Evidence map›Paper›PMID 37285006›Full record

ArticleJournal of nephrology2024

Real world evaluation of kidney failure risk equations in predicting progression from chronic kidney disease to kidney failure in an Australian cohort.

Sadia Jahan, Janine Hale, Eva Malacova, Cameron Hurst, Adrian Kark, Andrew Mallett

Open access · hybridAbstract read
In one paragraph

Article in Journal of nephrology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 33% 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

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 3 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. 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

6 authors at 4 institutions in 1 country.

Sadia JahanKidney Health Service, Royal Brisbane and Women's Hospital, Herston, Brisbane, QLD, 4029, Australia.
Janine HaleKidney Health Service, Royal Brisbane and Women's Hospital, Herston, Brisbane, QLD, 4029, Australia.
Eva MalacovaQIMR Berghofer Medical Research Institute, Herston Road, Herston, Brisbane, QLD, 4029, Australia.
Cameron HurstQIMR Berghofer Medical Research Institute, Herston Road, Herston, Brisbane, QLD, 4029, Australia.
Adrian KarkKidney Health Service, Royal Brisbane and Women's Hospital, Herston, Brisbane, QLD, 4029, Australia.
Andrew MallettKidney Health Service, Royal Brisbane and Women's Hospital, Herston, Brisbane, QLD, 4029, Australia. andrew.mallett@health.qld.gov.au.ORCID 0000-0002-8752-2551
QIMR Berghofer Medical Research Institute · AURoyal Brisbane and Women's Hospital · AURoyal Adelaide Hospital · AUThe University of Queensland · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChronic kidney disease progression to kidney failure is diverse, and progression may be different according to genetic aspects and settings of care. We aimed to describe kidney failure risk equation prognostic accuracy in an Australian population.

methodsA retrospective cohort study was undertaken in a public hospital community-based chronic kidney disease service in Brisbane, Australia, which included a cohort of 406 adult patients with chronic kidney disease Stages 3-4 followed up over 5 years (1/1/13-1/1/18). Risk of progression to kidney failure at baseline using Kidney Failure Risk Equation models with three (eGFR/age/sex), four (add urinary-ACR) and eight variables (add serum-albumin/phosphate/bicarbonate/calcium) at 5 and 2 years were compared to actual patient outcomes.

resultsOf 406 patients followed up over 5 years, 71 (17.5%) developed kidney failure, while 112 died before reaching kidney failure. The overall mean difference between observed and predicted risk was 0.51% (p = 0.659), 0.93% (p = 0.602), and - 0.03% (p = 0.967) for the three-, four- and eight-variable models, respectively. There was small improvement in the receiver operating characteristic-area under the curve from three-variable to four-variable models: 0.888 (95%CI = 0.819-0.957) versus 0.916 (95%CI = 0.847-0.985). The eight-variable model showed marginal receiver operating characteristic-area under the curve improvement: 0.916 (95%CI = 0.847-0.985) versus 0.922 (95%CI = 0.853-0.991). The results were similar in predicting 2 year risk of kidney failure.

conclusionsThe kidney failure risk equation accurately predicted progression to kidney failure in an Australian chronic kidney disease population. Younger age, male sex, lower estimated glomerular filtration rate, higher albuminuria, diabetes mellitus, tobacco smoking and non-Caucasian ethnicity were associated with increased risk of kidney failure. Cause-specific cumulative incidence function for progression to kidney failure or death, stratified by chronic kidney disease stage, demonstrated differences within different chronic kidney disease stages, highlighting the interaction between comorbidity and outcome.

Indexed as

Kidney Failure, ChronicRenal InsufficiencyRenal Insufficiency, ChronicAdultAustraliaCohort StudiesDisease ProgressionGlomerular Filtration RateHumansKidney Function TestsMaleRetrospective StudiesRisk FactorsKidney failureKidney failure risk equation KFREPredict progressionProgression prediction tool

Identifiers

PMID37285006
PMCPMC10920458
OpenAlexW4379599070

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.