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Production and validation of durable, high quality standardized malaria microscopy slides for teaching, testing and quality assurance during an era of declining diagnostic proficiency

机译:诊断能力下降的时代,用于教学,测试和质量保证的耐用,高质量标准化疟疾显微镜载玻片的生产和验证

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Background Sets of Giemsa-stained, blood smear slides with systematically verified composite diagnoses would contribute substantially to development of externally validated quality assurance systems for the microscopic diagnosis of malaria. Methods whole blood from Plasmodium-positive donors in Cambodia and Indonesia and individuals with no history of risk for malaria was collected. Using standard operating procedures, technicians prepared Giemsa-stained thick and thin smears from each donor. One slide from each of the first 35 donations was distributed to each of 28 individuals acknowledged by reputation as having expertise in the microscopic diagnosis of malaria. These reference readers recorded presence or absence of Plasmodium species and parasite density. A composite diagnosis for each donation was determined based on microscopic findings and species-specific small subunit ribosomal RNA (ssrRNA) DNA polymerase chain reaction (PCR) amplification. Results More than 12, 000 slides were generated from 124 donations. Reference readers correctly identified presence of parasites on 85% of slides with densities 350 parasites/μl. Percentages of agreement with composite diagnoses were highest for Plasmodium falciparum (99%), followed by Plasmodium vivax (86%). Conclusion Herein, a standardized method for producing large numbers of consistently high quality, durable Giemsa-stained blood smears and validating composite diagnoses for the purpose of creating a malaria slide repository in support of initiatives to improve training and competency assessment amidst a background of variability in diagnosis is described.
机译:背景技术吉姆萨染色的血涂片具有系统地经过验证的综合诊断,将大大有助于开发用于显微镜下诊断疟疾的外部验证质量保证系统。方法收集来自柬埔寨和印度尼西亚的疟原虫阳性供体以及没有疟疾风险史的个人的全血。使用标准的操作程序,技术人员从每个捐赠者处准备吉姆萨染色的厚薄涂片。前35笔捐赠中的每一张都分发给了28个个人,每个人都被誉为在微观诊断疟疾方面具有专业知识而受到声誉的认可。这些参考读者记录了疟原虫种类和寄生虫密度的存在与否。根据显微镜检查结果和特定于物种的小亚基核糖体RNA(ssrRNA)DNA聚合酶链反应(PCR)扩增,确定每项捐赠的综合诊断。结果124笔捐款产生了12千张幻灯片。参考读者正确地识别了密度为350寄生虫/μl的载玻片上85%的寄生虫。恶性疟原虫(99%)与综合诊断的一致性百分比最高,其次是间日疟原虫(86%)。结论本文的标准方法是产生大量一致,高质量,持久的吉姆萨染色的血液涂片并验证复合诊断,以建立疟疾载玻片库,以支持在环境变化的背景下改善培训和能力评估的计划。描述诊断。

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