埃塞俄比亚复检实验室疟疾显微镜工作人员的绩效评估。

MalariaWorld journal Pub Date : 2017-06-01 eCollection Date: 2017-01-01
Abnet Abebe, Meseret Belayneh, Habtamu Asrat, Wondwossen Kassa, Andargachew Gashu, Adino Desale, Getnet Hailu, Tesfaye Mekonnen, Feven Girmachew, Achamyeleh Mulugeta, Ebise Abose, Dereje Yenealem, Abeba G Tsadik, Adisu Kebede, Gonfa Ayana, Kassu Desta
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引用次数: 0

摘要

背景:吉姆萨染色的厚血膜和薄血膜的显微诊断仍然是诊断疟疾的标准实验室方法。在卫生设施中,检查血液玻片的显微镜的高质量性能仍然至关重要。材料和方法:对埃塞俄比亚23个疟疾复检实验室107名疟疾显微镜工作人员的工作性能进行了横断面研究。给每位显微镜师分发了12张血膜载玻片。收集数据并导出到SPSS version 20进行分析。计算卡方、敏感性、特异性、一致性百分比和kappa评分来评估检测和鉴定疟原虫种类的性能。结果:参与者的平均年龄为30±5岁,大多数(54;50.5%)在区域参考化验室工作。总体而言,参与者对疟疾寄生虫种类的检测和鉴定敏感性分别为96.8%和56.7%。对疟疾种类检测和鉴定的总体一致性分别为96.8% (Kappa = 0.9)和64.8% (Kappa = 0.33)。鉴定精度最低的疟原虫是疟原虫(3/107;2.8%),其次是卵形圆叶藻(35/107;32.7%)。在医院实验室工作的参与者物种识别准确率最高(72.3%,Kappa=0.51)。参加过疟疾显微镜和质量保证培训的研究参与者在寄生虫密度定量方面明显更好(结论:寄生虫鉴定和定量的准确性在参与者和专家显微镜之间存在明显差异。因此,对疟疾显微镜专家的定期能力评估和培训应该是强制性的,以确保埃塞俄比亚疟疾的正确诊断和管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Performance evaluation of malaria microscopists working at rechecking laboratories in Ethiopia.

Performance evaluation of malaria microscopists working at rechecking laboratories in Ethiopia.

Performance evaluation of malaria microscopists working at rechecking laboratories in Ethiopia.

Background: Microscopic diagnosis of Giemsa-stained thick and thin blood films has remained the standard laboratory method for diagnosing malaria. High quality performance of microscopists that examine blood slides in health facilities remains critically important.

Materials and methods: A cross-sectional study was conducted to assess the performance of 107 malaria microscopists working at 23 malaria rechecking laboratories in Ethiopia. A set of 12 blood film slides was distributed to each microscopist. Data was collected and exported to SPSS version 20 for analysis. Chi-square, sensitivity, specificity, percent agreement, and kappa scores were calculated to assess performance in detecting and identification of Plasmodium species.

Results: The mean age of the participants was 30 ± 5 yrs and most of them (54; 50.5%) were working at regional reference laboratories. Overall, the sensitivity of participants in detecting and identifying malaria parasite species was 96.8% and 56.7%, respectively. The overall agreement on detection and identification of malaria species was 96.8% (Kappa = 0.9) and 64.8% (Kappa = 0.33), respectively. The least accurately identified malaria parasite species was P. malariae (3/107; 2.8%) followed by P. ovale (35/107; 32.7%). Participants working at hospital laboratories had the highest percentage (72.3 %, Kappa=0.51) of accurate species identification. Study participants that had participated in malaria microscopy and quality assurance trainings were significantly better at quantifying parasite densities (P<0.001).

Conclusion: The accuracy of parasite identification and quantification differed strongly between participants and expert microscopists. Therefore, regular competency assessment and training for malaria microscopists should be mandatory to assure proper diagnosis and management of malaria in Ethiopia.

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