Evidence map›Paper›PMID 34231051›Full record

ArticleEuropean journal of pediatrics2022

Non-invasive assessment of liver abnormalities in pediatric Fontan patients.

Ruth De Bruyne, Kristof Vandekerckhove, Hazel Van Overschelde, Fabian Hendricx, Caroline Vande Walle, Katya De Groote, Joseph Panzer, Daniel De Wolf, Stephanie Van Biervliet, Thierry Bové and 1 more

Open access · greenAbstract read
PubMed Publisher
In one paragraph

Article in European journal of pediatrics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

10 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Observational
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. 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

11 authors at 1 institution in 1 country.

Ruth De BruyneDepartment of Pediatric Gastroenterology, Hepatology and Nutrition, Ghent University Hospital, Ghent University, Ghent, Belgium. ruth.debruyne@uzgent.be.ORCID http://orcid.org/0000-0002-5623-3300
Kristof VandekerckhoveDepartment of Pediatric Cardiology, Ghent University Hospital, Ghent University, Ghent, Belgium.
Hazel Van OverscheldeDepartment of Pediatrics, Ghent University Hospital, Ghent, Belgium.
Fabian HendricxDepartment of Pediatrics, University Hospital Brussels, Brussels, Belgium.
Caroline Vande WalleDepartment of Pediatric Radiology, Ghent University Hospital, Ghent, Belgium.
Katya De GrooteDepartment of Pediatric Cardiology, Ghent University Hospital, Ghent University, Ghent, Belgium.
Joseph PanzerDepartment of Pediatric Cardiology, Ghent University Hospital, Ghent University, Ghent, Belgium.
Daniel De WolfDepartment of Pediatric Cardiology, Ghent University Hospital, Ghent University, Ghent, Belgium.
Stephanie Van BiervlietDepartment of Pediatric Gastroenterology, Hepatology and Nutrition, Ghent University Hospital, Ghent University, Ghent, Belgium.
Thierry BovéDepartment of Cardiac Surgery, Ghent University Hospital, Ghent University, Ghent, Belgium.
Katrien FrançoisDepartment of Cardiac Surgery, Ghent University Hospital, Ghent University, Ghent, Belgium.
Ghent University Hospital · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Liver abnormalities are well known among long-term survivors of Fontan palliation, which remains the definite surgery for complex congenital heart disease and single ventricle physiology. Pediatric data however are scarce. We assessed the prevalence and degree of liver abnormalities in pediatric Fontan patients through non-invasive investigations suitable for longitudinal follow-up. Thirty-five patients with a median age of 11.8 years (5.2-16.6) and median time since Fontan of 6 years (1.17-13.83) were studied. Each child underwent a blood test, liver Doppler ultrasound (US), and transient elastography (TE). Healthy children were used as controls for TE measurement. AST, ALT, γGT, and direct bilirubin were abnormal in respectively 12 (34%), 5 (14%), 24 (69%), and 7 (20%) patients, while platelet count was decreased in 7 (20%). Splenomegaly was present in 7 (20%) patients. Portal vein mean flow velocity was < 15 cm/s in 19 (54%) patients indicative of portal hypertension. Twenty-two patients (63%) showed inferior vena cava collapsibility index values below 17%, indicating venous congestion. Hepatic artery and superior mesenteric artery resistance index were inversely correlated with time post Fontan (p < 0.05). TE values in Fontan patients were significantly higher than controls, with a median of 12.6 versus 4.6 kPa (p < 0.001) and were already increased shortly after Fontan completion. Conclusion: Liver abnormalities are frequently observed in pediatric Fontan patients. The non-invasive investigations used were not able to confirm liver fibrosis or differentiate hepatic congestion from fibrosis. Based on our findings, we propose a prospective screening protocol with serial measurements of laboratory, (Doppler) US, and TE parameters. What is Known: • Hepatic dysfunction is a well-known consequence of the Fontan circulation. • The natural history of Fontan-associated liver disease in the pediatric age group remains unclear. What is New: • Liver abnormalities are frequently observed in pediatric Fontan patients; however, differentiating liver fibrosis and hepatic congestion with non-invasive investigations remains challenging. Sonographic Doppler measurements may improve our insight in both Fontan-associated liver disease development and the functioning of the Fontan circulation. • A prospective screening protocol is proposed to improve our ability to detect Fontan-associated liver disease early on and understand its natural history.

Indexed as

Elasticity Imaging TechniquesFontan ProcedureHeart Defects, CongenitalLiver DiseasesChildHumansLiverLiver CirrhosisProspective StudiesChildrenFontanFontan-associated liver diseaseLiverNon-invasive assessment

Identifiers

PMID34231051
OpenAlexW2975233417

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.