Blood transfusions post kidney transplantation are associated with inferior allograft and patient survival-it is time for rigorous patient blood management.

anaemia blood calculated reaction frequency DSA donor specific antibody GFR glomerular filtration rate kidney transplant outcomes cRF transfusion

Journal

Frontiers in nephrology
ISSN: 2813-0626
Titre abrégé: Front Nephrol
Pays: Switzerland
ID NLM: 9918469487906676

Informations de publication

Date de publication:
2023
Historique:
received: 07 06 2023
accepted: 03 07 2023
medline: 7 9 2023
pubmed: 7 9 2023
entrez: 7 9 2023
Statut: epublish

Résumé

Patient Blood Management (PBM), endorsed by the World Health Organisation is an evidence-based, multi-disciplinary approach to minimise inappropriate blood product transfusions. Kidney transplantation presents a particular challenge to PBM, as comprehensive evidence of the risk of transfusion is lacking. The aim of this study is to investigate the prevalence of post-transplant blood transfusions across multiple centres, to analyse risk factors for transfusion and to compare transplant outcomes by transfusion status. This analysis was co-ordinated via the UK Transplant Registry within NHS Blood and Transplant (NHSBT), and was performed across 4 centres. Patients who had received a kidney transplant over a 1-year period, had their transfusion status identified and linked to data held within the national registry. Of 720 patients, 221(30.7%) were transfused, with 214(29.7%) receiving a red blood cell (RBC) transfusion. The proportion of patients transfused at each centre ranged from 20% to 35%, with a median time to transfusion of 4 (IQR:0-12) days post-transplant. On multivariate analysis, age [OR: 1.02(1.01-1.03), p=0.001], gender [OR: 2.11(1.50-2.98), p<0.0001], ethnicity [OR: 1.28(1.28-2.60), p=0.0008], and dialysis dependence pre-transplant [OR: 1.67(1.08-2.68), p=0.02], were associated with transfusion. A risk-adjusted Cox proportional hazards model showed transfusion was associated with inferior 1-year patient survival [HR 7.94(2.08-30.27), p=0.002] and allograft survival [HR: 3.33(1.65-6.71), p=0.0008], and inferior allograft function. RBC transfusions are common and are independently associated with inferior transplant outcomes. We urge that further research is needed to understand the mechanisms behind the outcomes, to support the urgent development of transplant-specific anaemia guidelines.

Sections du résumé

Background UNASSIGNED
Patient Blood Management (PBM), endorsed by the World Health Organisation is an evidence-based, multi-disciplinary approach to minimise inappropriate blood product transfusions. Kidney transplantation presents a particular challenge to PBM, as comprehensive evidence of the risk of transfusion is lacking. The aim of this study is to investigate the prevalence of post-transplant blood transfusions across multiple centres, to analyse risk factors for transfusion and to compare transplant outcomes by transfusion status.
Methods UNASSIGNED
This analysis was co-ordinated via the UK Transplant Registry within NHS Blood and Transplant (NHSBT), and was performed across 4 centres. Patients who had received a kidney transplant over a 1-year period, had their transfusion status identified and linked to data held within the national registry.
Results UNASSIGNED
Of 720 patients, 221(30.7%) were transfused, with 214(29.7%) receiving a red blood cell (RBC) transfusion. The proportion of patients transfused at each centre ranged from 20% to 35%, with a median time to transfusion of 4 (IQR:0-12) days post-transplant. On multivariate analysis, age [OR: 1.02(1.01-1.03), p=0.001], gender [OR: 2.11(1.50-2.98), p<0.0001], ethnicity [OR: 1.28(1.28-2.60), p=0.0008], and dialysis dependence pre-transplant [OR: 1.67(1.08-2.68), p=0.02], were associated with transfusion. A risk-adjusted Cox proportional hazards model showed transfusion was associated with inferior 1-year patient survival [HR 7.94(2.08-30.27), p=0.002] and allograft survival [HR: 3.33(1.65-6.71), p=0.0008], and inferior allograft function.
Conclusion UNASSIGNED
RBC transfusions are common and are independently associated with inferior transplant outcomes. We urge that further research is needed to understand the mechanisms behind the outcomes, to support the urgent development of transplant-specific anaemia guidelines.

Identifiants

pubmed: 37675353
doi: 10.3389/fneph.2023.1236520
pmc: PMC10479650
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1236520

Informations de copyright

Copyright © 2023 Hassan, Mumford, Robinson, Foukanelli, Torpey, Ploeg, Mamode, Murphy, Brown, Roberts, Regan and Willicombe.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Références

JAMA. 2019 Mar 12;321(10):983-997
pubmed: 30860564
J Am Soc Nephrol. 2007 Mar;18(3):975-84
pubmed: 17267740
N Engl J Med. 2006 Nov 16;355(20):2085-98
pubmed: 17108343
Transplantation. 2009 May 15;87(9):1381-6
pubmed: 19424040
Transplantation. 2012 Feb 15;93(3):314-8
pubmed: 22179407
PLoS One. 2021 Nov 12;16(11):e0259270
pubmed: 34767576
J Clin Med. 2021 Aug 23;10(16):
pubmed: 34442041
JAMA Netw Open. 2021 Nov 1;4(11):e2133935
pubmed: 34767026
N Engl J Med. 2019 Jan 31;380(5):447-458
pubmed: 30365356
N Engl J Med. 1998 Aug 27;339(9):584-90
pubmed: 9718377
BMJ. 2009 Oct 23;339:b4018
pubmed: 19854839
Am J Transplant. 2003 Jul;3(7):835-45
pubmed: 12814475
Nephron Clin Pract. 2011;117(2):c127-34
pubmed: 20693814
Ann Surg. 2019 May;269(5):794-804
pubmed: 30418206
Front Immunol. 2022 May 31;13:854850
pubmed: 35711440
Transplantation. 2016 Apr;100(4):719-26
pubmed: 26413991
Transfusion. 2017 Jun;57(6):1347-1358
pubmed: 28150313
Transpl Int. 2022 Mar 18;35:10279
pubmed: 35368637
BMC Nephrol. 2022 Jan 3;23(1):6
pubmed: 34979953
Thromb Res. 2006;118(3):417-22
pubmed: 15993929
Transfusion. 2018 Aug;58(8):1951-1957
pubmed: 30171817
Transplantation. 2012 May 15;93(9):923-8
pubmed: 22377790
N Engl J Med. 1989 Jul 20;321(3):151-7
pubmed: 2664510
Clin Nephrol. 2012 Jun;77(6):432-7
pubmed: 22595384
Am J Transplant. 2016 Sep;16(9):2661-9
pubmed: 26998676
Front Immunol. 2022 Mar 31;13:852079
pubmed: 35432350
Hum Immunol. 2020 Jul;81(7):323-329
pubmed: 32327243
Kidney Int. 2010 Feb;77(4):299-311
pubmed: 19847156
Am J Transplant. 2019 Jun;19(6):1720-1729
pubmed: 30582278
Nephrol Dial Transplant. 2016 Oct;31(10):1746-53
pubmed: 27387475
BMC Nephrol. 2018 Oct 5;19(1):252
pubmed: 30290796
N Engl J Med. 2009 Nov 19;361(21):2019-32
pubmed: 19880844
Transpl Immunol. 2013 Dec;29(1-4):22-7
pubmed: 24090807
Clin J Am Soc Nephrol. 2011 Jul;6(7):1794-801
pubmed: 21734096
N Engl J Med. 2006 Nov 16;355(20):2071-84
pubmed: 17108342

Auteurs

Sevda Hassan (S)

Centre for Inflammatory Disease, Department of Immunology and Inflammation, Imperial College London, London, United Kingdom.
Imperial College Renal and Transplant Centre, Imperial College Healthcare National Health Service (NHS) Trust, Hammersmith Hospital, London, United Kingdom.

Lisa Mumford (L)

Statistics and Clinical Studies, National Health Service (NHS) Blood and Transplant, Bristol, United Kingdom.

Susan Robinson (S)

Department of Haematology, Guys, Evelina and St Thomas National Health Service (NHS) Foundation Trust, London, United Kingdom.

Dora Foukanelli (D)

Department of Haematology, Addenbrooke's Hospital, Cambridge, United Kingdom.

Nick Torpey (N)

Department of Clinical Nephrology and Transplantation, Cambridge University Hospitals National Health Service (NHS) Foundation Trust, Cambridge, United Kingdom.

Rutger J Ploeg (RJ)

Department of Surgery, Nuffield Department of Surgical Science, University of Oxford, Oxford, United Kingdom.

Nizam Mamode (N)

Department of Transplantation, Guys, Evelina and St Thomas National Health Service (NHS) Foundation Trust, London, United Kingdom.

Michael F Murphy (MF)

National Health Service (NHS) Blood and Transplant, and Nuffield Department of Clinical and Laboratory Sciences, University of Oxford, Oxford, United Kingdom.

Colin Brown (C)

Haematology, National Health Service (NHS) Blood and Transplant, London, United Kingdom.

David J Roberts (DJ)

Haematology, National Health Service (NHS) Blood and Transplant, London, United Kingdom.

Fiona Regan (F)

Haematology, National Health Service (NHS) Blood and Transplant, London, United Kingdom.

Michelle Willicombe (M)

Centre for Inflammatory Disease, Department of Immunology and Inflammation, Imperial College London, London, United Kingdom.
Imperial College Renal and Transplant Centre, Imperial College Healthcare National Health Service (NHS) Trust, Hammersmith Hospital, London, United Kingdom.

Classifications MeSH