Evidence map›Paper›PMID 27075933›Full record

ReviewNephrology (Carlton, Vic.)2016

An expanded nationwide view of chronic kidney disease in Aboriginal Australians.

Wendy E Hoy, Susan A Mott, Stephen P Mc Donald

Erratum issuedOpen access · bronzeAbstract readReview
In one paragraph

Review in Nephrology (Carlton, Vic.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
4.4field-weighted citation impact, top 6% of its field
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

25 citing papers in PubMed, 66 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Supporting equitable access to kidney transplant in remote Western Australia using continuous quality improvement.International journal for quality in health care : journal of the International Society for Quality in Health Care · 2025
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Kidney failure in Samoa.The Lancet regional health. Western Pacific · 2020
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Observational
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Wendy E HoyCentre for Chronic Disease, School of Medicine, The University of Queensland, St Lucia, Queensland, Australia. w.hoy@uq.edu.au.
Susan A MottCentre for Chronic Disease, School of Medicine, The University of Queensland, St Lucia, Queensland, Australia.
Stephen P Mc DonaldUniversity of Adelaide and Australia and New Zealand Dialysis and Transplant Registry (ANZDATA), Adelaide, South Australia, Australia.
The University of Queensland · AUAustralia and New Zealand Dialysis and Transplant Registry · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We summarize new knowledge that has accrued in recent years on chronic kidney disease (CKD) in Indigenous Australians. CKD refers to all stages of preterminal kidney disease, including end-stage kidney failure (ESKF), whether or not a person receives renal replacement therapy (RRT). Recently recorded rates of ESKF, RRT, non-dialysis CKD hospitalizations and CKD attributed deaths were, respectively, more than sixfold, eightfold, eightfold and threefold those of non-Indigenous Australians, with age adjustment, although all except the RRT rates are still under-enumerated. However, the nationwide average Indigenous incidence rate of RRT appears to have stabilized. The median age of Indigenous people with ESKF was about 30 years less than for non-Indigenous people, and 84% of them received RTT, while only half of non-Indigenous people with ESKF did so. The first-ever (2012) nationwide health survey data showed elevated levels of CKD markers in Indigenous people at the community level. For all CKD parameters, rates among Indigenous people themselves were strikingly correlated with increasing remoteness of residence and socio-economic disadvantage, and there was a female predominance in remote areas. The burden of renal disease in Australian Indigenous people is seriously understated by Global Burden of Disease Mortality methodology, because it employs underlying cause of death only, and because deaths of people on RRT are frequently attributed to non-renal causes. These data give a much expanded view of CKD in Aboriginal people. Methodologic approaches must be remedied for a full appreciation of the burden, costs and outcomes of the disease, to direct appropriate policy development.

Indexed as

Health Services, IndigenousKidney Failure, ChronicRenal Replacement TherapyAustraliaHealth Services AccessibilityHumansIncidencePopulation GroupsQuality ImprovementSurvival Analysischronic kidney diseaseIndigenous Australiankidney failurerenal replacement therapy

Identifiers

PMID27075933
PMCPMC5157727
OpenAlexW2342205587

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.