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低成本聚酯头三维打印鼻咽拭子用于检测严重急性呼吸综合征相关冠状病毒 2(SARS-CoV-2)。

Low-Cost Polyester-Tipped Three-Dimensionally Printed Nasopharyngeal Swab for the Detection of Severe Acute Respiratory Syndrome-Related Coronavirus 2 (SARS-CoV-2).

机构信息

Department of Pediatrics, Amiri Hospital, Ministry of Health, Kuwait City, Kuwait

Department of Surgery, Jaber Al-Ahmad Hospital, Ministry of Health, Kuwait City, Kuwait.

出版信息

J Clin Microbiol. 2020 Oct 21;58(11). doi: 10.1128/JCM.01668-20.

Abstract

Case identification, isolation, and contact tracing are fundamental strategies used to control the spread of coronavirus disease 2019 (COVID-19). This has led to widespread testing that interrupted the supply chain for testing materials around the world. A prospective study was conducted to compare inexpensive and easily sourced 3-dimensionally (3D)-printed polylactic acid and polyester nasopharyngeal swabs to commercially manufactured swabs for the detection of severe acute respiratory syndrome-related coronavirus 2 (SARS-CoV-2). During the study period, 287 laboratory-confirmed hospitalized COVID-19 patients, at multiple stages of their illness, were enrolled. The median age for the study population was 47.6 years (interquartile range [IQR], 34.4 to 56.6 years), and two-thirds (67.6%) of the subjects were male. The median duration of hospitalization, at the time of sampling, was 13 days (IQR, 10 to 16 days). Overall concordance between the prototype and control swabs was 80.8% (Cohen's kappa coefficient, 0.61). Most discrepant results were due to prototype-positive control-negative results. When considering all positive results to be true positives, the prototype swab had a higher sensitivity (90.6% versus 80.8%; 95% confidence interval [CI], 85.7% to 94.0% and 74.7% to 85.7%, respectively; 0.015). The cost to produce the prototype swab was estimated to be $0.05 per swab. Polylactic acid 3D-printed polyester-tipped swabs were shown to be effective for nasopharyngeal sample collection. We believe that this design can easily be adopted in countries where commercial swabs are not readily available and can play a vital role in public health efforts for disease control in low-income countries.

摘要

病例识别、隔离和接触者追踪是控制 2019 年冠状病毒病(COVID-19)传播的基本策略。这导致了广泛的检测,从而中断了世界各地检测材料的供应链。一项前瞻性研究比较了廉价且易于获取的三维(3D)打印聚乳酸和聚酯鼻咽拭子与商业制造的拭子在检测严重急性呼吸综合征相关冠状病毒 2(SARS-CoV-2)方面的效果。在研究期间,共纳入了 287 名经实验室确诊的住院 COVID-19 患者,他们处于疾病的不同阶段。研究人群的中位年龄为 47.6 岁(四分位距[IQR],34.4 至 56.6 岁),三分之二(67.6%)的患者为男性。采样时的中位住院时间为 13 天(IQR,10 至 16 天)。原型和对照拭子之间的总体一致性为 80.8%(Cohen's kappa 系数,0.61)。大多数不一致的结果是由于原型阳性而对照阴性的结果。如果将所有阳性结果视为真阳性,那么原型拭子的灵敏度更高(90.6%对 80.8%;95%置信区间[CI],85.7%至 94.0%和 74.7%至 85.7%;0.015)。估计原型拭子的生产成本为每个拭子 0.05 美元。聚乳酸 3D 打印聚酯尖端拭子被证明可有效用于鼻咽样本采集。我们认为,这种设计可以很容易地在商业拭子不易获得的国家采用,并在低收入国家的疾病控制公共卫生工作中发挥重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2909/7587115/3052b905d83e/JCM.01668-20-f0001.jpg

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