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Impact of Blood Salvage Therapy on Outcomes After Oncologic Liver Surgery

Impact of Blood Salvage Therapy During Oncologic Liver Surgeries on Allogenic Transfusion Events, Survival and Recurrence

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05164406
Enrollment
106
Registered
2021-12-20
Start date
2018-01-01
Completion date
2021-02-28
Last updated
2023-05-31

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

Conditions

Liver Neoplasms

Keywords

Blood salvage therapy, Oncologic liver surgery

Brief summary

A before and after trial comparing the systematic use of blood salvage therapy with leucocyte filter during oncologic liver resections. Recurrence, survival, allogenic transfusion rates and surgical outcomes are compared with a representative historic cohort.

Detailed description

Blood salvage therapy in oncologic liver surgery is seldom used based on unproven concerns about the safety of the technique regarding potential cancer dissemination or recurrence. Nevertheless, the technique has proven advantages in other surgical settings regarding the allogenic transfusion outcomes. Allogenic blood transfusion has been scientifically proven to worsen prognosis in oncologic surgery. This study compares a cohort of patients systematically exposed the blood salvage therapy to one comparable cohort without the therapy and outcomes regarding transfusion rates, post-operative Hb measurement, recurrence, overall survival, and post-operative adverse events.

Interventions

PROCEDUREBlood salvage therapy

In the blood salvage group, blood is systematically given back when the minimal amount of blood loss required for reprocessing is met

Sponsors

Université de Sherbrooke
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years

Inclusion criteria

* Adult Oncologic liver surgery scheduled in our institution

Exclusion criteria

* Condition precluding consent for trial Pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Recurrence free survival18 months
Overall survival18 months
TransfusionUp to 30 days after surgeryAllogenic blood products requirements

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026