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药物对实验性梗死面积的限制。

Limitation of experimental infarct size by drugs.

作者信息

Flameng W, Vanhaecke J, Lesaffre E

机构信息

Department of Cardiovascular Surgery and Cardiology, University Clinic Gasthuisberg, Catholic University of Leuven, Belgium.

出版信息

J Cardiovasc Pharmacol. 1989;14 Suppl 9:S29-33.

PMID:2483229
Abstract

Testing drugs on their efficacy in limiting infarct size is difficult in the experimental setting because of the considerable variation in the sizes of infarcts produced in control animals, mainly in dogs. This variation in infarct size in the canine model is theoretically related to variations in the size of the ischemic bed or area at risk, in pre-existing collateral blood flow, and in myocardial metabolic demand. In this study, we identified the determinants of infarct size after different periods of coronary artery occlusion in unconscious dogs and constructed a mathematical model based on these determinants using stepwise logistic regression analysis. Eighty-nine percent of the variability in infarct size is accounted for by variations in the size of the ischemic bed and coronary collateral blood flow. Using this model, we were able to predict infarct size and to make valid comparisons between treated and control groups.

摘要

在实验环境中,由于对照动物(主要是狗)产生的梗死灶大小存在相当大的差异,因此测试药物在限制梗死灶大小方面的疗效很困难。犬模型中梗死灶大小的这种差异理论上与缺血床或危险区域的大小、预先存在的侧支血流以及心肌代谢需求的变化有关。在本研究中,我们确定了清醒犬冠状动脉闭塞不同时间段后梗死灶大小的决定因素,并使用逐步逻辑回归分析基于这些决定因素构建了一个数学模型。梗死灶大小89%的变异性可由缺血床大小和冠状动脉侧支血流的变化来解释。使用该模型,我们能够预测梗死灶大小,并对治疗组和对照组进行有效的比较。

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