Research on the Epidemiology of SARS-CoV-2 in Essential Response Personnel (RECOVER): Protocol for a Multisite Longitudinal Cohort Study.

COVID-19 SARS-CoV-2 cohort study essential and frontline workers first responder health care personnel incidence vaccine effectiveness

Journal

JMIR research protocols
ISSN: 1929-0748
Titre abrégé: JMIR Res Protoc
Pays: Canada
ID NLM: 101599504

Informations de publication

Date de publication:
03 Dec 2021
Historique:
received: 25 06 2021
accepted: 07 10 2021
revised: 06 10 2021
pubmed: 19 10 2021
medline: 19 10 2021
entrez: 18 10 2021
Statut: epublish

Résumé

Workers critical to emergency response and continuity of essential services during the COVID-19 pandemic are at a disproportionally high risk of SARS-CoV-2 infection. Prospective cohort studies are needed for enhancing the understanding of the incidence of symptomatic and asymptomatic SARS-CoV-2 infections, identifying risk factors, assessing clinical outcomes, and determining the effectiveness of vaccination. The Research on the Epidemiology of SARS-CoV-2 in Essential Response Personnel (RECOVER) prospective cohort study was designed to estimate the incidence of symptomatic and asymptomatic SARS-CoV-2 infections, examine the risk factors for infection and clinical spectrum of illness, and assess the effectiveness of vaccination among essential workers. The RECOVER multisite network was initiated in August 2020 and aims to enroll 3000 health care personnel (HCP), first responders, and other essential and frontline workers (EFWs) at 6 US locations. Data on participant demographics, medical history, and vaccination history are collected at baseline and throughout the study. Active surveillance for the symptoms of COVID-19-like illness (CLI), access of medical care, and symptom duration is performed by text messages, emails, and direct participant or medical record reports. Participants self-collect a mid-turbinate nasal swab weekly, regardless of symptoms, and 2 additional respiratory specimens at the onset of CLI. Blood is collected upon enrollment, every 3 months, approximately 28 days after a reverse transcription polymerase chain reaction (RT-PCR)-confirmed SARS-CoV-2 infection, and 14 to 28 days after a dose of any COVID-19 vaccine. From February 2021, household members of RT-PCR-confirmed participants are self-collecting mid-turbinate nasal swabs daily for 10 days. The study observation period began in August 2020 and is expected to continue through spring 2022. There are 2623 actively enrolled RECOVER participants, including 280 participants who have been found to be positive for SARS-CoV-2 by RT-PCR. Enrollment is ongoing at 3 of the 6 study sites. Data collected through the cohort are expected to provide important public health information for essential workers at high risk for occupational exposure to SARS-CoV-2 and allow early evaluation of COVID-19 vaccine effectiveness. DERR1-10.2196/31574.

Sections du résumé

BACKGROUND BACKGROUND
Workers critical to emergency response and continuity of essential services during the COVID-19 pandemic are at a disproportionally high risk of SARS-CoV-2 infection. Prospective cohort studies are needed for enhancing the understanding of the incidence of symptomatic and asymptomatic SARS-CoV-2 infections, identifying risk factors, assessing clinical outcomes, and determining the effectiveness of vaccination.
OBJECTIVE OBJECTIVE
The Research on the Epidemiology of SARS-CoV-2 in Essential Response Personnel (RECOVER) prospective cohort study was designed to estimate the incidence of symptomatic and asymptomatic SARS-CoV-2 infections, examine the risk factors for infection and clinical spectrum of illness, and assess the effectiveness of vaccination among essential workers.
METHODS METHODS
The RECOVER multisite network was initiated in August 2020 and aims to enroll 3000 health care personnel (HCP), first responders, and other essential and frontline workers (EFWs) at 6 US locations. Data on participant demographics, medical history, and vaccination history are collected at baseline and throughout the study. Active surveillance for the symptoms of COVID-19-like illness (CLI), access of medical care, and symptom duration is performed by text messages, emails, and direct participant or medical record reports. Participants self-collect a mid-turbinate nasal swab weekly, regardless of symptoms, and 2 additional respiratory specimens at the onset of CLI. Blood is collected upon enrollment, every 3 months, approximately 28 days after a reverse transcription polymerase chain reaction (RT-PCR)-confirmed SARS-CoV-2 infection, and 14 to 28 days after a dose of any COVID-19 vaccine. From February 2021, household members of RT-PCR-confirmed participants are self-collecting mid-turbinate nasal swabs daily for 10 days.
RESULTS RESULTS
The study observation period began in August 2020 and is expected to continue through spring 2022. There are 2623 actively enrolled RECOVER participants, including 280 participants who have been found to be positive for SARS-CoV-2 by RT-PCR. Enrollment is ongoing at 3 of the 6 study sites.
CONCLUSIONS CONCLUSIONS
Data collected through the cohort are expected to provide important public health information for essential workers at high risk for occupational exposure to SARS-CoV-2 and allow early evaluation of COVID-19 vaccine effectiveness.
INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID) UNASSIGNED
DERR1-10.2196/31574.

Identifiants

pubmed: 34662287
pii: v10i12e31574
doi: 10.2196/31574
pmc: PMC8647972
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e31574

Subventions

Organisme : NCATS NIH HHS
ID : UL1 TR002538
Pays : United States

Informations de copyright

©Laura J Edwards, Ashley L Fowlkes, Meredith G Wesley, Jennifer L Kuntz, Marilyn J Odean, Alberto J Caban-Martinez, Kayan Dunnigan, Andrew L Phillips, Lauren Grant, Meghan K Herring, Holly C Groom, Karley Respet, Shawn Beitel, Tnelda Zunie, Kurt T Hegmann, Archana Kumar, Gregory Joseph, Brandon Poe, Paola Louzado-Feliciano, Michael E Smith, Matthew S Thiese, Natasha Schaefer-Solle, Young M Yoo, Carlos A Silvera, Julie Mayo Lamberte, Josephine Mak, L Clifford McDonald, Matthew J Stuckey, Preeta Kutty, Melissa L Arvay, Sarang K Yoon, Harmony L Tyner, Jefferey L Burgess, Danielle Rentz Hunt, Jennifer Meece, Manjusha Gaglani, Allison L Naleway, Mark G Thompson. Originally published in JMIR Research Protocols (https://www.researchprotocols.org), 03.12.2021.

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Auteurs

Laura J Edwards (LJ)

Abt Associates, Inc, Atlanta, GA, United States.

Ashley L Fowlkes (AL)

Centers for Disease Control and Prevention, Atlanta, GA, United States.

Meredith G Wesley (MG)

Abt Associates, Inc, Atlanta, GA, United States.

Jennifer L Kuntz (JL)

Kaiser Permanente Northwest Center for Health Research, Portland, OR, United States.

Marilyn J Odean (MJ)

Whiteside Institute for Clinical Research, Duluth, MN, United States.
St. Luke's Regional Health Care System, Duluth, MN, United States.

Alberto J Caban-Martinez (AJ)

University of Miami, Miami, FL, United States.

Kayan Dunnigan (K)

Baylor Scott and White Health, Temple, TX, United States.

Andrew L Phillips (AL)

University of Utah, Salt Lake City, UT, United States.

Lauren Grant (L)

Centers for Disease Control and Prevention, Atlanta, GA, United States.

Meghan K Herring (MK)

Abt Associates, Inc, Atlanta, GA, United States.

Holly C Groom (HC)

Kaiser Permanente Northwest Center for Health Research, Portland, OR, United States.

Karley Respet (K)

St. Luke's Regional Health Care System, Duluth, MN, United States.

Shawn Beitel (S)

University of Arizona, Tucson, AZ, United States.

Tnelda Zunie (T)

Baylor Scott and White Health, Temple, TX, United States.

Kurt T Hegmann (KT)

University of Utah, Salt Lake City, UT, United States.

Archana Kumar (A)

Centers for Disease Control and Prevention, Atlanta, GA, United States.

Gregory Joseph (G)

Centers for Disease Control and Prevention, Atlanta, GA, United States.

Brandon Poe (B)

Abt Associates, Inc, Atlanta, GA, United States.

Paola Louzado-Feliciano (P)

University of Miami, Miami, FL, United States.

Michael E Smith (ME)

Baylor Scott and White Health, Temple, TX, United States.

Matthew S Thiese (MS)

University of Utah, Salt Lake City, UT, United States.

Natasha Schaefer-Solle (N)

University of Miami, Miami, FL, United States.

Young M Yoo (YM)

Centers for Disease Control and Prevention, Atlanta, GA, United States.

Carlos A Silvera (CA)

University of Miami, Miami, FL, United States.

Julie Mayo Lamberte (J)

Centers for Disease Control and Prevention, Atlanta, GA, United States.

Josephine Mak (J)

Centers for Disease Control and Prevention, Atlanta, GA, United States.

L Clifford McDonald (LC)

Centers for Disease Control and Prevention, Atlanta, GA, United States.

Matthew J Stuckey (MJ)

Centers for Disease Control and Prevention, Atlanta, GA, United States.

Preeta Kutty (P)

Centers for Disease Control and Prevention, Atlanta, GA, United States.

Melissa L Arvay (ML)

Centers for Disease Control and Prevention, Atlanta, GA, United States.

Sarang K Yoon (SK)

University of Utah, Salt Lake City, UT, United States.

Harmony L Tyner (HL)

St. Luke's Regional Health Care System, Duluth, MN, United States.

Jefferey L Burgess (JL)

University of Arizona, Tucson, AZ, United States.

Danielle Rentz Hunt (DR)

Abt Associates, Inc, Atlanta, GA, United States.

Jennifer Meece (J)

Marshfield Clinic Research Institute, Marshfield, WI, United States.

Manjusha Gaglani (M)

Baylor Scott and White Health, Temple, TX, United States.
Texas A&M University College of Medicine, Temple, TX, United States.

Allison L Naleway (AL)

Kaiser Permanente Northwest Center for Health Research, Portland, OR, United States.

Mark G Thompson (MG)

Centers for Disease Control and Prevention, Atlanta, GA, United States.

Classifications MeSH