首页> 美国政府科技报告 >Influence of Systemic Hypotension on Skeletal Muscle Ischemia-Reperfusion Injury After 4-Hour Tourniquet Application.
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Influence of Systemic Hypotension on Skeletal Muscle Ischemia-Reperfusion Injury After 4-Hour Tourniquet Application.

机译:系统性低血压对4小时止血带后骨骼肌缺血再灌注损伤的影响。

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OBJECTIVE: Tourniquet use for extremity hemorrhage control is common in military trauma. Tourniquet use may be accompanied by systemic hypotension, but this phenomenon has not been studied. We aimed to define the muscle effects of the combined insult of tourniquet-induced skeletal muscle ischemia-reperfusion injury (I-R) and hemorrhagic hypotension. DESIGN: After a 33% carotid arterial hemorrhage, Sprague-Dawley rats underwent 240-min hind limb ischemia induced by pneumatic tourniquet. Control animals were not hemorrhaged. No resuscitation was given. After tourniquet release, muscles were reperfused for 120 min and then dissected. Weights and mitochondrial viability assays (nitroblue tetrazolium method) were performed on the plantaris (PL), and soleus (SO). Histologic analysis was performed on the PL and SO. Muscle edema is expressed as the ratio of tourniquet limb to contralateral limb muscle weight. SETTING: Animal laboratories of the United States Army Institute of Surgical Research. STUDY ANIMALS: Twelve Sprague-Dawley rats. RESULTS: The mean arterial pressure of hemorrhaged animals was 38 + or - 3 mm Hg before tourniquet placement and 86 + or - 4 mm Hg before release, both significantly (p less than 0.05) lower than controls at the same time points. Pre- tourniquet mortality was 38% with hemorrhage and 0% without. All muscles experienced edema, with weight ratios greater than 1. The PL experienced significantly (p less than 0.05) less edema with hemorrhage. Viability was unaffected by hemorrhage in all muscles, as was tissue inflammation. No differences in inflammation were observed with hemorrhage. CONCLUSIONS: Systematic hypotension modulates the impact of 4 hours of tourniquet ischemia by decreasing muscle edema but minimally altering measures of muscle viability.

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