Impact of the Coronavirus Disease 2019 (COVID-19) Vaccine on Asymptomatic Infection Among Patients Undergoing Preprocedural COVID-19 Molecular Screening

Abstract Background Several vaccines are now available under emergency use authorization in the United States and have demonstrated efficacy against symptomatic COVID-19. Vaccine impact on asymptomatic severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection is largely unknown. Methods...

Full description

Saved in:
Bibliographic Details
Published inClinical infectious diseases Vol. 74; no. 1; pp. 59 - 65
Main Authors Tande, Aaron J, Pollock, Benjamin D, Shah, Nilay D, Farrugia, Gianrico, Virk, Abinash, Swift, Melanie, Breeher, Laura, Binnicker, Matthew, Berbari, Elie F
Format Journal Article
LanguageEnglish
Published US Oxford University Press 07.01.2022
Subjects
Online AccessGet full text
ISSN1058-4838
1537-6591
1537-6591
DOI10.1093/cid/ciab229

Cover

Abstract Abstract Background Several vaccines are now available under emergency use authorization in the United States and have demonstrated efficacy against symptomatic COVID-19. Vaccine impact on asymptomatic severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection is largely unknown. Methods We conducted a retrospective cohort study of consecutive, asymptomatic adult patients (n = 39 156) within a large US healthcare system who underwent 48 333 preprocedural SARS-CoV-2 molecular screening tests between 17 December 2020 and 8 February 2021. The primary exposure of interest was vaccination with ≥1 dose of an mRNA COVID-19 vaccine. The primary outcome was relative risk (RR) of a positive SARS-CoV-2 molecular test among those asymptomatic persons who had received ≥1 dose of vaccine compared with persons who had not received vaccine during the same time period. RR was adjusted for age, sex, race/ethnicity, patient residence relative to the hospital (local vs nonlocal), healthcare system regions, and repeated screenings among patients using mixed-effects log-binomial regression. Results Positive molecular tests in asymptomatic individuals were reported in 42 (1.4%) of 3006 tests and 1436 (3.2%) of 45 327 tests performed on vaccinated and unvaccinated patients, respectively (RR, .44; 95% CI, .33–.60; P < .0001). Compared with unvaccinated patients, risk of asymptomatic SARS-CoV-2 infection was lower among those >10 days after the first dose (RR, .21; 95% CI, .12–.37; P < .0001) and >0 days after the second dose (RR, .20; 95% CI, .09–.44; P < .0001) in the adjusted analysis. Conclusions COVID-19 vaccination with an mRNA-based vaccine showed a significant association with reduced risk of asymptomatic SARS-CoV-2 infection as measured during preprocedural molecular screening. Results of this study demonstrate the impact of the vaccines on reduction in asymptomatic infections supplementing the randomized trial results on symptomatic patients. Among asymptomatic adults undergoing preprocedural SARS-CoV-2 molecular screening, risk of a positive test was lower among those >10 days after the first dose and >0 days after the second dose of an mRNA COVID-19 vaccine, compared with those who were unvaccinated.
AbstractList Among asymptomatic adults undergoing preprocedural SARS-CoV-2 molecular screening, risk of a positive test was lower among those >10 days after the first dose and >0 days after the second dose of an mRNA COVID-19 vaccine, compared with those who were unvaccinated.
Abstract Background Several vaccines are now available under emergency use authorization in the United States and have demonstrated efficacy against symptomatic COVID-19. Vaccine impact on asymptomatic severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection is largely unknown. Methods We conducted a retrospective cohort study of consecutive, asymptomatic adult patients (n = 39 156) within a large US healthcare system who underwent 48 333 preprocedural SARS-CoV-2 molecular screening tests between 17 December 2020 and 8 February 2021. The primary exposure of interest was vaccination with ≥1 dose of an mRNA COVID-19 vaccine. The primary outcome was relative risk (RR) of a positive SARS-CoV-2 molecular test among those asymptomatic persons who had received ≥1 dose of vaccine compared with persons who had not received vaccine during the same time period. RR was adjusted for age, sex, race/ethnicity, patient residence relative to the hospital (local vs nonlocal), healthcare system regions, and repeated screenings among patients using mixed-effects log-binomial regression. Results Positive molecular tests in asymptomatic individuals were reported in 42 (1.4%) of 3006 tests and 1436 (3.2%) of 45 327 tests performed on vaccinated and unvaccinated patients, respectively (RR, .44; 95% CI, .33–.60; P < .0001). Compared with unvaccinated patients, risk of asymptomatic SARS-CoV-2 infection was lower among those >10 days after the first dose (RR, .21; 95% CI, .12–.37; P < .0001) and >0 days after the second dose (RR, .20; 95% CI, .09–.44; P < .0001) in the adjusted analysis. Conclusions COVID-19 vaccination with an mRNA-based vaccine showed a significant association with reduced risk of asymptomatic SARS-CoV-2 infection as measured during preprocedural molecular screening. Results of this study demonstrate the impact of the vaccines on reduction in asymptomatic infections supplementing the randomized trial results on symptomatic patients. Among asymptomatic adults undergoing preprocedural SARS-CoV-2 molecular screening, risk of a positive test was lower among those >10 days after the first dose and >0 days after the second dose of an mRNA COVID-19 vaccine, compared with those who were unvaccinated.
Several vaccines are now available under emergency use authorization in the United States and have demonstrated efficacy against symptomatic COVID-19. Vaccine impact on asymptomatic severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection is largely unknown.BACKGROUNDSeveral vaccines are now available under emergency use authorization in the United States and have demonstrated efficacy against symptomatic COVID-19. Vaccine impact on asymptomatic severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection is largely unknown.We conducted a retrospective cohort study of consecutive, asymptomatic adult patients (n = 39 156) within a large US healthcare system who underwent 48 333 preprocedural SARS-CoV-2 molecular screening tests between 17 December 2020 and 8 February 2021. The primary exposure of interest was vaccination with ≥1 dose of an mRNA COVID-19 vaccine. The primary outcome was relative risk (RR) of a positive SARS-CoV-2 molecular test among those asymptomatic persons who had received ≥1 dose of vaccine compared with persons who had not received vaccine during the same time period. RR was adjusted for age, sex, race/ethnicity, patient residence relative to the hospital (local vs nonlocal), healthcare system regions, and repeated screenings among patients using mixed-effects log-binomial regression.METHODSWe conducted a retrospective cohort study of consecutive, asymptomatic adult patients (n = 39 156) within a large US healthcare system who underwent 48 333 preprocedural SARS-CoV-2 molecular screening tests between 17 December 2020 and 8 February 2021. The primary exposure of interest was vaccination with ≥1 dose of an mRNA COVID-19 vaccine. The primary outcome was relative risk (RR) of a positive SARS-CoV-2 molecular test among those asymptomatic persons who had received ≥1 dose of vaccine compared with persons who had not received vaccine during the same time period. RR was adjusted for age, sex, race/ethnicity, patient residence relative to the hospital (local vs nonlocal), healthcare system regions, and repeated screenings among patients using mixed-effects log-binomial regression.Positive molecular tests in asymptomatic individuals were reported in 42 (1.4%) of 3006 tests and 1436 (3.2%) of 45 327 tests performed on vaccinated and unvaccinated patients, respectively (RR, .44; 95% CI, .33-.60; P < .0001). Compared with unvaccinated patients, risk of asymptomatic SARS-CoV-2 infection was lower among those >10 days after the first dose (RR, .21; 95% CI, .12-.37; P < .0001) and >0 days after the second dose (RR, .20; 95% CI, .09-.44; P < .0001) in the adjusted analysis.RESULTSPositive molecular tests in asymptomatic individuals were reported in 42 (1.4%) of 3006 tests and 1436 (3.2%) of 45 327 tests performed on vaccinated and unvaccinated patients, respectively (RR, .44; 95% CI, .33-.60; P < .0001). Compared with unvaccinated patients, risk of asymptomatic SARS-CoV-2 infection was lower among those >10 days after the first dose (RR, .21; 95% CI, .12-.37; P < .0001) and >0 days after the second dose (RR, .20; 95% CI, .09-.44; P < .0001) in the adjusted analysis.COVID-19 vaccination with an mRNA-based vaccine showed a significant association with reduced risk of asymptomatic SARS-CoV-2 infection as measured during preprocedural molecular screening. Results of this study demonstrate the impact of the vaccines on reduction in asymptomatic infections supplementing the randomized trial results on symptomatic patients.CONCLUSIONSCOVID-19 vaccination with an mRNA-based vaccine showed a significant association with reduced risk of asymptomatic SARS-CoV-2 infection as measured during preprocedural molecular screening. Results of this study demonstrate the impact of the vaccines on reduction in asymptomatic infections supplementing the randomized trial results on symptomatic patients.
Several vaccines are now available under emergency use authorization in the United States and have demonstrated efficacy against symptomatic COVID-19. Vaccine impact on asymptomatic severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection is largely unknown. We conducted a retrospective cohort study of consecutive, asymptomatic adult patients (n = 39 156) within a large US healthcare system who underwent 48 333 preprocedural SARS-CoV-2 molecular screening tests between 17 December 2020 and 8 February 2021. The primary exposure of interest was vaccination with ≥1 dose of an mRNA COVID-19 vaccine. The primary outcome was relative risk (RR) of a positive SARS-CoV-2 molecular test among those asymptomatic persons who had received ≥1 dose of vaccine compared with persons who had not received vaccine during the same time period. RR was adjusted for age, sex, race/ethnicity, patient residence relative to the hospital (local vs nonlocal), healthcare system regions, and repeated screenings among patients using mixed-effects log-binomial regression. Positive molecular tests in asymptomatic individuals were reported in 42 (1.4%) of 3006 tests and 1436 (3.2%) of 45 327 tests performed on vaccinated and unvaccinated patients, respectively (RR, .44; 95% CI, .33-.60; P < .0001). Compared with unvaccinated patients, risk of asymptomatic SARS-CoV-2 infection was lower among those >10 days after the first dose (RR, .21; 95% CI, .12-.37; P < .0001) and >0 days after the second dose (RR, .20; 95% CI, .09-.44; P < .0001) in the adjusted analysis. COVID-19 vaccination with an mRNA-based vaccine showed a significant association with reduced risk of asymptomatic SARS-CoV-2 infection as measured during preprocedural molecular screening. Results of this study demonstrate the impact of the vaccines on reduction in asymptomatic infections supplementing the randomized trial results on symptomatic patients.
Author Shah, Nilay D
Swift, Melanie
Berbari, Elie F
Farrugia, Gianrico
Pollock, Benjamin D
Tande, Aaron J
Breeher, Laura
Binnicker, Matthew
Virk, Abinash
AuthorAffiliation 5 Division of Preventive, Occupational Medicine, and Aerospace Medicine, Mayo Clinic , Rochester, Minnesota , USA
1 Division of Infectious Diseases, Mayo Clinic , Rochester, Minnesota , USA
4 Division of Gastroenterology, Mayo Clinic , Rochester, Minnesota , USA
3 Division of Health Care Delivery Research, Robert D. and Patricia E. Kern Center for the Science of Health Care Delivery, Mayo Clinic , Rochester, Minnesota , USA
2 Department of Quality, Experience, and Affordability, Mayo Clinic , Rochester, Minnesota , USA
6 Division of Clinical Microbiology, Department of Laboratory Medicine and Pathology, Mayo Clinic , Rochester, Minnesota , USA
AuthorAffiliation_xml – name: 3 Division of Health Care Delivery Research, Robert D. and Patricia E. Kern Center for the Science of Health Care Delivery, Mayo Clinic , Rochester, Minnesota , USA
– name: 2 Department of Quality, Experience, and Affordability, Mayo Clinic , Rochester, Minnesota , USA
– name: 4 Division of Gastroenterology, Mayo Clinic , Rochester, Minnesota , USA
– name: 6 Division of Clinical Microbiology, Department of Laboratory Medicine and Pathology, Mayo Clinic , Rochester, Minnesota , USA
– name: 5 Division of Preventive, Occupational Medicine, and Aerospace Medicine, Mayo Clinic , Rochester, Minnesota , USA
– name: 1 Division of Infectious Diseases, Mayo Clinic , Rochester, Minnesota , USA
Author_xml – sequence: 1
  givenname: Aaron J
  surname: Tande
  fullname: Tande, Aaron J
  email: tande.aaron@mayo.edu
  organization: Division of Infectious Diseases, Mayo Clinic, Rochester, Minnesota, USA
– sequence: 2
  givenname: Benjamin D
  surname: Pollock
  fullname: Pollock, Benjamin D
  organization: Department of Quality, Experience, and Affordability, Mayo Clinic, Rochester, Minnesota, USA
– sequence: 3
  givenname: Nilay D
  surname: Shah
  fullname: Shah, Nilay D
  organization: Division of Health Care Delivery Research, Robert D. and Patricia E. Kern Center for the Science of Health Care Delivery, Mayo Clinic, Rochester, Minnesota, USA
– sequence: 4
  givenname: Gianrico
  surname: Farrugia
  fullname: Farrugia, Gianrico
  organization: Division of Gastroenterology, Mayo Clinic, Rochester, Minnesota, USA
– sequence: 5
  givenname: Abinash
  surname: Virk
  fullname: Virk, Abinash
  organization: Division of Infectious Diseases, Mayo Clinic, Rochester, Minnesota, USA
– sequence: 6
  givenname: Melanie
  surname: Swift
  fullname: Swift, Melanie
  organization: Division of Preventive, Occupational Medicine, and Aerospace Medicine, Mayo Clinic, Rochester, Minnesota, USA
– sequence: 7
  givenname: Laura
  surname: Breeher
  fullname: Breeher, Laura
  organization: Division of Preventive, Occupational Medicine, and Aerospace Medicine, Mayo Clinic, Rochester, Minnesota, USA
– sequence: 8
  givenname: Matthew
  surname: Binnicker
  fullname: Binnicker, Matthew
  organization: Division of Clinical Microbiology, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA
– sequence: 9
  givenname: Elie F
  surname: Berbari
  fullname: Berbari, Elie F
  organization: Division of Infectious Diseases, Mayo Clinic, Rochester, Minnesota, USA
BackLink https://www.ncbi.nlm.nih.gov/pubmed/33704435$$D View this record in MEDLINE/PubMed
BookMark eNp9kd9r1TAUx4NM3A998l3yJBOpJk3TNi_CuNv0wmSCbq8hPT29i7RJl7SD_Sf-uabce0VFfAgJ3_M53-8h55gcOO-QkJecveNMifdg23RMk-fqCTniUlRZKRU_SG8m66yoRX1IjmP8zhjnNZPPyKEQFSsKIY_Ij_UwGpio7-h0h3Tlg3fmwYY50nMb0USkOeOKnq6ub9fnGVdv6K0BsA6pd_QsPg7j5AczWaBr1yFMdpEH7zb0S1LRTZHeuBbDxttFCzgGD9jOwfR070k_-x5h7k2gXyEguoQ-J08700d8sbtPyM3lxbfVp-zq-uN6dXaVQVHVU8Z5AaCE5FgXNZQVa1QtVSFSsYGybfJKSsFMqfIOO2wV5FDyrlQlq5qWd0qckA9b33FuBmwhTZxG02OwgwmP2hur_6w4e6c3_kFXqlaSLwanO4Pg72eMkx5sBOx749DPUeeSMVGJUi3oq9-zfoXs15EAvgUg-BgDdhrsZJY_TdG215zpZeVJbfVu5ann7V89e9t_06-3tJ_H_4I_AZ7tu_A
CitedBy_id crossref_primary_10_1016_j_ijid_2023_02_020
crossref_primary_10_1038_s41591_022_01679_5
crossref_primary_10_1016_j_ijid_2022_11_022
crossref_primary_10_1093_cid_ciad463
crossref_primary_10_1136_jim_2021_002131
crossref_primary_10_26633_RPSP_2022_203
crossref_primary_10_1093_ofid_ofab369
crossref_primary_10_2147_IDR_S356460
crossref_primary_10_1111_joim_13471
crossref_primary_10_1056_NEJMoa2110345
crossref_primary_10_1056_NEJMoa2113017
crossref_primary_10_15585_mmwr_mm7021e3
crossref_primary_10_3390_ijerph19074056
crossref_primary_10_1093_cid_ciab557
crossref_primary_10_1038_s41598_021_04428_9
crossref_primary_10_6000_1929_6029_2022_11_22
crossref_primary_10_1556_650_2022_32448
crossref_primary_10_1515_mr_2021_0034
crossref_primary_10_3389_fpubh_2023_1126461
crossref_primary_10_1172_JCI162282
crossref_primary_10_3390_vaccines10111896
crossref_primary_10_1177_21501351221085966
crossref_primary_10_1007_s11926_021_01037_3
crossref_primary_10_1093_ofid_ofac138
crossref_primary_10_3389_fpubh_2022_873596
crossref_primary_10_3390_pathogens10070911
crossref_primary_10_1053_j_gastro_2021_05_039
crossref_primary_10_1016_j_vaccine_2022_06_066
crossref_primary_10_3389_fimmu_2022_947602
crossref_primary_10_3390_vaccines10020157
crossref_primary_10_1080_21645515_2022_2027160
crossref_primary_10_1097_INF_0000000000003625
crossref_primary_10_12688_f1000research_53089_1
crossref_primary_10_3390_covid3020018
crossref_primary_10_1177_20503121231158981
crossref_primary_10_1007_s10787_021_00811_0
crossref_primary_10_1017_S1463423622000640
crossref_primary_10_1002_14651858_CD013665_pub3
crossref_primary_10_1038_s41598_024_53561_8
crossref_primary_10_1002_iid3_670
crossref_primary_10_3390_v13101921
crossref_primary_10_3390_vaccines9060591
crossref_primary_10_1186_s12879_022_07702_x
crossref_primary_10_3390_vaccines10101590
crossref_primary_10_1007_s00508_022_02067_2
crossref_primary_10_1016_j_celrep_2021_109664
crossref_primary_10_1017_ice_2022_301
crossref_primary_10_3390_vaccines10030393
crossref_primary_10_1017_ice_2021_399
crossref_primary_10_1038_s43856_024_00510_1
crossref_primary_10_3390_curroncol29010006
crossref_primary_10_3389_fpubh_2022_889311
crossref_primary_10_3390_vaccines10101639
crossref_primary_10_1016_j_mayocp_2021_04_012
crossref_primary_10_3390_jcm10132813
crossref_primary_10_3390_vaccines9070697
crossref_primary_10_3390_ijerph19127435
crossref_primary_10_1038_s41577_021_00578_z
crossref_primary_10_3389_phrs_2022_1604572
crossref_primary_10_1001_jama_2021_5283
crossref_primary_10_1056_NEJMoa2107456
Cites_doi 10.1001/jamanetworkopen.2020.35057
10.1016/j.mayocp.2020.05.039
10.1128/JCM.00590-20
10.1056/NEJMoa2034577
10.1016/S0140-6736(20)32661-1
10.1056/NEJMoa2035389
10.1016/j.mayocp.2020.06.010
10.1016/j.mayocp.2020.06.020
10.3201/eid2704.210016
ContentType Journal Article
Copyright The Author(s) 2021. Published by Oxford University Press for the Infectious Diseases Society of America. 2021
The Author(s) 2021. Published by Oxford University Press for the Infectious Diseases Society of America.
Copyright_xml – notice: The Author(s) 2021. Published by Oxford University Press for the Infectious Diseases Society of America. 2021
– notice: The Author(s) 2021. Published by Oxford University Press for the Infectious Diseases Society of America.
DBID TOX
AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
7X8
5PM
DOI 10.1093/cid/ciab229
DatabaseName Oxford Journals Open Access Collection
CrossRef
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
MEDLINE - Academic
PubMed Central (Full Participant titles)
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
MEDLINE - Academic
DatabaseTitleList

MEDLINE - Academic
MEDLINE
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
– sequence: 3
  dbid: TOX
  name: Oxford Journals Open Access Collection
  url: https://academic.oup.com/journals/
  sourceTypes: Publisher
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 1537-6591
EndPage 65
ExternalDocumentID PMC7989519
33704435
10_1093_cid_ciab229
10.1093/cid/ciab229
Genre Research Support, Non-U.S. Gov't
Journal Article
GeographicLocations United States
GeographicLocations_xml – name: United States
GrantInformation_xml – fundername: AHRQ HHS
  grantid: K12 HS026379
– fundername: FDA HHS
  grantid: U01 FD005938
– fundername: NHLBI NIH HHS
  grantid: R01 HL151662
– fundername: NIH HHS
  grantid: R56HL130496
– fundername: ;
– fundername: ;
  grantid: R01HS025164; R01HS025402; R03HS025517; K12HS026379
– fundername: ;
  grantid: U01FD005938
– fundername: ;
  grantid: R56HL130496; R01HL131535; R01HL151662
GroupedDBID ---
..I
.2P
.GJ
.I3
.ZR
08P
0R~
1KJ
1TH
29B
2AX
2WC
36B
3O-
4.4
48X
53G
5GY
5RE
5VS
5WD
6.Y
6J9
70D
AABZA
AACGO
AACZT
AAJKP
AAJQQ
AAMVS
AANCE
AAOGV
AAPGJ
AAPNW
AAPQZ
AAPXW
AAQQT
AARHZ
AASNB
AAUAY
AAUQX
AAVAP
AAWDT
AAYOK
ABBHK
ABEUO
ABIXL
ABJNI
ABKDP
ABLJU
ABNHQ
ABNKS
ABOCM
ABPLY
ABPTD
ABQLI
ABQNK
ABSAR
ABSMQ
ABTLG
ABWST
ABXSQ
ABXVV
ABZBJ
ACFRR
ACGFO
ACGFS
ACMRT
ACPQN
ACPRK
ACUFI
ACUTJ
ACUTO
ACYHN
ACZBC
ADACV
ADBBV
ADEYI
ADGZP
ADHKW
ADHZD
ADIPN
ADJQC
ADOCK
ADQBN
ADRIX
ADRTK
ADULT
ADVEK
ADYVW
ADZXQ
AEGPL
AEGXH
AEJOX
AEKPW
AEKSI
AEMDU
AENEX
AENZO
AEPUE
AETBJ
AEUPB
AEWNT
AEXZC
AFFNX
AFFZL
AFIYH
AFOFC
AFRAH
AFSHK
AFXAL
AFXEN
AFYAG
AGINJ
AGKEF
AGKRT
AGMDO
AGQXC
AGSYK
AGUTN
AHMBA
AHXPO
AI.
AIAGR
AIJHB
AJEEA
ALMA_UNASSIGNED_HOLDINGS
ALUQC
APIBT
APJGH
APWMN
AQDSO
AQKUS
AQVQM
ASPBG
ATGXG
AVNTJ
AVWKF
AXUDD
AZFZN
BAWUL
BAYMD
BCRHZ
BEYMZ
BHONS
BTRTY
BVRKM
BZKNY
C1A
C45
CDBKE
CS3
CZ4
DAKXR
DCCCD
DIK
DILTD
DOOOF
DU5
D~K
E3Z
EBS
EE~
EIHJH
EJD
EMOBN
ENERS
ESX
F5P
F9B
FECEO
FEDTE
FLUFQ
FOEOM
FOTVD
FQBLK
GAUVT
GJXCC
H13
H5~
HAR
HQ3
HTVGU
HVGLF
HW0
HZ~
IOX
IPSME
J21
J5H
JAAYA
JBMMH
JENOY
JHFFW
JKQEH
JLS
JLXEF
JPM
JSG
JSODD
JST
KAQDR
KBUDW
KOP
KSI
KSN
L7B
M49
MBLQV
MHKGH
MJL
ML0
N4W
N9A
NGC
NOMLY
NOYVH
NU-
NVLIB
O0~
O9-
OAUYM
OAWHX
OCZFY
ODMLO
ODZKP
OJQWA
OJZSN
OK1
OPAEJ
OVD
OWPYF
O~Y
P2P
P6G
PAFKI
PB-
PEELM
PQQKQ
Q1.
Q5Y
QBD
RD5
ROX
ROZ
RUSNO
RW1
RXO
SA0
SJN
TCURE
TEORI
TJX
TMA
TOX
TR2
VH1
W8F
X7H
Y6R
YAYTL
YKOAZ
YXANX
ZGI
~91
~S-
AAYXX
ABDFA
ABEJV
ABGNP
ABPQP
ABVGC
ADNBA
AEMQT
AGORE
AHGBF
AHMMS
AJBYB
AJNCP
ALXQX
CITATION
JXSIZ
CGR
CUY
CVF
ECM
EIF
NPM
7X8
5PM
ID FETCH-LOGICAL-c478t-114cc9351e848c670b985943478bc6db275530a692fefed9c2c61f69607bd1f93
IEDL.DBID TOX
ISSN 1058-4838
1537-6591
IngestDate Thu Aug 21 13:52:18 EDT 2025
Fri Jul 11 04:39:54 EDT 2025
Thu Apr 03 07:04:36 EDT 2025
Tue Jul 01 01:18:35 EDT 2025
Thu Apr 24 23:04:50 EDT 2025
Wed Aug 28 03:17:59 EDT 2024
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 1
Keywords COVID-19
SARS-CoV-2
asymptomatic
vaccination
Language English
License This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
https://creativecommons.org/licenses/by-nc-nd/4.0
The Author(s) 2021. Published by Oxford University Press for the Infectious Diseases Society of America.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c478t-114cc9351e848c670b985943478bc6db275530a692fefed9c2c61f69607bd1f93
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
A. J. T. and B. D. P. contributed equally to this work.
OpenAccessLink https://dx.doi.org/10.1093/cid/ciab229
PMID 33704435
PQID 2500373699
PQPubID 23479
PageCount 7
ParticipantIDs pubmedcentral_primary_oai_pubmedcentral_nih_gov_7989519
proquest_miscellaneous_2500373699
pubmed_primary_33704435
crossref_citationtrail_10_1093_cid_ciab229
crossref_primary_10_1093_cid_ciab229
oup_primary_10_1093_cid_ciab229
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2022-01-07
PublicationDateYYYYMMDD 2022-01-07
PublicationDate_xml – month: 01
  year: 2022
  text: 2022-01-07
  day: 07
PublicationDecade 2020
PublicationPlace US
PublicationPlace_xml – name: US
– name: United States
PublicationTitle Clinical infectious diseases
PublicationTitleAlternate Clin Infect Dis
PublicationYear 2022
Publisher Oxford University Press
Publisher_xml – name: Oxford University Press
References Storino (2022011123263012200_CIT0007) 2020; 95
World Health Organization. (2022011123263012200_CIT0001)
Rodino (2022011123263012200_CIT0010) 2020; 58
Voysey (2022011123263012200_CIT0012)
Voysey (2022011123263012200_CIT0005) 2021; 397
Amit (2022011123263012200_CIT0006) 2021; 27
Shah (2022011123263012200_CIT0008) 2020; 95
Johansson (2022011123263012200_CIT0002) 2021; 4
Baden (2022011123263012200_CIT0003) 2021; 384
Polack (2022011123263012200_CIT0004) 2020; 383
Pollock (2022011123263012200_CIT0009) 2020
Challener (2022011123263012200_CIT0011) 2020; 95
References_xml – volume: 4
  start-page: e2035057
  year: 2021
  ident: 2022011123263012200_CIT0002
  article-title: SARS-CoV-2 transmission from people without COVID-19 symptoms
  publication-title: JAMA Netw Open
  doi: 10.1001/jamanetworkopen.2020.35057
– volume: 95
  start-page: S17
  year: 2020
  ident: 2022011123263012200_CIT0008
  article-title: Diagnostic stewardship: an essential element in a rapidly evolving COVID-19 pandemic
  publication-title: Mayo Clin Proc
  doi: 10.1016/j.mayocp.2020.05.039
– volume: 58
  year: 2020
  ident: 2022011123263012200_CIT0010
  article-title: Evaluation of saline, phosphate-buffered saline, and minimum essential medium as potential alternatives to viral transport media for SARS-CoV-2 testing
  publication-title: J Clin Microbiol
  doi: 10.1128/JCM.00590-20
– ident: 2022011123263012200_CIT0012
  article-title: Single dose administration, and the influence of the timing of the booster dose on immunogenicity and efficacy of ChAdOx1 nCoV-19 (AZD1222) vaccine.
– volume: 383
  start-page: 2603
  year: 2020
  ident: 2022011123263012200_CIT0004
  article-title: Safety and efficacy of the BNT162b2 mRNA Covid-19 vaccine
  publication-title: N Engl J Med
  doi: 10.1056/NEJMoa2034577
– ident: 2022011123263012200_CIT0001
– volume: 397
  start-page: 99
  year: 2021
  ident: 2022011123263012200_CIT0005
  article-title: Safety and efficacy of the ChAdOx1 nCoV-19 vaccine (AZD1222) against SARS-CoV-2: an interim analysis of four randomised controlled trials in Brazil, South Africa, and the UK
  publication-title: Lancet
  doi: 10.1016/S0140-6736(20)32661-1
– year: 2020
  ident: 2022011123263012200_CIT0009
  article-title: Deployment of an interdisciplinary predictive analytics task force to inform hospital operational decision-making during the COVID-19 pandemic
  publication-title: Mayo Clinic Proc
– volume: 384
  start-page: 403
  year: 2021
  ident: 2022011123263012200_CIT0003
  article-title: Efficacy and safety of the mRNA-1273 SARS-CoV-2 vaccine
  publication-title: N Engl J Med
  doi: 10.1056/NEJMoa2035389
– volume: 95
  start-page: S44
  year: 2020
  ident: 2022011123263012200_CIT0007
  article-title: Revamping outpatient care for patients without COVID-19
  publication-title: Mayo Clin Proc
  doi: 10.1016/j.mayocp.2020.06.010
– volume: 95
  start-page: 1942
  year: 2020
  ident: 2022011123263012200_CIT0011
  article-title: Low utility of repeat real-time PCR testing for SARS-CoV-2 in clinical specimens
  publication-title: Mayo Clin Proc
  doi: 10.1016/j.mayocp.2020.06.020
– volume: 27
  year: 2021
  ident: 2022011123263012200_CIT0006
  article-title: Post-vaccination COVID-19 among healthcare workers, Israel
  publication-title: Emerg Infect Dis
  doi: 10.3201/eid2704.210016
SSID ssj0011805
Score 2.618544
Snippet Abstract Background Several vaccines are now available under emergency use authorization in the United States and have demonstrated efficacy against...
Several vaccines are now available under emergency use authorization in the United States and have demonstrated efficacy against symptomatic COVID-19. Vaccine...
Among asymptomatic adults undergoing preprocedural SARS-CoV-2 molecular screening, risk of a positive test was lower among those >10 days after the first dose...
SourceID pubmedcentral
proquest
pubmed
crossref
oup
SourceType Open Access Repository
Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 59
SubjectTerms Adult
Asymptomatic Infections - epidemiology
COVID-19
COVID-19 Vaccines
Humans
Major
Retrospective Studies
SARS-CoV-2
United States
Title Impact of the Coronavirus Disease 2019 (COVID-19) Vaccine on Asymptomatic Infection Among Patients Undergoing Preprocedural COVID-19 Molecular Screening
URI https://www.ncbi.nlm.nih.gov/pubmed/33704435
https://www.proquest.com/docview/2500373699
https://pubmed.ncbi.nlm.nih.gov/PMC7989519
Volume 74
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwhV3fS9xAEF6KD6Uvpdb-OLU6BR_aQmiSTbK7j3IqXkUtVOXewmayqweaHOau0P-kf64zSe7wRNrXZHZZMhvm252Z7xNiT1uvoyTCAHVsAz4xBITCXRAqDJEghLK2rfI9y44vkx_jdNwXyDbPpPCN_I7kFVpnEcfcp0fhl7fzxfl4mSyIdFupSEihvRvTfRvek7ErgWelme0RpnxaGvko1hy9Ea97kAj7nVfXxQtXvRUvT_s0-Ib4O2p7G6H2QPgNhsxCYH9P7ucNHHQJF6CIa-DL8PxqdBBE5itcWeSxUFew3_y5m87qlqsVRn0xFj1m2SH42fGsNtAKIl3XE37GzJcU50qm6IDFnHC6UNaFX8jVO2T6TlweHV4Mj4NeYiHAROlZQKchRCPTyOlEY6bCwuiUKeOULpClphTLCtnMxN55VxqMMYt8RsceVZSRN_K9WKvqyn0UUIYSjQ01ylQmpc-strErfemM9lmRlgPxbfH9c-z5x1kG4zbv8uAyZxHh3lkDsbc0nna0G8-b7ZIj_23xeeHknH4czobYytXzJifsF0olM0M2HzqnLyeSUoUJAcmBUCvbYWnApNyrb6rJTUvOrYwm0Go2_7uyLfEq5lYKvs5R22Jtdj93nwjgzIodgvajk512kz8A_yj7Ew
linkProvider Oxford University Press
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Impact+of+the+Coronavirus+Disease+2019+%28COVID-19%29+Vaccine+on+Asymptomatic+Infection+Among+Patients+Undergoing+Preprocedural+COVID-19+Molecular+Screening&rft.jtitle=Clinical+infectious+diseases&rft.au=Tande%2C+Aaron+J&rft.au=Pollock%2C+Benjamin+D&rft.au=Shah%2C+Nilay+D&rft.au=Farrugia%2C+Gianrico&rft.date=2022-01-07&rft.issn=1537-6591&rft.eissn=1537-6591&rft.volume=74&rft.issue=1&rft.spage=59&rft_id=info:doi/10.1093%2Fcid%2Fciab229&rft.externalDBID=NO_FULL_TEXT
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1058-4838&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1058-4838&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1058-4838&client=summon