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The Bone & Joint Journal
Vol. 96-B, Issue 7 | Pages 936 - 942
1 Jul 2014
Middleton C Uri O Phillips S Barmpagiannis K Higgs D Falworth M Bayley I Lambert S

Inherent disadvantages of reverse shoulder arthroplasty designs based on the Grammont concept have raised a renewed interest in less-medialised designs and techniques. The aim of this study was to evaluate the outcome of reverse shoulder arthroplasty (RSA) with the fully-constrained, less-medialised, Bayley–Walker prosthesis performed for the treatment of rotator-cuff-deficient shoulders with glenohumeral arthritis. A total of 97 arthroplasties in 92 patients (53 women and 44 men, mean age 67 years (standard deviation (sd) 10, (49 to 85)) were retrospectively reviewed at a mean follow-up of 50 months ((sd 25) (24 to 96)). The mean Oxford shoulder score and subjective shoulder value improved from 47 (sd 9) and 24 points (sd 18) respectively before surgery to 28 (sd 11) and 61 (sd 24) points after surgery (p <  0.001). The mean pain at rest decreased from 5.3 (sd 2.8) to 1.5 (sd 2.3) (p < 0.001). The mean active forward elevation and external rotation increased from 42°(sd 30) and 9° (sd 15) respectively pre-operatively to 78° (sd 39) and 24° (sd 17) post-operatively (p < 0.001). A total of 20 patients required further surgery for complications; 13 required revision of components. No patient developed scapular notching.

The Bayley–Walker prosthesis provides reliable pain relief and reasonable functional improvement for patients with symptomatic cuff-deficient shoulders. Compared with other designs of RSA, it offers a modest improvement in forward elevation, but restores external rotation to some extent and prevents scapular notching. A longer follow-up is required to assess the survival of the prosthesis and the clinical performance over time.

Cite this article: Bone Joint J 2014;96-B:936–42.


The Journal of Bone & Joint Surgery British Volume
Vol. 94-B, Issue 10 | Pages 1382 - 1389
1 Oct 2012
Sewell MD Kang SN Al-Hadithy N Higgs DS Bayley I Falworth M Lambert SM

There is little information about the management of peri-prosthetic fracture of the humerus after total shoulder replacement (TSR). This is a retrospective review of 22 patients who underwent a revision of their original shoulder replacement for peri-prosthetic fracture of the humerus with bone loss and/or loose components. There were 20 women and two men with a mean age of 75 years (61 to 90) and a mean follow-up 42 months (12 to 91): 16 of these had undergone a previous revision TSR. Of the 22 patients, 12 were treated with a long-stemmed humeral component that bypassed the fracture. All their fractures united after a mean of 27 weeks (13 to 94). Eight patients underwent resection of the proximal humerus with endoprosthetic replacement to the level of the fracture. Two patients were managed with a clam-shell prosthesis that retained the original components. The mean Oxford shoulder score (OSS) of the original TSRs before peri-prosthetic fracture was 33 (14 to 48). The mean OSS after revision for fracture was 25 (9 to 31). Kaplan-Meier survival using re-intervention for any reason as the endpoint was 91% (95% confidence interval (CI) 68 to 98) and 60% (95% CI 30 to 80) at one and five years, respectively.

There were two revisions for dislocation of the humeral head, one open reduction for modular humeral component dissociation, one internal fixation for nonunion, one trimming of a prominent screw and one re-cementation for aseptic loosening complicated by infection, ultimately requiring excision arthroplasty. Two patients sustained nerve palsies.

Revision TSR after a peri-prosthetic humeral fracture associated with bone loss and/or loose components is a salvage procedure that can provide a stable platform for elbow and hand function. Good rates of union can be achieved using a stem that bypasses the fracture. There is a high rate of complications and function is not as good as with the original replacement.


The Journal of Bone & Joint Surgery British Volume
Vol. 94-B, Issue 9 | Pages 1253 - 1259
1 Sep 2012
Sewell MD Higgs DS Al-Hadithy N Falworth M Bayley I Lambert SM

Scapulothoracic fusion (STF) for painful winging of the scapula in neuromuscular disorders can provide effective pain relief and functional improvement, but there is little information comparing outcomes between patients with dystrophic and non-dystrophic conditions. We performed a retrospective review of 42 STFs in 34 patients with dystrophic and non-dystrophic conditions using a multifilament trans-scapular, subcostal cable technique supported by a dorsal one-third semi-tubular plate. There were 16 males and 18 females with a mean age of 30 years (15 to 75) and a mean follow-up of 5.0 years (2.0 to 10.6). The mean Oxford shoulder score improved from 20 (4 to 39) to 31 (4 to 48). Patients with non-dystrophic conditions had lower overall functional scores but achieved greater improvements following STF. The mean active forward elevation increased from 59° (20° to 90°) to 97° (30° to 150°), and abduction from 51° (10° to 90°) to 83° (30° to 130°) with a greater range of movement achieved in the dystrophic group. Revision fusion for nonunion was undertaken in five patients at a mean time of 17 months (7 to 31) and two required revision for fracture. There were three pneumothoraces, two rib fractures, three pleural effusions and six nonunions. The main risk factors for nonunion were smoking, age and previous shoulder girdle surgery.

STF is a salvage procedure that can provide good patient satisfaction in 82% of patients with both dystrophic and non-dystrophic pathologies, but there was a relatively high failure rate (26%) when poor outcomes were analysed. Overall function was better in patients with dystrophic conditions which correlated with better range of movement; however, patients with non-dystrophic conditions achieved greater functional improvement.


Orthopaedic Proceedings
Vol. 94-B, Issue SUPP_XXXIX | Pages 125 - 125
1 Sep 2012
Templeton-Ward O Griffiths D Higgs D Falworth M Bayley I Lambert S
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Reverse polarity total shoulder arthroplasty (RTSA) has gained popularity over recent years for the treatment of the painful cuff deficient shoulder. Although proposed over 20 years ago and despite good clinical outcomes the RTSA has struggled to gain popularity due to reported high levels of complications.

One such complication is post-operative instability with frequencies of up to 30% (De Wilde 2002). The Bayley-Walker RTSA was designed specifically for patients with difficult reconstruction problems in whom an unconstrained prosthesis would not offer sufficient stability. It is a reverse anatomy fixed fulcrum constrained prosthesis. The glenoid component has a long HA-coated tapered helical screw, with large pitch and depth, fixation is augmented by a grooved HA coated glenoid plate.

The purpose of this study was to review the clinical experience from The Royal National Orthopaedic Hospital Stanmore and to ascertain the rate of glenoid component loosening. We also carried out a radiographic review to correlate loosening with patterns of lucency on post-operative radiographs. One hundred and five B-W TSRs in 103 patients were included, 24% of which were performed as revision of previous failed arthroplasty. In total, 8/105 glenoids required revision. Of those eight patients, two were cases of septic loosening. Of all nine specified areas of glenoid, tip lucency on x-ray appeared to be most strongly associated with need for glenoid revision. 5/9 cases with tip lucency progressed to loosening of the glenoid. Where tip lucency was not seen, 93/96 glenoid components remained secure, giving tip lucency a negative predictive value of 97%. Excluding the two infected cases, the glenoid remained secure in 97/103 patients undergoing BW-TSR with follow-up up to 13 years. The BW-TSR is a satisfactory and durable solution to the cuff-deficient shoulder in variety of challenging groups including younger patients and as a salvage procedure following failed, cuff-deficient arthroplasty.


Orthopaedic Proceedings
Vol. 93-B, Issue SUPP_I | Pages 52 - 53
1 Jan 2011
Griffiths D Templeton-Ward O Grange S Lambert S Bayley I Falworth M
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Arthroplasty as a salvage procedure for cuff and glenoid deficiency poses major problems due to the limitations in treatment options and debilitating symptoms. We hypothesized that computer aided deigned and manufactured (CADCAM) total shoulder arthroplasty, using a precisely fitted glenoid shell, can relieve the pain and poor function associated with irreparable rotator cuff pathology and severe glenoid deficiency in the shoulder.

Of the 127 cases so far performed, a prospective cohort study 79 consecutive subjects, with a mean 28.7 month follow-up, were evaluated by a single practitioner blinded to their group status. Outcome was assessed using a validated clinical shoulder scoring system and radiographic review.

The subjects had a mean age of 58 (41–82) and their indication (where recorded) was mainly revision total shoulder replacement (62%) with some cases for primary osteoarthritis (12%) and rheumatoid arthritis (9%) and a proportion for other reasons (19%) including 1 re-revision case for dislocation.

Clinical follow-up was limited in this population (n=58, 73%) The ‘CADCAM’ group’s mean Stanmore Percentage of Normal Shoulder Assessment scores (SPONSA) were relatively unchanged post surgery (47 to 42 p=0.3). The Oxford Shoulder scores improved significantly (15 to 33, p< 0.0001). Most significantly, and by way of explanation, post surgery subjects recorded a reduction in the Visual Analogue Scale (Pain) scores (6.6 to 2.9) p< 0.0001). Patient satisfaction was generally good.

Radiographic review of the 79 cases revealed glenoid component screw breakage (4%, n=5) which is a moderate correlate of glenoid loosening (r = 0.65, r2 = 0.42) and probably more accurate than radiographic lucent lines seen in 6% (n=7). Humeral lucency was seen in 10%, (n=8). These radiographic findings correlated well with the clinical findings.

Postoperative pain and function was significantly improved in subjects undergoing the ‘CADCAM’ technique of shoulder arthroplasty offering a consistent salvage option for situations where no alternative to glenoid reconstruction is feasible.


Orthopaedic Proceedings
Vol. 90-B, Issue SUPP_III | Pages 579 - 579
1 Aug 2008
Forster M Bauze A Bailie A Falworth M Oakeshott R
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The aim of this study was to assess the results of bilateral total knee replacement (TKR) staged one week apart during one hospital admission and compare these results with those of bilateral sequential TKRs and bilateral TKRs performed in 2 separate admissions by a single surgeon using a single prosthesis. Between 5th November 1997 and 10th August 2004, 104 patients underwent bilateral LCS TKRs using the Anteroposterior glide (APG) tibial component. The patients were analysed in 3 groups. The patients in Group 1 underwent bilateral sequential TKR under the same anaesthetic. The patients in Group 2 underwent bilateral TKRs under 2 separate anaesthetics, 7 days apart, during the same admission. The patients in Group 3 underwent bilateral TKR under 2 separate admissions, essentially 2 unilateral TKRs. The patients in Group 1 had shorter operations (p< 0.0001) and shorter hospital stays (p< 0.0001). Patients in Group 2 had less blood loss (p=0.004) but were not transfused any less than the other groups. The complication rate was low and comparable in all groups. There were no in hospital or 30 day deaths in any of the groups. Those patients in Group 3 had worse AKS function scores (p=0.02) and those patients in Group 2 had a significantly better HSS score (p=0.02). There was no significant difference between the groups in terms of range of motion or the AKS Knee score. This study has confirmed a shorter operation and hospital stay when the bilateral TKRs are carried out under the same anaesthetic. These patients also bled the most postoperatively. There was little difference in terms of complications and clinical outcome at a mean follow up of 4 years. With appropriate patient selection, both same anaesthetic and same admission bilateral TKR are safe methods to treat bilateral arthritis.


Orthopaedic Proceedings
Vol. 85-B, Issue SUPP_I | Pages 68 - 68
1 Jan 2003
Falworth M Clarke C Thomas M
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Purpose: To describe the characteristic examination findings post whiplash injury of relevance to the shoulder surgeon and an injection test, which can be used to abolish these signs and distinguish neck from shoulder pathology.

5A large amount has been written about whiplash injuries of the neck, but many of these patients are often referred to shoulder units for assessment either acutely or years after the accident because of continuing symptoms. Although neck pain is the commonest complaint tenderness on examination is sided and within the trapezius muscle in virtually all cases. Pain referred to the shoulder is also reported in 36 – 67% whilst interscapular pain occurs in 20 – 72%, depending on the time from injury.

We have reviewed a personal series of the senior author of over 700 cases. The consistent finding in these patients is tenderness localised to a specific part of the trapezius in the base of the neck, which is sided. Tenderness on the same side is also present along the vertebral border of the scapula to its lower pole in over 90%, provided the scapula is protracted. A further finding in some patients is a high arc of pain on abducting the arm, thus simulating an acromioclavicular joint problem, but in these cases the pain is localised to the trapezius. These findings are in addition to those of the neck, which may show some restricted movement due to pain.

The trapezius tenderness can be abolished by the injection of local anaesthetic into the trigger spot at the base of the neck (whiplash injection test), which also resolves most of the above signs and allows further assessment of the shoulder without the referred pain from the injected area.

Conclusions: Shoulder examination in patients who have suffered whiplash injuries is often difficult due to referred pain. Knowledge of the signs specifically due to the whiplash injury is required so that shoulder pathology is not assumed. A new whiplash injection test not previously described has been found very useful in abolishing the whiplash signs to enable accurate shoulder assessment in our practice.