Literature DB >> 21418533

Survival and morbidity following congenital heart surgery in a population-based cohort of children--up to 12 years of follow-up.

Signe Holm Larsen1, Kristian Emmertsen, Søren Paaske Johnsen, Jens Pedersen, Kirsten Hjortholm, Vibeke Elisabeth Hjortdal.   

Abstract

OBJECTIVES: The Risk Adjusted Classification for Congenital Heart Surgery can predict early mortality. However, the relation to long-term outcome in terms of mortality and morbidity is unknown.
DESIGN: We did a population-based follow-up study of 801 children undergoing congenital heart surgery between 1996 and 2002. All patients were followed from surgery until death or January 1, 2008. Operations were classified according to the Risk Adjusted Classification for Congenital Heart Surgery. Each patient was matched by age and sex with 10 population controls. Cox regression analysis, area under the receiver operator curve and competing risk analysis were used for the analyses.
RESULTS: Overall follow-up was 99.6%. The distribution of the Risk Adjusted Classification for Congenital Heart Surgery was: Category one 20%, category two 37%, category three 27%, category four 8%, category five 0% and category six 2%. Overall survival after a median follow-up of 8.2 years was 86% (95% confidence interval: 83-88%), with 54 early deaths occurring within 30 days after surgery and 57 late deaths. Long-term survival in those who were alive 30 days after surgery was 92% (90-94%); ranging from 98% (93-100%) in risk category one to 33% (5-68%) in category six. Survival overall and beyond 30 days was lower in each risk category than in controls (P < .001). During follow-up, 124 (15%) patients had new operations and 106 (13%) catheter-based interventions. These events were more frequent in category three, four, and six compared with category one, with no difference between category one and two. The area under the receiver operator curve for long-term mortality was 0.81 (95% confidence interval 0.75-0.87).
CONCLUSIONS: Children operated for congenital heart disease have impaired survival and often undergo new operations or catheter-based interventions. The risk of these events is related to the surgical complexity according to the Risk Adjusted Classification for Congenital Heart Surgery.
© 2011 Copyright the Authors. Congenital Heart Disease © 2011 Wiley Periodicals, Inc.

Entities:  

Mesh:

Year:  2011        PMID: 21418533     DOI: 10.1111/j.1747-0803.2011.00495.x

Source DB:  PubMed          Journal:  Congenit Heart Dis        ISSN: 1747-079X            Impact factor:   2.007


  5 in total

1.  Adolescents and adults with congenital heart diseases in oman.

Authors:  Asim Al-Balushi; Hamood Al-Kindi; Hamood Al-Shuaili; Suresh Kumar; Salim Al-Maskari
Journal:  Oman Med J       Date:  2015-01

2.  Circulating plasma circular RNAs as novel diagnostic biomarkers for congenital heart disease in children.

Authors:  Jinhuan Wu; Jiaqing Li; Heng Liu; Jiangwen Yin; Mengjie Zhang; Zhangbin Yu; Hongjun Miao
Journal:  J Clin Lab Anal       Date:  2019-08-20       Impact factor: 2.352

3.  Chronic kidney disease in patients with congenital heart disease: a nationwide, register-based cohort study.

Authors:  Mikaela Gillesén; Maria Fedchenko; Kok Wai Giang; Konstantinos Dimopoulos; Peter Eriksson; Mikael Dellborg; Zacharias Mandalenakis
Journal:  Eur Heart J Open       Date:  2022-09-02

4.  Modelling survival and mortality risk to 15 years of age for a national cohort of children with serious congenital heart defects diagnosed in infancy.

Authors:  Rachel L Knowles; Catherine Bull; Christopher Wren; Angela Wade; Harvey Goldstein; Carol Dezateux
Journal:  PLoS One       Date:  2014-09-10       Impact factor: 3.240

5.  Benefits of ultra-fast-track anesthesia for children with congenital heart disease undergoing cardiac surgery.

Authors:  Jing Xu; Guanghua Zhou; Yanpei Li; Na Li
Journal:  BMC Pediatr       Date:  2019-12-11       Impact factor: 2.125

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.