Atrial Fibrillation, Hypertension
Conditions
Keywords
Atrial Fibrillation, Hypertension, Renal Denervation
Brief summary
We propose a pilot study to assess safety and benefit of renal artery ablation at the time of planned atrial fibrillation ablation.
Detailed description
Symptomatic atrial fibrillation (AF) refractory to anti-arrhythmic drugs is commonly treated with ablation therapy. Pulmonary vein isolation along with additional substrate medication is commonly performed during ablation procedures is associated with 60-80% success rate for maintenance of sinus rhythm. After AF ablation hypertension (HTN) is a strong predictor for recurrence of atrial fibrillation. Drug resistant hypertension can be effectively treated with catheter based renal denervation therapy. Our primary hypothesis is concomitant renal denervation therapy along with AF ablation is associated with improvement in success rates of AF ablation along with adequate control of blood pressure. The specific objectives of this study are to prospectively compare success rates, time to AF recurrence, AF burden and blood pressure controls in patients randomized to concomitant renal denervation arm when compared to patients with AF ablation alone.
Interventions
PROCEDUREAF ablation with Renal Denervation
Pulmonary vein isolation (PVI) is performed as per operator preference by previously described techniques. Both mapping and ablation are performed under general anesthesia. The use of standard electrophysiology ablation catheter to perform renal artery ablation in hypertensive patients has been previously described. UP to 2 minutes of RF energy (10W with irrigation flow of 17 ml/min) are delivered at each location and up to 6 lesions for each artery on the longitudinal and rotational axis. Renal denervation is performed on both vascular pedicles after clinical AF ablation in patients assigned to the intervention arm.
PROCEDUREAF ablation alone
Pulmonary vein isolation (PVI) is performed as per operator preference by previously described techniques.
Sponsors
Siva Mulpuru
Study design
Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Paroxysmal and Persistent Atrial Fibrillation refractory eligible for AF ablation as per HRS/ECAS/EHRA consensus statement.\[23\] Paroxysmal AF is defined as two or more episodes of AF lasting less than 7 days in duration during the last 6 months before enrollment. Persistent AF is defined as AF lasting more than 7 days or requiring cardioversion for termination. 2. Hypertension (\>140/80 mm Hg) on treatment with at least 1 hypertensive medication. 3. GFR \>60ml/dl using Cockcroft- Gault equation
Exclusion criteria
1. Secondary causes of hypertension 2. Severe renal artery stenosis or dual renal arteries 3. Congestive heart failure with NYHA class III or IV status 4. EF\< 35% 5. LA Diameter \>6 cm 6. Previous AF ablation 7. Previous renal artery stent or angioplasty 8. Severe contrast allergy 9. Inability to give informed consent 10. Solitary kidney
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Atrial fibrillation (AF) Time to recurrence and Burden | 1 year | After 3 months of blanking period, time to recurrence of atrial arrhythmia lasting more than 30 seconds is measured during follow up. (Atrial fibrillation)AF burden is assessed on a 7 day duration event monitor. Electrocardiogram (EKG) or Event monitor strips will be evaluated by independent board certified physicians. |
| Hypertension control | 1 year | BP is obtained as per Joint National Committee (JNC 7) standards at 3, 6 and 12 month visits of follow up. Information regarding titration of antihypertensives or reduction in the number of medications to adequately control blood pressure is collected. |
Secondary
| Measure | Time frame |
|---|---|
| Glomerular Filtration Rate (GFR) at 3, 6 and 12 months | 1 year |
| Renal artery complications by Crosssectional Imaging (Magnetic Resonance Imaging or computed tomography | 3months |
| Quality of life scores (MAFSI- Mayo Atrial Fibrillation Symptom Index) | 1 year |
| Change in left atrial volume parameters | 1 year |
Countries
United States
Outcome results
None listed