Coronary heart diseaseCollateral function in early acute myocardial infarction☆
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Cited by (73)
Comparison of Myocardial Ischemia on the Ergocycle Versus the Treadmill in Patients With Coronary Heart Disease
2010, American Journal of CardiologyCitation Excerpt :However, we have no basis to assume this. Another possibility is that the greater blood pressure achieved during the ergocyle test resulted in improved coronary perfusion pressure through diseased coronary arteries and collateral vessels, with a favorable net effect on the supply–demand equation, despite the increased oxygen cost of a greater SBP.18 In support of this possibility, a recent study showed less exercise-induced myocardial ischemia during thallium-201 imaging in patients with greater, instead of lower, exercise diastolic blood pressure, despite a greater peak RPP and similar severity of CHD.19
Coronary collaterals improve prognosis in patients with ischemic heart disease
2009, International Journal of CardiologyCitation Excerpt :Notably, in some patients with adequate collateral flow, an acute coronary occlusion may be tolerated without signs of ischemia [4]. Functional observations confirmed that collaterals may preserve cardiac function during acute infarction [5–7], may limit infarct size [6] and may reduce post-infarct ventricular dilatation after 2 years [8] and post-infarct aneurysm formation after 4 years [9]. Subsequently, by exerting functional protection, collateral flow could alleviate the deleterious effects of atherosclerosis on morbidity and mortality in the long term.
Coronary collaterals-insights in molecular determinants and prognostic relevance
2007, International Journal of CardiologyUsefulness of Plasma Brain Natriuretic Peptide Concentration for Predicting Subsequent Left Ventricular Remodeling After Coronary Angioplasty in Patients With Acute Myocardial Infarction
2006, American Journal of CardiologyCitation Excerpt :Reocclusion might not accelerate left ventricular remodeling in cases with successful reperfusion limiting infarct size. Further, development of collateral circulation prevents left ventricular dilation, as previously reported.8–10 Third, the medications were different from those used in the previous study.
Reduced collateral circulation to the infarct-related artery in elderly patients with acute myocardial infarction
2004, Journal of the American College of CardiologyCitation Excerpt :Therefore, age-dependent endothelial dysfunction may contribute to impaired collateral development in the setting of myocardial ischemia. The presence of collateral circulation improves myocardial salvage (3–5)and prevents ventricular remodeling (6), thereby improving in-hospital prognosis independent of coronary reperfusion therapy (6,7,23–26). Because the aging heart might be expected to be less tolerant due to impaired biologic responses against myocardial ischemia, we compared the clinical effect of the presence of collateral circulation to the IRA in patients below and above 70 years of age.
Physiologically assessed coronary collateral flow and adverse cardiac ischemic events: A follow-up study in 403 patients with coronary artery disease
2002, Journal of the American College of CardiologyCitation Excerpt :Aside from the mentioned statistical and technical factors that are likely to have contributed to the fact that three of the 10 cited studies have described no effect or an adverse effect of collaterals on outcome (5–7), biological situations at variance to those chosen in our study design have probably caused contradicting results. Those conditions include selection of the study baseline during acute MI (7,13–15), of patients with chronic (3–6)or without infarction (8,12), focus on collaterals present at the time of (7,13–15)or developing after (3–6)acute MI, or investigation of patients with chronic total occlusions (3–5,12), balloon occluded vessels (8,15), or residual stenoses after thrombolysis (7). In the setting of acute MI, the rate of subsequent ischemic events during the first months of follow-up is much higher (cardiac mortality of 4% to 9% within six months after MI [14]), as compared with chronic stable CAD (mortality of 0.5% to 1%/1.8 years of follow-up in our study).
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This project was supported in part by Scientific Research Grant No 58570381 from the Ministry of Education of Japan.