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115

INTRODUCTION

Synthetic devices have been available since the

1970s for the treatment of anterior cruciate

ligament (ACL) injury. Such devices have a

number of potential benefits including the

avoidance of donor site morbidity, provision of

a strong stabilising construct – thereby allowing

aggressive rehabilitation and an early return to

sport – and the absence of the potential for

disease transmission. Despite these potential

benefits, the use of synthetic ligaments for ACL

reconstruction remains controversial. Devices

implanted in the late 1970s and 1980s had poor

outcomes including high failure rates and

significant complications such as synovitis,

osteolysis and osteoarthritis. More recent

devices appear to have better reported outcomes

in the short to mid-term, but have not gained

widespread support.

HISTORICAL OVERVIEW

A full historical account of the use of synthetic

devices in for ACL reconstruction is beyond

the scope of this chapter, but a brief summary is

provided as a background to current thinking.

A more detailed account can be found in the

article by Mascarenhas and MacDonald [6].

One of the major concerns with earlier synthetic

grafts was synovitis. It was attributed to

abrasion and breakage of the synthetic devices

resulting in free debris and particles within the

joint and there was concern that because of the

non-absorbable nature of the synthetic

ligaments, there was an increased risk of

developing osteoarthritis.

There was considerable interest in the potential

of carbon fiber as a scaffold for ligament

regeneration in the 1970s. A number of carbon

fiber devices were developed but were

associated with high failure rates, synovitis and

dissemination of carbon fiber to regional lymph

nodes. Modifications were made to include

polylactic acid and polycapralactone coating in

an ultimately unsuccessful attempt to reduce

problems with carbon wear particles.

Various devices have been developed from

polyester composites. The Leeds-Keio syn­

thetic ligament was woven from polyester and

was intended to serve as a scaffold for ingrowth

of ligamentous tissue. Conflicting results with

regard to ingrowth and clinical out come were

reported and concerns were raised about the

presence of foreign body giants cells containing

polyester debris. Like other synthetic ligaments,

the Leeds-Keio ligament fell into disuse.

The Dacron artificial ligament was made of

polyester strips and was designed as an

augmentation. It was nonetheless used by some

surgeons as a prosthetic ligament in “salvage”

IS THERE A PLACE FOR

A SYNTHETIC LIGAMENT?

J.A. FELLER