Spiess B D, McCarthy R J, Tuman K J, Woronowicz A W, Tool K A, Ivankovich A D
Department of Anesthesia, Rush Presbyterian-St. Luke's Medical Center, Chicago, IL 60612.
Undersea Biomed Res. 1988 Jan;15(1):31-7.
Decompression sickness is caused by the production of tissue and blood stream inert gas bubbles. Perfluorocarbon emulsions (PFC) have enhanced O2 and N2 solubilities as well as a small particle size as properties. The effects of treatment with a PFC (FC-43) and 100% oxygen on decompression sickness were investigated in 24 Sprague-Dawley rats compressed to 6.8 ATA and rapidly decompressed. Survival in animals receiving PFC and 100% oxygen was significantly longer (P = 0.01) than in those receiving a 6% hetastarch (H) treatment. The PFC survivors at 24 h did not demonstrate any neurologic deficits, whereas the 1 H animal surviving at 24 h was ataxic and not eating. Those animals who died most often did so within minutes after decompression, suggesting a hemodynamic demise. We conclude that PFC treatment when coupled with 100% oxygen breathing provides both hemodynamic and neurologic protection from decompression sickness.
减压病是由组织和血流中惰性气体气泡的产生引起的。全氟碳乳剂(PFC)具有增强的氧气和氮气溶解度以及小粒径的特性。在24只被压缩至6.8ATA并快速减压的Sprague-Dawley大鼠中,研究了用PFC(FC-43)和100%氧气治疗减压病的效果。接受PFC和100%氧气治疗的动物的存活时间显著长于接受6%羟乙基淀粉(H)治疗的动物(P = 0.01)。24小时时PFC治疗组存活的动物未表现出任何神经功能缺损,而24小时时存活的1只接受H治疗的动物出现共济失调且不进食。那些死亡最频繁的动物在减压后几分钟内死亡,提示为血流动力学衰竭。我们得出结论,PFC治疗与100%氧气吸入相结合可为减压病提供血流动力学和神经方面的保护。