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

Cardiology in the Young
Benjamin J LandisRobert B Hinton

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.

References

Apr 1, 1977·The Journal of Pediatrics·J D WaldmanA S Nadas
Aug 1, 1992·Australasian Radiology·K L Dawson-FalkR G Rosenfeld
Dec 1, 1992·American Journal of Diseases of Children·M B GoensJ W Wiggins
Nov 1, 1991·Archives of Disease in Childhood·V A StebbensD P Southall
Nov 1, 1991·The Journal of Pediatrics·J R Ingelfinger, J W Newburger
Nov 1, 1990·American Journal of Medical Genetics·A E LinJ M Graham
Feb 1, 1990·Archives of Disease in Childhood·K D BlakeR K Wyse
Jun 1, 1990·Journal of the American College of Cardiology·C WrenC Bull
Dec 1, 1987·Developmental Medicine and Child Neurology·D P SouthallE A Shinebourne
Nov 1, 1988·American Journal of Medical Genetics·N NiikawaH Umemoto
Oct 1, 1988·American Journal of Medical Genetics·D R WittJ G Hall
May 1, 1987·The American Journal of Cardiology·C WrenJ E Deanfield
Feb 1, 1987·American Journal of Medical Genetics·B R RollnickA O Martin
Jul 1, 1973·British Heart Journal·E C Martin, I F Moseley
Nov 4, 1982·The New England Journal of Medicine·T P Cooney, W M Thurlbeck
Aug 1, 1984·The Annals of Thoracic Surgery·L M MarmonJ M Dunn
Oct 1, 1984·Thorax·J R WoodK M Citron
Jul 1, 1984·Pediatric Cardiology·B BrandtE B Clark
Jan 1, 1980·AJR. American Journal of Roentgenology·R J HernandezA Rosenthal
Feb 1, 1983·The Journal of Pediatrics·C S Kitchens, J A Alexander
Nov 15, 1993·American Journal of Medical Genetics·A D KlineL G Jackson
May 1, 1995·Pediatric Cardiology·J I Hoffman
Jun 1, 1995·The Journal of Pediatrics·P KaplanB S Kaplan
Sep 1, 1994·American Journal of Medical Genetics·A WesselJ H Bürsch
Nov 1, 1994·Archives of Disease in Childhood·C O GøtzscheB O Kristensen
Jan 1, 1994·Urology·M L RitcheyD A Bloom
Nov 15, 1993·American Journal of Medical Genetics·L JacksonS Koch
Jan 1, 1993·Archives of Otolaryngology--head & Neck Surgery·D MorganR Wyse
Mar 1, 1993·Pediatric Cardiology·R K WyseK Blake
May 15, 1993·American Journal of Medical Genetics·B R PoberR L Teele
Jul 1, 1993·Journal of the American College of Cardiology·K J JenkinsS D Colan
Aug 1, 1996·The Annals of Thoracic Surgery·V Alexi-MeskishviliR Hetzer
May 3, 1996·American Journal of Medical Genetics·R PankauA Wessel
Apr 1, 1996·Journal of Medical Genetics·R A Newbury-EcobI D Young
Aug 1, 1996·Journal of Medical Genetics·S Tézenas Du MontcelN Philip
Mar 29, 1996·American Journal of Medical Genetics·F GreenbergJ R Lupski
Dec 1, 1996·The Journal of Pediatrics·L M BirdM C Jones
Jul 1, 1997·The Journal of Thoracic and Cardiovascular Surgery·C StammR H Anderson

❮ Previous
Next ❯

Citations

Aug 10, 2016·Frontiers in Cardiovascular Medicine·Benjamin J Landis, Stephanie M Ware
Dec 21, 2018·Circulation·Mary Ella PierpontUNKNOWN American Heart Association Council on Cardiovascular Disease in the Young; Council on Cardiovascular and Stroke Nursing; and
Dec 11, 2019·Cold Spring Harbor Perspectives in Biology·Shannon N Nees, Wendy K Chung
Jun 20, 2017·Birth Defects Research·Eric G JerniganJennifer S Nelson
Feb 8, 2020·Annals of Pediatric Cardiology·Subhrajit LahiriWelch Elizabeth
Dec 14, 2019·American Journal of Medical Genetics. Part C, Seminars in Medical Genetics·Joshua K Meisner, Donna M Martin
Oct 30, 2018·Journal of the American Heart Association·Shabnam PeyvandiMartina A Steurer
Oct 4, 2020·Current Opinion in Pediatrics·Gabrielle C GeddesStephanie M Ware
Jan 24, 2019·The Journal of Thoracic and Cardiovascular Surgery·Son Q DuongBrian Feingold
Aug 18, 2021·Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie·C La FayUNKNOWN Fédération des Equipes Ressources Régionales de Soins Palliatifs Pédiatriques (ERRSPP)

❮ Previous
Next ❯

Related Concepts

Related Feeds

Birth Defects

Birth defects encompass structural and functional alterations that occur during embryonic or fetal development and are present since birth. The cause may be genetic, environmental or unknown and can result in physical and/or mental impairment. Here is the latest research on birth defects.

22q11 Deletion Syndrome

22q11.2 deletion syndrome, also known as DiGeorge syndrome, is a congenital disorder caused by a partial deletion of chromosome 22. Symptoms include heart defects, poor immune system function, a cleft palate, complications related to low levels of calcium in the blood, and delayed development. Discover the latest research on this disease here.

Related Papers

Nederlands tijdschrift voor geneeskunde
W M A Verhoeven, S Tuinier
European Journal of Cardio-thoracic Surgery : Official Journal of the European Association for Cardio-thoracic Surgery
Roberto FormigariB Marino
Journal of the American Academy of Child and Adolescent Psychiatry
Jacob A S VorstmanHerman van Engeland
© 2021 Meta ULC. All rights reserved