Evidence map›Paper›PMID 39221095›Full record

ArticleWorld journal of hepatology2024

Successful treatment of acute liver failure due to Wilson's disease: Serendipity or fortuity?

Valeria Delle Cave, Fabiola Di Dato, Pier Luigi Calvo, Maria Immacolata Spagnuolo, Raffaele Iorio

Abstract read
In one paragraph

Article in World journal of hepatology, 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. 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.

Valeria Delle CaveDepartment of Translational Medical Science, Section of Pediatrics, University of Naples Federico II, Naples 80131, Italy.
Fabiola Di DatoDepartment of Translational Medical Science, Section of Pediatrics, University of Naples Federico II, Naples 80131, Italy.
Pier Luigi CalvoPediatric Gastroenterology Unit, Regina Margherita Children's Hospital, Azienda Ospedaliera-Universitaria Città della Salute e della Scienza, Turin 10126, Italy.
Maria Immacolata SpagnuoloDepartment of Translational Medical Science, Section of Pediatrics, University of Naples Federico II, Naples 80131, Italy.
Raffaele IorioDepartment of Translational Medical Science, Section of Pediatrics, University of Naples Federico II, Naples 80131, Italy. riorio@unina.it.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAcute liver failure (ALF) may be the first and most dramatic presentation of Wilson's disease (WD). ALF due to WD (WD-ALF) is difficult to distinguish from other causes of liver disease and is a clear indication for liver transplantation. There is no firm recommendation on specific and supportive medical treatment for this condition.

aimTo critically evaluate the diagnostic and therapeutic management of WD-ALF patients in order to improve their survival with native liver.

methodsA retrospective analysis of patients with WD-ALF was conducted in two pediatric liver units from 2018 to 2023.

resultsDuring the study period, 16 children (9 males) received a diagnosis of WD and 2 of them presented with ALF. The first was successfully treated with an unconventional combination of low doses of D-penicillamine and zinc plus steroids, and survived without liver transplant. The second, exclusively treated with supportive therapy, needed a hepatotransplant to overcome ALF.

conclusionSuccessful treatment of 1 WD-ALF patient with low-dose D-penicillamine and zinc plus steroids may provide new perspectives for management of this condition, which is currently only treated with liver transplantation.

Indexed as

24 hour-urinary copper excretionAutoimmune hepatitisChelatorCopperFulminant liver failureLiver transplantationNative liverPrognostic scoreSteroidsZinc

Identifiers

PMID39221095
PMCPMC11362907

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.