A Comparison of Steel and Bioabsorbable Screw Fixation of Lisfranc Foot Injuries

The Lisfranc ligaments are a group of ligaments that connect the bones of the middle portion
of the foot to each other. The Lisfranc ligaments allow for a normal and stable range of
motion and shape to the foot.

When the Lisfranc ligaments are disrupted, the stability it had given to the middle of the
foot is lost. Attempted activity at the foot will result in pain and abnormal motion. If
injury to the Lisfranc ligaments is left untreated, the eventual end result is foot
arthritis and deformity.

The current standard orthopaedic treatment of Lisfranc ligament injuries is surgery. The
Lisfranc ligaments are fixed by compressing the space between the middle bones of the foot
with steel screws. These screws allow for ligament healing. As the ligaments heal, the
patient should not resume activity with the fixed foot too soon as the screw may break. A
second surgical procedure is often recommended to remove the screw 6 months after surgery.
This allows for a complete return of normal foot range of motion, but at the cost of a
second procedure.

The use of materials that can be absorbed by the human body to fix the Lisfranc ligaments
has only been studied in 1 paper. One such material is the Smart Screw (Bionx, Blue Bell,
Pennsylvania) which is approved by the Food and Drug Administration (F.D.A.) and made of
polylevolactic acid (PLA). Absorbable screws could be ideal for the treatment of Lisfranc
ligament injuries.

Comparing the long-term results of fixing the Lisfranc ligaments with either a steel or
absorbable screw is important as there are no studies on the subject to date. There is only
1 published study regarding absorbable screws to fix the Lisfranc ligaments. The purpose of
this study is to compare the outcome of steel and absorbable screw fixation of the Lisfranc
ligaments in foot injuries in one surgeon's (J.A.) practice at Thomas Jefferson University
Hospital, Riddle Memorial Hospital, and Nazareth Hospital.

This study will be conducted in a prospective manner. This study does not focus on
experimental procedures or components, but rather involves the accepted management of a
select population of patients.

This study will be performed in a randomized, prospective manner involving 2 groups of
patients (steel vs. bioabsorbable screw populations) from 3 different hospitals. Power
analysis has been conducted to ensure an adequate patient population size.

The risks to patients will be minimal. The standard risks of fixing the Lisfranc ligaments
include bleeding, infection, nerve injury, recurrent foot instability, and the dangers of
administering anesthesia.

Study Groups Chosen patients for this study will be randomly assigned to one of two groups.
Group A will consist of patients that receive the steel screw. Group B will contain the
patients that receive the absorbable screw. Postoperative activity restrictions and
rehabilitation will be kept the same between the two groups.

Routine protocols for care of foot fracture patients will be utilized regarding infection,
wound care, pain control, and weightbearing restrictions. The involved foot will be placed
in a non-weight-bearing splint that patients are requested to avoid handling until it is
removed by the PI upon the first postoperative visit.

Patients who have their injury fixed using steel screws, need a second surgery in 6 months
for removal of the screw. This is the standard textbook treatment and is not a revision
surgery. Patients who will receive absorbable screw, wont need this surgery. This will be
discussed with the patient at the time of the approach for recruitment.

Outcome evaluation The PI will monitor and follow the patients during and after surgery.
Data collection will include the details of the surgery, intraoperative and postoperative
course including complications if applicable, and number of revision surgeries performed
should they occur. These patients received postoperative follow-up at 2 weeks, 6 weeks, 3
months, 6 months, 1 year, 2 years, and 3 years. Both groups of patients are prohibited from
bearing weight on the affected foot for six weeks. Patients will be instructed to gradually
increase weight-bearing starting at six weeks.

Postoperative satisfaction and function which will be scored according to the American
Orthopaedic Foot and Ankle Society (AOFAS) Midfoot scale which is highly accepted for its
validity, reliability, and reproducibility.

Patients will also be asked about their satisfaction with the surgical results using both
the 10 cm visual analog scale (VAS) and a four-point scale (poor, mild, good, and
excellent). Observed complications including need for further revision surgeries would be
documented. All of this information would have been gathered during the patients' follow-up
visits in the outpatient clinics after surgery. For those patients that receive a steel
screw, they will receive a second outpatient surgical procedure after the 6-month
postoperative follow-up to remove that screw using current standard orthopaedic technique.

Postoperative foot X-rays of these patients during their follow up in the outpatient setting
will also be examined to view proper alignment and compression of the middle portion of the
foot together which indicates healing of the Lisfranc ligaments. Radiographs are used to
evaluate the screw for breakage. In the case of the absorbable screw, radiographs are also
done to assess absorption.

Inclusion Criteria:

1. Subjects will be adults of any gender or race.

2. Subjects will be adults between 18 and 75 years of age.

3. The underlying diagnosis will be a Lisfranc foot injury.

4. The indication for fixing the Lisfranc ligaments is abnormal separation of the middle
part of the foot from each other.

5. Subjects will have received either a steel or absorbable screw to fix the Lisfranc
ligaments.

Exclusion Criteria:

1. Subjects may not have any cognitive impairment that would, in the investigator's
opinion, preclude study participation or compliance with protocol mandated
procedures.

2. Subjects may not have a history of known alcohol, analgesic, or narcotic substance
abuse within 12 months prior to pretreatment.

3. Subjects may not have a history of severe psychiatric illness such as depression or
psychosis that may influence the results of administered outcome questionnaires.

4. Subjects may not be pregnant.

5. Subjects may be excluded from this study for any reason that may pose unnecessary
risk or confounding of data, in the judgment of the investigator. This includes the 4
above points.

6. Subjects must not have intact or normal Lisfranc ligaments in the foot.

7. Subjects may not have a history of deep Lisfranc joint infection.