PIPJ replacement has become increasingly popular however, there is very little clinical data available apart from small studies and those from the originators of the prostheses. We present a review of our initial experience with the Acension(c) Pyro-carbon PIP joint. Data was collected from 62 joints in 39 patients with one patient lost to follow-up. Mean age was 61.6 years. 29 patients were female and 10 male. Mean follow up was 22.3 months (range 11 to 54). 7 patients or 11% needed further surgery. The majority were for stiffness with 3 operations for dislocation or component malposition. The total complication rate was 32%, again the biggest problem was stiffness. 4 joints have subluxed or dislocated, 2 had superficial infections. There was no statistical difference in the rate of complications compared to the operated finger or the pre-operative diagnosis. Post-operatively patients had a mean fixed flexion deformity of 19° and flexed to 76° (58° arc). However patients undergoing surgery following trauma do not do as well as the other groups with a decrease in ROM of 33°.Introduction
Results
We therefore compared the fixation strength achieved with simple suture, by bone anchor and by interference screw (Mini Bio-suture Tack and 3mm Biotenodesis interference screw, Arthrex, UK).
87 patients (51 male, 36 female; mean age 57, range 30 to 82) underwent arthroscopic subacromial decompression (SAD) and were followed up for one year. We calculated the ASES, the Constant, the DASH Disability/ Symptom, and the SF-36 Physical Function scores. All the scores improved throughout the follow-up period, although the SF36 score showed less marked improvement. Comparing the preoperative and one year values there were significant improvements at one year (p <
0.001) for the three upper-limb-specific scoring systems (ASES, Constant and DASH), and for the SF36, but less so (p = 0.001). Comparing the 6 months and one year scores there were significant improvements in the ASES, Constant and DASH scores, but not in the SF36 score. This suggests that improvement may still be continuing at one year. No significant differences in the postoperative scores for the four acromion operative appearance groups (normal, minor scuffing, marked damage, bare bone areas) were found, or for the operative cuff appearance groups (normal, minor scuffing, partial tear, full thickness tear, massive cuff tear). We also asked for the patients’ assessment of their outcome at one year, using a satisfaction visual analogue scale (VAS), and two category selection questions relating to satisfaction and to perceived room for further improvement respectively. Patients were coded as successes or failures on their responses to the VAS and the two questions. There seems to be an association with cuff appearance and success or failure as determined by the response to the room for improvement question. More specifically, this difference seems to be due the infraspinatus. A normal infraspinatus is associated with a successful outcome as perceived by the patient. In conclusion, with SAD recovery may not be complete at one year. The three limb-specific scores are equally useful in monitoring progress, whereas the more general SF36 score is less useful. The state of the acromion or cuff does not have an effect on outcome as measured by the commonly used scores. The appearance of the infraspinatus may be predictive of success as measured by the patient.
The study assesses the efficacy of commonly used suture materials with commonly described arthroscopic knotting techniques in as close a physiological pattern as possible. The investigation was carried out in three phases. Initially the suture material strength was tested. The suture was then tested to failure using the different knotting techniques. Finally the test was repeated after soaking the suture with normal saline. A Hounsfield tensometer was utilised with a load cell of 1000N, strain rate of 25mm/min, bar separation of 7.5mm and standard temperature and pressure. Suture material tested was 2 ethibond, 1 PDS and 1 Panacryl. Knotting techniques compared were the Tennessee slider, Tautline hitch, Duncan Loop, SMC knot and Surgeon’s knot. Two surgeons tied each knot 10 times after first becoming practiced with each technique. Each knot was tested to failure on 10 sequential experiments. Ultimate strength of the suture material and of the knotting techniques was assessed. In addition the mode of failure, whether the knot slipped or suture material fractured was investigated. As expected, 2 ethibond has a higher ultimate strength than either 1 PDS or 1 Panacryl. The Tautline hitch and Surgeon’s knot had a significantly lower slippage rate when compared to the other knotting techniques. (P value <
0.002). The Tennessee slider, Duncan Loop and SMC knots slipped in more than 50% of experiments. No difference was observed when the suture material had been soaked in normal saline. The number of half hitches required to provide maximum knot holding capacity was 3, confirming previous experimental findings by other investigators. The Tautline hitch is recommended for use with all suture materials due to low slippage rates, ease of tying, ease of sliding and overall high knot strength