Aprotinin prevents cardiopulmonary bypass-induced platelet dysfunction. A scanning electron microscope study
- PMID: 1385010
Aprotinin prevents cardiopulmonary bypass-induced platelet dysfunction. A scanning electron microscope study
Abstract
Background: Administration of aprotinin during extracorporeal circulation reduces blood loss and improves platelet function.
Methods and results: To evaluate the protective effect of aprotinin on platelets, 50 patients undergoing cardiopulmonary bypass were randomized before surgery to one of three groups. Seventeen patients (group A) received continuous high-dose aprotinin (7 x 10(6) KIU) during cardiopulmonary bypass, 17 (group B) received a single bolus of aprotinin in the pump prime (2 x 10(6) KIU), and 16 (group C) received placebo. Scanning electron microscopy was used to evaluate platelet aggregation on extracellular matrix. The platelet function was graded from 1 to 4, with grade 4 being normal aggregation. Immediately after cardiopulmonary bypass, 16 patients in group A (94%) reached preoperative aggregation grade (mean grade, 3.4 +/- 0.7) compared with nine of 17 in group B (52%) (mean grade, 2.9 +/- 1.2), and none in group C (0%) (mean grade, 1.4 +/- 0.5; p < 0.001). Postoperative platelet count did not differ significantly among the three groups. After surgery, group A bled less than groups B and C (395 +/- 120 versus 488 +/- 135 and 780 +/- 408 ml, respectively; p < 0.01). Patients in the aprotinin groups received fewer red blood cell units (0.9 +/- 1.2 and 1.9 +/- 1.2 versus 3.4 +/- 1.9, respectively; p < 0.01) and were exposed to less homologous blood products (1.3 +/- 1.7 and 2.1 +/- 1.1 versus 6.1 +/- 5, respectively; p < 0.001).
Conclusions: By preserving platelet function, aprotinin improves postoperative hemostasis in all patients who receive high dose and in most who receive low dose.
Similar articles
-
Aprotinin protects platelets against the initial effect of cardiopulmonary bypass.J Thorac Cardiovasc Surg. 1990 May;99(5):788-96; discussion 796-7. J Thorac Cardiovasc Surg. 1990. PMID: 1691806 Clinical Trial.
-
Effects of high-dose aprotinin on blood loss, platelet function, fibrinolysis, complement, and renal function after cardiopulmonary bypass.J Thorac Cardiovasc Surg. 1991 Jun;101(6):958-67. J Thorac Cardiovasc Surg. 1991. PMID: 1710008
-
Platelet protection by low-dose aprotinin in cardiopulmonary bypass: electron microscopic study.Ann Thorac Surg. 1993 Jan;55(1):114-9. doi: 10.1016/0003-4975(93)90484-y. Ann Thorac Surg. 1993. PMID: 7678061 Clinical Trial.
-
Activation of hemostasis during cardiopulmonary bypass and pediatric aprotinin dosage.Ann Thorac Surg. 1998 Jun;65(6 Suppl):S45-50; discussion S50-1, S74-6. doi: 10.1016/s0003-4975(98)00330-0. Ann Thorac Surg. 1998. PMID: 9647138 Review.
-
Platelet-sparing properties of aprotinin: A scoping review on mechanisms and clinical effects.Eur J Anaesthesiol. 2025 Jan 1;42(1):36-43. doi: 10.1097/EJA.0000000000002081. Epub 2024 Oct 11. Eur J Anaesthesiol. 2025. PMID: 39628415
Cited by
-
Why thrombin PAR1 receptors are important to the cardiac surgical patient.J Extra Corpor Technol. 2007 Dec;39(4):305-7. J Extra Corpor Technol. 2007. PMID: 18293826 Free PMC article. Review.
-
Combination of acute preoperative plateletpheresis, cell salvage, and aprotinin minimizes blood loss and requirement during cardiac surgery.J Extra Corpor Technol. 2005 Mar;37(1):9-14. J Extra Corpor Technol. 2005. PMID: 15804151 Free PMC article. Clinical Trial.
-
Aprotinin. A review of its pharmacology and therapeutic efficacy in reducing blood loss associated with cardiac surgery.Drugs. 1995 Jun;49(6):954-83. doi: 10.2165/00003495-199549060-00008. Drugs. 1995. PMID: 7543841 Review.
-
A risk-benefit assessment of aprotinin in cardiac surgical procedures.Drug Saf. 1998 Jan;18(1):21-41. doi: 10.2165/00002018-199818010-00003. Drug Saf. 1998. PMID: 9466086 Review.
-
Anti-fibrinolytic use for minimising perioperative allogeneic blood transfusion.Cochrane Database Syst Rev. 2011 Mar 16;2011(3):CD001886. doi: 10.1002/14651858.CD001886.pub4. Cochrane Database Syst Rev. 2011. PMID: 21412876 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources