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Lima SMR stemless reverse shoulder replacement

Learn the Lima SMR stemless reverse shoulder replacement surgical technique with step by step instructions on OrthOracle. Our e-learning platform contains high resolution images and a certified CME of the Lima SMR stemless reverse shoulder replacement surgical procedure.
Reverse geometry configuration total shoulder replacements are in widespread use for the treatment of patients with rotator cuff deficient shoulders but particularly for those with arthritic change so called ‘cuff tear arthropathy’. Such implants have also been used in the management of patients with unreconstructable proximal humeral fractures, a technique which has been described on Orthoracle at https://www.orthoracle.com/library/lima-smr-reverse-total-shoulder-replacement-for-proximal-humeral-fracture/
The design rationale in replacing a prosthetic ball on the glenoid (the glenosphere) and a socket on the humeral side in a semi-constrained construct, medialises the centre of rotation and increases the moment arm on which the large deltoid muscle can work, in the absence of the rotator cuff tendons which normally insert around the proximal humerus.
Many Orthopaedic companies have developed such shoulder replacement implants. In this case, I am using the stemless humeral implant on the reverse geometry system from the Italian company Lima. The stemless humeral component is constructed on a 3D printer to create a single piece of trabecular titanium. Hip surgeons have used the same trabecular titanium for successful reconstruction of the hip acetabulum with impressive bony ingrowth of the implant. In the shoulder, if the patient’s proximal humeral metaphyseal bone is not too soft then impaction of the trabacular titanium core humeral implant gives excellent primary fixation and promotes future bone ingrowth securing the platform component. This is a bone preserving procedure avoiding the need to use an intramedullary stem. The same humeral core component is used for anatomical total shoulder replacement and this facilitates revision of an anatomic replacement to reverse one. It is very straightforward to switch the articulating components leaving the glenoid baseplate and humeral core implants, which should be solidly fixed to bone, in place.
The patient in this case is an 80 year old female who presented with pain and dysfunction in her non dominant shoulder. Clinical assessment and investigations revealed the diagnosis of glenohumeral osteoarthritis with a thin and weak rotator cuff. She had exhausted conservative measures and felt that her shoulder was bad enough to consider major arthroplasty surgery.

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 it in any patient over the age of 60. In patients with osteoarthritis and poorly functioning or thin rotator cuff insertion, an anatomic configuration total shoulder replacement is likely to have poor outcome. In such cases it is worth considering sacrificing the superior rotator cuff and using a reverse geometry implant.
Patients with rheumatoid arthritis may also be considered for a reverse shoulder replacement as the natural history of their rotator cuff insertion is of poor function and degenerate tears.
All patients considered for a stemless humeral implant must have their proximal humeral metaphyseal bone assessed with cross-sectional imaging by MRI or CT scan. Whilst patients with acute proximal humerus fractures may be managed with a stemmed reverse shoulder replacement the likely deficiency in the proximal humeral metaphysis is a contraindication to stemless humeral implant.
SYMPTOMS & EXAMINATION
Patients usually present with gradual insidious deterioration in shoulder function and increasing pain. They will describe dysfunction, an inability to raise their arm and weakness with any lifting or loading of the shoulder. They will describe deep-seated pain within the shoulder girdle, perhaps radiating down the arm. On occasions there may be some swelling in comparison with the opposite shoulder indicating the presence of a joint effusion. They may describe previous history of an injury to the shoulder but often there has been complete absence of trauma. Usually the symptoms have come on gradually over a number of months or even years. Night pain is often a feature and they may describe 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 clinical assessment of rotator cuff strength reveals marked weakness. Neurological status in the upper limb is particularly important in documenting axillary nerve sensory function and the motor function of the deltoid muscle. I assess this by asking the patient to actively lift the flexed elbow away from their side, whilst palpating over the deltoid muscle to feel for contraction. The complete inability to elevate the neurologically intact arm due to rotator cuff weakness is referred to as ‘pseudoparalysis’. It is important to assess range of motion in their cervical spine, as well as elbow, wrist and hand function on the side in question. As with any patients considered for surgical management, their past medical history and comorbidities, including medication, should be taken into consideration and carefully documented.
IMAGING
Plain Xrays are mandatory and ideally these should be 3 views: AP, lateral and 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 important to look at subscapularis and compare this with clinical findings as I will try to preserve subscapularis or certainly repair it if it needs to be taken down to gain access to the shoulder. It is also possible to estimate adequacy of bone stock on MRI scan both within the glenoid and the humeral head to predict any potential concerns with respect to fixation of the metal components on both sides of the joint. Presence of geode cysts in either site may be picked up on the MRI when not easily seen on plain radiographs. Such finding may influence preoperative planning such as implant choice or need for bone grafting.
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 tears is technically not possible, then surgeons have considered debridement, tuberoplasty of the exposed greater tuberosity, in combination with long head of biceps tenotomy, or release of the suprascapular nerve. More recently, some surgeons have had success with interposition patch grafting of the rotator cuff tendon deficiencies, or more recent techniques, such as suprascapular reconstruction or insertion of an absorbable balloon spacer into the subacromial space, to depress the human head into the glenoid and facilitate physiotherapy management in strengthening the deltoid muscle. Traditionally, hemiarthroplasty replacing the proximal humerus would be considered in patients with arthritis but in absence of rotator cuff tendons or indeed poor function, this has notoriously poor outcome. Extended humeral heads on such implants whether stemmed or resurfacing were historically considered to allow prosthetic material to articulate with the undersurface of the acromion. These were known as cuff tear arthropathy or 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 would include education of the patient as to their condition, suitable oral analgesia and 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 a deltoid function to improve. In combination with physiotherapy exercise program, this can be very effective. If patients get good transient benefit from guided local anesthetic blockade of the suprascapular nerve, then they can be considered for percutaneous ablation of the nerve, using either a radio-frequency or a 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
General medical health and comorbidities must be taken into consideration in any patient being treated surgically for arthritic conditions. 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 anaesthetist, is recommended. Dysfunction of the deltoid muscle due to complete axillary nerve palsy is a contraindication to reverse geometry shoulder as the biomechanics 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 use of augmented or custom-built implants. Such techniques are not described here.

The procedure is performed under general anaesthetic 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 operated arm on a moveable narrow armboard. It 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 aneasthetist. The skin is prepared using Chlorhexidine solution, starting with 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 an 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.

Recommended surgeons apparel for joint replacement surgery includes an occlusive hood, eye protection and double gloves with waterproof gown

The patient is carefully placed into a semi-sitting position with head secured on an attached head ring.
Here I use the Velcro fastened bodybelt from the sling to secure the head to the ring (H). This is later used circumferentially around the patient’s waist and trunk as part of the sling immobilisation.
Note the moveable arm board (MA), which will be adjusted during the operation, and the small sandbag (S) placed beneath the scapula on the operation side.

Plain X-Ray shows bone on bone osteoarthritis of the glenohumeral joint with large proximal humeral osteophytes (O). The joint is well aligned with no proximal migration of the humeral head.

An axial image further confirms loss of gleno-humeral joint space with osteoarthritis and osteophytes. Here there appears to be adequate glenoid bone stock (G) for glenoid implant fixation. This needs to be confirmed with cross-sectional imaging (MRI or CT scan)

Whilst the supraspinatus insertion is intact, it is thin (SSp). Quality of humeral head bone (H) looks good with no cysts. Similarly the glenoid bone looks good.

This transverse section image shows subscapularis (SSc) intact anteriorly and infraspinatus (ISp) posteriorly intact although thin. Quality of humeral head bone (H) looks good with no cysts. Similarly the glenoid bone (G) looks good.

Start by preparing the hand with clear chlorhexidine solution

Hold the prepared hand with a cloth stockinette then continue to prepare the arm and shoulder girdle with pink staining Chlorhexidine solution finishing with the axilla.

Roll the cloth stockinette up the arm towards the elbow. Use adhesive edged waterproof drapes. First one should traverse the base of the neck protecting the anaesthetic tubing. Next a plastic U-drape is placed into the axilla.

Position of final sterile drapes. The forearm stockinette is secured with a crepe bandage. Note the quiver (Q) containing the diathermies & suction and secured to the drapes.

I inject 20ml 0.5% bupivacaine with adrenaline into the superficial soft tissues of the line of the incision. Not only does this help with analgesia but vasoconstriction by the adrenaline reduces bleeding from the soft and subcutaneous tissues after incision.

Palpate the coracoid process and mark proposed incision for the delto-pectoral approach from there, running 10-15cm distal down the line of the humeral shaft. Incise in this line.

The skin incision for a delto-pectoral approach

Spiked Jackson Burrows retractor in the superficial tissues.

A Jackson Burrows self-retaining retractor is used to hold open the fat layer and scissors are used to dissect the fat layer

Scissors are used to dissect the fat layer

The delto-pectoral interval is identified as a fatty streak between the muscles, pectoralis major medially and the deltoid laterally.

The cephalic vein (CV)is identified within deltopectoral interval.Pectoralis major (PM) sits medially and the deltoid (D) laterally.

The deltopectoral interval is easily developed digitially by sweeping the cephalic vein laterally with deltoid

After the cephalic vein is swept laterally with the deltoid, the deltopectoral interval is opened which exposes the upper edge of the pectoralis major insertion

Release the upper edge of of pectoralis major insertion using the cutting diathermy probe to incise the upper 2cm of tendon.

A forked retractor is placed onto the upper surface of the coracoid process and a release is performed under the deltoid muscle with digital dissection.

Use the sweep of a finger beneath deltoid to break down any subdeltoid adhesions and release under the deltoid muscle with digital dissection. Note the forked glenoid retractor (FGR) on top of coracoid process lifting soft tissues superiorly.

Take a Browne’s deltoid retractor (BDR)

Place the dish of the Browne’s retractor into subdeltoid space

Remove the Jackson Burrows self-retaining retractor

Take a Kolbel’s retractor (K).This has the advantage of having smooth metal blades which are minimally traumatic to the muscle they retract. A variety of depths of the blades are available.

Ensure the forked glenoid retractor (FGR) is on the coracoid process, Kolbel’s (K) self-retainer with blades sits under pec major and distal deltoid and Browne’s is in the proximal sub-deltoid space before proceeding to deeper dissection of the front of the shoulder.

Identify long head of biceps tendon in the bicipital groove

Cut intertubercular ligament overlying the biceps long head in its groove.Use scissors from inferior to superior to expose long head of biceps (LHB) tendon.

The long head of biceps tendon(LHB) identified with the forceps.

Palpate the upper edge of the subscaularis tendon.
A finger rolls easily over the upper edge of subscapularis and into the rotator interval.

Extend the split in intertubercular ligament proximally into the previously identified rotator interval then divide the LHB.

Mobilise the tenotomised long head of biceps.

Further distal dissection of the LHB tendon allows excision of the portion previously situated within bicipital groove.

With the upper edge of subscapularis already identified and rotator interval opened, the empty bicipital groove (BG) indicates lateral extent of subscapularis. The transversely running anterior circumflex humeral vessels know as the ‘three sisters’ (3S) indicate the lower border of subscapularis.

Use a 2.0 vicryl suture to tie off the anterior circumflex humeral vessels.

Tie off the anterior circumflex humeral vessels vessels to prevent bleeding during the next stage.

Use cutting a diathermy probe to perform vertical subscapularis tenotomy, ensuring a decent stump of tendon is left laterally to allow repair later.A variety of other techniques have also been described to manage subscapularis at this stage. Lesser tuberosity peel or osteotomy formally or with a fine slither of bone, Z lengthening of the tendon or a step cut.

The tenotomy is extended from the rotator interval proximally to the site where the 3 sisters were tied off distally.

Place a traction stay suture into the upper corner of the subscapularis tendon. Using this to guide completion of the tenotomy the proximal humerus is exposed.

Completion of the subscapularis tenotomy exposes the proximal humerus.

Squeeze the handle of moveable narrow arm board to drop it down.
This allows the arm to extend and facilitates dislocation of the shoulder glenohumeral joint and delivery of the humeral head into the wound.

Extension and external rotation of the arm and moving forked glenoid retractor from coracoid to medial edge of the articular surface delivers the arthritic humeral head into the wound.

Remove humeral head osteophytes with an osteotome and bone nibblers, to get back to the normal humeral head dimensions.

Use the osteotome to remove large rim osteophytes circumferentially, exposing the true humeral head.

Osteophytes being cleaved away from the original articular surface of the humeral head.

A bone nibbler being used to remove further osteophytes.

Removing osteophytes exposes the true humeral head.

Preoperative MRI imaging will have confirmed rotator cuff quality. Here the supraspinatus insertion is tenuous, thin and degenerate as suggested by the MRI scan.
The decision to sacrifice it and perform a reverse geometry total shoulder replacement is therefore confirmed to be correct.

Using cutting diathermy probe reflect residual supraspinatus insertion from the greater tuberosity footprint, given a reverse geometry shoulder is being implanted.The decision has been made in this case to use a reverse geometry implant despite the intact, although thin and degenerate, rotator cuff. To optimise postoperative function subscapularis has already been divided with a view to repair later and preservation of internal rotation and here only the superior supraspinatus insertion is released leaving infraspinatus more posteriorly on the greater tuberosity footprint hoping for active external rotation.

Release of the superior rotator cuff allows delivery of the humeral head into wound

Once the humeral head is delivered into the wound take the humeral cutting template.The humeral cutting template is used as an external jig. The alignment rod can be screwed into any of three positions of 0, 20 or 30 degrees. These degrees correspond to the amount of retroversion to be cut.
I tend to use 20 degrees retroversion option (as shown here, the central hole), and refer to the preoperative imaging to help me make that decision.
This template can also be used to make an initial assessment of core size with the depths of small, medium and large implants marked on the template.

Place the humeral cutting template so that it lines up the resection surface at the anatomical neck of the humerus and ensure the alignment rod (AR) handle is in line with the patients’ forearm with the elbow flexed at 90 degrees

Insert the 3mm pins into good bone to fix the cutting template


The pins are inserted using a mallet.

Two pins are required and the rod is removed before cutting commences.

Use the oscillating saw flush with the cutting template to resect the humeral head and remove it, followed by the jig.Note position of forked retractor (FR) behind humeral head protecting the skin, posterior rotator cuff (infraspinatus) and deeper the glenoid from saw blade.

Use a broad osteotome to elevate the cut humeral head.

Remove the resected humeral head.

Remove the cutting template.

The resected humeral metaphyseal surface exposed.

Confirm that humeral head metaphyseal bone is not too soft by palpating it firmly with thumb. The trabecular titanium of the core implant requires decent metaphyseal bone for primary impaction fixation.
If the bone is soft and there is concern that the core implant will not get adequate primary fixation then the decision to revert to the Lima SMR stemmed implant can be made.

Select an appropriately sized protection plate and impact onto the resected proximal humerus metaphyseal bone, once you have confirmed that the humeral head metaphyseal bone is not too soft.

The humeral protection plate in place.

Impacting the protection plate using a mallet.

Whilst holding forearm, squeeze handle of moveable narrow arm board.

Move arm board up to allow arm to rest in neutral in line with patient’s trunk.

Place a forked glenoid retractor (GR) behind the posterior glenoid rim displacing the proximal humerus posteriorly.Remove the subscapularis (SSc) on its traction stay suture from behind medial blade of the Kolbel retractor (K).

Pull the subscapularis stay suture laterally and use scissors to release soft tissue attachments of the rotator interval capsule adherent to upper border of the tendon.

Pull the subscapularis stay suture medially and dissect the anterior capsule off the subscapularis tendon using the scissors to open the tissue plane.

Using a finger palpate the axillary nerve as it passes posteriorly into the quadrilateral space. Its location should be revisited throughout the procedure to ensure awareness of its position.The axillary nerve is a terminal branch of the posterior cord of the brachial plexus carrying fibres from C5 & C6 nerve roots. It passes posteriorly through the quadrilateral (or quadrangular) space which is between the long head of triceps medially and the humeral shaft laterally and between the teres muscles, minor above and major below. It innervates teres minor and deltoid and the regimental badge patch sensation on the lateral aspect of the proximal arm. Damage to the nerve could result in altered sensation or numbness to this region and weakness or paralysis to deltoid which is hugely detrimental to function of a reverse geometry shoulder replacement which relies on medialisation of the centre of rotation of the shoulder and the increased moment arm with deltoid contraction.

Identify the stump of the long head of biceps tendon (LHB)

Use cutting diathermy to excise the residual biceps tendon and start to remove the capsulolabral soft tissues from around the circumference of the glenoid to allow access.Be constantly aware of the position of the axillary nerve as previously described.

Release and remove capsulolabral tissues to gain good access to the glenoid.

Use a No 15 scalpel blade on a long handle to complete 360 degree peri-glenoid soft tissue release. Don’t forget to continually review the position of the axillary nerve running from anterior to posterior directly below the inferior shoulder capsule at the inferior pole of the glenoid.

From the Lima set the “bunny ears” (BE) retractor is designed to fit under the inferior glenoid

With the fork of the ‘bunny ears’ (BE) retractor either side of the scapula blade under the inferior pole of the glenoid the axillary nerve is protected during further preparation of the glenoid. Re-position the forked (F) retractor around the posterior glenoid rim

Identify the subscapularis on its traction stay suture.

Tuck the subscapularis on its stay suture behind the medial blade of the Kolbel retractor

Mark the orientation of the glenoid, both “north to south” and also its central point.With the left index finger on the coracoid process the superior and inferior poles of the glenoid face can be identified. Use cutting diathermy to mark the North-South line.

Diathermy is used to mark the central point of the glenoid. The superior and inferior poles of the can also be marked at the perimeter of the glenoid at this stage. With reference to preoperative imaging the superior pole is usually just posterior to the base of the coracoid which can be palpated anterosuperiorly. The inferior pole is then estimated on the perimeter on a North-South line from superior pole through the central point

Assess the size of glenoid face and choose either the small or standard glenoid guide.

Place the cannulated gleniod guide guide of appropriate size onto the face of the glenoid, following this with insertion of a centrally placed guidewire into the glenoid.In this case I have used the small guide

Take the 2.5mm x 15cm long wire on a driver and insert it down the cannulated guide, into the marked centre of the glenoid.

Ones preoperative assessment of the glenoid “version” and wear by scrutiny of MRI or CT scan will influence the choice of wire position. In general for a reverse geometry metal glenoid baseplate the wire should be central and into a good volume of bone, with slight inferior inclination.

Remove the glenoid guide completely, leaving the wire in position.

Place the correctly sized glenoid reamer over guidewire, and ream under direct vision to subchondral bone.

The design feature of the cut out notch in the reamer(A) allows the easy passing of retractors.

Start the reamer and advance it down to bone

Gentle pressure on reamer starts to clear residual cartilage and subchondral bone.

Pull back the reamer to assess the glenoid preparation.
The aim is to just expose subchondral bone rather than excessive bone removal

There are two glenoid peg drill sizes: Small-R or Small/STD. Choose either small-R (R for reduced) for a small-R glenoid baseplate or Small/STD glenoid peg drill for small, standard or large (only available on special request) depending on the size of patient and the available bone seen on preoperative imaging.

Push the drill down until fully seated against glenoid face and ream using an appropriately sized glenoid drill for the central peg hole.

Remove both drill and guidewire to expose the central peg hole.

Choose the relevant definitive glenoid baseplate implant (size Small-R in this case) and attach to the glenoid impactor. There are four metal glenoid baseplates available: small-R (R for reduced), small, standard or large (the latter only available on special request) depending on the size of patient and the available bone seen on preoperative imaging. They are not sided for left and right.

Close-up of the glenoid baseplate on introducer. This is securely attached with the central rod screwed into the central hole of the face of the baseplate.

Insert glenoid baseplate into central peg hole and ensure long axis vertical orientation of the two drill holes along North-South line previously described.

Use a heavy mallet to impact the baseplate into the bone.

Press the button on the impactor shaft to release it from the implant
Having released the attachment, pull the shaft back to assess whether baseplate is completely down flush with the prepared glenoid face by looking at the exposed drill holes.

Inspect baseplate holes to assess whether it is fully seated. If not replace the impactor down on the baseplate and impact further with a heavy mallet.

Remove the impactor

Unscrew attachment handle

Drill through the holes in the baseplate for the glenoid fixation screws.Use 3.5 helix drill on flexible mandrel and drill guide. There are two length options of these drill bits but they are the only ones that fit on the flexible mandrel.

Angle the superior screw slightly anteriorly into the body of bone at base of coracoid process and drill the superior screw hole first.

Drill down as far as the drill guide allows
If not through the second cortex further depth on the drill can be achieved by removing the drill guide and re-drilling freehand

Take the depth gauge and measure the depth of first superior drill hole, then insert an appropriately sized 6.5mm screw, but do not tighten fully.

Take the first 6.5mm cancellous screw, here seen with screw holder.

The superior screw is inserted first.

Advance screw but stop shy of final tightening

Drill inferior screw hole perpendicular to baseplate aiming slightly posterior, then repeat the process of measuring and screw insertion.

Use depth gauge to assess length of inferior screw

Insert the inferior screw

Once both screws are in place tighten them dow sequentially to ensure the baseplate is evenly compressed into the glenoid.

Choose an appropriate glenosphere and adaptor, which are then assembled.Lima glenospheres(G) are available in 3 sizes: 36, 40 & 44mm. The 36 is made of Cobalt Chrome; the 40 & 44 are Polyethylene. Choice of glenosphere depends on size of patient, surgeon preference and joint stability. The latter can be assessed using trial implants. The adapter(A) choice is dependant on baseplate size.
Note here the thinner relatively longer end on the left which inserts into the Small-R baseplate, compared to the broader relatively shorter end on the right that inserts into the glenosphere.

Insert the short broad end of adaptor into glenosphere.

Take gauze swab to place over adaptor

Tap the covered adaptor with small mallet to engage the taper mechanism fully.

Take glenosphere insertion handle

Screw handle into glenosphere central hole

With the glenosphere screwed onto its insertion handle Insert the glenosphere adaptor into the baseplate central hole

Push glenosphere into position. The eccentric glenosphere has an extended lip which must be placed inferiorly on glenoid. This is designed to prevent glenoid notching. This is bony erosion of the inferior pole of the glenoid presumed due to repetitive impingement of the medial lip of the humeral implant with shoulder adduction. It has been reported in many of the reverse geometry shoulder replacement designs and theoretically may result in loosening of the glenoid component fixation.

Ensure the glenosphere rotation is correct with the extended lip inferiorly then tap the insertor to engage the taper mechanism.

Unscrew glenosphere insertion handle

Insert safety screw into glenosphere central hole

Advance the safety screw

The glenosphere is secured with a centrally located safety screw which is tightened down until a squeak is heard

Take glenosphere polyethylene button and its introducer

Insert the glenosphere button

Insert the Poly button that covers the central locking screw by pushing the button into the central hole until a click is heard then pull back the introducer.

The definitive glenosphere has been prepared.

Whilst holding the forearm squeeze the handle of arm board

Drop the arm board to allow the humerus to extend

Extension of humerus and replacing the Browne deltoid retractor (B) laterally and forked retractor (F) medially delivers the proximal humerus into wound

Four sizes of humeral core are available and the sizers are colour coded to guide surgical team. Extra small is grey/silver, small is yellow (YS), medium is orange (OM) and large is purple. The same handle is used for all sizers.

Apply the handle to the chosen humeral sizer. Take care not to drop as this is a loose fit. Next place it onto the cut humeral heads surface.It is cannulated to accept a K-wire.Note the depth marks (DM) on the handle indicating a short implant with an arrow. These are the marks used against a laser line on the wire to indicate if a short core implant is required. Here the orange and grey/silver marks for medium and extra small implants are seen. The coloured marks for small and large implants are found on the other side of the handle

Place humeral core sizer onto cut metaphyseal surface
Ensure that the circumference of the sizer is within the cut cortical bone

Take the 3.5mm humeral reamer guidewire. Note the laser line (LL) on the wire

Insert the wire down the cannulated sizer handle

A guide wire is drilled through the cannulated section of the humeral sizer. When wire comes up against lateral humeral cortex note position of laser line. This indicates the depth of the implant required, short or standard core section.Depth marks on handle have arrow pointing towards ‘short’ annotation. If laser line is the short side of the coloured mark then a short core implant is required. In this case the line is not on the short side of the orange medium mark so a standard depth implant is indicated

This shows the difference between the standard depth humeral reamer on the left compared to the equivalent short reamer on the right

Take the humeral reamer handle…

Fix the chosen reamer to the handle to the standard (not short) medium reamer (orange colour code) is used.

Place the reamer over the guidewire.

Advance the humeral reamer down the guide-wire and start the power reamer before touching bone

Advance the reamer over guide-wire into metaphyseal bone
Avoid wobbling or rocking the reamer handle to ensure a ‘clean’ reaming.

Advance the reamer using even pressure until its outer rim sits flush with the cut bone surface.

Gently withdraw the reamer up wire.

The reamed proximal humerus shows a good rim of cortical bone

Take the appropriate sized compactor for the chosen size of humeral core implant. Four sizes of humeral core are available and the sizers are colour coded to guide surgical team. Extra small is grey/silver, small is yellow, medium is orange and large is purple.

This makes the fin impactions for the humeral prosthesis and doubles as the trial implant

Attach the compactor handle

The compactor is Inserted over guidewire. It makes the fin impactions for the humeral prosthesis and doubles as the trial implant.Both fins should be placed into the greater tuberosity bone behind the bicipital groove. Here the forceps indicate the position of the groove.

Use the heavy mallet to impact the compactor into the metaphyseal bone

The compactor impacted into metaphyseal bone

Compactor handle has been removed.
Note here the rim of cortical bone is proud of the trial implant. This should be further resected

With the compactor handle resected use an oscillating saw to resect proud cortical bone rim flush with trial implant

A well seated trial implant.

There are three trial humeral liners available – short, medium or long.

Insertion pliers are used to squeeze the trial humeral implant as it’s pushed into position.Line up the small notch with superior humeral implant at the relevant R or L marking on the core for Right or Left shoulder.

Trial humeral liner in place

Reduce the trial shoulder replacement Do this with some gentle inferior and posterior pressure on the trial liner whilst elevating and internally rotating the arm.

The appearance of the reverse geometry articulation

Remove retractors and assess stability by moving the arm through a range of movement. Elevate, abduct and rotate at a variety of levels of elevation whilst palpating the shoulder and directly observing the articulation in the wound. If there is instability this needs to be assessed. Further use of trial liners could confirm most suitable size required for stable range of movement. Often it’s simply a need for a larger liner. Occasionally there is an unrecognised osteophyte around the cortical rim of the proximal humerus which needs resecting.

Once stability confirmed, dislocate joint, use pliers to remove trial liner then reattach core handle.

Dis-impact the core trial with a small mallet

Disimpact and then remove the core trial implantAvoid further hand wobble to ensure clean compacted fins

Note the clear, impacted fins in the prepared greater tuberosity bone

The definitive humeral core prosthesis.

Constructed on a 3D printer this trabecular titanium humeral core implant allows strong bone ingrowth.

Screw the impaction handle into the definitive core implant

Avoid contact of core implant with gauze swabs as they stick to the trabecular titanium

Wash the prepared humeral metaphysis.

The definitive humeral core implant is inserted once screwed onto the impaction handle, having lined up the fins.

Use the mallet to impact the implant

Controlled impaction continues until the implant sits flush with the bone resection of the humeral head.

Unscrew insertion handle

The definitive Cobalt Chrome humeral liner. Note the notch (N) indicating the superior aspect of this implant which will line up with R or L (for Right or Left shoulder) on the lateral edge of the humeral core implant.

Insert the definitive liner into humeral core

Ensure rotation of liner is accurate with the notch at the superior rim of the humeral core implant lining up with the marked R or L (for Right or Left shoulder).

Push the liner into position

The liner impactor is used to strike the humeral core liner so it engages with the humeral core.

Check solid fixation of the liner in its core.

The shoulder is reduced, the joint is thoroughly washed out and stability is confirmed.Final stability confirmed but should be no different from the same done with the trial implants.

Retrieve the subscapularis tendon on its traction stay suture.

Reduce the tendon to its lateral stump

Repair subscapularis tenotomy with interrupted Ethibond stitches

At least four heavy Ethibond stitches are required to get good apposition of the subscapularis tendon.

Check range of external rotation before excessive tension is placed onthe repair. This allows accurate instructions for postoperative physiotherapy

Close fascia and fat with continuous vicryl absorbable suture and also to the skin.

Running subcuticular monocryl stitch to close skin

Application of adhesive paper steristrips to protect skin closure

Position of metal implant components.
The polyethylene glenosphere is radiolucent and obviously not seen.

This modified axillary xray view shows position of glenoid baseplate screws in glenoid bone and core humeral implant impacted into proximal humerus metaphysis.

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
Ultimate aim is function rather than anatomical range of movement.

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
Results of a stemless reverse shoulder prosthesis at more than 58 months mean without loosening. R Ballas, L Begun. J Shoulder Elbow Surg. 2103 September; 22(9):e1-e6
Clinical and radiological outcome of the Total Evolutive Shoulder System (TESS) reverse shoulder arthroplasty: a prospective comparative non-randomised study. B Kadum, S Mukka, E Englund, A Sayed-Noor, G Sjoden. Int Orthopaedics. 2014 May; 38(5):1001-1006
The TESS reverse shoulder arthroplasty without a stem in the treatment of cuff-deficient shoulder conditions: clinical and radiographic results. P Teissier, J Teissier, P Kouyoumdjian, G Asencio. J Shoulder Elbow Surg. 2015 January; 24(1):45-51
Reverse shoulder arthroplasty with a cementless short metaphyseal humeral implant without a stem: clinical and radiologic outcomes in prospective 2- to 7-year follow-up study. O Levy, A Narvani, N Hous, R Abraham, J Relwani, R Pradhan, J Bruguera, G Sforza, E Atoun. J Shoulder Elbow Surg. 2016 August; 25(8):1362-1370
Short to mid-term results of stemless reverse shoulder arthroplasty in a selected patient population compared to a matched control group with stem. P Moroder, L Ernstbrunner, C Zweiger, M Schatz, G Seitlinger, R Skursky, J Becker, H Resch, R Krifter. Int Orthopaedics. 2016 October; 40(10):2115-2120


Reference

  • orthoracle.com
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