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作 者:王兴振[1] 朱声华[1] 刘庆[1] 胡安琪[1] 昝中学 余清贵 尹庆玲[1]
机构地区:[1]华西医科大学,四川卫生管理干部学院
出 处:《实用寄生虫病杂志》1995年第1期16-21,共6页Journal of Practical Parasitic Diseases
基 金:UNDP/World Bank/WHO/TDR提供基金
摘 要:作者等在间日疟流行区的四川筠连县四方村对QBC(Quantitativebuffycoat)法与姬姆萨厚血片染色法进行了现场应用诊断间日疟的对比研究。血液标本来自161名自愿供血的村民,其中男性83名,女性78名,年龄自必月至78岁。从指尖或耳垂刺取血液300μl。用10μl血均匀涂成直径12mm的圆形厚血膜,常规处理染色。将55ul血吸人QBC管,接操作规程离心备用。对每一厚血片均检查300视野(1000×油浸镜),对每-QBC管均观察5分钟(600×油浸镜),如尚未发现原虫,即停止观察,并判断该标本为阴性。用秒表准确记录各法查见原虫的最快时间,同时记录各期原虫在QBC管内的分布位置。结果发现,用姬姆萨厚片法查出带虫者34例,阴性127例,用QBC法查出带虫者32例,阴性129例。以姬姆萨厚片法为标准,计算QBC法的敏感性及特异性分别为79.41%及96.06%,符合率为92.55%。QBC法的阳性预期值及阴性预期值分别为84.36%及94.57%。姬姆萨厚片查见原虫的最快时间范围为1秒至30分钟,中数为10分钟。QBC法查见原虫的最快时间为2秒至4分15秒,中数为1分7秒。QBC管经离心后。The QBC technique in diagnosing vivax malaria was compared with that of the Giemsa stained thick smear under field conditions in Sifang Village, Junlian County, Sichuan Province, China. Blood samples were collected from 161 volunteer villagers. Each sample was examined with both the QBC and Giemsa techniques.Each stained Giemsa thick smear(GTS) was prepared by spreading 10μl blood over an appropriate area on a slide and examined for 300 oil immersion fields, and each QBC tube was observed for 5 min. before considering a sample to be negative. Results showed that 34 blood samples were positive for vivax malaria and 127 were negative by GTS,whereas, there were 32 positives and 129 negatives by QBC.Taking GTS as standard, the sensitivity and specficity of the QBC technique were 79.41% and 96.06% respectively, and the concordance was 92.55%.contributions of different developmental stages of P. vivax parasites in the centrifuged QBC tubed were observed and recorded, and the results revealed that all stages except schizonts,could be found in the lower part of the platelet zone, or the interphase between the monocyte and the platelet layers,especially the ring forms.
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