The examination of the ability of the OrthoPAT® blood collection device to decrease the transfusion rate and volume of adults undergoing posterior spine surgery for deformity correction of 6 levels or more.
The purpose of this study is to investigate the use of postoperative drains with blood salvage capabilities to determine if they decrease both the volume and rate of allogenic blood transfusion in adult patients undergoing multilevel spine surgery for deformity. In addition, the ability of these drains to decrease the complications that are associated with allogenic blood exposure (postoperative infection, volume overload and transfusion reactions) will also be evaluated.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
70
The Hospital for Special Surgery
New York, New York, United States
Volume of Allogenic Blood Transfused Postoperatively
The total volume of allogenic blood transfused postoperatively will be measured during the first 48 hours postoperatively while the drains are in place.
Time frame: 48 hours postoperative
Hemoglobin Levels, Post-Op Day 3
Hemoglobin levels will be measured post-operatively day 3
Time frame: 3 days postop
Hemoglobin Levels, Post-Op Day 2
Hemoglobin levels will be measured post-operatively day 2
Time frame: 2 days postop
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