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Corrosion Mechanisms in Orthopaedic Implants

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Corrosion Mechanisms in Orthopaedic Implants

Types of corrosion, electrochemistry, metal ion release, ALVAL, and clinical implications for orthopaedic implants

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Updated: 2025-12-25
High Yield Overview

CORROSION MECHANISMS IN ORTHOPAEDIC IMPLANTS

Electrochemical Degradation | Metal Ion Release | ALVAL | Implant Failure

4 Typesgalvanic, crevice, pitting, fretting
pH 3-4in crevice corrosion sites
1-100 ppbnormal serum metal ions
10-foldelevation in failed MoM hips

Four Major Types of Corrosion

Galvanic
PatternDissimilar metals in contact
TreatmentCoCr/Ti couples
Crevice
PatternOxygen depletion in gaps
TreatmentModular junctions
Pitting
PatternLocalized breakdown of passivation
TreatmentChloride exposure
Fretting
PatternMicro-motion plus corrosion
TreatmentTapers, poly wear

Critical Must-Knows

  • Corrosion is electrochemical degradation of metal in physiological environment
  • Passivation layer (TiO2, Cr2O3) protects implants - breakdown causes corrosion
  • MACC (mechanically-assisted crevice corrosion) is key mechanism at modular junctions
  • ALVAL (aseptic lymphocyte-dominated vasculitis-associated lesion) from metal hypersensitivity
  • MoM hip failures primarily from taper corrosion, not bearing surface wear

Examiner's Pearls

  • "
    Body fluid is corrosive: 0.9% NaCl, pH 7.4, 37°C, proteins
  • "
    Mixed metal couples (CoCr/Ti) have higher galvanic corrosion than matched materials
  • "
    Serum metal ions: Cobalt and chromium levels monitor MoM hips
  • "
    Taper assembly: clean, dry, single impaction reduces fretting corrosion

Critical Corrosion Exam Points

Electrochemical Process

Oxidation-reduction reaction. Metal loses electrons (oxidation: M → M+ + e-) at anode. Electrons flow to cathode where reduction occurs (O2 + 2H2O + 4e- → 4OH-). Passivation layer prevents this.

MACC at Modular Tapers

Mechanically-Assisted Crevice Corrosion is primary failure mode in modular hip implants. Micro-motion disrupts passivation + crevice environment creates low pH = accelerated corrosion.

ALVAL and Metal Hypersensitivity

Type IV delayed hypersensitivity to metal ions. Aseptic lymphocyte-dominated vasculitis causes soft tissue destruction (pseudotumor). Cobalt and chromium ions from corrosion products.

Prevention Strategies

Avoid mixed metals (match CoCr with CoCr), proper taper assembly (clean/dry/single impaction), use highly polished surfaces, consider ceramic heads to eliminate taper corrosion.

Clinical Imaging

Trunnion Surface Microscopy

5-panel SEM images of hip femoral taper trunnion surfaces
Click to expand
Scanning electron microscopy (SEM) of femoral taper trunnion surfaces demonstrating machining marks and surface characteristics. (A) TMZF alloy at 35x magnification. (B) Ti-6Al-4V at 100x showing machining grooves. (C-E) Various materials at different magnifications showing surface topography relevant to fretting corrosion and MACC mechanisms.Credit: Kurtz SM et al. Clin Orthop Relat Res 2013 (CC BY 4.0)

At a Glance

Corrosion is the electrochemical degradation of orthopaedic implants in the physiological environment (0.9% NaCl, pH 7.4, 37°C, proteins), occurring when the protective passivation layer (TiO₂, Cr₂O₃) breaks down. Four major corrosion types exist: Galvanic (dissimilar metal couples, e.g., CoCr/Ti), Crevice (oxygen depletion in gaps creating acidic pH 3-4), Pitting (localized passivation breakdown from chloride ions), and Fretting (micro-motion disrupting oxide layer). MACC (mechanically-assisted crevice corrosion) at modular taper junctions is the primary failure mechanism in modern hip implants, as micro-motion disrupts passivation within the crevice environment. Metal ion release leads to ALVAL (aseptic lymphocyte-dominated vasculitis-associated lesion), a Type IV delayed hypersensitivity reaction causing pseudotumor formation—serum cobalt and chromium levels monitor MoM hip patients. Prevention strategies include avoiding mixed metal couples, proper taper assembly (clean, dry, single impaction), polished surfaces, and ceramic femoral heads to eliminate head-taper corrosion.

Mnemonic

GCPFTypes of Corrosion

G
Galvanic
Dissimilar metals - electron flow from less noble to more noble
C
Crevice
Oxygen depletion in gaps creates acidic environment
P
Pitting
Localized breakdown of passivation layer
F
Fretting
Micro-motion disrupts passivation plus mechanical wear

Memory Hook:Get Careful, Prevent Failure - know your corrosion types!

Mnemonic

CHAMPSFactors Accelerating Corrosion

C
Chloride ions
Aggressive anion in body fluid attacks passivation
H
High stress
Stress corrosion cracking - tensile stress plus corrosive environment
A
Acidic pH
Low pH in crevices (pH 3-4) dissolves passivation layer
M
Motion (micro)
Fretting disrupts protective oxide layer
P
Proteins
Organic molecules affect corrosion kinetics
S
Surface roughness
Rough surfaces more susceptible than polished

Memory Hook:CHAMPS accelerate corrosion - control these factors!

Mnemonic

ALVALALVAL Features

A
Aseptic
Not infection - inflammatory reaction to metal debris
L
Lymphocyte-dominated
T-cell mediated Type IV hypersensitivity
V
Vasculitis-associated
Perivascular lymphocytic infiltration
A
Associated with metal
Cobalt and chromium ions from corrosion
L
Lesion (pseudotumor)
Soft tissue mass with tissue necrosis

Memory Hook:ALVAL describes the pathology of metal hypersensitivity reactions!

Overview and Electrochemistry

Corrosion is the electrochemical degradation of metallic materials in their environment. In orthopaedic implants, this occurs when metals are exposed to the aggressive physiological environment: aqueous solution with chloride ions (0.9% NaCl), pH 7.4, temperature 37°C, and organic molecules.

The body is a hostile environment for metals:

  • Chloride ions (aggressive anions) attack passivation layers
  • Proteins and amino acids affect electrochemical reactions
  • Cyclic mechanical loading creates stress and micro-motion
  • Oxygen gradients develop in crevices and gaps

Understanding corrosion mechanisms is essential because metal ion release can cause:

  1. Implant mechanical failure - material loss weakens structure
  2. Metal hypersensitivity - Type IV delayed hypersensitivity (ALVAL)
  3. Local tissue toxicity - soft tissue necrosis and pseudotumor
  4. Systemic metal elevation - unclear long-term effects

Electrochemical Principles

Oxidation at Anode

Metal loses electrons and goes into solution as ions:

M → M^n+ + ne^-

This is the corrosion reaction. Metal atoms become ions in solution (metal ion release).

Reduction at Cathode

Electrons are consumed in reduction reaction:

O2 + 2H2O + 4e^- → 4OH^-

Oxygen is reduced to hydroxyl ions. This completes the electrochemical circuit.

Passivation: The Key Defense

All orthopaedic metals (titanium, stainless steel, cobalt-chromium) rely on a thin oxide layer for corrosion resistance:

  • Titanium: Forms TiO2 layer (very stable, rapid self-healing)
  • Stainless steel: Forms Cr2O3 layer (chromium oxide)
  • Cobalt-chromium: Forms Cr2O3 layer (chromium oxide)

This passivation layer is typically 2-10 nm thick and prevents metal from contacting the corrosive environment. Corrosion occurs when passivation is disrupted.

Why Titanium is Corrosion Resistant

Titanium forms a tenacious TiO2 passivation layer that is extremely stable and self-healing - if scratched, it reforms in milliseconds in the presence of oxygen. This makes titanium highly corrosion-resistant despite being a reactive metal thermodynamically. CoCr relies on Cr2O3 which is less robust.

Principles and Mechanisms of Corrosion

Galvanic Corrosion

Galvanic Corrosion Mechanism

Occurs when two dissimilar metals are in electrical contact in an electrolyte. The less noble (more anodic) metal corrodes preferentially.

Galvanic series in physiological saline (most noble to least noble):

  1. Platinum (most noble - least corrodes)
  2. Cobalt-chromium alloys
  3. Titanium alloys
  4. Stainless steel 316L
  5. Magnesium (least noble - most corrodes)
Metal CoupleAnode (Corrodes)Cathode (Protected)Clinical Example
CoCr head / Ti stemTitanium stemCoCr headModular hip taper junction
CoCr / Stainless steelStainless steelCoCrMixed implants (rare)
CoCr / CoCrNeither (matched)Neither (matched)Preferred combination

Key principle: The larger the potential difference between metals (farther apart in galvanic series), the greater the corrosion rate of the anodic metal.

This principle explains why galvanic corrosion occurs at modular taper junctions in hip implants.

CoCr/Ti Modular Taper Corrosion

Scenario: CoCr femoral head on Ti alloy stem (modular hip)

Mechanism:

  1. CoCr is more noble than Ti in physiological environment
  2. At taper junction, Ti acts as anode and CoCr as cathode
  3. Ti oxidizes: Ti → Ti^4+ + 4e^-
  4. Micro-motion disrupts Ti passivation layer
  5. Galvanic current accelerates Ti corrosion
  6. Black debris accumulation at taper (Ti oxide and Cr oxide)

Evidence: Retrieval studies show worse corrosion at CoCr/Ti tapers than CoCr/CoCr tapers.

Prevention:

  • Match materials (CoCr on CoCr preferred)
  • Proper taper assembly (clean, dry, single impaction)
  • Minimize micro-motion (adequate taper engagement)

This demonstrates the clinical importance of galvanic corrosion in implant selection.

Crevice Corrosion

Definition: Localized corrosion within shielded areas (crevices, gaps) where oxygen is depleted.

Crevice Corrosion Development

Phase 1Initial State

Crevice exists between surfaces (modular taper, plate-bone interface). Initially passive.

Phase 2Oxygen Depletion

Oxygen consumed in crevice faster than it can diffuse in. Oxygen gradient develops - low inside crevice.

Phase 3pH Drop

Metal oxidation continues: M → M^n+ + ne^-. Hydrolysis: M^n+ + H2O → MOH + H^+. Produces H^+ ions. pH drops to 3-4 in crevice.

Phase 4Passivation Breakdown

Low pH dissolves protective oxide layer. Chloride ions migrate into crevice (charge balance). Acidic chloride environment is highly aggressive.

Phase 5Autocatalytic Corrosion

Corrosion accelerates and becomes self-sustaining. Metal ion release increases. Crevice pH stays low (autocatalytic).

Clinical sites of crevice corrosion:

  • Modular taper junctions (head-neck, neck-stem)
  • Screw-plate interfaces
  • Plate-bone interfaces
  • Modular knee tibial tray interfaces

MACC: Mechanically-Assisted Crevice Corrosion

When micro-motion is superimposed on crevice corrosion, the result is MACC:

  • Micro-motion continuously disrupts passivation layer
  • Fresh metal exposed to aggressive crevice environment
  • Mechanical wear debris plus corrosion products
  • Synergistic effect: corrosion rate much higher than either alone

MACC is the primary mechanism of modular taper corrosion in hip implants.

MACC at Modular Tapers

MACC is the leading cause of modular hip taper failures. Risk factors: large femoral heads (higher torque), offset head position (increased moment arm), patient factors (high BMI, activity). Prevention: proper assembly technique, avoid mixed metals, consider ceramic heads.

Pitting Corrosion

Definition: Highly localized breakdown of passivation creating small pits that propagate deep into metal.

Mechanism:

  1. Passivation layer has microscopic defect (inclusion, scratch)
  2. Chloride ions adsorb at defect site
  3. Local passivation breakdown creates micro-anode
  4. Pit propagates inward (autocatalytic like crevice)
  5. Small surface opening, deep penetration
  6. Can act as stress concentration site for fatigue crack initiation

Why chloride is aggressive: Cl^- is small anion that penetrates oxide layer and prevents re-passivation.

Clinical relevance:

  • Less common than fretting/crevice in orthopaedics
  • Can occur on stainless steel more than Ti or CoCr
  • Pits act as stress risers → fatigue crack initiation
  • Surface finishing reduces susceptibility

Fretting Corrosion

Definition: Combined mechanical wear and corrosion from small amplitude oscillatory motion between surfaces.

Mechanism:

  1. Micro-motion between surfaces (typically less than 100 microns)
  2. Passivation layer abraded away mechanically
  3. Fresh metal exposed to corrosive environment
  4. Oxidizes rapidly, forms debris
  5. Debris trapped between surfaces (third-body wear)
  6. Cycle repeats - synergistic mechanical + chemical degradation
FeaturePure WearPure CorrosionFretting Corrosion
MechanismMechanical removalChemical dissolutionSynergistic mech + chem
Motion requiredYes (sliding)NoYes (micro-motion)
Passivation roleNot relevantCriticalRepeatedly disrupted
DebrisMetallic particlesOxide/ionsOxide particles + ions
RateLinear with cyclesTime-dependentAccelerated (synergy)

Clinical examples:

  • Modular tapers: Fretting corrosion is dominant wear mode
  • Polyethylene backside: Fretting between poly and tibial tray
  • Screw-plate interfaces: Micro-motion causes fretting
  • Cerclage wires: Fretting against bone or plate

Visual appearance: Black debris (metal oxide particles) characteristic of fretting corrosion.

This completes the description of fretting mechanisms in orthopaedic implants.

Metal Ion Release and Biological Effects

Metal Ion Release Mechanisms

When corrosion occurs, metal ions are released into surrounding tissues and systemic circulation.

MetalNormal Serum LevelThreshold for ConcernSource of Elevation
Cobalt (Co)Less than 1 ppbGreater than 5 ppbCoCr implant corrosion, MoM bearing
Chromium (Cr)Less than 1 ppbGreater than 5 ppbCoCr implant corrosion
Titanium (Ti)Less than 5 ppbNo established thresholdTi implant corrosion (rare)
Nickel (Ni)Less than 1 ppbGreater than 5 ppbStainless steel corrosion

Routes of distribution:

  1. Local tissues - highest concentration, direct toxicity
  2. Regional lymph nodes - metal particles transported by macrophages
  3. Systemic circulation - ions absorbed into bloodstream
  4. Distant organs - liver, spleen, kidney accumulation

Biological Effects

Local tissue effects:

  • Metallosis: Macroscopic metal staining of tissues (black/gray discoloration)
  • Aseptic lymphocytic vasculitis-associated lesion (ALVAL): Type IV hypersensitivity
  • Pseudotumor: Soft tissue mass with necrosis, not true neoplasm
  • Osteolysis: Particle-induced bone resorption

ALVAL Pathophysiology:

ALVAL represents a Type IV delayed hypersensitivity reaction to metal ions:

ALVAL Development

Step 1Metal Ion Release

Corrosion releases Co and Cr ions into tissues.

Step 2Hapten Formation

Metal ions bind to proteins, creating metal-protein complexes (haptens).

Step 3T-Cell Sensitization

Antigen-presenting cells present hapten to T-cells. T-cells become sensitized (priming phase).

Step 4Re-exposure

Continued metal release re-exposes sensitized T-cells.

Step 5Immune Response

T-cells recruit macrophages and lymphocytes. Perivascular lymphocytic infiltration. Tissue destruction and necrosis.

Histology of ALVAL:

  • Perivascular lymphocytic infiltration
  • Aseptic fibrinoid necrosis
  • Diffuse lymphocytic infiltrate
  • Absence of infection

Clinical presentation:

  • Pain (most common)
  • Soft tissue mass (pseudotumor on imaging)
  • Instability or dislocation (soft tissue destruction)
  • Elevated serum metal ions (Co and Cr)

MoM Hip Surveillance

Monitor all MoM hip patients with serum cobalt and chromium levels annually. Threshold for concern: greater than 7 ppb for either metal. MRI for soft tissue evaluation if elevated or symptomatic. Consider revision if progressive elevation or pseudotumor.

Systemic Effects

Unclear long-term consequences:

  • Cobalt: Potential cardiomyopathy, thyroid dysfunction at very high levels
  • Chromium: Theoretical carcinogenic risk (Cr^6+ form)
  • Nickel: Known allergen, hypersensitivity common

Current evidence: Most patients with moderate metal elevation (5-10 ppb) do not have systemic symptoms, but long-term data limited.

This section completes the discussion of metal ion biological effects.

Anatomy of Corrosion Sites

Key Anatomical Sites of Implant Corrosion

Head-Neck Taper Junction

Most critical corrosion site in modern THA

  • Morse taper connection between femoral head and stem
  • Contact area: 50-150 mm² depending on design
  • Crevice geometry creates ideal environment for MACC
  • Micro-motion disrupts protective oxide layer

Anatomy:

  • Taper angle typically 5°40' (Morse taper)
  • Roughness affects seating and corrosion
  • Material couple (CoCr/Ti) critical factor

Stem-Sleeve Junction

Modular neck systems

  • Additional taper connection for neck modularity
  • Double modular systems have two corrosion sites
  • Higher failure rates led to some recalls

Key anatomy:

  • Neck angle and offset adjustability
  • Increased corrosion debris with two tapers
  • Greater surface area for metal ion release

Implant Regions Prone to Corrosion

LocationCorrosion TypeClinical Significance
Head-neck taperCrevice + fretting (MACC)Primary failure site in modular THA
Screw-plate interfaceCrevice + frettingHardware loosening, pain
Poly backsideFretting + third-body wearOsteolysis, loosening
MoM bearing surfaceTribocorrosionMetal ion release, ALVAL
Stem surfacePitting (rare)Usually minor clinical impact

Exam Pearl

FRACS Viva Point: "Why is the head-neck taper the most important corrosion site?" Answer: Crevice geometry + micro-motion creates MACC environment. The combination of oxygen depletion in the crevice (low pH 3-4), cyclic loading causing micro-motion, and mixed metal couples maximizes corrosion.

Understanding anatomical sites of corrosion helps identify at-risk implants and plan revision surgery.

Microscopic Anatomy of Corrosion

Passivation Layer Structure

Protective oxide layer:

  • Titanium: TiO₂ layer (2-10 nm thick)
  • CoCr: Cr₂O₃ layer (1-3 nm thick)
  • Self-healing in presence of oxygen

Layer characteristics:

  • Amorphous structure
  • Semiconductor properties
  • Dissolves in acidic environment (crevice)
  • Disrupted by mechanical abrasion

Crevice Microenvironment

Within the taper crevice:

  • Oxygen depleted (consumed at entrance)
  • pH drops to 3-4 (vs body pH 7.4)
  • Chloride ion concentration increases
  • Proteins denature and deposit

Electrochemistry:

  • Anodic reaction: M → M⁺ + e⁻
  • Metal dissolution accelerated
  • Autocatalytic process

Taper Design Factors

Design FeatureEffect on CorrosionOptimal Design
Taper angleSmaller angle = more contact, less micro-motion5°40' standard Morse taper
Taper lengthLonger = more contact area, better stabilityLonger tapers reduce fretting
Surface roughnessToo smooth = poor seating; too rough = frettingOptimal Ra 0.4-0.8 μm
Material matchMatched metals eliminate galvanic componentCoCr on CoCr preferred
Head diameterLarger head = more taper stress = more frettingKeep 36mm or less

Tissue Response at Corrosion Sites

ALVAL Histopathology

Histological features:

  • Dense perivascular lymphocytic infiltrate
  • T-cell predominant (Type IV reaction)
  • Vascular endothelial damage
  • Necrotic tissue with metal debris

Gross appearance:

  • Gray-black staining of tissues
  • Pseudotumor (soft tissue mass)
  • Fluid collection (sterile effusion)

Metal Debris Distribution

Local tissue accumulation:

  • Macrophages engulf metal particles
  • Metal ions bind to proteins
  • Debris accumulates in pseudocapsule
  • Can extend to bone causing osteolysis

Systemic distribution:

  • Metal ions enter bloodstream
  • Cobalt: neurological, cardiac toxicity
  • Chromium: renal accumulation

The microscopic anatomy of corrosion explains why certain implant designs and materials fail preferentially.

Classification

Four Major Types of Corrosion

Galvanic Corrosion

Definition: Corrosion when two dissimilar metals contact in an electrolyte

Mechanism:

  • Less noble metal = anode (corrodes)
  • More noble metal = cathode (protected)
  • Electron flow from anode to cathode

Clinical example:

  • CoCr head on Ti stem
  • Ti is less noble, corrodes at junction
  • Mixed metal couples show worse outcomes

Crevice Corrosion

Definition: Localized corrosion within shielded areas

Mechanism:

  • Oxygen depleted in crevice
  • pH drops to 3-4 (autocatalytic)
  • Chloride concentration increases
  • Passivation layer dissolves

Clinical example:

  • Modular taper junctions
  • Screw-plate interfaces
  • Under bone cement mantle

Pitting Corrosion

Definition: Highly localized passivation breakdown

Mechanism:

  • Chloride ions attack defects
  • Small surface pit, deep penetration
  • Self-propagating once initiated

Clinical example:

  • Stainless steel implants (most susceptible)
  • Surface contamination sites
  • Rare in Ti and CoCr

Fretting Corrosion

Definition: Mechanical wear + chemical corrosion

Mechanism:

  • Micro-motion disrupts oxide layer
  • Fresh metal exposed and oxidizes
  • Cyclic process with each loading cycle

Clinical example:

  • Modular tapers under load
  • Polyethylene liner backside
  • Screw-plate motion

MACC - The Key Mechanism

Mechanically-Assisted Crevice Corrosion (MACC) combines crevice + fretting corrosion. This is the PRIMARY failure mechanism at modular hip tapers. Micro-motion disrupts passivation within the crevice environment, accelerating metal dissolution.

Classification helps identify specific corrosion mechanisms and guide prevention strategies.

Corrosion Severity Classification

GradeVisual AppearanceMetal Ion LevelsClinical Action
Grade 1 (Mild)Minor discoloration, intact taperLess than 2 ppb Co/CrMonitor, annual review
Grade 2 (Moderate)Black debris, some surface damage2-7 ppb Co/CrIncrease surveillance, imaging
Grade 3 (Severe)Gross material loss, deep pitting7-20 ppb Co/CrConsider revision, MRI for soft tissue
Grade 4 (Catastrophic)Taper fracture, massive debrisGreater than 20 ppb Co/CrUrgent revision required

Goldberg Classification - Taper Corrosion

Type I - Fretting

Characteristics:

  • Burnished appearance
  • Material transfer between surfaces
  • No significant material loss
  • Early stage corrosion

Type II - Crevice

Characteristics:

  • Black debris deposition
  • Localized pitting
  • pH-driven dissolution
  • Moderate material loss

Type III - Mixed

Characteristics:

  • Combined fretting + crevice
  • This is true MACC
  • Most common severe pattern
  • Significant material loss

Type IV - Etching

Characteristics:

  • Generalized surface attack
  • Electrochemical dissolution
  • Severe material loss
  • Often with fatigue failure

Tribocorrosion Classification

TypeDefinitionPrimary Site
Type IWear-accelerated corrosionMoM bearing surfaces
Type IICorrosion-accelerated wearPolyethylene third-body wear
Type IIISynergistic tribocorrosionModular tapers (MACC)

Exam Pearl

FRACS Viva Point: "What distinguishes MACC from simple fretting corrosion?" Answer: MACC occurs specifically in crevice geometry (modular taper) where the crevice creates an acidic, chloride-rich, oxygen-depleted environment that accelerates passive layer breakdown when combined with micro-motion.

Understanding corrosion classification helps grade severity and guide clinical decision-making.

Clinical Implications and Prevention

Failed Metal-on-Metal Hips

Primary failure mode: Taper corrosion, NOT bearing surface wear in most modern MoM failures.

Evidence from retrieval studies:

  • Taper shows severe MACC with debris
  • Bearing surfaces often well-preserved
  • Mixed metal couples (CoCr/Ti) show worse corrosion
  • Large head diameter increases taper mechanical stress

Risk factors for taper corrosion:

  • Large femoral head diameter (greater than 36mm)
  • Increased offset (higher moment arm on taper)
  • High patient BMI and activity level
  • Mixed metal couples (CoCr on Ti)
  • Poor taper assembly (contamination, multiple impacts)

Taper Assembly Technique

Critical steps to minimize MACC:

Rationale:

  • Clean and dry: Contaminants prevent full seating and increase micro-motion
  • Single impaction: Multiple impacts damage taper surface
  • Adequate force: Ensures taper engagement and minimizes micro-motion
  • Matched materials: CoCr on CoCr eliminates galvanic component

Prevention Strategies

StrategyMechanismEffectivenessConsiderations
Ceramic headsEliminates metal taper corrosionExcellentFracture risk (historical concern, rare with modern ceramics)
Matched metalsEliminates galvanic corrosionGoodCoCr on CoCr preferred over CoCr on Ti
Dual mobilityReduces taper mechanical stressGoodAlternative bearing, not directly addressing corrosion
Avoid large headsReduces moment arm on taperModerateMay increase dislocation risk in some patients
Proper assemblyMinimizes micro-motionEssentialClean, dry, single impaction - surgeon dependent

Material selection considerations:

  • Titanium stems: Excellent corrosion resistance but weaker at taper when coupled with CoCr
  • CoCr stems: Stronger taper but heavier, more stiff
  • Ceramic heads: Eliminate taper corrosion but historical fracture concern
  • Modern approach: Ceramic head on Ti stem is popular compromise

This completes the prevention strategies discussion.

Investigations

Serum Metal Ion Testing

Cobalt and Chromium Levels

Primary biomarker for MoM monitoring:

  • Normal: Less than 1 ppb (μg/L)
  • Elevated: 2-7 ppb - increased surveillance
  • Concerning: Greater than 7 ppb - further investigation
  • Critical: Greater than 20 ppb - revision often indicated

Interpretation caveats:

  • Fasting sample (some foods contain metals)
  • Trace element tube (metal-free)
  • Recent activity may elevate levels

Sampling Protocol

Correct technique essential:

  • Fasting morning sample
  • Metal-free (trace element) tube
  • Avoid contamination from needle hub
  • Laboratory with validated assay (ICP-MS)

Frequency:

  • MoM hips: Annual minimum
  • Symptomatic: At presentation
  • Post-revision: 3, 12 months

Imaging for Corrosion-Related Pathology

ModalityFindingsRole
Plain radiographsOsteolysis, implant migration, looseningFirst-line, baseline comparison
MARS MRIPseudotumor, soft tissue necrosis, fluid collectionGold standard for ALVAL
UltrasoundFluid collections, pseudotumorScreening, guided aspiration
CT with MARSBone detail with metal suppressionOsteolysis assessment

Exam Pearl

FRACS Viva Point: "What is MARS MRI?" Answer: Metal Artifact Reduction Sequence MRI uses specialized pulse sequences and post-processing to reduce metal artifact, allowing visualization of periprosthetic soft tissues to detect ALVAL, pseudotumor, and fluid collections.

Serum metal ions and MARS MRI are the cornerstone investigations for suspected corrosion-related pathology.

Advanced Laboratory Testing

Lymphocyte Transformation Testing

Metal hypersensitivity assessment:

  • Tests T-cell reactivity to metal ions
  • Cobalt, chromium, nickel panels
  • Positive result suggests Type IV hypersensitivity

Clinical utility:

  • Pre-operative implant selection (controversial)
  • Post-revision persistent symptoms
  • Research tool, not routine practice

Synovial Fluid Analysis

Joint aspiration findings:

  • Turbid, gray-black fluid = corrosion debris
  • Rule out infection (culture, cell count)
  • Metal ion concentration in fluid very high

Cytology:

  • Macrophages with metal particles
  • Lymphocyte predominance in ALVAL
  • Helps differentiate from infection

Anderson ALVAL Classification (MRI)

TypeMRI FeaturesClinical Significance
Type 1 - CysticThin-walled fluid collectionMay be asymptomatic
Type 2a - Solid benignSolid mass, normal muscle signalOften symptomatic, consider revision
Type 2b - Solid destructiveSolid mass, muscle edema/atrophyRevision indicated, worse prognosis
Type 3 - MixedSolid and cystic componentsVariable prognosis

Intraoperative Assessment

Taper Inspection

Retrieval analysis:

  • Visual scoring of taper corrosion
  • Black debris = corrosion products
  • Measure material loss (weight, volume)
  • Photography for documentation

Tissue Sampling

Histopathology:

  • ALVAL classification (lymphocyte score)
  • Tissue necrosis extent
  • Metal debris quantification
  • Rule out infection (culture, frozen section)

Exam Pearl

Viva Trap: Elevated metal ions alone do NOT mandate revision. Clinical correlation is essential - assess symptoms, imaging, and patient factors. Many patients with moderately elevated levels remain asymptomatic.

Comprehensive investigation combines serology, imaging, and intraoperative assessment for accurate diagnosis.

Management

📊 Management Algorithm
Management algorithm for Corrosion Mechanisms
Click to expand
Management algorithm for Corrosion MechanismsCredit: OrthoVellum

Management Algorithm for Corrosion-Related Pathology

Asymptomatic with Normal Metal Ions

Metal ions less than 2 ppb:

  • Annual clinical review
  • Annual metal ion levels
  • Radiographs every 2 years
  • Patient education on symptoms

No intervention required unless:

  • Symptoms develop
  • Metal ions rise progressively
  • Imaging abnormalities appear

Asymptomatic with Elevated Metal Ions

Metal ions 2-7 ppb:

  • 6-monthly clinical review
  • MARS MRI to assess soft tissues
  • More frequent metal ion monitoring

Consider revision if:

  • Progressive elevation of ions
  • Imaging shows pseudotumor
  • Patient high-demand, long life expectancy

Indications for Revision Surgery

IndicationStrengthTiming
Symptomatic with Co/Cr greater than 7 ppbStrongElective revision planned
Pseudotumor on imaging (Type 2b)StrongSemi-urgent revision
Progressive osteolysisStrongBefore bone loss worsens
Metal ions greater than 20 ppbModerate-strongRevision recommended
Asymptomatic, rising ions 3-7 ppbModerateClose surveillance vs revision

Delay increases complexity. Early revision before extensive soft tissue or bone destruction improves outcomes. Waiting for severe symptoms often means worse tissue damage.

Management depends on symptoms, metal ion levels, imaging findings, and patient factors.

Surveillance Protocol - MoM Hips

Baseline Assessment

History, examination, metal ion levels (Co/Cr), radiographs, and MARS MRI if ions elevated or symptomatic.

Low-Risk Surveillance

Annual metal ions, 2-yearly radiographs, clinical review annually. Continue indefinitely.

Medium-Risk Surveillance

6-monthly metal ions, annual MARS MRI, consider revision discussion.

High-Risk Management

Revision surgery planning, specialist referral, pre-operative optimization.

Non-Operative Management

Activity Modification

Role:

  • Reduce loading cycles (fewer steps)
  • Lower impact activities
  • May reduce metal ion generation

Evidence:

  • Limited - theoretical benefit
  • Does not address underlying pathology
  • May delay inevitable revision

Medical Optimization

Pre-revision optimization:

  • Cardiac assessment if high cobalt
  • Neurological assessment if symptomatic
  • Nutritional status
  • Comorbidity management

Cobalt toxicity concerns:

  • Cardiomyopathy, thyroid dysfunction
  • Visual/hearing impairment
  • Neurological symptoms

Decision-Making Factors

FactorFavors RevisionFavors Surveillance
SymptomsPainful, functional limitationAsymptomatic
Metal ionsGreater than 7 ppb or risingStable less than 2 ppb
ImagingPseudotumor, osteolysisNormal soft tissues
Patient ageYoung, long life expectancyElderly, limited life expectancy
Activity levelHigh demandLow demand
Surgical riskLow operative riskHigh medical comorbidities

Exam Pearl

FRACS Viva Point: "What factors influence your decision to revise a MoM hip?" Answer: Symptoms, metal ion levels and trend, imaging findings (pseudotumor/ALVAL), bone stock, patient age/activity, surgical risk, and alternative implant options. A multidisciplinary approach with shared decision-making is essential.

Individualized management considers the balance between revision surgery risks and consequences of continued corrosion.

Surgical Technique

Revision Surgery for Corrosion-Related Failure

Head Exchange (If Stem Well-Fixed)

Indications:

  • Taper corrosion with well-fixed stem
  • Good bone stock
  • No extensive tissue destruction

Key steps:

  • Dislocate hip, remove head
  • Clean taper thoroughly (dry)
  • Inspect taper for damage
  • New ceramic head on clean, dry taper
  • Or sleeve adapter if taper damaged

Complete Revision

Indications:

  • Loose stem
  • Severe taper damage/fracture
  • Extensive osteolysis
  • Pseudotumor with bone destruction

Key steps:

  • Extended approach for exposure
  • Thorough debridement of necrotic tissue
  • Revise acetabulum if affected
  • New stem with modular options
  • Bone grafting if needed

Soft Tissue Management

Tissue FindingActionRationale
PseudotumorComplete excisionRemove source of inflammation
ALVAL-affected tissueThorough debridementRemove reactive tissue
Metallosis stainingLavage, debride what possibleMay not fully remove all staining
Necrotic abductorsDebride back to viable tissueDocument for prognosis

Exam Pearl

FRACS Viva Point: "How do you manage the taper at revision?" Answer: If taper undamaged: clean thoroughly, dry completely, place ceramic head with single firm impaction. If taper damaged: use a sleeve adapter system or revise the stem.

Careful debridement and appropriate component selection are essential for successful revision.

Approach Considerations

Extensile Approaches

May be required:

  • Large pseudotumors often extend posteriorly
  • Need visualization for complete excision
  • Posterior approach often best access

Options:

  • Extended posterior approach
  • Trochanteric osteotomy if needed
  • Combined approaches for large pseudotumors

Tissue Handling

Intraoperative principles:

  • Document tissue appearance (photos)
  • Send tissue for histology (ALVAL score)
  • Culture (rule out infection)
  • Assess abductor integrity/viability
  • Assess bone stock (classify defects)

Taper Management Options

Taper StatusOptionConsiderations
Pristine taperNew ceramic headClean/dry assembly, single impaction
Minor damageCeramic head with titanium sleeve adapterBypasses damaged taper surface
Significant damageSleeve adapter mandatoryMultiple systems available
Fractured taperStem revision requiredNo salvage possible

Implant Selection at Revision

Bearing Surface Choice

Recommendations:

  • Ceramic-on-ceramic: Eliminates metal ions
  • Ceramic-on-poly (XLPE): Very low wear
  • Metal-on-poly: Acceptable if ceramic taper used

Avoid:

  • Another metal-on-metal bearing
  • Mixed metal taper couples
  • Large metal heads on modular tapers

Stability Considerations

After ALVAL/pseudotumor:

  • Abductor function often compromised
  • Higher dislocation risk
  • Consider dual mobility cup
  • Larger head sizes (within reason)
  • Constrained liner if severe

Reconstruction:

  • May need soft tissue repair
  • Tendon transfers for abductor deficiency
  • Extended rehab protocol

Technical Pearls

Exam Pearl

Key Concept: Revision for corrosion has higher complication rates than routine revision due to tissue destruction. Dislocation rates 10-20% in severe ALVAL cases with abductor damage. Plan for this with bearing choice and soft tissue management.

Meticulous surgical technique addresses both component revision and soft tissue reconstruction.

Complications

Complications of Implant Corrosion

Local Tissue Destruction

ALVAL and Pseudotumor:

  • Soft tissue necrosis around implant
  • Pseudotumor (solid or cystic mass)
  • Abductor muscle destruction
  • Femoral nerve compression (rare)

Bone involvement:

  • Osteolysis from debris
  • Periprosthetic bone loss
  • May compromise revision fixation

Systemic Metal Toxicity

Cobalt toxicity syndrome:

  • Cardiomyopathy (cobalt cardiomyopathy)
  • Thyroid dysfunction
  • Neurological symptoms (peripheral neuropathy)
  • Visual and hearing impairment

Typically with very high levels:

  • Usually greater than 50-100 ppb
  • May be reversible with revision
  • Cardiac monitoring recommended

Complication Severity

ComplicationIncidenceSeverity
ALVAL/pseudotumor5-30% of MoM hipsModerate to severe
Aseptic loosening5-15% (corrosion-related)Moderate
Systemic toxicityLess than 1%Potentially severe
Implant fractureLess than 1%Severe - requires revision
Chronic pain10-20%Variable

Exam Pearl

Exam Viva Point: "What are the systemic effects of cobalt toxicity?" Answer: Cardiomyopathy, hypothyroidism, peripheral neuropathy, and visual/hearing impairment. Usually occurs with very high serum cobalt levels (greater than 50-100 ppb) and may be reversible after revision surgery.

Complications range from local tissue destruction to rare but serious systemic toxicity.

Complications of Revision Surgery

Intraoperative Complications

Increased difficulty:

  • Poor tissue quality for repair
  • Bone loss from osteolysis
  • Difficult exposure (scarring)
  • Bleeding from inflamed tissue

Specific risks:

  • Nerve injury (femoral, sciatic)
  • Fracture (weakened bone)
  • Incomplete debridement

Early Postoperative

Common complications:

  • Dislocation (10-20% with abductor damage)
  • Wound complications
  • Deep vein thrombosis
  • Infection

Contributing factors:

  • Poor tissue healing capacity
  • Metallosis affects wound healing
  • Abductor deficiency

Late Complications

ComplicationRisk FactorsManagement
Recurrent instabilityAbductor deficiency, large tissue resectionConstrained liner, revision, tendon transfer
Persistent symptomsIncomplete debridement, hypersensitivityConsider metal allergy testing, further revision
Recurrent pseudotumorIncomplete excision, new corrosion sourceRe-revision if significant
Functional limitationAbductor weakness, nerve injuryPhysiotherapy, assistive devices

Cobalt Cardiomyopathy

Rare but serious. Cobalt cardiomyopathy presents with heart failure symptoms, dilated cardiomyopathy on echo, and very high serum cobalt. May be reversible with urgent revision and supportive cardiac care. Requires urgent cardiology consultation.

Clinical Features

Presentation:

  • Dyspnea, fatigue, edema
  • Dilated cardiomyopathy on echo
  • May present as acute heart failure
  • Other toxic effects often present

Diagnosis:

  • High serum cobalt (often greater than 100 ppb)
  • Exclude other cardiomyopathy causes
  • ECG changes (conduction abnormalities)

Management

Treatment:

  • Urgent revision surgery
  • Cardiology involvement
  • Standard heart failure management
  • Monitor recovery of cardiac function

Prognosis:

  • Often reversible after source removed
  • Improvement over weeks to months
  • Some patients have residual damage

Exam Pearl

Key Learning: The worst complications are preventable with appropriate surveillance and timely revision. Delay until symptomatic often means worse tissue destruction and higher revision complexity.

Understanding complications guides surveillance protocols and revision decision-making.

Postoperative Care

Post-Revision Surveillance Protocol

Metal Ion Monitoring

Post-revision schedule:

  • 3 months: Baseline after revision
  • 12 months: Assess decline
  • Annually: Until levels normalize

Expected trajectory:

  • Rapid initial decline (first 3-6 months)
  • Gradual normalization over 1-2 years
  • May not return to normal in all patients

Clinical Review

Follow-up schedule:

  • 6 weeks: Wound check, weight-bearing
  • 3 months: Function assessment
  • 6 months: Metal ions, radiographs
  • 12 months: Comprehensive review
  • Annually: Ongoing surveillance

Assess at each visit:

  • Hip function (Oxford Hip Score)
  • Stability (dislocation precautions)
  • Symptoms (pain, clicking)

Rehabilitation Considerations

PhaseFocusSpecial Considerations
Week 0-6Protected weight-bearing, precautionsExtended hip precautions if abductor damage
Week 6-12Strengthening, gait trainingFocus on abductor rehabilitation
Month 3-6Progressive loading, functionMay need abductor brace if weak
Month 6+Return to activitiesSome permanent limitations expected

Exam Pearl

Exam Viva Point: "How do you follow up a patient after revision for ALVAL?" Answer: Serial metal ion levels (3, 12 months then annual), clinical review for function and stability, imaging if symptoms, and extended hip precautions due to abductor compromise.

Close surveillance ensures early detection of complications and guides rehabilitation.

Systemic Toxicity Monitoring

Cardiac Surveillance

If pre-revision cobalt toxicity:

  • Baseline echocardiogram
  • Cardiology follow-up
  • Serial monitoring of function
  • Usually improves after revision

Resolution expected:

  • Cardiac function often recovers
  • May take 6-12 months
  • Some patients have residual dysfunction

Neurological Recovery

Peripheral neuropathy:

  • Document pre-revision baseline
  • May improve after revision
  • Some sensory loss may persist
  • Nerve conduction studies if severe

Other symptoms:

  • Thyroid function monitoring
  • Visual/auditory assessment if affected
  • Most symptoms reversible

Persistent Symptoms

SymptomPossible CauseInvestigation
Persistent painIncomplete debridement, instability, infectionMRI, aspiration
Recurrent massIncomplete excision, new corrosionMARS MRI, metal ions
Elevated metal ionsResidual debris, new corrosion sourceImaging review, consider re-revision
InstabilityAbductor deficiency, component positionExamination, imaging, consider constrained revision

Long-Term Considerations

Implant Longevity

Revision implant survival:

  • Generally good if adequate debridement
  • May be compromised by bone loss
  • Depends on component choice
  • Ceramic bearings reduce re-corrosion risk

Functional Outcome

Expected outcomes:

  • Improvement in pain and function
  • May not return to pre-failure baseline
  • Abductor weakness often permanent
  • Some patients have persistent limitations

Vigilant postoperative care optimizes outcomes and detects complications early.

Outcomes

Outcomes After Revision for Corrosion

Metal Ion Decline

Post-revision trajectory:

  • Mean 50-70% reduction at 12 months
  • Normalization (less than 2 ppb) in most patients
  • Some patients have persistent elevation
  • Rate of decline varies

Factors affecting decline:

  • Extent of initial metallosis
  • Completeness of debridement
  • New implant bearing choice

Functional Outcomes

Clinical scores:

  • Oxford Hip Score: Significant improvement
  • Harris Hip Score: Mean improvement 20-30 points
  • Patient satisfaction: 70-85%

Limitations:

  • Often do not reach primary THA levels
  • Abductor weakness limits function
  • Some persistent pain common

Outcome Predictors

FactorBetter OutcomeWorse Outcome
Pre-revision tissue damageMinimal pseudotumorExtensive destruction
Abductor statusIntact abductorsNecrotic/absent abductors
Bone stockMinimal osteolysisSevere bone loss
Timing of revisionEarly (before extensive damage)Late (symptomatic, severe ALVAL)
Metal ion levelsModerately elevatedVery high (greater than 50 ppb)

Exam Pearl

Exam Viva Point: "What determines outcome after revision for ALVAL?" Answer: Pre-revision tissue destruction (especially abductor status), bone stock, timing of revision (earlier is better), and completeness of debridement. Patients with extensive destruction have worse functional outcomes.

Early revision before extensive tissue destruction optimizes outcomes.

Re-Revision Rates

Study/RegistryRe-revision RateNotes
AOANJRR (MoM revision)10-15% at 5 yearsHigher than primary revision rates
UK NJR (MoM revision)12-18% at 5 yearsDepends on reason for primary revision
With severe ALVAL15-25% at 5 yearsAbductor damage increases dislocation
Head exchange only5-10% at 5 yearsIf stem well-fixed, good outcome

Complication Rates

Dislocation

Post-revision rates:

  • 5-10% if minimal abductor damage
  • 15-25% with significant abductor loss
  • Constrained liners reduce but not eliminate

Risk factors:

  • Abductor muscle necrosis
  • Large tissue resection
  • Previous dislocation
  • Non-compliance with precautions

Infection

Post-revision rates:

  • 2-5% (higher than primary THA)
  • Compromised tissue increases risk
  • Prolonged surgery duration

Prevention:

  • Antibiotic prophylaxis
  • Meticulous technique
  • Avoid excessive tissue handling

Long-Term Survivorship

1-Year Outcomes

Most patients show significant pain and function improvement. Metal ions decline. Dislocation risk highest in first 6 months.

5-Year Outcomes

85-90% implant survival in most series. Functional outcomes stable. Some patients require re-revision for instability or other causes.

10-Year Outcomes

Limited data available. Appears comparable to other revision scenarios. Bone stock preservation at initial revision important.

Exam Pearl

Key Learning: Revision outcomes for corrosion are generally good but depend heavily on pre-revision tissue and bone damage. Early intervention preserves tissue and improves long-term results.

Outcome data supports early revision before extensive tissue destruction occurs.

Evidence Base

Gilbert et al - Corrosion at Modular Interfaces in Total Hip Arthroplasty

3
Gilbert JL, Buckley CA, Jacobs JJ • J Bone Joint Surg Am (2012)
Key Findings:
  • MACC (mechanically-assisted crevice corrosion) is primary mechanism at tapers
  • Mixed metal couples (CoCr/Ti) show significantly more corrosion than matched materials
  • Large femoral heads increase mechanical forces on taper, accelerating corrosion
  • Proper assembly technique (clean, dry, single impaction) critical to minimize micro-motion
Clinical Implication: MACC is the key failure mechanism in modular hip implants. Material selection (avoid mixed metals) and assembly technique are critical prevention strategies.
Limitation: Retrieval study - cannot establish causation, but mechanisms well-supported by electrochemical theory.

Langton et al - Blood Metal Ion Concentrations After Hip Resurfacing

3
Langton DJ, Jameson SS, Joyce TJ, et al • J Bone Joint Surg Br (2010)
Key Findings:
  • Cobalt and chromium levels elevated 10-100 fold in failed MoM hips vs normal
  • Threshold of 7 ppb for either metal associated with increased revision risk
  • Levels correlate with wear/corrosion at bearing and taper
  • Asymptomatic patients can have elevated levels - routine surveillance needed
Clinical Implication: Serum metal ions are biomarkers for MoM hip corrosion/wear. Annual surveillance with Co and Cr levels recommended. Threshold 7 ppb warrants further investigation.
Limitation: Correlation with revision risk, but optimal threshold for intervention debated.

Willert et al - Metal-on-Metal Bearings and Hypersensitivity

4
Willert HG, Buchhorn GH, Fayyazi A, et al • J Bone Joint Surg Am (2005)
Key Findings:
  • First description of ALVAL in failed MoM hips
  • Histology shows aseptic lymphocyte-dominated vasculitis, not infection
  • Type IV delayed hypersensitivity to metal debris (Co, Cr)
  • Soft tissue destruction can be extensive (pseudotumor)
Clinical Implication: ALVAL is distinct pathological entity from traditional aseptic loosening. Metal hypersensitivity can cause catastrophic soft tissue destruction requiring revision.
Limitation: Case series; prevalence of ALVAL in asymptomatic MoM patients unclear.

Exam Viva Scenarios

Practice these scenarios to excel in your viva examination

VIVA SCENARIOStandard

Scenario 1: Types of Corrosion

EXAMINER

"Examiner asks: Describe the four main types of corrosion in orthopaedic implants and give a clinical example of each."

EXCEPTIONAL ANSWER
The four main types of corrosion in orthopaedic implants are galvanic, crevice, pitting, and fretting corrosion. First, galvanic corrosion occurs when two dissimilar metals are in electrical contact in an electrolyte. The less noble metal acts as the anode and corrodes preferentially. A clinical example is a cobalt-chromium femoral head articulating with a titanium stem at the modular taper junction - titanium is less noble than CoCr and will corrode at the interface. Second, crevice corrosion is localized corrosion within shielded areas such as gaps or crevices where oxygen is depleted. This creates an acidic environment with pH as low as 3-4 that dissolves the protective passivation layer. This occurs at modular taper junctions and screw-plate interfaces. When micro-motion is added, this becomes MACC - mechanically-assisted crevice corrosion - which is the primary failure mode of modular hip tapers. Third, pitting corrosion is highly localized breakdown of passivation creating small pits that penetrate deep into the metal. Chloride ions in body fluid attack microscopic defects in the oxide layer. This is more common in stainless steel than titanium or CoCr. Fourth, fretting corrosion combines mechanical wear and chemical corrosion from small amplitude oscillatory motion. The micro-motion continuously disrupts the passivation layer, exposing fresh metal that rapidly oxidizes. This produces characteristic black debris seen at modular tapers and polyethylene backside wear.
KEY POINTS TO SCORE
Galvanic: dissimilar metals (CoCr/Ti taper)
Crevice: oxygen depletion in gaps (MACC at tapers)
Pitting: localized passivation breakdown (chloride attack)
Fretting: micro-motion plus corrosion (black debris)
All involve disruption of protective passivation layer
COMMON TRAPS
✗Confusing fretting with general wear (fretting is specific micro-motion plus corrosion)
✗Not mentioning MACC as the key clinical mechanism
✗Missing the electrochemical basis (oxidation-reduction)
LIKELY FOLLOW-UPS
"What is MACC and why is it important?"
"How do you prevent taper corrosion?"
"What is the galvanic series?"
VIVA SCENARIOChallenging

Scenario 2: ALVAL and Metal Hypersensitivity

EXAMINER

"Patient with painful MoM hip has serum cobalt 45 ppb, chromium 38 ppb, and MRI shows large pseudotumor. Examiner asks about pathophysiology and management."

EXCEPTIONAL ANSWER
This patient has ALVAL - aseptic lymphocyte-dominated vasculitis-associated lesion - which represents a Type IV delayed hypersensitivity reaction to metal debris. The pathophysiology involves several steps: First, corrosion at the bearing surface or more commonly the modular taper releases cobalt and chromium ions into the surrounding tissues. These metal ions bind to proteins forming metal-protein complexes called haptens. Antigen-presenting cells process these haptens and present them to T-cells, causing sensitization. Upon re-exposure to metal debris, the sensitized T-cells mount an immune response, recruiting macrophages and lymphocytes. This results in perivascular lymphocytic infiltration and tissue necrosis. The pseudotumor on MRI represents a soft tissue mass with extensive tissue destruction, not a true neoplasm. The markedly elevated serum metal levels over 5 ppb indicate significant ongoing corrosion and metal release. Management requires revision surgery. The goals are to remove the source of metal debris, debride necrotic tissue, and restore hip stability with a non-metal bearing. At revision, I would perform complete synovectomy, debride the pseudotumor, and revise to a ceramic-on-polyethylene or ceramic-on-ceramic bearing to eliminate metal ion release. The modular taper should be inspected - if corroded, the stem may need revision. I would send tissue for histology to confirm ALVAL and exclude infection. Postoperatively, I would monitor serum metal levels which should decline over 6-12 months, though complete normalization may take years. The prognosis after revision depends on the extent of soft tissue destruction - abductor damage may result in persistent limp and Trendelenburg gait.
KEY POINTS TO SCORE
ALVAL = Type IV delayed hypersensitivity to metal debris
Metal ions bind proteins forming haptens → T-cell sensitization
Pseudotumor = soft tissue mass with necrosis (not neoplasm)
Serum metals over 5 ppb concerning, over 7 ppb warrants action
Revision to non-metal bearing (ceramic head) essential
Debride pseudotumor, inspect/revise taper if corroded
Monitor metal levels post-revision (decline expected)
COMMON TRAPS
✗Calling it infection (it's aseptic - no bacteria)
✗Not recognizing this requires revision (symptomatic pseudotumor is surgical)
✗Revising to another MoM bearing (will recur)
✗Missing the taper as likely source of corrosion
LIKELY FOLLOW-UPS
"What histological findings distinguish ALVAL from infection?"
"What would you do if abductors completely destroyed?"
"How long do metal levels take to normalize after revision?"
VIVA SCENARIOStandard

Scenario 3: Taper Assembly Technique

EXAMINER

"Examiner asks: You are performing primary THA with a CoCr head on titanium stem. Describe your taper assembly technique and explain the rationale."

EXCEPTIONAL ANSWER
Proper taper assembly is critical to minimize the risk of fretting and crevice corrosion at the modular junction. My technique follows four key principles: clean, dry, single impaction, and adequate force. First, I ensure both the female taper on the stem and the male taper inside the femoral head are completely clean and dry. I inspect the tapers for any debris, wipe with a clean gauze, and ensure no blood or fluid contamination. The rationale is that any interposed material prevents full seating of the taper, increasing micro-motion which leads to mechanically-assisted crevice corrosion. Second, I align the head onto the taper and deliver a single firm impaction using the manufacturer's impactor. Multiple impacts can damage the taper surfaces and do not improve fixation - a single firm blow is sufficient. The goal is to achieve full taper engagement which minimizes micro-motion between the surfaces. Third, I use adequate impaction force - a firm mallet blow, not just hand pressure. Inadequate seating leads to micro-motion and accelerated corrosion. Finally, I understand that this is a mixed metal couple - CoCr on titanium - which has some galvanic corrosion risk. While matched materials would be ideal, if using a CoCr head on Ti stem, the assembly technique becomes even more critical. An alternative to eliminate taper corrosion risk would be to use a ceramic head, which I would consider in younger active patients where the implant must last many decades. The clean, dry, single firm impaction technique minimizes micro-motion which is the key factor in preventing MACC at the modular taper.
KEY POINTS TO SCORE
Clean and dry both male and female tapers completely
No fluid or blood contamination (prevents full seating)
Single firm impaction (multiple impacts damage surface)
Adequate force to achieve full taper engagement
Mixed metals (CoCr/Ti) at higher risk than matched
Ceramic head alternative to eliminate taper corrosion
Goal: minimize micro-motion to prevent MACC
COMMON TRAPS
✗Not emphasizing the clean and dry step (critical for full seating)
✗Suggesting multiple impacts improve fixation (opposite - damages taper)
✗Not knowing MACC mechanism (micro-motion disrupts passivation)
LIKELY FOLLOW-UPS
"What is MACC?"
"Why is CoCr on CoCr better than CoCr on Ti?"
"What are the pros and cons of ceramic heads?"

MCQ Practice Points

Passivation Layer Question

Q: What provides corrosion resistance to titanium implants? A: TiO2 passivation layer (titanium oxide). This thin (2-10 nm) oxide layer forms spontaneously and is self-healing. It prevents titanium metal from contacting the corrosive environment.

MACC Definition Question

Q: What is MACC and where does it occur? A: Mechanically-Assisted Crevice Corrosion - synergistic combination of micro-motion (disrupts passivation) and crevice environment (low pH, chloride). Primary failure mode at modular hip tapers.

Galvanic Series Question

Q: In a CoCr head on Ti stem taper, which metal corrodes? A: Titanium - Ti is less noble than CoCr in the galvanic series, so Ti acts as anode and corrodes preferentially. CoCr acts as cathode and is protected.

ALVAL Question

Q: What type of hypersensitivity reaction is ALVAL? A: Type IV delayed hypersensitivity (T-cell mediated). Metal ions bind proteins forming haptens, leading to T-cell sensitization and lymphocytic tissue infiltration.

Metal Ion Threshold Question

Q: What serum cobalt or chromium level warrants concern in MoM hips? A: Greater than 5-7 ppb for either metal. Levels above this threshold associated with increased corrosion/wear and revision risk. Normal is less than 1 ppb.

Crevice pH Question

Q: What is the pH inside a crevice undergoing crevice corrosion? A: pH 3-4 (highly acidic) - Metal hydrolysis produces H+ ions and oxygen depletion prevents neutralization. This low pH dissolves the passivation layer.

Fretting Debris Question

Q: What is the characteristic appearance of fretting corrosion debris? A: Black debris - mixture of metal oxide particles (FeO, TiO2, Cr2O3) from repeated disruption of passivation and oxidation. Distinguishes fretting from pure wear.

Australian Context

AOANJRR Data on Metal-on-Metal

MoM THA Outcomes

AOANJRR findings:

  • MoM THA has higher revision rates than other bearings
  • Large-head MoM (greater than 36mm) especially problematic
  • Led to significant decline in MoM use in Australia
  • Current MoM use less than 1% of primary THA

Revision rates:

  • MoM THA: 15-year revision rate approximately 25%
  • Ceramic-on-ceramic: approximately 8%
  • Ceramic-on-poly: approximately 6%

Hip Resurfacing

Australian registry data:

  • Better outcomes than large-head MoM THA
  • Still higher revision than standard THA
  • Patient selection critical (young, active males)
  • Declining use in Australia

Current indications:

  • Young male patients (less than 55 years)
  • High activity demands
  • Experienced surgeons only
  • Limited centres perform resurfacing

Australian MoM Surveillance Guidelines

CategoryRecommendationSource
All MoM hipsAnnual review minimumTGA, AOA
Symptomatic patientsMetal ions + MARS MRITGA
Metal ions greater than 7 ppbFurther investigation, consider revisionTGA
Large head (greater than 36mm)Higher surveillance intensityAOA, AOANJRR

Exam Pearl

Exam Viva Point: "What does AOANJRR data show about MoM hips?" Answer: Higher revision rates than other bearing couples, especially large-head MoM THA. This led to decline in MoM use to less than 1% of primary THA in Australia. Registry data influenced global practice changes.

Australian registry data significantly influenced worldwide practice changes for MoM implants.

TGA Recommendations

Therapeutic Goods Administration

Australian regulatory guidance:

  • Issued alerts on MoM hip implants
  • Surveillance recommendations for all MoM patients
  • Product recalls for high-risk devices
  • Mandatory reporting of adverse events

Key alerts:

  • ASR (DePuy) recall in 2010
  • Ongoing surveillance for all MoM devices
  • Reporting via DAEN system

Metal Ion Testing

Australian laboratory requirements:

  • ICP-MS recommended method
  • Accredited laboratories only
  • Standard trace element tubes
  • Fasting samples preferred

Medicare considerations:

  • Metal ion testing covered for MoM surveillance
  • MARS MRI may require specific referral
  • Specialist review for elevated levels

Australian Best Practice

SettingRecommendationNotes
Primary THAAvoid MoM bearingsCeramic or highly crosslinked poly preferred
SurveillanceAnnual metal ions if MoMMore frequent if elevated
RevisionExperienced tertiary centreAccess to MARS MRI, specialist support
Follow-upAOANJRR participationContributes to national outcomes data

Medicolegal Considerations

Documentation

Essential records:

  • Informed consent including corrosion risk
  • Surveillance plan documented
  • Metal ion results with interpretation
  • Timing of interventions

For revision:

  • Intraoperative photos
  • Tissue samples for histology
  • Explant analysis if possible

Recall Patients

Recalled device management:

  • Identify all affected patients
  • Implement surveillance protocol
  • Document all contacts and reviews
  • Report adverse events to TGA

Australian requirements:

  • Mandatory adverse event reporting
  • Participation in recall protocols
  • Patient notification obligations

Exam Pearl

Key Learning: Australia's AOANJRR provided some of the earliest and most robust data on MoM failure rates, influencing global practice. Australian surgeons should be familiar with TGA guidance and AOANJRR data on corrosion-related outcomes.

Australian surgeons benefit from world-leading registry data to guide corrosion-related decision-making.

CORROSION MECHANISMS IN ORTHOPAEDIC IMPLANTS

High-Yield Exam Summary

Electrochemistry Basics

  • •Corrosion = electrochemical degradation (oxidation-reduction)
  • •Anode: M → M^n+ + e^- (metal oxidizes, goes into solution)
  • •Cathode: O2 + 2H2O + 4e^- → 4OH^- (reduction)
  • •Passivation layer (TiO2, Cr2O3) prevents corrosion
  • •Body fluid aggressive: 0.9% NaCl, pH 7.4, chloride ions

Four Types of Corrosion

  • •GALVANIC: Dissimilar metals (CoCr/Ti) - less noble corrodes (Ti)
  • •CREVICE: Oxygen depletion → pH 3-4 → passivation dissolved
  • •PITTING: Localized chloride attack → small hole, deep penetration
  • •FRETTING: Micro-motion disrupts passivation + corrosion (synergy)
  • •MACC = Mechanically-Assisted Crevice Corrosion (taper failure mode)

ALVAL Pathophysiology

  • •Aseptic Lymphocyte-dominated Vasculitis-Associated Lesion
  • •Type IV delayed hypersensitivity to Co and Cr ions
  • •Metal ions + proteins = haptens → T-cell sensitization
  • •Perivascular lymphocytic infiltration, tissue necrosis
  • •Pseudotumor = soft tissue mass with necrosis (not tumor)
  • •Histology: lymphocytes, no bacteria (NOT infection)

Metal Ion Monitoring

  • •Normal: Co and Cr less than 1 ppb
  • •Concern threshold: greater than 5 ppb either metal
  • •Action threshold: greater than 7 ppb warrants investigation
  • •Annual surveillance for all MoM hips recommended
  • •Elevated levels: MRI for pseudotumor, consider revision
  • •Levels decline 6-12 months after revision (slow)

Taper Assembly (Prevent MACC)

  • •CLEAN: No debris on tapers
  • •DRY: No blood/fluid contamination (prevents full seating)
  • •SINGLE: One firm impaction (multiple damages surface)
  • •MATCH: CoCr on CoCr better than CoCr on Ti (no galvanic)
  • •CERAMIC: Ceramic head eliminates taper corrosion risk

Prevention Strategies

  • •Avoid mixed metals (galvanic corrosion)
  • •Proper taper assembly critical
  • •Ceramic heads eliminate metal taper corrosion
  • •Avoid large heads (reduce taper mechanical stress)
  • •Polish surfaces (reduce stress concentrations for pitting)
Quick Stats
Reading Time178 min
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