Evidence map›Paper›PMID 19714370›Full record

Trial reportPediatric nephrology (Berlin, Germany)2009

Cyclosporine and steroid therapy in children with steroid-resistant nephrotic syndrome.

Yuko Hamasaki, Norishige Yoshikawa, Shinzaburo Hattori, Satoshi Sasaki, Kazumoto Iijima, Koichi Nakanishi, Takeshi Matsuyama, Kenji Ishikura, Nahoko Yata, Tetsuji Kaneko and 2 more

Abstract readClinical TrialMulticenter Study
PubMed Publisher
In one paragraph

Trial report in Pediatric nephrology (Berlin, Germany), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 2 pooled it
2.4field-weighted citation impact, top 11% 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

36 citing papers in PubMed, 2 syntheses or guidelines pooled it, 77 citations in OpenAlex.

  1. Guideline
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  7. Review
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  13. Review
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  17. Article
  18. Rituximab for nephrotic syndrome in children.Clinical and experimental nephrology · 2017
    Review
  19. Steroid-resistant nephrotic syndrome: past and current perspectives.Pediatric health, medicine and therapeutics · 2017
    Review
  20. 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

12 authors at 5 institutions in 1 country.

Yuko HamasakiDepartment of Pediatric Nephrology, Tokyo Metropolitan Kiyose Children's Hospital, Kiyose-city, Japan. yu.hama@chp-kiyose-tokyo.jp
Norishige Yoshikawa
Shinzaburo Hattori
Satoshi Sasaki
Kazumoto Iijima
Koichi Nakanishi
Takeshi Matsuyama
Kenji Ishikura
Nahoko Yata
Tetsuji Kaneko
Masataka Honda
Japanese Study Group of Renal Disease
Tokyo Metropolitan Kiyose Children's Hospital · JPWakayama Medical University · JPKumamoto Health Science University · JPUniversity of Tokyo Health Sciences · JPHokkaido University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We conducted a prospective, multicenter trial to evaluate the efficacy and safety of a 12-month course of cyclosporine in children with steroid-resistant nephrotic syndrome (SRNS). Thirty-five patients were enrolled, of whom 28 had minimal change or diffuse mesangial proliferation (MC/DMP), and seven had focal segmental glomerulosclerosis (FSGS). All patients received cyclosporine and prednisolone; patients with FSGS additionally received methylprednisolone pulse therapy (MPT). The dose of cyclosporine was adjusted to maintain a trough level of 120-150 ng/ml during the initial 3 months of treatment, followed by 80-100 ng/ml during months 4-12. The primary end point was the remission rate at month 12. Remission was achieved in 23 of 28 (82.1%) patients in the MC/DMP group and in six of the seven (85.7%) patients in the FSGS group. Follow-up renal biopsies were performed in 26 patients (nine at month 12, 17 at month 24), and cyclosporine-related nephrotoxicity was detected in one (3.8%). Major adverse events comprised severe bacterial infections (two patients) and posterior reversible encephalopathy syndrome (one patient). In conclusion, a high remission rate was achieved in our patient cohort using a combined cyclosporine/ prednisolone treatment regimen in children with SRNS who had MC/DMP and a combined cyclosporine/prednisolone plus MPT regimen in children who had FSGS.

Indexed as

Administration, OralBiopsyChildChild, PreschoolCyclosporineDisease ProgressionDose-Response Relationship, DrugDrug Administration ScheduleDrug ResistanceDrug Therapy, CombinationFemaleFollow-Up StudiesGlucocorticoidsHumansImmunosuppressive AgentsInfusions, IntravenousCyclosporineGlucocorticoidsImmunosuppressive AgentsMethylprednisolonePrednisoloneSteroids

Identifiers

PMID19714370
OpenAlexW2083485009

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.