Multicentre clinical trial of low volume fresh frozen plasma therapy in acute pancreatitis
Version of Record online: 7 DEC 2005
Copyright © 1987 British Journal of Surgery Society Ltd.
British Journal of Surgery
Volume 74, Issue 10, pages 907–911, October 1987
How to Cite
Leese, T., Holliday, M., Heath, D., Hall, A. W. and Bell, P. R. F. (1987), Multicentre clinical trial of low volume fresh frozen plasma therapy in acute pancreatitis. Br J Surg, 74: 907–911. doi: 10.1002/bjs.1800741012
- Issue online: 7 DEC 2005
- Version of Record online: 7 DEC 2005
- Trent Regional Health Authority
- Acute pancreatitis;
- fresh frozen plasma;
- serum antiproteases
Fresh frozen plasma (FFP) has been proposed as a specific therapy for acute pancreatitis. Reduced mortality encountered in an uncontrolled clinical study and a controlled experimental study may be attributable to replenishment by FFP of the naturally occurring antiprotease system. To investigate this potential therapy further, 202 patients presenting with acute pancreatitis were randomized to receive FFP (2 units daily for 3 days) or a similar volume of colloid control as part of their intravenous fluid therapy. Clinical progress was monitored and the major serum antiproteases (α1-antiprotease and α2-macroglobulin) were measured on days 1, 3 and 7. There was no significant difference between the two groups in terms of clinical outcome. α1-Antiprotease levels rose significantly from day 1 to day 3 in both groups (P <0·0001) and remained elevated at day 7. α1-Antiprotease is an acute phase protein in man and raised serum levels would be anticipated. FFP appears to have no effect on the magnitude of this rise. Serum α2-macroglobulin levels were reduced in both groups on day 1 and continued to fall significantly from day 1 to day 3 in the colloid control group (P<0·005) whilst remaining substantially unaltered in patients receiving FFP (P = 0·6527). α2-Macroglobulin plays a central role in the elimination of proteases during acute pancreatitis and the ability of relatively low volumes of FFP to reduce the fall in serum α2-macroglobulin levels seen during the early stages of this disease may have therapeutic implications.