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Hepatic Artery Stenosis and Thrombosis After Liver Transplantation in Children

Hepatic Artery Stenosis and Thrombosis After Liver Transplantation in Children: a Multicenter, Retrospective, Observational Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05818644
Acronym
HEPATIC
Enrollment
583
Registered
2023-04-19
Start date
2023-09-28
Completion date
2025-12-23
Last updated
2026-06-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hepatic Artery Stenosis, Hepatic Artery Thrombosis, Liver Transplant; Complications, Pediatric ALL

Brief summary

The goal of this observational study is to investigate the incidence, current management practices, and outcomes in pediatric patients with HAC after liver transplantation. Research question: * What are the overall incidence of HAC and the effectiveness of all treatment strategies for HAC after pediatric LT? * What are the current management practices in the experience of centers, anticoagulant therapy, screening protocol, and assessment criteria for HAC after pediatric LT? The burden of participation is considered to be minimal, and limited to the questionnaires.

Interventions

None listed

Sponsors

University Medical Center Groningen
Lead SponsorOTHER
J. P. Garrahan Hospital
CollaboratorUNKNOWN
Hospital Italiano de Buenos Aires
CollaboratorOTHER
Royal Children's Hospital
CollaboratorOTHER
Medical University Innsbruck
CollaboratorOTHER
Hospital Sirio-Libanes
CollaboratorOTHER
Hospital Santo Antonio
CollaboratorUNKNOWN
Faculty of Medicine & Dentistry, University of Alberta
CollaboratorUNKNOWN
Zhejiang University
CollaboratorOTHER
Thomayer University Hospital
CollaboratorOTHER
Hôpital Bicêtre
CollaboratorUNKNOWN
University Children's Hospital
CollaboratorOTHER
Hannover Medical School
CollaboratorOTHER
Universitätsklinikum Hamburg-Eppendorf
CollaboratorOTHER
Dr Rela Institute and Medical Centre
CollaboratorUNKNOWN
Amrita Institute of Medical Sciences & Research Center
CollaboratorOTHER
Max Super Speciality Hospital
CollaboratorOTHER
Aster CMI Hospital
CollaboratorUNKNOWN
Papa Giovanni XXIII Hospital
CollaboratorOTHER
Bambino Gesù Children's Hospital
CollaboratorUNKNOWN
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
CollaboratorNIH
Auckland City Hospital
CollaboratorOTHER_GOV
Children's Memorial Health Institute
CollaboratorUNKNOWN
King Faisal Specialist Hospital & Research Center
CollaboratorOTHER
National University Hospital, Singapore
CollaboratorOTHER
Wits Donald Gordon Medical Centre
CollaboratorUNKNOWN
La Paz University Hospital
CollaboratorUNKNOWN
Vall d'Hebron Barcelona Hospital Campus
CollaboratorUNKNOWN
Karolinska Institutet
CollaboratorOTHER
University Hospital, Geneva
CollaboratorOTHER
Birmingham Women's and Children's Hospital
CollaboratorUNKNOWN
Primary Children's Hospital
CollaboratorOTHER
Children's Hospital of Philadelphia
CollaboratorOTHER
Children's Hospital Pittsburgh
CollaboratorUNKNOWN
Recanati-Miller Transplantation Institute, Mount Sinai Hospital
CollaboratorUNKNOWN
Ann & Robert H Lurie Children's Hospital of Chicago
CollaboratorOTHER
RenJi Hospital
CollaboratorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
0 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* Liver transplantation between January 1st 2002 and January 1st 2022, diagnoses of HAC after LT * The age of the patient is below 18 years at the time of diagnosis and intervention * The date of diagnosis of HAC or intervention was before January 1st 2023. HAC occurring after first or subsequent LTs are included.

Exclusion criteria

N/A

Design outcomes

Primary

MeasureTime frameDescription
Graft survival1-1-2001 and 1-1-2023Graft survival is defined as a functioning graft from transplantation to the end of follow-up data, re-transplantation, or death, whichever occurs first.
Patient survival1-1-2001 and 1-1-2023Patient survival is defined from the date of the primary LT until date of death. Causes of re-transplantation or death will be recorded.

Secondary

MeasureTime frameDescription
Technical success1-1-2001 and 1-1-2023Technical success is defined as the success of the intervention in re-establishing the arterial blood flow to the liver and will be assessed by each individual center.
Primary and secondary patency1-1-2001 and 1-1-2023Primary patency is defined as the time between the index treatment and re-intervention intended to restore patency in patients with a restenosis or re-occlusion. Secondary patency is the time between the index treatment and failure to re-establish flow by means of re-intervention. In case of re-transplantation or death due to other reasons, the patients will be censored if the treated vessel is patent. Kaplan-Meier curves will be plotted to visualize primary and secondary patency rates at various times after treatment for HAC, including 1, 3, 5, 10, 15 and 20 years.
Intra- and post-procedural complications1-1-2001 and 1-1-2023Procedural complications will be categorized into two main groups: transplant complications and procedural complications related to endovascular or surgical revascularization for HAC. Within these groups, intra-procedural complications predominantly consist of vascular issues, such as thrombosis, stenosis, compression, dissection, and rupture. In contrast, post-procedural complications encompass a broader range of issues, such as infection, rejection, bleeding, and vascular and biliary complications, including anastomotic stricture, non-anastomotic strictures, bile leak, biloma, or cholangitis. Re-interventions addressing both intra- and post-procedural complications will also be recorded.
Anticoagulant therapy after transplantation and after interventions1-1-2001 and 1-1-2023Anticoagulant therapy after transplantation and after interventions for HAC will be assessed according to the management practices of each participating site (center specific) and individual patient data (patient specific). Details about each anticoagulation regimen, including the specific anticoagulant, duration of anticoagulation, and upper and lower limits of target values, such as international normalized ratio, anti-factor Xa, and activated partial thromboplastin time, will be recorded. Patient-specific management will be documented for patients with HAC.
Center specific screening protocol1-1-2001 and 1-1-2023Local screening protocols to assess HAC after LT, such as the routine post-operative Doppler ultrasound policy, will be documented. Whether HAC screening is consistent for patients with and without risk factors will also be examined. The frequency of preferred radiological screening investigations within 2 weeks after LT will be determined, considering various risk factors.
Center specific diagnostic criteria1-1-2001 and 1-1-2023The diagnostic criteria section will cover the types of HAC, non-invasive radiological criteria, and interventional radiological criteria during invasive angiography. The center's definition of technical success after interventional radiological treatment will also be recorded.
Center specific radiological follow up1-1-2001 and 1-1-2023The radiological follow-up section will assess whether follow-up protocols are the same for all interventions or specific to each intervention type. The imaging methods and frequencies of radiological follow-up for different treatment modalities will be determined. Additionally, the experience years and level of seniority of the interventional radiologist will be recorded.
Incidence1-1-2001 and 1-1-2023The incidence of HAC will be determined by dividing the total number of patients diagnosed with HAC between 1st of January 2002 and 1st of January 2023, who had undergone LT between 1st of January 2002 and 1st of January 2022, by the total number of patients who underwent LT at pediatric age between 1st of January 2002 and 1st of January 2022. The study will present the overall incidence of HAC during the 20-year period of 2002 to 2022, as well as the incidence during specific 5-year intervals, namely 2002 to 2007, 2007 to 2012, 2012 to 2017, and 2017 to 2022, for each complication.

Countries

Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 17, 2026