Evidence map›Paper›PMID 30571778›Full record

ArticlePloS one2018

Views of ophthalmologists on the genetics of age-related macular degeneration: Results of a qualitative study.

Julika Loss, Daniel Müller, Johannes Weigl, Horst Helbig, Caroline Brandl, Iris M Heid, Robert P Finger, Bernhard H F Weber, Janina Curbach

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In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–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

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  4. Review
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.

Julika LossMedical Sociology, Institute for Epidemiology and Preventive Medicine, University of Regensburg, Regensburg, Germany.ORCID 0000-0002-9811-1002
Daniel MüllerMedical Sociology, Institute for Epidemiology and Preventive Medicine, University of Regensburg, Regensburg, Germany.
Johannes WeiglMedical Sociology, Institute for Epidemiology and Preventive Medicine, University of Regensburg, Regensburg, Germany.
Horst HelbigDepartment of Ophthalmology, University Hospital Regensburg, Regensburg, Germany.
Caroline BrandlDepartment of Ophthalmology, University Hospital Regensburg, Regensburg, Germany.ORCID 0000-0001-8223-6137
Iris M HeidDepartment of Genetic Epidemiology, University of Regensburg, Regensburg, Germany.
Robert P FingerUniversity Eye Hospital, University of Bonn, Bonn, Germany.
Bernhard H F WeberInstitute of Human Genetics, University of Regensburg, Regensburg, Germany.ORCID 0000-0002-8808-7723
Janina CurbachMedical Sociology, Institute for Epidemiology and Preventive Medicine, University of Regensburg, Regensburg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAge-related macular degeneration (AMD) is the leading cause of blindness in industrialized countries. It is a multifactorial disease of the retina modified by environmental/individual (e.g. smoking) and genetic factors. 34 independent genomic loci are associated with the risk to develop AMD; an interaction between smoking and genetics is currently investigated. It is unclear how the knowledge on the strong genetic component has entered the knowledge base of practicing ophthalmologists, and how they inform and counsel their (AMD) patients about it. In this study, we explore the ophthalmologists' view on AMD genetics, and their inclination towards communicating genetic risks to patients.

methodsWe recruited a purposive sample of thirty German ophthalmologists (office based: n = 15, hospital employees: n = 15, f:8/30), who took part in a recorded semi-standardized interview. Transcripts were analyzed using content analysis.

resultsThe majority of office-based ophthalmologists claimed to be unfamiliar with genetics of AMD, in contrast to hospital-affiliated ophthalmologists. Both office and hospital ophthalmologists were convinced that genetics lacks practical relevance in everyday patient care. Many withhold information on heritability or genetic background of AMD from patients and their relatives, for fear of unsettling those individuals. The relevance of the genetic component of AMD or an individuals' high genetic risk for prevention, e.g. screening or lifestyle modifications in persons with adverse genetic profile, was rated low.

conclusionDeveloping genetic educational programs tailored to the routine care of ophthalmologists may be indicated, as well as a better two-way communication between research and practice. Exploring patient views about their expectations to being informed about genetic disease etiology, or about their individual risk, would help inform communication strategies.

Indexed as

OphthalmologistsCommunicationCross-Sectional StudiesGenetic CounselingGenetic TestingGermanyHumansInterviews as TopicMacular DegenerationMultifactorial InheritancePatient Education as TopicQualitative ResearchRisk FactorsTranslational Research, Biomedical

Identifiers

PMID30571778
PMCPMC6301605

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