Abstract 4366567: Temporal Patterns and Regional Disparities in Congenital Heart Anomalies Across the European Union from 1990-2021: A Benchmarking Global Analysis

S Sandeep Sekar Lakshmisai (Department of Medicine, SRM Prime Hospital, Chennai, Tamil Nadu, India, 600087, Chennai, India) V Venkata Ramana Katikala (KIMS, Amalapuram, Tadepalle, India) G Gunjan Kochhar (university of oklahoma health sciences center, Oklahoma City, Oklahoma, United States) H Hassaan Imtiaz (Mclaren Bay Region, Saginaw, Michigan, United States) D deepika sanapala (Katuri medical college, Krishna, India) V Vaidheesh Varagantiwar (Internal medicine,Rajiv Gandhi institute of medical sciences, Adilabad,504001, India, Adilabad, India) J Jeel Patel (Gujarat Adani Institute of Medical Sciences, Bhuj, India) D Drumadala Gajbhiye (GMC Akola, Akola, India) J Jay Patel (NanoScience Technology Center, University of Central Florida) C Chandana Tummala (Internal Medicine, Vydehi Institute Of Medical Sciences and Research Centre, Whitefield-560066, Bangalore, Karnataka, India, Banglore, India) S SHAHZAD AHMED SAMI (DCH RMC/university of Alabama ,, Tuscaloosa, Alabama, United States) H Hardik Dineshbhai Desai

Abstract

Background: Congenital heart anomalies (CHA) remain one of the leading causes of childhood morbidity and mortality worldwide, with significant implications for long-term health outcomes and healthcare systems. Method: Utilizing global burden of disease 2021 study standardized methodology we estimated CHA burden for all 27 European Union countries from1990-2021. Age-standardized rates of deaths, prevalence, and years lived with disability (YLDs) were analyzed, and annualized percentage changes (APC) were calculated for multiple time intervals to assess temporal and sex-specific trends. Result: From 1990 to 2000, the APC in deaths due to CHA declined significantly by -5.72%, followed by a continued but less steep decline of -3.90% from 2000 to 2021. In contrast, the prevalence showed a slight annual decrease of -0.12% during 1990–2000, which reversed to a modest annual increase of 0.19% in the period 2000–2021. YLDs demonstrated a similar trend, with an annual decline of -0.58% from 1990 to 2000 and a slight increase of 0.12% annually from 2000 to 2021. The age-standardized death rate (ASMR) declined annually by -5.10% from 1990 to 2000 and -4.00% from 2000 to 2021, while the age-standardized prevalence rate (ASPR) remained largely stable during 1990–2000 (0.006% per year) and rose slightly thereafter (0.11% per year); similarly, YLDs (ASYLDsR) showed a mild decline in the first decade (-0.17%) followed by a gradual annual increase of 0.19% from 2000 to 2021. Nationally, the highest APC in ASPR observed in Austria by 0.66%, followed by Ireland 0.23%, Portugal 0.22%, Croatia 0.19%, Malta 0.16%. From 2000 to 2010, the ASMR declined annually by -4.30% in males and -4.58% in females, with a slower decline observed from 2010 to 2021 (-3.48% in males, -3.80% in females). The prevalence rate showed a modest annual increase in males (0.28%) and a slight decline in females (-0.05%) during 2000–2010, followed by a small rise in both sexes from 2010 to 2021 (0.02% in males, 0.18% in females). YLDs remained stable in females (-0.007%) and increased marginally in males (0.23%) from 2010 to 2021. Conclusion: While the mortality due to CHA has steadily declined across 3 decades and sexes, both prevalence and disability burden have shown a gradual upward trend since 2000, particularly among males. These findings highlight a shifting burden from fatal to non-fatal outcomes, underscoring the need for long-term care strategies and quality-of-life interventions.

Article Details

Journal Circulation
Volume / Issue Vol. 152, Issue Suppl_3
Published November 04, 2025
ISSN 0009-7322
Publisher Lippincott Williams & Wilkins

Journal Info

Circulation

Lippincott Williams & Wilkins

ISSN: 0009-7322 Health Sciences

Authors (12)

S

Sandeep Sekar Lakshmisai

Department of Medicine, SRM Prime Hospital, Chennai, Tamil Nadu, India, 600087, Chennai, India

V

Venkata Ramana Katikala

KIMS, Amalapuram, Tadepalle, India

G

Gunjan Kochhar

university of oklahoma health sciences center, Oklahoma City, Oklahoma, United States

H

Hassaan Imtiaz

Mclaren Bay Region, Saginaw, Michigan, United States

D

deepika sanapala

Katuri medical college, Krishna, India

V

Vaidheesh Varagantiwar

Internal medicine,Rajiv Gandhi institute of medical sciences, Adilabad,504001, India, Adilabad, India

J

Jeel Patel

Gujarat Adani Institute of Medical Sciences, Bhuj, India

D

Drumadala Gajbhiye

GMC Akola, Akola, India

J

Jay Patel

NanoScience Technology Center, University of Central Florida

C

Chandana Tummala

Internal Medicine, Vydehi Institute Of Medical Sciences and Research Centre, Whitefield-560066, Bangalore, Karnataka, India, Banglore, India

S

SHAHZAD AHMED SAMI

DCH RMC/university of Alabama ,, Tuscaloosa, Alabama, United States

H

Hardik Dineshbhai Desai