Introduction: Nicorandil may exert cardioprotective effects in ischemic heart disease. However, its efficacy in combination with early reperfusion is uncertain. The authors performed a meta-analysis of the short- and long-term clinical outcomes of nicorandil administration at the time of primary percutaneous coronary intervention (PCI) in patients with ST-elevated myocardial infarction (STEMI).
Methods: PubMed, MEDLINE, Embase, and the Cochrane Library databases were systematically searched for eligible randomized controlled studies. The primary endpoint was major adverse cardiovascular events (MACE), both in-hospital and post-discharge. The secondary endpoint was the incidence of no-reflow phenomenon.
Results: Ten studies were included (n = 1105). Mean patient age was 63.0 ± 10.0 years; 76.6% of patients were male. Compared with controls who received primary PCI, combined nicorandil/primary PCI significantly reduced in-hospital MACE (pooled odds ratio [OR] 0.16; 95% confidence interval [CI] 0.09–0.27), follow-up MACE (pooled OR 0.53; 95% CI 0.37–0.75), and total MACE (pooled OR 0.27; 95% CI 0.15–0.49). The combined treatment also reduced the incidence of no-reflow phenomenon (pooled OR 0.34; 95% CI 0.23–0.50).
Conclusion: Nicorandil administration at the time of primary PCI is associated with reduced MACE (both short- and long-term) and no-reflow phenomenon in patients with STEMI. 相似文献
Both animal models of experimental myocardial infarction and clinical studies on reperfusion therapy for acute myocardial
infarction have provided evidence of impaired tissue perfusion at the microvascular level after initiation of reperfusion
despite adequate restoration of epicardial vessel patency. Characteristics of this “no-reflow” phenomenon found in basic science
investigations, such as distinct perfusion defects, progressive decrease of resting myocardial flow with ongoing reperfusion
and functional vascular alterations are paralleled by clinical observations demonstrating similar features during the course
of reperfusion. In experimental animal investigations of coronary occlusion and reperfusion, this no-reflow phenomenon could
be characterized as a fundamental mechanism of myocardial ischemia and reperfusion. Major determinants of the amount of no-reflow
are the duration of occlusion, infarct size, but also the length of reperfusion, as rapid expansion of perfusion defects occurs
during reperfusion. Moreover, no-reflow appears to persist over a period of at least four weeks, a period when major steps
of infarct healing take place. The significant association of the degree of compromised tissue perfusion at four weeks and
indices of infarct expansion, found in chronic animal models of reperfused myocardial infarction, might be the pathoanatomic
correlate for the prognostic significance observed in the clinical setting. 相似文献
We assessed the prognostic value of the platelet to lymphocyte ratio (PLR) in primary percutaneous coronary intervention (pPCI). Patients (n?=?440) with acute myocardial infarction (AMI) who underwent pPCI were divided into 2 groups: low PLR (<137) and high PLR (>137). “Thrombolysis In Myocardial Infarction” (TIMI) flow grades and Syntax scores (SXS) were calculated from initial angiograms. In-hospital mortality rate and cardiac adverse events were obtained from medical records. Patients with high PLR had more no-reflow, higher SXS and higher mortality rate (p?<?0.001, p?<?0.001 and p?=?0.008, respectively). In receiver operating characteristic curve analysis, high PLR predicted development of no-reflow (specificity 71% and sensitivity 85%), SXS>22 (specificity 52% and sensitivity 61%) and adverse events (specificity 67% and sensitivity 63%). In multivariate regression analysis, PLR was an independent risk factor for no-reflow, SXS>22 and in-hospital adverse events. In addition to PLR, we present the relationship between mean platelet volume, red cell distribution width and neutrophil to lymphocyte ratio and no-reflow, SXS and in-hospital adverse events. 相似文献