干试剂床边裂解法快速检测链激酶耐药

K. A. Shwafi, J. Renkin, A. Meester, B. Pirenne, J. Col
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摘要

最近介绍了一种使用干试剂技术快速(3-5分钟)检测链激酶耐药(SKR)的新床边裂解法,该方法测量全血凝块对高和低链激酶(SK)浓度(100 U/ml (SK100)和10 U/ml (SK10))的裂解开始时间(LOT)。SKR的定义是LOT的延长,先前与标准SK反应性试验和急性心肌梗死(AMI) SK治疗患者的临床结果相关,SK100>50秒和SK10>120秒时SKR较高;SK10>120秒时部分SKR。在四所大学医院的心内科筛选了五个前瞻性临床组(325例患者),在先前接受过SK治疗的患者中,SKR患病率为87%(70%高,17%部分);在有记录的链球菌感染中,92%(75%高,17%部分);在患有风湿性心脏病的患者中,这一比例为76%(均为高)。近期呼吸道感染患者的SKR患病率为55%(33%高,22%部分)。在225例急性冠状动脉患者中,SKR为28%(高21%,部分7%),性别相同,但大于或等于65岁的患者SKR为36%(高32%,部分4%),而< 65岁的患者SKR为19%(高9%,部分10%)(P < 0.0001)。总之,我们证明了(通过快速功能分析)我们的结果与研究组中SKR的预期患病率的一致性,这指出了治疗前检测SKR以及在床边进行t-PA和SK之间的选择的可行性,而不会延迟治疗的开始。由于SKR在溶栓候选药物中很常见,治疗前检测SKR值得进一步研究。(C) 2000 Harcourt出版社有限公司
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rapid detection of streptokinase resistance using a bedside lytic assay of dry reagent technology
A new bedside lytic assay using dry reagent technology for rapid (3-5 min) detection of streptokinase resistance (SKR) was recently introduced, which measures lysis onset time (LOT) of whole blood clot in response to high and low streptokinase (SK) concentrations: 100 U/ml (SK100) and 10 U/ml (SK10). SKR was defined by prolongation of LOT, previously correlated with the standard SK Reactivity Test and with clinical outcome of acute myocardial infarction (AMI) SK-treated patients, high SKR when SK100>50 seconds and SK10>120 seconds; partial SKR when SK10>120 seconds. Five prospective clinical groups (325 patients) were screened in cardiac units of four university hospitals, In patients previously treated with SK, the prevalence of SKR was 87% (70% high, 17% partial); in those who had documented streptococcal infection, 92% (75% high, 17% partial); and in patients with rheumatic heart disease, 76% (all high). SKR prevalence was 55% (33% high, 22% partial) in those with recent respiratory tract infection. In 225 acute coronary patients, SKR was 28% (21% high, 7% partial), and was identical by gender, but was 36% (32% high, 4% partial) in patients greater than or equal to 65 years Versus 19% (9% high, 10% partial) in those < 65 years (P < 0.0001). In conclusion, we demonstrated (with a rapid functional assay) the consistence of our results with the expected prevalence of SKR in the groups studied, this points out to the feasibility of pre-therapeutic detection of SKR and choice between t-PA and SK made at bedside without delaying the onset of treatment. As SKR is common among candidates for thrombolysis, pre-therapeutic detection of SKR merits further investigation. (C) 2000 Harcourt Publishers Ltd.
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