Ottosson J, Dawidson I, Brandberg A, Idvall J, Sandor Z
Department of Surgery, University of Texas Southwestern Medical Center, Dallas 75235-9031.
Circ Shock. 1991 Sep;35(1):14-24.
Septic shock from intraperitoneal (i.p.) injection of live Escherichia coli bacteria in rats induces marked pathophysiological changes, including 40% decrease in plasma volume (PV), cardiac output, and oxygen consumption with 100% mortality within 24 hr. The present study evaluates cardiac output and organ blood flow before and after treatment of septic shock with an effective antibiotic (AB), plasma volume (PV) expansion, and corticosteroids (CS), alone and in combination. Treatment was initiated at 5.5 hr after bacterial injection, at a time when AB therapy did not improve 24 hr survival rate. Cardiac output decreased from 28.6 +/- 3.1 (SD) to 15.4 +/- 2.8 ml/min/kg (P less than .01) in septic rats concomitant with redistribution of blood flow from carcass to the heart, brain, intestines, liver, and adrenal glands. Absolute arterial blood flow increased only to the adrenal glands and the liver to 158% (P less than .01) and 167% (P less than .01) of control values, respectively. AB, CS, and Ringer's lactate (RL) alone or in combination did not significantly improve any organ blood flow compared to untreated septic animals but increased survival significantly to about 60% (P less than .01). Albumin (ALB) and CS in combination expanded PV to 138% (P less than .01), restored cardiac output to 100%, and achieved supranormal blood flow values to the brain (109%), liver (125%), small intestine (147%) (P less than .01), and kidneys (190%) (P less than .01) of preshock levels. More importantly, survival at 24 hr was 90% (9/10) (P less than .001). It is concluded that a colloid diluted in an electrolyte solution, combined with CS, and an effective antibiotic agent are necessary therapeutic ingredients for the successful recovery of experimental E. coli sepsis.
大鼠腹腔内注射活的大肠杆菌导致的感染性休克会引发显著的病理生理变化,包括血浆量(PV)、心输出量和氧耗量降低40%,且24小时内死亡率达100%。本研究评估了单独及联合使用有效抗生素(AB)、血浆量(PV)扩充剂和皮质类固醇(CS)治疗感染性休克前后的心输出量和器官血流情况。治疗在细菌注射后5.5小时开始,此时AB治疗并未提高24小时生存率。感染性休克大鼠的心输出量从28.6±3.1(标准差)降至15.4±2.8毫升/分钟/千克(P<0.01),同时伴随着血流从躯体重新分布至心脏、脑、肠、肝和肾上腺。绝对动脉血流仅在肾上腺和肝脏分别增加至对照值的158%(P<0.01)和167%(P<0.01)。与未治疗的感染动物相比,单独使用AB、CS和乳酸林格氏液(RL)或联合使用均未显著改善任何器官血流,但显著提高了生存率至约60%(P<0.01)。白蛋白(ALB)和CS联合使用可使PV扩充至138%(P<0.01),使心输出量恢复至100%,并使脑(109%)、肝(125%)、小肠(147%)(P<0.01)和肾(190%)(P<0.01)的血流值达到休克前水平的超常值。更重要的是,24小时生存率为90%(9/10)(P<0.001)。结论是,在电解质溶液中稀释的胶体、CS和有效的抗生素药物是成功恢复实验性大肠杆菌败血症的必要治疗成分。