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10.1016/j.jcv.2020.104712 http://scihub22266oqcxt.onion/10.1016/j.jcv.2020.104712 33338894!7716730!33338894     free     free     free Deprecated: Implicit conversion from float 231.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 231.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 231.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 231.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 231.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 231.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       J+Clin+Virol 2021 ; 134 (ä): 104712 Nephropedia Template TP {{tp|p=33338894|t=2021. Evaluation of rapid antigen detection kit from the WHO Emergency Use List for detecting SARS-CoV-2 |pdf=|usr=}}{{33338894}} gab.com Text Evaluation of rapid antigen detection kit from the WHO Emergency Use List for detecting SARS-CoV-2 JO: J Clin Virol http://www.kidney.de/pget.php?&tw=1&pmid=33338894 #FOAvip BACKGROUND: Currently, there are two rapid antigen detection (RAD) kits from the WHO Emergency Use List for detecting SARS-CoV-2. OBJECTIVE: The Panbio COVID-19 Ag Rapid Test Device was selected to evaluate the performance for detecting SARS-CoV-2. STUDY DESIGN: Analytical sensitivity for the detection of SARS-CoV-2 virus was determined by limit of detection (LOD) using RT-PCR as a reference method. Clinical sensitivity was evaluated by using respiratory specimens collected from confirmed COVID-19 patients. RESULTS: The LOD results showed that the RAD kit was 100 fold less sensitive than RT-PCR. Clinical sensitivity of the RAD kit was 68.6 % for detecting specimens from COVID-19 patients. CONCLUSIONS: The RAD kit evaluated in the present study shared similar performance with another kit from the WHO Emergency Use List, the Standard Q COVID-19 Ag. Understanding the clinical characteristics of RAD kits can guide us to decide different testing strategies in different settings. Twit Text FOAVip Evaluation of rapid antigen detection kit from the WHO Emergency Use List for detecting SARS-CoV-2 ????J Clin Virol http://www.kidney.de/pget.php?&tw=1&pmid=33338894 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=33338894 #FOAvip English Wikipedia <ref>{{Cite pmid|33338894}}</ref> Evaluation of rapid antigen detection kit from the WHO Emergency Use List for detecting SARS-CoV-2 #MMPMID33338894 Mak GCK; Lau SSY; Wong KKY; Chow NLS; Lau CS; Lam ETK; Chan RCW; Tsang DNC J Clin Virol 2021[Jan]; 134 (ä): 104712 PMID33338894show ga BACKGROUND: Currently, there are two rapid antigen detection (RAD) kits from the WHO Emergency Use List for detecting SARS-CoV-2. OBJECTIVE: The Panbio COVID-19 Ag Rapid Test Device was selected to evaluate the performance for detecting SARS-CoV-2. STUDY DESIGN: Analytical sensitivity for the detection of SARS-CoV-2 virus was determined by limit of detection (LOD) using RT-PCR as a reference method. Clinical sensitivity was evaluated by using respiratory specimens collected from confirmed COVID-19 patients. RESULTS: The LOD results showed that the RAD kit was 100 fold less sensitive than RT-PCR. Clinical sensitivity of the RAD kit was 68.6 % for detecting specimens from COVID-19 patients. CONCLUSIONS: The RAD kit evaluated in the present study shared similar performance with another kit from the WHO Emergency Use List, the Standard Q COVID-19 Ag. Understanding the clinical characteristics of RAD kits can guide us to decide different testing strategies in different settings. |Antigens, Viral/*analysis[MESH] |COVID-19 Testing/methods[MESH] |COVID-19/*diagnosis/pathology/virology[MESH] |Cross Reactions[MESH] |Hong Kong[MESH] |Humans[MESH] |Limit of Detection[MESH] |Nasopharynx/virology[MESH] |Pharynx/virology[MESH] |Reagent Kits, Diagnostic/*standards[MESH] |Reverse Transcriptase Polymerase Chain Reaction[MESH] |SARS-CoV-2/*immunology/pathogenicity[MESH]Evaluation of rapid antigen detection kit from the WHO Emergency Use L(epmc).pdf DeepDyve Pubget Overpricing