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Invasive Disease vs Urinary Antigen-Confirmed Pneumococcal Community-Acquired Pneumonia
Adrian Ceccato1, Antoni Torres2, Catia Cilloniz2
1Department of Pneumology, Institut Clinic del Tórax, Hospital Clinic of Barcelona-Institut d'Investigacions Biomèdiques August Pi i Sunyer, University of Barcelona, SGR 911, Centro de Investigación Biomédica en Red de Enfermedades Respiratorias (CIBERES), Barcelona, Spain; Sección Neumología, Hospital Nacional Alejandro Posadas, El Palomar, Argentina.
Background:
The burden of pneumococcal disease is measured only through patients with invasive pneumococcal disease. The urinary antigen test (UAT) for pneumococcus has exhibited high sensitivity and specificity. We aimed to compare the pneumococcal pneumonias diagnosed as invasive disease with pneumococcal pneumonias defined by UAT results.
Methods:
A prospective observational study of consecutive nonimmunosuppressed patients with community-acquired pneumonia was performed from January 2000 to December 2014. Patients were stratified into two groups: invasive pneumococcal pneumonia (IPP) defined as a positive blood culture or pleural fluid culture result and noninvasive pneumococcal pneumonia (NIPP) defined as a positive UAT result with negative blood or pleural fluid culture result.
Results:
We analyzed 779 patients (15%) of 5,132, where 361 (46%) had IPP and 418 (54%) had NIPP. Compared with the patients with IPP, those with NIPP presented more frequent chronic pulmonary disease and received previous antibiotics more frequently. Patients with IPP presented more severe community-acquired pneumonia, higher levels of inflammatory markers, and worse oxygenation at admission; more pulmonary complications; greater extrapulmonary complications; longer time to clinical stability; and longer length of hospital stay compared with the NIPP group. Age, chronic liver disease, mechanical ventilation, and acute renal failure were independent risk factors for 30-day crude mortality. Neither IPP nor NIPP was an independent risk factor for 30-day mortality.
Conclusions:
A high percentage of confirmed pneumococcal pneumonia is diagnosed by UAT. Despite differences in clinical characteristics and outcomes, IPP is not an independent risk factor for 30-day mortality compared with NIPP, reinforcing the importance of NIPP for pneumococcal pneumonia.
Insights
The urinary antigen test (UAT) identifies more pneumococcal pneumonia cases than traditional methods. Invasive and non-invasive pneumococcal pneumonia show different clinical features but similar mortality risks.
Area of Science:
- Infectious Diseases
- Pulmonology
- Clinical Microbiology
Background:
- Pneumococcal disease burden is often underestimated by focusing solely on invasive cases.
- The urinary antigen test (UAT) for Streptococcus pneumoniae demonstrates high sensitivity and specificity.
- Current diagnostic approaches may not fully capture the prevalence of pneumococcal pneumonia.
Purpose of the Study:
- To compare pneumococcal pneumonias diagnosed as invasive disease versus those identified by UAT.
- To evaluate the clinical characteristics and outcomes of invasive versus non-invasive pneumococcal pneumonia.
- To assess the diagnostic utility of UAT in community-acquired pneumonia.
Main Methods:
- A prospective observational study included 5,132 non-immunosuppressed patients with community-acquired pneumonia (2000-2014).
- Patients were classified into invasive pneumococcal pneumonia (IPP) (positive blood/pleural fluid culture) and non-invasive pneumococcal pneumonia (NIPP) (positive UAT, negative cultures).
- Clinical data, complications, and 30-day mortality were analyzed.
Main Results:
- Of 5,132 patients, 779 (15%) had pneumococcal pneumonia: 361 IPP (46%) and 418 NIPP (54%).
- NIPP patients more frequently had chronic lung disease and prior antibiotic use.
- IPP was associated with more severe pneumonia, higher inflammatory markers, worse oxygenation, more complications, and longer hospital stays.
- Independent risk factors for 30-day mortality included age, chronic liver disease, mechanical ventilation, and acute renal failure.
Conclusions:
- UAT identifies a significant proportion of pneumococcal pneumonia cases.
- Despite clinical differences, IPP is not an independent predictor of 30-day mortality compared to NIPP.
- NIPP plays a crucial role in the overall burden and management of pneumococcal pneumonia.
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