Evidence map›Paper›PMID 38007560›Full record

ArticleOrphanet journal of rare diseases2023

Educational needs of patients, families, and healthcare professionals to support the patient journey in haemophilia gene therapy in the UK.

Sara Boyce, Simon Fletcher, April Jones, Ruchika Kohli, Sarah Mangles, Min Ong, Debra Pollard, Sujan Sivasubramaniyam, David Stephensen, Nicola Stoner and 1 more

Open access · goldAbstract readLetter
In one paragraph

Article in Orphanet journal of rare diseases, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
1.2field-weighted citation impact, top 18% of its field
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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. Defining the Role of Nurses in Gene Therapy for Haemophilia.Haemophilia : the official journal of the World Federation of Hemophilia
    Article
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

11 authors at 8 institutions in 1 country.

Sara BoyceUniversity Hospital Southampton, Southampton, UK. sara.boyce@uhs.nhs.uk.ORCID 0000-0002-0671-3269
Simon FletcherOxford University Hospitals NHS Foundation Trust, Oxford, UK.
April JonesThe Royal Victoria Infirmary, Newcastle upon Tyne, UK.
Ruchika KohliCSL Behring, West Sussex, UK.ORCID 0000-0002-8683-326X
Sarah ManglesHaemophilia, Haemostasis and Thrombosis Centre, Hampshire Hospitals NHS Foundation Trust, Basingstoke, UK.
Min OngSheffield Children's NHS Foundation Trust, Sheffield, UK.
Debra PollardHaemophilia and Thrombosis Centre, Royal Free Hospital, London, UK.
Sujan SivasubramaniyamCSL Behring, West Sussex, UK.ORCID 0000-0002-0859-0370
David StephensenEast Kent Hospitals University NHS Foundation Trust, Kent, UK.
Nicola StonerOxford University Hospitals NHS Foundation Trust, Oxford, UK.ORCID 0000-0001-8132-7475
Rashid KazmiUniversity Hospital Southampton, Southampton, UK.
Oxford University Hospitals NHS Trust · GBEast Kent Hospitals University NHS Foundation Trust · GBHampshire Hospitals NHS Foundation Trust · GBRoyal Victoria Infirmary · GBSheffield Children's NHS Foundation Trust · GBSouthampton General Hospital · GBThe Royal Free Hospital · GBUniversity Hospital Southampton NHS Foundation Trust · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

With the first gene therapies for haemophilia approved by the European Commission, the US Food and Drug Administration, and the Medicines and Healthcare products Regulatory Agency, it is important to consider the remaining unmet needs and challenges that may arise throughout patients' treatment journeys. We discuss existing unmet needs and important considerations prior to, during, and following haemophilia gene therapy treatment in the UK, and propose potential next steps. Key areas for attention are education, psychological support, and guidance on implementation. Strategies are urgently required to fulfil these needs. An immediate priority for information providers should be comprehensive education for people with haemophilia (PWH) and healthcare professionals (HCPs). Greater access to resources and training in psychological services will be required throughout the treatment pathway. More specific guidance is required to define the implementation model, criteria for accreditation, and responsibilities of care centres. Furthermore, PWH may revisit discussions with HCPs multiple times pre-infusion, thus the patient journey is unlikely to be linear. Consideration of these challenges, and of potential strategies to address them, will be integral to optimising the future success of this promising therapy.

Indexed as

Hemophilia ADelivery of Health CareHealth PersonnelHumansUnited KingdomGene therapyHaemophilia AHaemophilia BHealth services needs and demandPatient navigation

Identifiers

PMID38007560
PMCPMC10676600
OpenAlexW4389002719

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.