Description of complaints/clinical symptoms and examination results of the SARS-CoV-2 rapid test in Brata Medika Laboratory Clinic Pare - Kediri in February 2021

A. M. Charisma, Arif Rahman Nurdianto, Rizal Fauzi Nurdianto, Fery Setiawan, Heribertus Agustinus B Tena
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Abstract

 SARS-CoV-2 antigen rapid test is one of the examinations widely used for early detection of Covid-19 infection. Rapid test is considered to have more advantages, is faster, and is cheaper than molecular PCR testing, and more accurate than rapid antibody tests. Its weakness is especially in detecting samples with small quantities of the virus. The study was conducted using a retrospective method. The data was taken from the patient's medical record of the SARS -CoV-2 antigen rapid swab test at Brata Medika Pare Clinical Laboratory for the period of February 2021. Data inclusion criteria including the examination, complete identity, results of anamnesis examination and rapid test examinations. Data were analyzed in a tabular form containing frequency and percentage. There were 18 (22.5%) patients with positive SARS-CoV-2antigen rapid swab test results, 16 (89%) with complaints/symptoms, and 2 (11%) without complaints/symptoms. Meanwhile, 62 (77.5%) were found with negative SARS-CoV-2 antigen rapid swab test results where 18 (29.0%) were patients with complaints/symptoms and 44 (71.0%) were patients without complaints/symptoms. The high percentage of negative SARS-CoV-2 antigen rapid swab test results in patients with complaints/symptoms (29.0%), it is recommended that a confirmatory examination with the molecular PCR test be carried out. 
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2021年2月Brata Medika实验室诊所Pare - Kediri SARS-CoV-2快速检测的主诉/临床症状和检查结果描述
SARS-CoV-2抗原快速检测是目前广泛应用的早期检测方法之一。快速检测被认为比分子PCR检测更有优势,更快,更便宜,比快速抗体检测更准确。它的弱点尤其在于检测含有少量病毒的样本。本研究采用回顾性方法进行。数据取自患者2021年2月期间在Brata Medika Pare临床实验室进行的SARS -CoV-2抗原快速拭子检测的病历。数据纳入标准包括检查、完整身份、记忆检查结果和快速检测检查。数据以包含频率和百分比的表格形式进行分析。sars - cov -2抗原快速拭子试验阳性18例(22.5%),有主诉/症状16例(89%),无主诉/症状2例(11%)。SARS-CoV-2抗原快速拭子检测阴性62例(77.5%),其中主诉/症状患者18例(29.0%),无主诉/症状患者44例(71.0%)。主诉/症状患者SARS-CoV-2抗原快速拭子试验阴性比例较高(29.0%),建议采用分子PCR检测进行确证性检查。
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审稿时长
8 weeks
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