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Laboratory diagnosis of malaria: Comparing giemsa stained thick blood films with rapid diagnostic test (RDT) in an endemic setting in North-west Nigeria

机译:疟疾的实验室诊断:在尼日利亚西北部流行地区比较吉姆萨染色厚厚的血膜与快速诊断测试(RDT)

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Malaria microscopy will continue to remain the gold standard for the diagnosis of malaria, but prolonged turnaround time and lack of malaria microscopist that are associated with this technique continue to impact on the quality of service rendered by the laboratory, especially the turnaround time, which is one of the quality indicators to measure laboratory quality systems. The prolonged turnaround time and lack of malaria microscopists identified with resource constraint setting in the midst of a period with high transmission of malaria prompted us to search for an alternative to the gold standard. Hence, multi-species were evaluated based on the rapid diagnostic test to determine its importance in the laboratory diagnosis of malaria. The rapid diagnostic test kit (SD Bioline – FK80) used in this study is based on the detection of Plasmodium falciparum, histidine rich protein-2 (HRP-2) and Plasmodium vivax-specific lactose dehydrogenase (Pv-pLDH), and was compared against traditional malaria microscopy. The evaluation was designed to provide data on the use of rapid diagnostic test and microscopy for malaria diagnosis in an urban secondary health facility with laboratory component. In total, 939 patients that consulted the out-patient department were clinically evaluated and suspected for malaria. Blood samples of those patients were subsequently tested using both techniques. The sensitivity and specificity for P. falciparum were 75.2 and 80.4%, respectively. The accuracy of the test was 76.8%. It was concluded that the rapid diagnostic test could be used as the first screening test for malaria diagnosis and have to be confirmed by microscopy if the outcome is negative. This will therefore improve on the current situation of treating patients for malaria without laboratory outcome to confirm clinical evaluation.
机译:疟疾显微镜将继续成为诊断疟疾的金标准,但延长的周转时间和缺乏与这种技术相关的疟疾显微镜专家继续影响实验室提供的服务质量,尤其是周转时间,即衡量实验室质量体系的质量指标之一。在疟疾传播高的时期中,周转时间延长和疟疾显微镜专家缺乏资源约束条件,这促使我们寻找替代金本位的方法。因此,基于快速诊断测试评估了多种物种,以确定其在疟疾实验室诊断中的重要性。本研究中使用的快速诊断测试试剂盒(SD Bioline – FK80)基于恶性疟原虫,富含组氨酸的蛋白2(HRP-2)和间日疟原虫间质特异性乳糖脱氢酶(Pv-pLDH)的检测,并进行了比较反对传统的疟疾显微镜。该评估旨在提供有关在具有实验室组件的城市二级医疗机构中使用快速诊断测试和显微镜检查进行疟疾诊断的数据。总共939例咨询了门诊部的患者经过了临床评估,并怀疑患有疟疾。随后使用两种技术测试了这些患者的血液样本。恶性疟原虫的敏感性和特异性分别为75.2%和80.4%。测试的准确性是76.8%。结论是,快速诊断测试可以作为疟疾诊断的首次筛查测试,如果结果阴性,则必须通过显微镜检查。因此,这将改善治疗疟疾而没有实验室结果以确认临床评估的当前状况。

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