CareStart™ G6PD缺乏症快速检测卡
发布时间:2017-4-6 10:00:53 浏览次数:
G6PD缺乏症
G6PD缺乏症是一种遗传疾病,导致没有或低G6PD活性。G6PD缺乏症患者不应该把伯氨喹,抗疟药物,高氧化应激和其他药物,因为它可能会导致急性溶血等严重的副作用。
真正的即时检测G6PD > 95%敏感性*世卫组织分类Ⅰ&Ⅱ(< 10%的正常活动)
CareStart™G6PD RDT视觉筛选试验,确定G6PD缺乏患者使用全血样品。
测试结果
Results of Access Bio's G6PD Performance Test :Institute Pasteur, Cambodi | ||
---|---|---|
Cutoff Value(%) | <30% | |
CareStart™ G6PD RDT | Sensitivity (95% CL) | 100% |
Specificity | 97% |
来源:
“现场试验来评估性能的现场即时诊断筛查G6PD缺乏症的恶性疟原虫和间日疟原虫疟疾流行地区的柬埔寨相融。《美国热带医学和卫生学会(2013年11月)
1Gently hold the bottom part of the pipette and touch the blood drop with the open end of the capillary tube.(CAUTION : Do not cover the hole!)
2Let the blood flow into the capillary tube.
3Cover and press the hole to release the blood into the sample well. Add 2 drops of Assay Buffer (100㎕) immediately after to the buffer well.
4Read result in 10 minutes.
检测结果
NORMALA distinct purple color appears in the reading window within 10 min.DEFICIENTNo color change or a very faint purple color appears in the reading window within 10 min(A borderline result is read as deficient.)INVALIDNo blood migration or incomplete blood migration in window.
Product | Cat. No. | Package Size | Components |
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CareStart™ G6PD RDT | RGP-M02582 | 25 tests/box | Alcohol, Lancets, Pipettes, Assay buffer, Instruction for use |
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