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疟疾快速诊断检测中的前带现象:漏检了多少病例?

Prozone in malaria rapid diagnostics tests: how many cases are missed?

机构信息

Department of Clinical Sciences, Unit of Tropical Laboratory Medicine, Institute of Tropical Medicine, Nationalestraat 155, B 2000 Antwerp, Belgium.

出版信息

Malar J. 2011 Jun 15;10:166. doi: 10.1186/1475-2875-10-166.

Abstract

BACKGROUND

Prozone means false-negative or false-low results in antigen-antibody reactions, due to an excess of either antigen or antibody. The present study prospectively assessed its frequency for malaria rapid diagnostic tests (RDTs) and Plasmodium falciparum samples in an endemic field setting.

METHODS

From January to April 2010, blood samples with P. falciparum high parasitaemia (≥ 4% red blood cells infected) were obtained from patients presenting at the Provincial Hospital of Tete (Mozambique). Samples were tested undiluted and 10-fold diluted in saline with a panel of RDTs and results were scored for line intensity (no line visible, faint, weak, medium and strong). Prozone was defined as a sample which showed no visible test line or a faint or weak test line when tested undiluted, and a visible test line of higher intensity when tested 10-fold diluted, as observed by two blinded observers and upon duplicate testing.

RESULTS

A total of 873/7,543 (11.6%) samples showed P. falciparum, 92 (10.5%) had high parasitaemia and 76 were available for prozone testing. None of the two Pf-pLDH RDTs, but all six HRP-2 RDTs showed prozone, at frequencies between 6.7% and 38.2%. Negative and faint HRP-2 lines accounted for four (3.8%) and 15 (14.4%) of the 104 prozone results in two RDT brands. For the most affected brand, the proportions of prozone with no visible or faint HRP-2 lines were 10.9% (CI: 5.34-19.08), 1.2% (CI: 0.55-2.10) and 0.1% (CI: 0.06-0.24) among samples with high parasitaemia, all positive samples and all submitted samples respectively. Prozone occurred mainly, but not exclusively, among young children.

CONCLUSION

Prozone occurs at different frequency and intensity in HRP-2 RDTs and may decrease diagnostic accuracy in the most affected RDTs.

摘要

背景

前带现象是指由于抗原或抗体过量,导致抗原-抗体反应出现假阴性或假低值结果。本研究前瞻性评估了前带现象在疟疾快速诊断检测(RDT)和恶性疟原虫样本中的频率,在一个流行地区进行。

方法

2010 年 1 月至 4 月,从在太特省医院就诊的患者中采集高疟原虫血症(≥4%红细胞感染)的恶性疟原虫血样。样本未经稀释和用盐水稀释 10 倍,用 RDT 试剂盒进行检测,并对线条强度(无可见线、模糊、弱、中、强)进行评分。前带现象定义为未经稀释时无可见检测线或模糊或弱检测线,而 10 倍稀释时出现更强检测线的样本,由两名盲法观察者观察并进行重复检测。

结果

共有 873/7543(11.6%)个样本显示恶性疟原虫,92(10.5%)个样本高疟原虫血症,76 个样本可用于前带检测。两种 Pf-pLDH RDT 均未显示前带现象,但六种 HRP-2 RDT 均显示前带现象,频率在 6.7%至 38.2%之间。在两个 RDT 品牌中,有四个(3.8%)和 15 个(14.4%)阴性和模糊 HRP-2 线的结果为前带现象。对于受影响最严重的品牌,高疟原虫血症样本、所有阳性样本和所有提交样本中无可见或模糊 HRP-2 线的前带比例分别为 10.9%(95%CI:5.34-19.08)、1.2%(95%CI:0.55-2.10)和 0.1%(95%CI:0.06-0.24)。前带现象主要发生在,但不仅限于,幼儿中。

结论

HRP-2 RDT 中前带现象的发生频率和强度不同,可能会降低受影响最严重的 RDT 的诊断准确性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19ad/3141590/674ce06f92dd/1475-2875-10-166-1.jpg

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