American Society of Hematology living guidelines on the use of anticoagulation for thromboprophylaxis in patients with COVID-19: January 2022 update on the use of therapeutic-intensity anticoagulation in acutely ill patients.


Journal

Blood advances
ISSN: 2473-9537
Titre abrégé: Blood Adv
Pays: United States
ID NLM: 101698425

Informations de publication

Date de publication:
13 09 2022
Historique:
received: 14 03 2022
accepted: 18 04 2022
pubmed: 4 5 2022
medline: 1 9 2022
entrez: 3 5 2022
Statut: ppublish

Résumé

COVID-19-related acute illness is associated with an increased risk of venous thromboembolism (VTE). These evidence-based guidelines from the American Society of Hematology (ASH) are intended to support patients, clinicians, and other health care professionals in making decisions about the use of anticoagulation in patients with COVID-19. ASH formed a multidisciplinary guideline panel that included patient representatives and applied strategies to minimize potential bias from conflicts of interest. The McMaster University GRADE Centre supported the guideline development process and performed systematic evidence reviews (through November 2021). The panel prioritized clinical questions and outcomes according to their importance for clinicians and patients. The panel used the Grading of Recommendations Assessment, Development and Evaluation (GRADE) approach to assess evidence and make recommendations, which were subject to public comment. This is an update to guidelines published in February 2021 as part of the living phase of these guidelines. The panel made one additional recommendation. The panel issued a conditional recommendation in favor of therapeutic-intensity over prophylactic-intensity anticoagulation in patients with COVID-19-related acute illness who do not have suspected or confirmed VTE. The panel emphasized the need for an individualized assessment of risk of thrombosis and bleeding. The panel also noted that heparin (unfractionated or low molecular weight) may be preferred because of a preponderance of evidence with this class of anticoagulants. This conditional recommendation was based on very low certainty in the evidence, underscoring the need for additional, high-quality, randomized controlled trials comparing different intensities of anticoagulation in patients with COVID-19-related acute illness.

Sections du résumé

BACKGROUND
COVID-19-related acute illness is associated with an increased risk of venous thromboembolism (VTE).
OBJECTIVE
These evidence-based guidelines from the American Society of Hematology (ASH) are intended to support patients, clinicians, and other health care professionals in making decisions about the use of anticoagulation in patients with COVID-19.
METHODS
ASH formed a multidisciplinary guideline panel that included patient representatives and applied strategies to minimize potential bias from conflicts of interest. The McMaster University GRADE Centre supported the guideline development process and performed systematic evidence reviews (through November 2021). The panel prioritized clinical questions and outcomes according to their importance for clinicians and patients. The panel used the Grading of Recommendations Assessment, Development and Evaluation (GRADE) approach to assess evidence and make recommendations, which were subject to public comment. This is an update to guidelines published in February 2021 as part of the living phase of these guidelines.
RESULTS
The panel made one additional recommendation. The panel issued a conditional recommendation in favor of therapeutic-intensity over prophylactic-intensity anticoagulation in patients with COVID-19-related acute illness who do not have suspected or confirmed VTE. The panel emphasized the need for an individualized assessment of risk of thrombosis and bleeding. The panel also noted that heparin (unfractionated or low molecular weight) may be preferred because of a preponderance of evidence with this class of anticoagulants.
CONCLUSION
This conditional recommendation was based on very low certainty in the evidence, underscoring the need for additional, high-quality, randomized controlled trials comparing different intensities of anticoagulation in patients with COVID-19-related acute illness.

Identifiants

pubmed: 35503027
pii: 485124
doi: 10.1182/bloodadvances.2022007561
pmc: PMC9068240
doi:

Substances chimiques

Anticoagulants 0

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

4915-4923

Subventions

Organisme : NHLBI NIH HHS
ID : K01 HL135466
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR001863
Pays : United States

Informations de copyright

© 2022 by The American Society of Hematology. Licensed under Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0), permitting only noncommercial, nonderivative use with attribution. All other rights reserved.

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Auteurs

Adam Cuker (A)

Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.

Eric K Tseng (EK)

Division of Hematology/Oncology, St. Michael's Hospital, University of Toronto, Toronto, ON, Canada.

Robby Nieuwlaat (R)

Department of Health Research Methods, Evidence, and Impact, Michael G. DeGroote Cochrane Canada and GRADE Centres, McMaster University, Hamilton, ON, Canada.

Pantep Angchaisuksiri (P)

Division of Hematology, Department of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.

Kathryn Dane (K)

Department of Pharmacy, The Johns Hopkins Hospital, Baltimore, MD.

Maria T DeSancho (MT)

Division of Hematology-Oncology, Department of Medicine, Weill Cornell Medicine, New York Presbyterian Hospital, New York, NY.

David Diuguid (D)

Division of Hematology, and.

Daniel O Griffin (DO)

Division of Infectious Diseases, College of Physicians & Surgeons of Columbia University, New York, NY.
Research and Development at United Health Group, Minnetonka, MN.
Prohealth NY, Lake Success, NY.

Susan R Kahn (SR)

Department of Medicine, McGill University, Montreal, QC, Canada.

Frederikus A Klok (FA)

Department of Medicine - Thrombosis and Hemostasis, Leiden University Medical Center, Leiden, the Netherlands.

Alfred Ian Lee (AI)

Section of Hematology, Yale School of Medicine, New Haven, CT.

Ignacio Neumann (I)

Department of Internal Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile.

Ashok Pai (A)

Division of Hematology & Oncology, Kaiser Permanente, Oakland/Richmond, CA.

Marc Righini (M)

Division of Angiology and Hemostasis, Geneva University Hospitals and Faculty of Medicine, Geneva, Switzerland.

Kristen M Sanfilippo (KM)

Washington University School of Medicine St. Louis, St. Louis, MO.

Deborah M Siegal (DM)

Department of Medicine and the Ottawa Hospital Research Institute, University of Ottawa, Ottawa, ON, Canada.

Mike Skara (M)

Cottage Grove, MN.

Deirdra R Terrell (DR)

Department of Biostatistics and Epidemiology, Hudson College of Public Health, University of Oklahoma Health Sciences Center, Oklahoma City, OK.

Kamshad Touri (K)

Toronto, ON, Canada.

Elie A Akl (EA)

Department of Internal Medicine, American University of Beirut, Beirut, Lebanon.

Reyad Al Jabiri (R)

University of Jordan, Amman, Jordan.

Yazan Al Jabiri (Y)

Lincoln Medical Center, Bronx, NY.

Angela M Barbara (AM)

Department of Health Research Methods, Evidence, and Impact, Michael G. DeGroote Cochrane Canada and GRADE Centres, McMaster University, Hamilton, ON, Canada.

Antonio Bognanni (A)

Department of Health Research Methods, Evidence, and Impact, Michael G. DeGroote Cochrane Canada and GRADE Centres, McMaster University, Hamilton, ON, Canada.

Mary Boulos (M)

Department of Health Research Methods, Evidence, and Impact, Michael G. DeGroote Cochrane Canada and GRADE Centres, McMaster University, Hamilton, ON, Canada.

Romina Brignardello-Petersen (R)

Department of Health Research Methods, Evidence, and Impact, Michael G. DeGroote Cochrane Canada and GRADE Centres, McMaster University, Hamilton, ON, Canada.

Rana Charide (R)

Clinical Research Institute, American University of Beirut, Beirut, Lebanon.

Luis E Colunga-Lozano (LE)

Department of Clinical Medicine, Health Science Center, Universidad de Guadalajara, Guadalajara, Jalisco, Mexico.

Karin Dearness (K)

Library Services, St. Joseph's Healthcare Hamilton, Hamilton, ON, Canada.

Andrea J Darzi (AJ)

Department of Health Research Methods, Evidence, and Impact, Michael G. DeGroote Cochrane Canada and GRADE Centres, McMaster University, Hamilton, ON, Canada.

Heba Hussein (H)

Oral Medicine and Periodontology Department, Faculty of Dentistry, Cairo University, Cairo, Egypt.

Samer G Karam (SG)

Department of Health Research Methods, Evidence, and Impact, Michael G. DeGroote Cochrane Canada and GRADE Centres, McMaster University, Hamilton, ON, Canada.

Razan Mansour (R)

Office of Scientific Affairs and Research, King Hussein Cancer Center, Amman, Jordan.

Gian Paolo Morgano (GP)

Department of Health Research Methods, Evidence, and Impact, Michael G. DeGroote Cochrane Canada and GRADE Centres, McMaster University, Hamilton, ON, Canada.

Rami Z Morsi (RZ)

Department of Neurology, University of Chicago, Chicago, IL.

Giovanna Muti-Schünemann (G)

Department of Health Research Methods, Evidence, and Impact, Michael G. DeGroote Cochrane Canada and GRADE Centres, McMaster University, Hamilton, ON, Canada.

Menatalla K Nadim (MK)

Department of Clinical Pathology, Faculty of Medicine, Ain Shams University, Cairo, Egypt.

Binu A Philip (BA)

Department of Health Research Methods, Evidence, and Impact, Michael G. DeGroote Cochrane Canada and GRADE Centres, McMaster University, Hamilton, ON, Canada.

Yuan Qiu (Y)

Department of Health Research Methods, Evidence, and Impact, Michael G. DeGroote Cochrane Canada and GRADE Centres, McMaster University, Hamilton, ON, Canada.

Yetiani Roldan Benitez (YR)

Department of Health Research Methods, Evidence, and Impact, Michael G. DeGroote Cochrane Canada and GRADE Centres, McMaster University, Hamilton, ON, Canada.

Adrienne Stevens (A)

Department of Health Research Methods, Evidence, and Impact, Michael G. DeGroote Cochrane Canada and GRADE Centres, McMaster University, Hamilton, ON, Canada.

Karla Solo (K)

Department of Health Research Methods, Evidence, and Impact, Michael G. DeGroote Cochrane Canada and GRADE Centres, McMaster University, Hamilton, ON, Canada.

Wojtek Wiercioch (W)

Department of Health Research Methods, Evidence, and Impact, Michael G. DeGroote Cochrane Canada and GRADE Centres, McMaster University, Hamilton, ON, Canada.

Reem A Mustafa (RA)

Department of Health Research Methods, Evidence, and Impact, Michael G. DeGroote Cochrane Canada and GRADE Centres, McMaster University, Hamilton, ON, Canada.
Department of Internal Medicine, Division of Nephrology, University of Kansas Medical Center, Kansas City, KS.

Holger J Schünemann (HJ)

Department of Health Research Methods, Evidence, and Impact, Michael G. DeGroote Cochrane Canada and GRADE Centres, McMaster University, Hamilton, ON, Canada.
Institut für Evidence in Medicine, Medical Center & Faculty of Medicine, University of Freiburg, Freiburg, Germany.

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