Patient blood management guideline for adults with critical bleeding.

Blood banks Blood cell count Critical care Hemostasis Resuscitation Shock Transfusion medicine

Journal

The Medical journal of Australia
ISSN: 1326-5377
Titre abrégé: Med J Aust
Pays: Australia
ID NLM: 0400714

Informations de publication

Date de publication:
28 Jan 2024
Historique:
received: 22 07 2023
accepted: 09 11 2023
medline: 29 1 2024
pubmed: 29 1 2024
entrez: 29 1 2024
Statut: aheadofprint

Résumé

The management of patients with critical bleeding requires a multidisciplinary approach to achieve haemostasis, optimise physiology, and guide blood component use. The 2011 Patient blood management guidelines: module 1 - critical bleeding/massive transfusion were updated and published. Systematic reviews were conducted for pre-specified research questions, and recommendations were based on meta-analyses of included studies. The critical bleeding/massive transfusion guideline includes seven recommendations and 11 good practice statements addressing: major haemorrhage protocols (MHPs) facilitating a multidisciplinary approach to haemorrhage control, correction of coagulopathy and normalisation of physiological derangement; measurement of physiological, biochemical and metabolic parameters in critical bleeding/massive transfusion; the optimal ratio of red blood cells to other blood components; the use of tranexamic acid; viscoelastic haemostatic assays; and cell salvage. The new guideline recommends MHPs be established as standard of care in all institutions managing patients with critical bleeding. In addition to routine physiological markers, the new guideline recommends temperature, biochemistry and coagulation profiles be measured early and frequently, providing parameters that define critical derangements. Ratio-based MHPs should include no fewer than four units of fresh frozen plasma and one adult unit of platelets for every eight units of red blood cells. In the setting of trauma and obstetric haemorrhage, administration of tranexamic acid within three hours of bleeding onset is recommended. The use of recombinant activated factor VII (rFVIIa) is not recommended. There was insufficient evidence to make recommendations on the use of viscoelastic haemostatic assays or cell salvage as part of MHPs.

Identifiants

pubmed: 38282333
doi: 10.5694/mja2.52212
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : National Blood Authority

Investigateurs

Don Campbell (D)
Shannon Farmer (S)
Craig J French (CJ)
Nichole Harvey (N)
Anthony Holley (A)
Anastazia Keegan (A)
Biswadev Mitra (B)
Mihcael Parr (M)
Michael C Reade (MC)
Cindy Schultz-Ferguson (C)
Richard Seigne (R)
James Winearls (J)

Informations de copyright

© 2024 The Authors. Medical Journal of Australia published by John Wiley & Sons Australia, Ltd on behalf of AMPCo Pty Ltd.

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Auteurs

Biswadev Mitra (B)

Emergency and Trauma Centre, Alfred Health, Melbourne, VIC.

Margaret Jorgensen (M)

Health Technology Analysts, Sydney, NSW.

Michael C Reade (MC)

Burns, Trauma and Critical Care Research Centre, University of Queensland, Brisbane, QLD.
Joint Health Command, Australian Defence Force, Canberra, ACT.

Anastazia Keegan (A)

PathWest Laboratory Medicine, King Edward Memorial Hospital, Perth, WA.
Australia Red Cross Lifeblood, Perth, WA.

Anthony Holley (A)

Royal Brisbane and Women's Hospital, Brisbane, QLD.

Shannon Farmer (S)

University of Western Australia, Perth, WA.

Nichole Harvey (N)

Centre for Nursing and Midwifery Research, James Cook University, Townsville, QLD.

James Winearls (J)

Gold Coast University Hospital, Gold Coast, QLD.

Michael Parr (M)

Liverpool Hospital, Sydney, NSW.
University of New South Wales, Sydney, NSW.

Craig J French (CJ)

Western Health, Melbourne, VIC.

Classifications MeSH