Evidence map›Paper›PMID 19672630›Full record

ArticlePediatric nephrology (Berlin, Germany)2009

Management patterns of childhood-onset nephrotic syndrome.

Nathaniel MacHardy, Paul V Miles, Susan F Massengill, William E Smoyer, John D Mahan, Larry Greenbaum, Sara Massie, Lynne Yao, Shashi Nagaraj, Jen-Jar Lin and 4 more

Abstract read
PubMed Publisher
In one paragraph

Article in Pediatric nephrology (Berlin, Germany), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 3 pooled it
1.5field-weighted citation impact, top 18% 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

34 citing papers in PubMed, 3 syntheses or guidelines pooled it, 54 citations in OpenAlex.

  1. Corticosteroid therapy for nephrotic syndrome in children.The Cochrane database of systematic reviews · 2024
    Pooled it
  2. Corticosteroid therapy for nephrotic syndrome in children.The Cochrane database of systematic reviews · 2020
    Pooled it
  3. Corticosteroid therapy for nephrotic syndrome in children.The Cochrane database of systematic reviews · 2015
    Pooled it
  4. Trial
  5. Trial
  6. Trial
  7. Extending prednisolone treatment does not reduce relapses in childhood nephrotic syndrome.Journal of the American Society of Nephrology : JASN · 2013
    Trial
  8. Trial
  9. Observational
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  12. Article
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  15. Atopic dermatitis as a risk factor for severe visual field loss in youth-a retrospective cohort study of glaucoma under steroid treatment.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2021
    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

14 authors at 11 institutions in 1 country.

Nathaniel MacHardyUniversity of North Carolina at Chapel Hill, 27599-7155, USA.
Paul V Miles
Susan F Massengill
William E Smoyer
John D Mahan
Larry Greenbaum
Sara Massie
Lynne Yao
Shashi Nagaraj
Jen-Jar Lin
Delbert Wigfall
Howard Trachtman
Yichun Hu
Debbie S Gipson
University of North Carolina at Chapel Hill · USAmerican Academy of Pediatrics · USChildren's Healthcare of Atlanta · USDuke Medical Center · USInova Children's Hospital · USLevine Children's Hospital · USNationwide Children's Hospital · USSchneider Children's Hospital · USUniversity Medical Center · USUniversity of Michigan–Ann Arbor · USWake Forest University · US

Funding

RATIONAL THERAPEUTICS FOR THE PEDIATRIC POPULATIONU18HS010397 · AHRQ · UNIV OF NORTH CAROLINA CHAPEL HILL · PI STILES, ALAN D · 1999 to 2006
$782k
AHRQ HHS U18HS10397-08
6 · The paper itself

Abstract

As an initial effort to identify opportunities to improve the management of children with nephrotic syndrome, the goal of this study was to assess the present-day management of children with primary nephrotic syndrome. A web-based survey was designed to assess the current management styles of all pediatric nephrology faculties at ten participating institutions. Ninety-one percent completed the initial survey. The duration of initial glucocorticoid therapy ranged from 4 to 24 weeks. Physicians reported that the recommendation for kidney biopsy was dependent on the response to initial corticosteroid therapy, with the minority always recommending a biopsy for frequently relapsing or steroid-dependent cases. All responding physicians recommended a kidney biopsy in steroid-resistant cases. Treatment strategies were reported to vary based upon the steroid response pattern and, where available, kidney histopathology. Striking variations in therapeutic preferences were described when alternatives to glucocorticoids were considered. The variability of management practices among pediatric nephrologists in the USA combined with the changing characteristics of our pediatric population raise concerns about our future strategies for improving healthcare for children coping with nephrotic syndrome. This variability is not unique to children's healthcare or to nephrology. However, a systematic approach to patient care and improvement in health outcomes has been shown to substantially improve morbidity and mortality outcomes in children with chronic health conditions.

Indexed as

Age of OnsetBiopsyChildData CollectionDrug ResistanceFemaleGlucocorticoidsHumansImmunosuppressive AgentsInternetKidneyMaleMulticenter Studies as TopicNephrologyNephrotic SyndromeRecurrenceGlucocorticoidsImmunosuppressive AgentsSteroids

Identifiers

PMID19672630
OpenAlexW1965888315

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.