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Published on: February 24, 2023
Clinical Features and Management Strategies in Children With Mycoplasma Pneumoniae
Tamara Garcia1, Todd A Florin2, Jan Leonard1
1Department of Pediatrics, Children's Hospital Colorado and University of Colorado, Aurora, CO.
Insights
Mycoplasma pneumoniae (Mp) community-acquired pneumonia (CAP) in children presents similarly to non-Mp CAP but may involve older children. Polymerase chain reaction testing is key for diagnosis, as clinical outcomes are comparable.
Area of Science:
- Pediatric infectious diseases
- Respiratory infections
- Microbiology
Background:
- Mycoplasma pneumoniae (Mp) is a frequent cause of community-acquired pneumonia (CAP) in children.
- Differentiating Mp CAP from other causes clinically is challenging.
Purpose of the Study:
- To compare clinical presentation, management, and outcomes of pediatric Mp CAP versus non-Mp CAP.
- To identify factors distinguishing Mp CAP in children.
Main Methods:
- Prospective multicenter cohort study of children (≥2 months) with CAP.
- Exclusion of children with complex chronic conditions.
- Polymerase chain reaction (PCR) testing for Mp detection.
- Analysis of clinical outcomes including hospitalization, PICU admission, and rehospitalization.
Main Results:
- 38 of 415 children (7.4%) had Mp detected.
- Children with Mp CAP were older and more likely to receive azithromycin or prior antibiotics.
- No statistical differences in symptom prevalence, lab values, or radiographic findings.
- Children with Mp CAP had a 33% shorter hospital stay.
Conclusions:
- Clinical presentation and outcomes for pediatric Mp CAP are similar to non-Mp CAP.
- PCR testing is crucial for accurate Mp CAP diagnosis.
- While symptom duration may be longer, clinical outcomes do not significantly differ.
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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