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MRI Cartilage Assessment

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MRI Cartilage Assessment

Comprehensive guide to MRI cartilage assessment including optimal sequences, grading systems, cartilage repair monitoring, and clinical decision-making for fellowship exam preparation.

High Yield
complete
Reviewed: 2026-03-11By OrthoVellum Medical Education Team

Reviewed by OrthoVellum Editorial Team

Orthopaedic clinicians and medical editors • Published by OrthoVellum Medical Education Team

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High Yield Overview

MRI Cartilage Assessment

Imaging Articular Cartilage for Surgical Decision-Making

2-4mmNormal articular cartilage thickness
PD-FSStandard cartilage sequence
Grade 0-4Modified Outerbridge MRI grading
T2 MapQuantitative early degeneration
dGEMRICGAG content assessment
3TPreferred field strength for cartilage
70-95%MRI sensitivity for full-thickness defects
40-70%MRI sensitivity for partial-thickness defects

Modified Outerbridge MRI Grading

Grade 0: Normal cartilage — smooth surface, uniform thickness, normal signal

Grade 1: Focal signal abnormality with intact surface (softening/swelling)

Grade 2: Partial-thickness defect involving less than 50% of cartilage depth

Grade 3: Partial-thickness defect involving more than 50% depth, or full-thickness without bone exposure

Grade 4: Full-thickness cartilage loss with exposed subchondral bone

Key: Arthroscopy remains the gold standard — MRI provides a non-invasive estimate of cartilage integrity but tends to underestimate partial-thickness lesions

Critical Must-Knows

  • Normal articular cartilage is 2-4mm thick and appears as a smooth, intermediate-signal layer on most sequences.
  • PD fat-suppressed and T2 fat-suppressed are the standard sequences for morphological cartilage assessment.
  • MRI is highly sensitive (70-95%) for full-thickness cartilage defects but less reliable (40-70%) for partial-thickness lesions.
  • T2 mapping and dGEMRIC are quantitative techniques that detect biochemical cartilage changes BEFORE morphological damage is visible.
  • The modified Outerbridge classification (Grades 0-4) is used to grade cartilage lesions on MRI.

Examiner's Pearls

  • "
    3T MRI provides superior cartilage imaging compared to 1.5T due to improved signal-to-noise ratio and spatial resolution.
  • "
    MR arthrography (direct, with intra-articular gadolinium) improves detection of partial-thickness cartilage lesions.
  • "
    Normal cartilage shows a layered appearance on high-resolution imaging: the deep radial zone has lower signal than the superficial transitional zone.
  • "
    Post-cartilage repair MRI (MOCART score) assesses: fill grade, integration, surface, signal, subchondral bone, effusion.
  • "
    Cartilage cannot heal spontaneously — even small defects will progress without intervention, making early detection critical.

Exam Warning

MRI cartilage assessment is commonly examined in the context of knee and hip pathology. You must be able to: explain optimal sequences for cartilage imaging, grade cartilage lesions using the modified Outerbridge classification, discuss the role of quantitative techniques (T2 mapping, dGEMRIC), and explain how MRI findings guide surgical decision-making between microfracture, OATS, and ACI. A common exam trap is overestimating the sensitivity of MRI for partial-thickness lesions.

Mnemonic

SOFBECartilage MRI Grading

S
Signal change only (Grade 1)
Focal increased signal within cartilage on PD/T2 with INTACT articular surface — corresponds to softening or early degeneration
O
One half affected (Grade 2)
Partial-thickness defect involves less than 50% of cartilage depth — the surface is disrupted but deep cartilage remains
F
Full of defect, more than half (Grade 3)
Partial-thickness defect involving more than 50% depth, or full-thickness without reaching bone
B
Bone exposed (Grade 4)
Full-thickness cartilage loss with exposed subchondral bone — often with associated subchondral oedema and cyst formation
E
Eburnation (sclerosis)
Grade 4 lesions often show secondary bone changes: sclerosis, cysts, and osteophyte formation

Memory Hook:SOFBE: Signal, One-half, Full, Bone, Eburnation — the progression of cartilage destruction on MRI.

Mnemonic

PIGOptimal Cartilage Sequences

P
PD fat-suppressed
Primary morphological sequence — high SNR, good cartilage-fluid contrast, standard for knee and ankle cartilage assessment
I
Intermediate echo 3D GRE
3D gradient echo sequences (SPGR, FLASH, DESS) provide thin isotropic slices for quantitative thickness mapping and surface assessment
G
Gadolinium arthrography
Direct MR arthrography improves partial-thickness lesion detection — dilute gadolinium outlines subtle surface defects

Memory Hook:PIG sequences for cartilage: PD fat-suppressed is the workhorse, 3D GRE for quantitative mapping, and Gadolinium arthrography for tricky partial-thickness defects.

Mnemonic

FISSBEMOCART Score Components

F
Fill grade
Percentage of defect filled by repair tissue: complete (100%), hypertrophic (over 100%), incomplete (less than 100%), or subchondral overgrowth
I
Integration to border
How well the repair tissue integrates with surrounding native cartilage: complete, incomplete (split visible), or deficient
S
Surface of repair
Smooth and intact, irregular, or fissured/eroded repair surface
S
Signal intensity
Normal signal (isointense to native cartilage) or abnormal signal (hyperintense on PD/T2 suggesting fibrocartilage)
B
Bone interface
Intact subchondral lamina, irregular subchondral bone, or subchondral bone overgrowth/cyst formation
E
Effusion
Presence and degree of joint effusion following cartilage repair — large effusions may indicate poor repair integrity

Memory Hook:FISSBE is the MOCART score framework for assessing cartilage repair on follow-up MRI.

Overview

Articular cartilage is a unique tissue that lacks intrinsic healing capacity due to its avascular nature and limited chondrocyte proliferative potential. Once damaged, cartilage defects tend to progress to larger lesions and eventually to osteoarthritis. MRI is the primary non-invasive modality for assessing articular cartilage, providing information about defect size, depth, location, and the condition of surrounding subchondral bone that guides surgical decision-making.

The challenge of cartilage MRI is that the tissue is thin (2-4mm), has subtle internal structural variation, and partial-thickness lesions can be difficult to distinguish from normal signal heterogeneity. This has driven the development of dedicated high-resolution cartilage sequences and quantitative imaging techniques that can detect biochemical changes in cartilage before macroscopic damage occurs.

Why Cartilage Assessment Matters

Cartilage defects of greater than 2cm² in the weight-bearing zone of the knee produce symptoms and risk progression to osteoarthritis. Treatment options depend on defect characteristics: microfracture for smaller defects (less than 2cm²), osteochondral autograft transfer (OATS) for 1-4cm² defects, and autologous chondrocyte implantation (ACI/MACI) for larger defects (greater than 2-4cm²). MRI provides the preoperative defect characterisation needed for surgical planning.

MRI vs Arthroscopy

Arthroscopy remains the gold standard for cartilage assessment — it allows direct visualisation, probing of the cartilage surface, and immediate treatment. However, MRI has the advantage of being non-invasive, showing the full extent of subchondral bone changes, revealing marrow oedema, and assessing areas inaccessible to the arthroscope. The correlation between MRI and arthroscopic findings is best for full-thickness defects (70-95% sensitivity) but less reliable for partial-thickness lesions (40-70% sensitivity).

Clinical Imaging

Imaging Gallery

MRI cartilage assessment showing articular cartilage layers and signal characteristics
Click to expand
MRI demonstrating articular cartilage assessment with the characteristic layered appearance of hyaline cartilage. The intermediate signal of normal cartilage is clearly differentiated from the bright signal of joint fluid — this contrast is essential for detecting surface defects and partial-thickness lesions.Credit: Open-i (NIH) (Open Access (CC BY))
MRI showing chondral defect with associated subchondral changes
Click to expand
MRI demonstrating a cartilage defect with associated subchondral bone changes. Note how the loss of the normal cartilage signal allows joint fluid (bright on T2/PD-FS) to track into the defect, clearly delineating the size and depth of the lesion. Subchondral oedema and cyst formation indicate a higher-grade lesion.Credit: Open-i (NIH) (Open Access (CC BY))

Systematic Approach

Systematic Cartilage Assessment on MRI

Systematic Cartilage Assessment Framework

StepAssessmentKey Considerations
1. Identify the sequencePD-FS or T2-FS is most appropriate for cartilage morphologyCartilage appears intermediate grey; fluid appears bright — this contrast is essential for detecting surface defects
2. Assess cartilage thicknessCompare thickness across the articular surface; note focal thinningNormal thickness varies by location: femoral condyle 2-3mm, patellar surface 3-5mm (thickest), tibial plateau 2-3mm
3. Grade the defectApply modified Outerbridge classification (Grades 0-4)Grade 1: signal change only. Grade 2: less than 50% depth. Grade 3: more than 50% depth. Grade 4: full-thickness with bone exposure
4. Measure defect dimensionsDocument the size (AP dimension, width, and depth in mm)Size determines treatment: less than 2cm² = microfracture, 1-4cm² = OATS, more than 2-4cm² = ACI/MACI
5. Assess subchondral boneLook for oedema, cysts, sclerosis beneath the cartilage defectSubchondral changes indicate chronicity and may affect surgical outcomes — large cysts may require bone grafting
6. Check for associated pathologyMeniscal tears, ligament injuries, loose bodies, alignmentCartilage defects rarely occur in isolation — associated pathology must be addressed simultaneously

Cartilage Imaging Sequences

Standard Cartilage Imaging

PD fat-suppressed is the workhorse sequence for cartilage morphological assessment. It provides:

  • High signal-to-noise ratio (long TR, short TE)
  • Good cartilage-fluid contrast (cartilage is intermediate; fluid is bright)
  • Sensitivity to surface defects and partial-thickness lesions
  • Fat suppression eliminates competing signal from epiphyseal fat and marrow

3D Gradient Echo sequences (SPGR, FLASH, DESS, MERGE) provide isotropic thin-slice acquisitions (0.5-1mm) that enable multiplanar reformatting and quantitative thickness mapping. These are increasingly used for:

  • Research studies requiring volumetric cartilage measurement
  • Pre- and post-operative cartilage repair monitoring
  • Cartilage thickness maps overlaid on 3D joint models

T2-weighted fat-suppressed can also be used for cartilage but has lower SNR than PD and may underestimate the extent of lesions that are better seen with PD contrast.

3T vs 1.5T: Higher field strength significantly improves cartilage imaging quality by increasing SNR and spatial resolution. 3T is preferred for dedicated cartilage assessment when available.

These remain the standard for clinical cartilage assessment.

Compositional Cartilage Mapping

Quantitative MRI techniques detect biochemical changes in cartilage at a molecular level, potentially identifying early degeneration before visible structural damage appears on standard sequences.

T2 Mapping: Measures the T2 relaxation time of cartilage voxel by voxel. T2 values reflect collagen fibre organisation and water content. In early degeneration, collagen fibre disruption and increased water content cause elevated T2 values. T2 maps are displayed as colour-coded images with elevated T2 (warm colours) indicating degeneration. Normal articular cartilage T2: 25-45ms.

dGEMRIC (delayed Gadolinium-Enhanced MRI of Cartilage): After IV gadolinium administration and a delay (approximately 90 minutes of exercise), gadolinium distributes into cartilage inversely proportional to the glycosaminoglycan (GAG) content. Low GAG content (early degeneration) leads to more gadolinium uptake and shorter T1, while healthy cartilage with high GAG content limits gadolinium penetration. dGEMRIC maps can identify areas of GAG depletion before morphological abnormality.

T1rho Mapping: Sensitive to proteoglycan content in cartilage. Elevated T1rho values correlate with proteoglycan loss. More sensitive to early changes than T2 mapping in some studies but requires specialised pulse sequences not available on all scanners.

Sodium MRI (23Na): Directly measures sodium concentration, which correlates with GAG content. Limited to research settings due to the need for specialised coils and ultra-high field strength (7T).

These techniques represent the future of cartilage assessment.

Cartilage Repair Assessment

Monitoring cartilage repair on MRI is increasingly importantas the number of cartilage repair procedures grows. The MOCART (Magnetic Resonance Observation of Cartilage Repair Tissue) score is the standardised tool for post-operative cartilage repair assessment.

MOCART Score Assessment Criteria

VariableBest OutcomeIntermediateWorst Outcome
Fill gradeComplete fill (100%)Over-fill (hypertrophic) or slight under-fill (75-100%)Significant under-fill (less than 50%) or complete graft failure
IntegrationComplete integration — no visible cleft between repair and native cartilagePartial integration — incomplete border with focal cleftNo integration — persistent cleft, delamination
SurfaceSmooth surface, flush with native cartilageIrregular surface, mild fibrillationFissured, severely irregular, or absent surface
Signal intensityIsointense to native cartilage on all sequencesMild hyperintensity (suggests more fibrous composition)Markedly abnormal signal (suggests failure or fibrocartilage only)
Subchondral boneIntact subchondral lamina with normal marrowMild irregularity or oedemaSubchondral overgrowth, large cysts, or persistent osteolysis

Repair Tissue vs Hyaline Cartilage

On MRI, true hyaline cartilage repair tissue is isointense to surrounding native cartilage on all sequences. Fibrocartilage repair (as produced by microfracture) tends to have slightly different signal characteristics: often mildly hyperintense on PD/T2 with a less distinct layered appearance. This signal difference can help distinguish the type of repair tissue, which has prognostic implications — hyaline-like repair (from ACI/MACI) generally has better long-term durability than fibrocartilage.

Evidence Base

Accuracy of MRI for Articular Cartilage Lesions in the Knee

Meta-Analysis
Defined by Quatman CE, Hettrich CM, Schmitt LC, Spindler KP • Journal of Bone and Joint Surgery (American) (2011)
Key Findings:
  • MRI sensitivity for full-thickness cartilage defects was 72-94% depending on the sequence and field strength.
  • Sensitivity for partial-thickness (Grade 1-2) lesions was significantly lower at 40-68%.
  • 3T MRI improved detection compared to 1.5T, particularly for partial-thickness lesions.
Clinical Implication: MRI reliably detects full-thickness cartilage defects but under-detects partial-thickness lesions — arthroscopy remains the gold standard for complete assessment.
Limitation: Meta-analysis heterogeneity was significant due to varying sequences, field strengths, and reader experience.
Source: Quatman CE et al. JBJS Am 2011;93(16):1513-20

MR Arthrography for Cartilage Assessment

Comparative Study
Disler DG, McCauley TR, Wirth CR, Fuchs MD • Radiology (1995)
Key Findings:
  • Direct MR arthrography improved sensitivity for partial-thickness cartilage defects to 85-92% compared to 55-65% for non-arthrographic MRI.
  • Intra-articular gadolinium provided a natural contrast agent that outlined subtle surface irregularities invisible on standard sequences.
  • Correlation with arthroscopy was excellent for defect location and depth grading.
Clinical Implication: When accurate cartilage assessment is critical (e.g., pre-operative planning for cartilage repair), direct MR arthrography should be considered.
Limitation: MR arthrography is invasive, requires injection, and adds cost and time to the imaging pathway.
Source: Disler DG et al. Radiology 1995;195(1):43-8

MRI is best for full-thickness defects; arthrography improves partial-thickness detection.

T2 Mapping for Early Cartilage Degeneration

Prospective Study
Mosher TJ, Dardzinski BJ • Seminars in Musculoskeletal Radiology (2004)
Key Findings:
  • T2 mapping detected elevated T2 values in cartilage with early degenerative changes before morphological changes were visible.
  • T2 values correlated with collagen fibre integrity and water content — both disrupted early in osteoarthritis.
  • Quantitative T2 maps provided reproducible, objective measurements for longitudinal monitoring.
Clinical Implication: T2 mapping may enable earlier detection and monitoring of cartilage degeneration than conventional morphological MRI it.
Limitation: T2 mapping requires post-processing software and there is no universally accepted threshold for abnormality.
Source: Mosher TJ, Dardzinski BJ. Semin Musculoskelet Radiol 2004;8(4):355-68

MOCART Score for Cartilage Repair Monitoring

Validation Study
Marlovits S, Singer P, Zeller P, Mandl I, Haller J, Trattnig S • European Journal of Radiology (2006)
Key Findings:
  • The MOCART score demonstrated good inter-reader reliability (kappa 0.72-0.85) for all scoring variables.
  • MOCART scores correlated with clinical outcomes (KOOS scores) at 2-year follow-up.
  • Fill grade and integration to native cartilage were the strongest predictors of clinical outcome.
Clinical Implication: MOCART provides a standardised, reproducible framework for post-operative cartilage repair assessment using MRI.
Limitation: MOCART has not been validated against long-term outcomes (more than 5 years) or histological analysis in all repair techniques.
Source: Marlovits S et al. Eur J Radiol 2006;57(1):16-23

dGEMRIC for Cartilage GAG Assessment

Prospective Study
Bashir A, Gray ML, Boutin RD, Burstein D • Magnetic Resonance in Medicine (1997)
Key Findings:
  • dGEMRIC index correlated strongly with GAG content measured biochemically (r = 0.85).
  • Areas of low GAG (early degeneration) showed shorter T1 after gadolinium, indicating increased gadolinium uptake.
  • dGEMRIC could detect GAG loss in macroscopically normal-appearing cartilage on arthroscopy.
Clinical Implication: dGEMRIC provides a validated non-invasive measure of cartilage GAG content, enabling detection of biochemical degeneration before structural failure.
Limitation: Requires gadolinium administration, exercise period, and significant delay before imaging — logistically challenging in clinical practice.
Source: Bashir A et al. Magn Reson Med 1997;38(5):857-66

Quantitative techniques detect early cartilage damage before morphological failure.

Australian Context

In Australia, MRI cartilage assessment is an integral part of the orthopaedic workup for osteochondral defects, particularly in the knee. Medicare-funded knee MRI is available for clinical indications including internal derangement and suspected cartilage damage, with 3T scanners increasingly available at major Australian imaging centres.

The Australian Orthopaedic Association has endorsed national guidelines for cartilage repair that recommend pre-operative MRI with dedicated cartilage sequences (PD-FS at minimum) to characterise defect size and subchondral bone quality before surgical planning. Quantitative cartilage imaging (T2 mapping, dGEMRIC) is available at Australian research institutions and selected tertiary imaging centres, though it is not yet part of routine clinical protocols.

The AOANJRR indirectly reflects cartilage health through its tracking of knee replacement rates — early detection and treatment of cartilage defects is a key strategy for delaying or preventing arthroplasty. Australian Medicare funds both microfracture and ACI/MACI procedures, with MACI (matrix-associated autologous chondrocyte implantation) being more widely available in Australia than in many other countries.

Exam Viva Scenarios

Practice these scenarios to excel in your viva examination

VIVA SCENARIOStandard

EXAMINER

"A 28-year-old footballer has an MRI showing a 3cm² full-thickness cartilage defect on the medial femoral condyle with underlying subchondral oedema."

EXCEPTIONAL ANSWER
This is a modified Outerbridge Grade 4 cartilage defect — full-thickness loss with exposed subchondral bone (evidenced by the subchondral oedema). The size (3cm²) and full-thickness nature are important for surgical planning. Treatment options for a young, active patient with a symptomatic 3cm² full-thickness defect include: (1) Microfracture: Suitable for defects less than 2cm², so this defect is at or beyond the upper limit. Microfracture creates channels in the subchondral bone to allow marrow elements to fill the defect, but the resulting repair tissue is predominantly fibrocartilage, which has inferior biomechanical properties and durability compared to hyaline cartilage. (2) OATS (Osteochondral Autograft Transfer): Suitable for 1-4cm² defects. Transfers plugs of hyaline cartilage and subchondral bone from a non-weight-bearing area (typically the superomedial trochlea or intercondylar notch edge) to the defect. Provides true hyaline cartilage at the repair site. Limited by donor site morbidity and difficulty matching surface contour for larger defects. (3) ACI/MACI (Matrix-Associated Autologous Chondrocyte Implantation): Preferred for larger defects (greater than 2-4cm²). Two-stage procedure: harvest chondrocytes, expand in culture, reimplant on a collagen scaffold. Produces hyaline-like repair tissue with the best long-term durability. Most appropriate for this patient given the defect size. I would also address contributing factors: alignment (consider HTO if varus malalignment focuses load on the medial compartment), meniscal status, and ligament stability.
KEY POINTS TO SCORE
Grade 4: full-thickness cartilage loss with subchondral bone exposure
3cm² defect — at the threshold for OATS and within the range for ACI/MACI
Microfracture produces fibrocartilage (inferior durability); OATS and ACI produce hyaline
ACI/MACI preferred for defects greater than 2-4cm² in young active patients
Must address contributing factors: alignment, meniscal status, ligament stability
COMMON TRAPS
✗Grading the lesion incorrectly (full-thickness with subchondral involvement = Grade 4)
✗Recommending microfracture alone for a 3cm² defect (exceeds its optimal size range)
✗Not mentioning the biomechanical difference between fibrocartilage and hyaline repair
✗Not addressing contributing malalignment (HTO consideration)
VIVA SCENARIOStandard

EXAMINER

"An examiner asks you about quantitative MRI techniques for assessing cartilage health beyond standard morphological imaging."

EXCEPTIONAL ANSWER
Both T2 mapping and dGEMRIC (delayed Gadolinium-Enhanced MRI of Cartilage) are compositional MRI techniques that detect biochemical changes in cartilage at the molecular level, potentially identifying degeneration before visible structural damage appears. T2 mapping measures the T2 relaxation time of cartilage voxel by voxel, displayed as a colour-coded map. Normal hyaline cartilage has T2 values of approximately 25-45ms. In early degeneration, disruption of the highly organised collagen fibre network and increased water content cause T2 values to increase — reflected as warmer colours on the map. T2 mapping is non-invasive, does not require contrast, and can be performed on standard clinical scanners with appropriate software. It is most sensitive to collagen fibre integrity and water content changes. dGEMRIC assesses glycosaminoglycan (GAG) content. After intravenous gadolinium and a 90-minute delay with exercise, the contrast agent distributes into cartilage inversely proportional to GAG concentration. Healthy cartilage with high GAG content resists gadolinium penetration (high T1), while degenerate cartilage with depleted GAG allows more gadolinium in (low T1). The resulting T1 map is called the dGEMRIC index. Both techniques are clinically valuable for: screening patients at risk of cartilage degeneration (e.g., after ACL reconstruction), monitoring cartilage repair tissue quality, detecting early osteoarthritis before radiographic changes, and evaluating cartilage health before and after joint-preserving procedures.
KEY POINTS TO SCORE
T2 mapping: detects collagen disruption and water content changes (non-invasive, no contrast)
dGEMRIC: measures GAG content — depleted GAG allows more gadolinium uptake (lower T1/dGEMRIC index)
Both detect biochemical changes BEFORE morphological damage visible on standard MRI
T2 mapping is more widely available; dGEMRIC requires gadolinium and 90-minute delay
Applications: early OA detection, post-repair monitoring, and research
COMMON TRAPS
✗Not knowing what T2 mapping and dGEMRIC measure specifically (collagen vs GAG)
✗Confusing the two techniques
✗Not mentioning the logistic challenges of dGEMRIC (gadolinium, exercise, delay)
✗Overstating clinical applicability — currently not routine in most clinical settings
VIVA SCENARIOChallenging

EXAMINER

"You review a follow-up MRI 12 months after ACI/MACI of the medial femoral condyle. The repair tissue is hyperintense on PD-FS compared to the surrounding native cartilage."

EXCEPTIONAL ANSWER
Hyperintense signal in the repair tissue on PD fat-suppressed images compared to native cartilage suggests the repair tissue has more fibrocartilaginous composition rather than mature hyaline cartilage. Native hyaline cartilage has intermediate signal on PD-FS; true hyaline repair should be isointense. Hyperintensity suggests increased water content and less organised collagen architecture, which may represent: immature repair tissue still undergoing remodelling (the repair tissue continues to mature for up to 24 months after ACI), predominantly fibrocartilage rather than hyaline repair, or early graft deterioration. Using the MOCART scoring system, I would assess: (1) Fill grade — is the defect completely filled, underfilled, or overfilled? Incomplete fill suggests graft failure; hypertrophy may indicate reactive fibrocartilage. (2) Integration — is there complete integration with the surrounding native cartilage or is there a visible cleft? Persistent clefts suggest poor incorporation and risk of delamination. (3) Surface — is the surface smooth and flush with the surrounding cartilage, or is it irregular/fibrillated? An irregular surface increases the risk of mechanical symptoms. (4) Signal intensity — the hyperintensity noted is a concern but at 12 months may still represent immature tissue. (5) Subchondral bone — is the subchondral lamina intact, or is there overgrowth or cyst formation? Subchondral bone changes are associated with worse outcomes. (6) Effusion — persistent effusion may indicate mechanical or inflammatory issues. I would recommend clinical correlation and repeat MRI at 24 months to assess maturation. If the signal normalises, the repair is maturing. If hyperintensity persists or worsens with other MOCART deterioration, revision may be needed.
KEY POINTS TO SCORE
Hyperintensity on PD-FS suggests fibrocartilage rather than mature hyaline repair
At 12 months, repair tissue may still be maturing — reassess at 24 months
MOCART score provides standardised assessment: fill, integration, surface, signal, bone, effusion
Fill grade and integration are the strongest predictors of clinical outcome
If signal normalises over time, indicates maturation; persistent change suggests failure
COMMON TRAPS
✗Interpreting hyperintense signal at 12 months as definitive graft failure (too early to conclude)
✗Not knowing the MOCART scoring system
✗Not assessing subchondral bone changes (important prognostic indicator)
✗Not recommending follow-up MRI if findings are equivocal

MRI Cartilage Assessment — Exam Day Reference

High-Yield Exam Summary

Optimal Sequences

  • •PD fat-suppressed: standard morphological cartilage sequence
  • •3D GRE (SPGR/FLASH/DESS): thin isotropic slices for quantitative mapping
  • •MR arthrography: improves partial-thickness defect detection (85-92% sensitivity)
  • •3T preferred over 1.5T for cartilage assessment

Outerbridge MRI Grading

  • •Grade 0: Normal cartilage
  • •Grade 1: Signal change, intact surface (softening)
  • •Grade 2: Partial-thickness less than 50% depth
  • •Grade 3: Partial-thickness more than 50% depth or full-thickness without bone
  • •Grade 4: Full-thickness with exposed subchondral bone

Treatment by Defect Size

  • •Less than 2cm²: Microfracture (fibrocartilage result)
  • •1-4cm²: OATS (true hyaline cartilage, donor site morbidity)
  • •More than 2-4cm²: ACI/MACI (hyaline-like repair, two-stage)
  • •Always address alignment (HTO), meniscal status, and ligament stability

Quantitative Techniques

  • •T2 mapping: collagen integrity and water content (non-invasive, no contrast)
  • •dGEMRIC: GAG content (requires IV gadolinium + 90-min delay)
  • •T1rho: proteoglycan content (research, not widely available)
  • •All detect biochemical changes BEFORE morphological damage

MOCART Score (Post-Repair)

  • •Fill grade, Integration, Surface, Signal, Bone interface, Effusion
  • •Isointense signal to native cartilage = best outcome
  • •Hyperintense signal = more fibrocartilaginous or immature
  • •Fill grade and integration are strongest outcome predictors
Quick Stats
Reading Time70 min
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