Evidence map›Paper›PMID 36892793›Full record

ReviewJournal of community genetics2023

An exemplary model of genetic counselling for highly specialised services.

Juliette Harris, Marion Bartlett, Duncan Baker, Cheryl Berlin, Jessica Bowen, Carole Cummings, Christina Fallows, Claire Green, Jared Griffin, Kay Julier and 8 more

Open access · greenAbstract readReview
In one paragraph

Review in Journal of community genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. 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

18 authors at 4 institutions in 1 country.

Juliette HarrisNational Ehlers-Danlos Syndrome Service, London North West University Healthcare NHS Trust, Harrow, London, HA1 3UJ, UK. juliette.harris1@nhs.net.
Marion BartlettNorth West Thames Regional Genetics Service, Northwick Park Hospital, London, UK.
Duncan BakerConnective Tissue Disorders Service, Sheffield Diagnostic Genetics Service, Sheffield Children's Hospital, Sheffield, UK.
Cheryl BerlinNorth West Thames Regional Genetics Service, Northwick Park Hospital, London, UK.
Jessica BowenNational Ehlers-Danlos Syndrome Service, Northern General Hospital, Sheffield, UK.
Carole CummingsNational Ehlers-Danlos Syndrome Service, London North West University Healthcare NHS Trust, Harrow, London, HA1 3UJ, UK.
Christina FallowsAnnabelle's Challenge Vascular EDS Charity, Bury, UK.
Claire GreenNational Ehlers-Danlos Syndrome Service, Northern General Hospital, Sheffield, UK.
Jared GriffinAnnabelle's Challenge Vascular EDS Charity, Bury, UK.
Kay JulierThe Ehlers-Danlos Support UK, Borehamwood, UK.
Tammy KamminNational Ehlers-Danlos Syndrome Service, Northern General Hospital, Sheffield, UK.
Ravinder SehraNational Ehlers-Danlos Syndrome Service, London North West University Healthcare NHS Trust, Harrow, London, HA1 3UJ, UK.
Clare StaceyAnnabelle's Challenge Vascular EDS Charity, Bury, UK.
Jan CobbenNorth West Thames Regional Genetics Service, Northwick Park Hospital, London, UK.
Neeti GhaliNational Ehlers-Danlos Syndrome Service, London North West University Healthcare NHS Trust, Harrow, London, HA1 3UJ, UK.
Diana JohnsonNational Ehlers-Danlos Syndrome Service, Northern General Hospital, Sheffield, UK.
Glenda SobeyNational Ehlers-Danlos Syndrome Service, Northern General Hospital, Sheffield, UK.
Fleur S van DijkNational Ehlers-Danlos Syndrome Service, London North West University Healthcare NHS Trust, Harrow, London, HA1 3UJ, UK.
London North West Healthcare NHS Trust · GBNorthern General Hospital · GBNorthwick Park Hospital · GBSheffield Children's Hospital · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

With genomic testing being increasingly integrated into every day clinical practice and a wide range of practitioners ordering genetic tests, it is important that the scope of the genetic counselling role continues to evolve alongside these changes. We present an exemplary role for genetic counsellors in a highly specialised service within England's National Health Service for people who have or are suspected to have rare genetic types of Ehlers Danlos syndrome. The service employs genetic counsellors and consultants from the fields of genetics and dermatology. The service also works closely with other specialists and related charities and patient organisations. The genetic counsellors in the service provide routine genetic counselling such as diagnostic and predictive testing, but their role also includes the writing of patient literature and emergency and well-being resources, delivering workshops and talks, and the development of qualitative and quantitative research on the patient experience. Data from such research has informed the development of patient self-advocacy and supportive resources, raised awareness amongst healthcare professionals and enhanced the standard of care and outcomes for patients. The service aims to be an example of innovation and accessibility and provides a model that can be potentially adopted by other highly specialised services of rare genetic diseases.

Indexed as

Ehlers Danlos syndrome (rare types)Genetic counsellingPatient self-advocacyRare genetic diseaseSpecialised services

Identifiers

PMID36892793
PMCPMC10104978
OpenAlexW4323652506

What OpenQuestion holds

Textmetadata
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.