Literature DB >> 27393478

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

Rohit S Loomba1, Peter C Kouretas2, Robert H Anderson3.   

Abstract

Isomerism, also known as heterotaxy, is a unique clinical entity in which there are mirror imaged findings in the thoracic. In the abdomen, the arrangement of organs can be random. The anatomic findings also have functional consequences. Isomerism has been known to increase morbidity and mortality in those with functionally univentricular hearts. The aim of this study was to determine the impact of isomerism on the Glenn hospitalization. Data from the 1997 to 2012 Kids' Inpatient Database were utilized for this cross-sectional study. Admissions during which a Glenn procedure was done were identified. Next, these admissions were separated into those with and without isomerism. Admission characteristics were then compared in a univariate fashion as well as by regression analysis. Length of hospitalization, cost of hospitalization, extracorporeal membrane oxygenation, and inpatient mortality were the outcomes of interest. A total of 4959 admissions with a Glenn procedure were identified. Of these, 450 were associated with isomerism. The median age at which the Glenn procedure was done was 10 and 13 months in those without and with isomerism, respectively. Neither univariate nor regression analysis demonstrated any significant difference in length of hospitalization, cost of hospitalization, need for extracorporeal membrane oxygenation, and inpatient mortality between those with and without isomerism. Isomerism does not impact the characteristics of the Glenn hospitalization. Those with isomerism did tend to be older when they underwent the Glenn procedure.

Keywords:  Cavoluplomonary anastomosis; Glenn; Heterotaxy; Isomerism

Mesh:

Year:  2016        PMID: 27393478     DOI: 10.1007/s00246-016-1449-9

Source DB:  PubMed          Journal:  Pediatr Cardiol        ISSN: 0172-0643            Impact factor:   1.655


  36 in total

1.  Thrombocytosis in asplenia syndrome with congenital heart disease: a previously unrecognized risk factor for thromboembolism.

Authors:  Kenichiro Yamamura; Kunitaka Joo; Shouichi Ohga; Hazumu Nagata; Kazuyuki Ikeda; Jun Muneuchi; Mamie Watanabe; Toshiro Hara
Journal:  Int J Cardiol       Date:  2012-06-22       Impact factor: 4.164

Review 2.  Observation versus prophylactic Ladd procedure for asymptomatic intestinal rotational abnormalities in heterotaxy syndrome: A systematic review.

Authors:  Rachel Landisch; Abdel-Hafeez Abdel-Hafeez; Roxanne Massoumi; Melissa Christensen; Amanda Shillingford; Amy J Wagner
Journal:  J Pediatr Surg       Date:  2015-08-08       Impact factor: 2.545

Review 3.  The nomenclature, definition and classification of cardiac structures in the setting of heterotaxy.

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

Review 4.  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

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

Authors:  Angela E Lin; Sergey Krikov; Tiffany Riehle-Colarusso; Jaime L Frías; John Belmont; Marlene Anderka; Tal Geva; Kelly D Getz; Lorenzo D Botto
Journal:  Am J Med Genet A       Date:  2014-08-06       Impact factor: 2.802

6.  Analysis of visceral heterotaxy according to splenic status, appendage morphology, or both.

Authors:  H Uemura; S Y Ho; W A Devine; R H Anderson
Journal:  Am J Cardiol       Date:  1995-10-15       Impact factor: 2.778

7.  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
Journal:  Circulation       Date:  2012-04-12       Impact factor: 29.690

8.  Heterotaxy syndrome and intestinal rotation abnormalities: a survey of institutional practice.

Authors:  Charissa R Pockett; Bryan J Dicken; Ivan M Rebeyka; David B Ross; Lindsay M Ryerson
Journal:  J Pediatr Surg       Date:  2013-10       Impact factor: 2.545

9.  Abnormalities of intestinal rotation in patients with congenital heart disease and the heterotaxy syndrome.

Authors:  Barbara Ferdman; Lisa States; J William Gaynor; Holly L Hedrick; Jack Rychik
Journal:  Congenit Heart Dis       Date:  2007 Jan-Feb       Impact factor: 2.007

10.  Arterial desaturation due to pulmonary arteriovenous malformations after the Kawashima Operation.

Authors:  Rohit S Loomba
Journal:  Ann Pediatr Cardiol       Date:  2016 Jan-Apr
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