Advanced heart failure in adult congenital heart disease: the role of renal dysfunction in management and outcomes

Author:

Krishnathasan Kaushiga1ORCID,Dimopoulos Konstantinos12ORCID,Duncan Neill34ORCID,Ricci Piera1,Kempny Alexander12,Rafiq Isma12ORCID,Gatzoulis Michael A12ORCID,Heng Ee Ling12,Blakey Sarah34,Montanaro Claudia12,Babu-Narayan Sonya V12ORCID,Francis Darrel P25,Li Wei12ORCID,Constantine Andrew12ORCID

Affiliation:

1. Adult Congenital Heart Centre and Centre for Pulmonary Hypertension, Royal Brompton Hospital, Royal Brompton and Harefield Hospitals, Guy’s and St Thomas’ NHS Foundation Trust , Sydney Street, London SW3 6NP , UK

2. National Heart and Lung Institute, Imperial College London , London , UK

3. Renal and Transplant Centre, Hammersmith Hospital, Imperial College Healthcare NHS Trust , London , UK

4. Department of Immunology and Inflammation, Imperial College London , London , UK

5. Hammersmith Hospital, Imperial College Healthcare NHS Trust, Imperial College London , London , UK

Abstract

Abstract Aims Previous studies in adult congenital heart disease (CHD) have demonstrated a link between renal dysfunction and mortality. However, the prognostic significance of renal dysfunction in CHD and decompensated heart failure (HF) remains unclear. We sought to assess the association between renal dysfunction and outcomes in adults with CHD presenting to our centre with acute HF between 2010 and 2021. Methods and results This retrospective analysis focused on the association between renal dysfunction, pre-existing and on admission, and outcomes during and after the index hospitalization. Chronic kidney disease (CKD) was defined as an estimated glomerular filtration rate <60 mL/min/1.73 m2. Cox regression analysis was used to identify the predictors of death post-discharge. In total, 176 HF admissions were included (mean age 47.7 ± 14.5 years, 43.2% females). One-half of patients had a CHD of great complexity, 22.2% had a systemic right ventricle, and 18.8% had Eisenmenger syndrome. Chronic kidney disease was present in one-quarter of patients. The median length of intravenous diuretic therapy was 7 (4–12) days, with a maximum dose of 120 (80–160) mg furosemide equivalents/day, and 15.3% required inotropic support. The in-hospital mortality rate was 4.5%. The 1- and 5-year survival rates free of transplant or ventricular assist device (VAD) post-discharge were 75.4% [95% confidence interval (CI): 69.2–82.3%] and 43.3% (95% CI: 36–52%), respectively. On multivariable Cox analysis, CKD was the strongest predictor of mortality or transplantation/VAD. Highly complex CHD and inpatient requirement of inotropes also remained predictive of an adverse outcome. Conclusion Adult patients with CHD admitted with acute HF are a high-risk cohort. CKD is common and triples the risk of death/transplantation/VAD. An expert multidisciplinary approach is essential for optimizing outcomes.

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine,Epidemiology

Reference22 articles.

1. Lifetime prevalence of congenital heart disease in the general population from 2000 to 2010;Marelli;Circulation,2014

2. Global, regional, and national burden of congenital heart disease, 1990–2017: a systematic analysis for the Global Burden of Disease Study 2017;Zimmerman;Lancet Child Adolesc Health,2020

3. Prevalence, predictors, and prognostic value of renal dysfunction in adults with congenital heart disease;Dimopoulos;Circulation,2008

4. Renal impairment, worsening renal function, and outcome in patients with heart failure: an updated meta-analysis;Damman;Eur Heart J,2014

5. 2018 AHA/ACC guideline for the management of adults with congenital heart disease: a report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice guidelines;Stout;Circulation,2018

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