Evidence map›Paper›PMID 38048591›Full record

ArticleBlood2024

Impaired O2 unloading from stored blood results in diffusion-limited O2 release at tissues: evidence from human kidneys.

Richard Dumbill, Julija Rabcuka, John Fallon, Simon Knight, James Hunter, Daniel Voyce, Jacob Barrett, Matt Ellen, Annemarie Weissenbacher, Tetuko Kurniawan and 6 more

Abstract read
In one paragraph

Article in Blood, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed.

  1. Trial
  2. Trial
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  9. Review
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  11. It's in your blood: The impact of age, sex, genetic factors and exposures on stored red blood cell metabolism.Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis · 2024
    Review
  12. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors.

Richard DumbillNuffield Department of Surgery, University of Oxford, Oxford, United Kingdom.ORCID 0000-0003-1907-4758
Julija RabcukaDepartment of Physiology, Anatomy & Genetics, University of Oxford, Oxford, United Kingdom.ORCID 0000-0002-2367-4636
John FallonNuffield Department of Surgery, University of Oxford, Oxford, United Kingdom.ORCID 0000-0002-8644-9380
Simon KnightNuffield Department of Surgery, University of Oxford, Oxford, United Kingdom.
James HunterNuffield Department of Surgery, University of Oxford, Oxford, United Kingdom.
Daniel VoyceOrganOx Limited, Oxford, United Kingdom.
Jacob BarrettOrganOx Limited, Oxford, United Kingdom.
Matt EllenOrganOx Limited, Oxford, United Kingdom.
Annemarie WeissenbacherDepartment of Visceral, Transplant and Thoracic Surgery, Center of Operative Medicine, Medical University of Innsbruck, Innsbruck, Austria.ORCID 0000-0002-0582-1815
Tetuko KurniawanInstitute of Fundamental Technological Research, Polish Academy of Sciences, Warsaw, Poland.ORCID 0000-0002-2227-8084
Slawomir BlonskiInstitute of Fundamental Technological Research, Polish Academy of Sciences, Warsaw, Poland.ORCID 0000-0002-6998-8198
Piotr Michal KorczykInstitute of Fundamental Technological Research, Polish Academy of Sciences, Warsaw, Poland.ORCID 0000-0002-5445-7933
Rutger PloegNuffield Department of Surgery, University of Oxford, Oxford, United Kingdom.ORCID 0000-0001-7801-665X
Constantin CoussiosOrganOx Limited, Oxford, United Kingdom.
Peter FriendNuffield Department of Surgery, University of Oxford, Oxford, United Kingdom.ORCID 0000-0003-0841-9685
Pawel SwietachDepartment of Physiology, Anatomy & Genetics, University of Oxford, Oxford, United Kingdom.ORCID 0000-0002-9945-9473

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

abstractThe volume of oxygen drawn from systemic capillaries down a partial pressure gradient is determined by the oxygen content of red blood cells (RBCs) and their oxygen-unloading kinetics, although the latter is assumed to be rapid and, therefore, not a meaningful factor. Under this paradigm, oxygen transfer to tissues is perfusion-limited. Consequently, clinical treatments to optimize oxygen delivery aim at improving blood flow and arterial oxygen content, rather than RBC oxygen handling. Although the oxygen-carrying capacity of blood is increased with transfusion, studies have shown that stored blood undergoes kinetic attrition of oxygen release, which may compromise overall oxygen delivery to tissues by causing transport to become diffusion-limited. We sought evidence for diffusion-limited oxygen release in viable human kidneys, normothermically perfused with stored blood. In a cohort of kidneys that went on to be transplanted, renal respiration correlated inversely with the time-constant of oxygen unloading from RBCs used for perfusion. Furthermore, the renal respiratory rate did not correlate with arterial O2 delivery unless this factored the rate of oxygen-release from RBCs, as expected from diffusion-limited transport. To test for a rescue effect, perfusion of kidneys deemed unsuitable for transplantation was alternated between stored and rejuvenated RBCs of the same donation. This experiment controlled oxygen-unloading, without intervening ischemia, holding all non-RBC parameters constant. Rejuvenated oxygen-unloading kinetics improved the kidney's oxygen diffusion capacity and increased cortical oxygen partial pressure by 60%. Thus, oxygen delivery to tissues can become diffusion-limited during perfusion with stored blood, which has implications in scenarios, such as ex vivo organ perfusion, major hemorrhage, and pediatric transfusion. This trial was registered at www.clinicaltrials.gov as #ISRCTN13292277.

Indexed as

ErythrocytesOxygenChildHumansKidneyOxygen

Identifiers

PMID38048591
PMCPMC10900257

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.