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dc.contributor.authorSabaz, Muhammed Nurullah
dc.contributor.authorAkın, Alper
dc.contributor.authorBilici, Meki
dc.contributor.authorDemir, Fikri
dc.contributor.authorTüre, Mehmet
dc.contributor.authorBalık, Hasan
dc.date.accessioned2021-09-23T10:56:23Z
dc.date.available2021-09-23T10:56:23Z
dc.date.issued2019en_US
dc.identifier.citationSabaz, M. N., Akın, A., Bilici, M., Demir, F., Türe, M. ve Balık, H. (2019). Factors affecting mortality in children with dilated cardiomyopathy. Turkish Journal of Pediatrics, 61(4), 485-492.en_US
dc.identifier.issn0041-4301
dc.identifier.urihttp://www.turkishjournalpediatrics.org/abstract.php?id=2014
dc.identifier.urihttps://hdl.handle.net/11468/7750
dc.descriptionPMID:31990464
dc.description.abstractDilated cardiomyopathy (DCMP) is a heart disease with high mortality rates that is often seen in children. Genetic and infectious reasons are primary in the etiology. The aim of this study was to investigate the etiology of DCMP and the parameters predicting mortality. A retrospective examination was made of 37 patients diagnosed with DCMP between January 2012 and October 2016. Data were recorded from the patient files of age, gender, complaints on presentation, findings of the physical examination, laboratory test results, echocardiography and electrocardiography findings at the time of diagnosis. These parameters were then compared between the surviving and non-surviving patients. The patients comprised 21 males with a mean age of 27.50±50 months. Diagnosis was made at the age of <12 months in 67.6% patients. Within mean 8 months of diagnosis, 16.2% of the patients were lost to mortality and 83.8% of the patients survived. In 83.3% of the non-surviving patients and in 29% of the surviving patients, sinus tachycardia was present at the time of diagnosis (p=0.023). Corrected QT (QTc) at the time of diagnosis was longer in the non-surviving patients (p=0.007). On ECG, the rate of ST-T wave change was higher in the non-surviving patients (80% vs. 17.8%, p=0.012). In conclusion, a significant proportion of the patients were diagnosed below the age of one year. In the non-surviving patients, as sinus tachycardia and ischaemic changes on ECG were seen more often and the QTc was longer, these findings could be considered to be predictors of mortality.en_US
dc.language.isoenen_US
dc.publisherTurkish Journal of Pediatricsen_US
dc.relation.ispartofTurkish Journal of Pediatricsen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectChilden_US
dc.subjectDilated cardiomyopathyen_US
dc.subjectMyocarditisen_US
dc.titleFactors affecting mortality in children with dilated cardiomyopathyen_US
dc.typeArticleen_US
dc.identifier.volume61en_US
dc.identifier.issue4en_US
dc.identifier.startpage485en_US
dc.identifier.endpage492en_US
dc.departmentDicle Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Çocuk Sağlığı ve Hastalıkları Ana Bilim Dalıen_US
dc.authorid0000000315879559en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.wosWOS:000508895200003en_US
dc.identifier.scopus2-s2.0-85078355764en_US
dc.identifier.trdizinidhttps://search.trdizin.gov.tr/yayin/detay/353127en_US
dc.identifier.pmid31990464en_US
dc.institutionauthorSabaz, Muhammed Nurullah
dc.institutionauthorAkın, Alper
dc.institutionauthorBilici, Meki
dc.institutionauthorDemir, Fikri
dc.institutionauthorTüre, Mehmet
dc.institutionauthorBalık, Hasan
dc.identifier.doi10.24953/turkjped.2019.04.003en_US
dc.identifier.scopusqualityQ3en_US
dc.identifier.wosqualityQ4en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.indekslendigikaynakTR-Dizinen_US


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