Evidence map›Paper›PMID 38212419›Full record

ArticlePediatric nephrology (Berlin, Germany)2024

Pediatric urogenital schistosomiasis diagnosed in France.

Lucas Percheron, Claire Leblanc, Tim Ulinski, Marc Fila, Denis Malvy, Justine Bacchetta, Vincent Guigonis, Cecile Debuisson, Elise Launay, Edouard Martinez and 4 more

Abstract read
PubMed Publisher
In one paragraph

Article in Pediatric nephrology (Berlin, Germany), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
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.

Lucas PercheronService de néphrologie, médecine interne pédiatrique, Hôpital des enfants, CHU de Toulouse, Avenue de grande Bretagne, 31000, Toulouse, France. percheron.l@chu-toulouse.fr.ORCID 0000-0002-2501-0462
Claire LeblancService de pédiatrie générale, maladies infectieuses et médecine interne Hôpital Robert Debré, Assistance Publique - Hôpitaux de Paris, Paris, France.
Tim UlinskiService de néphrologie et de transplantation pédiatrique, Université pierre marie curie, Assistance Publique - Hôpitaux de Paris, Paris, France.
Marc FilaService de néphrologie endocrinologie pédiatrique, Hôpital Arnaud de Villeneuve, Montpellier, France.
Denis MalvyService des maladies infectieuses et tropicales, Centre hospitalier universitaire, Bordeaux, France.
Justine BacchettaService de néphrologie rhumatologie pédiatrique, Centre hospitalier universitaire, Lyon, France.
Vincent GuigonisService de pédiatrie générale, centre hospitalier universitaire, Limoges, France.
Cecile DebuissonService de pédiatrie générale et de maladie infectieuse pédiatrique, Hôpital Purpan, Toulouse, France.
Elise LaunayService de pédiatrie générale et infectiologie pédiatrique, Centre hospitalier universitaire, Nantes, France.
Edouard MartinezService de pédiatrie, Centre hospitalier universitaire, Rouen, France.
Aurelie MorandPédiatrie spécialisée et médecine infantile, Hôpital de la Timone, AP-HM, Marseille, France.
Stéphane DecramerService de néphrologie, médecine interne pédiatrique, Hôpital des enfants, CHU de Toulouse, Avenue de grande Bretagne, 31000, Toulouse, France.
Joost-Peter SchanstraInstitut National de la Santé et de la Recherche Médicale (INSERM), U1048, Institute of Cardiovascular and Metabolic Disease, Toulouse, France.
Antoine BerryService de parasitologie-mycologie, Centre hospitalier universitaire de Toulouse, Toulouse, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSchistosomiasis affects approximately 230 million people worldwide. There is an increased incidence of schistosomiasis cases in France acquired from outside the country. This increases the risk of schistosomiasis outbreaks as observed in Corsica. Clinicians from non-endemic regions are not accustomed to diagnosing and managing this pathology. The objective of this study is to provide a better description of the clinical and paraclinical characteristics and disease evolution of affected children.

methodsThrough the French Pediatric Nephrology Society and the Pediatric Infectious Pathology Group, we contacted all French pediatric centers that may have treated children with urinary schistosomiasis between 2013 and 2019. Age, sex, comorbidities, and clinical, biological, and radiological data (at discovery and follow-up) were collected retrospectively.

resultsA total of 122 patients from 10 different centers were included. The median age was 14 years and the sex ratio M/F was 4:1. Hematuria was present in 82% of the patients while urinary tract abnormality was found in 36% of them. Fourteen patients (11%) displayed complicated forms of urinary schistosomiasis including 10 patients with chronic kidney disease. A total of 110 patients received treatment with praziquantel, which was well-tolerated and led to clinical resolution of symptoms in 98% of cases.

conclusionPatients with schistosomiasis present frequent kidney, urinary, or genital involvement. Systematic screening of patients returning from endemic areas is therefore recommended, especially since treatment with antiparasitic drugs is effective and well-tolerated. Enhancing medical knowledge of this pathology among all practitioners is essential to improve care and outcomes.

Indexed as

Schistosomiasis haematobiaAdolescentAnimalsChildFranceHematuriaHumansPraziquantelRetrospective StudiesSchistosoma haematobiumPraziquantelMigrantPediatricSchistosoma haematobiumSchistosomiasisUrogenital

Identifiers

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.