Evidence map›Paper›PMID 33619187›Full record

ArticleBMJ open2021

Are National Cancer Control Indicators for patient experiences being met in regional and remote Australia? A cross-sectional study of cancer survivors who travelled for treatment.

Jeff Dunn, Belinda Goodwin, Joanne F Aitken, Sonja March, Fiona Crawford-Williams, Michael Ireland, Nicholas Ralph, Leah Zajdlewicz, Arlen Rowe, Suzanne K Chambers

Abstract read
In one paragraph

Article in BMJ open, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

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

  1. Prevalence of unmet supportive care needs reported by individuals ever diagnosed with cancer in Australia: a systematic review to support service prioritisation.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2023
    Pooled it
  2. Review
  3. Article
  4. Understanding experiences of optimal survivorship care: findings from a population-based study of cancer survivors.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2025
    Article
  5. Article
  6. Article
  7. Article
  8. Survivorship care plans and information for rural cancer survivors.Journal of cancer survivorship : research and practice · 2023
    Article
  9. Article
  10. 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

10 authors.

Jeff DunnCancer Council Queensland, Queensland, Brisbane, Australia.
Belinda GoodwinCancer Council Queensland, Queensland, Brisbane, Australia belindagoodwin@cancerqld.org.au.ORCID 0000-0002-3425-4848
Joanne F AitkenCancer Council Queensland, Queensland, Brisbane, Australia.
Sonja MarchCentre for Health Research, University of Southern Queensland, Springfield, Queensland, Australia.
Fiona Crawford-WilliamsCentre for Health Research, University of Southern Queensland, Springfield, Queensland, Australia.
Michael IrelandCentre for Health Research, University of Southern Queensland, Springfield, Queensland, Australia.
Nicholas RalphCentre for Health Research, University of Southern Queensland, Springfield, Queensland, Australia.
Leah ZajdlewiczCancer Council Queensland, Queensland, Brisbane, Australia.
Arlen RoweCentre for Health Research, University of Southern Queensland, Springfield, Queensland, Australia.
Suzanne K ChambersCentre for Health Research, University of Southern Queensland, Springfield, Queensland, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo examine the health services experience of patients with cancer from regional and remote Australia using the Australian National Cancer Control Indicators (NCCI) guidelines as an assessment framework.

designCross-sectional.

settingQueensland non-for-profit cancer accommodation lodges.

participantsParticipants were patients with cancer who travelled for treatment from rural and remote Queensland to major urban centres (n=518; age mean=64.6, SD=11.18). OUTCOME MEASURES: Assessments included NCCI patient indicators, quality of life (QoL), psychological distress and unmet supportive care needs.

resultsThe frequency at which NCCI indicators were met ranged from 37.5% for receiving an assessment and care plan to 97.3% for understanding explanations about diagnosis. Geographical considerations did not impact patient experience, whereas middle school educated participants were more likely than those with senior-level education or higher to receive an assessment and care plan (OR=1.90, 95% CI 1.23 to 2.91) and to report having their views on treatment taken into account (OR=2.22, 95% CI 1.49 to 3.33). Patients with breast or prostate cancer reported better communication and patient involvement and information and services provision (

conclusionThe patient care experience varies across the NCCI indicators by sociodemographic and clinical factors that likely reflect healthcare system biases. Perceptions about communication and involvement appear most critical for optimal outcomes and should be a priority action area for cancer control.

Indexed as

Cancer SurvivorsNeoplasmsAustraliaCross-Sectional StudiesHumansMalePatient Outcome AssessmentQuality of LifeQueenslandadult oncologyhealth services administration & managementorganisation of health servicesquality in health care

Identifiers

PMID33619187
PMCPMC7903096

What OpenQuestion holds

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LicenceCC BY-NC
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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.