ReTSEACS: SvO2 Trigger in Transfusion Strategy After Cardiac Surgery

Sponsor
University Hospital, Montpellier (Other)
Overall Status
Completed
CT.gov ID
NCT02761564
Collaborator
(none)
100
1
2
24.3
4.1

Study Details

Study Description

Brief Summary

Current international guidelines suggest a restrictive transfusion strategy, setting that Hb level at 7 g/dl is a reasonable threshold. However, the idea of having only one threshold for all the patients has been challenged by authors, suggesting a more liberal strategy for certain cases. At the moment, there is no other parameter considered accurate enough to be taken into consideration for transfusion strategy management.

This study is to use ScVO2, a current, easily accessible parameter, before blood transfusion in order to stratify its indication after cardiac surgery.

Monocentric, randomised, single blind study (patient not aware of the group assignments) Patient inclusion will be made in ICU if the physician decides to perform blood transfusion according to standard transfusion strategy to treat a postoperative anemia (Hb<9g/dL).

Every patient will go through randomization to be placed in one of the two groups of the study: either the one whose transfusion strategy is adjusted by the pretransfusion ScvO2 (group ScvO2), or the control group.

Our main objective is to evaluate the impact of a new transfusion strategy founded on guidelines, but provided ScvO2 is less than 65%, on the incidence of red blood cells transfusion for anemia early after cardiac surgery.

Detailed Description

Currently, the rate of transfusion of cardiac surgery patients is approximately 50%. The decision to transfuse is based on the hemoglobin (Hb), the transfusion threshold from 7 to 9 g / dL seems to be reasonable, based on clinical parameters, as well as patient history, as the degree of coronary stenosis . Several randomized studies have shown that a restrictive transfusion strategy was superior to a liberal strategy.

ScvO2 is a parameter reflecting the balance between transport O2 and O2 in tissue consumption, which Hb is one of the determinants. It requires that a levy on central venous used frequently for such patients. ScvO2 could make better account of the actual tolerance of anemia that the only value of Hb and the patient's clinical characteristics.

We therefore hypothesize that ScvO2 can help with the decision of RBC transfusions after heart surgery.

Primary and secondary endpoints Principal: To assess the value of ScvO2 threshold (65%) in the restrictive transfusion strategy on the incidence of transfusion after cardiac surgery.

secondary:

  • Assess the impact of transfusion strategy based on ScvO2 on the number of transfused patients at D28

  • Assess the impact of transfusion strategy based on ScvO2 on the number of cells transfused concentrates.

  • Assess the impact of transfusion strategy based on ScvO2 on mortality or incidence of disease events such as cardiac complications, renal, respiratory or neurological dysfunction in the immediate aftermath of surgery.

Study Design

Study Type:
Interventional
Actual Enrollment :
100 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Other
Official Title:
Restrictive Transfusion Strategy Early After Cardiac Surgery
Actual Study Start Date :
Oct 6, 2016
Actual Primary Completion Date :
Sep 17, 2018
Actual Study Completion Date :
Oct 17, 2018

Arms and Interventions

Arm Intervention/Treatment
Experimental: ScVO2 group

Anemia (<9g/dL) requiring blood transfusion Measure of ScvO2 : ScVO2 is measured using the central venous catheter placed in the superior vena cava. Transfusion is performed if the ScVO2 is inferior or equal to 65%.

Other: ScvO2 measure
ScvO2 (oximetry) is measured at the distal lumen of the central venous catheter placed in the superior vena cava. Transfusion is performed if ScvO2 is inferior or equal to 65%.

Other: Control group

Anemia (<9g/dL) requiring blood transfusion : Transfusion is performed following national guidelines for red blood cell transfusion

Other: Red blood cell tranfusion
Red blood cell transfusion according to transfusion guidelines.

Outcome Measures

Primary Outcome Measures

  1. Number of patients transfused [Between 1 and 28 days (ICU stay)]

    Number of patients transfused during ICU stay

Secondary Outcome Measures

  1. Number of patients transfused [Day 28]

    Number of patients transfused on day 28

  2. Number of blood units transfused in ICU [Between 1 and 28 days (ICU stay)]

    Number of blood units transfused during ICU stay

  3. Number of blood units transfused on day 28 [Day 28]

    Number of blood units transfused

Other Outcome Measures

  1. Incidence of mortality [Day 28]

    Incidence of 28-day mortality

  2. total duration of mechanical ventilation [Day 1 to 28]

    total duration of mechanical ventilation on D28

  3. length of stay in ICU [Day 1 to 28]

    The length of stay in ICU

  4. length of hospital stay [Between 1 and 28 days]

    The length of stay during hospitalization (Between 1 and 28 days)

  5. Organ failure incidence [Day 1 to 28]

    incidence of organ failure at day 28

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 100 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Age over 18 years

  • Patients admitted to intensive care after heart surgery

  • Anemic patient (Hb < 9 g/dL)

  • Patient with a central venous catheter in the territory SVC

Exclusion Criteria:
  • Patient with acute bleeding defined as a postoperative bleeding over 1000 ml in 12 hours or the need for a recovery operation for hemostasis or the transfusion of blood units over 4

  • Patient with severe sepsis or septic shock criteria defined by the Surviving Sepsis compaign

Contacts and Locations

Locations

Site City State Country Postal Code
1 UHMontpellier Montpellier France

Sponsors and Collaborators

  • University Hospital, Montpellier

Investigators

  • Principal Investigator: Norddine ZEOURAL, MD, University Hospital, Montpellier

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University Hospital, Montpellier
ClinicalTrials.gov Identifier:
NCT02761564
Other Study ID Numbers:
  • 9655
First Posted:
May 4, 2016
Last Update Posted:
Mar 22, 2019
Last Verified:
May 1, 2016
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Keywords provided by University Hospital, Montpellier
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 22, 2019