Evidence map›Paper›PMID 18560903›Full record

ArticlePediatric nephrology (Berlin, Germany)2008

Clinical outcome of children with chronic kidney disease in a pre-dialysis interdisciplinary program.

Cristina M Bouissou Soares, José Silvério S Diniz, Eleonora M Lima, Jose M Penido Silva, Gilce R Oliveira, Monica R Canhestro, Enrico A Colosimo, Ana Cristina Simoes e Silva, Eduardo A Oliveira

Abstract read
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In one paragraph

Article in Pediatric nephrology (Berlin, Germany), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

21 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Multidisciplinary Chronic Kidney Disease Clinic Practices: A Scoping Review.Canadian journal of kidney health and disease · 2019
    Article
  9. Article
  10. Observational
  11. Observational
  12. Article
  13. Article
  14. Observational
  15. Article
  16. A predictive model of progression of CKD to ESRD in a predialysis pediatric interdisciplinary program.Clinical journal of the American Society of Nephrology : CJASN · 2014
    Article
  17. Article
  18. Article
  19. Clinical course of 822 children with prenatally detected nephrouropathies.Clinical journal of the American Society of Nephrology : CJASN · 2012
    Article
  20. 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

9 authors at 2 institutions in 1 country.

Cristina M Bouissou SoaresPediatric Nephrourology Unit, Federal University of Minas Gerais (UFMG), MG, Brazil.
José Silvério S Diniz
Eleonora M Lima
Jose M Penido Silva
Gilce R Oliveira
Monica R Canhestro
Enrico A Colosimo
Ana Cristina Simoes e Silva
Eduardo A Oliveira
Universidade Federal de Minas Gerais · BRHospital das Clínicas da Universidade Federal de Minas Gerais · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The purpose of this retrospective cohort study was to describe the outcome of 107 patients with chronic kidney disease (CKD) admitted to a pre-dialysis interdisciplinary management program from 1990 to 2006. The events of interest were progression to CKD stage 5 (renal survival), patient survival, hypertension, and somatic growth. Survival was studied by the Kaplan-Meier method. Patients were classified into four groups according to their primary renal disease: congenital nephro-uropathies; glomerular diseases; cystic disease, and miscellaneous. Median follow-up time was 94 months [Interquartile (IQ) range 38-145]. The probability of reaching CKD stage 5 was estimated to be 36% by 5 years after admission. As a whole, the mean estimated glomerular filtration rate (GFR) decrease per year was 5.8 ml/min per 1.73 m(2) body surface area [standard deviation (SD) 12.4]. The glomerular diseases group showed a median rate of GFR deterioration of 10 ml/min per 1.73 m(2) per year (IQ range -24 to -5.7), whereas the median rate of GFR deterioration for the groups with cystic diseases, congenital nephro-uropathies, and miscellanea were 2.5 ml/min (IQ range -10 to +0.34), 2.2 ml/min (IQ range -5.0 to -0.52), and 0.36 ml/min (IQ range -2.5 to +2.6), respectively (P < 0.001). The results of this study support the view that children and adolescents with glomerular diseases present a faster deterioration of renal function. Therefore, patients with glomerular diseases need to be referred early to a pediatric nephrology center so that suboptimal pre-dialysis care might possibly be avoided.

Indexed as

AdolescentChildChild, PreschoolCohort StudiesDisease ProgressionFemaleFollow-Up StudiesGlomerular Filtration RateGlomerulonephritisHumansHypertension, RenalKaplan-Meier EstimateMalePatient Care TeamProteinuriaRenal Dialysis

Identifiers

PMID18560903
OpenAlexW2161778465

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.