Evidence map›Paper›PMID 24458086›Full record

ArticleClinical journal of the American Society of Nephrology : CJASN2014

A predictive model of progression of CKD to ESRD in a predialysis pediatric interdisciplinary program.

Debora C Cerqueira, Cristina M Soares, Vanessa R Silva, Juliana O Magalhães, Isabella P Barcelos, Mariana G Duarte, Sergio V Pinheiro, Enrico A Colosimo, Ana Cristina Simões e Silva, Eduardo A Oliveira

Open access · hybridAbstract read
In one paragraph

Article in Clinical journal of the American Society of Nephrology : CJASN, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
8.6field-weighted citation impact, top 3% 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

19 citing papers in PubMed, 49 citations in OpenAlex.

  1. Review
  2. Review
  3. Chronic kidney disease in children: an update.Clinical kidney journal · 2023
    Review
  4. Article
  5. Kidney medicine · 2022
    Article
  6. Article
  7. Epidemiology and Outcome of CKD in Omani Children.Kidney international reports · 2019
    Article
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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 at 1 institution in 1 country.

Debora C CerqueiraDepartment of Pediatrics, Pediatric Nephrourology Unit,, †Nutrition Division, and, ‡Department of Statistics, National Institute of Science and Technology of Molecular Medicine, Faculty of Medicine, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Cristina M Soares
Vanessa R Silva
Juliana O Magalhães
Isabella P Barcelos
Mariana G Duarte
Sergio V Pinheiro
Enrico A Colosimo
Ana Cristina Simões e Silva
Eduardo A Oliveira
Universidade Federal de Minas Gerais · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesThe incidence of ESRD in children has increased over the last two decades. Nevertheless, there are still limited data on risk factors related to the emergence of ESRD among patients with CKD. The aim of this study was to develop a model of prediction of ESRD in children and adolescents with CKD (stages 2-4) enrolled in a predialysis interdisciplinary management program. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: In this retrospective cohort study, 147 patients with CKD admitted from 1990 to 2008 were systematically followed up at a tertiary pediatric nephrology unit for a median of about 4.5 years. The primary outcome was the progression to CKD stage 5. A predictive model was developed using Cox proportional hazards model and evaluated by c statistics.

resultsThe median renal survival was estimated at 98.7 months (95% confidence interval [95% CI], 68.7 to 129.6 months). The probability of reaching CKD stage 5 was estimated as 52% in 10 years. The most accurate model included eGFR, proteinuria at admission, and primary renal disease. Risk score ranged from 0 to 13 points (median, 4 points). The accuracy of the score applied to the sample was high, with c statistics of 0.865 (95% CI, 0.80 to 0.93) and 0.837 (95% CI, 0.76 to 0.91) at follow-up of 2 and 5 years, respectively. By survival analysis, it was estimated that at 10 years after admission, the probability of renal survival was about 63% for patients in the low-risk group and 43% for the medium-risk group; all patients assigned to the high-risk group had CKD stage 5 (P<0.001).

conclusionThe predictive model of progression of CKD might contribute to early identification of a subgroup of patients at high risk for accelerated renal failure.

Indexed as

AdolescentAge FactorsChildChild, PreschoolDisease ProgressionEarly DiagnosisFemaleGlomerular Filtration RateHumansInfantInfant, NewbornKaplan-Meier EstimateKidneyKidney Failure, ChronicMaleMultivariate Analysischronic kidney diseaseend-stage renal diseaseglomerulonephritispediatric nephrology

Identifiers

PMID24458086
PMCPMC3974357
OpenAlexW2103456128

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.