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急性心肌梗死静脉注射链激酶后长达866天的链激酶中和效价。

Streptokinase neutralisation titres up to 866 days after intravenous streptokinase for acute myocardial infarction.

作者信息

Patel S, Jalihal S, Dutka D P, Morris G K

机构信息

City Hospital, Nottingham.

出版信息

Br Heart J. 1993 Aug;70(2):119-21. doi: 10.1136/hrt.70.2.119.

Abstract

OBJECTIVE

To follow the change in streptokinase neutralisation titres in a group of patients after treatment with streptokinase for acute myocardial infarction.

DESIGN

Venous blood samples suitable for analysis were obtained up to 866 days after treatment with 1.5 million units of streptokinase in 189 patients. The ability of the patient's plasma to inhibit lysis of a thrombin clot by streptokinase was assessed.

SETTING

A coronary care unit in a district general hospital.

PATIENTS

A retrospective review of coronary care records and the district health authority computer showed that 329 patients who had received streptokinase were alive. All were invited for venepuncture and 220 (67%) attended. Satisfactory samples were obtained from 189 patients.

RESULTS

Raised titres of antibody sufficient to neutralise a standard dose of 1.5 million units of streptokinase were found in 90% of patients. There was a fall in streptokinase neutralisation titre with increasing time after administration of streptokinase (r = -0.35, P < 0.0001) and though there was considerable variation among the group the neutralisation titre was higher than in the general population in all patients, even those who had received streptokinase at least two years previously.

CONCLUSION

The ability of streptokinase to lyse a thrombin clot was appreciably inhibited in vitro by the plasma from patients who had received 1.5 million units of streptokinase. High streptokinase neutralisation titres persisted for a long time after the use of streptokinase as thrombolytic treatment for acute myocardial infarction. Readministration of streptokinase may not be efficacious for considerably longer than the one year currently advocated. Until the in vivo effects of streptokinase readministration are known a non-antigenic thrombolytic agent should be used instead.

摘要

目的

追踪一组急性心肌梗死患者接受链激酶治疗后链激酶中和抗体滴度的变化。

设计

在189例接受150万单位链激酶治疗的患者中,于治疗后长达866天采集适合分析的静脉血样本。评估患者血浆抑制链激酶溶解凝血酶凝块的能力。

地点

一家地区综合医院的冠心病监护病房。

患者

对冠心病监护记录及地区卫生当局计算机系统进行回顾性分析发现,329例接受链激酶治疗的患者仍存活。所有患者均被邀请接受静脉穿刺,220例(67%)前来就诊。从189例患者中获得了满意的样本。

结果

90%的患者体内存在足以中和150万单位标准剂量链激酶的抗体滴度升高情况。链激酶中和抗体滴度随链激酶给药后时间的延长而下降(r = -0.35,P < 0.0001),尽管该组患者之间存在相当大的差异,但所有患者的中和抗体滴度均高于一般人群,即使是那些至少在两年前接受过链激酶治疗的患者。

结论

接受150万单位链激酶治疗患者的血浆在体外可显著抑制链激酶溶解凝血酶凝块的能力。在将链激酶用作急性心肌梗死溶栓治疗后,高链激酶中和抗体滴度会持续很长时间。再次使用链激酶可能在比目前所提倡的一年时间长得多的时间内都无效。在了解再次使用链激酶的体内效应之前,应改用非抗原性溶栓剂。

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