Evidence map›Paper›PMID 24398793›Full record

ArticleEuropean journal of human genetics : EJHG2014

Current understanding of genetics and genetic testing and information needs and preferences of adults with inherited retinal disease.

Martin McKibbin, Mushtaq Ahmed, Matthew J Allsop, Louise Downey, Richard Gale, Hilary Louise Grant, Barbara Potrata, Thomas A Willis, Jenny Hewison

Abstract read
In one paragraph

Article in European journal of human genetics : EJHG, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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.

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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Willingness to pay for genetic testing for inherited retinal disease.European journal of human genetics : EJHG · 2015
    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

9 authors.

Martin McKibbinEye Clinic, Leeds Teaching Hospitals NHS Trust, St James's University Hospital, Leeds, UK.
Mushtaq AhmedYorkshire Regional Genetics, Chapel Allerton Hospital, Leeds, UK.
Matthew J AllsopLeeds Institute of Health Sciences, University of Leeds, Leeds, UK.
Louise DowneyHull and East Yorkshire Eye Hospital, Hull, UK.
Richard GaleEye Clinic, The York Hospital, York, UK.
Hilary Louise GrantLeeds Institute of Health Sciences, University of Leeds, Leeds, UK.
Barbara PotrataLeeds Institute of Health Sciences, University of Leeds, Leeds, UK.
Thomas A WillisLeeds Institute of Health Sciences, University of Leeds, Leeds, UK.
Jenny HewisonLeeds Institute of Health Sciences, University of Leeds, Leeds, UK.

Funding

Department of Health PB-PG-0909-20228
6 · The paper itself

Abstract

Advances in sequencing technology and the movement of genetic testing into all areas of medicine will increase opportunities for molecular confirmation of a clinical diagnosis. For health-care professionals without formal genetics training, there is a need to know what patients understand about genetics and genetic testing and their information needs and preferences for the disclosure of genetic testing results. These topics were explored during face-to-face interviews with 50 adults with inherited retinal disease, selected in order to provide a diversity of opinions. Participants had variable understanding of genetics and genetic testing, including basic concepts such as inheritance patterns and the risk to dependents, and many did not understand the term 'genetic counselling'. Most were keen for extra information on the risk to others, the process for genetic testing and how to share the information with other family members. Participants were divided as to whether genetic testing should be offered at the time of the initial diagnosis or later. Many would prefer the results to be given by face-to-face consultation, supplemented by further information in a format accessible to those with visual impairment. Health-care professionals and either leaflets or websites of trusted agencies were the preferred sources of information. Permission should be sought for disclosure of genetic information to other family members. The information needs of many patients with inherited retinal disease appear to be unmet. An understanding of their information needs and preferences is required to help health-care professionals provide optimal services that meet patient expectations.

Indexed as

Patient Education as TopicAdolescentAdultChildFemaleGenetic CounselingHumansMaleRetinal Diseases

Identifiers

PMID24398793
PMCPMC4135409

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.