Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/22728
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dc.date.accessioned2021-11-19T08:46:36Z-
dc.date.available2021-11-19T08:46:36Z-
dc.date.issued2006-
dc.identifier.citationKöksal, N. vd. (2006). ''Nonbronchoscopic bronchoalveolar lavage for diagnosing ventilator-associated pneumonia in newborns''. Turkish Journal of Pediatrics, 48(3), 213-220.en_US
dc.identifier.issn0041-4301-
dc.identifier.urihttps://www.turkishjournalpediatrics.org/uploads/pdf_TJP_339.pdf-
dc.identifier.urihttp://hdl.handle.net/11452/22728-
dc.description.abstractThe appropriate treatment of ventilator-associated pneumonia (VAP) must be based on accurate diagnosis, which can be done by microbiological examination of the samples obtained from the respiratory tract by nonbronchoscopic bronchoalveolar lavages (NB-BAL). This study was designed to determine the effectiveness of NB-BAL in diagnosing VAP in newborns. Two hundred and seven NB-BAL samples were obtained from 145 intubated neonates for microbiologic and cytologic evaluation of the distal air-way. The NB-BAL samples were processed for microscopic quantification of the polymorphonuclear cells (PMN) containing intracellular bacteria (ICB) and quantitative culture (positive threshold, 10(5) cfu/ml). VAP was defined as a new, progressive, or persistent (>24 hrs) infiltrate on the chest radiograph, with two or more of the following criteria: a) macroscopically purulent tracheal secretions, b) fever or hypothermia, c) leukocytosis or leukopenia, and d) worsening of respiratory status with a Pa O-2/F IO2 ratio of <240. Colonization was defined as mechanical ventilation for more than seven days, no signs of infection, and isolation of the same bacteria species in two previously obtained NB-BAL samples. Of the 145 neonates, 40 (27.5%) were infected and 12 (8.3%) were colonized. Forty-four patients (30%) developed VAP according to diagnostic categories based on clinical and radiologic criteria. Forty newborns with VAP (90%) had positive NB-BAL culture. The sensitivity, specificity, and positive and negative predictive values of NB-BAL fluid culture for VAP diagnosis were 90%, 90%, 70%, and 97%, respectively. The percentage of ICB was significantly higher in newborns with VAP. The presence of ICB in 2% or more on Giemsa-stained smears corresponded to a sensitivity of 94%, specificity of 83%, positive predictive value of 94%, and negative predictive value of 83%. The sensitivity and specificity of combination of ICB and NB-BAL quantitative culture in diagnostic samples were 94% and 90%, respectively. The positive and negative predictive values were 71% and 98%. In our study, the presence of leukocytes in the NB-BAL fluid smear of infants with VAP was higher than that of the colonized babies (84%, 26%). This difference was statistically significant (p<0.0001). The sensitivity and specificity of PMNs in NB-BAL fluid for the diagnosis were 86% and 75%, respectively, and the positive and negative predictive values were 89% and 69%. We conclude that NB-BAL lavage is well tolerated and clinically useful in mechanically ventilated newborns. These results suggest that NB-BAL fluid microscopic examination and cultures can offer a sensitive and specific means to diagnose VAP in newborns and may provide relevant information about the causative pathogens.en_US
dc.language.isoenen_US
dc.publisherTürk Milli Pediatri Derneğien_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.subjectPediatricsen_US
dc.subjectVentilator-associated pneumoniaen_US
dc.subjectSepsisen_US
dc.subjectPrematureen_US
dc.subjectMechanical ventilationen_US
dc.subjectNewbornen_US
dc.subjectNonbronchoscopic bronchoalveolar lavagen_US
dc.subjectFluiden_US
dc.subjectAccuracyen_US
dc.subjectRisk-factorsen_US
dc.subjectNosocomial pneumoniaen_US
dc.subjectProtected specimen brushen_US
dc.subject.meshSensitivity and specificityen_US
dc.subject.meshRespiration, artificialen_US
dc.subject.meshProspective studiesen_US
dc.subject.meshPredictive value of testsen_US
dc.subject.meshBronchoalveolar lavageen_US
dc.subject.meshPneumonia, bacterialen_US
dc.subject.meshMaleen_US
dc.subject.meshInfant, newbornen_US
dc.subject.meshHumansen_US
dc.subject.meshFemaleen_US
dc.subject.meshCross infectionen_US
dc.subject.meshChi-square distributionen_US
dc.subject.meshBronchoalveolar lavage fluiden_US
dc.titleNonbronchoscopic bronchoalveolar lavage for diagnosing ventilator-associated pneumonia in newbornsen_US
dc.typeArticleen_US
dc.identifier.wos000242293400006tr_TR
dc.identifier.scopus2-s2.0-33750706525tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Pediatri Anabilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Enfeksiyon Hastalıkları ve Mikrobiyoloji Anabilim Dalı.tr_TR
dc.identifier.startpage213tr_TR
dc.identifier.endpage220tr_TR
dc.identifier.volume48tr_TR
dc.identifier.issue3tr_TR
dc.relation.journalTurkish Journal of Pediatricsen_US
dc.contributor.buuauthorKöksal, Nilgün-
dc.contributor.buuauthorHacımustafaoğlu, Mustafa-
dc.contributor.buuauthorÇelebi, Solmaz-
dc.contributor.buuauthorÖzakın, Cüneyt-
dc.indexed.trdizinTrDizintr_TR
dc.identifier.pubmed17172064tr_TR
dc.subject.wosPediatricsen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubmeden_US
dc.wos.quartileQ4en_US
dc.contributor.scopusid7003323615tr_TR
dc.contributor.scopusid6602154166tr_TR
dc.contributor.scopusid7006095295tr_TR
dc.contributor.scopusid57200678942tr_TR
dc.subject.scopusVentilator Associated Pneumonia; Intensive Care Units; Piperacillin Plus Tazobactamen_US
dc.subject.emtreeAntibiotic agenten_US
dc.subject.emtreeVentilator associated pneumoniaen_US
dc.subject.emtreeTrachea mucusen_US
dc.subject.emtreeThorax radiographyen_US
dc.subject.emtreeTherapy effecten_US
dc.subject.emtreeStenotrophomonas maltophiliaen_US
dc.subject.emtreeStatistical significanceen_US
dc.subject.emtreeStaphylococcus epidermidisen_US
dc.subject.emtreeStaphylococcus aureusen_US
dc.subject.emtreeSmearen_US
dc.subject.emtreeSensitivity and specificityen_US
dc.subject.emtreeRadiodiagnosisen_US
dc.subject.emtreeSeudomonas aeruginosaen_US
dc.subject.emtreePredictionen_US
dc.subject.emtreePolymorphonuclear cellen_US
dc.subject.emtreeNewbornen_US
dc.subject.emtreeMicrobiological examinationen_US
dc.subject.emtreeMaleen_US
dc.subject.emtreeMajor clinical studyen_US
dc.subject.emtreeLung minute volumeen_US
dc.subject.emtreeLung lavageen_US
dc.subject.emtreeLung infiltrateen_US
dc.subject.emtreeLower respiratory tracten_US
dc.subject.emtreeLeukopeniaen_US
dc.subject.emtreeLeukocytosisen_US
dc.subject.emtreeKlebsiella pneumoniaeen_US
dc.subject.emtreeIntubationen_US
dc.subject.emtreeHypothermiaen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeGiemsa stainen_US
dc.subject.emtreeFeveren_US
dc.subject.emtreeFemaleen_US
dc.subject.emtreeEdwardsiella ictalurien_US
dc.subject.emtreeDisease durationen_US
dc.subject.emtreeDiagnostic valueen_US
dc.subject.emtreeControlled studyen_US
dc.subject.emtreeColony forming uniten_US
dc.subject.emtreeClinical featureen_US
dc.subject.emtreeCell counten_US
dc.subject.emtreeCandida albicansen_US
dc.subject.emtreeBacterium isolationen_US
dc.subject.emtreeBacterium identificationen_US
dc.subject.emtreeBacterium detectionen_US
dc.subject.emtreeBacterium cultureen_US
dc.subject.emtreeBacterial colonizationen_US
dc.subject.emtreeArtificial ventilationen_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeArterial oxygen tensionen_US
dc.subject.emtreeAcinetobacter baumanniien_US
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