Evidence map›Paper›PMID 42243888›Full record

ArticleBMC health services research2026

Empirical estimate for the indirect healthcare costs of sickle cell disease from a retrospective cohort study in England between 2007 and 2019.

Caoimhe T Rice, Martin Besser, Christine L Baker, Carmine Colavecchia, Jennifer A Davidson, Jeremy P Brown, Giovanna Tedesco Barcelos

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Article in BMC health services research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Caoimhe T RiceThermo Fisher Scientific, London, UK. Caoimhe.rice@thermofisher.com.
Martin BesserAddenbrooke's Hospital, Cambridge, UK.
Christine L BakerPfizer Inc, New York, NY, USA.
Carmine ColavecchiaPfizer Inc, New York, NY, USA.
Jennifer A DavidsonThermo Fisher Scientific, London, UK.
Jeremy P BrownThermo Fisher Scientific, London, UK.
Giovanna Tedesco BarcelosPfizer AG, Zurich, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSickle cell disease (SCD) imposes a considerable burden on patients and their families while also exerting economic pressure on high-prevalence countries. This retrospective cohort study estimated the societal cost of SCD in England, including productivity loss (PL) and loss of future income (LFI).

methodsIn this retrospective cohort study, individuals aged ≥ 12 years with SCD were identified between 01 April 2007 and 31 March 2019 using linked healthcare data from the Clinical Practice Research Datalink Aurum, Hospital Episode Statistics, and Office for National Statistics death registrations. PL was calculated based on time spent hospitalised, attending healthcare appointments, or on certified sick days, using average wages for England stratified by age for the same year the PL occurred. LFI due to unemployment, medical retirement, or death was calculated from the age at first occurrence until age 68 years. Average annual earnings for FY2021/2022 were applied by age decile and discounted at 3.5%. Expected income increased with age decile.

resultsOverall, 9,272 patients with SCD were included, with a mean age of 35.5 years and a median follow-up of 7 years. Mean annualised (per patient per year [PPPY]) productive time lost due to hospital stays was 5.5 days. Individuals spent 2.7 days PPPY in outpatient care, 3.6 days PPPY attending primary care appointments, 3.3 days PPPY in emergency departments, and 2.2 days PPPY sick at home. The mean annualised PL for these sickness and healthcare attendances was £1,821 PPPY, equivalent to 3.1 weeks of average UK weekly earnings in 2021. For the 6% of patients (555/9,272) who experienced an LFI event, they were estimated to lose an average of £511,236 over their lifetime.

conclusionsPatients with SCD and their families had an estimated PL equivalent to 3.1 weeks of average UK weekly earnings in 2021 per individual annually. For patients with SCD who died or were incapacitated before retirement age, lifetime LFI was more than half a million pounds.

trial registrationNot applicable.

Indexed as

Anemia, Sickle CellCost of IllnessHealth Care CostsAdolescentAdultAgedEnglandFemaleHumansMaleMiddle AgedRetrospective StudiesYoung AdultCostHemoglobinopathyIndirect costLoss of future incomeProductivity lossSickle cell diseaseSocietal burden

Identifiers

PMID42243888
PMCPMC13460019

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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.