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低渗非离子型和离子型造影剂的止血作用:一项双盲对照研究。

Haemostatic effects of low osmolar non-ionic and ionic contrast media: a double-blind comparative study.

作者信息

Hoffmann J J, Tielbeek A V, Krause W

机构信息

Department of Clinical Laboratories, Catharina Hospital, Eindhoven, The Netherlands.

出版信息

Br J Radiol. 2000 Mar;73(867):248-55. doi: 10.1259/bjr.73.867.10817039.

Abstract

In this prospective, double-blind, randomized study the effects of a non-ionic contrast medium (Iopromide) on the haemostatic system were compared with those of a low osmolar ionic medium (Ioxaglate). The aim was to investigate in vivo whether a non-ionic contrast agent is less anticoagulant or more pro-thrombotic than an ionic medium. A large number of haemostatic parameters, including activation markers, were measured. Either Iopromide (n = 16; median volume 102 ml; 95% confidence interval 90-108 ml) or Ioxaglate (n = 15; median 105 ml; 95% confidence interval 95-114 ml) was given to 31 patients scheduled for abdominal and femoral arteriography. Blood for laboratory investigations was collected before, and 5 and 30 min after, administering the contrast medium. Indications for activation of coagulation and platelets were already found in nearly 50% of the patients before any contrast medium was given. Both Iopromide and Ioxaglate caused further increases in thrombin-antithrombin complex, prothrombin fragments 1 + 2 and beta-thromboglobulin. The degree of activation was similar for both agents. Anticoagulant effects were not observed. The haemorheological effects were compatible with haemodilution by 5-8%, again without differences between the contrast agents. Contrary to the findings from in vitro studies, we found no significant differences between the effects of the non-ionic Iopromide and the ionic Ioxaglate on coagulation and platelets. Both agents activated these systems to a limited, but identical, degree. Our results support the notion that the catheterization procedure per se may represent a source of haemostatic activation and that the ionic contrast agent studied has insufficient anticoagulant effect to prevent clotting activation being induced by the contrast medium.

摘要

在这项前瞻性、双盲、随机研究中,将一种非离子型造影剂(碘普罗胺)对止血系统的影响与一种低渗离子型造影剂(碘克沙醇)进行了比较。目的是在体内研究非离子型造影剂是否比离子型造影剂具有更低的抗凝作用或更强的促血栓形成作用。测量了大量止血参数,包括激活标志物。对31例计划进行腹部和股动脉造影的患者给予碘普罗胺(n = 16;中位体积102 ml;95%置信区间90 - 108 ml)或碘克沙醇(n = 15;中位体积105 ml;95%置信区间95 - 114 ml)。在给予造影剂之前、之后5分钟和30分钟采集用于实验室检查的血液。在给予任何造影剂之前,近50%的患者已出现凝血和血小板激活的指征。碘普罗胺和碘克沙醇均导致凝血酶 - 抗凝血酶复合物、凝血酶原片段1 + 2和β - 血小板球蛋白进一步升高。两种造影剂的激活程度相似。未观察到抗凝作用。血液流变学效应与5 - 8%的血液稀释相符,造影剂之间同样没有差异。与体外研究结果相反,我们发现非离子型碘普罗胺和离子型碘克沙醇对凝血和血小板的影响没有显著差异。两种造影剂均在有限但相同的程度上激活这些系统。我们的结果支持这样一种观点,即导管插入术本身可能是止血激活的一个来源,并且所研究的离子型造影剂的抗凝作用不足以防止造影剂诱导的凝血激活。

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