Prevalence and Etiology of Community-acquired Pneumonia in Immunocompromised Patients

dc.contributor.authorPasquale, Marta Francesca Di
dc.contributor.authorSotgiu, Giovanni
dc.contributor.authorGramegna, Andrea
dc.contributor.authorRadovanovic, Dejan
dc.contributor.authorTerraneo, Silvia
dc.contributor.authorReyes, Luis F.
dc.contributor.authorRupp, Jan
dc.contributor.authorGonzález del Castillo, Juan
dc.contributor.authorBlasi, Francesco
dc.contributor.authorAliberti, Stefano
dc.contributor.authorRestrepo, Marcos I.
dc.contributor.authorCillóniz, Catia
dc.contributor.authorTorres Martí, Antoni
dc.contributor.authorGLIMP Investigators
dc.date.accessioned2019-07-09T10:58:35Z
dc.date.available2019-08-23T05:10:19Z
dc.date.issued2018-08-23
dc.date.updated2019-07-02T19:30:21Z
dc.description.abstractBackground: The correct management of immunocompromised patients with pneumonia is debated. We evaluated the prevalence, risk factors, and characteristics of immunocompromised patients coming from the community with pneumonia. Methods: We conducted a secondary analysis of an international, multicenter study enrolling adult patients coming from the community with pneumonia and hospitalized in 222 hospitals in 54 countries worldwide. Risk factors for immunocompromise included AIDS, aplastic anemia, asplenia, hematological cancer, chemotherapy, neutropenia, biological drug use, lung transplantation, chronic steroid use, and solid tumor. Results: At least 1 risk factor for immunocompromise was recorded in 18% of the 3702 patients enrolled. The prevalences of risk factors significantly differed across continents and countries, with chronic steroid use (45%), hematological cancer (25%), and chemotherapy (22%) the most common. Among immunocompromised patients, community-acquired pneumonia (CAP) pathogens were the most frequently identified, and prevalences did not differ from those in immunocompetent patients. Risk factors for immunocompromise were independently associated with neither Pseudomonas aeruginosa nor non–community-acquired bacteria. Specific risk factors were independently associated with fungal infections (odds ratio for AIDS and hematological cancer, 15.10 and 4.65, respectively; both P = .001), mycobacterial infections (AIDS; P = .006), and viral infections other than influenza (hematological cancer, 5.49; P < .001). Conclusions: Our findings could be considered by clinicians in prescribing empiric antibiotic therapy for CAP in immunocompromised patients. Patients with AIDS and hematological cancer admitted with CAP may have higher prevalences of fungi, mycobacteria, and noninfluenza viruses.
dc.format.extent12 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idimarina5651482
dc.identifier.issn1537-6591
dc.identifier.pmid31222287
dc.identifier.urihttps://hdl.handle.net/2445/136778
dc.language.isoeng
dc.publisherOxford University Press
dc.relation.isformatofReproducció del document publicat a: https://dx.doi/10.1093/cid/ciy723
dc.relation.ispartofClinical Infectious Diseases, 2019, vol. 68, num. 9, p. 1482-1493
dc.relation.urihttps://dx.doi/10.1093/cid/ciy723
dc.rights(c) Pasquale et al., 2019
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.sourceArticles publicats en revistes (IDIBAPS: Institut d'investigacions Biomèdiques August Pi i Sunyer)
dc.subject.classificationPneumònia adquirida a la comunitat
dc.subject.classificationEtiologia
dc.subject.otherCommunity-acquired pneumonia
dc.subject.otherEtiology
dc.titlePrevalence and Etiology of Community-acquired Pneumonia in Immunocompromised Patients
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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