The FDA has approved Medtronic's Symplicity Spyral renal denervation system for treating hypertension. The system uses radiofrequency energy to denervate renal arteries. The approval follows the FDA's Circulatory System Devices Panel's split decision on the system's efficacy and risk-benefit analysis. The SPYRAL HTN Global Clinical Program treated over 25,000 patients with and without medication, showing a significant reduction in ambulatory systolic blood pressure. The system was evaluated in the SPYRAL HTN-OFF and SPYRAL HTN-ON studies, demonstrating varying results in blood pressure reduction. Key opinion leaders emphasize the safety and effectiveness of the procedure, highlighting its potential to transform hypertension treatment. Patient preference and shared decision-making play crucial roles in considering the Symplicity blood pressure procedure.
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