Literature DB >> 19322890

Aortic dissection in childhood and adolescence: an analysis of occurrences over a 10-year interval in New York State.

Charles R Fikar1, Ronald Fikar.   

Abstract

BACKGROUND: Rarely occurring in the pediatric and adolescent population, aortic dissection is a condition with many predisposing factors. Previous studies have suggested that congenital cardiovascular disorders are the most common predisposing conditions. Trauma-associated aortic dissection is considered a rare occurrence.
METHODS: The Statewide Planning and Research Cooperative System database of New York State was used to retrieve cases of aortic dissection in persons < or = 21 years old over a 10-year period. A retrospective analysis for risk or associated conditions was undertaken.
RESULTS: Forty-five of a total of 12,142 cases of aortic dissection (0.37%) occurred in persons < or = 21 years old. No patient was younger than 15 years of age. Six of the 45 died (13%). Most patients were male (37 of 45, or 82%). Contrary to previous reports, the most common associated condition was trauma (19 of 45, or 42%), with Marfan syndrome the second most common (11 of 45, or 24%). Ten of 45 adolescent and young adult patients (22%) had no apparent risk factors.
CONCLUSIONS: Traumatic aortic disruptions must be considered in children and adolescents who survive serious chest trauma. Family members of pediatric and young adult patients with trauma-associated aortic dissection may need to be evaluated for possible risk of aortic dissection. 2009 Wiley Periodicals, Inc.

Entities:  

Mesh:

Year:  2009        PMID: 19322890      PMCID: PMC6652935          DOI: 10.1002/clc.20383

Source DB:  PubMed          Journal:  Clin Cardiol        ISSN: 0160-9289            Impact factor:   2.882


  6 in total

1.  Aortic dissection and rupture in an 11-year-old child: A case report.

Authors:  Lucy Youngmin Eun; Deok Kyu Cho; Yun Hyeong Cho; Ki Hyun Byun
Journal:  J Cardiol Cases       Date:  2010-10-15

2.  Impact of aortic aneurysm on hospitalizations in patients with marfan syndrome: a multi-institutional study.

Authors:  R Thomas Collins; Venusa Phomakay; Yuri A Zarate; Xinyu Tang
Journal:  Pediatr Cardiol       Date:  2014-08-06       Impact factor: 1.655

Review 3.  Bicuspid aortic valve: identifying knowledge gaps and rising to the challenge from the International Bicuspid Aortic Valve Consortium (BAVCon).

Authors:  Hector I Michelena; Siddharth K Prakash; Alessandro Della Corte; Malenka M Bissell; Nandan Anavekar; Patrick Mathieu; Yohan Bossé; Giuseppe Limongelli; Eduardo Bossone; D Woodrow Benson; Patrizio Lancellotti; Eric M Isselbacher; Maurice Enriquez-Sarano; Thoralf M Sundt; Philippe Pibarot; Artur Evangelista; Dianna M Milewicz; Simon C Body
Journal:  Circulation       Date:  2014-06-24       Impact factor: 29.690

4.  Aortic dissection and rupture in a child.

Authors:  Yun Ju Jo; Eun Jeong Lee; Jin Won Oh; Chang Min Moon; Deok Kyu Cho; Yun Hyeong Cho; Ki Hyun Byun; Lucy Youngmin Eun
Journal:  Korean Circ J       Date:  2011-03-31       Impact factor: 3.243

5.  Aortic Root Dilatation in Mucopolysaccharidosis I-VII.

Authors:  Meena Bolourchi; Pierangelo Renella; Raymond Y Wang
Journal:  Int J Mol Sci       Date:  2016-11-29       Impact factor: 5.923

6.  Case Report: Management of a 10-Year-Old Patient Who Presented With Infective Endocarditis and Stanford Type A Aortic Dissection.

Authors:  Yanxiao Liang; Mingzhi Wan; Lijie Wang; Ni Yang; Dongyu Li
Journal:  Front Cardiovasc Med       Date:  2022-01-28
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.