Rapid detection of streptokinase resistance using a bedside lytic assay ofdry reagent technology

Citation
K. Al Shwafi et al., Rapid detection of streptokinase resistance using a bedside lytic assay ofdry reagent technology, FIBRINOL PR, 14(6), 2000, pp. 351-357
Citations number
30
Categorie Soggetti
Cardiovascular & Hematology Research
Journal title
FIBRINOLYSIS & PROTEOLYSIS
ISSN journal
13690191 → ACNP
Volume
14
Issue
6
Year of publication
2000
Pages
351 - 357
Database
ISI
SICI code
1369-0191(200011)14:6<351:RDOSRU>2.0.ZU;2-3
Abstract
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 st andard SK Reactivity Test and with clinical outcome of acute myocardial inf arction (AMI) SK-treated patients, high SKR when SK100>50 seconds and SK10> 120 seconds; partial SKR when SK10>120 seconds. Five prospective clinical g roups (325 patients) were screened in cardiac units of four university hosp itals, In patients previously treated with SK, the prevalence of SKR was 87 % (70% high, 17% partial); in those who had documented streptococcal infect ion, 92% (75% high, 17% partial); and in patients with rheumatic heart dise ase, 76% (all high). SKR prevalence was 55% (33% high, 22% partial) in thos e 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 Vers us 19% (9% high, 10% partial) in those < 65 years (P < 0.0001). In conclusion, we demonstrated (with a rapid functional assay) the consiste nce of our results with the expected prevalence of SKR in the groups studie d, this points out to the feasibility of pre-therapeutic detection of SKR a nd choice between t-PA and SK made at bedside without delaying the onset of treatment. As SKR is common among candidates for thrombolysis, pre-therape utic detection of SKR merits further investigation. (C) 2000 Harcourt Publi shers Ltd.