Medical Evaluation of Test Results Related to Covid 19 in Iranian Hospitals Using QUADAS-2 to Evaluate the Quality of Studies and Meta-Analysis Using Stata / MP v.16 Software
H. Danesh, S. R. Ghasabeh, R. Rounasi, E. Zarepur, A. Abdolrazaghnejad
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Abstract
The aim of current study was to evaluate the outcome of some laboratory tests and accuracy of diagnostic tests for patients with COVID-19. The QUADAS-2 tool was utilized to quality assessment of diagnostic accuracy studies. For data extraction, two reviewers blind and independently extracted data from and full text of studies that included. 95% confidence interval for effect size with fixed effect model and Inver-variance method were calculated. Meta-analysis was performed using Stata/MP v.16 software. 469 studies were reviewed, of which the full text of 52 studies was reviewed and finally twenty-two studies were selected for meta-analysis. Mean differences of Alanine transaminase was 3.40 U/L (MD, 95% CI -2.45, 9.25), correlation between Alanine transaminase and severe COVID-19 was not significantly. Stool, feces, rectal swabs 25% (ES, 95% CI 0.32, 0.82), Urine 1% (ES, 95% CI 0.05, 0.58), overall sensitivity of PCR for detection of COVID-19 was 44% (ES, 95% CI 0.19, 0.68), less sensitive observerd when PCR detection of COVID-19. Evidence revealed that at the time of admission of patients with COVID-19, a specific laboratory model can be used to perform relevant tests and make decisions about patients. PCR using sputum samples was highly sensitive for detecting COVID-19 and after that computed tomography of the chest was identified with high sensitivity. © 2022 by SPC (Sami Publishing Company).
使用QUADAS-2评估研究质量和使用Stata / MP v.16进行荟萃分析对伊朗医院Covid - 19相关检测结果的医学评价软件
本研究的目的是评估一些实验室检查的结果和COVID-19患者诊断检查的准确性。QUADAS-2工具用于诊断准确性研究的质量评估。在数据提取方面,两位审稿人采用盲法,独立地从纳入的研究中提取数据和全文。用固定效应模型和反方差法计算了效应大小的95%置信区间。采用Stata/MP v.16软件进行meta分析。共对469项研究进行综述,其中52项研究的全文进行综述,最后选取22项研究进行meta分析。谷丙转氨酶的平均差异为3.40 U/L (MD, 95% CI -2.45, 9.25),谷丙转氨酶与重症COVID-19的相关性无统计学意义。粪便、粪便、直肠拭子25%(可信区间,95% CI 0.32, 0.82),尿液1%(可信区间,95% CI 0.05, 0.58), PCR检测COVID-19的总灵敏度为44%(可信区间,95% CI 0.19, 0.68), PCR检测COVID-19时敏感性较低。有证据表明,在新冠肺炎患者入院时,可以使用特定的实验室模型进行相关测试并做出有关患者的决策。痰标本PCR检测COVID-19灵敏度高,胸部ct检测灵敏度高。©2022 by SPC (Sami Publishing Company)。
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