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Joint replacement- Stryker SR Metal on Poly PIP joint

This is a detailed step by step instruction through a Middle finger Proximal interphalangeal joint (PIPJ) cemented joint replacement with the Styker SR PIP joint implant via a dorsal ulnar approach.
This is a procedure usually performed for osteoarthritis of the PIPJ with stable collateral ligaments. It can also be performed for post-traumatic or well controlled inflammatory arthritis as long as the bone stock and soft tissue stability can support the joint.
The procedure can be performed as a day case under local, regional or general anaesthetic and take around 1 hour.
Following a period of 1 week in plaster cast the patient then starts mobilisation with a Bedford finger splint and is provided with a night resting splint at 30 degrees MCPJ flexion and straight PIPJs. The patient should achieve their pre-operative range of movement with minimal pain by 6 weeks and at this point should start strengthening exercises. The joint will always appear slightly swollen however the majority of post operative swelling will resolve by 3 months.

Indications
Articular damage causing pain in the PIPJ.
Failure of non-operative treatment.
Causes would include: osteoarthritis, inflammatory arthritis or post-traumatic arthritis.
Symptoms
The symptoms experienced are pain and stiffness which leads to reduced function and grip strength. In more severe cases night pain may be a problem for the patient. The operation is carried out in the main for pain. It will usually not improve the range of movement unless there is a specific bony block to the range. This is due to the progressive tightening of the soft tissues around the joint which remain in place and are repaired once the implants are inserted.
The patient’s job and hobbies often play a major role in their symptoms and therefore discussing these details and realistic expectations of the post-operative outcomes are essential in treatment selection especially if they have a very good grip strength despite the pain. Very heavy manual work is often a cause for the arthritis and exacerbation of the pain.
Examination
A patient with PIPJ arthritis who requires surgery will usually have a swelling around the joint which will be a combination of synovitis and osteophytes. The will often have a restricted range of movement in both flexion and extension and a reduced grip strength.
There is often some angulation at the joint due to an uneven collapse of the proximal phalanx condyles or erosion into the middle phalanx base. This is likely to be angulation in an ulnar direction due to the forces exerted on the joint by the thumb during tripod pinch in the index and middle fingers.
The joint may be painful to palpate and certainly be painful at extremes of movement. If they have considerable joint deformity and angulation (common in inflammatory arthritis) this would suggest poor soft tissue support and they would not usually be considered for this type of joint replacement. A single piece plastic joint replacement is usually more appropriate.
They may have other arthritc joints however it is not uncommon to have isolated PIPJ arthritis due to trauma.
Investigations
Investigations include plain PA and lateral radiographs of the effected joint.
Non-operative Management
Non-operative management for arthritis includes, analgesia, activity modification, Bedford splinting (which may be worn during certain activities and prevent accidental deviation and pain), physiotherapy with grip strengthening and steroid and local anaesthetic injections.
The injections treat the synovitis not the wear to the joint.
Alternative operative Management
Alternative procedures for PIPJ arthritis include:
Silastic single piece joint replacements, other bicomponent replacements.
Arthrodesis.
Denervation.
Contraindications
Absolute contra-indications
Infection, skeletal immaturity and joint instability.
Relative contra-indications
A very stiff joint which an arthrodesis may be a better option with fewer risks (particularly of revision surgery).
A heavy manual job – which is likely to cause early failure (often when patients are a couple of years from retirement it may be advisable for them to delay surgery until retirement to prolong the life of the implant).
A very distorted/collapsed joint – the soft tissues may be intact but very tight in this case and may require release to insert an implant- this group of patients may be best to be also consented for joint fusion or silastic single piece replacements with the option to convert inter-operatively if excessive soft tissue release required to insert a trial has made the joint unstable.

Pre-operative preparations and Equipment
The operation can be performed under local, regional or general anaesthetic. The duration of surgery is around 1 hour. An upper arm tourniquet is applied and inflated to 250mmHg (a digital tourniquet may also be used if performing the procedure under local anaesthetic and if it will not interfere with operative technique).
A clean air flow theatre is recommended for implant surgery and a change of gloves prior to implant insertion to reduce infection risk.
Equipment – Stryker SR PIP implant tray with range of implants XS-XL, narrow saw blade, Fine bone nibblers, bone cement, an image intensifier, plaster cast.
A single dose of antibiotics are given pre-operatively.

Dorso-lateral skin incision marked on ulnar border of PIPJ.
With the limb anaesthetised, prepped and drapped on an arm board and tourniquet inflated the skin incision is marked.
The line of the incision is on the dorso-ulnar border (dorso-radial in the little finger). It roughly lies over the junction of the lateral bands and the central tendon. It extends from mid-proximal phalanx to mid-middle phalanx.

Skin is incised and then blunt dissection performed down to the extensor hood.Once the skin is incised the skin, fat and dorsal branches of the digital nerves are elevated as one layer to the level of the extensor tendon to maintain skin vascularity and protection of the nerves.
The junction between the lateral band (interossei tendons) and central tendon is marked.

The extensor hood is incised between the lateral band and the central tendon.The capsule will be incised as a separate layer.

The capsule is incised.The capsule is incised in line with the tendon incision and is then released from the middle phalanx starting on the ulnar border working gradually volar to the insertion of the true collateral ligament which is attached to the volar 30-40% of the lateral border of the middle phalanx.

The capsule is reflected radially as is part of the insertion of the central slip.The central slip which is also partially elevated with the periosteum of the middle phalanx.
Occasionally the central slip may completely detach at this point, if this occurs it will need to be reattached at the end of the procedure. NB – a bony suture must be inserted before cementing if this is the case.

The scissors are pointing to the ulna collateral ligament of the PIPJ travelling from the centre of rotation of the proximal phalanx head to the volar 30-40% of the middle phalanx.

The true and accessory ulnar collateral ligaments and volar plate are released.The ligaments are sharply dissected off the middle phalanx as a sheet continuous with the periosteum, the ulnar two thirds of volar plate is also released. The release is made easier by pronating the middle phalanx as the dissection proceeds dorsal to volar as this keep the tension on the tissues for a cleaner dissection.
The collateral ligaments are elevated in a sheet in this way to allow them to stick back down and provide lateral stability in the post operative period without the need for a formal repair.

The joint is shotgunned radially.Once the joint is released as described the lateral shotgun of the joint is attempted. It often takes a few attempts to complete this manoeuvre with a little further release required between each attempt. In joints which have marked erosion of the joint the whole volar plate may need to be released to shotgun the joint.

The joint is now shotgunned revealling a clear view of both articular surfaces.
MP – Middle phalanx
PP – Proximal phalanx

Be aware that the lateral bands seperated of the central tendon in the initial dissection can be under tension on the ulnar side of the joint (shown by the scissors) and therefore are at risk of iatrogenic damage if care is not taken.

The proximal phalanx head is cut perpendicular to the diaphysis just distal to the collateral ligament insertion.This cut can be difficult execute correctly if the phalanx condyle are unevenly worn therefor it is best to firstly remove and large dorsal osteophytes, clear soft tissue around the head allowing both origins of the collateral ligaments to be clearly identified and drawing a line along the long axis of the bone as seen in the image. Following this a cut line on the distal edge of the collateral insertions and perpendicular to the long axis is drawn (also shown).
It can be seen that on this image the radial condyle (highlighted by the metal pointer) is less eroded and therefore relatively more bone will be cut from this side.

The bone cut is undertaken with the appropriate size saw and the collateral are protected.

The cut is made. Often is the cut is at the level of the collaterals the insertion of the the ligaments can be seen indenting into the bone at the cut level.

The starter awl is inserted centrally in both radio-ulnar and volar-dorsal directions.

A 45 degree volar bone cut is performed at the lower level of the awl entry point. The cut is easiest to perform with the proximal phalanx vertical and the blade at 45 degrees to the table.
The collateral ligaments and lateral bands are protected with skin hooks.

The starter awl is then used on the middle phalanx.The awl is inserted centrally from radial to ulnar and slightly dorsal of central in the volar-dorsal direction.

The middle phalanx is cut perpendicular to the diaphysis.The site of the starter awl entry can be seen.
A sliver of bone is removed with the saw from the ulnar aspect of the middle phalanx where the collateral was excised from. This bone sliver aims to create enough space for the implant and its thickness will depend on the severity of erosion of the base of the phalanx.
If still attached the central slip should be protected also at this point.

The joint gap is assessed in finger extension.Once both bone sections have been cut there should be an even joint space able to fit the implant when the finger is pulled straight. Clearly the joint gap will open more on the ulnar side if stressed as no collateral ligament is attached.

A burr is used to widen the awl hole if the bone is sclerotic.When reaming PIP joints the surgeon must be aware whether the implant being used can mix sizes of proximal and distal implants or whether one size is used, as in the case of this implant.
Where one size for both proximal and middle phalanx is used then the largest implant is used which fits the smallest bone.
As it can vary whether the canal of the middle or proximal phalanx is largest is is best to ream sequentially to avoid over reaming of one bone.
When starting reaming a burr may be required initially if the bone is sclerotic.

The initial reamer is sited in the middle phalanx.The initial reamer is sited in the middle phalanx.

A radiograph is taken to check central placement on the AP and lateral images.

It can be seen from this view that the reamer is slightly volar in its placement and therefore on subsequent reamer insertions a dorsal pressure can be applied to ream more dorsal than volar and correct the reaming position prior to trial insertion.

The initial reamer is placed in the proximal phalanx.

The initial reamer position is checked on the AP and lateral images.

Again the reamer is slightly volar in placement and therefore this should be corrected on subsequent reams prior to trial insertion.

Trial implants are inserted.Once both bones have been sequentially reamed up to the largest size of the smallest bone (if the proximal phalanx is reamed maximally to a size 2 and the middle phalanx could be easily reamed to a size 3 – stop at a size 2 in both bones so that the sizes match).
The trials (in this case size 2) can now be inserted.
The tension is tested to assess for over stuffing of the joint. If the correct size is inserted the PIPJ should fully extend with ease and flex without the trial being too unstable (if a significant preoperative flexion contracture was present this assessment may vary).


Range of movement assessed with trial implants in situ.The rotational alignment is also assessed. Make sure the shapes of the 2 components of the trial sea nicely and align with the pen line previously drawn down the proximal phalanx. Rotation can often look abnormal in this approach due to the one sided joint release. If there is any concern them place a tacking suture attaching the central slip to the lateral band and reassess – this will usually correct any abnormal rotation caused by the operative dissection.

Radiographs of the trials are taken.

The trial is removed and the bone washed and dried to prepare for cementing.At this point, if the central slip was completely lifted off the middle phalanx then two osseous tunnels can be drilled with a 1.2mm k-wire into the insertion on the middle phalanx and a suture passes through the holes before cementing enabling reattachment during closure.
The area is prepared with a clean drape or towel, change of gloves, implant (which has been checked and opened), implant impactors, forceps and Watson-Cheyne dissector for removal of excess cement.

An antibiotic impregnated cement is inserted.In this case a standard cement is used and after 2-3 mins when easy to handle the cement is rolled into a small sausage shape and pushed into the canal of both bones and the impacted it with a thumb.

The proximal phalanx implant is inserted.

The middle phalanx implant is inserted.

The appropriate impactor is used to firm in the two implants.

The excess cement is removed, the joint relocated and radiographs taken.

AP radiograph of the implant in situ

Manufacturers box showing the size 2 implant.

The ulnar collateral ligament is laid back into position and the capsule and tendon repaired.The collateral ligament is left to heal in place and is not formally sutured down.
The central slip is sutured back if necessary with the pre-prepared interosseous suture and the lateral band is sutured back to the central tendon with 4/0 PDS.
This will then correct any rotational deformity and instability seen following the initial dissection.
To note in this patient, the marked ulnar angulation of the DIPJ made intra-operative alignment (often referenced off the nailbed) more difficult and must be appreciated pre-operatively.

The skin is closed using a 4/0 vicryl rapide.

An occlusive dry dressing is applied.

A volar plaster slab, wool and crepe are applied in extension. This cast will be removed at 1 week in clinic.

Pre-operative AP radiograph showing marked erosion of the ulnar condyle of both the proximal and middle phalanges.

Pre-operative lateral radiograph revealing PIPJ and DIPJ arthritis.

The procedure is performed as a day case and the patients are discharge with a sling and return within a week for wound review and hand therapy.
We provide paracetamol, ibuprofen, codeine and a laxative (senna) on discharge.
The wound is redressed and a Bedford splint applied to the finger. The Bedford splint is applied to the operated finger and its ulna neighbour to protect the elevated ulnar collateral ligaments. (taping may be required for a 5th PIPJ replacement to prevent excessive ulnar deviation as a Bedford splint will be a poor fit to its neighbour the ring finger).
At 2 weeks the dressing removed.
The Bedford splint is worn full time for 6 weeks and is used to prevent excessive radial or ulnar deviation and aid in mobilisation supported by the adjacent digit. A volar resting splint in 30 degrees MCPJ flexion and straight PIPJs is also provided for night time wear for 6 weeks.
At 6 weeks a PA and lateral radiograph of the joint is taken this is repeated at 6, 12 and 24 months.
Strengthening exercises can begin at 6 weeks and most patients should expect to have most of their grip strength and final range of movement by 3 months.
It will usually take patients 6-8 weeks to return to light work and 3-6 months to return to heavier work.

Results
Complications include infection, stiffness, continued pain, fracture and implant failure/loosening.
For some figures on these complications please read the following articles:
Thomas E. Trumble and Dennis J. Heaton. Outcomes of Surface Replacement Proximal Interphalangeal Joint Arthroplasty Through a Volar Approach: A Prospective Study. Hand (N Y). 2017 May; 12(3): 290–296.
This paper describes a series of 21 patients using the Stryker SR PIPJ as show in this operation but using a volar approach. There was a mean of 34 months follow up, a mean arc of motion at the PIPJ of 87 degrees which was an improvement from pre-operatively of 58 degrees. There were no implant failures, 4 (20%) extensor tenolysis and 1 superficial skin infection.
Murray PM1, Linscheid RL, Cooney WP 3rd, Baker V, Heckman MG. Long-term outcomes of proximal interphalangeal joint surface replacement arthroplasty. J Bone Joint Surg Am. 2012 Jun 20;94(12):1120-8.
This paper reviews the long term follow up of a similar metal on polyethylene 2 component prosthesis. 67 implants were followed up for a mean of 8.8 years. The majority were implanted for osteoarthritis via the dorsal approach and cemented in situ.
This paper reviews the long term follow up of a similar metal on polyethylene 2 component prosthesis. 67 implants were followed up for a mean of 8.8 years. The majority were implanted for osteoarthritis via the dorsal approach and cemented in situ.
At follow up the mean range of movement at the PIPJ was 40 degrees. Eight prostheses had failed. This equated to implant failure of 3% at one year, 8% at three years, 11% at five years, and 16% at fifteen through twenty-five years. Volar implanted joints failed more frequently than those inserted via a dorsal approach. The were no infections and overall 2 patients underwent amputation and 4 PIPJ fusions due to failures.

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