Evidence map›Paper›PMID 42165217›Full record

ArticleHaemophilia : the official journal of the World Federation of Hemophilia

Real-World Unmet Treatment Needs for Patients With Haemophilia: Results From the Global Adelphi Disease Specific Programme Database.

Víctor Jiménez Yuste, Cléa Percier, Shwetha Prashanth, Nathan Ball, Ella Morton, Giancarlo Castaman

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Article in Haemophilia : the official journal of the World Federation of Hemophilia. 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

What it found

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2 · The registry

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3 · Its place in the literature

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0 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.

Víctor Jiménez YusteHospital Universitario La Paz-IdiPaz, Servicio de Hematología, Autonoma University, Madrid, Spain.
Cléa PercierNovo Nordisk Health Care AG, Zürich, Switzerland.
Shwetha PrashanthNovo Nordisk Service Centre India Private Limited, Bangalore, India.
Nathan BallAdelphi Real World, Bollington, UK.
Ella MortonAdelphi Real World, Bollington, UK.
Giancarlo CastamanCenter For Bleeding Disorders and Coagulation, Careggi University Hospital, Florence, Italy.

Funding

Novo NordiskNovo Nordisk Health Care AG
6 · The paper itself

Abstract

introductionProphylactic factor replacement and non-factor therapy has improved bleed prevention and clinical outcomes for people with haemophilia (PwH). The remaining burdens faced by PwH in real-world settings, despite availability of newer therapies, are not well documented.

aimWe aimed to describe the haemophilia patient population, assess clinical and humanistic burden of disease, and identify unmest needs associated with current treatments.

methodsData were drawn from the Adelphi Real World Haemophilia Disease Specific Programme, a cross-sectional survey of haemophilia-treating physicians, their patients with haemophilia A (HA) or B (HB), and caregivers. Data were collected in multiple countries from July 2023 to October 2024. Physicians reported patient demographics, disease characteristics, treatment details, bleeding episodes and joint health status. Patients and caregivers reported health-related quality of life (HRQoL). Analyses were descriptive.

resultsOverall, 283 physicians reported on 2227 patients, with 67% of PwH aged 18-49 years. Prophylactic compliance was high: 94% of patients were either fairly or fully compliant (taking 50%-‍80% or >80% of prescribed dose, respectively). However, physicians were not completely satisfied with prophylaxis for 56% of patients with HA and 59% with HB, citing concerns about administration methods, dosing schedules, and efficacy. Joint problems were experienced by 49% of patients; 57% reported ≥1 bleed annually despite prophylaxis. HRQoL impairment was reported by patients on all types of prophylaxis.

conclusionDespite current treatment, many PwH continue to experience limitations to their daily activities, productivity, and physical independence. A patient-centred approach is needed to ensure clinical effectiveness can be balanced with lifestyle priorities.

Indexed as

Hemophilia AAdolescentAdultChildCross-Sectional StudiesDatabases, FactualFemaleHumansMaleMiddle AgedQuality of LifeYoung Adulthaemophiliaoutcomesprophylaxisreal‐worldtreatment burdentreatment satisfaction

Identifiers

PMID42165217
PMCPMC13378624

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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.