Ellison N, Behar M, MacVaugh H, Marshall B E
Ann Thorac Surg. 1980 Jan;29(1):15-9. doi: 10.1016/s0003-4975(10)61619-0.
A directive from the Food and Drug Administration indicates that the use of plasma protein fraction (PPF) is contraindicated during cardiopulmonary bypass because of possible hypotension. Bradykinin has been implicated as the cause of this hypotension. Bradykinin levels were measured by radioimmunoassay in PPF and in 5% albumin and were found to be consistently elevated in the former and occasionally in the latter. The addition of PPF to pump primes resulted in significantly elevated levels of bradykinin, which rapidly cleared, indicating that extrapulmonary sites of bradykinin inactivation were efficient. The potential hypotensive effect of PPF was observed by determining the change in mean perfusion pressure in two groups of patients: one group with a 3,000 ml crystalloid prime and the other with a prime of 2,000 ml of crystalloid and 1,000 ml of PPF. There was no significant difference in the perfusion pressure between the two groups at any point, and the hypotensive effects seen in both groups were readily treated, suggesting that the directive against the use of PPF during cardiopulmonary bypass may be unnecessarily restrictive.
美国食品药品监督管理局发布的一项指令表明,由于可能导致低血压,在体外循环期间禁止使用血浆蛋白部分(PPF)。缓激肽被认为是导致这种低血压的原因。通过放射免疫分析法测定了PPF和5%白蛋白中的缓激肽水平,发现前者中的缓激肽水平持续升高,后者中偶尔也会升高。将PPF添加到灌注液中会导致缓激肽水平显著升高,且其会迅速清除,这表明肺外缓激肽失活部位的作用有效。通过测定两组患者平均灌注压的变化来观察PPF的潜在降压作用:一组使用3000ml晶体预充液,另一组使用2000ml晶体和1000ml PPF的预充液。两组在任何时间点的灌注压均无显著差异,且两组出现的低血压效应都易于处理,这表明在体外循环期间禁止使用PPF的指令可能限制过度。