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Published on: April 2, 2014
Inflammatory rebound and postinfectious inflammatory response in children with pleural infection: A single-center
Clément Poirault1, Alice Hadchouel1, Charlotte Roy1
1Department of Pediatric Pulmonology and Allergology, University Hospital Necker-Enfants Malades, AP-HP, Paris, France.
Insights
An inflammatory rebound occurred in 38% of children with pleural infection (PI). This suggests corticosteroids may benefit children with PI if given early, between days 2 and 5.
Area of Science:
- Pediatric Infectious Diseases
- Critical Care Medicine
- Inflammation Research
Background:
- Pleural inflammation is central to pediatric pleural infection (PI).
- Corticosteroid therapy is being explored for PI, but optimal timing and patient selection are unclear.
- Investigating inflammatory trajectories in pediatric PI is crucial for treatment optimization.
Purpose of the Study:
- To analyze inflammatory patterns in children diagnosed with pleural infection (PI).
- To identify factors associated with disease progression and treatment response.
- To inform the timing of potential corticosteroid interventions in pediatric PI.
Main Methods:
- Retrospective single-center study of pediatric PI cases (3 months to 17 years, 11 months).
- Included patients with PI caused by Streptococcus pyogenes, Streptococcus pneumoniae, and Staphylococcus aureus.
- Defined inflammatory rebound as a C-reactive protein (CRP) increase of ≥50 mg/L after an initial decrease of ≥50 mg/L.
Main Results:
- Fifty-three pediatric PI cases were analyzed.
- An inflammatory rebound was observed in 20 patients (38%), particularly those with S. pyogenes.
- Patients experiencing inflammatory rebound had prolonged fever and longer hospital stays.
Conclusions:
- Nearly 40% of pediatric PI patients exhibited an inflammatory rebound.
- This rebound may represent an early postinfectious inflammatory response.
- Corticosteroids might be most effective in pediatric PI if administered early (Days 2-5).
Introduction:
As pleural inflammation plays a central role in pleural infection (PI), corticosteroids are increasingly being considered as a potential therapy. However, the timing of treatment and the identification of patients who might benefit most remain unresolved. The aim of this study was therefore to investigate the inflammatory trajectories of children with PI.
Methods:
This retrospective single-center study included children aged 3 months to 17 years and 11 months hospitalized for PI due to Streptococcus pyogenes, Streptococcus pneumonia, and Staphylococcus aureus over 10 years. An inflammatory rebound was defined biologically as a reincrease in C-reactive protein (CRP) of at least 50 mg/L after an initial decrease in CRP of at least 50 mg/L.
Results:
We included 53 cases of PI, including 16 due to S. pyogenes, 27 due to S. pneumonia, and 10 due to S. aureus. An inflammatory rebound occurred in 20 patients (38%) after a median of 4.5 (3-6) days. This inflammatory rebound occurred in 9 (56%) children with S. pyogenes, 8 (30%) children with S. pneumonia, and 3 (30%) children with S. aureus. Children with an inflammatory rebound also had a higher rate of persistent fever after Day 7 and a longer length of stay (p = .01 for both).
Conclusion:
We postulate that the inflammatory rebound identified in nearly 40% of our patients corresponds to an early postinfectious inflammatory response, and thus that corticosteroids may be most beneficial for children with PI if administered early (between Days 2 and 5).
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