binomial and logistic regression were performed to determine the association of Mp with clinical outcomes.
Of the 415 children included, 38 (7.4%) had Mp detected. Children with Mp were older [median interquartile range age 8.8 (3.1, 13.0) vs. 4.6 (interquartile range: 2, 8.2) y], more likely to receive azithromycin (68.4% vs. 22.2%) and more likely to receive antibiotics in the prior 2 weeks (63.2% vs. 35.7%) versus those with non-Mp CAP. Children with Mp CAP were 33% less likely to stay in the hospital for an additional day (95% CI: 0.48-0.94).
Children with Mp CAP are more likely to have a longer duration of symptoms, but there are no statistical differences in symptom prevalence, laboratory values, or radiographic findings. There was no statistical difference in clinical outcomes for children with Mp CAP suggesting that clinical presentation and outcomes are similar between Mp and non-Mp CAP. Polymerase chain reaction testing for Mp CAP may be the only way to discriminate between non-Mp and Mp CAP.
肺炎支原体(Mp)是社区获得性肺炎(CAP)患儿中检测到的最常见细菌病原体。我们的主要目的是比较6家儿童医院中患Mp CAP和未患Mp CAP患儿的临床表现、临床管理及预后。
在一项前瞻性多中心队列研究中,纳入年龄2个月及以上且诊断为CAP的合格患儿,研究时间为2015年10月1日至2018年6月31日。患有复杂慢性病的患儿被排除。通过聚合酶链反应检测患儿是否感染Mp。临床结局包括住院情况,以及住院患儿的住院时间、入住儿科重症监护病房(PICU)情况和出院后8周内再次住院情况。采用负二项回归和逻辑回归分析来确定Mp与临床结局之间的关联。
纳入的415名患儿中,38名(7.4%)检测出Mp。与未患Mp CAP的患儿相比,患Mp的患儿年龄更大[年龄中位数(四分位间距)8.8(3.1,13.0)岁 vs. 4.6(四分位间距:2,8.2)岁],更有可能接受阿奇霉素治疗(68.4% vs. 22.2%),且在前2周内更有可能接受抗生素治疗(63.2% vs. 35.7%)。患Mp CAP的患儿住院时间延长一天的可能性降低33%(95%置信区间:0.48 - 0.94)。
患Mp CAP的患儿症状持续时间更有可能更长,但在症状发生率、实验室检查值或影像学表现方面无统计学差异。患Mp CAP患儿的临床结局无统计学差异,这表明Mp CAP与非Mp CAP的临床表现和结局相似。Mp CAP的聚合酶链反应检测可能是区分非Mp CAP和Mp CAP的唯一方法。