A Controlled Trial of Renal Denervation for Resistant Hypertension

被引:1623
作者
Bhatt, Deepak L. [1 ,2 ]
Kandzari, David E. [5 ]
O'Neill, William W. [6 ]
D'Agostino, Ralph [3 ,4 ]
Flack, John M. [7 ,8 ]
Katzen, Barry T. [9 ]
Leon, Martin B. [10 ,11 ]
Liu, Minglei [12 ]
Mauri, Laura [1 ,2 ,4 ]
Negoita, Manuela [12 ]
Cohen, Sidney A. [12 ,15 ]
Oparil, Suzanne [13 ]
Rocha-Singh, Krishna [14 ]
Townsend, Raymond R. [15 ]
Bakris, George L. [16 ]
机构
[1] Brigham & Womens Hosp, Heart & Vasc Ctr, 75 Francis St, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Boston, MA USA
[3] Boston Univ, Sch Publ Hlth, Boston, MA USA
[4] Harvard Clin Res Inst, Boston, MA USA
[5] Piedmont Heart Inst, Atlanta, GA USA
[6] Henry Ford Hosp, Div Cardiol, Detroit, MI 48202 USA
[7] Wayne State Univ, Detroit, MI USA
[8] Detroit Med Ctr, Detroit, MI USA
[9] Baptist Cardiac & Vasc Inst, Miami, FL USA
[10] Columbia Univ, New York Presbyterian Hosp, Med Cen ter, New York, NY USA
[11] Cardiovasc Res Fdn, New York, NY USA
[12] Medtron CardioVasc, Santa Rosa, CA USA
[13] Univ Alabama Birmingham, Birmingham, AL USA
[14] Prairie Heart Inst, Springfield, IL USA
[15] Univ Penn, Perelman Sch Med, Philadelphia, PA 19104 USA
[16] Univ Chicago Med, Chicago, IL USA
关键词
SYMPATHETIC DENERVATION; STATEMENT; EDUCATION; THERAPY; COUNCIL; DESIGN;
D O I
10.1056/NEJMoa1402670
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Prior unblinded studies have suggested that catheter-based renal-artery denervation reduces blood pressure in patients with resistant hypertension. Methods We designed a prospective, single-blind, randomized, sham-controlled trial. Patients with severe resistant hypertension were randomly assigned in a 2:1 ratio to undergo renal denervation or a sham procedure. Before randomization, patients were receiving a stable antihypertensive regimen involving maximally tolerated doses of at least three drugs, including a diuretic. The primary efficacy end point was the change in office systolic blood pressure at 6 months; a secondary efficacy end point was the change in mean 24-hour ambulatory systolic blood pressure. The primary safety end point was a composite of death, end-stage renal disease, embolic events resulting in end-organ damage, renovascular complications, or hypertensive crisis at 1 month or new renal-artery stenosis of more than 70% at 6 months. Results A total of 535 patients underwent randomization. The mean (SD) change in systolic blood pressure at 6 months was -14.1323.93 mm Hg in the denervation group as compared with -11.7425.94 mm Hg in the sham-procedure group (P<0.001 for both comparisons of the change from baseline), for a difference of -2.39 mm Hg (95% confidence interval [CI], -6.89 to 2.12; P=0.26 for superiority with a margin of 5 mm Hg). The change in 24-hour ambulatory systolic blood pressure was -6.7515.11 mm Hg in the denervation group and -4.79 +/- 17.25 mm Hg in the sham-procedure group, for a difference of -1.96 mm Hg (95% CI, -4.97 to 1.06; P=0.98 for superiority with a margin of 2 mm Hg). There were no significant differences in safety between the two groups. Conclusions This blinded trial did not show a significant reduction of systolic blood pressure in patients with resistant hypertension 6 months after renal-artery denervation as compared with a sham control. (Funded by Medtronic; SYMPLICITY HTN-3 ClinicalTrials.gov number, NCT01418261.)
引用
收藏
页码:1393 / 1401
页数:9
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