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G6PD缺乏癥

G6PD缺乏癥是一種遺傳疾病,導(dǎo)致沒有或低G6PD活性。G6PD缺乏癥患者不應(yīng)該把伯氨喹,抗瘧藥物,高氧化應(yīng)激和其他藥物,因?yàn)樗赡軙?dǎo)致急性溶血等嚴(yán)重的副作用。

真正的即時(shí)檢測G6PD > 95%敏感性*世衛(wèi)組織分類Ⅰ&Ⅱ(< 10%的正常活動)

CareStart?G6PD RDT視覺篩選試驗(yàn),確定G6PD缺乏患者使用全血樣品。

測試結(jié)果

來源:

“現(xiàn)場試驗(yàn)來評估性能的現(xiàn)場即時(shí)診斷篩查G6PD缺乏癥的惡性瘧原蟲和間日瘧原蟲瘧疾流行地區(qū)的柬埔寨相融?！睹绹鵁釒пt(yī)學(xué)和衛(wèi)生學(xué)會(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.

檢測結(jié)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.