Lacerations of the FDP tendon in zone one may be reattached to bone with a modified Bunnell pullout suture or with suture anchors. Eleven cadaveric fingers were submitted to cyclical testing of five hundred cycles with either a modified Bunnell pullout suture of 3-0 polypropylene or a micro-Mitek suture anchor with 3-0 Ethibond. Gap formation was 6.6mm in the modified Bunnell group and 2.0mm in the micro-Mitek group (p<
0.001). Load to failure was 37.6N in the pullout group and 28.5N in the anchor group (p<
0.005). Gap in the pullout group and low failure load in the anchor group are of concern. Distal zone one FDP tendon lacerations are usually re-attached to bone by a modified Bunnell pullout suture of 3-0 polypropylene. This treatment may lead to moderate to severe losses of DIP joint motion in up to 50% of patients. Suture anchors have recently been introduced as a fixation alternative. Cyclical testing simulating five days of a passive mobilisation protocol was used to compare the Micro-Mitek anchor to the modified-Bunnell pullout suture in FDP tendon fixation. Eleven cadaveric fingers FDP tendons were repaired to bone using a modified Bunnell pullout suture of 3-0 polypropylene or a micro-Mitek anchor with 3-0 Ethibond. Testing was done from 2N to 15N at 5N/sec, for a total of five hundred cycles. Gap formation at the tendon bone interface was measured. Load-to-failure was performed on all specimens. No specimens failed during cyclic testing. Gap formation was 6.6mm (SD 1.2, range 4.9–8.2mm) and 2.0mm (SD = 0.4, range 1.7–2.7mm) for the pullout technique and the micro-Mitek anchor repair respectively (p<
0.001). Load to failure data was 37.6N (SD 4.7, range 31.8–45.1N) for the pullout group and 28.5N (SD 4.0, range 21.8–33.4N) for the micro-Mitek group (p<
0.005). This data suggests that both fixation techniques may be adequate to sustain five days of simulated passive rehabilitation therapy. Significant gap formation in the modified Bunnell pullout group is of concern although this needs to be correlated in the clinical setting. The lower failure rate of the micro-Mitek group may leave a narrow margin of safety for passive rehabilitation.
In relation to the conduct of this study, one or more of the authors is in receipt of a research grant from a non-commercial source.
The use of plates and screws for the treatment of certain metacarpal fractures is well established. Securing plates with bicortical screws has been considered an accepted practice. However, no study has questioned this. This study biomechanically assessed the use of bicortical versus unicortical screws in metacarpal plating. Eighteen fresh frozen cadaveric metacarpals were subject to midshaft transverse osteotomies and randomly divided into two groups. Using dorsally applied Leibinger 2.3mm 4 hole plates, one group was secured using 6mm unicortical screws, while the second group had bicortical screws. Metacarpals were tested to failure using a four point bending protocol in an apex dorsal direction on a servo-hydraulic testing machine with a 1kN load cell. Load to failure, rigidity, and mechanism of failure were all assessed. Each group had three samples that did not fail after a 900 N load was applied. Of those that failed, the mean load to failure was 596N and 541 N for the unicortical and bicortical groups respectively. These loads are well in excess of those experienced by the in-vivo metacarpal. The rigidity was 446N/mm and 458N/mm of the uni-cortical and bicortical groups respectively. Fracture at the screw/bone interface was the cause of failure in all that failed, with screw pullout not occurring in any. This study suggests that there may be no biomechanical advantage in using bicortical screws when plating metacarpal fractures. Adopting a unicortical plating method simplifies the operation, and avoids potential complications associated with overdrilling and oversized screws.
The behaviour of two different methods of reattachment of the flexor digitorum profundus tendon insertion was assessed. Cyclical testing simulating the first 5 days of a passive mobilisation protocol was used to compare the micro Mitek anchor to the modified-Bunnell pull-out suture. Twelve fresh-frozen cadaveric fingers were dissected to the insertion of the FDP tendon. The FDP insertion was then sharply dissected from the distal phalanx and repaired using one of two methods: group 1 -modified Bunnell pullout suture using 3/0 Prolene; group 2 micro Mitek anchor loaded with 3/0 Ethibond inserted into the distal phalanx. Each repaired finger was mounted on to a material testing machine using pneumatic clamps. We cyclically tested the repair between 2N and 15N using a load control of 5N/s for a total of 500 cycles. Gap formation at the tendon bone interface was measured every 100 cycles. No specimens failed during cyclical testing. After 500 cycles, gap formation of the tendon-bone interface was 6.6mm (SD = 1.2mm), and 2.1 mm (SD = 0.3mm) for the pullout technique and the micro Mitek anchor repair respectively. Concerns related to suture anchors, such as anchor failure or protrusion, joint penetration, and anchor-suture junction failure, were not encountered in this study. Cyclical loading results suggest that the repair achieved with both methods of fixation is sufficient to avoid failure. However, significant gap formation at the tendon-bone interface in the modified Bunnell group is of concern, suggesting it may not be the ideal fixation method.