scholarly journals Positive rate of RT-PCR detection of SARS-CoV-2 infection in 4880 cases from one hospital in Wuhan, China, from Jan to Feb 2020

2020 ◽  
Vol 505 ◽  
pp. 172-175 ◽  
Author(s):  
Rui Liu ◽  
Huan Han ◽  
Fang Liu ◽  
Zhihua Lv ◽  
Kailang Wu ◽  
...  
Keyword(s):  
Rt Pcr ◽  
2021 ◽  
Vol 104 (2) ◽  
pp. 003685042110261
Author(s):  
Sungwoo Choi ◽  
Hyo Jeong Choi ◽  
Ho Jung Kim

The most common method for SARS-CoV-2 testing is throat or nasal swabbing by real-time reverse transcription polymerase chain reaction (RT-PCR) assay. In South Korea, drive-through swab test is used for screening system and community treatment centers (CTCs), which admit and treat confirmed COVID-19 patients with mild symptoms, are being used. This retrospective study was conducted on patients admitted to a CTC on March 6, 2020. A total of 313 patients were admitted. The nasal and throat swabs were collected from the upper respiratory tract, and a sputum test was performed to obtain lower respiratory samples. The positive rate of the first set of test, sputum test was higher than that of the swab test ( p = 0.011). In the second set of test, 1 week after the first ones, the rate of positive swab tests was relatively high ( p = 0.026). In the first set of test, 66 of 152 (43.4%) patients showed 24-h consecutive negative swab test results, when the sputum test results were considered together, that number fell to 29 patients (19.1%) ( p < 0.001). Also, in the second set of test, 63 of 164 (38.4%) patients met the discharge criteria only when the swab test was considered; that number fell to 30 (18.3%) when the sputum test results were also considered ( p < 0.001). Using the swab test alone is insufficient for screening test and discharge decision. Patients who may have positive result in the sputum test can be missed.


2021 ◽  
pp. 114286
Author(s):  
Xiaoqin Li ◽  
Yu Li ◽  
Wenli Hu ◽  
Yingjuan Li ◽  
Yan Li ◽  
...  
Keyword(s):  

2011 ◽  
Vol 175 (2) ◽  
pp. 236-245 ◽  
Author(s):  
Oliver Lung ◽  
Mathew Fisher ◽  
Anne Beeston ◽  
Kimberley Burton Hughes ◽  
Alfonso Clavijo ◽  
...  

2011 ◽  
Vol 27 (3) ◽  
pp. 291-296 ◽  
Author(s):  
Jong-Seung Lee ◽  
Won-Kyong Cho ◽  
Hong-Soo Choi ◽  
Kook-Hyung Kim
Keyword(s):  

Author(s):  
Ying Zhang ◽  
Xue Cai ◽  
Weigang Ge ◽  
Donglian Wang ◽  
Guangjun Zhu ◽  
...  

2018 ◽  
Vol 68 (3) ◽  
pp. 321-332 ◽  
Author(s):  
Chun-Mei Han ◽  
Rong Chen ◽  
Tao Li ◽  
Xiao-Li Chen ◽  
Yong-Fu Zheng ◽  
...  

AbstractThe aims of this study were to establish whether the sex-determining region Y gene and its mRNA transcript are present in the Y sperm and X sperm of bulls and, if present, determine their cellular localization. Semen was collected from three bulls and sorted by flow cytometry into X- and Y-chromosome populations. Reverse transcription-polymerase chain reaction (RT-PCR) was used to determineSrymRNA expression in X sperm and Y sperm. The presence and localization ofSryDNA and RNA were investigated by fluorescence in situ hybridization (FISH). RT-PCR detected a singleSrytranscript of 142 bp in Y sperm but not in X sperm. In Y sperm, the FISH-positive rates forSryDNA andSryRNA did not differ significantly from the re-analyzed Y sperm purity. In further experiments, there were no significant differences between the FISH-positive rate forSryRNA and the re-analyzed Y sperm purity for X-sorted, Y-sorted, or unsorted sperm. In conclusion, FISH analysis revealed thatSrytranscripts are present at the edges of the sperm heads of Y sperm but are absent from X sperm.


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