Complex metaphyseal reconstruction for AORI Type 2B/3 bone loss · High-difficulty revision arthroplasty
- Porous metal tibial cones are indicated for AORI Type 2B and Type 3 bone defects where the metaphysis can no longer support a standard baseplate.
- The cone is press-fit (cementless) into host bone to achieve biological fixation by osseointegration, while the tibial baseplate is cemented INTO the cone. Never cement the cone directly to host bone — it defeats biological fixation.
- Ream to bleeding bone, select a cone so the trial is 2mm undersized, and aim for 60 to 70 percent surface contact with flush seating. A cone sitting 5mm proud has inadequate contact and will fail.
- The stem bypasses the cone by two cortical diameters (typically 100 to 150mm) for diaphyseal load sharing — the Morgan-Jones three-zone fixation concept (zone 1 epiphysis, zone 2 metaphysis, zone 3 diaphysis).
- Aseptic survivorship of metaphyseal cones is approximately 97 percent at midterm (Zanirato systematic review, 927 cones), and the Mayo series showed over 95 percent cone survival at five to nine years (Kamath).
When & Why
Indication. A painful, loose revision total knee arthroplasty with AORI Type 2B or Type 3 tibial bone loss — metaphyseal bone too damaged to support a standard baseplate — where a porous metal cone can provide biological (zone 2) fixation. The cone is the workhorse when augments alone are insufficient and a structural allograft or custom implant is not yet warranted. Primary indications - AORI Type 2B defects — damaged metaphyseal bone with both tibial condyles compromised but some structural support remaining.
- AORI Type 3 defects — deficient metaphyseal bone with loss of structural support; both condyles lost.
- Periprosthetic fracture with metaphyseal bone loss requiring fixation and support.
- Failed structural allograft with a residual cavitary defect.
- Septic revision after debridement, staged once infection is eradicated. Relative indications - AORI Type 2A with poor bone quality (osteoporosis, multiple prior revisions).
- A hinged or constrained revision requiring enhanced tibial support. Contraindications - Absolute: active infection (stage a spacer and treat infection first), inadequate host bone for a cone press-fit (severely deficient cortices), uncorrectable vascular insufficiency, a non-ambulatory patient with low functional demand.
- Relative: severe osteoporosis (consider cemented augments and longer stems), extensor mechanism disruption (repair or reconstruct first), medical comorbidity precluding a greater-than-two-hour operation, a patient under 50 years (consider structural allograft if young and active). Pre-operative imaging - Weight-bearing AP and lateral radiographs (full-length) — assess alignment, component position, defect extent and stem trajectory.
- CT with 3D reconstruction — quantifies bone stock, defect morphology, cortical integrity and prior screw holes; the basis for cone templating.
- Metal-artifact-reduction (MARS) MRI — if infection is suspected or soft-tissue and extensor-mechanism integrity must be assessed. Templating - Cone: measure the metaphyseal width on CT (mediolateral and AP) and choose a cone 2 to 5mm smaller than the metaphyseal diameter (available 35–55mm for the tibia, most common 40–50mm). Larger cones give more fixation surface but sacrifice more host bone.
- Stem: length to bypass the cone by two cortical diameters (typically 100–150mm total), diameter to fill 80 percent of the canal at the isthmus (10–18mm). Choose cemented for poor bone or an older patient, cementless for good bone and biological fixation.
- Augments: wedge augments for peripheral/slope defects (5–20mm) and block augments for central defects (5–15mm); plan for a minimum 10mm tibial polyethylene. The reconstruction decision. A cone is one of several ways to rebuild a deficient metaphysis — choose it deliberately:
Porous tantalum or titanium scaffold (80 percent porosity) giving cementless biological fixation in zone 2. Press-fit to host bone, baseplate cemented into the cone. The default for AORI 2B/3.
A diaphyseally-engaging porous sleeve giving equivalent zone-2 fixation (97.8 percent aseptic survivorship vs 97.3 percent for cones, Zanirato). Choice is driven by implant system and defect geometry, not survivorship.
Wedges and blocks cemented to the baseplate — suitable for contained peripheral defects (AORI 2A) but do not address central cavitary metaphyseal loss.
Biology-friendly for very large uncontained defects in younger patients, but carries resorption and non-union risk; now largely reserved where cones or sleeves cannot gain fixation.
A custom triflange or distal-femoral-replacement-type prosthesis for massive bone loss, or a rotating hinge when global instability coexists.
For the poor-bone, low-demand patient where biological fixation is not realistic — immediate stability at the cost of late loosening risk.
Setup. Supine on a radiolucent table, padded proximal-thigh tourniquet, bump under the ipsilateral hip for 15 to 20 degrees of internal rotation, C-arm from the contralateral side for cone position and stem trajectory. Laminar flow, double-gloving, pulsatile lavage (6 to 9L). Antibiotic prophylaxis: cefazolin 2g IV (3g if weight greater than 120kg) within 60 minutes, vancomycin 15mg/kg over one hour for MRSA risk or beta-lactam allergy, redose cefazolin if the case exceeds four hours. Consent specifically for the higher wound-complication and infection rates of revision surgery, stiffness, and the possibility of needing a more constrained insert or a staged second stage if infection is found.
The Operation
The goal is to remove the loose components while preserving every scrap of host bone, expose and classify the tibial defect, then rebuild the metaphysis with a press-fit porous cone that osseointegrates, locking a stemmed baseplate into it and sharing load to the diaphysis through a stem that bypasses the cone by two cortical diameters. The exposure is everything in a stiff, multiply-operated knee — it is laid out first below (and in depth on the medial parapatellar approach to the knee page).

Lies 10 to 15mm posterior to the posterior capsule at the joint line. Protect with a bent Hohmann retractor resting on bone (not soft tissue), flex the knee to relax the bundle, and avoid posterior power-burr work.
Posterolateral, winding around the fibular neck 30 to 40mm distal to the joint. At risk with valgus correction — release contractures slowly, limit valgus correction to gradual increments, decompress at the fibular neck if a large correction is planned.
Origin on the medial femoral condyle about 10mm proximal and posterior to the joint line. Preserve by subperiosteal dissection during medial exposure and avoid excessive medial stripping.
The quadriceps tendon, patella and patellar tendon. Use an extensile approach early if the patella will not evert, protect the lateral geniculate blood supply, and avoid aggressive lateral release.
The metaphyseal-diaphyseal junction is the stress riser during removal and reaming. Avoid aggressive osteotome use, ream stems with flexible reamers in 0.5mm increments, and confirm trajectory with fluoroscopy.
Operative sequence
- Use the prior midline incision (the most lateral of several scars, to preserve lateral genicular blood supply), and excise any intermediate scar en bloc with the arthrotomy rather than raising a bridge.
- Raise full-thickness flaps only — no subcutaneous beveling — and handle skin gently with skin hooks, never crushing clamps. Skin ischaemia occurs in 8 to 12 percent of revisions.
- Extend proximally to mid-thigh and distally to the tibial tubercle or beyond.
Attempt a standard medial parapatellar arthrotomy first. Release the medial capsule and deep MCL fibres subperiosteally and try to evert the patella with the knee flexed to 90 degrees. If the patella will not evert lateral to the midline without tension, extend the exposure rather than forcing it: - Rectus snip (preferred, lowest complication rate 2 to 3 percent): a 45-degree proximal-lateral incision 2 to 3cm long in the quadriceps tendon from the superomedial patellar pole, preserving the VMO. Repair directly at closure with a figure-of-8 of number-2 FiberWire.
- Tibial tubercle osteotomy (severe stiffness, younger patient): a 5 to 6cm by 1.5cm osteotomy lateral to the tibial crest, cut with a microsagittal saw to 4 to 5mm depth preserving the posterior cortex, cracked with a thin osteotome, and reflected proximally with the patellar tendon. Fix at closure with 2 to 3 bicortical screws or cerclage wires.
- V-Y quadricepsplasty (last resort, ankylosed knee in a low-demand elderly patient): an inverted V with the apex 6 to 8cm proximal to the patella, gaining 3 to 5cm of length. High complication rate (10 to 15 percent disruption); protected weight-bearing for six weeks.
- Disrupt the cement-bone interface with narrow osteotomes; use curved osteotomes posteriorly under direct vision to avoid the popliteal bundle.
- An oscillating saw clears the anterior flange cement; extract the femoral component with a universal extractor.
- Remove all cement with a high-speed burr and ultrasonic device, preserving host bone — do not gouge.
- Flex the knee maximally and elevate the medial and lateral sleeves, preserving the MCL and LCL origins.
- Place bent Hohmann retractors posteromedially and posterolaterally resting on bone, not soft tissue, to protect the popliteal bundle.
- Cut the cement peripherally with a microsagittal saw, then osteotomes at the bone-cement interface working anterior to posterior; a Gigli saw reaches the posterior cement.
- Remove the stem with flexible osteotomes down the canal (cemented) or a slotted extractor (press-fit). Gentle mallet taps only — violent impaction fractures the cortex. Periprosthetic fracture during removal occurs in 5 to 8 percent.
- Clear all cement to bleeding bone (essential for cone osseointegration) using hand tools, burr and ultrasonic removal with pulse lavage between steps.
- Classify the defect by AORI: Type 1 intact metaphysis (no cone), 2A one condyle damaged (augment), 2B both condyles damaged (cone indicated), 3 deficient metaphysis with loss of structural support (cone required).
- Porous tantalum or titanium cone, 80 percent porosity, modulus about 3 GPa (close to bone, low stress-shielding).
- Measure the metaphyseal diameter on CT and choose a cone 2 to 5mm smaller; balance maximising contact against sacrificing healthy bone.
- Begin with the smallest reamer (usually 30 to 35mm) and advance in 2.5mm increments.
- Ream to the bleeding-bone endpoint: punctate bleeding with a firm cortical rim. Non-bleeding sclerotic bone will not osseointegrate.
- Preserve the cortical rim; avoid eccentric reaming that perforates the thin metaphyseal cortex.
- Insert a trial cone 2mm smaller than the planned final size; rotate to optimise contact in asymmetric defects.
- Burr high spots rather than over-reaming (preserves bone). Accept only flush seating or at most 2mm proud — a proud cone has poor contact and will fail.
- Impact the final cone to a stable endpoint, then stress it: it must not rotate under the impactor, subside under axial load, or toggle mediolaterally.
- Fluoroscopy confirms symmetric AP position, correct depth parallel to the joint line, and no occult fracture.
- Target 60 to 70 percent surface contact and no micromotion.
- Pack morselised autograft (reaming debris, preferred) or allograft chips around the cone periphery to fill gaps and enhance ingrowth.
- Keep graft out of the cone-to-baseplate interface, where it would cause instability.
- Trial the baseplate with stem on the cone: rotation aligned to the tibial tubercle, central mediolateral position, no rocking.
- Stem length to bypass the cone by two cortical diameters (100 to 150mm); diameter to fill 80 percent of the isthmus. Use flexible reamers that follow the canal, confirming trajectory fluoroscopically.
- Aim for fixation in at least two of the three Morgan-Jones zones (zone 1 epiphysis via the baseplate, zone 2 metaphysis via the cone, zone 3 diaphysis via the stem), ideally all three.
- The stem shares load with the cone and protects against subsidence if cone ingrowth is incomplete; the load fraction is implant- and construct-dependent rather than fixed.
- Cemented technique (commonest): a thin 1 to 2mm cement mantle on the cone's superior surface, insert the baseplate with stem, hold compression 8 to 10 minutes, remove extruded cement.
- Cementless technique: direct impaction or a central screw through the baseplate into the cone, relying on taper-lock and osseointegration.
- A baseplate-cone gap greater than 2mm causes micromotion and failure — ensure flush contact.
- Trial then cement wedge augments (peripheral, 5 to 20mm) or block augments (central, 5 to 15mm) to the baseplate, avoiding cement at the augment-bone interface.
- Restore the joint line: normally 25mm distal to the medial femoral epicondyle and 10mm distal to the fibular head. Elevation risks patella baja (Insall-Salvati ratio less than 0.8).
- Minimum 10mm polyethylene (highly cross-linked preferred); thicker inserts (12 to 25mm) for laxity or bone loss.
- Choose constraint by ligament status: posterior-stabilised if collaterals intact, constrained condylar (CCK) for 5 to 10mm collateral laxity in extension, rotating hinge for gross instability. Avoid over-constraining.
- Trial and assess stability, balance flexion-extension gaps within 2mm, range of motion to 110 to 120 degrees, and central patellar tracking. Lock the insert, irrigate copiously, and re-check stability.
- Repair the medial arthrotomy with interrupted number-1 Vicryl or PDS; repair a rectus snip with figure-of-8 number-2 FiberWire; fix a tibial tubercle osteotomy with 2 to 3 bicortical screws or cerclage.
- Confirm central patellar tracking and a strong straight-leg-raise against resistance. Close in layers over drains if dead space is a concern, with an occlusive compressive dressing.
The popliteal neurovascular bundle lies only 10 to 15mm posterior to the capsule. During femoral and tibial component removal use curved osteotomes and a posterior retractor resting on bone, keep the knee flexed, and never use a power burr posteriorly. The metaphyseal-diaphyseal junction is the stress riser for fracture — if a crack is seen or heard, stop, stabilise with cerclage cables and a longer stem (bypassing by two cortical diameters), and consider a lateral locking plate if it propagates.
Use one full-thickness flap and excise intermediate scars en bloc; handle skin with hooks only. If the patella will not evert without tension, extend the exposure early — a rectus snip is the lowest-morbidity option. Extensor mechanism rupture occurs in 1 to 2 percent of standard and 5 to 8 percent of extensile approaches and is catastrophic.
With the knee flexed to 90 degrees, attempt to evert the patella. If it will not pass lateral to the midline without tension, extend: a rectus snip for mild-to-moderate stiffness (2 to 3 percent complication rate), a tibial tubercle osteotomy for severe stiffness or patella baja in a younger patient, and a V-Y quadricepsplasty only for an ankylosed knee in a low-demand elderly patient (10 to 15 percent disruption rate).
The cone is press-fit and cementless to host bone for osseointegration; the baseplate is cemented into the cone for immediate stability. These are not contradictory — the cone-bone interface is biological, the cone-implant interface is cemented. Cementing the cone directly to host bone defeats biological fixation. Published series report near-universal radiographic osseointegration and around 97 percent aseptic cone survivorship at midterm.
Non-bleeding sclerotic bone will not osseointegrate. If you cannot reach bleeding bone with a firm cortical rim, switch to a cemented technique or structural allograft. A cone sitting 5mm proud has roughly 40 to 50 percent contact (the minimum is 60 to 70 percent), will micromove, and will subside — remove it, ream 2 to 3mm deeper or upsize 2.5mm, and if it still will not seat, abandon the cone for augments or allograft.
Aftercare & Complications
Rehabilitation | Phase | Timing | Weight-bearing | Therapy | |-------|--------|----------------|---------| | 1 | 0–6 weeks | Touch weight-bearing (allows cone osseointegration) | CPM 0–90 degrees, quadriceps sets, straight-leg raises; goal 0–90 degrees by discharge | | 2 | 6–12 weeks | Advance to weight-bearing as tolerated if radiographs stable | Progressive strengthening, proprioception, gait | | 3 | 3–6 months | Full weight-bearing, wean aids | Goal 0–110 degrees minimum, 0–120 degrees ideal | | 4 | 6 months+ | Unrestricted | Low-impact activities (golf, swimming, cycling) | If an intraoperative fracture occurred, protect with non- to partial weight-bearing for 12 weeks. Continue chemical thromboprophylaxis for 4 to 6 weeks and use multimodal analgesia (adductor canal block, paracetamol, opioids; NSAIDs short-term if renal function allows). Radiographic surveillance. AP and lateral at 6 weeks assessing for subsidence (greater than 2mm is concerning) and lucencies (progressive radiolucency greater than 2mm indicates loosening); repeat at 3 months if symptomatic, then at 6 months, 1 year, and annually. Outcomes. Knee Society Score improves roughly 40 to 50 points (about 52 to 85 in the landmark series); patient satisfaction is 70 to 80 percent, lower than primary TKA.
Pooled aseptic survivorship of metaphyseal cones at midterm — Zanirato systematic review (927 cones, mean 3.6 years).
Revision-free cone survival at five to nine years in the Mayo series — Kamath (66 cones, mean 70 months).
Periprosthetic infection — the leading reason for failure in pooled cone series, exceeding aseptic loosening.
Complications
- Recognition
- Progressive pain, radiolucencies greater than 2mm at the bone-cone or cone-baseplate interface, subsidence greater than 5mm, component migration
- Prevention
- Adequate press-fit (60–70 percent contact), ream to bleeding bone, stem bypass of 2 cortical diameters, avoid cementing the cone to host bone
- Management
- Revision: larger cone if bone stock allows, structural allograft or custom implant for massive loss (AORI 3), hinged prosthesis if instability coexists
- Recognition
- Wound drainage beyond 5–7 days, fever, aspiration WBC greater than 3000 with PMN greater than 80 percent, positive cultures, ESR greater than 30 or CRP greater than 10
- Prevention
- Prophylactic antibiotics, minimal operative time, copious irrigation (9L), occlusive dressing, aspirate pre-operatively if any concern
- Management
- Acute (less than 4 weeks): DAIR if components stable and organism sensitive. Chronic: two-stage revision (spacer 6–12 weeks then reimplantation). Suppression if non-surgical
- Recognition
- Giving way, recurrent effusions, varus-valgus laxity greater than 10mm at 20 degrees, flexion-extension gap mismatch greater than 3mm
- Prevention
- Appropriate constraint (CCK for 5–10mm laxity, hinge if greater than 10mm), balance gaps within 2mm, restore the joint line
- Management
- Exchange polyethylene to higher constraint, revise to a rotating hinge if severe, address bone loss or collateral deficiency
- Recognition
- Acute pain, inability to bear weight, fracture around the cone or stem
- Prevention
- Gentle removal technique, sequential stem reaming in 0.5mm increments, fluoroscopy, cemented stems in osteoporotic bone, adequate stem length
- Management
- Stable component: cerclage cables or screws. Around the stem: longer stem bypassing the fracture by 2 cortical diameters plus possible locking plate or strut allograft. Distal to the stem: ORIF
- Recognition
- Foot drop, loss of ankle dorsiflexion, dorsal foot sensory loss
- Prevention
- Gradual correction of valgus, decompress at the fibular neck if correction greater than 15 degrees, monitor nerve function
- Management
- Observe 6 to 12 months (80 percent recover if neurapraxia), AFO for foot drop, explore or transfer if no recovery
- Recognition
- Inability to straight-leg-raise, extensor lag, palpable defect
- Prevention
- Extensile approach early if stiff, protect the lateral geniculate vessels, heavy-suture repair of any extensile approach
- Management
- Acute primary repair, augment with mesh or allograft if attenuated; chronic reconstruction with extensor-mechanism allograft or medial gastrocnemius flap
- Recognition
- Range of motion less than 90 degrees at 3 months, progressive flexion loss
- Prevention
- Adequate soft-tissue balancing, avoid joint-line elevation, early aggressive therapy
- Management
- Manipulation under anaesthesia at 6 to 12 weeks, arthroscopic then open arthrolysis, component revision if malalignment
- Recognition
- Persistent drainage beyond 7 days, dehiscence or necrosis, superficial infection
- Prevention
- Full-thickness flaps, excise intermediate scars, optimise diabetes and nutrition, plastic surgery if concern
- Management
- Oral antibiotics and local care for superficial infection; early debridement, negative-pressure therapy, gastrocnemius flap for deeper problems
Viva & Exam Focus
CONESCONES — when to use a porous metal tibial cone
STABLESTABLE — cone fixation principles
Clinical Decision Scenarios
Practise clinical reasoning and management decisions out loud
“A 68-year-old presents with pain and loosening of their tibial component 8 years after primary TKA. Radiographs show 15mm of medial tibial subsidence with both condyles compromised. How would you classify this defect and what reconstruction options would you consider?”
“During cone impaction for a Type 3 tibial defect, you achieve what appears to be good press-fit stability. However, fluoroscopy shows the cone is 5mm proud relative to the metaphyseal rim. How would you address this?”
“Post-operatively, a patient with a tibial cone reconstruction develops progressive pain, and radiographs at 1 year show a 2mm lucent line around the entire cone-bone interface with 3mm of subsidence compared with 6-week films. How would you manage this patient?”
Indication
- AORI Type 2B (both condyles damaged) or Type 3 (deficient metaphysis) tibial bone loss
- Also: periprosthetic fracture with metaphyseal loss, failed structural allograft, staged septic revision
Exposure (the heart)
- Standard medial parapatellar first; extend if the patella will not evert at 90 degrees
- Rectus snip (lowest morbidity, 2 to 3 percent), tibial tubercle osteotomy (severe stiffness, young), V-Y last resort (ankylosed, elderly)
- Full-thickness flaps only; excise intermediate scars; protect the lateral geniculate supply
Cone technique
- Ream to bleeding bone in 2.5mm increments, firm cortical rim
- Trial cone 2mm undersized; target 60 to 70 percent contact, flush seating
- Cone press-fit (cementless) to host bone; baseplate cemented INTO the cone — never cement the cone to host bone
Stem and load sharing
- Stem bypasses the cone by 2 cortical diameters (100 to 150mm), fills 80 percent of the isthmus
- Morgan-Jones three zones: 1 epiphysis (baseplate), 2 metaphysis (cone), 3 diaphysis (stem) — fix at least two, ideally all three
Complications (Big 4)
- Aseptic loosening 5 to 8 percent at 5 years
- Infection 3 to 5 percent (the leading failure mode, around 10 percent in pooled series)
- Instability 3 to 5 percent
- Periprosthetic fracture 2 to 4 percent
Postoperative
- Touch weight-bearing for 6 weeks to allow osseointegration
- Range of motion 0 to 90 degrees by discharge, 0 to 110 minimum by 3 months
- Radiographs at 6 weeks, 3 months, 6 months, 1 year then annual; subsidence greater than 2mm or lucencies greater than 2mm are concerning
Background & Evidence
Epidemiology. Bone loss is the defining challenge of revision TKA, and the metaphyseal cone was developed for the defects augments cannot solve — AORI Type 2B and 3 — where the metaphyseal shell can no longer support a baseplate. Tantalum and titanium porous cones exploit a high-porosity (80 percent) scaffold whose modulus (about 3 GPa) is close to bone, allowing reliable bone ingrowth (osseointegration) and ongrowth. The AORI bone-defect classification (Anderson Orthopaedic Research Institute) drives the reconstruction:
- Metaphyseal bone
- Intact
- Structural support
- Preserved
- Reconstruction
- Standard revision baseplate, no cone
- Metaphyseal bone
- Damaged, one condyle
- Structural support
- Partial
- Reconstruction
- Modular augments usually suffice
- Metaphyseal bone
- Damaged, both condyles
- Structural support
- Compromised
- Reconstruction
- Metaphyseal cone indicated
- Metaphyseal bone
- Deficient
- Structural support
- Lost
- Reconstruction
- Cone required; consider sleeve, allograft or custom implant
Key evidence. Meneghini established the technique (15 knees, AORI 2B/3, KSS 52 to 85, all osseointegrated at a mean 34 months). Kamath provided intermediate-term durability (66 cones, mean 70 months, only one aseptic loosening, revision-free cone survival over 95 percent). Long confirmed independent osseointegration with alignment restoration but showed infection as the dominant failure mode. The Zanirato systematic review pooled 927 cones and 1801 sleeves and found near-equivalent aseptic survivorship (97.3 percent vs 97.8 percent) — cones and sleeves are interchangeable, choice driven by implant system and defect geometry. Byttebier's meta-analysis (4391 knees) found no significant difference in 10-year failure between porous implants and grafting, though tantalum cones showed the largest patient-reported outcome gains.
References
Use of porous tantalum metaphyseal cones for severe tibial bone loss during revision total knee replacement
- 15 revision TKAs (8 Type-3, 7 Type-2B AORI defects) with porous tantalum tibial cones; mean 3.5 prior knee replacements
- Mean Knee Society clinical score improved from 52 to 85 at a mean 34 months follow-up
- All 15 cones showed radiographic osseointegration with reactive trabeculation; no loosening or migration
Porous tantalum metaphyseal cones for severe tibial bone loss in revision knee arthroplasty: a five to nine-year follow-up
- 66 tibial cones in 63 patients (24 Type-3, 25 Type-2B, 17 Type-2A); mean 70 months follow-up (range 60 to 106)
- Mean Knee Society Score improved from 55 to 80 (p less than 0.0001); 49 percent had a prior periprosthetic infection
- Only one aseptic loosening; revision-free survival of the tibial cone component greater than 95 percent at latest follow-up
Porous tantalum cones for large metaphyseal tibial defects in revision total knee arthroplasty: a minimum 2-year follow-up
- 16 revision TKAs with tantalum tibial cones for AORI 2A/2B/3 defects; mean 31 months follow-up, none lost
- Reconstruction restored the joint line and a near-neutral mechanical axis (mean 5.4 degrees valgus) with radiographic osseointegration
- Two well-fixed cones required removal for recurrent infection; the remaining 14 functioned well with no reoperation
Metaphyseal cones and sleeves in revision total knee arthroplasty: two sides of the same coin? A systematic review
- Systematic review of 37 studies: 927 cones (mean 3.6 years) and 1801 sleeves (mean 4.5 years)
- Aseptic implant survivorship 97.3 percent for cones and 97.8 percent for sleeves — statistically overlapping
- Both provide stable metaphyseal (zone 2) fixation for AORI Type 2B and 3 defects in aseptic and septic revision
Comparison of different strategies in revision arthroplasty of the knee with severe bone loss: a systematic review and meta-analysis
- Meta-analysis of 77 articles and 4391 knees comparing porous cones/sleeves with morselised and structural grafting
- No significant difference in failure at 10 years between all porous implants and all grafting procedures (OR 0.91, 95 percent CI 0.70 to 1.19)
- Tantalum cones showed the largest improvement in patient-reported outcome measures of the strategies analysed
Early results of the use of tantalum femoral cones for revision total knee arthroplasty
- Companion femoral cone series (24 knees) extending the porous-cone concept to the femoral side
- Mean Knee Society Score improved from 55 to 81 at a mean 33 months
- All cones were well-fixed radiographically with no loosening
Bone loss with revision total knee arthroplasty: defect classification and alternatives for reconstruction
- Classic reference defining the AORI bone-defect classification (Types 1, 2A, 2B, 3)
- Sets out the reconstruction algorithm — augments, structural allograft, custom implants — that cones later slot into
Management of bone loss: augments, cones, offset stems
- Practical algorithm for selecting augments, cones, stems and offset stems in revision TKA
- Describes how to combine zone-1 (augments), zone-2 (cones) and zone-3 (stems) fixation