Evidence map›Paper›PMID 35469261›Full record

ArticleInternational journal of general medicine2022

Pathological and Evolutive Correlations in Steroid Resistant Nephrotic Syndrome in Children.

Iuliana Magdalena Starcea, Roxana Alexandra Bogos, Georgiana Scurtu, Mihaela Munteanu, Radu Russu, Vasile Valeriu Lupu, Ancuta Lupu, Laura Trandafir, Ingrith Crenguta Miron, Maria Adriana Mocanu

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In one paragraph

Article in International journal of general medicine, 2022. 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
0.4field-weighted citation impact, top 41% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Review
  3. A rare cause of steroid-resistant nephrotic syndrome - a case report.Central-European journal of immunology · 2023
    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

10 authors at 2 institutions in 1 country.

Iuliana Magdalena StarceaPediatrics Department, "Grigore T. Popa" University of Medicine and Pharmacy, Iasi, Romania.
Roxana Alexandra BogosPediatrics Department, "Grigore T. Popa" University of Medicine and Pharmacy, Iasi, Romania.
Georgiana ScurtuPediatrics Department, "Grigore T. Popa" University of Medicine and Pharmacy, Iasi, Romania.
Mihaela MunteanuNephrology Division, St. Mary's Emergency Children Hospital, Iasi, Romania.
Radu RussuNephrology Division, St. Mary's Emergency Children Hospital, Iasi, Romania.
Vasile Valeriu LupuPediatrics Department, "Grigore T. Popa" University of Medicine and Pharmacy, Iasi, Romania.ORCID 0000-0003-2640-8795
Ancuta LupuPediatrics Department, "Grigore T. Popa" University of Medicine and Pharmacy, Iasi, Romania.
Laura TrandafirPediatrics Department, "Grigore T. Popa" University of Medicine and Pharmacy, Iasi, Romania.
Ingrith Crenguta MironPediatrics Department, "Grigore T. Popa" University of Medicine and Pharmacy, Iasi, Romania.
Maria Adriana MocanuPediatrics Department, "Grigore T. Popa" University of Medicine and Pharmacy, Iasi, Romania.
Grigore T. Popa University of Medicine and Pharmacy · RORomanian Academy · RO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Nephrotic syndrome (NS) is the term used for the association of edema and massive proteinuria. From a therapeutic point of view, it is important to distinguish between primitive and secondary kidney damage. The clinical evolution, prognosis and therapeutic response in the NS in children are directly determined by the anatomopathological aspect. Steroid resistant nephrotic syndrome was diagnosed in patients with idiopathic NS based on lack of complete remission despite treatment with steroids. Purpose: To analyse the anatomopathological aspects of steroid resistant nephrotic syndrome (SRNS) and their correlation with evolution. Materials and Methods: We made a retrospective study with the aim to analyze the anatomo-pathological aspects and their correlations with evolution in 68 cases of steroid resistant nephrotic syndrome (SRNS) hospitalized in the Pediatric Nephrology Department in Iaşi, Romania. We defined SRNS in all cases without response to corticosteroids after the first month of therapy. For all the cases selected, the period of follow-up was the minimal 6 months. Results and Discussions: A 36% case of nephrotic syndrome was corticoresistant, with the mean age at onset of patients with SRNS being 9.18 years, compared to KDIGO studies in which the corticosteroid resistance is 10-20%. Renal biopsy was performed in 80.88% children with SRNS and was allowed the evaluation of the activity and chronicity index. Total remission was obtained in 44.01% children with SRNS. The correlation of the anatomopathological aspects with the evolution is not statistically significant (p = 0.76), observing different therapeutic responses to all the analyzed histological types. Conclusion: Almost half of NS in children are cortico resistant. Remission was obtained in 44% of cases of SRNS. Predicting the response to long-term treatment in SRNS is difficult using only renal biopsy; it is necessary to introduce genetic molecular analyses to establish a judicious therapeutic attitude.

Indexed as

childrenevolutionnephrotic syndromesteroid resistance

Identifiers

PMID35469261
PMCPMC9034867
OpenAlexW4224252699

What OpenQuestion holds

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Registered trials

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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.