Evidence map›Paper›PMID 41060359›Full record

ArticlePharmacoEconomics - open2025

The Economic and Clinical Impact of Recurring Automated Red Blood Cell Exchange to Manage Sickle Cell Disease in the UK.

Sarah M Medland, Jamie Bainbridge, Matthew Cawson, Stuart J Mealing, Anna Yudina, Isabel Eastwood, Arne de Kreuk, Martin Besser, Eva Tsouana

Abstract read
In one paragraph

Article in PharmacoEconomics - open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Sarah M MedlandYork Health Economics Consortium Ltd, University of York, Enterprise House, Innovation Way, Heslington, York, YO10 5NQ, UK. sarah.medland@york.ac.uk.ORCID http://orcid.org/0009-0000-1312-8458
Jamie BainbridgeYork Health Economics Consortium Ltd, University of York, Enterprise House, Innovation Way, Heslington, York, YO10 5NQ, UK.ORCID http://orcid.org/0009-0005-0903-3604
Matthew CawsonTerumo BCT Europe N.V., Ikaroslaan 41, 1930, Zaventem, Belgium.ORCID http://orcid.org/0000-0001-7175-0720
Stuart J MealingYork Health Economics Consortium Ltd, University of York, Enterprise House, Innovation Way, Heslington, York, YO10 5NQ, UK.ORCID http://orcid.org/0000-0002-2564-1440
Anna YudinaTerumo BCT Europe N.V., Ikaroslaan 41, 1930, Zaventem, Belgium.
Isabel EastwoodYork Health Economics Consortium Ltd, University of York, Enterprise House, Innovation Way, Heslington, York, YO10 5NQ, UK.ORCID http://orcid.org/0009-0007-3959-9101
Arne de KreukKing's College Hospital, Denmark Hill, London, SE5 9RS, UK.ORCID http://orcid.org/0000-0002-9715-9063
Martin BesserDepartment of Haematology, Cambridge University Hospitals, Hills Road, Cambridge, CB2 0QQ, UK.ORCID http://orcid.org/0000-0003-1004-6232
Eva TsouanaMid and South Essex NHS Foundation Trust, Basildon University Hospital, Nether Mayne, Basildon, Essex, SS16 5NL, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

objectiveSickle cell disease (SCD) is a group of inherited health conditions affecting 7.74 million people worldwide. Regular automated red blood cell exchange (aRBCX) transfusions have been shown to improve control and management of SCD compared with manual RBCX (mRBCX). The aim of this study was to estimate the lifetime clinical and economic impact of aRBCX versus mRBCX in two United Kingdom-based populations with SCD (paediatrics initiated aged 5 years and adults initiated aged 38 years) that were clinically indicated for chronic disease-modifying transfusions (DMTs).

methodsAn individual patient-level simulation model was developed to estimate lifetime quality-adjusted life years (QALYs) and healthcare costs. DMT administration programmes aligned with recommended treatment schedules. Monte Carlo methods determined baseline characteristics and clinical event occurrence. Pragmatic review findings and expert opinion informed model parameters and assumptions. Second-order probabilistic sensitivity analysis (PSA) was performed for 1000 individuals' lifetimes over 500 iterations.

resultsPer individual, aRBCX reduced acute clinical events by 19% in both populations versus mRBCX. The time spent receiving chelation therapy reduced by 63 and 32 months for paediatric-initiated and adult-initiated individuals, respectively. Total lifetime DMT costs were reduced by £71,217 and £30,740 for paediatric-initiated and adult-initiated individuals, respectively. Overall, aRBCX increased QALYs and reduced costs by 0.29 and £112,811 in paediatric-initiated individuals and 0.24 and £61,895 in adult-initiated individuals. aRBCX was cost-effective in 100% of PSA iterations for both populations.

conclusionaRBCX shows potential to improve health outcomes and reduce healthcare costs for individuals with SCD initiating a chronic DMT programme.

Identifiers

PMID41060359
PMCPMC12559512

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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.