Evidence map›Paper›PMID 31250206›Full record

ArticlePediatric nephrology (Berlin, Germany)2019

LDL-apheresis-induced remission of focal segmental glomerulosclerosis recurrence in pediatric renal transplant recipients.

Lokesh Shah, David K Hooper, Daryl Okamura, Dean Wallace, Divya Moodalbail, Caroline Gluck, Ania Koziell, Joshua J Zaritsky

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Pediatric nephrology (Berlin, Germany), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 3 pooled it
4.0field-weighted citation impact, top 6% 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

17 citing papers in PubMed, 3 syntheses or guidelines pooled it, 43 citations in OpenAlex.

  1. Pooled it
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  6. Safety and Efficacy of Therapeutic Plasma Exchange in Pediatric Non-Neurological Diseases.International journal of nephrology and renovascular disease · 2026
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  13. Favorable therapeutic efficacy of low-density lipoprotein apheresis for nephrotic syndrome with impaired renal function.Therapeutic apheresis and dialysis : official peer-reviewed journal of the International Society for Apheresis, the Japanese Society for Apheresis, the Japanese Society for Dialysis Therapy · 2022
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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

8 authors at 6 institutions in 3 countries.

Lokesh ShahLucile Packard Children's Hospital, Stanford University School of Medicine, 300 Pasteur Drive, G306, MC 5208, Stanford, CA, 94305, USA. Lokesh.shah.md@gmail.com.ORCID 0000-0001-5452-3796
David K HooperCincinnati Children's Hospital Medical Center, 3333 Burnet Ave, Cincinnati, OH, 45229, USA.
Daryl OkamuraSeattle Children's Hospital, 4800 Sand Point Way NE, Seattle, WA, 98105, USA.
Dean WallaceRoyal Manchester Children's Hospital, Hathersage Road, Manchester, M13 9WL, UK.
Divya MoodalbailAlfred I. duPont Hospital for Children, 1600 Rockland Rd, Wilmington, DE, 19803, USA.
Caroline GluckAlfred I. duPont Hospital for Children, 1600 Rockland Rd, Wilmington, DE, 19803, USA.
Ania KoziellKing's College London, Guy's Hospital, Great Maze Pond, London, SE1 9RT, UK.
Joshua J ZaritskyAlfred I. duPont Hospital for Children, 1600 Rockland Rd, Wilmington, DE, 19803, USA.
Alfred I. duPont Hospital for Children · USCincinnati Children's Hospital Medical Center · USGuy's Hospital · GBLucile Packard Children's Hospital · USRoyal Manchester Children's Hospital · GBSeattle Children's Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFocal segmental glomerulosclerosis (FSGS) in pediatric patients is typically difficult to treat and will progress to end-stage renal disease (ESRD) in about 10% of cases. Following kidney transplantation, FSGS can recur in up to 56% of renal allografts-with a near 100% recurrence in subsequent transplants.

methodsFour different pediatric centers across the USA and the UK employed a protocol using LDL-apheresis (LDL-A) and pulse solumedrol to treat recurrent FSGS after transplantation in seven patients. All the patients included in this series demonstrated immediate, or early, recurrence of FSGS, which clinically presented as nephrotic-range proteinuria within hours to days after implantation of the kidney.

resultsAll patients experienced reductions in urinary protein to creatinine ratios resulting in partial or complete remission. All patients demonstrated improvements in their estimated GFRs at their most recent follow-up since LDL-A discontinuation.

conclusionsThis case series describes the successful treatment, across four different pediatric centers, of seven pediatric patients with recurrent post-transplant FSGS using the Liposorber® LA-15 in combination with pulse solumedrol.

Indexed as

Kidney TransplantationAllograftsBlood Component RemovalChildChild, PreschoolCombined Modality TherapyCreatinineDisease ProgressionFemaleFollow-Up StudiesGlomerular Filtration RateGlomerulosclerosis, Focal SegmentalHumansInfantKidney Failure, ChronicKidney GlomerulusCreatinineLipoproteins, LDLMethylprednisolone HemisuccinateEnd-stage renal disease (ESRD)Focal segmental glomerulosclerosis (FSGS)Lipoprotein LDL-apheresis (LDL-A)Plasma exchange (PE)Steroid-resistant nephrotic syndrome (SRNS)

Identifiers

PMID31250206
OpenAlexW2953592240

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.