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Interest of Oxygenated Hypothermic Perfusion (PHO) in Preservation of Hepatic Grafts From Expanded Criteria Donors

Interest of Oxygenated Hypothermic Perfusion in Preservation of Hepatic Grafts From Expanded Criteria Donors. A Prospective Monocentric Study.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03376074
Acronym
PERPHO
Enrollment
25
Registered
2017-12-18
Start date
2018-02-19
Completion date
2019-02-07
Last updated
2019-03-11

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

Conditions

Hepatocellular Injury

Keywords

liver transplantation, hypothermic machine liver perfusion, extended criteria liver grafts

Brief summary

Interest of oxygenated hypothermic perfusion in preservation of hepatic grafts from expanded criteria donors.

Detailed description

The excellent results of liver transplantation (LT) have led to a significant increase in the number of patients awaiting transplantation. At the same time, the number of grafts remains stable. To extend the donor pool, the use of Extended Criteria Donor (ECD) donors graft increased each year despite the fact that these graft are known to be more vulnerable to ischemia-reperfusion injuries induced by cold storage preservation (CS). Their use is therefore associated with a greater risk of postoperative dysfunction of the graft. This risk can be reduced by improving preservation quality. The preservation by hypothermic oxygenated perfusion (HOPE) consists of keeping the graft in hypothermia (4 to 12 °C) on an machine perfusion (MP) using a specific solution, saturated with oxygen. In kidney transplantation, the use of MP has been shown to improve graft function as well as graft survival, especially for ECD grafts. In liver transplantation, experimental studies on animal models have demonstrated the superiority of HOPE over CS regarding graft function and survival. These results have been confirmed in humans on small retrospective series. As HOPE is an expensive procedure, obtaining evidence of its effectiveness could result in a reimbursement of the additional cost.

Interventions

25 patients: Application of HOPE for 2 hours, perfusion rate 100-150 ml/min, pressure controlled, perfusion pressure \< 3 mm Hg, perfusion route portal vein, recirculating system, perfusion volume 2 L, perfusate solution (UWMP®), perfusate temperature 4-12 °C, perfusate oxygenation 40 KPa

75 patients transplanted in Rennes between 2010 and 2015 with a cold stored grafts, matched (ratio 1: 3) using a propensity score calculated according to some parameters

Sponsors

Rennes University Hospital
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Months to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients older than 18 years * Candidates for a first orthotopic liver transplantation, without transplantation of another associated organ (kidney, pancreas, heart, lung, intestine) * With cirrhosis whatever its etiology and gravity * With or without hepatocarcinoma * Having given free, informed and written consent * LT made from a whole graft, harvested from a brain-dead donor with ECD criteria, defined as the presence of at least one of the following criteria: * Age\> 65 years * BMI\> 30 kg / m2 * Duration of hospitalization in intensive care unit\> 7 days * Natremia\> 155 mmol / l * AST\> 150 IU / ml * ALT\> 170 IU / ml * Occurrence of cardiac arrest before harvesting * Macrovacuolar steatosis\> 30% on liver histology

Exclusion criteria

* History of organ transplantation * Transplantation in emergency * Transplantation from a living donor, a reduced graft or a graft from a deceased donor by cardiac arrest (DCD) * Major persons subject to legal protection (safeguard of justice, guardianship), persons deprived of their liberty

Design outcomes

Primary

MeasureTime frameDescription
Evaluation of the performance of HOPE in the preservation of ECD liver grafts on graft function recoveryDay 7Occurrence of early allograft dysfunction and / or primary non function

Secondary

MeasureTime frameDescription
Evaluation of the impact of PHO during the conservation of ECD liver grafts on postoperative morbidityDay 7
Evaluation of graft's survivalMonth 3Occurrence of a vascular and biliary complication
Number of days of hospitalization (initial stay) after transplantationPostoperative course
Evaluation of the impact of PHO during the conservation of ECD liver grafts on intraoperative morbidityDay 1Number of intraoperative transfusions
Cost of the initial stayPostoperative course
Cost of the hospitalization stayMonth 3
Number of days of hospitalization after transplantationMonth 3

Countries

France

Outcome results

None listed

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