Literature DB >> 26944361

Bodily isomerism is an independent risk factor for pulmonary hypertension in adults with congenital heart disease.

Rohit S Loomba1, Saurabh Aggarwal2, Rohit R Arora3, Robert Anderson4.   

Abstract

INTRODUCTION: Bodily isomerism, or heterotaxy is a unique entity on which there is mirror imagery in various organ systems, leading to a deviation from the normal lateral arrangements of the viscera. Adults with such isomerism and associated congenital malformations of the heart are now reaching adulthood and developing long-term complications. This study investigates the prevalence and characteristics of pulmonary hypertension in adults with isomerism.
METHODS: The 2012 iteration of the Nationwide Inpatient Sample was utilized and patients were identified as having or not having bodily isomerism and having or not having pulmonary hypertension. Univariate analysis utilizing Chi-square tabulation was done to assess characteristics associated with pulmonary hypertension. Next, a multivariate analysis was done on all patients to identify predictors of pulmonary hypertension followed by a multivariate analysis of patients with only isomerism to identify predictors of pulmonary hypertension specific to this subset.
RESULTS: A total of 6,907,109 admissions were included in the analysis. Of these, 861 had isomerism (0.01%). Of those with isomerism, 5.6% were found to have pulmonary hypertension. When all patients were included in the multivariate analysis, isomerism was found to be an independent risk factor for pulmonary hypertension with an odds ratio of approximately 1.79. When only patients with isomerism were included in the multivariate analysis, advanced age, obesity, and history of anomalous pulmonary venous connection were independent risk factors of pulmonary hypertension.
CONCLUSION: Pulmonary hypertension is more common in those with isomerism, with isomerism being an independent risk factor for pulmonary hypertension. The prevalence of pulmonary hypertension is 5.6% in the setting of isomerism. Independent risk factors for pulmonary hypertension in patients with isomerism include age, obesity, and history of anomalous pulmonary venous connection.
© The Author(s), 2016.

Entities:  

Keywords:  atrioventricular septal defect; congenital heart disease; double outlet right ventricle; heterotaxy; isomerism; malformations; pulmonary hypertension

Mesh:

Year:  2016        PMID: 26944361      PMCID: PMC5933610          DOI: 10.1177/1753465816636810

Source DB:  PubMed          Journal:  Ther Adv Respir Dis        ISSN: 1753-4658            Impact factor:   4.031


  17 in total

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Authors:  Jeffrey P Jacobs; Robert H Anderson; Paul M Weinberg; Henry L Walters; Christo I Tchervenkov; Danny Del Duca; Rodney C G Franklin; Vera D Aiello; Marie J Béland; Steven D Colan; J William Gaynor; Otto N Krogmann; Hiromi Kurosawa; Bohdan Maruszewski; Giovanni Stellin; Martin J Elliott
Journal:  Cardiol Young       Date:  2007-09       Impact factor: 1.093

2.  Atrial appendages and venoatrial connections in hearts from patients with visceral heterotaxy.

Authors:  H Uemura; S Y Ho; W A Devine; L L Kilpatrick; R H Anderson
Journal:  Ann Thorac Surg       Date:  1995-09       Impact factor: 4.330

Review 3.  Isomerism or heterotaxy: which term leads to better understanding?

Authors:  Rohit S Loomba; Anthony M Hlavacek; Diane E Spicer; Robert H Anderson
Journal:  Cardiol Young       Date:  2015-06-19       Impact factor: 1.093

4.  Heterotaxy in southern Nevada: prenatal detection and epidemiology.

Authors:  William N Evans; Ruben J Acherman; Humberto Restrepo
Journal:  Pediatr Cardiol       Date:  2015-01-14       Impact factor: 1.655

5.  Laterality defects in the national birth defects prevention study (1998-2007): birth prevalence and descriptive epidemiology.

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6.  The diverse cardiac morphology seen in hearts with isomerism of the atrial appendages with reference to the disposition of the specialised conduction system.

Authors:  Audrey Smith; Siew Yen Ho; Robert H Anderson; M Gwen Connell; Robert Arnold; James L Wilkinson; Andrew C Cook
Journal:  Cardiol Young       Date:  2006-10       Impact factor: 1.093

Review 7.  Pulmonary arterial hypertension associated with congenital heart disease: recent advances and future directions.

Authors:  Michael A Gatzoulis; Maurice Beghetti; Michael J Landzberg; Nazzareno Galiè
Journal:  Int J Cardiol       Date:  2014-09-28       Impact factor: 4.164

8.  High prevalence of respiratory ciliary dysfunction in congenital heart disease patients with heterotaxy.

Authors:  Nader Nakhleh; Richard Francis; Rachel A Giese; Xin Tian; You Li; Maimoona A Zariwala; Hisato Yagi; Omar Khalifa; Safina Kureshi; Bishwanath Chatterjee; Steven L Sabol; Matthew Swisher; Patricia S Connelly; Mathew P Daniels; Ashok Srinivasan; Karen Kuehl; Nadav Kravitz; Kimberlie Burns; Iman Sami; Heymut Omran; Michael Barmada; Kenneth Olivier; Kunal K Chawla; Margaret Leigh; Richard Jonas; Michael Knowles; Linda Leatherbury; Cecilia W Lo
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Review 9.  The Fontan operation: the long-term outlook.

Authors:  Daphne T Hsu
Journal:  Curr Opin Pediatr       Date:  2015-10       Impact factor: 2.856

10.  Racial disparities in heterotaxy syndrome.

Authors:  Keila N Lopez; Lisa K Marengo; Mark A Canfield; John W Belmont; Heather A Dickerson
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2015-09-02
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  2 in total

1.  Characteristics of Hospitalizations for the Glenn Procedure in Those With Isomerism Compared to Those Without.

Authors:  Rohit S Loomba; Peter C Kouretas; Robert H Anderson
Journal:  Pediatr Cardiol       Date:  2016-07-08       Impact factor: 1.655

2.  Cardiopulmonary Exercise Testing in Fontan Patients With and Without Isomerism (Heterotaxy) as Compared to Patients With Primary Ciliary Dyskinesia and Subjects With Structurally Normal Hearts.

Authors:  Rohit S Loomba; Michael Danduran; Kim G Nielsen; Astrid M Ring; Joshua Kovach; Robert H Anderson
Journal:  Pediatr Cardiol       Date:  2016-11-23       Impact factor: 1.655

  2 in total

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