Evidence map›Paper›PMID 18821034›Full record

ArticleFamilial cancer2009

Patient preferences and National Health Service costs: a cost-consequences analysis of cancer genetic services.

Gethin L Griffith, Rhiannon Tudor Edwards, J Mark G Williams, Jonathon Gray, Val Morrison, Clare Wilkinson, Jim Turner, Barbara France, Paul Bennett

Abstract read
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In one paragraph

Article in Familial cancer, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 3 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

9 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
  2. Preferences for Genetic Testing to Predict the Risk of Developing Hereditary Cancer: A Systematic Review of Discrete Choice Experiments.Medical decision making : an international journal of the Society for Medical Decision Making · 2024
    Pooled it
  3. Pooled it
  4. Article
  5. Article
  6. Value of Genetic Testing for Hereditary Colorectal Cancer in a Probability-Based US Online Sample.Medical decision making : an international journal of the Society for Medical Decision Making · 2015
    Article
  7. Article
  8. Article
  9. 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.

Gethin L GriffithHealth Economics Research Group, Brunel University, Uxbridge, Middlesex UB8 3PH, UK. Gethin.Griffith@brunel.ac.uk
Rhiannon Tudor Edwards
J Mark G Williams
Jonathon Gray
Val Morrison
Clare Wilkinson
Jim Turner
Barbara France
Paul Bennett

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The study has three aims; firstly to establish if, having been informed of their risk status and that gene testing is inappropriate for them, low and moderate risk patients have misunderstood or failed to grasp this and want a test that is inappropriate for them. Secondly, to elicit patients' willingness to pay for cancer genetic services. Thirdly, to ascertain the aspects of cancer genetics services that are important to high risk patients and present service configurations prioritised in terms of preferences accompanied by their costs (cost-consequences analysis). Patient preferences were gathered from 120 patients returning a self-administered discrete choice questionnaire issued post genetic risk assessment. Patients at low and moderate risk of developing breast cancer desired inappropriate testing. Patients at high, moderate and low risk of developing genetic cancer were willing to pay up to 3,000 pounds for genetic serviced, which exceeds the current estimated cost of providing testing and counselling. Counselling by a genetics associate accompanied by favourable levels of other attributes provided high utility and substantial cost savings.

Indexed as

Breast NeoplasmsCosts and Cost AnalysisFemaleGenetic Predisposition to DiseaseGenetic ServicesHumansNational Health ProgramsPatient PreferenceUnited Kingdom

Identifiers

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.