Literature DB >> 24343877

Analysis of cardiac anomalies in VACTERL association.

Bridget K Cunningham1, Donald W Hadley, Hwaida Hannoush, Andrew C Meltzer, Nickie Niforatos, Daniel Pineda-Alvarez, Vandana Sachdev, Nicole Warren-Mora, Benjamin D Solomon.   

Abstract

BACKGROUND: Congenital heart disease (CHD) is estimated to affect between 3 and 5% of all newborns. Extra-cardiac malformations are observed in 7 to 50% of patients with CHD. One relatively well-known association that can occur in the context of CHD is VACTERL. Controversy still remains regarding the definition of VATER association and its expansion to VACTERL, the appropriate diagnostic criteria and the overall incidence.
METHODS: We conducted a description of a case series to characterize the cardiac findings present in a cohort of patients meeting the criteria for VACTERL association.
RESULTS: Forty-six of 220 were eligible for inclusion into the study, 67% (31 of 46) had CHD. The most common CHD was ventricular septal defect, present in 18 of 31 patients (58%). There was no statistically significant association between CHD severity and the presence or absence of other VACTERL component features, specifically anorectal malformation (p = 0.18) or tracheo-esophageal fistula (p = 0.72). CHD presence also did not correlate with the presence of tracheo-esophageal fistula or anorectal malformation.
CONCLUSION: Although this study does not, by design, provide further evidence toward the questions of whether CHD is a defining feature of VACTERL association, the frequency of CHD in our cohort does lend support to it being an important medical consideration in patients with VACTERL association. Based on our experience, we strongly recommend a screening echocardiogram to evaluate for CHD in individuals with a potential diagnosis of VACTERL association.
Copyright © 2013 Wiley Periodicals, Inc.

Entities:  

Keywords:  VACTERL; VACTERL association; VATER; VATER association; congenital heart defects

Mesh:

Year:  2013        PMID: 24343877     DOI: 10.1002/bdra.23211

Source DB:  PubMed          Journal:  Birth Defects Res A Clin Mol Teratol        ISSN: 1542-0752


  8 in total

Review 1.  CHD associated with syndromic diagnoses: peri-operative risk factors and early outcomes.

Authors:  Benjamin J Landis; David S Cooper; Robert B Hinton
Journal:  Cardiol Young       Date:  2015-09-08       Impact factor: 1.093

2.  Aortic dilation, genetic testing, and associated diagnoses.

Authors:  Yuri A Zarate; Elizabeth Sellars; Tiffany Lepard; Xinyu Tang; R Thomas Collins
Journal:  Genet Med       Date:  2015-07-02       Impact factor: 8.822

3.  Variabilities in the mortality-related resource utilisation for congenital heart disease.

Authors:  David A Danford; Quentin Karels; Shelby Kutty
Journal:  Open Heart       Date:  2016-05-06

4.  Role of Genetic Factors in the Pathogenesis of Radial Deficiencies in Humans.

Authors:  Amira Elmakky; Ilaria Stanghellini; Antonio Landi; Antonio Percesepe
Journal:  Curr Genomics       Date:  2015-08       Impact factor: 2.236

5.  Incidence rate of congenital scoliosis estimated from a nationwide health insurance database.

Authors:  Ji-Won Kwon; Hyun Wook Chae; Hye Sun Lee; Sinae Kim; Sahyun Sung; Soo Bin Lee; Seong-Hwan Moon; Hwan-Mo Lee; Byung Ho Lee
Journal:  Sci Rep       Date:  2021-03-09       Impact factor: 4.379

6.  Right Pulmonary Artery Originating from Ascending Aorta (Hemitruncus Arteriosus) with VACTERL Association in a Neonate: A Case Report.

Authors:  Byeong-Su Shin; Taehong Kim; Hyoung Doo Lee; Hoon Ko; Joung-Hee Byun
Journal:  Children (Basel)       Date:  2022-02-03

7.  VACTERL association in a fetus with multiple congenital malformations - Case report.

Authors:  Paul Costin Pariza; Irina Stavarache; Vasile Adrian Dumitru; Octaviana Munteanu; Tiberiu Augustin Georgescu; Valentin Varlas; Consuela-Mădălina Gheorghe; Roxana Elena Bohîlțea
Journal:  J Med Life       Date:  2021 Nov-Dec

8.  Severe caudal regression syndrome with overlapping features of VACTERL complex: antenatal detection and follow up.

Authors:  K Kanagasabai; Venkatraman Bhat; G K Pramod; Siddaramappa J Patil; S Kiranmayi
Journal:  BJR Case Rep       Date:  2016-12-08
  8 in total

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