败血症
医学
多粘菌素B
多粘菌素
右旋糖酐
穿孔
盲肠
安慰剂
右旋糖酐70
胃肠病学
腹膜炎
内科学
麻醉
外科
病理
抗生素
微生物学
生物
冶金
冲孔
生物化学
材料科学
替代医学
作者
Gordon S. Doig,Claudio M. Martin,William J. Sibbald
标识
DOI:10.1097/00003246-199712000-00009
摘要
Objective To test the hypothesis that adult sheep pretreated with polymyxin-dextran and then made septic by cecal ligation and perforation would have fewer changes in microvascular integrity and cellular architecture in extrapulmonary organs. Design Prospective, randomized, double-blind, placebo-controlled animal study. Setting An animal research facility in a university-affiliated hospital. Subjects Mature, male Suffolk sheep (32 to 67 kg). Interventions Animals with chronic indwelling catheters were pretreated with polymyxin B-dextran (6 mg/kg) or placebo (dextran) and an intra-abdominal focus of infection was then produced by cecal ligation and perforation. Treatment (polymyxin B or placebo) was continued every 8 hrs for 48 hrs. Measurements and Main Results Forty-eight hours after randomization, the polymyxin B-dextran group manifested significantly less pyrexia (p = .04), higher mean arterial pressures (p = .02), less variable serum albumin concentrations (p = .05), and a trend toward decreased lactate concentrations (p = .10). Qualitative morphometry and semiquantitative scoring of tissue from gastrocnemius muscle demonstrated that polymyxin B-dextran-treated sheep had significantly increased total capillary (p = .04) and capillary luminal areas (p = .038) and less mitochondrial swelling and damage (p = .03) compared with the placebo sheep. Conclusions Pretreatment of sheep in a polymicrobial, peritonitis model of sepsis with polymyxin B-dextran resulted in a significant amelioration of sepsis-induced ultrastructural damage. In placebo-treated control animals, these ultrastructural lesions were associated with a greater severity of sepsis, as measured by the presence of pyrexia, increased lactate concentrations, and less stable blood pressures. These findings justify the investigation of the effects of polymyxin B-dextran in a post onset model of sepsis. (Crit Care Med 1997; 25:1956-1961)
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