Evidence map›Paper›PMID 34408148›Full record

ReviewNPJ genomic medicine2021

Queensland Genomics: an adaptive approach for integrating genomics into a public healthcare system.

Miranda E Vidgen, Dayna Williamson, Katrina Cutler, Claire McCafferty, Robyn L Ward, Keith McNeil, Nicola Waddell, David Bunker

Abstract readReview
In one paragraph

Review in NPJ genomic medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Article
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  4. Article
  5. Review
  6. Review
  7. Culture intelligent workflow, structure, and steps.Frontiers in artificial intelligence · 2023
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. 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

8 authors.

Miranda E VidgenQIMR Berghofer Medical Research Institute, Herston, QLD, Australia. miranda.vidgen@qimrberghofer.edu.au.ORCID http://orcid.org/0000-0003-4131-0390
Dayna WilliamsonQueensland Genomics, Queensland Health, Herston, QLD, Australia.
Katrina CutlerQueensland Genomics, Queensland Health, Herston, QLD, Australia.
Claire McCaffertyQueensland Genomics, Queensland Health, Herston, QLD, Australia.
Robyn L WardFaculty of Medicine, The University of Queensland, Herston, QLD, Australia.ORCID http://orcid.org/0000-0002-6877-8906
Keith McNeilOffices of Chief Medical Officer and Chief Clinical Information Officer, Queensland Health, Brisbane, QLD, Australia.
Nicola WaddellQIMR Berghofer Medical Research Institute, Herston, QLD, Australia. nic.waddell@qimrberghofer.edu.au.ORCID http://orcid.org/0000-0002-3950-2476
David BunkerQueensland Genomics, Queensland Health, Herston, QLD, Australia.

Funding

Department of Health | National Health and Medical Research Council (NHMRC) APP1139071
6 · The paper itself

Abstract

The establishment of genomics in health care systems has been occurring for the past decade. It is recognised that implementing genomics within a health service is challenging without a system-wide approach. Globally, as clinical genomics implementation programs have matured there is a growing body of information around program design and outcomes. Program structures vary depending on local ecosystems including the health system, politics and funding availability, however, lessons from other programs are important to the design of programs in different jurisdictions. Here we describe an adaptive approach to the implementation of genomics into a publicly funded health care system servicing a population of 5.1 million people. The adaptive approach enabled flexibility to facilitate substantial changes during the program in response to learnings and external factors. We report the benefits and challenges experienced by the program, particularly in relation to the engagement of people and services, and the design of both individual projects and the program as a whole.

Identifiers

PMID34408148
PMCPMC8373904

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.