Autologous Chondrocyte Implantation: Transarthroscopic Implantation of Hyalograft (Hyaff 11) with Autologous Chondrocytes

Published on 11/03/2015 by admin

Filed under Orthopaedics

Last modified 22/04/2025

Print this page

rate 1 star rate 2 star rate 3 star rate 4 star rate 5 star
Your rating: none, Average: 0 (0 votes)

This article have been viewed 1685 times

Chapter 9D Autologous Chondrocyte Implantation

Transarthroscopic Implantation of Hyalograft (Hyaff 11) with Autologous Chondrocytes

Introduction

To facilitate the implantation of cultured chondrocytes and make it possible to perform an autologous chondrocyte implantation (ACI) procedure transarthroscopically, different porous scaffolds have been developed. One such material is based on the benzylic ester of hyaluronic acid (Hyaff 11, Fidia Advanced Biopolymers, Abano Terme, Italy) and consists of a network of 20-μm-thick fibers with interstices of variable sizes.

It has been demonstrated to be an optimal physical support to allow cell-cell contacts, cluster formation, and extracellular matrix deposition and to deliver differentiated chondrocytes.1,2

The cells harvested from the patient are expanded and then seeded onto the scaffold where the cells are able to redifferentiate and retain a chondrocytic phenotype even after a long period of in vitro expansion in monolayer culture1,2 (Fig. 9D-1). The Hyalograft with cultured chondrocytes may be implanted by press fitting directly into the lesion as described by Kon et al.3 The scaffold has self-adhesive properties, but most often additional fibrin glue is needed for a secure positioning. In this chapter, the authors describe a modified implantation technique: the “folded blanket” technique for the knee and for the ankle.

Technical Overview

Cartilage is harvested as described in Chapter 9C. The cell culture takes a longer time to grow compared to when cells are transplanted as suspension. After 4 to 5 weeks, the scaffold is delivered as 2 × 2 cm large patches (Fig. 9D-2). Depending on the quality of the cultured cells, the seeded scaffolds have different strength.

Operative Technique for the Knee

A high anteromedial or anterolateral portal is created, and a standard arthroscopy is performed in supine position.

The arthroscopic Hyalograft-chondrocyte technique is applicable for defects at the medial and lateral femoral condyle, trochlea, tibial plateau, and in some rare cases when reachable also for the patella.

For a defect at the medial femoral condyle, a medial suprameniscal portal is created. This portal is needed to introduce the matrix into the joint.

A half pipe introducer may be used to introduce the scaffold into the joint.

The defect has already been debrided as described in Chapter 3. The central part of the defect is treated by a microfracture awl to get a fixation point (mushroom fixation) (Fig. 9D-3).

The chondrocyte-seeded matrix is then cut with a scissor or scalpel to the approximate size of the defect (Fig. 9D-4).

The scaffold is covered with a thin fibrin glue layer (Fig. 9D-5), grasped with an arthroscopic grasp instrument with plain surfaces (Fig. 9D-6), and introduced into the joint along the half pipe intruder to reach the defect (Fig. 9D-7).

The pressure controlled pump may be stopped intermittently during the procedure. (The operation may also be done in CO2.)

The scaffold is released from the grasper and with a smooth arthroscopy obturator caught and moved into the defect. The central part of the scaffold is pressed gently into the fixation point.

Some extra fibrin glue is injected over the implanted scaffold, and the scaffold is compressed toward the defect bottom with a curved smooth tonsil elevator. If the scaffold is oversized, the edges may be folded like a blanket into the defect to fill it up entirely (Fig. 9D-8).

If too small, additional pieces of the scaffold are implanted to fill the defect like a patchwork quilt. Several layers of Hyalograft may be needed to fill the defect up to surrounding cartilage (mille feuille technique) (Fig. 9D-9).

Excess glue is taken away with a gentle move of the shaver. Care should be taken not to catch the implant with the shaver.

Graft adherence and integration are controlled by moving the knee joint with flexion and extension movements. The scaffold should either be in level with surrounding cartilage or slightly below (Fig. 9D-10).

Hyalograft with Seeded Chondrocytes and Bone Grafting for Osteochondral Defects

When a bone grafting is needed for deep and large osteochondral defects such as osteonecrosis and osteochondritis dissecans (OCD), the seeded scaffold may be used directly in conjunction with bone grafts. The bone grafts may be harvested from the crista iliaca anterior superior region or from the proximal tibia (Fig. 9D-13).

The bone grafts are mixed with fibrin glue to a putty-like consistency, forming bone paste (Fig. 9D-14). The bone grafts are put into a 2-ml syringe where the top of syringe has been cut off leaving a round opening (Fig. 9D-15). The bone grafts may be mixed with an artificial bone substitute if needed.

The bony defect has been prepared by excision and subchondral drilling to stimulate the sclerotic bone region.

Finally, the bone paste is implanted via the syringe into the osteochondral defect (Fig. 9D-16). The bone paste is compressed to fill the osseous part of the defect (Figs. 9D-17 and 9D-18).

The cell seeded scaffold is implanted and put over the top of the bone grafts, saturated with fibrin glue (Fig. 9D-19). Extension-flexion motions are used to test the stability of the dual graft (Fig. 9D-20).