The purpose of the study was to test the hypothesis that cellular mechanisms of fibroblasts derived from primary frozen shoulder (PFS) exhibit similar activity in terms of contraction, response to cytokine transforming growth factor-beta1 (TGF beta1) and mechanical stimulation similar to that generated by fibroblasts derived from Dupuytren’s disease. Frozen shoulder has been postulated to be Dupuytren’s disease of the shoulder with an association inferred since 1936. Primary explant cultures of fibroblasts from seven patients with PFS and five control patients were obtained using standard tissue culture techniques. Fibroblasts were seeded in 3-D collagen constructs and contraction force generated over 24 hours measured using a culture force monitor (CFM) in real time. Increasing concentrations of TGF-beta1 were added to cell seeded gels and force generated measured using the CFM over 24 hours. These mechanical output data were statistically compared to data available from Dupuytren’s disease. Compared to Dupuytren’s fibroblasts, PFS fibroblasts showed a statistically reduced ability to contract a 3-D collagen gel over 24 hours (p< 0.01). In Dupuytren’s disease, fibroblasts derived from nodules and cords generate peak forces of 140 dynes and 110 dynes respectively, while PFS fibroblasts generated peak force of 8 dynes The response to TGF-beta1 stimulation, which has been shown to enhance peak force contraction in Dupuytren’s fibroblasts had no effect on PFS fibroblasts and this was statistically significant (p< 0.01). These data suggest intrinsic differences in cellular activity and mechanisms between Dupuytren’s and Primary Frozen Shoulder even though clinically they both manifest with a contracted extracellular matrix affecting function and requiring surgical intervention. This may explain increased post surgical recurrence in Dupuytren’s as compared to Primary Frozen Shoulder release.

Aim. To identify and quantify the reasons for failure of primary shoulder arthroplasty.

Materials. Seventy-nine Revision Shoulder Arthroplasties (RSA) in 75 patients were performed between January 1990 and July 2003. Twelve patients underwent more than one revision. Five patients were lost to follow-up. The indications for PSA (38 total shoulder arthroplasties, 37 hemiarthroplasties) were trauma (22), osteoarthritis (13), rheumatoid arthritis (11), avascular necrosis (9), cuff tear arthropathy (9), traumatic arthritis (5), capsulorraphy arthropathy (4),and instability (2). Glenoid and humeral bone stock, and rotator cuff integrity were analysed and the reasons for failure of the index procedure were determined.

Results. The median interval between PSA and RSA was 46 months (1 month to 22.8 years; mean 28 months). Thirty-six (58.1%) PSAs (of which 26 of 37 hemiarthroplasties (70%)) failed in the first three years. Failure of the PSA was caused by rotator cuff deficiency (24), glenoid bone erosion (19), glenoid component loosening (25), humeral bone erosion (3), infection of the implant (3) and periprosthetic fracture (1). Revision of a loose humeral component was performed in 6 cases, but 31 humeral components were revised in order to deal with glenoid or rotator cuff conditions.

Conclusion. When faced with a limited surgical armamentarium or tactic, there is a predictable rate of failure of shoulder replacement involving the interaction of the failed or failing rotator cuff and the evolution of glenoid deficiency.

Aim: To evaluate the role and outcome of FFTSA in shoulders with arthritis and/or irreparable rotator cuff tears.

Materials. The records of 60 consecutive patients with FFTSA were retrospectively reviewed. Primary FFTSA (group 1) was performed in 29 (48%), revision FFTSA (group 2) in 26 (43%), and re-revision FFTSA (group 3) in 5 (9%) patients. The mean age at primary FFTSA was 70 years (37 – 82), and at revision FFTSA, 67.6 years (38 – 89) at a mean interval of 38 months after primary intervention. In re-revision FFTSA the interval between the primary (mean age 64 years) and final (mean age 68.4 years) interventions varied from 20 to 148 months. Primary FFTSA was performed for cuff arthropathy in 18 (62%) and after trauma in 5 (17%): all 29 patients had rotator cuff insufficiency. Revision FFTSA was performed for failure of humeral head replacement (HHR) after fracture in 17 (65%) of which 14 had rotator cuff insufficiency. All those in group 3 had rotator cuff insufficiency. The dominant indication for intervention was pain in 59 cases. The glenoid component was uncemented in all cases. The humeral component was cemented in 27 of the 29 Primary FFTSA. CADCAM variations of the standard humeral design were used in 8 cases.

Results. At a mean follow-up of 25 months, 81% of primary FFTSA had no or mild pain, and 87.5% were satisfied or very satisfied with the outcome: both outcomes were independent of the original rotator cuff defect. At a mean follow-up of 41 months, 69% of revision FFTSA had no or mild pain, and 68 % were satisfied or very satisfied: the least satisfied patients were those in which a previous HHR for fracture had been the primary intervention. There were 3 complications in group 1, 2 in group 2, and 2 in group 3. In 4 patients with deficient deltoid function, 3 were satisfied with the eventual outcome

Conclusion. FFTSA has a clear role in the management of shoulders in which the rotator cuff has failed and a joint replacement is required for pain relief.

Aim: To demonstrate that inappropriate sequencing of activation of shoulder muscles can cause shoulder instability.

Methods. The records of 933 cases of recurrent shoulder instability referred to a specialist shoulder service between 1993 and 2003 were reviewed. All patients were assessed clinically. Muscle patterning abnormality (Bayley 1986) was identified in 428 patients (46%). Confirmatory functional electromyography was performed in 166 (36%). Inappropriate pectoralis major activation was identified in 73% of anterior instability. In posterior instability, inappropriate activation of latissimus dorsi and anterior deltoid was present in 72% and infra-spinatus was suppressed in 19%. Arthroscopic assessment was performed in 141 (33%), identifying structural lesions of instability in 86 (20%).

All patients diagnosed with muscle patterning disorder received specilalist physical therapy using biofeedback. Symptomatic improvement or stability was achieved in 76% of patients with anterior instability but with no previous surgery, and in 53% of patients with previous surgery. Posterior instability was eliminated in 85% of cases.

Conclusion. Muscle patterning abnormalities contribute to recurrent instability of the shoulder in 46% of cases. The success of physical therapy in these patients is high.

In 1991 15% of the UK population that travelled abroad required medical assistance. We have been treating more patients with lower limb injuries requiring repatriation via aircraft. Recommendations from Airlines were unavailable. 357 Consultants replied to a questionnaire about transportation of patients with a lower limb injury wearing a plaster cast. There was no consensus on safe transportation of these patients. No scientific data is available on the dynamics of transportation of patients with lower limb trauma. In order to assess the safest method of transportation an experiment was conducted. Ethical committee approval was granted. Five volunteers wearing above leg plaster casts were placed in a decompression chamber. The effects on anterior compartment pressures, Doppler venous return, ambient pressure between plaster and skin were assessed in different positions with and without plasters being split. In the normal population we have shown a trebling of intracompartmental pressures from an average of under 10mmHg to 30mmHg. Intracompartmental pressures are more raised with 90 degrees of hip flexion rather than 45 degrees. We recommend patients be transferred with their legs at 45 degrees to the ground with a split plaster cast.

To devise an operative approach to the management of acute posterior fracture-dislocation of the shoulder which restores or retains normal proximal humeral anatomy and allows the early restoration of a complete, stable range of motion.

Since 1996 we have treated four male patients (five shoulders) aged between 19 and 54 years at the time of first dislocation with autogenous iliac grafting of the anterior humeral head defect for acute and acuteon-chronic posterior dislocation of the shoulder. Two patients had epilepsy: one of these patients had bilateral dislocations. Two patients had motorbike RTAs. The deltopectoral approach with vertical division of the subscapularis tendon was used in all cases. The defects comprised 20– 25% of the volume of the humeral head at the equator after preparation for grafting. Grafts were fixed with compression screws. The subscapularis tendon was repaired anatomically. Active-assisted rehabilitation was started immediately, restricting external rotation to the neutral position for six weeks, thereafter allowing full rotation and elevation as comfort allowed.

The patient with bilateral dislocations died of unrelated causes 18 months after surgery. He was reported to have had no further dislocations, complete pain free functional use of both shoulders and no complications of the procedure. The remaining three patients were reviewed at a minimum of 20 months after surgery (average 35 months). All grafts had incorporated. There was no graft collapse or boundary arthrosis. The absolute Constant scores were 85.1, 90.9, and 89.2; the subjective shoulder scores were 98%, 90%, and 99%; the Oxford rating scale for pain scores were 14 out of 60, 13 out of 60, and 14 out of 60; and the Oxford rating scale for instability scores were 14 out of 60, 15 out of 60 and 15 out of 60. There were no redislocations, or complications of the procedures.

Posterior stability appears more dependant on surface arc of contact than on capsular integrity, in contrast to the anteriorly unstable shoulder. Restoration of the articular surface arc of contact by segmental autogenous grafting retains normal humeral anatomy, allows normal motion with excellent cuff function, and a return to normal daily activities. The procedure has been shown to be safe at a minimum of 20 months.