Clinical Practice Guidelines From the Association for the Advancement of Blood and Biotherapies (AABB): COVID-19 Convalescent Plasma.


Journal

Annals of internal medicine
ISSN: 1539-3704
Titre abrégé: Ann Intern Med
Pays: United States
ID NLM: 0372351

Informations de publication

Date de publication:
09 2022
Historique:
pubmed: 16 8 2022
medline: 23 9 2022
entrez: 15 8 2022
Statut: ppublish

Résumé

Coronavirus disease 2019 convalescent plasma (CCP) has emerged as a potential treatment of COVID-19. However, meta-analysis data and recommendations are limited. The Association for the Advancement of Blood and Biotherapies (AABB) developed clinical practice guidelines for the appropriate use of CCP. These guidelines are based on 2 living systematic reviews of randomized controlled trials (RCTs) evaluating CCP from 1 January 2019 to 26 January 2022. There were 33 RCTs assessing 21 916 participants. The results were summarized using the GRADE (Grading of Recommendations Assessment, Development and Evaluation) method. An expert panel reviewed the data using the GRADE framework to formulate recommendations. The AABB suggests CCP transfusion in addition to the usual standard of care for outpatients with COVID-19 who are at high risk for disease progression (weak recommendation, moderate-certainty evidence). The AABB recommends against CCP transfusion for unselected hospitalized persons with moderate or severe disease (strong recommendation, high-certainty evidence). This recommendation does not apply to immunosuppressed patients or those who lack antibodies against SARS-CoV-2. The AABB suggests CCP transfusion in addition to the usual standard of care for hospitalized patients with COVID-19 who do not have SARS-CoV-2 antibodies detected at admission (weak recommendation, low-certainty evidence). The AABB suggests CCP transfusion in addition to the usual standard of care for hospitalized patients with COVID-19 and preexisting immunosuppression (weak recommendation, low-certainty evidence). The AABB suggests against prophylactic CCP transfusion for uninfected persons with close contact exposure to a person with COVID-19 (weak recommendation, low-certainty evidence). CCP is most effective when transfused with high neutralizing titers to infected patients early after symptom onset.

Identifiants

pubmed: 35969859
doi: 10.7326/M22-1079
pmc: PMC9450870
doi:

Types de publication

Journal Article Practice Guideline Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1310-1321

Subventions

Organisme : NHLBI NIH HHS
ID : K23 HL151826
Pays : United States

Commentaires et corrections

Type : CommentIn

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Auteurs

Lise J Estcourt (LJ)

NHS Blood and Transplant and Radcliffe Department of Medicine, University of Oxford, United Kingdom (L.J.E.).

Claudia S Cohn (CS)

University of Minnesota, Department of Laboratory Medicine and Pathology, Minneapolis, Minnesota (C.S.C.).

Monica B Pagano (MB)

University of Washington, Department of Laboratory Medicine and Pathology, Seattle, Washington (M.B.P.).

Claire Iannizzi (C)

Evidence-based Oncology, Department of Internal Medicine, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany (C.I., N.K., N.S.).

Nina Kreuzberger (N)

Evidence-based Oncology, Department of Internal Medicine, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany (C.I., N.K., N.S.).

Nicole Skoetz (N)

Evidence-based Oncology, Department of Internal Medicine, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany (C.I., N.K., N.S.).

Elizabeth S Allen (ES)

University of California San Diego, Department of Pathology, La Jolla, California (E.S.A.).

Evan M Bloch (EM)

The Johns Hopkins University School of Medicine, Department of Pathology, Baltimore, Maryland (E.M.B., R.G., A.A.R.T.).

Gregory Beaudoin (G)

Minneapolis, Minnesota (G.B.).

Arturo Casadevall (A)

The Johns Hopkins University School of Public Health, Department of Molecular Microbiology and Immunology, Baltimore, Maryland (A.C.).

Dana V Devine (DV)

Canadian Blood Services, Vancouver, British Columbia, Canada (D.V.D.).

Farid Foroutan (F)

University Health Network, Ted Rogers Centre for Heart Research, Toronto, and Department of Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, Ontario, Canada (F.F.).

Thomas J Gniadek (TJ)

NorthShore University Health System, Department of Pathology and Laboratory Medicine, Evanston, Illinois (T.J.G.).

Ruchika Goel (R)

The Johns Hopkins University School of Medicine, Department of Pathology, Baltimore, Maryland (E.M.B., R.G., A.A.R.T.).

Jed Gorlin (J)

Innovative Blood Resources, Division of New York Blood Center Enterprises, St. Paul, Minnesota (J.G.).

Brenda J Grossman (BJ)

Washington University in St. Louis School of Medicine, Department of Pathology and Immunology, St. Louis, Missouri (B.J.G.).

Michael J Joyner (MJ)

Mayo Clinic, Department of Anesthesiology and Perioperative Medicine, Rochester, Minnesota (M.J.J.).

Ryan A Metcalf (RA)

University of Utah, Department of Pathology, Salt Lake City, Utah (R.A.M.).

Jay S Raval (JS)

University of New Mexico, Department of Pathology, Albuquerque, New Mexico (J.S.R.).

Todd W Rice (TW)

Vanderbilt University Medical Center, Division of Allergy, Pulmonary, and Critical Care Medicine, Nashville, Tennessee (T.W.R.).

Beth H Shaz (BH)

Duke University, Department of Pathology, Durham, North Carolina (B.H.S.).

Ralph R Vassallo (RR)

Vitalant, Medical Affairs, Scottsdale, Arizona (R.R.V.).

Jeffrey L Winters (JL)

Mayo Clinic, Department of Laboratory Medicine and Pathology, Rochester, Minnesota (J.L.W.).

Aaron A R Tobian (AAR)

The Johns Hopkins University School of Medicine, Department of Pathology, Baltimore, Maryland (E.M.B., R.G., A.A.R.T.).

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