1540 Osteochondral Allograft
Transcript of 1540 Osteochondral Allograft
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OSTEOCHONDRALALLOGRAFT
RECONSTRUCTION FOR MASSIVE BONE DEFECT
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-Head Orthopaedic Surgeon University of Cincinnati Athletics
-Director of Sports Medicine University of Cincinnati Medical Center
-Associate Professor of UC College of Medicine
-Medical Director Holmes Sports Medicine
Angelo J. Colosimo, MD
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“Ulcerated cartilage is a troublesome thing, once it is destroyed it is not repaired”
Hunter, 1743
“Ulcerated cartilage is a troublesome thing, once it is destroyed it is not repaired”
Hunter, 1743
INTRODUCTION
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INTRODUCTION
Focal cartilage defects in the knee pose a difficult clinical challengeRepair, regeneration
and transplantationTreatment remains an
unsolved clinical and scientific problem
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INTRODUCTION
The goal of articular cartilage repair is to: Restore joint congruityProvide full pain-free motion Prevent further tissue deteriorationStimulate healing
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INTRODUCTION
Despite numerous attempts at addressing the problem of chondrallesions, treatment options remain limited and the long-term outcomes uncertain.
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INTRODUCTION
Current treatment options provide, at best:Temporary pain relief
Diminished clinical symptoms
Temporary functional improvement
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INTRODUCTION
Articular cartilage functional properties:Load bearing distribution
Reduces peak stresses on subchondral bone
Joint lubrication
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ARTICULAR CARTILAGE - COMPOSITION
Hyaline Cartilage:Resists compressive forcesThe collagen structure gives
the tissue its form, strength and durabilityType II CollagenPrimary function is load
bearingWithstands cyclic load and
shearing forcesArticular cartilage is designed
for long term performance
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ARTICULAR CARTILAGE - COMPOSITION
Fibrocartilage (repair cartilage): Resists tension forcesHistological studies show
unorganized cellular patternNot structured for efficient load
bearingLower concentration of
proteoglycansLong-term performance is inferior
to normal articular cartilageNo type II collagen
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Two Categories:Partial thickness Defects
Full thickness Defects
ARTICULAR CARTILAGE LESIONS
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I. Debridement & CurettageII. DrillingIII. Microfracture TechniqueIV. Osteochondral Autograft
Transplantation V. Osteochondral Allograft TransplantationVI. Autologous Chondrocyte ImplantationVII. Growth Factors
AVAILABLE SURGICAL OPTIONS
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FULL-THICKNESS INJURY
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AUTOLOGOUS OSTEOCHONDRAL
TRANSPLANTATION(MOSAICPLASTY)
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AUTOLOGOUS OSTEOCHONDRAL TRANSPLANTATION
Mosaicplasty:Osteochondral plugs
transplanted from non-weight bearing articular cartilage to chondral defect in weight bearing area
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The closer repair cartilage comes to restoring hyaline cartilage the more durableLimited surgical techniquesOsteochondral autograft
transplantation (OATS): Restore height Restore shape Hyaline cartilage Intact tidemark Firm carrier – subchondral bone –
nutritionOBI Plugs
OATS - MOSAICPLASTY
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OATS - MOSAICPLASTY
No disease transmissionGood chondrocyte survivalReliable bony unionLimited donor sizeGraft size
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Ideal Lesion:Small (10-30mm)
Full thickness
Femoral condyle (medial or lateral)
Stable surrounding articular cartilage
INDICATIONS FOR OATS
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Why OATS???Microfracture and abrasion easierOATS:Repair with autologous hyaline
cartilageCell viability/survivalRestore height and shape of
defectLong term survival (tidemark)
INDICATIONS FOR OATS
30 months s/p OATS
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Contra-indications:Deep, crater like defect
Loss of subchondral bone
Difficult to cover large defect
No appropriate harvest sites
Severe Malalignment
INDICATIONS FOR OATS
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OATS - SURGICAL TECHNIQUE
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Step 1: Selection of donor site
OATS SURGICAL TECHNIQUE
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Step 2: Chondral defect sizing
OATS SURGICAL TECHNIQUE
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Step 3: Recipient defect preparation
OATS SURGICAL TECHNIQUE
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Step 3: Recipient Defect Preparation
OATS SURGICAL TECHNIQUE
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Step 4: Determine depth of recipient defect
OATS SURGICAL TECHNIQUE
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Step 5: Donor core harvesting
OATS SURGICAL TECHNIQUE
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Step 6: Donor core insertion
OATS SURGICAL TECHNIQUE
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Step 7: Final donor core seating
OATS SURGICAL TECHNIQUE
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OATS – Plug placement
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OATS SURGICAL VIDEO
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Mosaicplasty appears to be a viable alternative for full-thickness cartilage defects
Regeneration of hyaline or hyaline-like cartilage
Longevity???
OATS SUMMARY
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OSTEOCHONDRALALLOGRAFTS
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First used in 1908 by Lexer He reported a 50% success rate
In the 1940s and 1950s they were thought to be a biologic alternative to the total joint replacement
In the 1970s fresh osteochondralallografts were used for limb salvage after large tumor resections
Today they are used more widely due to increased availability
INTRODUCTION
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OSTEOCHONDRAL ALLOGRAFTS
Used for Large focal osteo-articular defects and bone lossMature hyaline
cartilage and boneSuccess = cell viabilityFresh, Fresh frozen or
cryopreserved
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OSTEOCHONDRAL ALLOGRAFTS
Immunology:Studied extensively
Intact hyaline cartilage
Immunologically privileged
No donor match
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Cell ViabilityFresh (99%)Fresh Frozen (10-15%)Cryopreserved (35-40%)
Use of cryoprotective agents increases chondrocyte viability compared to fresh frozen grafts
Cell viability decreases over time
OSTEOCHONDRAL ALLOGRAFTS
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IncorporationAllograft bone is replaced by Host bone in 2-3 yearsCreeping substitutionGross et al reported 85% success rate in 126 knees with fresh allografts
OSTEOCHONDRAL ALLOGRAFTS
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ImmunologyChondrocytes are immuno-
privelaged
Humoral antibodies cannot penetrate into the matrix
Rejection is insignificant
Tissue typing and immunosuppressants are unnecessary
Possibility of immune response to allograft cells and marrow
OSTEOCHONDRAL ALLOGRAFTS
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Considerations:Size of defect
Availability of size-matched quality donor
Extremity alignment
Monopolar vs bipolar defects
Ligamentous stability
Meniscal injury
OSTEOCHONDRAL ALLOGRAFTS
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Indications:Large, deep, extensive
osteochonrdal lesions
Bone loss
Skeletal maturity
No arthritic changes
<50 years old
Correctable alignment and ligamentous laxity
OSTEOCHONDRAL ALLOGRAFTS
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Optimal Outcomes:Single defect
>2cm
1 compartment
No angular deformity
OSTEOCHONDRAL ALLOGRAFTS
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Contraindications:Inflammatory arthropathy
Uncorrected ligamentous instability
Uncorrected malalignment
Diffuse arthrosis
AVN
OSTEOCHONDRAL ALLOGRAFTS
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OSTEOCHONDRAL ALLOGRAFTS
Grafts work best in post-traumatic changes and osteochondritisdissecans
Age and size match
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OSTEOCHONDRAL ALLOGRAFTS
Advantages:Readily available
Lack of donor site morbidity
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OSTEOCHONDRAL ALLOGRAFTS
Disadvantages: Disease transmission
Donor procurement expense
Chondrocyte survival
Open procedure
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OSTEOCHONDRAL ALLOGRAFT KS CASE
Pre-operative findings
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OSTEOCHONDRAL ALLOGRAFT KS CASE
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OSTEOCHONDRAL ALLOGRAFT KS CASE
Follow-up at 6 weeks
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OSTEOCHONDRAL ALLOGRAFT KS CASE
Follow-up at 1 year
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OSTEOCHONDRAL ALLOGRAFT MH CASE
Pre-operative radiographs
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OSTEOCHONDRAL ALLOGRAFT MH CASE
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OSTEOCHONDRAL ALLOGRAFT MH CASE
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OSTEOCHONDRAL ALLOGRAFT MH CASE
Follow-up 1 year
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OSTEOCHONDRAL ALLOGRAFT NH CASE
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OSTEOCHONDRAL ALLOGRAFT NH CASE
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OSTEOCHONDRAL ALLOGRAFT NH CASE
Follow-up at 2 months post-operatively for an osteochondralallograft of the LFC
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OSTEOCHONDRALALLOGRAFT
KF CASE
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OSTEOCHONDRAL ALLOGRAFTS
Gross (1996): 92 fresh allografts for traumatic articular defects:
75% successful at 5 yrs 64% successful at 10 yrs 63% successful at 14 yrs
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OSTEOCHONDRAL ALLOGRAFTS
Garrett (1994)17 patients with osteochondritisdissecansAges 16-46Lateral femoral condylar defectsAll had fresh frozen allografts
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OSTEOCHONDRAL ALLOGRAFTS
Garrett (1994) Transplantation within 4 days of harvestHerbert screw fixation and NWB 6 weeksFollow-up 2 to 9 years16/17 (94%) had successful results
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AUTOLOGOUS CHONDROCYTE IMPLANTATION
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AUTOLOGOUS CHONDROCYTE IMPLANTATION
Introduced: Sweden (1987) US (1995)
Two stage procedureOpen procedureLaboratory dependantMACI Patch FDA December 2016
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AUTOLOGOUS CHONDROCYTE IMPLANTATION
Indications:Lesions 1- 10 cmAge < 50-55Only femoral lesions
are FDA approvedOsteochondritis
dissecansConcomitant
correction of instability or malalignment
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Approved by FDA December 2016 Currently only for knees
Cellular sheet 3 cm x 5 cm ACI cells on a resorbable
porcine collagen membraneType I/III collagenAt least 500,000 cells/cm2
Clinical OutcomesSUMMIT Trial144 patients (18-54)MACI vs MFX137 pts with FU @ 2yearsKOOS scalesMACI was clinically and
statistically better for treating symptomatic cartilage defects than MFX
MACI PATCH
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Growth Factors Insulin-Like Growth Factor-1(ILGF-1)Fibroblast Growth Factor (FGF)Transforming Growth Factor-beta (TGF-beta)Hepatocyte Growth Factor (HGF)Platelet-Derived Growth Factor (PDGF)Bone Morphogenetic Proteins (BMP)Interleukin-1 Receptor Antagonist (ILRA)
FUTURE CONSIDERATIONS
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ARTICULAR CARTILAGE KEY POINTS
Hyaline cartilage lasts longer than fibrocartilageHyaline cartilage
restores the normal function and durability of the jointHyaline cartilage is
better able to redistribute joint stress
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ARTICULAR CARTILAGE KEY POINTS
Fibrocartilage will fill the defect and promote relief of symptoms up to a given point in timeFibrocartilage lacks
the composition, structure and durability of normal hyaline cartilage
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SUMMARY
Challenging problemTraditional treatment
allows for only temporary reliefNew attempts at
regeneration not reliableStudies must be > 6 mo.
F/U
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