Atrial fibrillation Circulatory System Atrial fibrillation and flutter
Conditions
Interventions
The study is a single-center cohort study with a prospective design using different questionnaires at baseline to investigate quality of life (QoL), symptoms and referral experiences before atrial fib
Sponsors
Karolinska Institute
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients referred for a de novo PVI
Exclusion criteria
Exclusion criteria: 1. Inability to read or understand Swedish 2. Cognitive impairment
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| Referral history, experience of information given in regard to the arrhythmia, number of years with symptomatic atrial fibrillation (AF), and previous evaluations and diagnoses of their arrhythmia symptoms, measured with a supplementary questionnaire at baseline | — |
Primary
| Measure | Time frame |
|---|---|
| 1. Symptoms measured using the Symptom Checklist-Frequency and Severity Scale (SCL) at baseline and 6 months 2. QoL measured using the Short Form-36 (SF-36) health survey questionnaire at baseline and 6 months 3. Functional impairment measured using the Sick Impact Profile at baseline and 6 months | — |
Countries
Sweden
Outcome results
None listed