Analytical sensitivity and clinical sensitivity of the three rapid antigen detection kits for detection of SARS-CoV-2 virus
Copyright © 2020 Elsevier B.V. All rights reserved..
BACKGROUND: Numerous rapid antigen detection (RAD) kits for diagnosing COVID-19 patients are available in the market recently.
OBJECTIVE: To compare analytical sensitivity and clinical sensitivity for the three commercially available RAD kits.
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 three RAD kits varied from 102-105 fold less sensitive than RT-PCR. Clinical sensitivity of RAD kits ranged from 22.9 %-71.4 % for detecting specimens from COVID-19 patients.
CONCLUSIONS: Although RAD kits were less sensitive than RT-PCR, understanding the clinical characteristics of different RAD kits can guide us to obtain suitable specimens for testing. The likelihood of positive results for RAD kits will be higher.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2020 |
---|---|
Erschienen: |
2020 |
Enthalten in: |
Zur Gesamtaufnahme - volume:133 |
---|---|
Enthalten in: |
Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology - 133(2020) vom: 16. Dez., Seite 104684 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Mak, Gannon Ck [VerfasserIn] |
---|
Links: |
---|
Themen: |
2019 novel coronavirus |
---|
Anmerkungen: |
Date Completed 29.12.2020 Date Revised 10.01.2021 published: Print-Electronic Citation Status MEDLINE |
---|
doi: |
10.1016/j.jcv.2020.104684 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM317438352 |
---|
LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
001 | NLM317438352 | ||
003 | DE-627 | ||
005 | 20231225163254.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231225s2020 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1016/j.jcv.2020.104684 |2 doi | |
028 | 5 | 2 | |a pubmed24n1058.xml |
035 | |a (DE-627)NLM317438352 | ||
035 | |a (NLM)33176236 | ||
035 | |a (PII)S1386-6532(20)30426-1 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Mak, Gannon Ck |e verfasserin |4 aut | |
245 | 1 | 0 | |a Analytical sensitivity and clinical sensitivity of the three rapid antigen detection kits for detection of SARS-CoV-2 virus |
264 | 1 | |c 2020 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 29.12.2020 | ||
500 | |a Date Revised 10.01.2021 | ||
500 | |a published: Print-Electronic | ||
500 | |a Citation Status MEDLINE | ||
520 | |a Copyright © 2020 Elsevier B.V. All rights reserved. | ||
520 | |a BACKGROUND: Numerous rapid antigen detection (RAD) kits for diagnosing COVID-19 patients are available in the market recently | ||
520 | |a OBJECTIVE: To compare analytical sensitivity and clinical sensitivity for the three commercially available RAD kits | ||
520 | |a 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 | ||
520 | |a RESULTS: The LOD results showed that the three RAD kits varied from 102-105 fold less sensitive than RT-PCR. Clinical sensitivity of RAD kits ranged from 22.9 %-71.4 % for detecting specimens from COVID-19 patients | ||
520 | |a CONCLUSIONS: Although RAD kits were less sensitive than RT-PCR, understanding the clinical characteristics of different RAD kits can guide us to obtain suitable specimens for testing. The likelihood of positive results for RAD kits will be higher | ||
650 | 4 | |a Comparative Study | |
650 | 4 | |a Journal Article | |
650 | 4 | |a 2019 novel coronavirus | |
650 | 4 | |a COVID-19 | |
650 | 4 | |a RT-PCR | |
650 | 4 | |a Rapid antigen detection | |
650 | 4 | |a SARS-CoV-2 | |
650 | 7 | |a Antigens, Viral |2 NLM | |
650 | 7 | |a Reagent Kits, Diagnostic |2 NLM | |
700 | 1 | |a Lau, Stephen Sy |e verfasserin |4 aut | |
700 | 1 | |a Wong, Kitty Ky |e verfasserin |4 aut | |
700 | 1 | |a Chow, Nancy Ls |e verfasserin |4 aut | |
700 | 1 | |a Lau, C S |e verfasserin |4 aut | |
700 | 1 | |a Lam, Edman Tk |e verfasserin |4 aut | |
700 | 1 | |a Chan, Rickjason Cw |e verfasserin |4 aut | |
700 | 1 | |a Tsang, Dominic Nc |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology |d 1997 |g 133(2020) vom: 16. Dez., Seite 104684 |w (DE-627)NLM097223964 |x 1873-5967 |7 nnns |
773 | 1 | 8 | |g volume:133 |g year:2020 |g day:16 |g month:12 |g pages:104684 |
856 | 4 | 0 | |u http://dx.doi.org/10.1016/j.jcv.2020.104684 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 133 |j 2020 |b 16 |c 12 |h 104684 |