E989 JACC April 5, 2011 Volume 57, Issue 14
MYOCARDIAL ISCHEMIA AND INFARCTION IMPACT OF SINGLE INTRACORONARY NICORANDIL ADMINISTRATION ON MICROCIRCULATORY DISTURBANCE AFTER SUCCESSFUL PRIMARY PERCUTANEOUS INTERVENTION IN ST-SEGMENT ELEVATION MYOCARDIAL INFARCTION ACC Poster Contributions Ernest N. Morial Convention Center, Hall F Sunday, April 03, 2011, 3:30 p.m.-4:45 p.m.
Session Title: Acute Myocardial Infarction -- Pharmacological, Stem Cell and other Adjunctive Therapies Abstract Category: 3. Acute Myocardial Infarction—Therapy Session-Poster Board Number: 1037-316 Authors: Yasuji Doi, Noritoshi Ito, Shinsuke Nanto, Hirotaka Sawano, Tomoaki Natsukawa, Yuma Kurozumi, Daisuke Tonomura, Noriaki Yamada, Ken-ichiro Okada, Yasuyuki Hayashi, Tatsuro Kai, Toru Hayashi, Osaka Saiseikai Senri Hospital, Suita, Japan, Osaka University Graduate School of Medicine, Suita, Japan Background: Index of Microcirculatory Resistance (IMR) is an on-site parameter for the assessment of microcirculatory disturbance after primary percutaneous coronary intervention (PCI) in patients with ST-segment elevation myocardial infarction (STEMI). High IMR has been shown to be a predictor of poor left ventricular (LV) function recovery. We sought to investigate the effects of intracoronary nicorandil administration after primary PCI on microvascular injury and chronic phase LV function. Methods: A total of 44 patients with first STEMI were studied. IMR in the infarct related artery was measured using PressureWire™ Certus (St. Jude Medical, USA) immediately after successful stenting of the culprit lesion (baseline) and after intracoronary nicorandil administration of 2 mg. LV ejection fraction (EF) was obtained just after successful primary PCI and at six months after. Results: Mean IMR of STEMI patients after successful primary PCI was very high (33U). Single intracoronary nicorandil administration significantly decreased the baseline IMR both in 14 patients with baseline-high IMR (>32U) and in the other 30 patients with baseline-low IMR (≤32U) (66±32U vs. 30±14U, p<0.01; 18±7 U vs. 14±5 U, p<0.01, respectively). The 14 baseline-high IMR patients were subdivided into two groups according to median IMR after nicorandil (29U). There was no difference in LVEF immediately after primary PCI among the patients with baseline-low IMR, those with baseline-high and after-nicorandil-low IMR and those with baseline-high and after-nicorandil-low IMR. As compared with LVEF at six months in the baseline-low IMR patients, it was maintained in 7 baseline-high and after-nicorandil-low IMR patients (61±9% vs. 62±10%, p=NS), but was significantly reduced in 7 patients with baseline-high and after-nicorandil-low IMR (51±9%, p<0.01). IMR levels after nicorandil correlated positively with peak creatinine kinase levels (r=0.39, p=0.01) and negatively with LVEF at 6 months (r=0.37, p=0.01). Conclusions: High IMR levels after primary PCI in patients with STEMI can be improved by intracoronary nicorandil administration, which may at least partly contribute to maintained LV function at 6 months.