Development and Validation of the Atrial Fibrillation Effect on QualiTy-of-Life (AFEQT) Questionnaire in Patients With Atrial Fibrillation

Author:

Spertus John1,Dorian Paul1,Bubien Rosemary1,Lewis Steve1,Godejohn Donna1,Reynolds Matthew R.1,Lakkireddy Dhanunjaya R.1,Wimmer Alan P.1,Bhandari Anil1,Burk Caroline1

Affiliation:

1. From the Mid America Heart Institute (J.S., A.P.W.), Kansas City, MO; St Michael's Hospital (P.D.), Toronto, Ontario, Canada; the University of Alabama at Birmingham (R.B.), Birmingham, AL; St Jude Medical (S.L., D.G., C.B.), Atrial Fibrillation Division, St Paul, MN; the Division of Cardiology (M.R.R.), Beth Israel Deaconess Medical Center, Boston, MA; the University of Kansas Hospital (D.R.L.), Kansas City, KS; MDCC (S.L.), San Diego, CA; Outcomes Research Consultant (C.B.), Laguna Beach, CA; and...

Abstract

Background— Atrial fibrillation (AF) has a deleterious impact on health-related quality-of-life (HRQoL), but measuring this outcome is difficult. A comprehensive, validated, disease-specific questionnaire to measure the spectrum of QoL domains affected by AF and its treatment is not available. We developed and validated a 20-item questionnaire, Atrial Fibrillation Effect on QualiTy-of-life (AFEQT), in a 6-center, prospective, observational study. Methods and Results— Factor analyses established 4 conceptual domains (Symptoms, Daily Activities, Treatment Concern, and Treatment Satisfaction) from which individual domain and global scores were calculated. Participants from 6 centers completed the AFEQT at baseline, at month 1, and at month 3. Psychometric analyses included internal consistency and known-group validity. Test-retest reliability was assessed by comparing 1-month changes in scores among those with no change in therapy. Effect size was used to assess responsiveness after intervention. Among 219 patients age 62±11.9 years, 94% completed the AFEQT at baseline and 3 months; 66% had paroxysmal, 24% persistent, 5% longstanding persistent, and 5% permanent AF. Internal consistency was >0.88 for all scales. Lower AFEQT scores were observed with increased AF severity, categorized as asymptomatic, mild, moderate and severe, respectively: 71.2±20.6, 71.3±19.2, 57.9±19.0, and 42.0±21.2. Intraclass correlations for Overall, Symptoms, Daily Activities, Treatment Concern, and Satisfaction scores were 0.8, 0.5, 0.8, 0.7, and 0.7, respectively. Changes in 3-month scores were larger after ablation than with pharmacological adjustments, and both were greater than those observed in stable patients. Conclusions— This initial validation of AFEQT supports its use as an outcome in studies and a means to clinically follow patients with AF.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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