Academic Medical Centre, Department of Medical Microbiology, Parasitology Unit, Amsterdam University Medical Centres, Meibergdreef 9, 1105, AZ, Amsterdam, The Netherlands.
Queen Elizabeth Central Hospital, Blantyre, Malawi.
Infect Dis Poverty. 2019 Nov 28;8(1):96. doi: 10.1186/s40249-019-0609-6.
There is significant need for accurate diagnostic tools for Cryptosporidium spp. and Giardia duodenalis infections in resource limited countries where diarrhoeal disease caused by these parasites is often prevalent. The present study assessed the diagnostic performance of three commercially available rapid diagnostic tests (RDTs) based on faecal-antigen detection for Cryptosporidium spp. and/or G. duodenalis infections in stool samples of children admitted with severe acute malnutrition (SAM) and diarrhoea. An established multiplex PCR was used as reference test.
Stool samples from children with SAM and diarrhoea enrolled in a randomized controlled trial (registered at clinicaltrials.gov/ct2/show/NCT02246296) in Malawi (n = 175) and Kenya (n = 120) between December 2014 and December 2015 were analysed by a multiplex PCR for the presence of Cryptosporidium spp., G. duodenalis or Entamoeba histolytica parasite DNA. Cryptosporidium-positive samples were species typed using restriction fragment length polymorphism analysis. A sub-sample of the stool specimens (n = 236) was used for testing with three different RDTs. Diagnostic accuracy of the tests under evaluation was assessed using the results of PCR as reference standard using MedCalc software. Pearson Chi-square test and Fisher's exact test were used to determine (significant) difference between the number of cryptosporidiosis or giardiasis cases found by PCR in Malawi and Kenya. The overall diagnostic accuracy of each RDT was calculated by plotting a receiver operating characteristic (ROC) curve for each test and to determine the area under the curve (AUC) using SPSS8 software.
Prevalence of Cryptosporidium spp. by PCR was 20.0 and 21.7% in Malawi and Kenya respectively, mostly C. hominis. G. duodenalis prevalence was 23.4 and 5.8% in Malawi and Kenya respectively. E. histolytica was not detected by PCR. RDT testing followed the same pattern of prevalence. RDT sensitivities ranged for cryptosporidiosis from 42.9 to 76.9% and for G. duodenalis from 48.2 to 85.7%. RDT specificities ranged from 88.4 to 100% for Cryptosporidium spp. and from 91.2 to 99.2% for G. duodenalis infections. Based on the estimated area under the curve (AUC) values, all tests under evaluation had an acceptable overall diagnostic accuracy (> 0.7), with the exception of one RDT for Cryptosporidium spp. in Malawi.
All three RDTs for Cryptosporidium spp. and Giardia duodenalis evaluated in this study have a moderate sensitivity, but sufficient specificity. The main value of the RDTs is within their rapidness and their usefulness as screening assays in surveys for diarrhoea.
在资源有限的国家,迫切需要准确的诊断工具来检测隐孢子虫和贾第鞭毛虫感染,因为这些寄生虫引起的腹泻在这些国家很常见。本研究评估了三种基于粪便抗原检测的商业快速诊断检测(RDT)在因严重急性营养不良(SAM)和腹泻住院的儿童粪便样本中检测隐孢子虫和/或贾第鞭毛虫感染的诊断性能。采用建立的多重 PCR 作为参考试验。
2014 年 12 月至 2015 年 12 月,马拉维(n=175)和肯尼亚(n=120)的一项随机对照试验(在 clinicaltrials.gov/ct2/show/NCT02246296 注册)中,对患有 SAM 和腹泻的儿童的粪便样本进行了基于多重 PCR 的隐孢子虫、贾第鞭毛虫或溶组织内阿米巴寄生虫 DNA 检测。采用限制性片段长度多态性分析对隐孢子虫阳性样本进行种型鉴定。使用三种不同的 RDT 对粪便标本的亚样本(n=236)进行检测。使用 MedCalc 软件,以 PCR 结果为参考标准,评估试验的诊断准确性。使用 Pearson Chi-square 检验和 Fisher's exact 检验来确定马拉维和肯尼亚 PCR 检测到的隐孢子虫病或贾第鞭毛虫病病例数之间的差异(有统计学意义)。使用 SPSS8 软件对每个 RDT 的整体诊断准确性进行计算,为每个测试绘制接收者操作特征(ROC)曲线,并确定曲线下面积(AUC)。
马拉维和肯尼亚的 PCR 检测到的隐孢子虫 spp. 的流行率分别为 20.0%和 21.7%,主要是 C. hominis。贾第鞭毛虫的流行率分别为马拉维和肯尼亚的 23.4%和 5.8%。PCR 未检测到溶组织内阿米巴。RDT 检测遵循相同的流行模式。隐孢子虫病的 RDT 敏感性范围为 42.9%至 76.9%,贾第鞭毛虫病的敏感性范围为 48.2%至 85.7%。隐孢子虫病的 RDT 特异性范围为 88.4%至 100%,贾第鞭毛虫病的特异性范围为 91.2%至 99.2%。基于估计的曲线下面积(AUC)值,所有评估的测试均具有可接受的整体诊断准确性(>0.7),除了马拉维的一种隐孢子虫病 RDT 除外。
本研究评估的三种用于隐孢子虫和贾第鞭毛虫的 RDT 均具有中等敏感性,但特异性足够。RDT 的主要价值在于其快速性及其作为腹泻调查中筛查检测的有用性。