4.7 Article

First Report of the Global SYMPLICITY Registry on the Effect of Renal Artery Denervation in Patients With Uncontrolled Hypertension

期刊

HYPERTENSION
卷 65, 期 4, 页码 766-+

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/HYPERTENSIONAHA.114.05010

关键词

denervation; hypertension; sympathetic nervous system

资金

  1. Medtronic, Inc
  2. German Society of Cardiology (Deutsche Gesellschaft fur Kardiologie)
  3. National Institute for Health Research [NF-SI-0514-10011] Funding Source: researchfish

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This study aimed to assess the safety and effectiveness of renal denervation using the Symplicity system in realworld patients with uncontrolled hypertension (NCT01534299). The Global SYMPLICITY Registry is a prospective, open-label, multicenter registry. Office and 24-hour ambulatory blood pressures (BPs) were measured. Change from baseline to 6 months was analyzed for all patients and for subgroups based on baseline office systolic BP, diabetic status, and renal function; a cohort with severe hypertension (office systolic pressure, >= 160 mm Hg; 24-hour systolic pressure, = 135 mm Hg; and = 3 antihypertensive medication classes) was also included. The analysis included protocol-defined safety events. Six-month outcomes for 998 patients, including 323 in the severe hypertension cohort, are reported. Mean baseline office systolic BP was 163.5 +/- 24.0 mm Hg for all patients and 179.3 +/- 16.5 mm Hg for the severe cohort; the corresponding baseline 24-hour mean systolic BPs were 151.5 +/- 17.0 and 159.0 +/- 15.6 mm Hg. At 6 months, the changes in office and 24-hour systolic BPs were -11.6 +/- 25.3 and -6.6 +/- 18.0 mm Hg for all patients (P<0.001 for both) and -20.3 +/- 22.8 and -8.9 +/- 16.9 mm Hg for those with severe hypertension (P<0.001 for both). Renal denervation was associated with low rates of adverse events. After the procedure through 6 months, there was 1 new renal artery stenosis >70% and 5 cases of hospitalization for a hypertensive emergency. In clinical practice, renal denervation resulted in significant reductions in office and 24-hour BPs with a favorable safety profile. Greater BP-lowering effects occurred in patients with higher baseline pressures.

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