Invasive Disease vs Urinary Antigen-Confirmed Pneumococcal Community-Acquired Pneumonia

dc.contributor.authorCeccato, Adrian
dc.contributor.authorTorres Martí, Antoni
dc.contributor.authorCillóniz, Catia
dc.contributor.authorAmaro, Rosanel
dc.contributor.authorGabarrús, Albert
dc.contributor.authorPolverino, Eva
dc.contributor.authorPrina, Elena
dc.contributor.authorGarcia Vidal, Carolina
dc.contributor.authorMuñoz Conejero, Eva
dc.contributor.authorMéndez, Cristina
dc.contributor.authorCifuentes, Isabel
dc.contributor.authorPuig de la Bellacasa, Jordi
dc.contributor.authorMenéndez, Rosario
dc.contributor.authorNiederman, Michael S.
dc.date.accessioned2019-11-12T10:14:44Z
dc.date.available2019-11-12T10:14:44Z
dc.date.issued2017-06
dc.date.updated2019-11-12T10:14:45Z
dc.description.abstractBackground: 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.
dc.format.extent9 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec675111
dc.identifier.idimarina2804709
dc.identifier.issn0012-3692
dc.identifier.pmid28093269
dc.identifier.urihttps://hdl.handle.net/2445/144559
dc.language.isoeng
dc.publisherAmerican College of Chest Physicians
dc.relation.isformatofVersió postprint del document publicat a: https://doi.org/10.1016/j.chest.2017.01.005
dc.relation.ispartofChest, 2017, vol. 151, num. 6, p. 1311-1319
dc.relation.urihttps://doi.org/10.1016/j.chest.2017.01.005
dc.rights(c) American College of Chest Physicians, 2017
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.sourceArticles publicats en revistes (Medicina)
dc.subject.classificationPneumònia adquirida a la comunitat
dc.subject.classificationInfeccions per pneumococs
dc.subject.otherCommunity-acquired pneumonia
dc.subject.otherPneumococcal Infections
dc.titleInvasive Disease vs Urinary Antigen-Confirmed Pneumococcal Community-Acquired Pneumonia
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/acceptedVersion

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