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Transfusion of Fresh Frozen Plasma in Non-bleeding Intensive Care Unit (ICU) Patients (TOPIC)

Primary Purpose

Blood Coagulation Disorders, Hemorrhage

Status
Completed
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
omitting FFP transfusion before an intervention
Sponsored by
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Blood Coagulation Disorders focused on measuring Fresh frozen plasma, Coagulopathy, Intensive care, Adverse effects, Lung injury

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 18 years and older
  • INR >1.5 and <3.0
  • undergoing invasive procedure (insertion of a central venous catheter, a chest drain, percutaneous tracheostomy)

Exclusion Criteria:

  • clinically overt bleeding at the time of the procedure (excludes minor epistaxis, minor gum bleeding, microscopic hematuria, superficial bruises, or normal menses)
  • thrombocytopenia of < 30 x 109/L.
  • use of abciximab, tirofiban, ticlopidine or activated protein C
  • use of heparin < 1 hour prior to the procedure, or low molecular weight heparin in therapeutic doses < 12 hours prior to procedure
  • history of congenital or acquired coagulation factor deficiency or bleeding diathesis
  • no informed consent

Sites / Locations

  • Academic Medical Centre - University of Amsterdam
  • Ter Gooi Ziekenhuizen
  • Leids Universitair Medisch Centrum
  • Diakonessenhuis

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

No FFP transfusion prior to intervention

FFP transfusion prior to intervention

Arm Description

Patients with a coagulopathy (INR 1,5-3,0), who are randomized to omitting transfusion of fresh frozen plasma before they undergo an intervention.

Patients with a coagulopathy (INR 1,5-3,0), who are randomized to transfusion of fresh frozen plasma before they undergo an intervention. This is considered standard care.

Outcomes

Primary Outcome Measures

Procedure-related relevant bleeding, occurring within 24 hours after the procedure.
Relevant bleeding will be defined using a validated tool for assessment of bleeding in the critically ill. An assessment of bleeding will be standardized and performed by an independent research physician or intensivist blinded to the transfusion strategy 1 and 24 hours after the procedure and when clinically indicated.

Secondary Outcome Measures

minor bleeding within 24 hours
onset of acute lung injury within 48 hours.
Lung injury will be evaluated by P/F ratio, change in ventilator settings, chest x-ray and Lung Injury Score.
effect of FFP transfusion on coagulation parameters
a range of coagulation parameters will be evaluated to assess efficacy of FFP transfusion in these patients
evaluation of costs
Evaluation of costs in the two different groups will be made. Length of stay, number of ventilation days, differences in medication use, all will be taken into account.

Full Information

First Posted
June 14, 2010
Last Updated
June 14, 2013
Sponsor
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Collaborators
ZonMw: The Netherlands Organisation for Health Research and Development
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1. Study Identification

Unique Protocol Identification Number
NCT01143909
Brief Title
Transfusion of Fresh Frozen Plasma in Non-bleeding Intensive Care Unit (ICU) Patients
Acronym
TOPIC
Official Title
Transfusion of Fresh Frozen Plasma in Non-bleeding ICU Patients
Study Type
Interventional

2. Study Status

Record Verification Date
June 2010
Overall Recruitment Status
Completed
Study Start Date
May 2010 (undefined)
Primary Completion Date
June 2013 (Actual)
Study Completion Date
June 2013 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Collaborators
ZonMw: The Netherlands Organisation for Health Research and Development

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
With the aim to restrict inappropriate fresh frozen plasma (FFP) transfusions to critically ill patients, a randomized clinical trial will be conducted in a subgroup of intensive care (ICU) patients undergoing an invasive procedure. The objective is to assess the effectiveness and costs of omitting prophylactic FFP transfusion compared to current practice of prophylactic transfusion, in non-bleeding ICU patients with a coagulopathy.
Detailed Description
Rationale: Fresh frozen plasma (FFP) is an effective therapy to correct for a deficiency of multiple coagulation factors during bleeding. In past years, use of FFP has increased, in particular in patients on the Intensive Care Unit (ICU), and has expanded to include prophylactic use in patients with a coagulopathy prior to undergoing an invasive procedure. Retrospective studies suggest that prophylactic use of FFP does not prevent bleeding, but carries the risk of transfusion-related morbidity. However, up to 50% of FFP is administered to non-bleeding ICU patients. Objective: With the aim to restrict inappropriate FFP transfusions to critically ill patients, a randomized clinical trial will be conducted in a subgroup of ICU patients with a coagulopathy undergoing an invasive procedure. The objective is to assess the effectiveness and costs of prophylactic FFP transfusion (current practice) compared to no prophylactic transfusion, in non-bleeding ICU patients with a coagulopathy, prior to undergoing an invasive procedure (e.g. placement of central venous catheter, tracheostomy, chest tube). Study design: Prospective, multicentre, randomized, open-label, blinded end point evaluation (PROBE) design.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Blood Coagulation Disorders, Hemorrhage
Keywords
Fresh frozen plasma, Coagulopathy, Intensive care, Adverse effects, Lung injury

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
81 (Actual)

8. Arms, Groups, and Interventions

Arm Title
No FFP transfusion prior to intervention
Arm Type
Experimental
Arm Description
Patients with a coagulopathy (INR 1,5-3,0), who are randomized to omitting transfusion of fresh frozen plasma before they undergo an intervention.
Arm Title
FFP transfusion prior to intervention
Arm Type
No Intervention
Arm Description
Patients with a coagulopathy (INR 1,5-3,0), who are randomized to transfusion of fresh frozen plasma before they undergo an intervention. This is considered standard care.
Intervention Type
Other
Intervention Name(s)
omitting FFP transfusion before an intervention
Intervention Description
In the interventional group FFP transfusion is omitted before performing a procedure (e.g. placement of central venous catheter, tracheostomy, chest tube)
Primary Outcome Measure Information:
Title
Procedure-related relevant bleeding, occurring within 24 hours after the procedure.
Description
Relevant bleeding will be defined using a validated tool for assessment of bleeding in the critically ill. An assessment of bleeding will be standardized and performed by an independent research physician or intensivist blinded to the transfusion strategy 1 and 24 hours after the procedure and when clinically indicated.
Time Frame
24 hours after the procedure
Secondary Outcome Measure Information:
Title
minor bleeding within 24 hours
Time Frame
within 24 hours of the procedure
Title
onset of acute lung injury within 48 hours.
Description
Lung injury will be evaluated by P/F ratio, change in ventilator settings, chest x-ray and Lung Injury Score.
Time Frame
48 hours within the intervention
Title
effect of FFP transfusion on coagulation parameters
Description
a range of coagulation parameters will be evaluated to assess efficacy of FFP transfusion in these patients
Time Frame
within 24 hours of transfusion of FFP
Title
evaluation of costs
Description
Evaluation of costs in the two different groups will be made. Length of stay, number of ventilation days, differences in medication use, all will be taken into account.
Time Frame
up to 28 days after inclusion

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 18 years and older INR >1.5 and <3.0 undergoing invasive procedure (insertion of a central venous catheter, a chest drain, percutaneous tracheostomy) Exclusion Criteria: clinically overt bleeding at the time of the procedure (excludes minor epistaxis, minor gum bleeding, microscopic hematuria, superficial bruises, or normal menses) thrombocytopenia of < 30 x 109/L. use of abciximab, tirofiban, ticlopidine or activated protein C use of heparin < 1 hour prior to the procedure, or low molecular weight heparin in therapeutic doses < 12 hours prior to procedure history of congenital or acquired coagulation factor deficiency or bleeding diathesis no informed consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nicole P Juffermans, MD, PhD
Organizational Affiliation
Academic Medical Centre - University of Amsterdam
Official's Role
Principal Investigator
Facility Information:
Facility Name
Academic Medical Centre - University of Amsterdam
City
Amsterdam
ZIP/Postal Code
1105 AZ
Country
Netherlands
Facility Name
Ter Gooi Ziekenhuizen
City
Hilversum
ZIP/Postal Code
1231 XZ
Country
Netherlands
Facility Name
Leids Universitair Medisch Centrum
City
Leiden
ZIP/Postal Code
2333 XZ
Country
Netherlands
Facility Name
Diakonessenhuis
City
Utrecht
ZIP/Postal Code
3582 KE
Country
Netherlands

12. IPD Sharing Statement

Citations:
PubMed Identifier
25880761
Citation
Straat M, Muller MC, Meijers JC, Arbous MS, Spoelstra-de Man AM, Beurskens CJ, Vroom MB, Juffermans NP. Effect of transfusion of fresh frozen plasma on parameters of endothelial condition and inflammatory status in non-bleeding critically ill patients: a prospective substudy of a randomized trial. Crit Care. 2015 Apr 15;19(1):163. doi: 10.1186/s13054-015-0828-6.
Results Reference
derived
PubMed Identifier
25809519
Citation
Muller MC, Straat M, Meijers JC, Klinkspoor JH, de Jonge E, Arbous MS, Schultz MJ, Vroom MB, Juffermans NP. Fresh frozen plasma transfusion fails to influence the hemostatic balance in critically ill patients with a coagulopathy. J Thromb Haemost. 2015 Jun;13(6):989-97. doi: 10.1111/jth.12908. Epub 2015 Apr 18.
Results Reference
derived
PubMed Identifier
22196464
Citation
Muller MC, de Jonge E, Arbous MS, Spoelstra-de Man AM, Karakus A, Vroom MB, Juffermans NP. Transfusion of fresh frozen plasma in non-bleeding ICU patients--TOPIC trial: study protocol for a randomized controlled trial. Trials. 2011 Dec 23;12:266. doi: 10.1186/1745-6215-12-266.
Results Reference
derived

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Transfusion of Fresh Frozen Plasma in Non-bleeding Intensive Care Unit (ICU) Patients

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