ABSTRACT
Objective To investigate the harmonization of results of Prothrombin time(PT),International Normalized Ratio(INR),activated partial thromboplastin time(APTT),fibrinogen(FIB)and thrombin time(TT)with different coagulation analyzers in different or sanle clinical laboratory.Methods PT,INR,Am,FIB and TT for the same quality control material were detected with 14 different coagulation analyzers,which are distributed in 12 clinical laboratories and classified into A,B and C group.MeaJlwhile,PT,INR,APTT,FIB of 139 samples were detected with two different coagulation aJlalyzers in the same laboratory.Results There was no significant difference for detection of level 3 of both INR and TT among the three group analyzers(P＞0.05),but there was significant difference for other tests (P＜0.05).The comparison between groups showed that there was high percentage(66.7%)of consistency for detection of INR,FIB-C and TT between group B and C.The results of two different coagulation analvzers ( ACL Futura and CA 510)in same laboratory showed that there was no significant difference(P＞0.05)for detection of PT,INR,PT-FIB and FIB-C between them,and there was good eorrelation for them in detecting PT,INR,APTT,PT-FIB and FIB-C(r＞0.975).Analysis of bias showed that the bias of PT,INR,PT-FIB and FIBC between the two different coagulation analyzers was acceptable according to CLIA'88.Conclusion There are good agreement for the results between different coagulation analyzers based upon the similar Drinciple in coagulation analysis.
ABSTRACT
ve To study the mutagenecity of volatile organic compounds (VOCs) emitted from decoration materials to experimental animals and human subjects so as to provide some technical basis for the management of safety and hygienic quality of indoor decoration materials. Methods The micronucleus test was carried out in mice exposed to the tested toxicants in an experimental cabinet, in which the tested VOCs were prepared at the various concentrations which were 5, 10, 20 and 40 times as high as the concentrations of VOCs in decorated rooms monitored on site respectively. The frequencies of micronucleus of peripheral blood lymphocytes were examined among waitress working in decorated indoor environment. Results The concentrations of formaldehyde, benzene, methylbenzene, ethyl acetate, butyl acetate in decorated rooms were significantly higher than those in un-decorated rooms and the related national standards within half a year after decoration. The frequencies of micronucleus of mice exposed to tested VOCs with concentration being 40 times as high as those in decorated rooms were significantly higher than those of negative control group at the 15 th day after exposure. There were no significant differences in frequencies of mi-cronucleus in peripheral blood lymphocytes between waitress working in decorated rooms and un-decorated rooms. Conclusion VOCs emitted from decoration materials were uneasily diffused in air-conditioned airtight environment. The higher concentrations of VOCs simulated based on their levels in decorated rooms revealed mutagenecity to ex-perimental animals.