19 июня 2002 00:00    |    
	
	
	Aprotinin in coronary operation with cardiopulmonary bypass: does «low-dose»  aprotinin inhibit the inflammatory response?
	
		
	
		
	
	
						         Background. Cardiopulmonary bypass induces a systemic inflammatory response. Aprotinin, a nonspecific proteinase inhibitor is known to improve postoperative hemostasis and may modify the inflammatory reaction. This study evaluates the effects of low-dose  aprotinin on inflammatory markers in patients scheduled for elective coronary artery bypass grafting. 
 Methods. Patients were prospectively randomized into two groups: the control group © (n = 14) and the low-dose  aprotinin group (A) (n = 15) with (2 x 106 KIU = 280 mg) aprotinin added to the pump prime. Cytokine response (interleukin-6,  soluble TNF II receptor), terminal complement production (SC5b−9), and neutrophil activation (lactoferrin) were assessed up to 6 hours postoperatively. Clinical data and hemostatic factors including fibrinopeptide A, thrombin-antithrombin  complex, D-dimer,  and plasmin/  
 Results. In both study groups, a significant increase of all inflammatory markers was seen (IL-6,  sTNF-IIR,  SC5b−9, lactoferrin), p less than 0.001. Peak levels of complement production occurred after protamine administration, whereas cytokine increases were more pronounced postoperatively with marked elevation up to 6 hours. The markers did not differ significantly between groups throughout the study period (p > 0.05 at each time of determination). However, after protamine administration reduced fibrinolysis (D-dimer,  plasmin/  2−antiplasmin) was detected in group A. Measurements for coagulation (fibrinopeptide A, thrombin-antithrombin  complex) were not significantly influenced by aprotinin. The total amount of blood loss during the first 24 hours was significantly reduced in group A (p < 0.02). 
 Conclusions. Low-dose  aprotinin added to the pump prime does not inhibit the inflammatory response caused by cardiopulmonary bypass, but improves postoperative hemostasis. A potential effect of high-dose  aprotinin on inflammatory markers remains to be elucidated. 
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