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Background: Peak oxygen consumption (V̇O ) is used to predict outcomes and the timing of transplantation in patients with heart failure with reduced ejection fraction (HFrEF); V̇O also has predictive utility in patients with adult congenital heart disease (ACHD). However, the predictive value of a given V̇O in patients with ACHD compared to those with HFrEF, especially after adjustment for age and sex, is not clear.
Methods: To address this, we performed a longitudinal cohort study comparing patients with ACHD to patients with HFrEF. The ACHD and HFrEF cohorts were matched for sex and age (+/- 10 y). V̇O tests were conducted between 1993 and 2012. Events were defined as death, cardiac transplantation, or left ventricular assist device placement. Outcome data were obtained via electronic medical record, Social Security Death Index, and phone interview. Cox proportional-hazard regressions were used to evaluate relationships of event-free survival with predictor variables.
Results: Patients with ACHD (N=137) and HFrEF (N=137) with a median follow-up time of 14.5 (13.4-15.6) y in the ACHD cohort and 19 (14.8-21.1) y in the HFrEF cohort. Higher V̇O was associated with lower risk for a cardiac outcome, independent of age and sex, in both ACHD (HR 0.89, 95% CI 0.83-0.96, =0.002) and HFrEF (HR 0.85, 95% CI 0.81-0.89, <0.001Male sex was associated with greater risk of a cardiac outcome ( =0.001) in ACHD (HR 3.34) and HFrEF (HR 1.83). After multivariable adjustment (that included age, sex, and V̇O ) having ACHD conferred a 66% lower risk of a cardiovascular event compared to a HFrEF diagnosis (HR 0.34, 95% CI 0.22-0.53, <0.001).
Conclusions: V̇O independently predicts event-free survival among adults with ACHD or HFrEF and has clinical utility in the outpatient setting. Patients with ACHD, however, have a better prognosis for any given V̇O compared to those with HFrEF.
What Is New?: In an age- and sex-matched longitudinal cohort study with over 7 y of follow-up, adults with congenital heart disease (ACHD) were found to have a better event-free (no transplant or LVAD) survival than adults with heart failure with reduced ejection fraction (HFrEF) even after multivariable adjustment that included age, sex, and V̇O . Thus, for any given V̇O a better event-free survival would be expected in ACHD compared with HFrEF. For both groups, a higher V̇O did still confer an improved event-free survival and male sex conferred a worse event-free survival.
What Are The Clinical Implications?: Patients with HFrEF commonly undergo V̇O testing to evaluate clinical status, exercise capabilities, and timing for transplantation. Less commonly, patients with ACHD undergo V̇O testing. This study confirmed that a higher V̇O is still an excellent predictor of freedom from cardiac events and survival in both groups; however, for a given V̇O , a patient with ACHD would be expected to have a markedly improved event-free survival vs. a patient with HFrEF even after adjusting for age and sex. Moreover, our analysis adds to the understanding of how much of an advantage a higher V̇O confers for each mL·min ·kg confers in each group, with a slightly greater incremental benefit for the ACHD group. This finding has implications for timing of referral to cardiac transplantation for patients with ACHD. Future studies are needed to determine the optimal V̇O cut-off for transplantation for those with ACHD. Furthermore, more studies are needed to investigate the potential mechanism(s) for the ACHD survival advantage.
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http://dx.doi.org/10.1101/2024.10.11.24315308 | DOI Listing |
Cureus
August 2025
Physiology, Alkindy College of Medicine, Baghdad University, Baghdad, IRQ.
Cor triatriatum is a rare congenital heart defect that divides the right or left atrium into three chambers. Although the diagnosis is typically made within the first years of birth, it can occasionally be made later in adulthood and is frequently associated with other cardiac defects but may be present in isolation. Clinical manifestations range from lung congestion, exhaustion, coughing, and dyspnea to the onset of heart failure.
View Article and Find Full Text PDFObjective: Our objective was to build classifiers for multiple phenotypes that categorize a cohort of adults with congenital heart disease (ACHD), that can be used to populate variables in a biobank.
Materials And Methods: A dataset of 1492 ACHD patients, with expert-created labels for eight phenotypes, was created and used to train classifiers with three different architectures. A larger unlabeled dataset containing 15869 patients was used to pre-train the classifiers, and a 20% subset of the unlabeled dataset was used to validate the classifier predictions.
Cureus
July 2025
Cardiovascular Surgery, Kitasato University School of Medicine, Sagamihara, JPN.
Ebstein's anomaly (EA) is a rare congenital defect of the tricuspid valve (TV), typically characterized by downward displacement of the septal and posterior leaflets into the right ventricle, resulting in tricuspid regurgitation (TR), right heart enlargement, and heart failure. While surgical outcomes for EA have improved significantly in pediatric and young adult populations, data on surgical intervention in elderly patients remain limited. Elderly patients often present with comorbidities and diminished physiological reserve, which complicate both surgical decision-making and perioperative management.
View Article and Find Full Text PDFJ Am Coll Cardiol
September 2025
Mount Sinai Fuster Heart Hospital, Kravis Children's Hospital, Icahn School of Medicine at Mount Sinai, New York, New York, USA. Electronic address:
Background: Adults with congenital heart disease (ACHD) undergo repeated cardiac interventions, develop cardiac complications including atrial fibrillation, heart failure, and stroke, and may have genetic vulnerabilities for neurocognitive deficits (NCDs). However, NCDs have not been well studied in this population.
Objectives: The aim of this study was to examine the prevalence and risk factors associated with NCDs in young adults with moderate and severe complex congenital heart disease (CHD).
Cardiol Young
August 2025
Division of Pediatric Cardiology, Department of Pediatrics, Lucile Packard Children's Hospital, Stanford University, Stanford, CA, USA.
Introduction: Although the importance of advance care planning (ACP) for individuals with adult congenital heart disease (ACHD) has been established, there is no consensus regarding the optimal age to initiate ACP discussions. We asked ACHD patients their opinions about the timing of the first ACP discussion.
Materials/methods: Adult patients seen in an outpatient ACHD clinic from April to August 2018 completed a self-administered questionnaire that evaluated opinions regarding the content and timing of ACP discussions, end-of-life communication preferences, and anticipated emotional responses to ACP discussions.