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Recurrent invasive pneumococcal disease in children: underlying clinical conditions, and immunological and
Laia Alsina1, Maria G Basteiro2, Hector D de Paz3
1Allergy and Clinical Immunology Department, Hospital Sant Joan de Déu, University of Barcelona, Barcelona, Spain; Functional Unit of Immunology, Hospital Sant Joan de Déu and Hospital Clinic. Barcelona, Spain.
Insights
Recurrent invasive pneumococcal disease (IPD) in children is rare. Reinfection often has identifiable risk factors, while relapses, especially with pleuropneumonia, suggest a persistent infection.
Area of Science:
- Pediatric Infectious Diseases
- Microbiology
- Immunology
Background:
- Invasive pneumococcal disease (IPD) can recur in children, necessitating differentiation between relapse and reinfection.
- Understanding risk factors for recurrent IPD is crucial for effective management and prevention.
Purpose of the Study:
- To evaluate clinical, immunological, and microbiological characteristics of recurrent IPD in children.
- To differentiate between relapse and reinfection in recurrent IPD cases.
- To identify specific risk factors associated with both relapse and reinfection.
Main Methods:
- Retrospective evaluation of pediatric patients (<18 years) with recurrent IPD from 2004-2011.
- IPD defined by clinical findings and pathogen detection in sterile body fluids.
- Recurrent IPD defined as ≥2 episodes ≥1 month apart; relapse vs. reinfection distinguished by isolate analysis.
Main Results:
- 10 out of 593 IPD patients (1.7%) experienced recurrent IPD.
- Meningitis and empyema were the most frequent forms of recurrent IPD.
- Relapse (0.5%) occurred in 3 patients with recurrent empyema (clone ST306); reinfection (1.2%) in 7 patients, with identifiable risk factors in 5 (CSF leak, chemotherapy, MyD88 mutation).
Conclusions:
- Recurrent IPD in children is uncommon.
- Reinfection is associated with identifiable risk factors in nearly 80% of cases.
- Recurrent IPD presenting as pleuropneumonia is typically a relapse of infection.
Purpose:
Clinical, immunological and microbiological characteristics of recurrent invasive pneumococcal disease (IPD) in children were evaluated, differentiating relapse from reinfection, in order to identify specific risk factors for both conditions.
Methods:
All patients <18 years-old with recurrent IPD admitted to a tertiary-care pediatric center from January 2004 to December 2011 were evaluated. An episode of IPD was defined as the presence of clinical findings of infection together with isolation and/or pneumococcal DNA detection by Real-Time PCR in any sterile body fluid. Recurrent IPD was defined as 2 or more episodes in the same individual at least 1 month apart. Among recurrent IPD, we differentiated relapse (same pneumococcal isolate) from reinfection.
Results:
593 patients were diagnosed with IPD and 10 patients died. Among survivors, 23 episodes of recurrent IPD were identified in 10 patients (1.7%). Meningitis was the most frequent form of recurrent IPD (10 episodes/4 children) followed by recurrent empyema (8 episodes/4 children). Three patients with recurrent empyema caused by the same pneumococcal clone ST306 were considered relapses and showed high bacterial load in their first episode. In contrast, all other episodes of recurrent IPD were considered reinfections. Overall, the rate of relapse of IPD was 0.5% and the rate of reinfection 1.2%. Five out of 7 patients with reinfection had an underlying risk factor: cerebrospinal fluid leak (n = 3), chemotherapy treatment (n = 1) and a homozygous mutation in MyD88 gene (n = 1). No predisposing risk factors were found in the remainder.
Conclusions:
recurrent IPD in children is a rare condition associated with an identifiable risk factor in case of reinfection in almost 80% of cases. In contrast, recurrent IPD with pleuropneumonia is usually a relapse of infection.
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