Oral Nicorandil to Reduce Cardiac Death After Coronary Revascularization in Hemodialysis Patients: A Randomized Trial

被引:23
作者
Nishimura, Masato [1 ]
Tokoro, Toshiko [2 ]
Nishida, Masasya [3 ]
Hashimoto, Tetsuya [3 ]
Kobayashi, Hiroyuki [3 ]
Imai, Ryo [4 ]
Yamazaki, Satoru [5 ]
Okino, Koji [6 ]
Iwamoto, Noriyuki [3 ]
Takahashi, Hakuo [7 ]
Ono, Toshihiko [3 ]
机构
[1] Toujinkai Hosp, Div Cardiovasc, Fushimi Ku, Momoyama, Kyoto 6128026, Japan
[2] Toujinkai Hosp, Div Nephrol, Momoyama, Kyoto 6128026, Japan
[3] Toujinkai Hosp, Div Urol, Momoyama, Kyoto 6128026, Japan
[4] Toujinkai Hosp, Div Orthoped, Momoyama, Kyoto 6128026, Japan
[5] Toujinkai Clin, Kyoto, Japan
[6] Toujinkai Satellite Clin, Kyoto, Japan
[7] Kansai Med Univ, Dept Clin Sci & Lab Med, Osaka, Japan
关键词
End-stage renal disease; microcirculation; ischemia; potassium channel; preconditioning; sudden death; SENSITIVE POTASSIUM CHANNELS; STABLE ANGINA-PECTORIS; LONG-TERM SURVIVAL; DIALYSIS PATIENTS; 2-NICOTINAMIDOETHYL NITRATE; DISTAL EMBOLIZATION; INSULIN-RESISTANCE; INTERVENTION; ANGIOPLASTY; ACTIVATION;
D O I
10.1053/j.ajkd.2009.03.025
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: Survival after invasive coronary revascularization is worse in patients with chronic kidney disease than in patients without chronic kidney disease. We examined whether oral administration of nicorandil, a hybrid nitrate and adenosine triphosphate-sensitive potassium channel opener, could improve outcome after coronary revascularization in hemodialysis patients. Study Design: Open-labeled prospective randomized trial. Setting & Participants: Maintenance hemodialysis patients who underwent percutaneous coronary artery intervention and had complete coronary revascularization (absence of both restenosis and de novo coronary lesion) at coronary arteriography 6 months later. Enrollment occurred between January 1, 2002, and December 31, 2004. Interventions: Treatment with or without oral administration of nicorandil, 15 mg/d. Outcomes & Measurements: The primary end point was cardiac death (sudden cardiac death or death from acute myocardial infarction or congestive heart failure). The secondary end point was all-cause death. End-point adjudication was performed masked to the intervention. Results: 129 patients (91 men, 38 women) with a mean age of 66 +/- 9 (SD) years. During a 2.7 +/- 1.5-year follow-up, 26 died of cardiac events (acute myocardial infarction, 6; congestive heart failure, 5; sudden cardiac death, 15), and 12 died of noncardiac causes. Cardiac death-free survival rates were greater in the nicorandil group than in the control group (P = 0.009; at 3 years, 86.6% in the nicorandil group and 70.7% in the control group). All-cause death-free survival rates were also greater in the nicorandil group than in the control group (P = 0.01; at 3 years, 79.2% in the nicorandil group versus 60.5% in the control group). Additional percutaneous coronary artery intervention was performed in 6 participants in the nicorandil group and 2 participants in the control group. No serious side effects of nicorandil were reported during the course of the study. Limitations: Small sample size and open-label design. Conclusions: Oral administration of nicorandil may reduce cardiac death and improve the survival of hemodialysis patients after coronary revascularization. Am J Kidney Dis 54:307-317. (C) 2009 by the National Kidney Foundation, Inc.
引用
收藏
页码:307 / 317
页数:11
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