Adolescent Idiopathic Scoliosis Clinical Trial
Official title:
Effectiveness Of Gelatin Matrix With Human Derived Thrombin On Blood Loss, Surgical Time, Hospital Stay And Complications In Adolescents Undergoing Spine Surgery For Adolescent Idiopathic Scoliosis: A Randomized Clinical Trial.
The Finnish Paediatric Orthopaedic Study Group will perform a prospective randomized, multicenter, clinical trial comparing Gelatin matrix with human derived thrombin (Floseal, Baxter) and without use of Floseal in adolescents undergoing posterior spinal deformity surgery for AIS (adolescent idiopathic scoliosis between 45 and 90 degrees) in Turku, Tampare and Helsinki Children's Hospitals. Sixty patients will be randomized into the intervention group receiving Floseal (n=30) and control group not receiving Floseal (n=30). Each University Hospital will treat 10 Floseal and 10 conventional treated scoliosis patients (block randomization). Both treatment groups will be allowed to use conventional blood saving methods.
Background: Posterior spinal deformity surgery can be associated with major blood loss,
especially from cancellous bone or epidural venous plexus. Products such as Gelatin Matrix
with bovine derived thrombin (Floseal) can be used to prevent blood loss in adult patients
undergoing spine surgery.
Aim: To document and compare effectiveness of Gelatin matrix with human derived thrombin with
conventional blood loss control methods in adolescents undergoing posterior spinal deformity
surgery for adolescent idiopathic scoliosis (AIS), who do not need vertebral column
resection.
Methods: The Finnish Paediatric Orthopaedic Study Group will perform a prospective
randomized, multicenter, clinical trial comparing Gelatin matrix with human derived thrombin
(Floseal, Baxter) and without use of Floseal in adolescents undergoing posterior spinal
deformity surgery for AIS (adolescent idiopathic scoliosis between 45 and 90 degrees) in
Turku, Tampere and Helsinki Children's Hospitals. Sixty patients will be randomized into the
intervention group receiving Floseal (n=30) and control group not receiving Floseal (n=30).
Each University Hospital will treat 10 Floseal and 10 conventional treated scoliosis patients
(block randomization). Both treatment groups will be allowed to use conventional blood saving
methods.
Main outcome measures:
Blood loss during surgery (millilitres) Drain output during 24 hours (millilitres) Total
blood loss (Blood loss during surgery + drain output, millitres) Used blood products (Red
cell, frozen plasma, and thrombocyte units) Time of surgery Hospital stay Cost benefit
analysis (blood product use, surgical time, hospital stay) Complications related to use of
Floseal as a secondary outcome measure.
Primary Hypothesis and expected outcomes: Use of Floseal will reduce blood loss and surgical
time in patients undergoing spine surgery for adolescent idiopathic scoliosis (Level-I
evidence). Cost benefit analysis will most probably show that the use of Floseal is cost
effective. E.g. the value of one allogenic Red Blood Cell unit is 400€. If no red blood cell
units are needed instead of the usual three, the reduced blood product use alone will cover
the extra costs of Floseal use. In addition, if no allogenic blood infusions are needed, the
risk of infections will probably be significantly less. Reduced surgical time and shorter
hospital stay may also be cost reducing findings in patients receiving Floseal.
Safety Aspects: Gelatin Matrix with human derived thrombin (Floseal, Baxter Biosurgery) is
indicated for blood loss control in patients undergoing spine surgery when other methods are
less effective.
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