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Unipolar voltage abnormality is associated with greater left ventricular dysfunction in ischemic cardiomyopathy
B. Aldhoon, DS. Frankel, MD. Hutchinson, DJ. Callans, AE. Epstein, S. Dixit, MP. Riley, D. Lin, FC. Garcia, GE. Supple, JM. Cooper, R. Bala, R. Deo, ES. Zado, FE. Marchlinski,
Language English Country United States
Document type Journal Article, Research Support, Non-U.S. Gov't
NLK
CINAHL Plus with Full Text (EBSCOhost)
from 1990-02-01 to 1 year ago
Medline Complete (EBSCOhost)
from 1990-02-01 to 1 year ago
PubMed
24237590
DOI
10.1111/jce.12315
Knihovny.cz E-resources
- MeSH
- Ventricular Dysfunction, Left diagnosis physiopathology surgery MeSH
- Myocardial Ischemia diagnosis physiopathology surgery MeSH
- Cardiomyopathies diagnosis physiopathology surgery MeSH
- Catheter Ablation methods MeSH
- Middle Aged MeSH
- Humans MeSH
- Body Surface Potential Mapping methods MeSH
- Aged MeSH
- Treatment Outcome MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
INTRODUCTION: Following myocardial infarction (MI), left ventricular function is determined by cardiac remodeling occurring in both infarcted and noninfarcted myocardium (NIM). Unipolar voltage mapping may detect remodeling changes in NIM that are associated with the left ventricular ejection fraction (LVEF). We aimed to identify (1) unipolar voltage characteristics in patients with chronic MI, and (2) association of voltage abnormalities with degree of left ventricular dysfunction (LVD). METHODS AND RESULTS: Two groups of patients with ischemic cardiomyopathy (ICM) who underwent LV endocardial mapping during catheter ablation for ventricular tachycardia (VT) between January 2010 and December 2012 were studied. The first group (19 males) had mild to moderate LVD (M-LVD, LVEF >35%) and was matched for age, sex, infarction size, and infarction location with 10 males who had severe LVD (S-LVD, LVEF <35%). Both bipolar and unipolar endocardial abnormal voltage areas were measured and compared between groups. Abnormal bipolar area was comparable in both groups (30 ± 8% in the S-LVD group vs 28 ± 8% in the M-LVD group; P = 0.5). Total abnormal unipolar voltage area was significantly larger in the S-LVD group (57 ± 14% vs 43 ± 13%; P = 0.02). The abnormal unipolar voltage area within the normal bipolar voltage area was greater in the S-LVD group (26 ± 11% vs 15 ± 16%; P = 0.03). In receiver operating characteristic curve analysis, an 18.0% cut-off value for abnormal unipolar area within NIM identified severe LVD, with 90% sensitivity and 79% specificity (area under the curve 0.821). CONCLUSIONS: Patients with ICM and severe LVD have larger areas of unipolar voltage abnormality in the noninfarcted tissue than patients with M-LVD.
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