Transfusion Savings in Heart Surgery: Impact of Individual Strategy by Erythropoietin and Metabolic Adjustment (ScvO2)

Cardiac Surgery Clinical Trial

— BLOOCOST  

Official title:

Patient Blood Management in Cardiac Surgery by Erythropoietin, Ferric Carboxymaltose and Metabolic Adjustment (ScvO2): A Randomized Controlled Study

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04141631
• Other study ID #: RECHMPL19_0042
• Status: Completed
• Phase: N/A
• Start date: January 13, 2020
• Est. completion date: June 15, 2022

Study information

• Verified date: September 2022
• Source: University Hospital, Montpellier
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Preoperative anemia, bleeding and transfusions have been recognized as a "Deadly triad" in cardiac surgery associated with an increased morbidity,mortality, and costs related. Thus strategies to reduce unnecessary RBC transfusions and to optimize preoperative anemia must be developed .The study evaluate an individual blood conservation strategy based on patient blood management bundles in cardiac surgery patients: optimisation perioperative hemoglobin level by erythropoietin and ferric carboxymaltose (Ferinject) associated with the use of ScV02 to guide perioperative erythrocyte transfusion.

Description:

Preoperative anemia is the most common haematological abnormalities in cardiac surgery affecting 20 to 40% of patients and is becoming increasingly prevalent due to an ageing population with more chronic diseases.Preoperative anemia is independently associated with increased risk of adverse outcome following cardiac surgery but also implies blood transfusions which, associated with anemia, increase significantly perioperative cardiac morbidity and mortality. Therefore, strategies of blood conservation to optimize anemia and to minimize transfusion have been developped in the concept of the Blood Patient Management (BPM). To correct anemia, intravenous iron has been shown to be an effective treatment with increase hemoglobin (Hb) level in the perioperative period. It is now established that intravenous iron, as ferric carboxymaltose (Ferinject) is better tolerated compared to oral supplementation with better stimulation of erythropoiesis and,consequently, higher Hb levels. Based on promising results in the orthopedic surgery patients, the use of recombinant human erythropoietin (EPO) has also been proposed in cardiac surgery. Secondly, because even one red blood cells products (RBC) compromises postoperative outcome, guidelines suggest to adopt restrictive threshold of Hb levels to decide RBC transfusion. However, beyond the fact that RBC transfusion correct Hb level, the final goal of blood transfusion is to improve oxygen delivery to hypoxemic tissue. In this respect, the relevance of the use of a Hb threshold to guide transfusion have been questioned. Venous oxygen saturation (SvO2) and ScvO2 (central oxygen venous saturation), global parameters of tissue oxygenation, in stable hemodynamic and respiratory conditions, may be an relevant marker of anemia tolerance. Recently, the investigators demonstrated the lack of benefit in terms of ScvO2 increase during erythrocyte transfusion if ScvO2 was > 65%. In order to reduce exposure to transfusion, the management of anemia with EPO and perioperative intravenous FCM associated with the use of ScvO2 could be interesting to both improve Hb levels and reduce RBC transfusion.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 128
• Est. completion date: June 15, 2022
• Est. primary completion date: May 10, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 90 Years

Eligibility

Inclusion Criteria:

• Scheduled Cardiac surgery for more than 24 hours
• High risk of perioperative transfusion defined by a TRUST Score = 3
• Veno-Venous catheter in Superior vena cava territory
• Patient Affiliate or beneficiary of social security
• Collection on free, informed and written consent

Exclusion Criteria:

• EPO and FCM contraindication
• Patients already treated by EPO at the time of inclusion
• Non controlled Infectious endocarditis defined by ESC guidelines 2015
• Patients including in an other research
• Patients whose physical and/or psychological health is severely impaired and who, according to the investigator, may affect the participant's compliance with the study.
• Patients deprived from his rights (guardianship or tutelage measure)
• Patients who refuses to sign the consent
• pregnant or lactating woman

Related Conditions & MeSH terms

• Cardiac Surgery
• Perioperative Anemia
• Transfusion

Intervention

Drug:
• EPO (600UI/Kg, sub-cutaneous) and Ferric Carboxymaltose (FCM) (20 mg/kg in 250 mL of saline solution 0.9% over 15 min)
EPO (600UI/Kg, sub-cutaneous) and Ferric Carboxymaltose (FCM) (20 mg/kg in 250 mL of saline solution 0.9% over 15 min) will be administered if Hb < 13g/dL the day before surgery Hb = 7g/dL AND ScvO2 > 65% in postoperative ICU stay Postoperative Transfusion will be guided by ScvO2 values : if Hb = 8 g/dL AND ScvO2 = 65% or if Hb < 7g/dL independently of ScVO2 value

Locations

Country	Name	City	State
France	DEpartement d'anesthésie et réanimation D - Arnaud de Villeneuve	Montpellier

Sponsors (1)

Lead Sponsor	Collaborator
University Hospital, Montpellier

Country where clinical trial is conducted

France, 

References & Publications (4)

Alghamdi AA, Davis A, Brister S, Corey P, Logan A. Development and validation of Transfusion Risk Understanding Scoring Tool (TRUST) to stratify cardiac surgery patients according to their blood transfusion needs. Transfusion. 2006 Jul;46(7):1120-9. — View Citation

Plicht B, Lind A, Erbel R. [Infective endocarditis : New ESC guidelines 2015]. Internist (Berl). 2016 Jul;57(7):675-90. doi: 10.1007/s00108-016-0086-y. Review. German. — View Citation

Ranucci M, Baryshnikova E, Castelvecchio S, Pelissero G; Surgical and Clinical Outcome Research (SCORE) Group. Major bleeding, transfusions, and anemia: the deadly triad of cardiac surgery. Ann Thorac Surg. 2013 Aug;96(2):478-85. doi: 10.1016/j.athoracsur.2013.03.015. Epub 2013 May 11. — View Citation

Task Force on Patient Blood Management for Adult Cardiac Surgery of the European Association for Cardio-Thoracic Surgery (EACTS) and the European Association of Cardiothoracic Anaesthesiology (EACTA), Boer C, Meesters MI, Milojevic M, Benedetto U, Bolliger D, von Heymann C, Jeppsson A, Koster A, Osnabrugge RL, Ranucci M, Ravn HB, Vonk ABA, Wahba A, Pagano D. 2017 EACTS/EACTA Guidelines on patient blood management for adult cardiac surgery. J Cardiothorac Vasc Anesth. 2018 Feb;32(1):88-120. doi: 10.1053/j.jvca.2017.06.026. Epub 2017 Sep 30. Review. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Transfusion incidence at hospital discharge	Number of patients transfused of blood units	up to Day 28
Secondary	ICU transfusion incidence	Number of blood units transfused during ICU stay	at ICU discharge or up to Day 28
Secondary	total of blood units transfused	number of blood units administered per patient	up to day 28
Secondary	Hemoglobin level at surgery discharge and Hemoglobin level at 1 month after discharge from hospital	the last hemoglobin value at surgery discharge and the hemoglobin value at 1 month after discharge from hospital	at surgery discharge (or at Day 28) and at 1 month after discharge from hospital
Secondary	The total duration of mechanical ventilation	The total duration of mechanical ventilation in ICU	at ICU discharge or up to Day 28
Secondary	length of stay in ICU	numbers of days in ICU	up to day 28
Secondary	Length of hospital stay	Length of stay during hospitalization (Between 1 and 28 day)	at day 28
Secondary	Incidence of Mortality	Incidence of 28-day mortality	at day 28
Secondary	Incidence of postoperative events in ICU	AKI (KDIGO criteria), Cardiac dysfunction (acute heart failure requiring inotrope or extracorporeal life support (ECLS), arrythmia), vascular dysfunction (norepinephrine support without sepsis), respiratory dysfunction (non invasive ventilation devices, secondary intubation,mechanical ventilation more than 12 hours), septic complications (sepsis/septic shock)	at day 28