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Local electrogram delay recorded from left ventricular lead at implant predicts response to cardiac resynchronization therapy: retrospective study with 1 year follow up
R. Polasek, P. Kucera, P. Nedbal, T. Roubicek, T. Belza, J. Hanuliakova, D. Horak, D. Wichterle, J. Kautzner,
Language English Country England, Great Britain
Document type Journal Article, Research Support, Non-U.S. Gov't
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BioMedCentral
from 2001-12-01
BioMedCentral Open Access
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Directory of Open Access Journals
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Free Medical Journals
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- MeSH
- Biomarkers blood MeSH
- Bundle-Branch Block physiopathology therapy MeSH
- Time Factors MeSH
- Equipment Design MeSH
- Adult MeSH
- Electrophysiologic Techniques, Cardiac * MeSH
- Ventricular Function, Left * MeSH
- Risk Assessment MeSH
- Middle Aged MeSH
- Humans MeSH
- Linear Models MeSH
- Multivariate Analysis MeSH
- Natriuretic Peptide, Brain blood MeSH
- Peptide Fragments blood MeSH
- Predictive Value of Tests MeSH
- Cardiac Resynchronization Therapy Devices * MeSH
- Ventricular Remodeling MeSH
- Retrospective Studies MeSH
- Risk Factors MeSH
- Chi-Square Distribution MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Heart Block blood physiopathology therapy MeSH
- Cardiac Resynchronization Therapy * adverse effects MeSH
- Heart Failure blood physiopathology therapy MeSH
- Treatment Outcome MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Geographicals
- Czech Republic MeSH
BACKGROUND: Considerable proportion of patients does not respond to the cardiac resynchronization therapy (CRT). This study investigated clinical relevance of left ventricular electrode local electrogram delay from the beginning of QRS (QLV). We hypothesized that longer QLV indicating more optimal lead placement in the late activated regions is associated with the higher probability of positive CRT response. METHODS: We conducted a retrospective, single-centre analysis of 161 consecutive patients with heart failure and LBBB or nonspecific intraventricular conduction delay (IVCD) treated with CRT. We routinely intend to implant the LV lead in a region with long QLV. Clinical response to CRT, left ventricular (LV) reverse remodelling (i.e. decrease in LV end-systolic diameter - LVESD ≥10%) and reduction in plasma level of NT-proBNP >30% at 12-month post-implant were the study endpoints. We analyzed association between pre-implant variables and the study endpoints. RESULTS: Clinical CRT response rate reached 58%, 84% and 92% in the lowest (≤105 ms), middle (106-130 ms) and the highest (>130 ms) QLV tertile (p < 0.0001), respectively. Longer QRS duration (p = 0.002), smaller LVESD and a non-ischemic cardiomyopathy (both p = 0.02) were also univariately associated with positive clinical CRT response. In a multivariate analysis, QLV remained the strongest predictor of clinical CRT response (p < 0.00001), followed by LVESD (p = 0.01) and etiology of LV dysfunction (p = 0.04). Comparable predictive power of QLV for LV reverse remodelling and NT-proBNP response rates was observed. CONCLUSION: LV lead position assessed by duration of the QLV interval was found the strongest independent predictor of beneficial clinical response to CRT.
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