Evidence map›Paper›PMID 30552564›Full record

ArticlePediatric nephrology (Berlin, Germany)2019

Five-year outcome of children with idiopathic nephrotic syndrome: the NEPHROVIR population-based cohort study.

Claire Dossier, Jean-Daniel Delbet, Olivia Boyer, Patrick Daoud, Bettina Mesples, Beatrice Pellegrino, Helène See, Gregoire Benoist, Anne Chace, Anis Larakeb and 2 more

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Pediatric nephrology (Berlin, Germany), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

22 citing papers in PubMed, 40 citations in OpenAlex.

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  19. Podocytopathies.Nature reviews. Disease primers · 2020
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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

12 authors at 8 institutions in 1 country.

Claire DossierDepartment of Pediatric Nephrology, Hôpital Armand-Trousseau, APHP, Paris, France. claire.dossier@aphp.fr.ORCID 0000-0001-7918-2879
Jean-Daniel DelbetDepartment of Pediatric Nephrology, Hôpital Armand-Trousseau, APHP, Paris, France.
Olivia BoyerDepartment of Pediatric Nephrology, Hôpital Necker-Enfants-Malades, APHP, Paris, France.
Patrick DaoudDepartment of Pediatrics and Neonatology, Centre Hospitalier Intercommunal André-Grégoire, Montreuil, France.
Bettina MesplesDepartment of Pediatrics, Hôpital Louis-Mourier, APHP, Colombes, France.
Beatrice PellegrinoDepartment of Pediatrics, CH Francois-Quesnay, Mantes-La-Jolie, France.
Helène SeeDepartment of Pediatrics, Centre Hospitalier Intercommunal Robert-Ballanger, Aulnay Sous Bois, France.
Gregoire BenoistDepartment of Pediatrics, Hôpital Ambroise-Paré, APHP, Boulonge-Billancourt, France.
Anne ChaceDepartment of Pediatrics, Centre Hospitalier Intercommunal de Villeneuve Saint-Georges, Villeneuve Saint-Georges, France.
Anis LarakebDepartment of Pediatrics, Centre Hospitalier de Meaux, Meaux, France.
Julien HoganDepartment of Pediatric Nephrology, Hôpital Robert-Debré, APHP, 48 Bd Serurier, 75019, Paris, France.
Georges DeschênesDepartment of Pediatric Nephrology, Hôpital Robert-Debré, APHP, 48 Bd Serurier, 75019, Paris, France.
Assistance Publique – Hôpitaux de Paris · FRSorbonne Université · FRCentre Hospitalier Intercommunal André Grégoire Montreuil · FRCentre Hospitalier Intercommunal de Villeneuve-Saint-Georges · FRCentre hospitalier Robert-Ballanger · FRHôpital Ambroise-Paré · FRHôpital Louis-Mourier · FRHôpital Necker-Enfants Malades · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe optimal therapeutic regimen for children at onset of idiopathic nephrotic syndrome (INS) is still under debate. A better knowledge of the disease's course is necessary to design more appropriate and/or personalized treatment protocols.

methodsWe report the 5-year outcome of patients included from December 2007 to May 2010 in the prospective multicentric and multiethnic population-based NEPHROVIR study. Patients were treated at onset according to the French steroid protocol (3990 mg/m

resultsOut of the 188 children with nephrotic syndrome (121 boys, 67 girls; median age 4.1 years), 174 (93%) were steroid-sensitive. Six percent of steroid-sensitive patients required intravenous steroid pulses to get into remission. Relapse-free rate for steroid-sensitive patients was 21% (36/174) at last follow-up (median 72 months). A first relapse occurred in138 steroid sensitive patients (79%) with a median time of 8.3 months (IQ 3.4-11.3). Out of the 138 relapsers, 43 were frequent relapsers. Age at onset below 4 years was the only predictive factor of relapse, while gender, ethnicity, and delay to first remission were not. At 96 months of follow-up, 83% of frequent relapsers were still under steroids and/or immunosuppressive drugs.

conclusionsThe treatment of the first flare deserves major improvements in order to reduce the prevalence of relapsers and the subsequent long-lasting exposure to steroids and immunosuppression.

Indexed as

Administration, IntravenousAdolescentCase-Control StudiesChildChild, PreschoolFemaleFranceHumansImmunosuppressive AgentsIncidenceInfantMaleNephrotic SyndromeProspective StudiesPulse Therapy, DrugRecurrenceImmunosuppressive AgentsSteroidsChildrenFrequent relapserImmunosuppressive drugMethylprednisolone pulseNephrotic syndromeNephrovirSteroid-sensitive

Identifiers

PMID30552564
OpenAlexW2905370020

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.