CHD associated with syndromic diagnoses: peri-operative risk factors and early outcomes

Cardiol Young. 2016 Jan;26(1):30-52. doi: 10.1017/S1047951115001389. Epub 2015 Sep 8.

Abstract

CHD is frequently associated with a genetic syndrome. These syndromes often present specific cardiovascular and non-cardiovascular co-morbidities that confer significant peri-operative risks affecting multiple organ systems. Although surgical outcomes have improved over time, these co-morbidities continue to contribute substantially to poor peri-operative mortality and morbidity outcomes. Peri-operative morbidity may have long-standing ramifications on neurodevelopment and overall health. Recognising the cardiovascular and non-cardiovascular risks associated with specific syndromic diagnoses will facilitate expectant management, early detection of clinical problems, and improved outcomes--for example, the development of syndrome-based protocols for peri-operative evaluation and prophylactic actions may improve outcomes for the more frequently encountered syndromes such as 22q11 deletion syndrome.

Keywords: CHD; genetic; syndrome.

Publication types

  • Review

MeSH terms

  • 22q11 Deletion Syndrome / complications
  • Alagille Syndrome / complications
  • Heart Defects, Congenital / complications
  • Heart Defects, Congenital / genetics
  • Heart Defects, Congenital / surgery*
  • Heart Diseases / complications
  • Heart Diseases / congenital*
  • Heart Diseases / genetics
  • Heart Diseases / surgery*
  • Heterotaxy Syndrome / complications
  • Humans
  • Infant
  • Marfan Syndrome / complications
  • Noonan Syndrome / complications
  • Risk Factors
  • Syndrome
  • Time Factors
  • Treatment Outcome
  • Turner Syndrome / complications
  • Williams Syndrome / complications