Department of Parasitology and Mycology, Faculty of Pharmacy, Animal Biology and Zoology, Felix Houphouët-Boigny University, BPV 34, Abidjan, Côte d'Ivoire.
Laboratory of Parasitology and Mycology, Diagnosis and Research Centre On AIDS and Other Infectious Diseases, 01 BPV 13, Abidjan, Côte d'Ivoire.
Acta Parasitol. 2024 Mar;69(1):541-548. doi: 10.1007/s11686-023-00754-2. Epub 2024 Jan 16.
Microscopic diagnosis of Giemsa-stained thick and thin blood films remained the gold standard laboratory method for the diagnosis of malaria. In this context, we felt it was important to conduct this evaluation with 40 public medical biology laboratories (MBLs) in the Abidjan 1 health region that perform blood parasitology tests to improve their implementation process.
This descriptive and analytical study took place in July 2020 and involved participating laboratories (PLs) from the public sector in Abidjan. A set of 3 blood smear slides of variable parasite densities (PDs) with assigned values (AVs) of parasite densities and assigned Plasmodium species was used. The criterion for establishing the parasite density compliance interval was assigned values of ± 25%, and the performance rates were compared to the 80% recommended by the WHO for the African region.
Nearly a quarter (11/40) of the participating laboratories had a compliance rate greater than 80%, including 10 with a performance of 100% for the ability to identify parasites. Regarding identifying plasmodial species, a concordance rate of 100% was obtained for slide 1 for Plasmodium falciparum, while this rate was 20% for slide 2 for Plasmodium ovale. For parasite densities < 200/µl, 87.5% of the participating laboratories (PLs) had a performance rate lower than 80%, while 95% of these PLs had a performance rate higher than 80% for parasitaemia > 2000/µl.
There is a need to strengthen adapted to low parasitaemia, to improve the biological confirmation of malaria in Côte d'Ivoire.
吉氏染色厚、薄血涂片的显微镜诊断仍然是疟疾诊断的金标准实验室方法。在这种情况下,我们认为对阿比让 1 区的 40 家进行血液寄生虫学检测的公共医学生物学实验室(MBL)进行这项评估非常重要,以改善其实施过程。
这是一项描述性和分析性研究,于 2020 年 7 月在阿比让进行,涉及公共部门的参与实验室(PL)。使用了一套 3 张具有指定寄生虫密度(PD)值和指定疟原虫种的可变寄生虫密度(PD)的血涂片。寄生虫密度符合率的标准是指定值的±25%,性能率与世界卫生组织(WHO)推荐的 80%进行比较,适用于非洲地区。
近四分之一(11/40)的参与实验室符合率大于 80%,其中 10 家实验室对识别寄生虫的能力达到了 100%的性能。关于识别疟原虫种,对于恶性疟原虫,第 1 张载玻片的符合率为 100%,而对于卵形疟原虫,第 2 张载玻片的符合率为 20%。对于密度<200/µl 的寄生虫,87.5%的参与实验室(PL)的性能率低于 80%,而对于密度>2000/µl 的寄生虫,这些 PL 的 95%的性能率高于 80%。
有必要加强对低寄生虫血症的适应,以改善科特迪瓦的疟疾生物学确认。