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DOS Kongressen 2017 ·

101

Prevention of Bone Bridge Formation using Autologous

Cartilage in an Experimental Porcine Model

Ahmed Abdul-Hussein Abood, Bjarne Møller-Madsen, Juan Manuel Shiguetomi-

Medina, Hans Stødkilde-Jørgensen, Casper Bindzus Foldager, Ole Rahbek

Children’s Orthopaedics, Aarhus University Hospital; Children’s Orthopaedics,

Aarhus University Hospital; Orthopaedic Research Laboratory, Aarhus University

Hospital; MR Center Skejby, Aarhus University Hospital; Orthopaedics, Aarhus

University Hospital; Children’s Orthopaedics, Aarhus University Hospital

Background:

Bone bridges can occur due to physeal injury. This can lead to

partial growth arrest and bone deformities. The current treatment is ineffective.

Purpose / Aim of Study:

Investigate efficacy of autologous cartilage for phy-

seal repair in a porcine experimental gap model.

Materials and Methods:

Five immature pigs were included in the study. At

baseline the medial part of the distal femoral physis was injured in both legs us-

ing a 6 mm cannulated drill. The drill was inserted 1.5 cm into the bone creating

a standardized gap mimicking a defect after resection of a physeal bone bridge.

The defects were rinsed with sterile saline. Upon randomization, the right leg

was selected for either filling of defect with cartilage chips and Tiseel® (Group

A, n =5) or Tiseel only (Group B, n=5). Cartilage was harvested from low-

weight-bearing parts of the femoral condyle of the leg randomized for cartilage

treatment. A sharp incision through the skin, patellar ligament and Hoffa’s fat

pad was made. The articular surface was exposed. Through two 6 mm punches

sites were designated and harvested. The cartilage fragments were cut with a

scalpel perioperatively into smallest possible sized chips. The chips were molted

with the Tisseel® and inserted into the empty defect. Tiseel® was inserted into

the contralateral empty defect. The animals were housed for 14 weeks. MRI

was performed at 14 weeks.

Findings / Results:

No bone bridges were found on MRI in Group A. In Group B

one case of bone bridge formation was verified. The water- content measured

on MRI, showed a greater mean value (9,5%) in Group B.

Conclusions:

Bone bridges were prevented when autologous cartilage chips

were added to the Tiseel®. This suggests that transplantation of autologous

cartilage chips may play a role in preventing bone bridge formation.

No conflicts of interest reported

53.