Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/25589
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dc.date.accessioned2022-04-06T06:42:45Z-
dc.date.available2022-04-06T06:42:45Z-
dc.date.issued2012-04-
dc.identifier.citationGüler, E. vd. (2012). "Evaluation of a clinical pulmonary infection score in the diagnosis of ventilator-associated pneumonia". Signa Vitae, 7(1), 32-37.en_US
dc.identifier.issn1334-5605-
dc.identifier.urihttps://doi.org/10.22514/SV71.042012.6-
dc.identifier.urihttps://www.signavitae.com/articles/10.22514/SV71.042012.6-
dc.identifier.urihttps://www.mendeley.com/catalogue/d7f11c9b-cb2d-3455-bbb6-81c2a088b306/-
dc.identifier.urihttp://hdl.handle.net/11452/25589-
dc.description.abstractThe most important dilemma in the diagnosis of ventilator-associated pneumonia (VAP) based on only clinical findings is overdiagnosis. The aim of the study is to prospectively evaluate the Clinical Pulmonary Infection Score (CPIS) in relation to VAP diagnosis. Design. Prospective, in a cohort of mechanically ventilated patients. Setting. The intensive care unit of a university hospital. Patients. Fifty patients, on mechanical ventilation therapy for more than 48 hours, suspected of having VAP were enrolled in the study and bacteriologic confirmation was done by bronchoalveolar lavage (BAL) culture. Interventions. Bronchoscopy with BAL fluid culture after establishing a clinical suspicion of VAP in patients having no prior antibiotic therapy or no change in current antibiotic therapy within last three days before BAL. CPIS scores during diagnosis were 6+/-2 (3-9) (median+/-QR, maximum-minimum) and it was 7+/-2 (2-9) at the 72nd hour, in 41 cases with a diagnosis of VAP. In cases with no diagnosis of VAP, the CPIS scores were found to be 6+/-2 (4-8) and 5+/-3 (2-7), respectively. There was no significant difference between the VAP group and the non-VAP group at diagnosis, but was significant at 72nd hour (respectively, p=0.551 and p=0.025). CPIS scores during diagnosis were 6+/-3 (4-8) (median+/-QR, maximum-minimum) and 7+/-4 (2-8) at the 72nd hour, in 14 cases with a diagnosis of early-onset VAP. In cases with a diagnosis of late-onset VAP, the CPIS scores were found to be 6+/-2 (3-9) and 7+/-2 (3-9), respectively. There was no significant difference between the early-onset VAP group and the late-onset VAP group. In conclusion, the CPIS results should be evaluated carefully in the clinical setting during the diagnosis.en_US
dc.language.isoenen_US
dc.publisherMre Pressen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.rightsAtıf Gayri Ticari Türetilemez 4.0 Uluslararasıtr_TR
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectEmergency medicineen_US
dc.subjectVentilator associated pneumoniaen_US
dc.subjectCpisen_US
dc.subjectVap diagnosisen_US
dc.subjectManagementen_US
dc.subjectEpidemiologyen_US
dc.subjectCriteriaen_US
dc.subjectCulturesen_US
dc.subjectOutcomesen_US
dc.titleEvaluation of a clinical pulmonary infection score in the diagnosis of ventilator-associated pneumoniaen_US
dc.typeArticleen_US
dc.identifier.wos000304326700006tr_TR
dc.identifier.scopus2-s2.0-84860998082tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Anesteziyoloji ve Reanimasyon Anabilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Mikrobiyoloji ve Enfeksiyon Hastalıkları Anabilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Göğüs Cerrahisi Anabilim Dalı.tr_TR
dc.contributor.orcid0000-0003-4820-2288tr_TR
dc.identifier.startpage32tr_TR
dc.identifier.endpage37tr_TR
dc.identifier.volume7tr_TR
dc.identifier.issue1tr_TR
dc.relation.journalSigna Vitaeen_US
dc.contributor.buuauthorGüler, Emre-
dc.contributor.buuauthorKahveci, Ferda-
dc.contributor.buuauthorAkalın, Halis-
dc.contributor.buuauthorSınırtaş, Melda-
dc.contributor.buuauthorBayram, Sami-
dc.contributor.buuauthorÖzcan, Berin-
dc.contributor.researcheridAAG-9356-2021tr_TR
dc.contributor.researcheridAAU-8952-2020tr_TR
dc.subject.wosEmergency medicineen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.wos.quartileQ4en_US
dc.contributor.scopusid57198133515tr_TR
dc.contributor.scopusid6602405968tr_TR
dc.contributor.scopusid57207553671tr_TR
dc.contributor.scopusid6505818048tr_TR
dc.contributor.scopusid8705640100tr_TR
dc.contributor.scopusid6603825848tr_TR
dc.subject.scopusVentilator Associated Pneumonia; Intensive Care Units; Piperacillin Plus Tazobactamen_US
dc.subject.emtreeAntibiotic agenten_US
dc.subject.emtreeAdulten_US
dc.subject.emtreeAgeden_US
dc.subject.emtreeAntibiotic therapyen_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeArtificial ventilationen_US
dc.subject.emtreeBronchoscopyen_US
dc.subject.emtreeClinical articleen_US
dc.subject.emtreeClinical effectivenessen_US
dc.subject.emtreeClinical evaluationen_US
dc.subject.emtreeClinical pulmonary infection scoreen_US
dc.subject.emtreeControlled clinical trialen_US
dc.subject.emtreeControlled studyen_US
dc.subject.emtreeDiagnostic accuracyen_US
dc.subject.emtreeDrug effecten_US
dc.subject.emtreeEarly diagnosisen_US
dc.subject.emtreeFemaleen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeIntensive care uniten_US
dc.subject.emtreeLung lavageen_US
dc.subject.emtreeMaleen_US
dc.subject.emtreePredictive valueen_US
dc.subject.emtreeScoring systemen_US
dc.subject.emtreeSensitivity and specificityen_US
dc.subject.emtreeTreatment durationen_US
dc.subject.emtreeVentilator associated pneumoniaen_US
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