Clinical Features and Management Strategies in Children With Mycoplasma Pneumoniae

医学 四分位间距 社区获得性肺炎 肺炎支原体 儿科 肺炎 阿奇霉素 前瞻性队列研究 队列 儿科重症监护室 逻辑回归 队列研究 内科学 抗生素 生物 微生物学
作者
Tamara García‐Salum,Todd A. Florin,Jan Leonard,Samir S. Shah,Richard M. Ruddy,Rebecca Wallihan,Ankita P. Desai,Sherman J. Alter,Osama El Assal,Sarah Marzec,Meghan Keaton,Ki Wook Yun,Amy L. Leber,Asunción Mejías,Daniel M. Cohen,Octavio Ramilo,Lilliam Ambroggio
出处
期刊:Pediatric emergency care [Lippincott Williams & Wilkins]
卷期号:41 (4): 305-310 被引量:4
标识
DOI:10.1097/pec.0000000000003338
摘要

Objective: 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. Methods: 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. Results: 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). Conclusion: 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.
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