Future cardiology · 2019
Dilated cardiomyopathy in a pediatric population: etiology and outcome predictors - a single-center experience.
СтатьяНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
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Ошибки и ограничения
История · было → стало
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Ciuca Cristina, Ragni Luca, Hasan Tammam, Balducci Anna, Angeli Emanuela, Prandstraller Daniela, Egidy-Assenza Gabriele, Donti Andrea, Bonvicini Marco, Gargiulo Gaetano D
Аннотация
AIM: The aim of the study was to assess predictors of outcome in patients hospitalized for dilated cardiomyopathy (DCM) and severe left ventricular dysfunction. Patients & methods: 83 pediatric patients hospitalized for heart failure due to DCM with coexistent left ventricular dysfunction were enrolled.
RESULTS: Overall, 5-year survival free from heart transplantation was 69.8%. Normalization of left ventricular function was achieved in 39.8% of patients during follow-up: younger age, less necessity of inotropic support and other than idiopathic DCM predicted left ventricular function, while familial history for cardiac disease or sudden death and inotropic support during hospitalization were associated with poorer outcome.
CONCLUSION: Almost 40% of patients with DCM experienced a complete normalization of cardiac function. Outcome was extremely variable according to the type of DCM.
RESULTS: Overall, 5-year survival free from heart transplantation was 69.8%. Normalization of left ventricular function was achieved in 39.8% of patients during follow-up: younger age, less necessity of inotropic support and other than idiopathic DCM predicted left ventricular function, while familial history for cardiac disease or sudden death and inotropic support during hospitalization were associated with poorer outcome.
CONCLUSION: Almost 40% of patients with DCM experienced a complete normalization of cardiac function. Outcome was extremely variable according to the type of DCM.
Предметные рубрики MeSH
BiostatisticsCardiomyopathy, DilatedChild, PreschoolElectrocardiographyFemaleFollow-Up StudiesHeart Defects, CongenitalHumansItalyMaleMuscular DystrophiesPrevalencePrognosisProspective StudiesRegistriesRisk AssessmentRisk FactorsStroke VolumeSurvival RateVentricular Function, LeftVentricular Remodeling