Evidence map›Paper›PMID 39091324›Full record

ArticleTherapeutic advances in hematology2024

Long-term efmoroctocog alfa prophylaxis improves perceived pain, mental, and physical health in patients with hemophilia A:

Priyanka Raheja, Nana Kragh, Linda Bystrická, Daniel Eriksson, Khaoula Aroui, Marwa Mezghani, Sylvaine Barbier, Silvia Linari

3 registry-linked trialsAbstract read
In one paragraph

Article in Therapeutic advances in hematology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this 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.

NCT01181128 phase3completednot on this map

A-LONG: An Open-Label, Multicenter Evaluation of the Safety, Pharmacokinetics, and Efficacy of Recombinant Factor VIII Fc Fusion Protein (rFVIIIFc) in the Prevention and Treatment of Bleeding in Previously Treated Subjects With Severe Hemophilia A

TypeinterventionalSponsorBioverativ Therapeutics Inc.Ran2010 to 2012Enrolled165ConditionsSevere Hemophilia AArmsFactor VIII (rFVIIIFc), Advate®
NCT01454739 phase3completednot on this map

An Open-Label, Multicenter Evaluation of the Long-Term Safety and Efficacy of Recombinant Human Coagulation Factor VIII Fusion Protein (rFVIIIFc) in the Prevention and Treatment of Bleeding Episodes in Previously Treated Subjects With Hemophilia A

TypeinterventionalSponsorBioverativ Therapeutics Inc.Ran2011 to 2017Enrolled240ConditionsHemophilia AArmsrFVIIIFc
NCT01458106 phase3completednot on this map

An Open-Label, Multicenter Evaluation of Safety, Pharmacokinetics, and Efficacy of Recombinant Coagulation Factor VIII Fc Fusion Protein, BIIB031, in the Prevention and Treatment of Bleeding Episodes in Pediatric Subjects With Hemophilia A

TypeinterventionalSponsorBioverativ Therapeutics Inc.Ran2012 to 2013Enrolled71ConditionsHemophilia AArmsBIIB031 (rFVIIIFc), FVIII (PK subgroup only)
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

8 authors.

Priyanka RahejaHaematology Department, Haemophilia Centre, The Royal London Hospital, Barts Health NHS Trust, Whitechapel Road, London E1 1FR, UK.
Nana KraghSobi, Stockholm, Sweden.
Linda BystrickáSobi, Stockholm, Sweden.
Daniel ErikssonSobi, Stockholm, Sweden.ORCID https://orcid.org/0000-0001-7699-242X
Khaoula ArouiPutnam, Les Berges du lac, Tunisia.
Marwa MezghaniPutnam, Les Berges du lac, Tunisia.
Sylvaine BarbierPutnam, Lyon, France.
Silvia LinariDepartment of Oncology, Center for Bleeding Disorders and Coagulation, Careggi University Hospital, Florence, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Hemophilia-associated bleeding and resultant joint pain and mobility restrictions can predispose patients to poor health-related quality of life (HRQoL). Therefore, efficacy of a treatment needs to address more than just annualized bleed rates. Objectives: Describe the evolution of HRQoL, pain, and activity in patients with hemophilia A, treated with efmoroctocog alfa prophylaxis. Design: A Methods: Physical health, pain, and HRQoL were assessed by PROs for a cumulative treatment duration of up to ~6 years. The primary endpoint was change from baseline in EuroQoL (EQ)-5D and Haemophilia Quality of Life Questionnaire (Haem-A-QoL). Results: 118 adult/adolescents and 71 pediatric patients were included. The proportion of adults and adolescents reporting no problem in the EQ-5D analysis of ' Conclusion: Long-term efmoroctocog alfa prophylaxis reduces pain and improves HRQoL in adult and adolescent patients with hemophilia A. In pediatric patients, it reduces perceived pain and maintains satisfaction levels. Trial registration: NCT01458106, NCT01181128, NCT01454739.

Indexed as

hemophilia Apainpatient-reported outcomes measuresquality of liferFVIIIFc protein

Identifiers

PMID39091324
PMCPMC11292708

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

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.