CARDIAC RESYNCHRONIZATION AND DEFIBRILLATOR THERAPY (CRT-D) OR CRT ALONE (CRT-P) IN PATIENTS WITH DILATED CARDIOMYOPATHY AND HEART FAILURE WITHOUT LATE GADOLINIUM ENHANCEMENT (LGE) CARDIAC MAGNETIC RESONANCE IMAGING (CMRI) HIGH-RISK MARKERS - CRT-REALITY STUDY - STUDY DESIGN AND RATIONALE
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F27283933%3A_____%2F21%3A00009786" target="_blank" >RIV/27283933:_____/21:00009786 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/00669806:_____/22:10435465 RIV/00159816:_____/22:00077899 RIV/00023001:_____/22:00083421 RIV/00098892:_____/22:10157606 a 5 dalších
Výsledek na webu
<a href="https://biomed.papers.upol.cz/pdfs/bio/2022/02/08.pdf" target="_blank" >https://biomed.papers.upol.cz/pdfs/bio/2022/02/08.pdf</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.5507/bp.2021.015" target="_blank" >10.5507/bp.2021.015</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
CARDIAC RESYNCHRONIZATION AND DEFIBRILLATOR THERAPY (CRT-D) OR CRT ALONE (CRT-P) IN PATIENTS WITH DILATED CARDIOMYOPATHY AND HEART FAILURE WITHOUT LATE GADOLINIUM ENHANCEMENT (LGE) CARDIAC MAGNETIC RESONANCE IMAGING (CMRI) HIGH-RISK MARKERS - CRT-REALITY STUDY - STUDY DESIGN AND RATIONALE
Popis výsledku v původním jazyce
Background: Primary preventive implantation of implantable defibrillator (ICD) is according to current guidelines indicated in patients with heart failure NYHA (New York Heart Association) class II/III and LVEF b35%. Thanks to advances in heart failure pharmacotherapy, a decrease in mortality could render a benefit of ICD insufficient to justify its implantation in some patients. Methods: Study design: multicenter, prospective, randomized, controlled trial evaluating the benefit of implantation of Cardiac Resynchronization and Defibrillator Therapy (CRT-D) or CRT Alone (CRT-P) in non-ischemic patients with reduced left ventricle ejection fraction (LVEF) and optimal pharmacotherapy without significant mid-wall myocardial fibrosis detected by cardiac magnetic resonance (CMR). The primary end-point: Re-hospitalization for heart failure, ventricular tachycardia, major adverse cardiac events (MACE). The secondary end-points: Sudden cardiac death, cardiovascular death, resuscitated cardiac arrest or sustained ventricular tachycardia, device-related complications, and change in quality of life. Course of the study: After a pharmacotherapy is optimized and significant mid-wall myocardial fibrosis excluded, patients will be randomized 1:1 to CRT-P or CRT-D implantation. Discussion: If our hypothesis is confirmed, this could provide evidence for the management of these patients with a significant impact on common daily praxis and health care expenditures.
Název v anglickém jazyce
CARDIAC RESYNCHRONIZATION AND DEFIBRILLATOR THERAPY (CRT-D) OR CRT ALONE (CRT-P) IN PATIENTS WITH DILATED CARDIOMYOPATHY AND HEART FAILURE WITHOUT LATE GADOLINIUM ENHANCEMENT (LGE) CARDIAC MAGNETIC RESONANCE IMAGING (CMRI) HIGH-RISK MARKERS - CRT-REALITY STUDY - STUDY DESIGN AND RATIONALE
Popis výsledku anglicky
Background: Primary preventive implantation of implantable defibrillator (ICD) is according to current guidelines indicated in patients with heart failure NYHA (New York Heart Association) class II/III and LVEF b35%. Thanks to advances in heart failure pharmacotherapy, a decrease in mortality could render a benefit of ICD insufficient to justify its implantation in some patients. Methods: Study design: multicenter, prospective, randomized, controlled trial evaluating the benefit of implantation of Cardiac Resynchronization and Defibrillator Therapy (CRT-D) or CRT Alone (CRT-P) in non-ischemic patients with reduced left ventricle ejection fraction (LVEF) and optimal pharmacotherapy without significant mid-wall myocardial fibrosis detected by cardiac magnetic resonance (CMR). The primary end-point: Re-hospitalization for heart failure, ventricular tachycardia, major adverse cardiac events (MACE). The secondary end-points: Sudden cardiac death, cardiovascular death, resuscitated cardiac arrest or sustained ventricular tachycardia, device-related complications, and change in quality of life. Course of the study: After a pharmacotherapy is optimized and significant mid-wall myocardial fibrosis excluded, patients will be randomized 1:1 to CRT-P or CRT-D implantation. Discussion: If our hypothesis is confirmed, this could provide evidence for the management of these patients with a significant impact on common daily praxis and health care expenditures.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
30201 - Cardiac and Cardiovascular systems
Návaznosti výsledku
Projekt
—
Návaznosti
V - Vyzkumna aktivita podporovana z jinych verejnych zdroju
Ostatní
Rok uplatnění
2021
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Biomedical Papers
ISSN
1213-8118
e-ISSN
—
Svazek periodika
—
Číslo periodika v rámci svazku
2
Stát vydavatele periodika
CZ - Česká republika
Počet stran výsledku
7
Strana od-do
173-179
Kód UT WoS článku
000731340300001
EID výsledku v databázi Scopus
—