Evidence map›Paper›PMID 34224002›Full record

ArticlePediatric nephrology (Berlin, Germany)2022

To biopsy or not to biopsy: Henoch-Schönlein nephritis in children, a 5-year follow-up study.

Marina Avramescu, Annie Lahoche, Julien Hogan, Rémi Salomon, Gwenaëlle Roussey, Justine Bacchetta, Stéphane Decramer, Tim Ulinski, Coralie Barbe, Christine Pietrement

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Pediatric nephrology (Berlin, Germany), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 22% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Guideline
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  4. Review
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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 8 institutions in 1 country.

Marina AvramescuService de Néphrologie Pédiatrique, AP-HP, Hôpital Universitaire Necker-Enfants Malades, Paris, France.
Annie LahocheService de Néphrologie Pédiatrique, Hôpital Jeanne de Flandre, Centre Hospitalier Régional Universitaire de Lille, Lille, France.
Julien HoganService de Néphrologie Pédiatrique, AP-HP, Hôpital Universitaire Robert Debré, Paris, France.
Rémi SalomonService de Néphrologie Pédiatrique, AP-HP, Hôpital Universitaire Necker-Enfants Malades, Paris, France.
Gwenaëlle RousseyService de Néphrologie Pédiatrique, Centre Hospitalier Universitaire de Nantes, Nantes, France.
Justine BacchettaService de Néphrologie Pédiatrique, Hôpital Femme Mère Enfants, Bron, Lyon, France.
Stéphane DecramerService de Néphrologie Pédiatrique, Centre Hospitalier Universitaire de Toulouse, Toulouse, France.
Tim UlinskiService de Néphrologie Pédiatrique, AP-HP, Hôpital Universitaire Armand Trousseau, Paris, France.
Coralie BarbeNéphrologie Pédiatrique, CHU Reims, 45 rue Cognacq Jay, 51092, Reims CEDEX, France.
Christine PietrementNéphrologie Pédiatrique, CHU Reims, 45 rue Cognacq Jay, 51092, Reims CEDEX, France. cpietrement@chu-reims.fr.ORCID http://orcid.org/0000-0002-3234-5105
Centre Hospitalier Universitaire de Reims · FRHôpital Necker-Enfants Malades · FRAssistance Publique – Hôpitaux de Paris · FRCentre Hospitalier Universitaire de Nantes · FRCentre Hospitalier Universitaire de Toulouse · FRHôpital Femme Mère Enfant · FRHôpital Jeanne de Flandre · FRSorbonne Université · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe prognosis of Henoch-Schönlein purpura (HSP), IgA vasculitis, depends on kidney involvement. There is no consensus on the initiation of treatment for HSP nephritis (HSPN). Some centres start treatment before performing a kidney biopsy (KB) while in others, treatment is dictated by the importance of the clinical, biological and histological signs. The aim of this study was to evaluate which of these two approaches is associated with a better kidney outcome at 5-year follow-up.

methodsThis multicentre, retrospective, nonrandomised study included children treated for HSPN between 2006 and 2010 in a French paediatric nephrology unit. One group had an early KB at diagnosis (before starting treatment or in the 15 following days). In the second group, initial treatment was decided without performing a KB.

resultsAmong the 107 children included, 63.5% had an early KB at diagnosis. Follow-up at 5 years was completed in 44 children (28 KB at diagnosis, 16 no KB at diagnosis). Median urine protein/creatinine at 5 years was 2.5 mg/mmol in the early biopsy diagnosis group and 12.5 mg/mmol in the non-biopsy group. An antiproteinuric treatment was given, at 5 years, to 35.7% of the early biopsy at diagnosis children and in 62.5% of the non-biopsied children.

conclusionsChildren with early KB at diagnosis seem to have a better renal outcome at 5 years compared to those without an early biopsy at diagnosis or biopsied later. However, this is a small patient cohort and data are missing. Further work is needed to build consensual guidelines on the management of HSPN in children.

Indexed as

NephritisBiopsyChildFollow-Up StudiesHumansRetrospective StudiesHenoch-Schönlein purpuraIgA vasculitisKidney biopsyNephropathyProteinuria

Identifiers

PMID34224002
OpenAlexW3181876865

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.