Patients with Single-Ventricle Physiology over the Age of 40 Years
Background: Single-ventricle physiology (SVP) is associated with significant morbidity and mortality at a young age. However, survival prospects have improved and risk factors for a negative outcome are well described in younger cohorts. Data regarding older adults is scarce. Methods: In this study,...
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doaj-0dd21620e2d64fa9b7642ec17cf8dca02020-12-19T00:00:19ZengMDPI AGJournal of Clinical Medicine2077-03832020-12-0194085408510.3390/jcm9124085Patients with Single-Ventricle Physiology over the Age of 40 YearsClaudia Pujol0Sandra Schiele1Susanne J. Maurer2Julia Hock3Celina Fritz4Alfred Hager5Peter Ewert6Oktay Tutarel7Department of Congenital Heart Disease and Paediatric Cardiology, German Heart Centre Munich, Technical University of Munich, 80636 Munich, GermanyDepartment of Congenital Heart Disease and Paediatric Cardiology, German Heart Centre Munich, Technical University of Munich, 80636 Munich, GermanyDepartment of Electrophysiology, German Heart Centre Munich, Technical University of Munich, 80636 Munich, GermanyDepartment of Congenital Heart Disease and Paediatric Cardiology, German Heart Centre Munich, Technical University of Munich, 80636 Munich, GermanyDepartment of Congenital Heart Disease and Paediatric Cardiology, German Heart Centre Munich, Technical University of Munich, 80636 Munich, GermanyDepartment of Congenital Heart Disease and Paediatric Cardiology, German Heart Centre Munich, Technical University of Munich, 80636 Munich, GermanyDepartment of Congenital Heart Disease and Paediatric Cardiology, German Heart Centre Munich, Technical University of Munich, 80636 Munich, GermanyDepartment of Congenital Heart Disease and Paediatric Cardiology, German Heart Centre Munich, Technical University of Munich, 80636 Munich, GermanyBackground: Single-ventricle physiology (SVP) is associated with significant morbidity and mortality at a young age. However, survival prospects have improved and risk factors for a negative outcome are well described in younger cohorts. Data regarding older adults is scarce. Methods: In this study, SVP patients under active follow-up at our center who were ≥40 years of age at any point between January 2005 and December 2018 were included. Demographic data, as well as medical/surgical history were retrieved from hospital records. The primary end-point was all-cause mortality. Results: Altogether, 49 patients (19 female (38.8%), mean age 49.2 ± 6.4 years) were included. Median follow-up time was 4.9 years (interquartile range (IQR): 1.8–8.5). Of these patients, 40 (81.6%) had undergone at least one cardiac surgery. The most common extracardiac comorbidities were thyroid dysfunction (<i>n</i> = 27, 55.1%) and renal disease (<i>n</i> = 15, 30.6%). During follow-up, 10 patients (20.4%) died. On univariate analysis, renal disease and liver cirrhosis were predictors of all-cause mortality. On multivariate analysis, only renal disease (hazard ratio (HR): 12.5, 95% confidence interval (CI): 1.5–106.3, <i>p</i> = 0.021) remained as an independent predictor. Conclusions: SVP patients ≥40 years of age are burdened with significant morbidity and mortality. Renal disease is an independent predictor of all-cause mortality.https://www.mdpi.com/2077-0383/9/12/4085single-ventricle physiologymortalityrenal diseaseadult congenital heart diseaseFontan |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Claudia Pujol Sandra Schiele Susanne J. Maurer Julia Hock Celina Fritz Alfred Hager Peter Ewert Oktay Tutarel |
spellingShingle |
Claudia Pujol Sandra Schiele Susanne J. Maurer Julia Hock Celina Fritz Alfred Hager Peter Ewert Oktay Tutarel Patients with Single-Ventricle Physiology over the Age of 40 Years Journal of Clinical Medicine single-ventricle physiology mortality renal disease adult congenital heart disease Fontan |
author_facet |
Claudia Pujol Sandra Schiele Susanne J. Maurer Julia Hock Celina Fritz Alfred Hager Peter Ewert Oktay Tutarel |
author_sort |
Claudia Pujol |
title |
Patients with Single-Ventricle Physiology over the Age of 40 Years |
title_short |
Patients with Single-Ventricle Physiology over the Age of 40 Years |
title_full |
Patients with Single-Ventricle Physiology over the Age of 40 Years |
title_fullStr |
Patients with Single-Ventricle Physiology over the Age of 40 Years |
title_full_unstemmed |
Patients with Single-Ventricle Physiology over the Age of 40 Years |
title_sort |
patients with single-ventricle physiology over the age of 40 years |
publisher |
MDPI AG |
series |
Journal of Clinical Medicine |
issn |
2077-0383 |
publishDate |
2020-12-01 |
description |
Background: Single-ventricle physiology (SVP) is associated with significant morbidity and mortality at a young age. However, survival prospects have improved and risk factors for a negative outcome are well described in younger cohorts. Data regarding older adults is scarce. Methods: In this study, SVP patients under active follow-up at our center who were ≥40 years of age at any point between January 2005 and December 2018 were included. Demographic data, as well as medical/surgical history were retrieved from hospital records. The primary end-point was all-cause mortality. Results: Altogether, 49 patients (19 female (38.8%), mean age 49.2 ± 6.4 years) were included. Median follow-up time was 4.9 years (interquartile range (IQR): 1.8–8.5). Of these patients, 40 (81.6%) had undergone at least one cardiac surgery. The most common extracardiac comorbidities were thyroid dysfunction (<i>n</i> = 27, 55.1%) and renal disease (<i>n</i> = 15, 30.6%). During follow-up, 10 patients (20.4%) died. On univariate analysis, renal disease and liver cirrhosis were predictors of all-cause mortality. On multivariate analysis, only renal disease (hazard ratio (HR): 12.5, 95% confidence interval (CI): 1.5–106.3, <i>p</i> = 0.021) remained as an independent predictor. Conclusions: SVP patients ≥40 years of age are burdened with significant morbidity and mortality. Renal disease is an independent predictor of all-cause mortality. |
topic |
single-ventricle physiology mortality renal disease adult congenital heart disease Fontan |
url |
https://www.mdpi.com/2077-0383/9/12/4085 |
work_keys_str_mv |
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