Does heparin coating improve biocompatibility? A study on complement, blood cells and postoperative morbidity during cardiac surgery

被引:24
作者
Belboul, Ali [1 ]
Al-Khaja, Najib [1 ]
机构
[1] Univ Gothenbourg, Sahlgrenska Hosp, Dept Thorac & Cardiovasc Surg, S-41345 Gothenburg, Sweden
来源
PERFUSION-UK | 1997年 / 12卷 / 06期
关键词
D O I
10.1177/026765919701200607
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To evaluate whether the effect of heparin coating the extracorporeal circuit resulted in differences in patient outcome and haemostatic alteration, 24 patients undergoing elective, isolated coronary artery bypass were randomized prospectively to cardiopulmonary bypass (CPB) with heparin-coated circuits (group H, n = 12) or uncoated circuits (group C, n = 12). The technique of CPB, heparinization and its reversal were the same in both groups. We studied complement status (C3d, C3, C3d/C3, C4 and C-function), white blood cell counts with differentiation and the postoperative morbidity. The results confirmed that CPB activates complement and increases neutrophils in both the H and C groups. A significantly lower level of leucocytosis was seen in group H compared to the C group (p < 0.05). The complement function via the classical pathway (C-function), expressed as a percentage of the function of a reference serum pool (the values of normal sera were 75-125%), was significantly reduced in both heparin-coated and uncoated circuits (p < 0.05). There was no significant intergroup difference regarding C3, C3d/C3, C4 and C-function during the study period. A lower frequency of postoperative morbidity was present in the H group. We conclude that heparin-coated surfaces elicit less leucocytosis and decrease postoperative morbidity in patients undergoing cardiac surgery but do not cause a significant difference regarding activation of the complement system as reported by many other investigators.
引用
收藏
页码:385 / 391
页数:7
相关论文
共 49 条
[21]   AUTO-TRANSFUSION OF MEDIASTINAL BLOOD IN CARDIAC-SURGERY [J].
LEPORE, V ;
RADEGRAN, K .
SCANDINAVIAN JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 1989, 23 (01) :47-49
[22]  
LEW PD, 1985, B EUR PHYSIOPATH RES, V21, P231
[23]   CHANGES IN MACROMOLECULAR PERMEABILITY BY INTRAVASCULAR GENERATION OF OXYGEN-DERIVED FREE-RADICALS [J].
LEY, K ;
ARFORS, KE .
MICROVASCULAR RESEARCH, 1982, 24 (01) :25-33
[24]   THE EFFECT OF PROTAMINE SULFATE ON PLATELET-FUNCTION [J].
LINDBLAD, B ;
WAKEFIELD, TW ;
WHITEHOUSE, WM ;
STANLEY, JC .
SCANDINAVIAN JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 1988, 22 (01) :55-59
[25]   DETECTION OF SERUM FIBRINOGEN AND FIBRIN DEGRADATION PRODUCTS - COMPARISON OF 6 TECHNICS USING PURIFIED PRODUCTS AND APPLICATION IN CLINICAL STUDIES [J].
MARDER, VJ ;
MATCHETT, MO ;
SHERRY, S .
AMERICAN JOURNAL OF MEDICINE, 1971, 51 (01) :71-&
[26]   OXIDANT INJURY OF LUNG PARENCHYMAL-CELLS [J].
MARTIN, WJ ;
GADEK, JE ;
HUNNINGHAKE, GW ;
CRYSTAL, RG .
JOURNAL OF CLINICAL INVESTIGATION, 1981, 68 (05) :1277-1288
[27]   FORMATION OF C5A DURING CARDIOPULMONARY BYPASS - INHIBITION BY PRECOATING WITH HEPARIN [J].
MOLLNES, TE ;
VIDEM, V ;
GOTZE, O ;
HARBOE, M ;
OPPERMANN, M .
ANNALS OF THORACIC SURGERY, 1991, 52 (01) :92-97
[28]   C5A AND THROMBOXANE GENERATION ASSOCIATED WITH PULMONARY VASO-CONSTRICTION AND BRONCHO-CONSTRICTION DURING PROTAMINE REVERSAL OF HEPARIN [J].
MOREL, DR ;
ZAPOL, WM ;
THOMAS, SJ ;
KITAIN, EM ;
ROBINSON, DR ;
MOSS, J ;
CHENOWETH, DE ;
LOWENSTEIN, E .
ANESTHESIOLOGY, 1987, 66 (05) :597-604
[29]  
NILSSON L, 1990, ARTIF ORGANS, V14, P46
[30]   SIMPLIFIED ASSAYS OF HEMOLYTIC-ACTIVITY OF THE CLASSICAL AND ALTERNATIVE COMPLEMENT PATHWAYS [J].
NILSSON, UR ;
NILSSON, B .
JOURNAL OF IMMUNOLOGICAL METHODS, 1984, 72 (01) :49-59