Evidence map›Paper›PMID 37154959›Full record

Observational studyPediatric nephrology (Berlin, Germany)2023

Outcome of children with IgA vasculitis with nephritis treated with steroids: a matched controlled study.

Anne-Lise Mary, Stéphanie Clave, Caroline Rousset-Rouviere, Etienne Berard, Olivia Boyer, Stéphane Decramer, Marc Fila, Vincent Guigonis, Sylvie Cloarec, Jérôme Harambat and 7 more

Abstract readObservational Study
PubMed Publisher
In one paragraph

Observational study in Pediatric nephrology (Berlin, Germany), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 25% 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

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

  1. Guideline
  2. 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

17 authors at 14 institutions in 1 country.

Anne-Lise MaryIntensive Care Unit, Armand Trousseau Hospital, AP-HP, 75012, Paris, France.
Stéphanie ClaveDepartment of Multidisciplinary Pediatrics, Pediatric Nephrology Unit, Assistance Publique Des Hôpitaux de Marseille, Marseille, France.
Caroline Rousset-RouviereDepartment of Multidisciplinary Pediatrics, Pediatric Nephrology Unit, Assistance Publique Des Hôpitaux de Marseille, Marseille, France.
Etienne BerardDepartment of Pediatrics, Hôpital de L'Archet, University Hospital of Nice, Nice, France.
Olivia BoyerDepartment of Pediatric Nephrology, Reference Center for Idiopathic Nephrotic Syndrome in Children and Adults, Necker Hospital, APHP, 75015, Paris, France.
Stéphane DecramerDepartment of Pediatric Nephrology, Hôpital Des Enfants, Reference Center for Rare Kidney Diseases SORARE, University Hospital of Toulouse, Toulouse, France.
Marc FilaDepartment of Pediatric Nephrology, Reference Center for Rare Kidney Diseases SORARE, Hôpital Arnaud-de-Villeneuve, University Hospital of Montpellier, Montpellier, France.
Vincent GuigonisDepartment of Pediatrics, Hôpital Mère-Enfant, University Hospital of Limoges, Reference Center for Rare Kidney Diseases SORARE, Limoges, France.
Sylvie CloarecDepartment of Pediatric Nephrology and Hemodialysis, Clocheville Hospital, University Hospital of Tours, Tours, France.
Jérôme HarambatDepartment of Pediatrics, Hôpital Pellegrin-Enfants, University Hospital of Bordeaux, Reference Center for Rare Kidney Diseases SORARE, Bordeaux, France.
Julien HoganPediatric Nephrology Department, Robert Debré Hospital, APHP and French Reference Center for Rare Diseases (CRMR) Idiopathic Nephrotic Syndrome, Paris, France.
Annie LahochePediatric Nephrology Unit Jeanne de Flandre Hospital, Regional University Hospital of Lille, Lille, France.
Gwenaelle Roussey-KeslerPediatric Department, Nantes University Hospital, Nantes, France.
Ariane ZaloszycDepartment of Pediatrics 1, University Hospital of Strasbourg, Strasbourg, France.
Tim UlinskiPediatric Nephrology Department, Armand Trousseau Hospital, DMU Origyne, APHP and French Reference Center for Rare Diseases MARHEA, Paris, France.
Cyrielle ParmentierPediatric Nephrology Department, Armand Trousseau Hospital, DMU Origyne, APHP and French Reference Center for Rare Diseases MARHEA, Paris, France.
Jean-Daniel DelbetPediatric Nephrology Department, Armand Trousseau Hospital, DMU Origyne, APHP and French Reference Center for Rare Diseases MARHEA, Paris, France. jean-daniel.delbet@aphp.fr.ORCID http://orcid.org/0000-0002-9892-5663
Sorbonne Université · FRAssistance Publique Hôpitaux de Marseille · FRAssistance Publique – Hôpitaux de Paris · FRCentre Hospitalier Universitaire de Montpellier · FRHôpital des Enfants · FRHôpital Jeanne de Flandre · FRHôpital l'Archet · FRHôpital Mère-Enfant · FRHôpital Necker-Enfants Malades · FRHôpital Pellegrin · FRNantes Université · FRUniversité de Strasbourg · FRUniversité de Tours · FRUniversité Sorbonne Nouvelle · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIgA vasculitis (IgAV) is the most common vasculitis in children. IgAV long-term prognosis depends on kidney involvement or IgA vasculitis with nephritis (IgAVN). To date, steroid treatment (oral steroids or methylprednisolone pulses) has not proven to be formally efficient. This study aimed to assess the role of steroids on IgAVN outcome.

methodsAll children with IgAVN diagnosed 2000-2019 in 14 French pediatric nephrology units with minimal follow-up of 6 months were retrospectively included. Outcomes of patients treated with steroids were compared with those of a control group of untreated patients matched for age, sex, proteinuria, eGFR, and histological features. The primary endpoint was IgAVN remission defined as urine protein-to-creatinine ratio < 20 mg/mmol without impaired eGFR one year after disease onset.

resultsA total of 359 patients with IgAVN were included with a median follow-up time of 249 days (range 43-809). One hundred eight (30%) patients received oral steroids alone, 207 (51%) patients received three methylprednisolone pulses followed by oral steroids, and 44 patients (12.5%) did not receive steroids. Thirty-two children treated with oral steroids alone were compared with 32 matched control patients who did not receive steroids. One year after disease onset, IgAVN remission proportion was not different between these two groups: 62% versus 68%, respectively. Ninety-three children treated with oral steroids alone were compared with 93 matched patients treated with three methylprednisolone pulses followed by oral corticosteroids. IgAVN remission proportion was not different between these two groups: 77% versus 73%, respectively.

conclusionThe benefit of oral steroids alone and methylprednisolone pulses could not be established based on this observational study. Randomized controlled trials are thus required to determine the efficacy of steroids in IgAVN. A higher resolution version of the Graphical abstract is available as Supplementary information.

Indexed as

IgA VasculitisNephritisChildHumansImmunoglobulin AKidneyMethylprednisoloneRetrospective StudiesImmunoglobulin AMethylprednisoloneHenoch–Schonlein purpura nephritisIgA vasculitis with nephritisRenal outcomeSteroids

Identifiers

PMID37154959
OpenAlexW4375850366

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.