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LEFT VENTRICULAR DYSSYNCHRONY IN PATIENTS WITH MODERATE CORONARY STENOSIS AND BORDER LINE FRACTIONAL FLOW RESERVE
The cutoff values of fractional flow reserve (FFR) to detect physiological myocardial ischemia are still controversial. Some studies have reported that left ventricular (LV) dyssynchrony occurs in patients with coronary artery disease (CAD). The purpose of this study was to investigate LV dyssynchro...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nagoya University
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4361517/ https://www.ncbi.nlm.nih.gov/pubmed/25797980 |
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author | SHIBATA, YOHEI SONE, TAKAHITO TSUBOI, HIDEYUKI ISOBE, SATOSHI ISHII, HIDEKI SUZUKI, SUSUMU HAYASHI, MUTSUHARU MUROHARA, TOYOAKI |
author_facet | SHIBATA, YOHEI SONE, TAKAHITO TSUBOI, HIDEYUKI ISOBE, SATOSHI ISHII, HIDEKI SUZUKI, SUSUMU HAYASHI, MUTSUHARU MUROHARA, TOYOAKI |
author_sort | SHIBATA, YOHEI |
collection | PubMed |
description | The cutoff values of fractional flow reserve (FFR) to detect physiological myocardial ischemia are still controversial. Some studies have reported that left ventricular (LV) dyssynchrony occurs in patients with coronary artery disease (CAD). The purpose of this study was to investigate LV dyssynchrony in patients with moderate coronary stenosis and borderline FFR, using stress electrocardiographically-gated myocardial perfusion single-photon emission computed tomography (SPECT). The study population comprised 10 patients with moderate (50–75% diameter) stenosis and an FFR in the range 0.75–0.90, who were compared to 10 control subjects. All underwent stress myocardial (99m)Tc-sestamibi (MIBI) or tetrofosmin SPECT imaging. The regional time to end systole (TES), time to peak ejection (TPE), and time to peak filling (TPF) were obtained as indexes of perfusion and function, using gated SPECT (pFAST) in combination with Cardio Gated SPECT Regional Assessment for LV Function (cardioGRAF). The dyssynchrony index (DI) was also calculated. The DI of post-stress TES was significantly greater than that of rest in patients with moderate CAD (4.8 ± 2.8 vs. 2.7 ± 1.5, P = 0.01), but there were no significant differences in the control subjects (3.0 ± 1.7 vs. 2.9 ± 1.9, P = 0.99). There were no significant differences in TPE and TPF between the groups. In conclusion, LV dyssynchrony may occur after stress in patients with coronary stenosis and borderline FFR, even without a significant reduction in perfusion. |
format | Online Article Text |
id | pubmed-4361517 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nagoya University |
record_format | MEDLINE/PubMed |
spelling | pubmed-43615172015-03-20 LEFT VENTRICULAR DYSSYNCHRONY IN PATIENTS WITH MODERATE CORONARY STENOSIS AND BORDER LINE FRACTIONAL FLOW RESERVE SHIBATA, YOHEI SONE, TAKAHITO TSUBOI, HIDEYUKI ISOBE, SATOSHI ISHII, HIDEKI SUZUKI, SUSUMU HAYASHI, MUTSUHARU MUROHARA, TOYOAKI Nagoya J Med Sci Original Paper The cutoff values of fractional flow reserve (FFR) to detect physiological myocardial ischemia are still controversial. Some studies have reported that left ventricular (LV) dyssynchrony occurs in patients with coronary artery disease (CAD). The purpose of this study was to investigate LV dyssynchrony in patients with moderate coronary stenosis and borderline FFR, using stress electrocardiographically-gated myocardial perfusion single-photon emission computed tomography (SPECT). The study population comprised 10 patients with moderate (50–75% diameter) stenosis and an FFR in the range 0.75–0.90, who were compared to 10 control subjects. All underwent stress myocardial (99m)Tc-sestamibi (MIBI) or tetrofosmin SPECT imaging. The regional time to end systole (TES), time to peak ejection (TPE), and time to peak filling (TPF) were obtained as indexes of perfusion and function, using gated SPECT (pFAST) in combination with Cardio Gated SPECT Regional Assessment for LV Function (cardioGRAF). The dyssynchrony index (DI) was also calculated. The DI of post-stress TES was significantly greater than that of rest in patients with moderate CAD (4.8 ± 2.8 vs. 2.7 ± 1.5, P = 0.01), but there were no significant differences in the control subjects (3.0 ± 1.7 vs. 2.9 ± 1.9, P = 0.99). There were no significant differences in TPE and TPF between the groups. In conclusion, LV dyssynchrony may occur after stress in patients with coronary stenosis and borderline FFR, even without a significant reduction in perfusion. Nagoya University 2015-02 /pmc/articles/PMC4361517/ /pubmed/25797980 Text en http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license, please visit (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Paper SHIBATA, YOHEI SONE, TAKAHITO TSUBOI, HIDEYUKI ISOBE, SATOSHI ISHII, HIDEKI SUZUKI, SUSUMU HAYASHI, MUTSUHARU MUROHARA, TOYOAKI LEFT VENTRICULAR DYSSYNCHRONY IN PATIENTS WITH MODERATE CORONARY STENOSIS AND BORDER LINE FRACTIONAL FLOW RESERVE |
title | LEFT VENTRICULAR DYSSYNCHRONY IN PATIENTS WITH MODERATE CORONARY STENOSIS AND BORDER LINE FRACTIONAL FLOW RESERVE |
title_full | LEFT VENTRICULAR DYSSYNCHRONY IN PATIENTS WITH MODERATE CORONARY STENOSIS AND BORDER LINE FRACTIONAL FLOW RESERVE |
title_fullStr | LEFT VENTRICULAR DYSSYNCHRONY IN PATIENTS WITH MODERATE CORONARY STENOSIS AND BORDER LINE FRACTIONAL FLOW RESERVE |
title_full_unstemmed | LEFT VENTRICULAR DYSSYNCHRONY IN PATIENTS WITH MODERATE CORONARY STENOSIS AND BORDER LINE FRACTIONAL FLOW RESERVE |
title_short | LEFT VENTRICULAR DYSSYNCHRONY IN PATIENTS WITH MODERATE CORONARY STENOSIS AND BORDER LINE FRACTIONAL FLOW RESERVE |
title_sort | left ventricular dyssynchrony in patients with moderate coronary stenosis and border line fractional flow reserve |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4361517/ https://www.ncbi.nlm.nih.gov/pubmed/25797980 |
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