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Lima stemmed SMR reverse geometry shoulder replacement (nickel free implants)

Learn the Lima stemmed SMR reverse geometry shoulder replacement (nickel free implants) surgical technique with step by step instructions on OrthOracle. Our e-learning platform contains high resolution images and a certified CME of the Lima stemmed SMR reverse geometry shoulder replacement (nickel free implants) surgical procedure.
Reverse geometry configuration total shoulder replacements are in widespread use for the treatment of patients with rotator cuff deficient shoulders associated with significant arthritic change, known as cuff tear arthropathy. Such implants have also been used in the management of patients with irreparable proximal humeral fractures, a technique which has been described elsewhere in Orthoracle.
The design rationale in placing a prosthetic ball on the glenoid (the glenosphere) and a socket on the humeral side in a semi-constrained construct, is to medialise the joints centre of rotation and so increase the moment arm of the large deltoid muscle. This potentially optimises its function in the absence of the deficient rotator cuff tendons.
Many companies have developed such shoulder replacement implant systems. In this case, I am using the stemmed reverse geometry system, known as SMR from the Italian company Lima. The patient in this case is a female in her 70s, who presented with pain and disfunction in her non dominant left shoulder. Clinical assessment and investigations revealed a rotator cuff tear arthropathy. She had exhausted conservative measures and felt that her shoulder was bad enough to consider major arthroplasty surgery. During her history, she revealed that she had a significant allergy to nickel. Whilst there is little evidence that patients with nickel allergies or sensitivities have significant reaction to orthopaedic implants containing nickel, this is a risk to which the patient does not need to be exposed.
In the standard Lima shoulder replacement implants, the cobalt chrome components do contain nickel, although this is less than 1%. The Lima system does have options to avoid using any nickel and the implants used in this case are titanium, with a polyethylene humeral insert.


INDICATIONS
Cuff tear arthropathy is the prime indication for this operation. Whilst such reverse geometry arthroplasty has historically been reserved for an older population, I would consider using it in any patient over the age of 60.
SYMPTOMS & EXAMINATION
Patients will present with gradual insidious deterioration in shoulder function and increasing pain. The dysfunction usually manifests as an inability to raise their arm and weakness with any lifting or loading in the shoulder. They will often describe deep-seated pain within the shoulder girdle, perhaps radiating down their arm. On occasion there may be some swelling in comparison with the opposite shoulder. They may describe a previous history of injury to the shoulder but often there is a complete absence of a trauma. Usually the symptoms have come on gradually over a number of months or even years. Debilitating night pain is often a feature and they may describe a crunching or clicking within the shoulder.
Clinical examination is important, to compare both shoulders looking for symmetry, with respect to swelling and muscle wasting. Active and passive range of motion should be assessed and it is most likely that a clinical assessment of rotator cuff strength will reveal marked weakness. Neurological status in the upper limb is particularly important with documentation of axillary nerve sensory function and the motor function in the deltoid muscle. I assess this by asking the patient to actively abduct the flexed elbow away from their side, whilst palpating over the deltoid muscle to feel for adequate contraction. It is important to assess range of motion of the cervical spine, as well as elbow, wrist and hand function on the effected side. As with any patients considered for any surgical management, their past medical history and co-morbidities, including medication, should be taken into consideration and carefully documented.
IMAGING
Plain X-rays are mandatory and ideally these should be 3 views: an A-P, lateral and an axillary (or modified axial views). I recommend MRI scanning in all patients undergoing shoulder replacement and I use this to confirm my clinical findings, with respect to the rotator cuff deficiency. It is in particular important to look at the subscapularis muscle and compare this with clinical findings. I will try to preserve the subscapularis or certainly repair it if it needs to be taken down to gain access to the shoulder. The adequacy of bone stock can be well assessed on the MRI images, particularly within the glenoid.
ALTERNATIVE OPERATIVE TREATMENT
Patients with rotator cuff deficiency and minimal arthritis could be considered for arthroscopic assessment of the shoulder, with a view to rotator cuff repair. Such repair surgery could also be performed as an open operation. If repair of the rotator cuff tear is technically not possible, then surgeons have described arthroscopic debridement, tuberoplasty of the exposed greater tuberosity, in combination with long headed bicep tenotomy, or release of the suprascapular nerve.
More recently, some surgeons have had success with interposition patch grafting of rotator cuff deficiencies, or more recently described techniques, such as superior capsular reconstruction or insertion of an absorbable balloon spacer to the subacromial space to depress the humeral head into the glenoid (which can facilitate physiotherapy strengthening of the deltoid muscle). Traditionally, a hemi-arthroplasty of the proximal humerus would be considered in patients with arthritis but in absence of rotator cuff tendons, though this has had notoriously poor outcomes. Extended humeral heads on such implants (either stemmed or resurfacing) were also developed to allow prosthetic material to articulate with the undersurface of the acromion . These were known as cuff tear arthropathy(CTA) implants.
NON-OPERATIVE MANAGEMENT
As with all patients considered for any joint replacement surgery, conservative non-operative management should have been exhausted. Such treatment includes education of the patient as to their condition, suitable oral analgesia or anti-inflammatory medication (taking into account their medical comorbidities) and physiotherapy to optimise their function. Therapists will concentrate on an anterior deltoid strengthening program, which can be very successful in a motivated patient, to improve range of motion, function, strength and hence reduce pain. Some doctors will consider steroid and local anesthetic injection to the shoulder, which can certainly help with acute inflammatory synovitis or arthritis. In my practice, we use ultrasound guided suprascapular nerve blocks with local anesthetic, instilled into the suprascapular notch around the suprascapular nerve. This can be very beneficial in helping shoulder pain and then allowing deltoid function to improve. In combination with physiotherapy exercise program, this can be very effective. If patients get good transient benefit from guided local anaesthetic blockade of the suprascapular nerve, then they can be considered for percutaneous ablation of the nerve, using either a radio-frequency or cryoablation probe. Studies are ongoing as to the effectiveness of such treatment but should be considered in the non-operative management of such patients.
CONTRAINDICATIONS
As with any patient treated surgically for arthritic conditions, their general medical health and comorbidities must be taken into consideration. Patients must be able to comply with relatively straightforward physiotherapy in the post-operative period and ongoing rehabilitation instructions to optimise their function. In patients with significant medical comorbidities then a multidisciplinary approach with a pre-operative assessment team, often lead by a senior anesthetist, is recommended. Dysfunction of the deltoid muscle due to complete axillary nerve palsy is a contraindication to reverse geometry shoulder, as the bio-mechanics of the implant are reliant on function of the deltoid muscle. Relative contraindications are lack of bone stock within the glenoid and scapula but this can be addressed with either a bone grafting techniques or augmented implants. Such technique is not described here.

The procedure is performed under general anesthetic usually supplemented with interscalene local anaesthetic nerve block performed by the anaesthetist. The patient is placed in the semi-sitting beach chair position, with the arm on a moveable narrow armboard. This is often appropriate to perform a social wash of the affected shoulder and axilla prior to routine skin preparation. Unless there are contraindications, I use Flowtron intermittent calf compression during surgery to reduce the risk of thromboembolic disease. Intravenous antibiotics are administered by anaesthetist. The skin is prepared using Chlorhexidine solution, starting at the hand and preparing the whole of the upper limb and shoulder, across to the patient’s midline. Standard adhesive drapes are used to protect the patient’s airway tubing and to allow adequate exposure for approach to the shoulder from anterior incision. With the help of a company representative, the nurses should be familiarised with the sets required for shoulder arthroplasty. I also use a standard set of shoulder retractors which significantly facilitate the operation.

An AP Radiograph indicating arthritis of the glenohumeral joint with proximal migration of the humeral head which is now articulating with the sclerotic undersurface of the acromion. There is significant irregularity of the greater tuberosity. Of note, there is also arthritic change in the acromioclavicular joint but this was clinically asymptomatic. The quality of the bone in the proximal humerus looks normal

An axillary X-ray showing arthritic change in the gleno-humeral joint and complete loss of joint space. There is irregularity of the humeral head and this sits relatively posteriorly subluxed on the back of the glenoid. There appears to be adequate bone stock within the glenoid.

Single coronal cut of an MRI scan confirming complete loss of superior rotator cuff with the greater tuberosity articulating with the undersurface of the acromion. The white indicates the fluid of the intra-articular effusion. The bone quality within the humeral head looks good and uniform in appearance. The same can be said of the bone seen in the glenoid. Of note (when considering the seating and osseo-integration of the implant)there are no significant cysts within the glenoid.

A transverse MRI image across the shoulder. This confirms a large effusion and fluid around the long head of biceps tendon anteriorly. Of note, on this view, there is adequate glenoid bone stock (G) for the implantation of the glenoid component and anteriorly the subscapularis tendon appears intact. There is also intact posterior rotator cuff indicating reasonable infraspinatus. The deltoid muscle (D) surrounding the shoulder is a little thin but intact.

The patient is placed on an operating table which allows positioning in the semi-sitting position. The head is on a moveable head ring and supported with a simple strap, which attaches to itself with Velcro. I use the body belt from the simple sling used in the post-operative period. A moveable armboard is attached to the side of the operating table. This allows the arm to be moved during surgery. It is important during positioning of the patient to ensure that the arm can be moved across the side of the operating table and the humerus can be positioned vertically to allow intramedullary reaming down the humeral shaft.

This shows a small sandbag that I use to place underneath the patient’s scapula on the operated shoulder.

The skin preparation starts with using colourless Chlorhexidine solution for the hand, which is prepared whilst an assistant holds the proximal forearm.

Once the hand is prepared with Chlorhexidine, it can be covered with a cloth stockingette and held by the surgeon to allow the assistant to let go of the proximal forearm.

The hand can then be elevated to allow preparation of the rest of the upper limb, axilla and shoulder girdle, with pink staining Chlorhexidine solution.

Once the skin is fully prepared, the first adhesive drape crosses the base of the neck, protecting the patient’s head and anaesthetic airway tubing.

Further adhesive drapes are then applied around the shoulder, this shows a waterproof U-shaped drape into the axilla, isolating the shoulder. The cloth stockinette can then be rolled up to the elbow.

Further drapes are then placed around the shoulder, to close off the axilla and allow access to the front of the shoulder girdle and down the arm.

Further drapes are applied.

The final exposure of the operative field, surrounded by the blue adhesive drapes.

The cloth stockingette along the arm is then secured by overwrapping with a crepe bandage.

Final position prior to starting surgery.

The proposed surgical incision site is marked on the skin, from just lateral of the coracoid process and extending 10-15 cms down the shaft of the humerus. The skin and superficial tissues are then instilled with 20 mls 0.5% bupivacaine with adrenaline to act as a vasoconstrictor and help with haemostasis.

The skin is incised.

I use a Jackson Burrows shallow Gelpi-type retractor to facilitate dissection of the superficial tissues.

The cephalic vein should be identified within the fatty streak of the deltopectoral interval.

The cephalic vein clearly identified within the deltopectoral interval.

A curved retractor with the 2 small forks on the tip is then used.

This retractor is then placed on top of the coracoid process(A) to retract the superior tissues. Using an index finger gently open the deltopectoral interval down to the clavi-pectoral fascia and the conjoint tendon.

The index finger is beneath the superior edge of the pectoralis major tendon insertion and this can be incised 1-2 cm to facilitate an access. In this image the Kolbel self-retaining retractor (with atraumatic metal blades) has been placed beneath deltoid laterally and pectoralis major medially.

This image shows the Browne’s retractor, which is useful for protecting deltoid and placing behind the humeral head

This shows Browne’s retractor about to be placed beneath deltoid, around the back of the humeral head.

This image shows the 3 retractors used to identify the proximal humerus. The curved retractor (A) is on top of the coracoid, the self-retaining Kolbel’s retractor (B) and Browne’s retractor (C) behind the humeral head protecting the deltoid muscle laterally. This gives good exposure to the proximal humerus. The anterior circumflex humeral vessels can be seen running transversely from medial to lateral (3S), these vessels can be dissected out and tied off to prevent bleeding

The tendon of long head of biceps is identified and dissected out.

The long head of biceps tendon is then divided as a tenotomy. The distal tendon can be subsequently tenodesed to the pectoralis major. The proximal tendon is then excised with a detachment from the superior glenoid labrum, if this is still intact. In patients with significant cuff tear arthropathy the long head of biceps tendon may be chronically ruptured.

After assessment of the subscapularis tendon anteriorly inserting onto the lesser tuberosity, just medial to the long head of biceps and the bicipital groove, the rotator interval can be opened. This may release thick synovial fluid from an intra articular effusion. In this image I am incising the upper edge of subscapularis to get access to the shoulder.

Subscapularis is incised exposing the white articular cartilage of the humeral head.

A heavy vicryl stitch is placed into the upper edge of subscapularis tendon, to act as a traction stay suture.

Pulling on the traction stay suture allows further release of subscapularis, extending the tenotomy.

Further inferior release of subscapularis exposes the articular cartilage of the humeral head.

Reflection of subscapularis and the adherent anterior shoulder capsule reveals a small ossific lose body which can be excised. The anterior capsular tissue should be released from the undersurface of the subscapularis tendon.

The subscapularis is then placed beneath the medial blade of the Kolbel’s retractor. These stay sutures can be seen overlying that blade. External rotation to the shoulder and extension of the elbow, with use of the moveable armboard, then allows dislocation of the arthritic humeral head, which is delivered into the wound as seen.

A bone nibbler is used to remove the prominent osteophytes from around the rim of the proximal humerus. An osteotome may also be used to excise osteophytes and reveal the true proximal humerus.

The sharp spiked initial awl is placed onto the superior surface of the articular cartilage, just medial to the edge of the greater tuberosity footprint from which the superior rotator cuff is torn and detached.

The position of the awl should be half way between the front and back of the humeral head articular surface, in line with the shaft of the humerus.

A few blows with a mallet impacts the awl into the proximal humeral metaphyseal bone.

The initial awl is removed and the sharp intramedullary reamer is then placed into this entry hole.

With firm rotation the reamer is advanced down the humeral shaft.

Further advancement of the reamer into humerus.

Keeping the reamer in position, take the extramedullary cutting guide. This clips onto the slot on the reamer shaft. Twisting the small brass dial(as shown) will allow the guide to be raised and lowered to get optimal position for the cut across the humeral head.

Screw in the alignment rod into the appropriate hole either at neutral or at 20 degrees retroversion. This choice comes with experience but can be estimated by looking at the preoperative imaging. Axillary view plain xrays or the transverse axial MRI cuts should be used to assess whether glenohumeral alignment is neutral or more retroverted.

Further fine adjustment of the height of the extramedullary jig.

Rotate the jig, so that the alignment rod is directly in line with the patients’ forearm.

Place 2 pins into the appropriate holes to securely fix the jig in position in good bone.

These are secured using a mallet, ensuring that the rotation of the jig is maintained with alignment of the rod and forearm.

A final check of the height and rotation of the cutting jig is made.

Pull down the brass handle to release the extramedullary jig, leaving the cutting slot in place with the pins.

Remove the jig attachment and intramedullary reamer leaving the cutting slot in place with the pins.

Take an oscillating saw with a 2cm flat blade, which is used within the slot to resect the proximal humerus.

The humeral resection cut has been made, with the humeral head fragment shown elevated away from the cutting slot.

Remove the pins from the cutting slot.

Ensure a flat surface of the cut proximal humerus.

Position the flat proximal humeral plate to protect the humeral bone during preparation of the glenoid.

Replace retractors to retract the humeral head laterally under the deltoid. Tension on the subscapularis stay suture (S) allows further mobilisation of the tendon.

Digitally break down the adhesions around the tendon of subscapularis.

Using a pair of scissors, the capsule can be released from around subscapularis tendon and the tendon is further mobilised from the anterior glenoid. The rotator interval capsular tissue can be freed from the upper edge of the tendon using sharp dissection. Laterally the capsule is adherent to the Subscapularis tendon but the interval between the two can be easily identified. Always be conscious of the position of the axillary nerve running posteriorly towards the quadrilateral space under the lower border of subscapularis (upper border of the space) with the neck of the humerus laterally, long head of triceps medially and teres major below. I personally don’t dissect out the nerve but it’s position can be palpated.

Check the mobility of subscapularis tendon following the releases. Traction on the stay suture will reveal improved excursion of the tendon and muscle. Careful palpation allows passage of the surgeons index finger along the front of the subscapularis muscle and behind along the glenoid neck.

Again palpate and protect the axillary nerve inferior to the inferior glenoid rim as it runs posteriorly into the quadrilateral space.

Having palpated the axillary nerve to confirm it’s proximity, perform a 360 degree peri-glenoid release of capsulo-labral soft tissues. Start superiorly with the stump of the long head of biceps tendon and release the superior labrum to which it attaches. USing either cutting diathermy or a No15 scalpel blade stick to bone and release and excise all the capsulo-labral soft tissues from the bony glenoid rim.

Peri-glenoid releases are performed using a combination of scalpel blade, scissors and cutting diathermy. As per previous steps continually reassure yourself as to the proximity of the axillary nerve by palpation.

Retractors can be adjusted to facilitate access to the glenoid during the releases. Kolbel’s self-retainer (K) is under deltoid laterally and the conjoint tendon (of coracobrachialis & short head of biceps) medially. The Lima forked retractor (L) is under the inferior glenoid with the fork either side of the scapula blade if possible. The curved glenoid retractor (C) is behind the posterior glenoid rim.

Posterior capsulolabral structures are also released and excised, here using a No. 15 scalpel blade on a long knife handle.

A sharp edged Cobb is used to scrape the residual articular cartridge from the glenoid and clear the glenoid rim of soft tissues.

Further adjustment of the retractors’ positions to give excellent access to the glenoid.

Decide whether small or standard glenoid component required. In this case the small sizing device fits the glenoid well. Analysis of the preoperative imaging will help decide whether reamer needs to be used to relatively change the version. This would usually mean preferentially reaming down the front edge of a relatively retroverted glenoid. Review of the MRI (or CT) axial cuts will confirm position of the best volume of glenoid bone.

A wire is placed down the centre of the cannulated small glenoid guide and the guidewire is advanced into the centre of the bony glenoid, taking into account the assessment of the pre-operative cross sectional imaging. I aim to insert the wire tilted very slightly inferiorly.

Wire in position in the glenoid jig.

Remove the glenoid guide, leaving the wire in position.

Insert the small reamer over the guidewire.

Ream the glenoid with gentle pressure.

Reamings of cortical bone seen around the glenoid reamer.

Remove the loose bone reamings to assess adequacy of reaming. It is important to clear residual articular cartilage and have a smooth surface of sub-chondral bone but not to breach the sub-condral plate into cancellous bone.

When glenoid preparation is complete, the central peg drill is used over the guidewire. In this case the small-R metalback glenoid component is to be used and this is the small-R peg drill. R stands for ‘reduced’ indicating smaller size, diameter and length, of the central peg of the glenoid baseplate.

Advance until the drill is well seated against the glenoid bone.

Remove the peg drill.

Use chlorhexidine solution wash to ensure that the peg hole is clear of bone debris.

This shows the central peg drill with the wire in place.

Remove the wire from the central peg hole. This shows completed glenoid preparation.

Take the definitive small-R metalback glenoid component and its introducer.

Screw the introducer onto the definitive implant.

Slide the outer component of the introducer over the initial rod.

This clicks into position in the implant drill holes.

Insert the peg of the metalback glenoid into the prepared bone.

Impact using a mallet against the strikeplate of the introducer.

Press the button on the outer sheath of the glenoid component introducer and pull back along the rod, to assess whether the component is seated down against the bone by inspecting through the component drill holes.

Take the drill and drill guide.

Insert the drill with it’s flexible driver into the drill guide.

Drill each of the 2 holes in the metalback component. The superior hole should be aimed slightly anterior into the body of bone at the base of the coracoid process. Second inferior drill hole is perpendicular to the plate or angled slightly posterior. Measure each drill hole to confirm screw length.

Take each screw with the screw-holder and screwdriver.

Screws are inserted into the metal back glenoid component and tightened.

Tighten the screws sequentially to ensure that the metal base plate is seated and fixed firmly to the glenoid bone.

This shows the screw holder at the insertion of the second superior screw.

Screwdriver being inserted into the screw.

Final position of the metalback glenoid component.

In this case, given the patients small stature and small shoulder, the decision was made to use a 36mm glenosphere component. This shows the nickel free titanium glenosphere and connector peg. Note the extended lip which will be placed under the inferior glenoid rim to prevent inferior glenoid notching.

Place the thick end of the connector peg into the hole on the glenoid component.

Cover the top of the peg with a gauze swab or folded drape material and gently tap to fix the peg taper to the glenosphere.

Screw the insertion handle on to the glenoid component.

Glenosphere ready for insertion to the metal base plate. Note the extended lip which will be placed under the inferior glenoid rim to prevent inferior glenoid notching.

Insert the glenosphere peg into the metalback glenoid component and gently impact using the mallet ensuring implant rotation correct with lipped edge under inferior glenoid rim.

Take the screw for glenosphere fixation.

Insert the screw into the hole in the glenosphere and tighten.

Final position of glenosphere with the lip under the inferior aspect of the glenoid.

Remove the glenoid retractors and adjust the Kolbel’s self-retainer position.

Use Browne’s retractor to protect the deltoid muscle whilst delivering the proximal humerus into the wound.

Elevate the arm to facilitate manoeuvring the proximal humerus.

Deliver the proximal humerus into the wound and place the forked glenoid retractor behind the humerus.

Sequentially take the humeral stem trial components mounted on the introducers. They act as medullary canal tamps.

Insert down the shaft of the humerus and impact in position.

Take the height guide and clip onto introducer. This allows estimation of adequate depth of stem tamp when height guide plate is flush with the humeral metaphyseal cut.

Rotate the guide so that it sits down onto the cut bony surface.

Tap each humeral trial down until a good fit is achieved within the humeral diaphysis. This can be heard by a change in the pitch noise of impaction with the mallet.

This shows the insertion handle with the height guide in position.

Once the diameter of the stem component has been confirmed, attach the chosen trial stem to the handle and take the version bar, which can be screwed into the 0 degree or 20 degree hole.

Insert chosen trial component and rotate until version bar is in line with forearm. Remove the insertion device.

Take the hand held metaphyseal reamer.

This shows the sharp semi conical end of the metaphyseal reamer.

Place the hand reamer over the peg of the trial humeral component.

Rotate the hand reamer alternately clockwise and anticlockwise to clear the proximal humeral metaphysis.

Remove the hand reamer.

Reapply the insertion handle to remove the trial stem.

Construct the trial humeral implant by applying the trial humeral body (HB) onto the chosen stem (S) and fixing with a quarter turn of the screwdriver. Apply the introducer to the humeral body.

Introducer attached to humeral trial.

Insert the trial component once again using the version bar in the appropriate hole lined up with the patient’s forearm.

Ensure rotation is accurate, then remove the introducer.

This shows the trial humeral component in place.

Insert the plastic trial humeral insert and click into position.

Reduce the humeral cup to articulate with the glenosphere.

Remove all retractors and put the shoulder through a passive range of motion, including elevation, extension and rotational movements, to ensure stability. Different depth and offset plastic humeral cup inserts can be trialled to optimise stability and range of motion.

Once the stability is confirmed with trial implants then retractors are reinserted and the shoulder is dislocated.

The insert is removed and the introducer is reapplied to the humeral trial component.

Remove the humeral trial and wash out and ensure there is no debris within the humeral shaft.

Take definitive Lima SMR reverse geometry humeral components. In this case, the uncemented stem and humeral body are chosen.

Push the humeral components together.

The humeral components assemled.

Take the introducer and apply to the humeral body.

Once again use the version rod during insertion and ensure it is in line with the forearm. Insert the component to the humerus.

Push the implant down to the level at which the trial had been stable.

Gentle impaction using a mallet ensures that the humeral component seats down within the bone.

Remove the handle of the insertion device by unscrewing it but leave the barrel in place.

Take the screw and drop it down the barrel.

Insert the screw using the screwdriver until the component is tight. The version bar can be repositioned to facilitate some counter-torque during tightening.

Remove the introducer barrel.

Further trial insert cups can be used to confirm stability and then take the definitive polyethylene insert and place into the humeral component.

Push on digitally and then click in to ensure seated in correct position using the impactor and the mallet.

Final view of the definitive humeral components.

Reduce the glenohumeral joint. This shows the white polyethylene insert articulating with the titanium glenosphere.

Perform a thorough washout and ensure haemostasis. I use a regular wash with Chlorhexidine solution during total arthroplasty surgery. Retrieve stay suture from subscapularis to ensure that this can oppose the stump.

Repair subscapularis tenotomy using interrupted No 2 Ethibond stitches.

Several interrupted stitches are used to repair subscapularis, to optimise range of motion and function.

Final stitch placed into subscapularis tendon. At the end of subscapularis repair, tension on the tendon can be checked with external rotation of the shoulder to be able to advise the physiotherapists of the safe early range of motion without risk of disrupting the repair.

After thorough washout and haemostasis, the superficial fascia and fat are closed with continuous 0 Vicryl stitch.

Skin is closed with a running continuous subcuticular 3/0 Monocryl absorbable suture, to give a good skin apposition.

Skin closure is protected with adhesive paper steri-strips.

Standard adhesive dressing is applied to the wound.

Post-operative AP radiograph showing the metal base plate on the glenoid, with the 2 screws into the body of the glenoid bone and the titanium glenosphere. The titanium humeral component is noted within the humeral shaft and articulating with the glenosphere.

Lateral post-operative x ray showing the implants correctly aligned.

Axillary post-operative xray.

General points
• The surgery is primarily performed for pain relief, function can improve but it is often secondary to a reduction in pain –allowing improved Deltoid function.
• Patient progress and outcome will ultimately depend on the condition of the joint and soft tissue pre-operatively.
• Improvement can continue for 18-24 month’s post-operatively, it is therefore important to encourage patient to continue with rehabilitation until no further improvement.
• Aim of rehabilitation is good quality of movement, and maximal function, however in this group of patients increased scapula motion is to be expected and maybe encouraged,
• Don’t sacrifice quality of movement and function for ROM
• The principles of the Deltoid Rehabilitation Programme for irreparable rotator cuffs should be utilised.
Precautions
The underlying pathology is one of chronic degenerative rotator cuff rupture; it varies from patient to patient as to what if any rotator cuff remains intact. If any tendons were repaired then this will be stated in the op notes and the rehabilitation will be guided by this.
Repetitive overhead activities and loaded activities above shoulder height may be limited long term and should not be forced with rehabilitation.
Lifting weights above shoulder height with more than 2-4 kg should be avoided unless otherwise instructed by the surgeon.
Hand behind back (HBB) should not be forced and may not be regained There is likely to be a chronic deficit in rotator cuff strength, particularly in ER
Immobilisation
• Patient to wear sling for 3 weeks 24 hours a day, only removing for physiotherapy exercises • At 3 weeks, start to wean out of sling but to continue wearing at night for a further 3 weeks
• Total sling usage – 6 weeks
Post-Operative
0-6 weeks: Pendular exercises; Active assisted ER to neutral (ONLY IF THERE IS NO SUBSCAPULARIS REPAIR); Active assisted elevation in supine as comfort allows – consider use of table slides or walk backs
3 weeks: Gradually wean out of sling – light activities only (weight of a cup of tea within the field of vision, short lever)
6 weeks: Start to increase ER, as ER increases gradually increase elevation ROM; Active assisted exercises progressing to active exercises – utilise short lever, supine & CKC if appropriate; Don’t force HBB position; No long lever open chain exercises until 8 weeks
8 weeks: Consider use of the principles of the Deltoid Rehabilitation programme Sub maximal isometrics in neutral – avoiding any repaired tendons
12 weeks+: Isometrics in variable starting positions; Progressing to resisted through range strengthening – consider weight of arm, varied starting position & functional weights as well as theraband. REMEMBER FUNCTIONAL GOAL and the underlying pathology is massive irreparable rotator cuff tear
The Ultimate Aim is Function rather than anatomical normal movement.

Nickel sensitivity and the implantation of orthopaedic prostheses. D Gawkrodger. Contact Dermatitis. 1993;28:257-259
Intolerance reactions to knee arthroplasty in patients with nickel/cobalt allergy and disappearance of symptoms after revision surgery with titanium-based endoprostheses. K Dietrich, F Mazoochian, B Summer, M Reinert, T Ruzicka, P Thomas. J German Soc Dermatology. 2009 May;7(5):410-412
The SMR reverse shoulder prosthesis in the treatment of cuff-deficient shoulder conditions. S Young, N Everts, C Ball, T Astley, P Poon. J Shoulder Elbow Surg. 2009 July;18(4):622-626
Mid-term results of a metalbacked glenoid component in total shoulder replacement. A Castagna, M Randelli, R Garofalo, L Maradei, A Giardella, M Borroni. J Bone Joint Surg [Br] 2010;92(10):1410-1415
Biomechanical evaluation of different designs of glenospheres in the SMR reverse shoulder prosthesis: micromotion of the baseplate and risk of loosening. P Poon, J Chou, D Young, S Malak, I Anderson. Shoulder & Elbow. 2010.2:94-99
Shoulder arthroplasty in the patient with metal hypersensitivity. M Morwood, G Garrigues. J Shoulder Elbow Surg. 2015 May;24:1156-1164


Reference

  • orthoracle.com
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