Evidence map›Paper›PMID 35840992›Full record

ArticleOrphanet journal of rare diseases2022

Burden associated with Fabry disease and its treatment in 12-15 year olds: results from a European survey.

Lisa Bashorum, Gerard McCaughey, Owen Evans, Ashley C Humphries, Richard Perry, Alasdair MacCulloch

Open access · goldAbstract read
In one paragraph

Article in Orphanet journal of rare diseases, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 16% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Article
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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

6 authors at 2 institutions in 1 country.

Lisa BashorumAmicus Therapeutics UK, One Globeside, Fieldhouse Lane, Marlow, SL7 1HZ, UK.
Gerard McCaugheyAmicus Therapeutics UK, One Globeside, Fieldhouse Lane, Marlow, SL7 1HZ, UK.
Owen EvansAdelphi Values PROVE, Adelphi Mill, Grimshaw Lane, Macclesfield, SK10 5JB, UK.
Ashley C HumphriesAdelphi Values PROVE, Adelphi Mill, Grimshaw Lane, Macclesfield, SK10 5JB, UK.
Richard PerryAdelphi Values PROVE, Adelphi Mill, Grimshaw Lane, Macclesfield, SK10 5JB, UK.
Alasdair MacCullochAmicus Therapeutics UK, One Globeside, Fieldhouse Lane, Marlow, SL7 1HZ, UK. amacculloch@amicusrx.com.ORCID 0000-0001-9904-9063
Adelphi Group (United Kingdom) · GBAmicus Therapeutics (United Kingdom) · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFabry Disease (FD) is a rare X-linked metabolic lysosomal disorder. FD has a broad range of symptoms which vary markedly between patients. The heterogenous nature of the disease makes diagnosis difficult for health care professionals (HCPs), which in turn has a significant effect on the patient's quality of life (QoL). As few adolescent patients are eligible for treatment, to date there has been little published data on the burden of disease and impact of treatment on these patients and their caregivers. This study was developed to provide some insight into these groups.

methodsAn online-based survey was performed to gather further insights on the burden of FD in 14 adolescents aged 12-15 years old across three European countries, from the perspective of the patients, caregivers and HCPs.

resultsSymptom burden was found to be high in the adolescent population, with 'pain' and 'intolerance to heat or cold' commonly reported symptoms, both by patients and to HCPs. Eleven of the 14 patients surveyed were receiving enzyme replacement therapy (ERT), with their post-ERT symptomology showing improvement when compared to symptoms before receiving ERT. The majority of caregivers believe their child's overall health has improved since starting ERT. While there was a positive outlook towards ERT noted by the patients and caregivers, 4/5 HCPs believed there is 'a need for more efficacious treatment options' and all HCPs noted that there is 'a need for more manageable treatment options'. FD was shown to place a burden on caregivers, who reported feelings of guilt and absences from work.

conclusionsData show there is a significant symptom burden for the adolescent, which affects their QoL and mental health, as well as placing a burden on the wider family. While ERT is an effective treatment and provides symptom relief for many of the respondents in the survey, they still reported symptom burden. Additionally, there was reporting of reluctance to engage in treatment or difficulties associated with the treatment. Heterogeneity in symptom presentation suggests that the treatment regimen needs to be tailored to the individual. Physicians therefore need to have a choice of treatment options available to help them manage symptoms and disease where the benefit to risk ratio is in favour of undergoing treatment.

Indexed as

Fabry DiseaseAdolescentCaregiversChildEnzyme Replacement TherapyHumansQuality of LifeSurveys and QuestionnairesAdolescent burdenCaregiver burdenEnzyme replacement therapyFabry disease

Identifiers

PMID35840992
PMCPMC9287883
OpenAlexW4285491963

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.