Atrial Arrhythmia, Atrial Fibrillation
Conditions
Keywords
Atrial fibrillation, Mediterranean Diet, Extra Virgin Olive Oil, Ablation
Brief summary
Background: Atrial fibrillation (AF) is the most frequent cardiac arrhythmia and represents a high priority public health problem, as in a few decades it will become a possibly unsustainable load for the national health system. Preventive and therapeutic strategies based on the best possible scientific evidence are required. Ablation therapy, despite being the most effective approach, is associated with a 30-35% arrhythmic recurrence rate. An intervention with Mediterranean diet and extra virgin olive oil (EVOO) has proven effective in primary prevention and reduced the incidence of AF in high-risk subjects in a recent, large, randomized trial (PREDIMED). Methods: Parallel, randomized, multicenter nutritional intervention trial in 640 patients with AF treated with catheter ablation. Two groups will be randomized in a 1:1 ratio: 1) intervention with Mediterranean diet and EVOO; 2) usual care (control group). The primary objective will be the incidence of atrial tachyarrhythmias for two years after ablation. At least 190 recurrences are expected after 2 years (median) of follow-up. A relative risk of 0.7 is assumed and statistical power of 80%. Follow-up visits will be scheduled at 3, 6, 12, 18 and 24 months. In addition to the in-person visits, event monitors will be used to document episodes. Dietary intervention will be carried out by nutritionists who will use methods adapted from the PREDIMED trial with contacts every 2 months. 1 liter of EVOO per week will be provided for free in the intervention arm. Inflammatory markers will be analyzed in both groups during follow-up. Cox models will be used to estimate adjusted hazard ratios.
Interventions
DIETARY_SUPPLEMENTMediterranean diet plus extra virgin olive oil
The patients in the intervention group will receive 1 liter of EVOO per week free of charge and dietary advice on how to follow a Mediterranean diet with contacts every two months. Dietary intervention will be carried out by nutritionists with previous experience in the PREDIMED study. All of them were registered, trained and certified for developing the PREDIMED intervention protocol that is similar to the one to be carried out in this study. The theoretical sessions with patients about dietary education shall be conducted in telephone form, using the internet and sending comprehensive written material to their homes that includes recipes, shopping lists, menus and explanations of typical food in the Mediterranean diet
Sponsors
University of Navarra
University Hospital Virgen de las Nieves
Hospital General Universitario de Alicante
Fundación de investigación HM
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)
Eligibility
Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No
Inclusion criteria
* Patients with symptomatic paroxysmal AF (with evidence of more than one symptomatic episode in the last year and at least one documented episode) upon whom catheter ablation is performed. * Patients with persistent symptomatic AF upon whom catheter ablation is performed.
Exclusion criteria
* Serious medical condition that prevents dietary intervention (gastrointestinal disease with intolerance to fats, advanced malignancy, neurological, psychiatric or severe endocrine disease) * Any other pathology or medical condition that limits survival to less than one year; Immunodeficiency or HIV-positive, * Consumption of illegal drugs, * Chronic alcoholism or total consumption of alcohol \>80 g/d * Body mass index \> 40 kg/m 2, * Difficulty or major inconvenience with changing dietary habits, inability to follow a style of Mediterranean diet, low probability of changing dietary habits according to the models of Prochaska and Diciemente (Nigg, 1999) * History of food allergy or hypersensitivity to any component of EVOO * Participation in a clinical trial carried out with drugs or use of a drug in experimental state during the year prior to inclusion * Institutionalized patients for chronic treatment, with lack of autonomy and with inability to perform the clinical follow-up, * Impossibility of telephone contact * Patients with acute infection or inflammatory process (e.g. pneumonia) may be included in the study three months after the resolution of the infectious symptoms.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| atrial tachyarrhythmias documented by electrocardiogram or recorder device | mean follow up of 2 years | Atrial tachyarrhythmia is defined at any fast rate (\>100 bpm) of supraventricular origin lasting more than 30 seconds and that is documented by ECG, Holter or event monitor. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Atrial fibrillation documented by electrocardiogram or recorder device | mean follow up of 2 years | AF is defined at any irregular atrial rhythm lasting more than 30 seconds and that is documented by ECG, Holter or event monitor. AF may or may not be symptomatic. |
| changes in Inflammatory markers in blood samples | 1 year follow up | Prior to ablation blood samples will be collected for determination of inflammatory parameters in a subsample of the study (neutrophil to lymphocyte ratio, TNF-alpha, fibrinogen, IL-2, IL6, IL-8, C-reactive protein). At 3 and 12 months of follow-up the determination of these parameters will be repeated. |
| Changes in quality of life measured by SF-36 questionnaire | mean follow up of 2 years | Change in quality of life during the follow up measured by SF-36 questionnaire |
Countries
Spain
Outcome results
None listed