RiaSTAP vs. Conventional Transfusion in Patients Having Heart Valve Surgery

Phase 2

Terminated

• Conditions: Heart Valve Disease; Coronary Artery Disease
• Interventions: Drug: Human fibrinogen concentrate; Other: apheresis platelets

• Registration Number: NCT01283321
• Lead Sponsor: Emory University

Brief Summary

Heart surgery involving valve replacement often involves the use of the heart-lung machine for over 90 minutes, and bleeding tendency is frequently seen. Conventionally, platelet transfusion has been the primary therapy to treat bleeding after this type of procedure. More recently, perioperative supplementation of purified fibrinogen (RiaSTAP, CSL Behring) was shown to reduce bleeding and blood product use (plasma or platelets) after heart surgery. The objective of this trial is to demonstrate the clinical equivalency and economic utility of using fibrinogen concentrate, RiaSTAP for the mitigation of post-operative bleeding in patients in lieu of platelet transfusion.

Purified fibrinogen concentrate has been approved by FDA, and it has been used for the treatment of acute bleeding episodes in patients with low fibrinogen due to hereditary causes (e.g., afibrinogenemia). Compared to the transfusion of platelets which may be associated with volume overload, bacterial/viral infection, immunological effects and excess blood clotting, purified fibrinogen has several advantages. First, it contains no liquid plasma allowing for low volume infusion. Several viral inactivation/reduction steps are used to prepare the fibrinogen concentrate, increasing its viral safety. No antibodies or white blood cells are contained in the fibrinogen concentrate; therefore transfusion reactions are rare. Although platelet transfusion is widely used after heart surgery, there has been no randomized study to endorse this practice. In this study, patients undergoing heart valve replacement will be randomized to receive either platelet (1 unit) transfusion or fibrinogen concentrate (4g) after heparin anticoagulation is reversed. Subjects will be treated only if there is evidence of significant microvascular bleeding. Fifteen minutes after the initial treatment, subjects will be reevaluated for bleeding. If bleeding continues, subjects will be treated with blood transfusion per institutional standard of care.

The primary endpoints for this study are the hemostatic condition of the surgical field and 24-hour total of blood product transfusion.

Detailed Description

Platelet and plasma transfusion remain in the mainstay hemostatic therapy for perioperative bleeding. Several studies indicate that acquired fibrinogen deficiency can be the primary cause of bleeding after cardiac surgery. The aim of the study is to compare hematologica and transfusion profiles between the first-line fibrinogen replacement and platelet transfusion in post-cardiac surgical bleeding. In this prospective randomized, open-lable study, 20 adult patients undergoing valve replacement or repair, and fulfilling preset visual bleeding scale (0=excellent hemostasis; 1=oozing; 2=moderate bleeding; 3=severe bleeding from multiple bleeding sites) are randomized to 4 g of fibrinogen or 1 unit of apheresis platelet transfusion. After the initial randomized intervention, additional transfusions are given in the presence of bleeding (\>200 ml/hour) according to the institutional practie as follows; 1 apheresis platelet unit if platelet count is less than 100 x 10\^9 /L, 2 units of plasma if international normalized ratio is \>1.6, or 10 units of cryoprecipitate if fibrinogen level is \<200 mg/dL. Primary endpoints include hemostatic condition in the surgical field and 24-hour hemostatic product usage. Hematologica data, clinical outcome, and safety date are collected up to the 28th day postoperative visit.

Basic Information
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Recruitment & Eligibility
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Study & Design
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Trial Locations

Study Timeline

• Study Start: 2011-01
• Study First Submitted: 2011-01-24
• Study First Submitted QC: 2011-01-24
• Study First Posted: 2011-01-25
• Primary Completion: 2013-05
• Study Completion: 2013-05
• Results First Submitted: 2015-01-20
• Results First Submitted QC: 2015-02-02
• Results First Posted: 2015-02-16
• Status Verified: 2018-05
• Last Update Submitted: 2018-05-23
• Last Update Posted: 2018-06-21

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 26

Inclusion Criteria

• Willing and able to provide written informed consent

• Age >17 and < 86 years

• Patients undergoing planned cardiopulmonary bypass (CPB) for:

  1. combined coronary artery bypass grafting and valve replacement/repair surgery

  2. single valve replacement surgery

  3. mitral valve repair surgery

  4. or double valve surgery (aortic and mitral)

• Presence of clinically relevant microvascular bleeding after protamine administration (hemostasis assessment score of 2-3)

• Patients should fulfill the following parameters prior to the study intervention:

  • Body temperature > 35.0°C
  • Blood pH > 7.2
  • Hb > 7.0 mg/dL
  • Activated clotting time (ACT) < 155 seconds
  • CPB time > 60 minutes

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Exclusion Criteria

• Replacement of aorta
• Planned valve replacement without median sternotomy
• Previous valve replacement surgery (previous coronary artery bypass graft (CABG) acceptable)
• History or suspicion of a congenital or acquired coagulation disorder such as hemophilia, von Willebrand disease, and liver disease
• Hemodialysis dependent renal failure
• Liver dysfunction (aspartate aminotransferase (AST) or alanine aminotransferase (ALT) increased ≥ 2-fold above the upper limit of local laboratory normal ranges)
• Known allergy/anaphylaxis to fibrinogen concentrate or apheresis platelet units
• Clopidogrel administration within 5 days of surgery
• Coumadin (warfarin) administration within 5 days of surgery
• Participation in another clinical study in the 4 weeks preceding surgery
• Any indication that a potential subject did not comprehend the study restrictions, procedures, or consequences therein an informed consent cannot be convincingly given
• Life expectancy less than 48 hours

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Group A: RiaSTAP	Human fibrinogen concentrate	Human fibrinogen concentrate
Group B: apheresis platelets	apheresis platelets	single apheresis unit

Primary Outcome Measures

Name	Time	Method
Bleeding Scores	intra-operatively and up to 24 hours postoperatively	Bleeding scores are scored on a four-point scale. A visual assessment of surgical field was performed by the senior surgical staff as follows: 0 = excellent hemostasis (dry field), 1 = mild bleeding (oozing), 2 = moderate bleeding (controllable with applied pressure), and 3 = severe bleeding (multiple diffuse bleeding sites). If the visual bleeding scale was 2 to 3, the subjects were randomly assigned to a study intervention using a closed envelope method.

Secondary Outcome Measures

Name	Time	Method
Number of Participants in Whom Transfusion of Platelet Concentrate is Required During or After Surgery.	Operative period up to 60 minutes
Volume (mL) of Fresh-frozen Plasma (FFP) Transfused-during Surgery and up to 24 Hours After Surgery	Operative period up to 60 minutes and up to 24 hours after surgery
Volume (mL) of Platelets Transfused- During Surgery and up to 24 Hours After Surgery	Operative period up to 60 minutes and up to 24 hours after surgery
Median Blood Loss (mL) at 12 Hours After Surgery	From end of surgery to 12 hours after surgery

Trial Locations

Locations (1)

Emory University Hospital; 🇺🇸 Atlanta, Georgia, United States