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Background: Congenital heart operations are categorized into risk categories based on The Society of Thoracic Surgeons-European Association of Cardio-Thoracic Surgery Congenital Heart Surgery (STAT) Mortality Categories. The adjusted mortality rate should adjust for case mix.
Methods: The Society of Thoracic Surgeons Congenital Heart Surgery Public Reporting data were extracted for the top 50 U.S. News & World Report Cardiology and Heart Surgery Programs in 2021 (operations from January 2015 to December 2018). Variability in STAT 1 as a percentage of total operations and as a ratio to STAT 4+5 operations was evaluated.
Results: STAT 1 cases varied between centers from 18% to 37% of total. The ratio of STAT 1 to STAT 4+5 varied from 0.52 to 1.97. There was an inverse relationship between the STAT 1:STAT 4+5 ratio and adjusted mortality rate that did not reach statistical significance (P = .12). When programs (n = 12) in the quartiles with the highest vs lowest STAT 1:STAT 4+5 ratio were compared, a significant difference was found in the median adjusted mortality rate (2.2% vs 2.95%, P = .03).
Conclusions: There is a 4-fold difference in the ratio of STAT 1 to STAT 4+5 cases among congenital heart surgery programs, even when smaller programs are excluded, suggesting significant differences in the decision-making philosophy. Programs with the highest proportion of STAT 1 cases had lower adjusted mortality rate, suggesting that The Society of Thoracic Surgery Congenital Heart Surgery Database mortality risk model adjusts well but not completely for case-mix variability between programs.
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http://dx.doi.org/10.1016/j.athoracsur.2022.08.012 | DOI Listing |
Eur J Case Rep Intern Med
August 2025
Cardiac Sciences Division, Department of Medicine, King Abdulaziz Hospital, Ministry of National Guard Health Affairs (MNGHA), Al Ahsa, Saudi Arabia.
Unlabelled: Anomalous origin of the coronary arteries is a rare congenital condition that can present as non-specific chest pain or shortness of breath or remain asymptomatic. Early identification is critical as certain variants are linked with a high risk of sudden cardiac death. Here, we report the case of a 53-year-old female with hypertension, hypothyroidism, obesity (class II) and a history of intermittent chest pain radiating to the left arm for two years.
View Article and Find Full Text PDFCase Rep Pediatr
September 2025
Department of Thoracic Surgery, Avicenna Tajik State Medical University, Dushanbe, Tajikistan.
Ectopia cordis is an exceptionally uncommon congenital condition where the heart develops outside its normal position due to incomplete closure of the ventral chest wall during embryogenesis. The anomaly may occur in isolation or with other structural defects, often resulting in a poor prognosis despite advancements in medical and surgical care. This report discusses a preterm neonate delivered at 33 weeks of gestation following an uneventful pregnancy in a dizygotic twin gestation.
View Article and Find Full Text PDFRev Cardiovasc Med
August 2025
Department of Cardiology, University Hospitals of Leicester NHS Trust, Glenfield Hospital, LE3 9QP Leicester, UK.
Adult congenital heart disease (ACHD) constitutes a heterogeneous and expanding patient cohort with distinctive diagnostic and management challenges. Conventional detection methods are ineffective at reflecting lesion heterogeneity and the variability in risk profiles. Artificial intelligence (AI), including machine learning (ML) and deep learning (DL) models, has revolutionized the potential for improving diagnosis, risk stratification, and personalized care across the ACHD spectrum.
View Article and Find Full Text PDFEClinicalMedicine
October 2025
Department of Cardiothoracic Surgery, Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine, China.
Background: Paediatric patients who underwent surgery for mitral regurgitation (MR) have a high risk of recurrence or death; however, no prediction tool has been developed to risk-stratify this challenging subpopulation.
Methods: In this multicentre cohort study, paediatric patients undergoing surgery for congenital MR in Shanghai Children's Medical Center in January 1st, 2009-December 31st, 2022 were included for analysis while those had a combination with infective endocarditis, anomalous left coronary artery from the pulmonary artery, rheumatic valvular disease, connective tissue disease, or single ventricle were excluded. A Cox regression model predictive of the primary outcome (a composite of mortality or mitral valve [MV] re-operation) was derived and converted to a point-based risk score.
Eur Heart J Qual Care Clin Outcomes
September 2025
Adult Congenital Heart Centre and Centre for Pulmonary Hypertension, Royal Brompton Hospital, Guy's and St Thomas' NHS Foundation Trust, Sydney Street, London SW3 6NP, UK.