Abstract | BACKGROUND/AIMS: METHODS: RESULTS: Over a mean duration of follow-up of 2.8 +/- 1.6 years in the 82 propensity-matched patients (41 in the nicorandil group and 41 in the non- nicorandil group), we observed 17 cardiac deaths and 12 cases of nonfatal myocardial infarction. The incidence of MACE was lower (p = 0.0365) in the nicorandil group (10/41, 24.4%) than in the non- nicorandil group (19/41, 46.3%). On stepwise Cox hazard analysis, MACE was significantly inhibited by administration of nicorandil (hazard risk, 0.387; 95% CI 0.178-0.842; p = 0.0168). Kaplan-Meier survival estimates revealed that MACE-free survival rates at 3 years were 80.5 and 58.5% in patients with and without nicorandil, respectively. CONCLUSIONS:
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Authors | Masato Nishimura, Toshiko Tokoro, Masaya Nishida, Tetsuya Hashimoto, Hiroyuki Kobayashi, Satoru Yamazaki, Ryo Imai, Koji Okino, Noriyuki Iwamoto, Hakuo Takahashi, Toshihiko Ono |
Journal | Nephron. Clinical practice
(Nephron Clin Pract)
Vol. 111
Issue 3
Pg. c212-21
( 2009)
ISSN: 1660-2110 [Electronic] Switzerland |
PMID | 19225237
(Publication Type: Comparative Study, Journal Article)
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Chemical References |
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Topics |
- Aged
- Death
- Female
- Follow-Up Studies
- Humans
- Kidney Diseases
(complications, drug therapy, mortality)
- Male
- Middle Aged
- Myocardial Ischemia
(complications, mortality, prevention & control)
- Nicorandil
(therapeutic use)
- Renal Dialysis
(adverse effects, mortality)
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