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Albumin vs. Plasma for PEdiAtric pRiming Trial (APPEAR)

Primary Purpose

Hemorrhage

Status
Completed
Phase
Phase 4
Locations
Italy
Study Type
Interventional
Intervention
Albumin
Fresh Frozen Plasma
Sponsored by
IRCCS Policlinico S. Donato
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Hemorrhage focused on measuring albumin, fresh frozen plasma, extracorporeal circulation, cardiovascular surgery, pediatric population

Eligibility Criteria

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

Inclusion Criteria:

  • weight under 10 kg
  • cardiovascular surgery procedure with extracorporeal circulation
  • need for hematic priming solution
  • elective surgery
  • informed consent signed

Exclusion Criteria:

  • congenital disorders of coagulation system
  • emergency surgery

Sites / Locations

  • IRCCS San Donato

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Albumin

Fresh Frozen Plasma

Arm Description

5% Albumin to be added to the priming solution composed of concentrated red cells to reach a target of 28-30% hematocrit and albumin to reach the standard volume administered to these patients (400 ml)

Fresh Frozen Plasma to be added to the priming solution composed of concentrated red cells to reach a target of 28-30% hematocrit and plasma to reach the standard volume administered to these patients (400 ml)

Outcomes

Primary Outcome Measures

Volume of postoperative bleeding
Postoperative bleeding in ml/kg, as measured by chest drainage

Secondary Outcome Measures

Number of units of blood components transfused
All kind of blood products (packed red cells, fresh frozen plasma, platelet concentrate) transfused from the extracorporeal circulation beginning
Hours on artificial ventilation
Artificial ventilation duration from the ICU admission till extubation
Days of hospital stay
Hospital stay duration from ICU admission till discharge
Thromboembolic complications
All kind of thromboembolic complication (peripheric, pulmonary, mesenteric) from ICU admission till discharge from the hospital

Full Information

First Posted
March 15, 2016
Last Updated
August 29, 2016
Sponsor
IRCCS Policlinico S. Donato
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1. Study Identification

Unique Protocol Identification Number
NCT02738190
Brief Title
Albumin vs. Plasma for PEdiAtric pRiming Trial
Acronym
APPEAR
Official Title
Albumin vs. Plasma for PEdiAtric pRiming Trial
Study Type
Interventional

2. Study Status

Record Verification Date
August 2016
Overall Recruitment Status
Completed
Study Start Date
January 2015 (undefined)
Primary Completion Date
May 2016 (Actual)
Study Completion Date
May 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
IRCCS Policlinico S. Donato

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This is a randomized controlled trial that compares two different priming composition (albumin vs. fresh frozen plasma) for extracorporeal circulation of pediatric patients under 10 kg of weight. The two approaches are both employed at the moment but there is actually no evidence on the superiority of one over the other. This study is aimed to test the hypothesis that Albumin is superior to fresh frozen plasma in terms of minor bleeding and transfusional requirements.
Detailed Description
Extracorporeal circulation (ECC) in neonates and infants undergoing cardiac surgery for the correction or palliation of cardiac defects is characterized by temperature variation, activation of coagulation and inflammatory cascades, hemodilution. An excessive dilution of circulating mass determines a variation in colloid-oncotic pressure (COP) that, together with hydrostatic pressure, induces liquids exchange between interstitial space and plasma. COP variation together with inflammatory response due to extracorporeal circulation and temperature variation is the main determinant of interstitial and pulmonary edema occurrence. Intravascular albumin is responsible for 80% for the COP. Golab et al. randomized a population of neonates and infants undergoing to pediatric cardiac surgery procedures in order to reach two different targets of COP through administration of different albumin amounts. His results didn't show significant differences for primary and secondary endpoints except for postoperative ventilation duration. Trials on adult patients undergoing cardiac surgery haven't showed differences in bleeding when varying colloid solution employed. Albumin is preferred to artificial colloids due to reduced risk of anaphylactic reactions and for its capacity to maintain COP. Hemodilution is associated to a reduction in hematocrit, platelet count, fibrinogen and other coagulation factor concentration. Solutions employed for ECC (Extracorporeal Circulation) circuits priming also contain components that could impair hemostasis. In order to reduce the negative effects on the coagulation, many centers for pediatric surgery employ fresh frozen plasma (FFP) for priming solution. Oliver et al randomized a population of 51 cardiopathic, acyanotic children under 10 kg of weight to receive either albumin or FFP as ECC priming. The authors showed a reduction of postoperative bleeding in the group receiving FFP. No significant differences were detected in postoperative coagulation tests. Other studies with small cohorts weren't able to detect significant differences between the two regimens applied by Oliver and colleagues. Currently the patients receiving blood priming are treated with either FFP or albumin in order to maintain a correct COP. Comparative studies are very limited by small populations and haven't yet provided definitive conclusions about eventual superiority of one regimen over another. This is a randomized controlled trial that compares the employment of 5% Albumin (ALB group) versus Fresh Frozen Plasma (FFP group) for priming as per standard protocol of extracorporeal circulation procedure. No modifications to the normal clinical management of the patient are planned. The primary endpoint is to reduce postoperative bleeding (registered as ml/kg in the first 12 postoperative hours). The secondary endpoints are to reduce transfusional requirements for all the blood products (packed red cells, fresh frozen plasma and platelets registered as ml/kg from the beginning of the extracorporeal circulation for up to 48 hours from the termination of the surgery), ventilation support and hospital stay duration. Safety endpoint is represented by the percentage of thromboembolic complications (stroke, peripheric, pulmonary and mesenteric thromboembolisms). Both the treatments employed in this trial are to be considered standard.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hemorrhage
Keywords
albumin, fresh frozen plasma, extracorporeal circulation, cardiovascular surgery, pediatric population

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
80 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Albumin
Arm Type
Active Comparator
Arm Description
5% Albumin to be added to the priming solution composed of concentrated red cells to reach a target of 28-30% hematocrit and albumin to reach the standard volume administered to these patients (400 ml)
Arm Title
Fresh Frozen Plasma
Arm Type
Active Comparator
Arm Description
Fresh Frozen Plasma to be added to the priming solution composed of concentrated red cells to reach a target of 28-30% hematocrit and plasma to reach the standard volume administered to these patients (400 ml)
Intervention Type
Drug
Intervention Name(s)
Albumin
Other Intervention Name(s)
Albumina, Human Albumin
Intervention Description
Albumin 5% added to blood priming solution
Intervention Type
Biological
Intervention Name(s)
Fresh Frozen Plasma
Intervention Description
Fresh Frozen Plasma added to blood priming solution
Primary Outcome Measure Information:
Title
Volume of postoperative bleeding
Description
Postoperative bleeding in ml/kg, as measured by chest drainage
Time Frame
24 hours
Secondary Outcome Measure Information:
Title
Number of units of blood components transfused
Description
All kind of blood products (packed red cells, fresh frozen plasma, platelet concentrate) transfused from the extracorporeal circulation beginning
Time Frame
48 hours
Title
Hours on artificial ventilation
Description
Artificial ventilation duration from the ICU admission till extubation
Time Frame
hours until extubation, an average of 72 hours
Title
Days of hospital stay
Description
Hospital stay duration from ICU admission till discharge
Time Frame
days until discharge, an average of 10 days
Title
Thromboembolic complications
Description
All kind of thromboembolic complication (peripheric, pulmonary, mesenteric) from ICU admission till discharge from the hospital
Time Frame
Postoperative hospital stay until discharge, an average of 10 days

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: weight under 10 kg cardiovascular surgery procedure with extracorporeal circulation need for hematic priming solution elective surgery informed consent signed Exclusion Criteria: congenital disorders of coagulation system emergency surgery
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marco Ranucci, MD, FESC
Organizational Affiliation
IRCCS Policlinico S. Donato
Official's Role
Principal Investigator
Facility Information:
Facility Name
IRCCS San Donato
City
San Donato Milanese
State/Province
MI
ZIP/Postal Code
20097
Country
Italy

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
436426
Citation
Weil MH, Henning RJ, Puri VK. Colloid oncotic pressure: clinical significance. Crit Care Med. 1979 Mar;7(3):113-6. doi: 10.1097/00003246-197903000-00006. No abstract available.
Results Reference
background
PubMed Identifier
21055963
Citation
Golab HD, Scohy TV, de Jong PL, Kissler J, Takkenberg JJ, Bogers AJ. Relevance of colloid oncotic pressure regulation during neonatal and infant cardiopulmonary bypass: a prospective randomized study. Eur J Cardiothorac Surg. 2011 Jun;39(6):886-91. doi: 10.1016/j.ejcts.2010.09.040. Epub 2010 Nov 5.
Results Reference
background
PubMed Identifier
16085250
Citation
Chandler WL. Effects of hemodilution, blood loss, and consumption on hemostatic factor levels during cardiopulmonary bypass. J Cardiothorac Vasc Anesth. 2005 Aug;19(4):459-67. doi: 10.1053/j.jvca.2004.11.046.
Results Reference
background
PubMed Identifier
12735570
Citation
Oliver WC Jr, Beynen FM, Nuttall GA, Schroeder DR, Ereth MH, Dearani JA, Puga FJ. Blood loss in infants and children for open heart operations: albumin 5% versus fresh-frozen plasma in the prime. Ann Thorac Surg. 2003 May;75(5):1506-12. doi: 10.1016/s0003-4975(02)04991-3.
Results Reference
background
PubMed Identifier
14992912
Citation
McCall MM, Blackwell MM, Smyre JT, Sistino JJ, Acsell JR, Dorman BH, Bradley SM. Fresh frozen plasma in the pediatric pump prime: a prospective, randomized trial. Ann Thorac Surg. 2004 Mar;77(3):983-7; discussion 987. doi: 10.1016/j.athoracsur.2003.09.030.
Results Reference
background
PubMed Identifier
28510741
Citation
Bianchi P, Cotza M, Beccaris C, Silvetti S, Isgro G, Pome G, Giamberti A, Ranucci M; Surgical and Clinical Outcome REsearch (SCORE) group. Early or late fresh frozen plasma administration in newborns and small infants undergoing cardiac surgery: the APPEAR randomized trial. Br J Anaesth. 2017 May 1;118(5):788-796. doi: 10.1093/bja/aex069.
Results Reference
derived

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Albumin vs. Plasma for PEdiAtric pRiming Trial

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