Evidence map›Paper›PMID 31269922›Full record

ArticleBMC nephrology2019

Immunosuppressive therapy in children with primary nephrotic syndrome: single center experience, Karachi, Pakistan.

Khemchand Netaram Moorani, Harnam Moolchand Hotchandani, Aasia Mohammad Zubair, Neelesh Chander Lohana, Nanga Ram Veerwani

Open access · goldAbstract read
In one paragraph

Article in BMC nephrology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 31% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. 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

5 authors at 2 institutions in 1 country.

Khemchand Netaram MooraniDepartment of Pediatric Nephrology, National Institute of Child Health (NICH), Jinnah Sindh Medical University, Karachi, Pakistan. khemchandn@hotmail.com.ORCID 0000-0002-4692-284X
Harnam Moolchand HotchandaniDepartment of Pediatric Nephrology, The Kidney Center Postgraduate Training Institute (TKC-PGTI), Karachi, Sindh, 75500, Pakistan.
Aasia Mohammad ZubairDepartment of Pediatric Nephrology, National Institute of Child Health (NICH), Jinnah Sindh Medical University, Karachi, Pakistan.
Neelesh Chander LohanaDepartment of Pediatric Nephrology, The Kidney Center Postgraduate Training Institute (TKC-PGTI), Karachi, Sindh, 75500, Pakistan.
Nanga Ram VeerwaniDepartment of Pediatric Nephrology, The Kidney Center Postgraduate Training Institute (TKC-PGTI), Karachi, Sindh, 75500, Pakistan.
Kidney Centre · PKJinnah Sindh Medical University · PK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMajority of children with nephrotic syndrome are steroid sensitive, but treatment of difficult to treat nephrotic (frequent relapsing, steroid dependent and steroid resistant) syndrome is challenging. Low dose steroid, levamisole, cyclophosphamide (CPM), mycophenolate mofetil (MMF) and calcineurin inhibitors (CNIs) are the common options of treatment. Objective of the study was to determine the response to steroid and alternative immunosuppressive agents (ISAs) in children with difficult nephrotic syndrome (DNS).

methodsThis is a retrospective cohort study of 176 children with DNS, managed over 12 years at The Kidney Center-Postgraduate Training Institute, Karachi- Pakistan from 2005 to 2017. Initial episode was treated with daily oral prednisolone (OP) for 4-8 weeks followed by alternate day OP for 12-24 weeks. Subsequently low dose OP, levamisole (Leva)and cyclophosphamide was used for frequent relapsing (FR)/ steroid dependent (SD). All with initial steroid resistance and non- responders to leva and or cyclophosphamide were biopsied and treated with CNIs and MMF. Data was analyzed using descriptive statistics.

resultsThere were 130(73.86%) children with FR/SD and 46(26.13%) with SRNS. All children with SR (46) and 86 with FR/SD were biopsied. Minimal change disease (60.60%) and focal segmental glomerulosclerosis (FSGS 23%) were the two common lesions. Majority (73.86%) received single OP whereas divided doses were administered in 26.13% cases. Daily OP was used for 4, 6 and 8 weeks in 61.36,28.4 and10.22% respectively. Steroids were tapered over 3 (31.81%),4 (52.27%) and 6 months (15.90%). Levamisole, CPM, cyclosporin (CS) and MMF were used sequentially in 45, 54.23, 50 and 20% respectively. Combination of MMF and CS was used in 11.29% of cases. Levamisole was effective in 80%, CPM induced complete remission (CR, 57.77%) or partial remission (PR, 22.22%), CS induced CR 46.59% and PR 39.77%. MMF showed PR and CR 69 and 12.82% respectively. At last follow up, 46% were maintaining remission while off treatment, whereas 35% are maintaining remission on therapy,10.23% lost- to-follow, 5.68% progressed to chronic kidney disease. Mortality was 2.84% and it was due to infection and uremia.

conclusionMajority had steroid sensitive MCD. Levamisole and cyclophosphamide were effective in maintaining remission in FR/ SD. FSGS was responsible for resistance to steroid and alternative ISAs. Cyclosporin was effective in inducing remission in SRNS. Mortality was less than 3%.

Indexed as

Adjuvants, ImmunologicAdolescentChildChild, PreschoolCohort StudiesFemaleHumansImmunosuppression TherapyImmunosuppressive AgentsInfantMaleNephrotic SyndromePakistanRetrospective StudiesAdjuvants, ImmunologicImmunosuppressive AgentsCyclophosphamideCyclosporinLevamisoleMinimal change diseaseMycophenolate mofitilNephrotic syndromeOral prednisolone

Identifiers

PMID31269922
PMCPMC6607530
OpenAlexW2953869249

What OpenQuestion holds

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LicenceCC BY
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.