TY - JOUR
T1 - Defining clinically important difference in the atrial fibrillation effect on quality-of-life score
T2 - Results from the outcomes registry for better informed treatment of atrial fibrillation
AU - Holmes, Dajuanicia N.
AU - Piccini, Jonathan P.
AU - Allen, Larry A.
AU - Fonarow, Gregg C.
AU - Gersh, Bernard J.
AU - Kowey, Peter R.
AU - O'Brien, Emily C.
AU - Reiffel, James A.
AU - Naccarelli, Gerald V.
AU - Ezekowitz, Michael D.
AU - Chan, Paul S.
AU - Singer, Daniel E.
AU - Spertus, John A.
AU - Peterson, Eric D.
AU - Thomas, Laine
N1 - Funding Information:
Dr Piccini reports research support from Boston Scientific, ResMed, ARCA Bio-pharma, St Jude Medical Center, Gilead Sciences, Johnson & Johnson, Spec-tranetics, and Janssen (all significant) and consultancies for Janssen Scientific Affairs (significant), Spectranetics (significant), Medtronic (significant), Forest Laboratories (modest), Pfizer (modest), Glaxo SmithKline (modest), and Am-gen and Allergan. Dr Allen reports research grants from PCORI, NIH/NHLBI and American Heart Association (all significant) and consultancies for ACI clinical (significant), Boston Scientific (modest), Cytokinetics/Amgen (modest), Duke Clinical Research Institute (modest) and Janssen (modest). Dr Fonarow reports consulting for Janssen (significant). Dr Gersh reports consultancies with Janssen Scientific Affairs (significant), Cipla Limited and Armetheon Inc. Data Safety Monitoring Board for Mount Sinai St Lukes, Boston Scientific Corporation (modest), Teva Pharmaceutical Industries, St Jude Medical, Janssen Research & Development, Baxter Healthcare Corporation, Thrombosis Research Institute, Duke Clinical Research Institute, Duke University, Kowa Research Institute and Cardiovascular Research Foundation (all modest) and advisory board member for Medtronic (modest). Dr Kowey reports consulting for Johnson & Johnson (significant), Daiichi-Sankyo (modest), Bristol-Myers Squibb, and Boehringer Ingelheim. Dr O’Brien reports research grants from Janssen Scientific Affairs, BMS, Novartis (significant) and Sanofi (modest). Dr Reiffel reports research grants from Medtronic and Janssen and is a consultant for Medtronic, Portola, InCardia Therapeutics, and Acesion. Dr Naccarelli reports a research grant from Janssen Scientific Affairs (significant) and is a consultant to Janssen (significant), Glaxo Smith Kline (significant), Sanofi (modest), Novartis (modest), Portola (modest), Acesion (modest), and Omeicos (modest). Dr Ezekowitz reports research grants from Bristol-Myers Squibb, Boehringer Ingelheim and Pfizer (all significant) and is a consultant for Medtronic, Boehringer Ingelheim, Pfizer, Sanofi, Portota, Daiichi-Sankyo, Johnson and Johnson, Janssen Scientific Affairs, Merck, Pfizer, and Bristol-Myers Squibb (all modest). Dr Chan is supported by the National Heart Blood and Lung Institute (1R01HL123980). Dr Singer reports contract research with Bristol-Myers Squibb and Boehringer Ingelheim (both significant) and is a consultant/advisory board member for Boehringer Ingelheim (significant), Bristol-Myers Squibb (significant), Medtronic (modest), Johnson and Johnson (modest), Merck (modest), Pfizer (modest), and CVS Health (modest). Dr Spertus reports research support from Bayer (significant) and consultant for Janssen Scientific Affairs, Bayer, Novartis, United Healthcare, AstraZeneca (all modest). Dr Peterson reports significant research support from Eli Lilly & Company, Dai-ichi Sankyo, and Janssen. Dr Thomas reports research support with Novartis, Boston Scientific, Gilead Sciences, Inc, and Janssen Scientific Affairs (all modest). The other author reports no conflicts.
Publisher Copyright:
© 2019 American Heart Association, Inc.
PY - 2019/5/1
Y1 - 2019/5/1
N2 - Background: The Atrial Fibrillation Effect on Quality-of-Life (AFEQT) questionnaire has recently been validated to measure the impact of atrial fibrillation on quality of life, but a clinically important difference in AFEQT score has not been well defined. Methods and Results: To determine the clinically important difference in overall AFEQT (score range= 0 [worst] to 100 [best]) and selected subscales, we analyzed data in the Outcomes Registry for Better Informed Treatment of Atrial Fibrillation (ORBIT-AF) registry, a United States-based outpatient atrial fibrillation registry. AFEQT was assessed at baseline and 1 year in a subset of 1347 ORBIT-AF patients from 80 US sites participating in ORBIT-AF from June 2010 to August 2011. The mean change method was used to relate changes in 1-year AFEQT scores to clinically important changes in the physician assessment of European Heart Rhythm Association functional status (1 class improvement and separately 1 class deterioration). Clinically important differences and 95% CI corresponding to either a 1 European Heart Rhythm Association class improvement or deterioration were 5.4 (3.6-7.2) and-4.2 (-6.9 to-1.5) AFEQT points, respectively. Similarly, clinically important difference values were seen for a 1 European Heart Rhythm Association class improvement for the AFEQT subscales Activities of Daily Living and Symptoms: 5.1 (2.5-7.6) and 7.1 (5.3-9.0) AFEQT points, respectively. Conclusions: Based on the anchor of 1 European Heart Rhythm Association class change, changes in AFEQT score of + or-5 points are clinically important changes in patients' health. Clinical Trial Registration: URL: https://clinicaltrials.gov. Unique identifier: NCT01165710.
AB - Background: The Atrial Fibrillation Effect on Quality-of-Life (AFEQT) questionnaire has recently been validated to measure the impact of atrial fibrillation on quality of life, but a clinically important difference in AFEQT score has not been well defined. Methods and Results: To determine the clinically important difference in overall AFEQT (score range= 0 [worst] to 100 [best]) and selected subscales, we analyzed data in the Outcomes Registry for Better Informed Treatment of Atrial Fibrillation (ORBIT-AF) registry, a United States-based outpatient atrial fibrillation registry. AFEQT was assessed at baseline and 1 year in a subset of 1347 ORBIT-AF patients from 80 US sites participating in ORBIT-AF from June 2010 to August 2011. The mean change method was used to relate changes in 1-year AFEQT scores to clinically important changes in the physician assessment of European Heart Rhythm Association functional status (1 class improvement and separately 1 class deterioration). Clinically important differences and 95% CI corresponding to either a 1 European Heart Rhythm Association class improvement or deterioration were 5.4 (3.6-7.2) and-4.2 (-6.9 to-1.5) AFEQT points, respectively. Similarly, clinically important difference values were seen for a 1 European Heart Rhythm Association class improvement for the AFEQT subscales Activities of Daily Living and Symptoms: 5.1 (2.5-7.6) and 7.1 (5.3-9.0) AFEQT points, respectively. Conclusions: Based on the anchor of 1 European Heart Rhythm Association class change, changes in AFEQT score of + or-5 points are clinically important changes in patients' health. Clinical Trial Registration: URL: https://clinicaltrials.gov. Unique identifier: NCT01165710.
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U2 - 10.1161/CIRCOUTCOMES.118.005358
DO - 10.1161/CIRCOUTCOMES.118.005358
M3 - Article
C2 - 31092022
AN - SCOPUS:85066876327
SN - 1941-7713
VL - 12
JO - Circulation: Cardiovascular Quality and Outcomes
JF - Circulation: Cardiovascular Quality and Outcomes
IS - 5
M1 - e005358
ER -