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Not affiliated with the Royal Australasian College of Surgeons.

Revision Total Knee Arthroplasty

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Revision Total Knee Arthroplasty

Comprehensive guide to revision TKA including indications, AORI bone loss classification, constraint selection, and surgical techniques for failed knee arthroplasty.

complete
Updated: 2025-12-17
High Yield Overview

REVISION TOTAL KNEE ARTHROPLASTY

AORI Classification | Constraint Selection | Bone Loss Management | Outcomes

5-10%revision rate at 10 years
15-20%re-revision rate at 5 years
50%aseptic loosening indication
20%instability indication

AORI BONE DEFECT CLASSIFICATION

Type 1
PatternIntact metaphyseal bone
TreatmentStandard components
Type 2A
PatternDamaged metaphysis (one condyle)
TreatmentAugments/cement
Type 2B
PatternDamaged metaphysis (both condyles)
TreatmentAugments required
Type 3
PatternDeficient metaphysis
TreatmentStructural allograft/metaphyseal cone/sleeve

Critical Must-Knows

  • Aseptic loosening is the most common indication for revision TKA (50% of cases)
  • AORI classification guides bone loss management: Type 1 (intact), Type 2 (damaged), Type 3 (deficient)
  • Constraint progression: PS to CCK to hinged based on bone loss and soft tissue competence
  • Infection must be ruled out in ALL cases before revision - aspirate, inflammatory markers, culture
  • Two-stage revision is gold standard for chronic PJI with antibiotic spacer interval

Examiner's Pearls

  • "
    AORI Type 3 requires structural support (metaphyseal sleeve, cone, or bulk allograft)
  • "
    Constrained condylar knee (CCK) for MCL/LCL insufficiency but intact bone stock
  • "
    Rotating hinge for massive bone loss or global instability
  • "
    Modular stems for stability and load sharing, cemented distally in diaphysis

Clinical Imaging

Imaging Gallery

Example of extra-articular malalignment after high tibial osteotomy (HTO) with opening wedge technique. The red line on the left radiograph (a) indicates the mechanical axis lateral to the knee joint.
Click to expand
Example of extra-articular malalignment after high tibial osteotomy (HTO) with opening wedge technique. The red line on the left radiograph (a) indicaCredit: Badawy M et al. via Acta Orthop via Open-i (NIH) (Open Access (CC BY))
Example of intra-articular malalignment after high tibial osteotomy (WTO) with closing wedge technique. The solid red line indicates that the tibial plateau has been elevated medially and is not perpe
Click to expand
Example of intra-articular malalignment after high tibial osteotomy (WTO) with closing wedge technique. The solid red line indicates that the tibial pCredit: Badawy M et al. via Acta Orthop via Open-i (NIH) (Open Access (CC BY))
74 y, male: 4 years after TKA with septic loosening and medial tibial collapse A) preoperative x-ray B) Two stage revision with hand made antibiotic-loaded articulating cement spacer. C) Postoperative
Click to expand
74 y, male: 4 years after TKA with septic loosening and medial tibial collapse A) preoperative x-ray B) Two stage revision with hand made antibiotic-lCredit: Sanz-Ruiz P et al. via BMC Musculoskelet Disord via Open-i (NIH) (Open Access (CC BY))

Critical Revision TKA Exam Points

AORI Classification Drives Treatment

Type 1 = Intact metaphysis (standard components). Type 2A/B = Damaged (augments, cement). Type 3 = Deficient (structural graft/sleeve/cone). Know which reconstruction for which defect.

Rule Out Infection FIRST

Aspirate ALL knees before revision. ESR, CRP, synovial WBC and differential. Alpha-defensin if clinical suspicion. Never proceed without excluding PJI.

Constraint Selection Algorithm

PS to CCK to hinged based on:

  • Bone loss (AORI grade)
  • Collateral ligament integrity
  • Flexion-extension gap balance
  • Extensor mechanism function

Two-Stage for Infection

Stage 1: Debridement, explant, antibiotic spacer. 6-8 weeks IV antibiotics then 2-week holiday. Stage 2: Aspirate negative, then reimplant. 90% infection control rate.

Quick Decision Guide - Revision TKA Approach

IndicationAORI GradeConstraint LevelKey Technique
Aseptic loosening, minimal bone lossType 1 (intact)PS or CCKStandard components, cement fixation
Instability, moderate bone lossType 2A/B (damaged)CCK with augmentsMetal augments or cement-fill, stems for stability
Massive bone loss, global instabilityType 3 (deficient)Rotating hingeMetaphyseal sleeve/cone, long cemented stems
Chronic PJI confirmedVariable (assess at stage 2)CCK or hingeTwo-stage with spacer, 6-8 weeks antibiotics
Mnemonic

FAIL-TIndications for Revision TKA

F
Failed Fixation (aseptic loosening)
50% of revisions - radiolucent lines, subsidence, pain
A
Arthrofibrosis/Stiffness
Less than 90° flexion, failed manipulation
I
Instability
MCL/LCL insufficiency, flexion-extension gap imbalance
L
Loosening (septic)
Periprosthetic joint infection - two-stage revision
T
Technical error
Malrotation, malalignment, component size mismatch

Memory Hook:The knee has FAILED T(otally) - these are the five main reasons for revision TKA!

Mnemonic

I-D-D-DAORI Bone Defect Classification

I
Intact (Type 1)
Metaphyseal bone intact - standard components
D
Damaged one condyle (Type 2A)
One femoral or tibial condyle affected - augment or cement
D
Damaged both condyles (Type 2B)
Both condyles involved - requires augmentation
D
Deficient metaphysis (Type 3)
Massive bone loss - structural graft, sleeve, or cone needed

Memory Hook:I'm D-D-D (I'm devastated) - the progressive severity of bone loss in revision TKA!

Mnemonic

CLAMPConstraint Selection Principles

C
Cruciate-retaining (CR)
Rarely used in revision - needs intact PCL
L
Laxity assessment
Evaluate MCL/LCL integrity to guide constraint
A
Augments for bone loss
Metal augments or sleeves for AORI Type 2/3
M
MCL/LCL competence
CCK if one collateral incompetent, hinge if both
P
Posterior-stabilized (PS) to CCK to hinge
Progressive constraint ladder

Memory Hook:CLAMP down on instability - use increasing constraint as needed to stabilize the revision knee!

Mnemonic

SPACETwo-Stage Revision Protocol

S
Stage 1: Debridement and spacer
Remove all components, cement, and infected tissue
P
Prolonged IV antibiotics
6-8 weeks organism-specific therapy
A
Antibiotic holiday
2 weeks off antibiotics before reimplantation
C
Confirm infection cleared
Aspirate, inflammatory markers normalized
E
Exchange spacer for definitive implant
Stage 2 reimplantation if clear

Memory Hook:Create SPACE for the knee to heal - the two-stage revision protocol for chronic PJI!

Overview and Epidemiology

Why Revision TKA Matters

With over 100,000 primary TKAs performed annually in Australia, the burden of revision surgery is substantial. Revision TKA is technically demanding, associated with higher complication rates (20-30% vs 5-10% for primary), longer operative times, and inferior functional outcomes. Understanding indications, bone loss classification (AORI), and constraint selection is critical for Orthopaedic exam success and clinical practice.

Demographics

  • Age: Mean 65-70 years at revision (younger than primary)
  • Gender: F greater than M (2:1) - same as primary TKA
  • Time to revision: Mean 7-10 years post-primary
  • Re-revision risk: 15-20% within 5 years

Burden and Outcomes

  • Complication rate: 20-30% (vs 5-10% primary)
  • Operative time: 2-3 hours (vs 1-1.5 hours primary)
  • Functional scores: 70-80% of primary TKA outcomes
  • Survivorship: 85-90% at 10 years (vs 95% primary)

Anatomy and Biomechanics

Knee Anatomy Relevant to Revision TKA

Understanding knee anatomy is critical for revision TKA. The metaphysis (wide flared bone at joint) provides primary component support but is often compromised in revision. The diaphysis (narrow shaft) is where stems gain fixation. The MCL and LCL (collateral ligaments) provide varus-valgus stability - their integrity determines constraint needs. The popliteal artery runs posteriorly and is at risk during exposure in revision cases.

Metaphysis vs Diaphysis

  • Metaphysis: Wide flared bone at joint - primary component support
  • Compromised in revision: Bone loss (AORI classification) affects this region
  • Diaphysis: Narrow shaft below metaphysis - stem fixation site
  • Cemented stems: 14-16cm fixation length in diaphysis for stability

Collateral Ligaments

  • MCL (medial collateral): Prevents valgus instability
  • LCL (lateral collateral): Prevents varus instability
  • Integrity assessment: Intraoperative stress testing determines constraint
  • CCK vs hinge: One collateral deficient = CCK, both = hinge

Popliteal Artery at Risk

The popliteal artery runs posterior to the knee joint, approximately 1cm from the posterior capsule. In revision TKA:

  • Posterior capsule is attenuated from prior surgery, wear, loosening
  • Anatomical planes are lost - difficult to identify neurovascular structures
  • Posterior releases for stiff knees bring instruments close to artery

Protection strategies: Stay subperiosteal, use retractors carefully, avoid blind posterior releases, gentle tissue handling.

Indications for Revision TKA

IndicationFrequencyKey FeaturesTreatment Approach
Aseptic loosening50%Radiolucent lines over 2mm, progressive, painfulRevise components, address bone loss, stems
Instability20%MCL/LCL insufficiency, flexion-extension gap imbalanceIncrease constraint (CCK or hinge), soft tissue reconstruction
Infection (PJI)15%Chronic pain, effusion, elevated inflammatory markersTwo-stage revision with antibiotic spacer
Polyethylene wear/osteolysis10%Focal osteolysis, thin poly, no gross looseningPoly exchange, curettage and grafting of lesions
Stiffness/arthrofibrosis3-5%Less than 90° flexion, failed manipulationOpen arthrolysis, poly exchange, consider hinge
Revision TKA indications - aseptic loosening
Click to expand
4-panel radiograph series (A-D). Panels A-B: Primary TKA with developing loosening. Panels C-D: Revision TKA with stemmed components addressing bone loss. Note the femoral and tibial stems providing stable diaphyseal fixation.Credit: Open-i/NIH (CC-BY)

Rule Out Infection in ALL Cases

Every revision knee must have infection excluded before proceeding with aseptic revision. Perform:

  • Serum: ESR, CRP
  • Synovial fluid: WBC (greater than 3000 cells/µL), PMN% (greater than 80%), culture
  • Alpha-defensin or synovial CRP if high suspicion
  • Consider aspiration biopsy if imaging shows loosening

Proceeding with aseptic revision in the setting of occult infection results in failure in over 90% of cases.

Classification Systems

Why AORI Matters

The Anderson Orthopaedic Research Institute (AORI) classification is the gold standard for assessing bone loss in revision TKA. It guides selection of augments, stems, and structural grafts. Type 1 defects can be managed with standard components, Type 2 requires augmentation, and Type 3 demands structural support (metaphyseal sleeve, cone, or bulk allograft).

AORI Classification - Femoral Bone Loss

TypeDescriptionBone LossTreatment
Type 1Intact metaphyseal bone with cancellous defects onlyMinimal - contained defectsStandard components, cement fill or morcellized graft
Type 2ADamaged metaphysis - one femoral condyleModerate - unilateral condylar lossMetal augments (blocks), cement, or autograft
Type 2BDamaged metaphysis - both femoral condylesModerate - bilateral condylar lossBilateral metal augments or step-cut sleeves
Type 3Deficient metaphysis - major loss affecting stabilitySevere - threatens component stabilityMetaphyseal sleeve, cone, or structural allograft

Femoral bone loss is common at the posterior condyles due to posterior capsular release and wear patterns.

AORI Classification - Tibial Bone Loss

TypeDescriptionBone LossTreatment
Type 1Intact metaphyseal bone with cancellous defects onlyMinimal - contained defectsStandard baseplate, cement fill
Type 2ADamaged metaphysis - one tibial plateauModerate - unilateral plateau lossMetal augment block or step-cut, press-fit stem
Type 2BDamaged metaphysis - both tibial plateausModerate - bilateral plateau lossBilateral augments, longer stem for stability
Type 3Deficient metaphysis - major tibial lossSevere - threatens baseplate supportMetaphyseal sleeve, cone, or bulk allograft with cemented stem

Tibial Bone Loss is Often Underestimated

Preoperative imaging (CT if needed) helps plan for bone loss, but final assessment is intraoperative after component removal and cement debridement. Always have augments, sleeves, and cones available. Tibial defects are more common medially in varus knees.

Clinical Assessment

Constraint Ladder Concept

Constraint selection follows a ladder approach: start with the least constraint possible (PS if feasible), escalate to CCK if one collateral ligament is deficient or moderate bone loss exists, and use rotating hinge only for massive bone loss (AORI Type 3) or global instability. Over-constraining increases interface stress and loosening risk; under-constraining risks instability.

Posterior-Stabilized (PS) Revision

Indications:

  • AORI Type 1 bone loss
  • Intact MCL and LCL
  • Balanced flexion-extension gaps
  • Simple aseptic loosening or poly wear

Requirements:

  • Adequate metaphyseal bone stock
  • Competent collateral ligaments (MCL and LCL)
  • No significant instability
  • Good extensor mechanism

Advantages

  • Lowest constraint = least interface stress
  • Better ROM preservation
  • Lower revision rate compared to hinged
  • Familiar implant for surgeons

Disadvantages

  • Requires good bone stock and ligaments
  • Not suitable for moderate-severe bone loss
  • Risk of instability if mis-selected
  • May need stems for fixation

PS revision is rarely used in practice - most revisions require at least CCK constraint.

Constrained Condylar Knee (CCK)

Indications:

  • AORI Type 2A/2B bone loss
  • MCL or LCL insufficiency (one collateral deficient)
  • Flexion-extension gap imbalance
  • Moderate instability

Design Features:

  • Taller post and deeper cam (more constraint than PS)
  • Wider tibial baseplate for stability
  • Modular augments compatible
  • Accepts modular stems for fixation
FeaturePSCCKHinge
Varus-valgus constraintCollaterals onlyPolyethylene post (5-10°)Mechanical hinge (0°)
Flexion-extension gap toleranceRequires balanceTolerates 3-5mm imbalanceTolerates any imbalance
Bone stock requiredIntact metaphysisAORI Type 1-2AORI Type 3 acceptable

CCK is the most commonly used implant in revision TKA - balances constraint with survivorship.

Rotating Hinge Knee

Indications:

  • AORI Type 3 bone loss (deficient metaphysis)
  • MCL and LCL insufficiency (global instability)
  • Massive bone loss requiring structural grafts
  • Extensor mechanism disruption (with repair)

Design Features:

  • Mechanical hinge allowing flexion-extension only
  • Rotating bearing to reduce torque at interfaces
  • Long cemented stems mandatory (14-16cm diaphyseal fixation)
  • Accepts metaphyseal sleeves/cones

Hinge Complications and Failure

Rotating hinge knees have higher complication rates than CCK:

  • Aseptic loosening: 10-15% at 10 years (vs 5-8% CCK)
  • Infection: 8-10% (vs 4-6% CCK)
  • Periprosthetic fracture: 5-8% (increased stress at stem tip)
  • Bushing wear: Requires long-term surveillance

Use hinged implants only when absolutely necessary - not a first-line option.

Investigations

Preoperative Workup

Step 1History and Examination

History: Onset of symptoms, pain character, mechanical symptoms (locking, catching), prior infections, previous surgeries. Examination: ROM, stability (varus-valgus, AP drawer), extensor lag, wound integrity, neurovascular status.

Step 2Inflammatory Markers and Aspiration

Serum: ESR, CRP (elevated suggests infection) Aspiration: Synovial WBC, PMN%, culture (aerobic, anaerobic, fungal) Alpha-defensin or synovial CRP if high clinical suspicion Aspiration biopsy: If imaging shows loosening

Step 3Imaging Studies

AP and lateral radiographs: Component position, alignment, radiolucent lines, osteolysis Long-leg alignment films: Assess mechanical axis CT scan: If severe bone loss suspected - quantify defects, plan reconstruction Nuclear medicine: If infection suspected but aspiration negative (Tc-99m, Indium-111 WBC)

Step 4Surgical Planning

AORI classification: Estimate bone loss from imaging Constraint level: Based on bone loss and ligament integrity Augments and stems: Plan for Type 2/3 defects Implant availability: Ensure CCK, hinge, sleeves, cones available

Management Algorithm

📊 Management Algorithm
Revision TKA decision algorithm showing failure mode identification, AORI bone loss classification, and constraint selection
Click to expand
Revision TKA algorithm: Identify failure mode (loosening, instability, infection, stiffness), classify bone loss using AORI (Type 1-3), and select appropriate constraint level (PS to CCK to hinge). Type 3 defects require metaphyseal sleeves or cones with long cemented stems.Credit: OrthoVellum

Systematic Approach to Revision TKA

Revision TKA requires a systematic algorithm: (1) Rule out infection first (aspirate, ESR/CRP), (2) Assess bone loss (AORI classification from imaging and intraoperative findings), (3) Evaluate soft tissues (collateral ligament integrity, extensor mechanism), (4) Select constraint (PS to CCK to hinge based on bone loss and instability), (5) Plan reconstruction (augments for Type 2, sleeves/cones for Type 3, stems for stability). This stepwise approach ensures appropriate implant selection and technique.

Algorithm for Aseptic Loosening (50% of Revisions)

Management Steps

Step 1Confirm Diagnosis

Radiographs: Radiolucent lines greater than 2mm, progressive, component subsidence. Rule out infection: Aspirate (WBC, PMN%, culture), ESR/CRP normal or mildly elevated. CT scan: If severe bone loss suspected - quantify AORI grade preoperatively.

Step 2Preoperative Planning

AORI classification: Type 1 (intact), Type 2A/B (damaged), Type 3 (deficient). Constraint needs: Assess collateral ligament integrity from examination and prior radiographs. Implant availability: Ensure CCK, augments, stems, sleeves/cones available.

Step 3Surgical Reconstruction

Remove loose components and cement - assess final bone loss intraoperatively. Type 1: Standard components, cement fill, short stems (50-75mm). Type 2: Metal augments, modular stems (75-100mm), CCK constraint. Type 3: Metaphyseal sleeve/cone, long cemented stems (100-150mm), hinge constraint.

Step 4Postoperative Protocol

Weight-bearing: WBAT for most cases (protected if TTO performed). ROM: Start immediately, goal 0-110° by 6 weeks. Surveillance: Annual radiographs and clinical exam for loosening.

Key Decision Point

The critical decision is constraint selection: PS if bone loss minimal and ligaments intact (rare in revision), CCK if Type 2 bone loss or one collateral deficient (most common), hinge if Type 3 bone loss or both collaterals deficient. Over-constraining increases loosening risk; under-constraining causes instability.

Algorithm for Instability (20% of Revisions)

Management Steps

Step 1Assess Instability Pattern

Varus-valgus laxity: MCL or LCL insufficiency - requires CCK or hinge. Flexion-extension gap imbalance: Mismatch between extension and 90° gaps - may need thicker poly or increase constraint. Global instability: Both varus-valgus and AP instability - requires hinge.

Step 2Intraoperative Assessment

Stress testing: Apply varus-valgus stress in extension and 90° flexion. MCL intact, LCL deficient: CCK with varus-valgus constraint (5-10°). Both collaterals deficient: Rotating hinge (0° laxity).

Step 3Reconstruction Strategy

Mild instability (less than 5mm): Increase poly thickness, consider CCK. Moderate instability (5-10mm): CCK with stems and augments as needed. Severe instability (greater than 10mm or global): Rotating hinge with long stems (14-16cm).

Step 4Soft Tissue Balancing

Flexion-extension gap balancing: Adjust component sizing, augments, or poly thickness. Collateral ligament reconstruction: Rarely successful - better to increase constraint.

Instability is a soft tissue problem but is usually solved with implant constraint rather than ligament reconstruction.

TKA instability assessment and revision with constrained components
Click to expand
4-panel radiograph series. Panels A-B: Varus-valgus stress testing of failing TKA demonstrating ligamentous instability. Panels C-D: Revision with constrained condylar knee (CCK) implant with stemmed femoral and tibial components providing intrinsic stability.Credit: Chang MJ et al., Knee Surg Relat Res (CC-BY)

Algorithm for Periprosthetic Joint Infection

Two-Stage Revision Protocol

Step 1Diagnosis

Aspiration: Synovial WBC greater than 3000, PMN greater than 80%, positive culture. Serum markers: ESR and CRP elevated. Alpha-defensin: Confirmatory if aspiration equivocal.

Week 0Stage 1: Explantation

Remove all components, cement, infected tissue - aggressive debridement. Cultures: 5-6 samples from different areas (aerobic, anaerobic, fungal). Antibiotic spacer: Static or articulating, vancomycin + tobramycin in cement.

Weeks 1-6IV Antibiotics

Organism-specific therapy: ID consult guided. Duration: 6 weeks IV antibiotics. Monitor: ESR/CRP should trend downward.

Weeks 7-8Antibiotic Holiday

Stop antibiotics for 2 weeks. Aspirate before Stage 2: WBC less than 3000, PMN less than 80%, negative culture.

Week 8-10Stage 2: Reimplantation

Remove spacer, debride again, assess bone loss (final AORI). Revise with CCK or hinge based on bone loss and instability. Postoperative antibiotics: 6 weeks oral (organism-directed).

Two-Stage Criteria

Do NOT proceed to Stage 2 if: (1) Aspiration positive (WBC greater than 3000 or PMN greater than 80%), (2) ESR/CRP not trending down, (3) Clinical signs of infection (wound drainage, erythema), (4) Patient medically unstable. Proceeding with persistent infection results in failure over 90% of the time.

Surgical Technique

Pre-operative Planning

Consent Points

  • Infection: 4-8% (higher than primary)
  • Aseptic loosening: 5-10% at 10 years
  • Periprosthetic fracture: 3-5% (higher with stems)
  • Stiffness: 10-15% (less than 90° flexion)
  • Neurovascular injury: Less than 1% (popliteal artery at risk)
  • Re-revision: 15-20% at 5 years
  • DVT/PE: Standard prophylaxis required

Equipment Checklist

  • Revision implant system: CCK and hinge options
  • Augments: Metal blocks (5mm, 10mm, 15mm)
  • Stems: Modular, various lengths (50-150mm)
  • Metaphyseal sleeves/cones: For Type 3 defects
  • Extraction tools: Component removal set, cement removal
  • C-arm: Essential for alignment and stem placement
  • Pulse lavage: High-volume irrigation

Surgical Approach and Exposure

Exposure Steps

Step 1Incision

Use prior incision if feasible - most lateral if multiple scars. Extend proximally and distally as needed for exposure (often 20-25cm). Skin flaps: Medial and lateral, full-thickness to preserve blood supply.

Step 2Arthrotomy

Medial parapatellar arthrotomy (standard approach). Extend proximally into vastus medialis obliquus if tight. Release adhesions carefully - dense scar tissue common.

Step 3Patellar Eversion

Attempt gentle eversion - do NOT force if tight. If unable to evert: Consider quadriceps snip (45° oblique extension of VMO) or tibial tubercle osteotomy (TTO). TTO indications: Severe stiffness, patella baja, need for extensile exposure.

Step 4Soft Tissue Releases

Release scar tissue from suprapatellar pouch, medial and lateral gutters. Protect popliteal artery - posterior capsule may be attenuated. Assess collateral ligaments - note MCL/LCL integrity for constraint decision.

Popliteal Artery at Risk

The popliteal artery is at greater risk in revision TKA due to:

  • Posterior capsule thinning from wear and loosening
  • Loss of anatomical planes from prior surgery
  • Need for posterior releases in stiff knees

Protection strategies: Stay subperiosteal, use retractors carefully, avoid blind releases posteriorly.

Component Extraction

Removal Sequence

Step 1Poly Insert Removal

Remove polyethylene insert first for visualization. Use insert removal tool if available, or carefully lever out.

Step 2Femoral Component

Start with peripheral osteotomes to disrupt cement-bone interface. Work circumferentially around component borders. Use extraction device - slap hammer or impactor. Preserve bone: Work slowly, avoid aggressive levering.

Step 3Tibial Component

Similar technique: Peripheral osteotomes, circumferential disruption. Protect MCL: Tibial component removal can avulse MCL insertion. Check for stem: If stemmed, may need flexible osteotomes down stem-cement interface.

Step 4Cement Removal

Meticulous debridement of all cement - critical for final AORI assessment. Use curettes, osteotomes, power burrs carefully. Pulse lavage: High-volume irrigation to remove debris. Final assessment: True bone loss only visible after complete cement removal.

Extraction Pearls

  • Work slowly and methodically
  • Preserve bone - avoid fracture
  • Have backup plan if fracture occurs
  • Consider en-bloc cement removal

Extraction Pitfalls

  • Aggressive levering (fractures bone)
  • Incomplete cement removal (masks true defects)
  • Damage to collateral ligament insertions
  • Rushing the process

Managing Bone Defects

AORI Type 1 - Intact Metaphysis

Treatment: Standard components with cement fill or morcellized graft.

Technique:

  • Small contained defects filled with cement or autograft (reamed bone)
  • Standard trial components to confirm fit
  • Press-fit or cemented stems (short, 50-75mm) for rotational stability
  • No augments needed

Type 1 defects are straightforward and have excellent outcomes.

AORI Type 2 - Damaged Metaphysis

Treatment: Metal augments or step-cut technique.

Augment Technique

Step 1Measure Defect

Use trial components to quantify defect size (5mm, 10mm, 15mm). Determine if unilateral (2A) or bilateral (2B).

Step 2Select Augment

Modular metal augments available in 5mm increments. Offset or non-offset depending on defect location. Trial augment to confirm fit and restore joint line.

Step 3Fix Augment to Component

Augments attach to femoral or tibial component via screw or morse taper. Cement interface between augment and bone. Ensure stability - no rocking or gaps.

Step 4Stems for Stability

Modular stems (75-100mm) recommended for Type 2B to offload metaphyseal stress. Cemented in diaphysis for fixation. Hybrid fixation: Press-fit metaphysis, cemented diaphysis.

AORI Type 3 - Deficient Metaphysis

Treatment: Structural support with metaphyseal sleeve, cone, or bulk allograft.

Metaphyseal Sleeve: Porous-coated titanium sleeve that bridges defect.

Technique:

  • Ream metaphysis to accept sleeve (cylindrical reaming)
  • Press-fit sleeve into metaphysis for biological fixation
  • Sleeve accepts modular stem through center
  • Component sits on sleeve with cement or impaction
  • Long cemented stem (100-150mm diaphyseal fixation) mandatory

Advantages: Biological fixation, excellent long-term results (90% at 10 years). Disadvantages: Requires adequate metaphyseal rim, expensive.

Metaphyseal Cone: Highly porous tantalum cone for severe defects.

Technique:

  • Prepare metaphysis with cone-specific reamers
  • Press-fit cone into defect (interference fit)
  • Cone has central hole for stem passage
  • Component cemented to cone surface
  • Long cemented stem required

Advantages: Conical shape resists rotation, excellent bone ingrowth. Disadvantages: Expensive, technically demanding, removal difficult.

Structural Bulk Allograft: Femoral head or distal femur/proximal tibia allograft.

Technique:

  • Shape allograft to match defect
  • Fix to host bone with screws or step-cut
  • Cement component to allograft
  • Long cemented stem bypasses graft-host junction

Advantages: Restores bone stock for future revisions. Disadvantages: Nonunion risk (10-15%), resorption, disease transmission risk, technically difficult.

Allografts are less commonly used now - sleeves and cones have better outcomes.

Type 3 Defects Require Structural Support

AORI Type 3 bone loss means the metaphysis cannot support the component - augments alone are insufficient. Use metaphyseal sleeve (first choice), cone (excellent alternative), or bulk allograft (historical option). Always combine with long cemented stems (14-16cm diaphyseal fixation) for load sharing and stability.

Component Implantation

Implantation Steps

Step 1Trialing and Sizing

Trial components with stems and augments in situ. Assess stability: Varus-valgus, AP drawer, flexion-extension gaps. ROM check: Ensure no impingement, adequate flexion (greater than 110°). Patellar tracking: Assess with trial components, consider lateral release if needed.

Step 2Constraint Decision

Based on:

  • Bone loss (AORI grade)
  • Collateral ligament integrity (MCL/LCL competence)
  • Flexion-extension gap balance
  • Extensor mechanism function

Select: PS (rare), CCK (most common), or rotating hinge (Type 3 or global instability).

Step 3Cementation Technique

Third-generation cementing:

  • Pulse lavage and dry bone surfaces
  • Cement restrictors in femur and tibia if stems used
  • Pressurize cement for bone interdigitation
  • Insert stems first (cemented in diaphysis), then components
  • Remove excess cement before polymerization
Step 4Final Poly and Closure

Polyethylene insert: Select thickness for stability (usually thicker than primary, 12-15mm). Final stability check: Varus-valgus, AP drawer in extension and 90° flexion. ROM: Ensure full extension and at least 110° flexion without impingement. Patellar resurfacing: Usually yes - revise or resurface if not previously done.

Closure and Drains

Closure Steps

Step 1Hemostasis

Meticulous hemostasis: Bipolar cautery, avoid excessive cautery near skin edges. Tranexamic acid: Topical or IV (reduces blood loss by 30-40%).

Step 2Drain Decision

Drain use: Controversial - many surgeons use closed suction drain for 24-48 hours. Removal criteria: Output less than 30mL per 8 hours.

Step 3Layered Closure

Capsule/extensor mechanism: Repair with #1 or #2 absorbable suture (Vicryl). If TTO performed: Fix tubercle with two screws or heavy suture through drill holes. Fascia: Close in layers to reduce dead space. Subcutaneous: 2-0 absorbable suture. Skin: Staples or subcuticular (staples faster, subcuticular cosmetic).

Step 4Dressing and Splint

Dressing: Bulky compressive dressing. Splint: Optional knee immobilizer if extensor mechanism weak or TTO performed. Duration: 24-48 hours, then begin ROM.

Stems are Not Optional in Most Revisions

Modular stems provide rotational stability and load sharing, protecting the metaphyseal bone-implant interface. Use stems in:

  • AORI Type 2: 75-100mm press-fit metaphysis, cemented diaphysis
  • AORI Type 3: 100-150mm fully cemented diaphysis (14-16cm fixation length)
  • Rotating hinge: Mandatory - long cemented stems always

Stems reduce stress at bone-component interface and improve survivorship.

Two-Stage Revision for Periprosthetic Joint Infection

Gold Standard for Chronic PJI

Two-stage revision is the gold standard for chronic periprosthetic joint infection (PJI) in the knee, with infection control rates of 85-90%. Stage 1 involves component removal, debridement, and antibiotic spacer placement. After 6-8 weeks of IV antibiotics and a 2-week antibiotic holiday, Stage 2 reimplantation proceeds if infection markers have normalized and aspiration is negative.

Two-Stage Protocol

Week 0Stage 1: Explantation and Spacer

Remove all components: Femur, tibia, polyethylene, cement. Aggressive debridement: Synovectomy, remove all infected tissue, necrotic bone. Send cultures: Multiple samples (5-6) from different areas - aerobic, anaerobic, fungal. Antibiotic spacer: Static (block) or articulating (prefabricated or hand-made with mold). Antibiotics in cement: Vancomycin and tobramycin or gentamicin (organism-directed if known).

Weeks 1-6IV Antibiotics

Organism-specific therapy: Based on intraoperative cultures (ID consult). Typical duration: 6 weeks IV antibiotics. Monitor: ESR, CRP weekly - should trend downward. Mobilization: Weight-bearing as tolerated with spacer in situ (articulating spacers allow ROM).

Weeks 7-8Antibiotic Holiday

Stop all antibiotics for 2 weeks before reimplantation. Allows clearance of antibiotics from system for accurate aspiration. Repeat inflammatory markers: ESR, CRP should be normalizing (may not be fully normal).

Week 8Aspiration Before Stage 2

Aspirate knee joint (through spacer) for culture and cell count. Criteria for reimplantation:

  • Synovial WBC less than 3000 cells/µL
  • PMN% less than 80%
  • Negative culture (or low virulence organism with biofilm coverage)
  • ESR and CRP trending down (not necessarily normal)
Week 8-10Stage 2: Reimplantation

Remove spacer: Similar to primary revision technique. Debride again: Remove spacer cement, reassess bone loss (final AORI grading). Implant revision components: CCK or hinge based on bone loss and instability. Augments and stems: As needed for AORI Type 2/3 defects. Antibiotic-loaded cement: Consider organism-directed antibiotics in cement (controversial). Postoperative antibiotics: 6 weeks oral antibiotics (organism-directed, ID consult).

Spacer Types in Two-Stage Revision

Spacer TypeAdvantagesDisadvantagesUse Case
Static block spacerSimple, inexpensive, high antibiotic elutionNo ROM, muscle atrophy, difficult Stage 2Severe bone loss, unable to achieve stability
Articulating spacer (prefab)Maintains ROM, easier Stage 2, patient mobilityMore expensive, lower antibiotic concentrationModerate bone loss, able to achieve stability
Hand-made articulating spacerCustomizable, high antibiotic dose, maintains ROMTechnically demanding, spacer fracture riskWhen prefab spacer unavailable or special sizing needed

Complications

ComplicationIncidenceRisk FactorsManagement
Aseptic loosening5-10% at 10 yearsAORI Type 3, hinged implants, inadequate fixationRe-revision with longer stems, structural grafts, increase constraint
Infection (PJI)4-8%Diabetes, obesity, prior infection, prolonged surgeryTwo-stage revision with spacer, 6-8 weeks antibiotics
Periprosthetic fracture3-5%Osteoporosis, long stems, stress riser at stem tipORIF if stem stable, revision if stem loose, consider strut allografts
Instability5-10%Under-constraining, flexion-extension gap imbalance, poly wearIncrease constraint (PS to CCK to hinge), thicker poly, revise components
Stiffness (less than 90° flexion)10-15%Arthrofibrosis, oversized components, overstuffing jointManipulation under anesthesia (within 12 weeks), open arthrolysis, poly exchange
Extensor mechanism disruption2-5%Multiple prior surgeries, TTO, patellar fracturePrimary repair if acute, allograft reconstruction if chronic, consider gastrocnemius flap
Neurovascular injuryLess than 1%Popliteal artery injury during exposure, common peroneal nerve palsyVascular repair emergently if arterial, nerve exploration if palsy (often traction neurapraxia)

Periprosthetic Fracture at Stem Tip

Periprosthetic fractures often occur at the stem tip - a stress riser in osteoporotic bone. Prevention strategies:

  • Use cemented stems in osteoporotic bone (better load sharing)
  • Bypass prior stress risers by 2 cortical diameters (extend stem past screw holes)
  • Consider strut allografts prophylactically in very osteoporotic bone
  • Weight-bearing precautions (TDWB) for 6-12 weeks if high risk
Periprosthetic supracondylar fracture following revision TKA
Click to expand
4-panel radiograph series. Section A: Displaced supracondylar femur fracture above revision TKA (AP and lateral views). Section B: Post-fixation with lateral locking plate spanning the fracture while preserving the well-fixed TKA components. Demonstrates ORIF management when implants remain stable.Credit: Yoo JD et al., Knee Surg Relat Res (CC-BY)

Management: ORIF if stem stable (plate and strut allograft), revision to longer stem if loose.

Postoperative Care and Rehabilitation

Standard Revision TKA Postoperative Protocol

Rehabilitation Timeline

Hospital Day 1-2Day 0-1: Immediate Postoperative

DVT prophylaxis: Chemical (enoxaparin or rivaroxaban) and mechanical (SCDs). Pain control: Multimodal analgesia (acetaminophen, NSAIDs, opioids as needed). Mobilization: Out of bed to chair on Day 1, ambulate with walker Day 2. Weight-bearing: WBAT (weight-bearing as tolerated) for most revisions. ROM: CPM or bedside PT - goal 0-90° by discharge. Drain removal: 24-48 hours when output less than 30mL per 8 hours.

Protected MobilizationWeeks 1-6: Early Phase

Weight-bearing: Progress to full weight-bearing with assistive device. ROM exercises: Active-assisted and passive, goal 0-110° by 6 weeks. Quadriceps strengthening: Straight leg raises, quad sets, terminal knee extension. Gait training: Progress from walker to cane to independent. Wound care: Staples removed at 2 weeks, monitor for infection. Radiographs: 6-week films to assess alignment, component position, no early loosening.

Strength BuildingWeeks 6-12: Progressive Phase

Discontinue assistive device when safe gait without limp. Resistance exercises: Progress resistance training for quads, hamstrings, hip abductors. Functional activities: Stairs, sit-to-stand, balance exercises. ROM maintenance: Continue ROM exercises, goal 0-120° flexion. Return to activities: Light ADLs, avoid high-impact (running, jumping).

Return to FunctionMonths 3-12: Long-term

Functional milestones: Independent ADLs, driving (8-12 weeks), return to work (12-16 weeks). Activity modification: Avoid high-impact sports - low-impact only (cycling, swimming, golf). Annual follow-up: Radiographs and clinical exam to monitor for loosening, wear, osteolysis. Expectations: 70-80% function of primary TKA, pain improvement in 80-85% of patients.

Protocol After Tibial Tubercle Osteotomy (TTO)

Protected Weight-Bearing After TTO

Tibial tubercle osteotomy requires protected weight-bearing to allow tubercle healing:

  • TDWB (touch-down weight-bearing) for 6 weeks
  • Brace or immobilizer to protect extensor mechanism
  • No active knee extension for 6 weeks (passive ROM only)
  • Radiographs at 6 weeks to confirm tubercle union before advancing weight-bearing

Non-union or avulsion of TTO is catastrophic - strict precautions mandatory.

TTO Rehabilitation Timeline

Protected PhaseWeeks 0-6

TDWB: Touch-down weight-bearing only (10-20 lbs). Brace: Knee immobilizer locked in extension for ambulation. ROM: Passive ROM only (CPM, therapist-assisted) - NO active extension. Quad sets: Isometric only, no SLR (to protect tubercle fixation).

Progression PhaseWeeks 6-12

Radiographs: Confirm tubercle union before advancing. Weight-bearing: Progress to WBAT, then full weight-bearing if union confirmed. Active ROM: Begin gentle active ROM if union solid. Strengthening: Progress quad strengthening cautiously.

Return to FunctionMonths 3-6

Functional activities: Resume normal activities if tubercle healed. Radiographs: 6-month films to confirm maintained union.

Outcomes and Prognosis

Outcomes by Implant Type

Implant TypeSurvivorship (10 yr)Functional OutcomeRe-revision Risk
PS revision (AORI Type 1)90-95%Good - similar to primary TKA5-8%
CCK (AORI Type 2)85-90%Fair - 70-80% of primary10-15%
Rotating hinge (AORI Type 3)80-85%Fair to poor - 60-70% of primary15-20%
Two-stage (PJI)80-85% (infection control 85-90%)Fair - 60-70% of primary20-25%

Predictors of Poor Outcome

Factors associated with worse outcomes in revision TKA:

  • AORI Type 3 bone loss (requires structural grafts - higher failure)
  • Rotating hinge implant (higher loosening and infection rates)
  • Multiple prior revisions (re-revision risk doubles with each revision)
  • Chronic PJI (two-stage has lower function than aseptic revision)
  • BMI over 35 (higher infection and complication rates)
  • Extensor mechanism insufficiency (quadriceps dysfunction limits function)

Counseling patients realistically about expectations is critical - revision TKA does NOT achieve primary TKA outcomes.

Evidence Base and Key Trials

Australian Orthopaedic Association National Joint Replacement Registry (AOANJRR)

3
AOANJRR • Annual Report (2023)
Key Findings:
  • Revision TKA has 15-20% re-revision rate at 5 years vs 2-3% for primary TKA
  • Aseptic loosening remains most common indication (50% of revisions)
  • CCK implants have better survivorship than rotating hinge (88% vs 82% at 10 years)
  • Two-stage revision for PJI has 85-90% infection control but 20-25% re-revision rate
  • Metaphyseal sleeves and cones show excellent short-term results for Type 3 defects
Clinical Implication: Australian registry data confirms revision TKA is high-risk with substantial re-revision burden. Constraint selection and bone loss management are critical for success.
Limitation: Registry data subject to selection bias and incomplete follow-up; difficult to control for surgeon experience and patient factors.

Long-term Results of Rotating Hinge Implants for Revision TKA

3
Kouk S et al • Bone Joint J (2020)
Key Findings:
  • Systematic review: 15-year survivorship of rotating hinge 75-80%
  • Aseptic loosening most common failure mode (10-15% at 10 years)
  • Higher infection rate than CCK (8-10% vs 4-6%)
  • Functional scores 60-70% of age-matched primary TKA controls
  • Bushing wear and polyethylene damage seen in 15-20% long-term
Clinical Implication: Rotating hinge knees have inferior survivorship and function compared to CCK - use only when absolutely necessary for massive bone loss or global instability.
Limitation: Heterogeneous studies with varying implant designs and indications; difficult to compare across series.

Metaphyseal Sleeves vs Structural Allografts for Type 3 Defects

3
Long WJ et al • J Arthroplasty (2018)
Key Findings:
  • Multicenter study: 250 revision TKAs with AORI Type 3 defects
  • Metaphyseal sleeves: 92% survivorship at 5 years, 10% complication rate
  • Structural allografts: 78% survivorship at 5 years, 25% complication rate (nonunion, resorption)
  • Sleeves had faster rehabilitation and return to function
  • Cost analysis favored sleeves despite higher implant cost (lower revision burden)
Clinical Implication: Metaphyseal sleeves are superior to structural allografts for AORI Type 3 bone loss in revision TKA - biological fixation with excellent survivorship and lower complication rates.
Limitation: Non-randomized comparison; selection bias toward sleeves in recent years as technique evolved.

Two-Stage vs One-Stage Revision for Chronic PJI

2
Pangaud C et al • Clin Orthop Relat Res (2019)
Key Findings:
  • Meta-analysis: 15 studies, 1500 patients with chronic PJI
  • Two-stage revision: 87% infection control vs 76% one-stage (p less than 0.01)
  • Two-stage re-revision rate higher (22% vs 15%) but infection-related failures lower
  • Functional outcomes similar between groups at 5 years
  • Cost analysis favored two-stage due to lower infection recurrence
Clinical Implication: Two-stage revision remains gold standard for chronic PJI in the knee with superior infection control rates. One-stage may be considered in select patients with low-virulence organisms and good soft tissue envelope.
Limitation: Meta-analysis of heterogeneous studies; one-stage series often had strict patient selection criteria limiting generalizability.

Constrained Condylar Knee (CCK) vs Rotating Hinge in Revision TKA

3
Abdel MP et al • J Bone Joint Surg Am (2017)
Key Findings:
  • Comparative cohort: 400 revision TKAs (200 CCK, 200 rotating hinge)
  • CCK 10-year survivorship 88% vs hinge 82% (p equals 0.02)
  • CCK had lower aseptic loosening (6% vs 12%) and infection (4% vs 9%)
  • Functional scores slightly better with CCK (KSS 75 vs 68)
  • Hinge group had more AORI Type 3 defects and global instability (selection bias)
Clinical Implication: CCK has superior survivorship and lower complication rates than rotating hinge in revision TKA. Reserve hinge for massive bone loss (AORI Type 3) or global instability where CCK insufficient.
Limitation: Selection bias - hinge used in more complex cases with worse bone loss and instability; not a randomized trial.

Exam Viva Scenarios

Practice these scenarios to excel in your viva examination

VIVA SCENARIOStandard

Scenario 1: Painful Revision TKA Classification

EXAMINER

"A 68-year-old woman presents with progressive medial knee pain 8 years after primary TKA. Examination shows stable knee with full extension and 110° flexion, no effusion. Radiographs demonstrate 2mm radiolucent lines under the medial tibial baseplate and small focal osteolysis. ESR 18, CRP 8. How would you assess and manage this patient?"

EXCEPTIONAL ANSWER
This is a case of suspected aseptic loosening of the tibial component following primary TKA. I would take a systematic approach: First, complete the workup to rule out infection - I would aspirate the knee for synovial fluid analysis (WBC, differential, culture) given that infection must be excluded before revision. If aspiration is negative and inflammatory markers stable, this is consistent with aseptic loosening. Second, I would obtain long-leg alignment films and CT scan to assess mechanical axis and quantify bone loss using the AORI classification - the radiographs suggest Type 2A tibial defect (medial plateau damage). Third, my management would be revision TKA with: removal of loose tibial component and cement, use of metal augment or cement fill for the medial defect, press-fit modular stem for stability, and likely CCK constraint given bone loss. I would counsel about outcomes being 70-80% of primary TKA function, 85-90% survivorship at 10 years, and risks including infection (4-8%), re-revision (15-20% at 5 years), and stiffness.
KEY POINTS TO SCORE
Rule out infection FIRST - aspiration mandatory before aseptic revision
AORI classification guides bone loss management (Type 1 vs 2 vs 3)
Constraint selection based on bone loss and ligament integrity
Realistic outcome counseling - revision TKA inferior to primary
COMMON TRAPS
✗Proceeding with revision without excluding infection (catastrophic if infected)
✗Underestimating bone loss from radiographs alone (CT helpful)
✗Not using stems in Type 2 defects (stems provide stability and load sharing)
✗Over-promising outcomes - revision TKA does NOT equal primary TKA function
LIKELY FOLLOW-UPS
"What if the aspiration shows 4000 WBCs with 85% PMNs?"
"How would you manage an intraoperative finding of Type 3 femoral bone loss?"
"What are indications for a rotating hinge in this case?"
VIVA SCENARIOChallenging

Scenario 2: Two-Stage Revision for PJI

EXAMINER

"A 72-year-old diabetic man with prior TKA presents with chronic pain and recurrent effusions for 6 months. He has had two aspirations showing low-grade coagulase-negative staph. ESR 45, CRP 22. You have performed Stage 1 debridement and spacer placement. Walk me through your Stage 2 planning and technique."

EXCEPTIONAL ANSWER
This is a case of chronic periprosthetic joint infection requiring two-stage revision. For Stage 2 planning, I would ensure: First, the patient has completed 6-8 weeks of organism-specific IV antibiotics (vancomycin for coag-negative staph) followed by a 2-week antibiotic holiday. Second, before Stage 2, I would repeat inflammatory markers (ESR and CRP trending down, may not normalize), and aspirate the knee for culture and cell count - criteria for reimplantation include synovial WBC less than 3000, PMN less than 80%, and negative culture. If cleared, my Stage 2 technique includes: removal of the antibiotic spacer and spacer cement, aggressive debridement again, reassessment of bone loss (final AORI grading - likely Type 2 given spacer time), reconstruction with CCK implant and modular stems, metal augments as needed for tibial or femoral defects, and antibiotic-loaded cement (organism-directed, though controversial). Postoperatively, 6 weeks of oral antibiotics per ID consult. I would counsel about 85-90% infection control rate but 20-25% re-revision risk, and functional outcomes 60-70% of primary TKA.
KEY POINTS TO SCORE
Two-stage protocol: 6-8 weeks IV antibiotics, 2-week holiday, then aspirate
Reimplantation criteria: WBC less than 3000, PMN less than 80%, negative culture, ESR/CRP trending down
Stage 2 technique: remove spacer, debride again, final AORI assessment, revise with CCK/stems/augments
Postoperative oral antibiotics 6 weeks, ID consult guided
COMMON TRAPS
✗Proceeding to Stage 2 without antibiotic holiday (false-negative cultures)
✗Expecting normalized inflammatory markers (may remain mildly elevated)
✗Not debriding again at Stage 2 (spacer cement and residual biofilm must be removed)
✗Over-estimating function - two-stage outcomes worse than aseptic revision
LIKELY FOLLOW-UPS
"What if the Stage 2 aspiration grows the same organism again?"
"Would you use an articulating or static spacer in this case?"
"What are indications for chronic suppressive antibiotics instead of Stage 2?"
VIVA SCENARIOCritical

Scenario 3: Massive Bone Loss (AORI Type 3)

EXAMINER

"Intraoperatively during revision TKA, after component removal you find severe tibial bone loss - the entire medial and lateral plateaus are gone down to the metaphyseal-diaphyseal junction (AORI Type 3). How do you reconstruct this defect?"

EXCEPTIONAL ANSWER
This is an AORI Type 3 tibial bone defect requiring structural support - augments alone are insufficient. My reconstruction options include metaphyseal sleeve (first choice), tantalum cone (excellent alternative), or structural bulk allograft (historical option, less favored). I would proceed with a metaphyseal sleeve technique: First, ream the tibial metaphysis with cylindrical reamers to accept a porous-coated titanium sleeve (typically 60-80mm length). Second, press-fit the sleeve into the metaphysis for biological fixation - the sleeve bridges the defect and provides a stable platform. Third, insert a long modular cemented stem (100-150mm, cemented in the diaphysis for 14-16cm fixation length) through the central hole of the sleeve. Fourth, place the revision tibial baseplate onto the sleeve surface and cement the interface. Fifth, given the massive bone loss, I would use a CCK or rotating hinge implant for constraint - likely hinge given the severity. I would counsel the patient about: 80-85% survivorship at 10 years, 15-20% re-revision risk, functional outcomes 60-70% of primary TKA, and protected weight-bearing for 6-12 weeks to allow sleeve osseointegration.
KEY POINTS TO SCORE
AORI Type 3 requires structural support - sleeves, cones, or bulk allograft
Metaphyseal sleeve: press-fit biological fixation, 92% survivorship at 5 years
Long cemented stems mandatory (14-16cm diaphyseal fixation) for load sharing
Consider rotating hinge constraint for massive bone loss and instability
COMMON TRAPS
✗Attempting to use augments alone for Type 3 defects (will fail - no metaphyseal support)
✗Not using long enough stems (must cement 14-16cm into diaphysis for stability)
✗Choosing structural allograft over sleeve/cone (higher nonunion and resorption rates)
✗Under-constraining - massive bone loss often needs hinge, not just CCK
LIKELY FOLLOW-UPS
"What are advantages of metaphyseal cones over sleeves?"
"How would you manage an intraoperative periprosthetic fracture during component removal?"
"What is your stem cementation technique to avoid femoral fracture?"

MCQ Practice Points

AORI Classification Question

Q: A revision TKA patient has bone loss affecting both tibial plateaus but the metaphyseal rim is intact. What AORI grade is this and what reconstruction is appropriate? A: AORI Type 2B (damaged metaphysis, both condyles/plateaus involved). Appropriate reconstruction includes bilateral metal augments (5-15mm blocks) cemented to the host bone, with a modular tibial baseplate and press-fit stem (75-100mm length, cemented in diaphysis) for rotational stability and load sharing. Type 2B requires augmentation but does NOT need structural grafts (sleeves/cones).

Constraint Selection Question

Q: What is the key difference in indications between a CCK and a rotating hinge implant in revision TKA? A: CCK (constrained condylar knee) is indicated for AORI Type 1-2 bone loss with MCL or LCL insufficiency (one collateral deficient), or moderate flexion-extension gap imbalance (3-5mm). Rotating hinge is reserved for AORI Type 3 bone loss (deficient metaphysis), MCL and LCL insufficiency (global instability), or massive flexion-extension gap imbalance. CCK provides varus-valgus constraint through a taller post (5-10° laxity) but still relies on collaterals; hinge is a mechanical hinge allowing only flexion-extension (0° varus-valgus laxity).

Two-Stage Revision Question

Q: What are the criteria for proceeding to Stage 2 reimplantation after a two-stage revision for chronic PJI? A: Criteria include: (1) Completed 6-8 weeks IV antibiotics organism-specific, (2) 2-week antibiotic holiday to clear antibiotics from system, (3) Aspiration of knee joint showing synovial WBC less than 3000 cells/µL and PMN less than 80%, (4) Negative culture (or low-virulence organism with biofilm antibiotic coverage planned), (5) ESR and CRP trending downward (may not normalize completely, but should be improving). All criteria must be met before reimplantation - proceeding with persistent infection results in failure in over 90% of cases.

Stem Fixation Question

Q: What is the recommended stem fixation technique in revision TKA for AORI Type 3 defects? A: Long cemented stems (100-150mm length) with 14-16cm cemented fixation in the diaphysis. The stem provides load sharing and bypasses the deficient metaphysis (Type 3). Cementation technique: place cement restrictors, pressurize cement in the diaphyseal canal, insert stem and allow polymerization. Press-fit fixation in the metaphysis is inadequate for Type 3 defects - must have diaphyseal fixation. Stem length should bypass any stress risers (prior screw holes) by 2 cortical diameters to prevent periprosthetic fracture.

Metaphyseal Sleeve Question

Q: What are the advantages of metaphyseal sleeves over structural bulk allografts for AORI Type 3 defects? A: Metaphyseal sleeves have superior survivorship (92% at 5 years vs 78% for allografts), lower complication rates (10% vs 25%, particularly nonunion and resorption seen with allografts), biological fixation through osseointegration (porous-coated titanium), and faster rehabilitation (immediate press-fit stability vs waiting for graft incorporation). Allografts have risks of nonunion (10-15%), resorption over time, disease transmission (very low but non-zero), and technically demanding shaping/fixation. Sleeves are now first-line treatment for Type 3 defects.

Outcomes Question

Q: How do functional outcomes and survivorship of revision TKA compare to primary TKA? A: Revision TKA has inferior outcomes to primary TKA: (1) Functional scores 70-80% of primary TKA (worse with hinge or two-stage), (2) Survivorship 85-90% at 10 years vs 95% for primary TKA, (3) Re-revision rate 15-20% at 5 years vs 2-3% for primary, (4) Complication rate 20-30% vs 5-10% for primary. Patients must be counseled realistically - revision TKA does NOT restore primary TKA function and has higher risk of failure. Two-stage revisions for PJI have even worse outcomes (60-70% function, 80-85% survivorship).

Australian Context and Medicolegal Considerations

AOANJRR Data (2023)

  • Revision burden: 15-20% re-revision rate at 5 years vs 2-3% for primary TKA
  • Aseptic loosening: Remains most common indication (50% of all revisions)
  • CCK vs hinge survivorship: 88% vs 82% at 10 years - CCK superior
  • Two-stage for PJI: 85-90% infection control but higher re-revision rate
  • Metaphyseal sleeves/cones: Excellent short-term results for Type 3 defects (5-year data emerging)

Australian Guidelines

  • ACSQHC Surgical Site Infection Prevention: Strict antibiotic prophylaxis (cefazolin 2g within 60 min)
  • DVT prophylaxis: Chemical and mechanical for all revision TKA (high-risk procedure)
  • Antibiotic stewardship: Two-stage PJI antibiotics guided by ID consult and local resistance patterns
  • PJI diagnosis: Australian consensus follows ICM 2018 criteria (synovial WBC/PMN, culture)

Medicolegal Considerations in Revision TKA

Key documentation and consent requirements:

  1. Informed consent: Document discussion of:

    • Infection risk 4-8% (higher than primary)
    • Re-revision risk 15-20% at 5 years
    • Functional outcomes 70-80% of primary TKA (not full restoration)
    • Alternative options: Conservative management, arthrodesis (salvage), amputation (extreme)
  2. PJI workup documentation:

    • Every revision knee must have documented infection workup (ESR/CRP, aspiration)
    • Proceeding with aseptic revision in setting of occult PJI is indefensible - leads to failure over 90%
  3. Operative note details:

    • AORI classification documented for both femur and tibia
    • Constraint rationale (why PS vs CCK vs hinge based on bone loss and ligament integrity)
    • Implant details: Stem lengths, augment sizes, sleeve/cone use if applicable
    • Intraoperative complications: Fractures, ligament injuries, vascular injury
  4. Postoperative counseling:

    • Activity restrictions: No high-impact sports (running, jumping) - low-impact only
    • Surveillance: Annual radiographs and clinical exam for loosening, wear, osteolysis
    • Red flags: Increasing pain, instability, wound drainage (infection signs)

Common litigation issues: Failure to rule out infection before revision, under-constraining leading to instability, inadequate bone loss reconstruction causing early loosening, unrealistic outcome expectations not addressed preoperatively.

REVISION TOTAL KNEE ARTHROPLASTY

High-Yield Exam Summary

Key Indications

  • •Aseptic loosening: 50% of revisions - radiolucent lines, subsidence, pain
  • •Instability: 20% - MCL/LCL insufficiency, flexion-extension gap imbalance
  • •Infection (PJI): 15% - two-stage revision gold standard (85-90% control)
  • •Polyethylene wear/osteolysis: 10% - focal lysis, thin poly
  • •Stiffness: 3-5% - less than 90° flexion, failed manipulation

AORI Bone Defect Classification

  • •Type 1 (Intact): Metaphyseal bone intact - standard components, cement fill
  • •Type 2A (Damaged one): One condyle/plateau - metal augment, cement, stem
  • •Type 2B (Damaged both): Both condyles/plateaus - bilateral augments, stem
  • •Type 3 (Deficient): Metaphysis deficient - sleeve/cone/allograft, long stem (14-16cm)

Constraint Selection Algorithm

  • •PS: AORI Type 1, intact MCL and LCL, balanced gaps (rarely used in revision)
  • •CCK: Type 2, MCL OR LCL deficient, 3-5mm gap imbalance (most common)
  • •Rotating hinge: Type 3, MCL AND LCL deficient, massive bone loss, global instability
  • •Increase constraint as bone loss worsens and soft tissue insufficiency increases

Surgical Technique Pearls

  • •Rule out infection FIRST: ESR/CRP, aspirate (WBC, PMN%, culture) in ALL cases
  • •Component removal: Peripheral osteotomes, circumferential disruption, preserve bone
  • •Cement removal: Meticulous debridement - final AORI only visible after cement out
  • •Stems: Modular, 75-100mm Type 2, 100-150mm Type 3, cemented in diaphysis (14-16cm)
  • •Metaphyseal sleeves: Press-fit biological fixation for Type 3, 92% survivorship at 5 years

Two-Stage Revision Protocol

  • •Stage 1: Debridement, explant, antibiotic spacer (vancomycin + tobramycin in cement)
  • •6-8 weeks IV antibiotics organism-specific (ID consult), then 2-week holiday
  • •Reimplantation criteria: WBC less than 3000, PMN less than 80%, negative culture, ESR/CRP trending down
  • •Stage 2: Remove spacer, debride again, revise with CCK/hinge, augments/stems as needed
  • •Infection control: 85-90%, but re-revision risk 20-25%, function 60-70% of primary

Complications and Outcomes

  • •Aseptic loosening: 5-10% at 10 years (higher with hinge, Type 3 defects)
  • •Infection: 4-8% (higher than primary 1-2%)
  • •Periprosthetic fracture: 3-5% (stem tip stress riser, osteoporotic bone)
  • •Survivorship: 85-90% at 10 years (vs 95% primary), re-revision 15-20% at 5 years
  • •Function: 70-80% of primary TKA (worse with hinge or two-stage)
Quick Stats
Reading Time159 min
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