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Prevalence of myocardial perfusion abnormalities in end-stage liver disease
BACKGROUND: The prevalence of coronary artery disease (CAD) in end-stage liver disease (ESLD) being evaluated for orthotopic liver transplantation (OLT) is unclear based on variable definition used for CAD. OBJECTIVE: The aim of this study to investigate the prevalence of abnormal stress myocardial...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3180729/ https://www.ncbi.nlm.nih.gov/pubmed/21969772 http://dx.doi.org/10.4103/0972-3919.84588 |
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author | Fathala, Ahmed Safar, Bander Al Muhaideb, Ahmed |
author_facet | Fathala, Ahmed Safar, Bander Al Muhaideb, Ahmed |
author_sort | Fathala, Ahmed |
collection | PubMed |
description | BACKGROUND: The prevalence of coronary artery disease (CAD) in end-stage liver disease (ESLD) being evaluated for orthotopic liver transplantation (OLT) is unclear based on variable definition used for CAD. OBJECTIVE: The aim of this study to investigate the prevalence of abnormal stress myocardial perfusion single-photon emission computed tomography (MPS) imaging, as a marker for CAD, among patients with ESLD who were referred for stress MPS imaging as a routine work up before OLT. MATERIALS AND METHODS: This was a single-center, retrospective study. We reviewed data on 167 patients who were referred for MPS as a routine work up before OLT over the last 2 years. All patients underwent evaluation for CAD risk factors [age, hypercholesterolemia, diabetes mellitus (DM), hypertension (HTN), and smoking], and stress MPS as per standard protocol. RESULTS: The total number of patients referred for stress MPS was 167. Seven patients (4% of total study population) were excluded from the study due to poor and/or nondiagnostic studies. 147 patients (92%) had normal, but only 13 patients (8%) had abnormal MPS scans. DM and male gender were the most independent risk factors for abnormal MPS with P value of 0.046, and 0.26, respectively. There was no significant association between the abnormal MPS result and HTN, hypercholesterolemia, smoking, age or etiology of the liver disease. CONCLUSION: Based on our data, the prevalence of abnormal MPS and left ventricular ejection fraction in patients with ESLD was found to be 8%. DM and male gender were the most independent predictor factors for abnormal MPS. True prevalence of CAD and usefulness of MPS in patients with ESLD can only be studied using a very large and randomized prospective study. |
format | Online Article Text |
id | pubmed-3180729 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Medknow Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-31807292011-10-03 Prevalence of myocardial perfusion abnormalities in end-stage liver disease Fathala, Ahmed Safar, Bander Al Muhaideb, Ahmed Indian J Nucl Med Original Article BACKGROUND: The prevalence of coronary artery disease (CAD) in end-stage liver disease (ESLD) being evaluated for orthotopic liver transplantation (OLT) is unclear based on variable definition used for CAD. OBJECTIVE: The aim of this study to investigate the prevalence of abnormal stress myocardial perfusion single-photon emission computed tomography (MPS) imaging, as a marker for CAD, among patients with ESLD who were referred for stress MPS imaging as a routine work up before OLT. MATERIALS AND METHODS: This was a single-center, retrospective study. We reviewed data on 167 patients who were referred for MPS as a routine work up before OLT over the last 2 years. All patients underwent evaluation for CAD risk factors [age, hypercholesterolemia, diabetes mellitus (DM), hypertension (HTN), and smoking], and stress MPS as per standard protocol. RESULTS: The total number of patients referred for stress MPS was 167. Seven patients (4% of total study population) were excluded from the study due to poor and/or nondiagnostic studies. 147 patients (92%) had normal, but only 13 patients (8%) had abnormal MPS scans. DM and male gender were the most independent risk factors for abnormal MPS with P value of 0.046, and 0.26, respectively. There was no significant association between the abnormal MPS result and HTN, hypercholesterolemia, smoking, age or etiology of the liver disease. CONCLUSION: Based on our data, the prevalence of abnormal MPS and left ventricular ejection fraction in patients with ESLD was found to be 8%. DM and male gender were the most independent predictor factors for abnormal MPS. True prevalence of CAD and usefulness of MPS in patients with ESLD can only be studied using a very large and randomized prospective study. Medknow Publications 2011 /pmc/articles/PMC3180729/ /pubmed/21969772 http://dx.doi.org/10.4103/0972-3919.84588 Text en Copyright: © Indian Journal of Nuclear Medicine http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Fathala, Ahmed Safar, Bander Al Muhaideb, Ahmed Prevalence of myocardial perfusion abnormalities in end-stage liver disease |
title | Prevalence of myocardial perfusion abnormalities in end-stage liver disease |
title_full | Prevalence of myocardial perfusion abnormalities in end-stage liver disease |
title_fullStr | Prevalence of myocardial perfusion abnormalities in end-stage liver disease |
title_full_unstemmed | Prevalence of myocardial perfusion abnormalities in end-stage liver disease |
title_short | Prevalence of myocardial perfusion abnormalities in end-stage liver disease |
title_sort | prevalence of myocardial perfusion abnormalities in end-stage liver disease |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3180729/ https://www.ncbi.nlm.nih.gov/pubmed/21969772 http://dx.doi.org/10.4103/0972-3919.84588 |
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