External Quality Assessment Program for SARS-COV-2 Molecular Detection in Pakistan

IF 4.3 4区 医学 Q1 INFECTIOUS DISEASES Influenza and Other Respiratory Viruses Pub Date : 2024-07-11 DOI:10.1111/irv.13316
Nazish Badar, Aamer Ikram, Muhammad Salman, Sidra Saeed, Hamza Ahmed Mirza, Abdul Ahad, Asiya Ashraf, Umer Farooq
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Abstract

Introduction

Amid coronavirus disease 2019 (COVID-19) pandemic, accurate detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is critical for diagnosis management and breaking down transmission chains. We designed a national external quality assessment panel (EQAP) for SARS-CoV-2 molecular detection comprising working laboratories nationwide.

Methods

A molecular diagnostic EQA panel that consists of five samples for SARS CoV-2 testing was distributed to 141 public and private sector laboratories across country. These samples contain different concentrations of SARS-CoV-2 to evaluate the sensitivity of commercial kits available.

Results

Sensitivity among public and private sector laboratories was variable, particularly lower SARS-CoV-2 concentrations significantly increased the risk of false-negative tests, whereas Ct values of accurately tested SARS-CoV-2 specimens increased as concentration decreased. These findings highlighted that performance of used commercial kits was not significantly correlated to various extraction or PCR methods.

Conclusion

This study highlights the need for a national external quality assessment panel (EQAP) in the country to improve the quality of the healthcare system while ensuring the accuracy and reliability of results. Furthermore, EQAPs can help laboratories meet accreditation and regulatory requirements. However, continued participation in EQAP is recommended for quality enhancement of laboratories.

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巴基斯坦 SARS-COV-2 分子检测外部质量评估计划。
导言:在冠状病毒病 2019(COVID-19)大流行期间,准确检测严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)对于诊断管理和切断传播链至关重要。我们设计了一个全国性的 SARS-CoV-2 分子检测外部质量评估小组(EQAP),由全国范围内的工作实验室组成:方法:我们向全国 141 家公共和私营实验室分发了由五份 SARS CoV-2 检测样本组成的分子诊断 EQA 面板。这些样本含有不同浓度的 SARS-CoV-2 以评估现有商业试剂盒的灵敏度:结果:公共和私营实验室的灵敏度各不相同,特别是较低的 SARS-CoV-2 浓度会显著增加假阴性检测的风险,而准确检测 SARS-CoV-2 标本的 Ct 值会随着浓度的降低而增加。这些发现突出表明,使用的商业试剂盒的性能与各种提取或 PCR 方法没有明显的相关性:本研究强调了在该国建立国家外部质量评估小组(EQAP)的必要性,以提高医疗保健系统的质量,同时确保结果的准确性和可靠性。此外,EQAP 还能帮助实验室满足认证和监管要求。不过,为了提高实验室的质量,建议继续参与 EQAP。
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来源期刊
CiteScore
7.20
自引率
4.50%
发文量
120
审稿时长
6-12 weeks
期刊介绍: Influenza and Other Respiratory Viruses is the official journal of the International Society of Influenza and Other Respiratory Virus Diseases - an independent scientific professional society - dedicated to promoting the prevention, detection, treatment, and control of influenza and other respiratory virus diseases. Influenza and Other Respiratory Viruses is an Open Access journal. Copyright on any research article published by Influenza and Other Respiratory Viruses is retained by the author(s). Authors grant Wiley a license to publish the article and identify itself as the original publisher. Authors also grant any third party the right to use the article freely as long as its integrity is maintained and its original authors, citation details and publisher are identified.
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