Evidence map›Paper›PMID 39075533›Full record

ArticleHealth and quality of life outcomes2024

Exploring the relationship between condition severity and health-related quality of life in people with haemophilia A across Europe: a multivariable analysis of data from the CHESS II study.

Enrico Ferri Grazzi, Charles Hawes, Charlotte Camp, David Hinds, Jamie O'Hara, Tom Burke

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Article in Health and quality of life outcomes, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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3citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Enrico Ferri GrazziHCD Economics, Keckwick Lane, Daresbury, Cheshire, WA4 4FS, UK. enrico.ferrigrazzi@primeglobalpeople.com.
Charles HawesBioMarin Europe, London, UK.
Charlotte CampBioMarin Europe, London, UK.
David HindsBioMarin Pharmaceutical, San Rafael, CA, USA.
Jamie O'HaraHCD Economics, Keckwick Lane, Daresbury, Cheshire, WA4 4FS, UK.
Tom BurkeHCD Economics, Keckwick Lane, Daresbury, Cheshire, WA4 4FS, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHaemophilia A (HA; Factor VIII deficiency) is a congenital X-linked bleeding disorder characterized by trauma-related or spontaneous bleeding events, most notably arising within the intraarticular space and resulting in chronic inflammation and degeneration of affected joints. Endogenous clotting factor activity relative to normal levels determines the severity of HA symptoms, as mild (> 5-40%), moderate (1-5%), or severe (< 1%). Within the current environment of rapid evolution in HA management, we seek to understand the interplay of condition severity and health-related quality of life (HRQoL) to characterise and differentiate unmet needs among people with HA (PwHA).

methodsA generalised linear regression model (GLM) was developed to explore the relationship between HA severity and EQ-5D-5 L index score from adult HA patients sampled in the "Cost of Haemophilia across Europe - a Socioeconomic Survey II" (CHESS II) cross-sectional, retrospective burden of illness study among adults with hereditary haemophilia A or B from eight European countries. HA patients of any severity with no active inhibitors during the 12 months prior to data capture and a completeEQ-5D-5 L response were included. A base GLM model was specified with covariates for demographic and clinical characteristics (age, body mass index, country, employment, HA severity, annual bleeding rate, problem joints, and chronic pain).

resultsOf 381 evaluable patients, 221 (58.0%) had severe HA, 96 (25.2%) had moderate HA, and 64 (16.8%) had mild HA. Among the covariates included in the GLM model and after controlling for haemophilia-related outcomes, a significant association was observed between mild HA and higher EQ-5D-5 L index score (average marginal effects, 0.084; p = 0.016) relative to severe HA. Patient country of residence and magnitude of HA-related chronic pain were also associated with significant differences in index scores, with the latter showing a negative relationship with HRQoL outcomes.

conclusionsCondition severity and chronic pain are significant predictors of HRQoL in PwHA. Durable bleeding protection and effective management of chronic pain have the potential to address unmet treatment needs in this population.

Indexed as

Hemophilia AQuality of LifeSeverity of Illness IndexAdolescentAdultAgedCross-Sectional StudiesEuropeFemaleHumansMaleMiddle AgedMultivariate AnalysisRetrospective StudiesSurveys and QuestionnairesYoung AdultAnnual bleeding rateClotting factor VIIIHaemophilia AHealth-related quality of lifePainPatient-reported outcomesProblem jointsSevere haemophilia

Identifiers

PMID39075533
PMCPMC11288067

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