.Patient Blood Management Program in Liver Transplantation

Last updated: March 29, 2023
Sponsor: Hospital Universitari de Bellvitge
Overall Status: Active - Recruiting

Phase

N/A

Condition

Anemia

Treatment

N/A

Clinical Study ID

NCT05187637
EOM025/21
  • Ages > 18
  • All Genders

Study Summary

Transfusion management improvement programs, generally known as patient blood management (PBM) programs, are based on a set of perioperative measures aimed at improving clinical outcomes by avoiding unnecessary exposure to blood components.

In a recent series of liver transplants (LT) performed in Spanish centers belonging to the Spanish Liver Transplant Society, despite optimal hemostasis management and preservation of the vena cava, around 20% of patients required massive transfusion (considered as the administration of 6 or more red blood cell concentrates intraoperatively). In addition, 63% of the patients were transfused with at least one packed red cells during the operation.

By correcting the iron deficiency in patients who meet the criteria of the anemia study (transferrin saturation less than 20%), we could improve the hemoglobin level, which would allow a wider margin for the transfusion of red cell concentrates.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • liver cirrhosis on the liver transplant waiting list
  • haemoglobin lower than 11.5g/dL
  • transferrin saturation index below 40%
  • ferritin below 800mcg/L

Exclusion

Exclusion Criteria:

  • refusal to participate
  • Known hypersensitivity to Ferinject
  • current infection

Study Design

Total Participants: 66
Study Start date:
March 23, 2022
Estimated Completion Date:
April 24, 2023

Study Description

This is a prospective observational multicenter study to evaluate the efficacy of iron administration in patients candidates to LT. Inclusion criteria Patients with Hb < 11.5 g/dL

  • and transferrin saturation index < 40%+ferritina <800mcg/L will receive Fe carboxymaltose iv* *Ganzoni formula modified (total iron dose = [actual body weight × (11.5-actual Hb)] × 2.4 + 500), and represent the intervention group. Those patients with Hb < 11.5 g/dL and transferrin saturation index > 40% will constitute the control group. The Intraoperative managed protocol was standardized within groups and Teams. Demographic and liver function test after iron administration will be registered; perioperative transfusion data will be recorded. Recruitment, treatment and follow-up will be conducted by monitored by an independent audit to assure the quality of data. Specific Data Unit not related to the participated Teams will do statistical analysis. The primary outcome is the feasibility of apply the first pillar of the patient blood management programs (PBM) in LT candidates. Secondary outcomes are the response rate (increase in Hb > 1 g/dL) to the intervention, and red blood cell requirements in both, intervention and control group

Connect with a study center

  • HUBellvitge

    Hospitalet de Llobregat, Barcelona 08907
    Spain

    Active - Recruiting

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