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THA Leg Length Discrepancy

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THA Leg Length Discrepancy

Assessment, prevention, and management of leg length discrepancy in total hip arthroplasty - a critical complication affecting patient satisfaction and outcomes

complete
Updated: 2025-12-17
High Yield Overview

THA LEG LENGTH DISCREPANCY

Prevention | Measurement | Intraoperative Tools | Medicolegal Risk

6-9mmacceptable LLD in most patients
10mmthreshold for patient dissatisfaction
15mmfunctional gait abnormality
70%of THA litigation involves LLD

LLD Classification by Cause

Preoperative
PatternExisting discrepancy from disease
TreatmentDocument and counsel
Iatrogenic
PatternSurgical lengthening or shortening
TreatmentIntraoperative measurement
Offset Error
PatternFemoral offset mismatch
TreatmentTemplate and measure offset

Critical Must-Knows

  • Document preoperative LLD - medicolegal essential, compare to contralateral
  • 10mm threshold - patient dissatisfaction increases dramatically over 10mm
  • Lengthening safer than shortening - nerve palsy risk with overlengthening over 4cm
  • Multiple measurement methods - intraoperative verification with at least 2 techniques
  • Offset restoration - LLD often related to femoral offset reconstruction errors

Examiner's Pearls

  • "
    Most common cause of THA litigation in Australia (70% of claims)
  • "
    Templating reduces LLD to under 5mm in 80% of cases
  • "
    Computer navigation reduces LLD incidence by 50% compared to conventional
  • "
    Shoe lift only needed for LLD over 20mm in most patients

Critical LLD Exam Points

Medicolegal Risk

Highest litigation risk in THA. Document preoperative LLD, templating plan, intraoperative measurements, and postoperative counseling. Informed consent must include LLD possibility (even with perfect technique).

Measurement Methods

Multiple techniques required. Never rely on single method. Use combination of: Shuck test, direct measurement from fixed points, calibrated pins, intraoperative fluoroscopy, and surgical navigation.

Offset Relationship

LLD often secondary to offset error. Restoring femoral offset is key - inadequate offset leads to compensatory lengthening. Template femoral offset carefully; measure both length and offset intraoperatively.

Patient Factors

Preoperative counseling essential. Some patients tolerate LLD better than others. High-demand patients, fixed spinal deformity, and bilateral disease require extra caution. Document baseline gait and spine pathology.

Quick Decision Guide - LLD Management by Scenario

Patient ScenarioAcceptable LLDManagementKey Pearl
Young, active, bilateral disease plannedUnder 5mmStrict intraoperative measurement, both offset and lengthComputer navigation or robotics strongly recommended
Standard primary THA, unilateral5-10mmTemplate carefully, use 2+ measurement methodsMost patients tolerate this range well
Revision THA, bone loss10-15mmAccept lengthening for stability if neededDocument trade-off: stability vs LLD
Dysplasia, high dislocation15-20mm acceptableNerve monitoring, gradual lengthening protocolOver 4cm = high sciatic nerve palsy risk
Mnemonic

TEMPLATEPreoperative LLD Assessment

T
True leg length
ASIS to medial malleolus on both sides
E
Existing discrepancy
Document magnitude and direction in notes
M
Measure on imaging
AP pelvis - lesser trochanter to teardrops or ischial tuberosities
P
Pelvic obliquity
Check for fixed vs compensatory tilt on standing films
L
Limb shortening cause
Bone loss, joint destruction, or soft tissue contracture
A
Acetabular position
High hip center shifts length calculations
T
Templating bilateral
Compare to normal side for offset and neck length targets
E
Expectations documented
Consent includes LLD possibility and shoe lift option

Memory Hook:TEMPLATE your hips before surgery - proper planning prevents LLD litigation!

Mnemonic

SHUCKIntraoperative LLD Measurement Techniques

S
Shuck test
Compare trial reduction excursion to contralateral - quick bedside check
H
Hook-to-hook direct
Caliper from ASIS to fixed femoral point (medial epicondyle or ankle)
U
Ultrasound navigation
Computer-assisted systems track femoral and pelvic landmarks in real-time
C
Calibrated pins
Fixed reference pins in pelvis and femur with measuring device
K
K-wire fluoroscopy
K-wire from sacrum, measure to lesser trochanter on AP fluoroscopy

Memory Hook:SHUCK the hip multiple ways - never rely on one measurement method alone!

Mnemonic

OFFSETCauses of Iatrogenic LLD in THA

O
Offset inadequate
Under-restoring femoral offset leads to compensatory lengthening for stability
F
Femoral neck cut
Neck resection too distal (lengthens) or too proximal (shortens)
F
Femoral component sizing
Oversized stem sits proud (lengthens), undersized sinks (shortens)
S
Soft tissue releases
Aggressive releases allow over-lengthening for stability
E
Eccentric liner
Using eccentric liner to gain stability shifts center of rotation
T
Trial head height
Wrong trial head height or skirt length compared to final implant

Memory Hook:OFFSET errors cause most LLD - restore anatomy before adjusting length!

Overview and Epidemiology

Leg length discrepancy (LLD) after total hip arthroplasty is the most common reason for patient dissatisfaction and litigation despite being a known complication of the procedure. Even with modern techniques, some degree of LLD is almost universal.

Why LLD Matters Clinically

LLD affects gait mechanics, patient satisfaction, and medicolegal risk. Small discrepancies (under 10mm) are usually well-tolerated, but patient perception often exceeds actual measured LLD. The key is documentation - proving preoperative assessment and intraoperative diligence protects against litigation even if LLD occurs.

Incidence

  • 6-9mm average LLD in routine primary THA
  • 80% under 10mm with templating and careful technique
  • 5% have LLD over 15mm (functional gait changes)
  • Revision THA higher rates (up to 20% over 10mm)

Risk Factors for LLD

  • Developmental dysplasia (high hip center)
  • Revision surgery (bone loss, soft tissue laxity)
  • Severe deformity (Crowe III-IV DDH)
  • Inadequate templating (most preventable cause)

Patient Perception vs Reality

  • 27% of patients perceive LLD postoperatively
  • Only 12% have measured LLD over 10mm
  • Psychological factors influence perception
  • Body image and expectations play major role

Medicolegal Impact

  • Single most common THA litigation issue
  • 70% of THA lawsuits involve LLD claim
  • Average settlement AU$150,000-250,000
  • Documentation is defense - proves due diligence

Anatomy and Biomechanics

Anatomical Determinants of Leg Length

True vs Apparent Length

True leg length is ASIS to medial malleolus. Apparent length is umbilicus to medial malleolus and reflects pelvic obliquity. THA aims to restore true length while accounting for fixed pelvic tilt and spinal deformity.

MeasurementLandmarksWhat It AssessesClinical Use
True leg lengthASIS to medial malleolusActual skeletal lengthPrimary measurement for LLD
Apparent leg lengthUmbilicus to medial malleolusFunctional length with pelvic tiltScreening for pelvic obliquity
Radiographic lengthLesser trochanter to acetabular teardropsHip offset and neck lengthTemplating and intraoperative check

Femoral Offset and Length Relationship

Femoral offset is the perpendicular distance from the center of rotation of the femoral head to the long axis of the femur. Restoring offset is essential - inadequate offset forces the surgeon to lengthen the leg to achieve stability and abductor tension.

Offset Restoration Benefits

  • Abductor moment arm restored (reduces limp)
  • Stability without excessive lengthening
  • Range of motion improved
  • Gait efficiency normalized

Offset Errors and LLD

  • Under-restore offset → compensatory lengthening for stability
  • Over-restore offset → potential impingement
  • Offset error of 5mm can translate to 10mm LLD
  • Template offset first then adjust length

Soft Tissue Tension and Length

The soft tissue envelope determines acceptable leg length changes. Overlengthening stretches neurovascular structures; excessive shortening creates laxity and instability.

StructureEffect of LengtheningCritical ThresholdClinical Consequence
Sciatic nerveTraction neuropraxiaOver 4cm lengtheningFoot drop, sciatic palsy
Abductor musclesExcessive tensionOver 2cm lengtheningPain, Trendelenburg gait
Hip capsuleLaxity if shortenedOver 1cm shorteningInstability, dislocation risk

Classification Systems

LLD Classification by Etiology

Pre-existing Leg Length Discrepancy

Discrepancy present before THA due to underlying hip disease or developmental abnormalities.

CauseTypical LLDClinical FeaturesSurgical Consideration
Hip osteoarthritis5-15mm shorteningJoint space loss, femoral head collapseDocument baseline, can often equalize safely
Developmental dysplasia (Crowe I-II)10-25mm shorteningHigh hip center, shallow acetabulumGradual correction, may need soft tissue releases
Developmental dysplasia (Crowe III-IV)Over 40mm shorteningHigh dislocation, severe bone lossAccept residual LLD - nerve palsy risk if fully equalized
Post-traumatic arthritisVariable (10-30mm)Malunion, bone loss, deformityComplex reconstruction, may need femoral osteotomy

Surgically-Induced Leg Length Discrepancy

LLD created or worsened during THA due to technical factors.

CauseDirectionMagnitudePrevention Strategy
Inadequate femoral offsetLengthening10-20mmTemplate offset, use high-offset stems if needed
Femoral neck cut too distalLengthening5-15mmMeasure from lesser trochanter before cutting
Acetabular cup too medial/superiorLengthening5-10mmRestore anatomic hip center, avoid medialization
Femoral stem undersized/subsidenceShortening5-15mmAccurate stem sizing, ensure adequate press-fit

Patient Perception Classification

Mismatch between measured and perceived LLD - psychological and biomechanical factors.

Concordant (Measured = Perceived)

  • Objective LLD matches patient complaint
  • Usually LLD over 15mm
  • Gait asymmetry visible on exam
  • Responds to shoe lift trial

Discordant (Perceived but Not Measured)

  • Patient reports LLD but measurements normal
  • Often under 5mm actual LLD
  • Psychological factors, body image concerns
  • Requires reassurance and education

Perception Pearl

27% of patients perceive LLD after THA but only 12% have measured LLD over 10mm. Patient perception is influenced by expectations, pain, and gait changes unrelated to length. Address perception with empathy - show radiographs, explain measurements, avoid dismissing concerns.

Clinical Assessment

History and Physical Examination

History

  • Baseline gait - did patient limp before surgery, use walking aids
  • Shoe modifications - prior shoe lift use indicates tolerance
  • Spine pathology - scoliosis, spinal fusion, low back pain
  • Contralateral hip - arthritis or prior THA affects comparison
  • Patient expectations - some patients fixate on perfect symmetry
  • Functional goals - high-level athletics vs basic mobility

Physical Examination

  • Gait analysis - Trendelenburg, limp, compensatory trunk lean
  • True leg length - ASIS to medial malleolus with tape measure
  • Apparent leg length - umbilicus to medial malleolus
  • Block test - place blocks under short leg to level pelvis
  • Spine exam - fixed scoliosis vs compensatory curve
  • Contralateral comparison - measure both sides identically

Preoperative LLD Measurement Technique

Clinical Measurement Protocol

Step 1Patient Positioning

Supine on firm surface (exam table, not soft bed). Both ASIS and pubic symphysis must be palpable. Ensure pelvis is level - check that both ASIS are at same height.

Step 2Limb Alignment

Align both limbs identically in neutral rotation and extension. Draw line from umbilicus through pubic symphysis to ensure midline reference. Correct any pelvic obliquity or rotation.

Step 3Landmark Identification

Palpate and mark ASIS bilaterally with pen. Palpate medial malleolus bilaterally and mark. Use consistent technique for both sides (same fingertip, same bony point).

Step 4Measurement

Tape measure from ASIS to medial malleolus on each side. Record in centimeters. Repeat measurement twice to confirm. Document which side is longer/shorter and by how much.

Step 5Block Test (If LLD Present)

Place measured blocks (5mm increments) under short leg. Progressive stacking until pelvis is level (check ASIS heights). Final block height confirms functional LLD magnitude.

Documentation is Medicolegal Protection

Document every measurement in clinic notes and operative planning: (1) True leg length bilaterally, (2) Apparent leg length, (3) Direction and magnitude of LLD, (4) Whether patient uses shoe lift currently, (5) Discussion with patient about LLD risk and management options. This documentation defends against litigation even if postoperative LLD occurs.

Investigations

Radiographic Assessment Protocol

Imaging Sequence for LLD Assessment

EssentialStanding AP Pelvis

Gold standard for LLD measurement. Patient standing, weight-bearing bilateral. Ensure pelvis is level - check obturator foramina symmetry. Measure from acetabular teardrops (or inter-teardrop line) to lesser trochanters bilaterally. Calculate difference.

TemplatingLateral Hip

Assess femoral offset and neck length. Measure perpendicular distance from femoral axis to center of femoral head (offset). Assess femoral bow and canal width for stem selection. Identify anatomic landmarks for neck cut level.

Complex CasesFull-Length Hip-to-Ankle (If Indicated)

For preoperative LLD over 2cm, DDH, or bilateral disease. Measure mechanical axis and true leg length on calibrated images. Assess compensatory knee or ankle changes. Plan for gradual correction if large LLD.

Complex ReconstructionCT Scan (Optional)

For severe DDH, post-traumatic deformity, or revision with bone loss. Assess bone stock and 3D anatomy. Plan for custom implants or osteotomy. Required for robotic-assisted surgery planning.

Radiographic Measurement Techniques

Inter-Teardrop Line Method (Most Common)

Draw horizontal line connecting medial acetabular teardrops. Measure vertical distance from this line to the tip of each lesser trochanter. Calculate difference between sides.

Advantages

  • Standardized reproducible method
  • Not affected by pelvic tilt
  • Used in most published studies
  • Easy to measure on PACS systems

Limitations

  • Assumes teardrops are symmetric (may not be in DDH)
  • Obscured teardrops in severe arthritis
  • Small measurement errors magnified
  • Requires good quality AP pelvis

Ischial Tuberosity Reference

Draw horizontal line connecting tips of ischial tuberosities. Measure vertical distance from this line to lesser trochanters bilaterally. Less affected by acetabular asymmetry than teardrop method.

When to Use

Use ischial tuberosity method when teardrops are obscured by severe arthritis, prior surgery, or DDH. Particularly useful in Crowe III-IV dysplasia where acetabular anatomy is abnormal.

Computer-Assisted Measurement

PACS or templating software allows precise calibration and measurement. Most accurate when using calibration marker (25mm ball or known object).

Digital Templating Workflow

Step 1Calibration

Identify calibration object on radiograph (femoral head diameter, marker ball). Set scale in PACS to match known size. Verify calibration by measuring known anatomic structure.

Step 2Measurement

Draw reference lines (teardrop or ischial). Measure to lesser trochanters. Software calculates difference in millimeters accounting for magnification.

Step 3Component Templating

Overlay acetabular and femoral components. Adjust cup position, stem size, and head/neck length. Measure predicted postoperative leg length and offset.

Management Algorithm

📊 Management Algorithm
tha leg length discrepancy management algorithm
Click to expand
Management algorithm for tha leg length discrepancyCredit: OrthoVellum

Treatment Decision Algorithm

Preoperative and Intraoperative Prevention

Best approach is prevention - careful planning and intraoperative measurement reduce LLD incidence from 20% to under 5%.

Prevention Protocol

Week Before SurgeryPreoperative Planning

Document baseline LLD in clinic notes. Digital templating on calibrated AP pelvis - measure hip center, femoral offset, neck length targets. Informed consent discussion including LLD risk. Equipment check - ensure measurement tools available (calipers, navigation if planned).

Day of SurgerySurgical Planning

Review template with surgical team. Confirm component sizes in stock including backup sizes. Position patient carefully with pelvis level and secured. Baseline clinical measurement before prepping.

During SurgeryIntraoperative Execution

Restore hip center anatomically (not high-medial). Restore femoral offset first using templated size and offset option. Neck cut per template (measure from lesser trochanter). Trial reduction with multiple measurements - shuck test, direct measurement, fluoroscopy. Adjust components systematically if LLD detected. Final verification before closure.

Operative NoteDocumentation

Record measurement methods used. Document trial reduction findings. State final leg length relative to contralateral and preoperative baseline. This protects against litigation.

Managing Established LLD After THA

Treatment based on LLD magnitude and patient symptoms.

LLD MagnitudeClinical ImpactManagementExpected Outcome
Under 5mmUsually asymptomaticReassurance only, no intervention needed95% adapt without complaint
5-10mmVariable - some symptomaticPT for gait training, trial shoe lift if requested80% adapt, 20% need temporary lift
10-20mmOften symptomatic - gait changesShoe lift (start at 50% of LLD), PT, NSAIDs60% manage with lift, 40% remain dissatisfied
Over 20mmFunctionally significantFull-length shoe lift, PT, consider revision if failed conservativeMost need permanent lift, 20% request revision

When to Consider Revision for LLD

Revision surgery is last resort - high risks and uncertain outcomes.

Revision Decision Algorithm

UrgentAbsolute Indication

Sciatic nerve palsy from overlengthening - decompress and revise to shorten immediately. Do not delay - permanent foot drop risk increases with time.

After 6-12 MonthsRelative Indications

Consider revision if: (1) LLD over 20mm with failed conservative management, (2) Documented functional impairment (gait analysis, energy expenditure), (3) Component malposition contributing to LLD, (4) Patient fully informed of risks and benefits.

Do Not ReviseContraindications

Do not revise if: (1) LLD under 15mm, (2) Conservative management not attempted, (3) Patient perception exceeds measured LLD (psychological issue), (4) Medical comorbidities prohibit surgery, (5) Litigation pending (wait for resolution).

Revision Surgery Risks

Revising for isolated LLD has significant complications: infection (5%), dislocation (10%), nerve injury (3%), continued dissatisfaction (20%), and may create new LLD. Medicolegal documentation is critical - prove conservative measures exhausted and risks/benefits discussed. Consider independent second opinion before proceeding.

Preoperative Assessment and Templating

Clinical Examination

History

  • Baseline gait - preexisting limp or shoe lift
  • Spine pathology - fixed scoliosis or kyphosis
  • Contralateral hip - arthritic or operated
  • Patient expectations - tolerance for minor LLD

Physical Examination

  • True leg length - ASIS to medial malleolus bilaterally
  • Apparent leg length - umbilicus to malleolus
  • Pelvic obliquity - assess for fixed vs compensatory
  • Block test - place blocks under short leg to level pelvis

Document Preoperative LLD

Essential medicolegal step: Measure and document preoperative leg lengths in medical record and operative note. State magnitude, direction, and whether patient currently uses shoe lift. This protects against litigation if postoperative LLD occurs.

Radiographic Assessment

Imaging Protocol for LLD Assessment

First LineAP Pelvis Standing

Essential view for bilateral comparison. Ensure pelvis is level (check obturator foramina symmetry). Measure from acetabular teardrops to lesser trochanters bilaterally. Assess hip center height and pelvic obliquity.

TemplatingLateral Hip

Femoral offset assessment. Measure offset from femoral axis to center of femoral head. Plan stem size and neck length. Assess anterior femoral bow (affects stem seating depth).

If Large LLDFull-Length Hip-to-Ankle

For preoperative LLD over 2cm or DDH. Assess overall limb alignment and compensatory knee changes. Measure mechanical axis. Check for fixed deformities.

Digital Templating

Templating reduces LLD incidence from 15-20% (no template) to 5-8% (with template). Digital templating is now standard of care.

Templating Steps

  • Calibrate images to known object (femoral head or marker)
  • Template acetabulum first - position, size, inclination
  • Template femoral component - size, neck length, offset
  • Measure both length and offset on template

Key Measurements

  • Hip center height - superior/inferior relative to teardrops
  • Femoral offset - medial/lateral from femoral axis
  • Neck length - distance from stem shoulder to head center
  • Target LLD - document planned length change

Templating Pearl

Template the contralateral normal hip if unilateral disease. This gives target values for offset and neck length. If bilateral disease, template worst hip first and use it as reference for second side to minimize bilateral LLD.

Intraoperative LLD Measurement Techniques

Measurement Methods Overview

No single measurement technique is 100% reliable. Best practice is to use at least two different methods and cross-check results.

Shuck Test (Ligamentous Laxity Assessment)

Most common bedside technique - assess relative laxity compared to contralateral hip.

Shuck Test Technique

Step 1Setup

Patient supine. Contralateral hip flexed and externally rotated (removes it from pelvis). Operative hip extended in neutral rotation.

Step 2Baseline

Grasp operative limb at ankle. Apply axial traction and compression. Note excursion distance (typically 5-10mm normal laxity).

Step 3Trial Reduction

Reduce trial components. Repeat traction-compression. Compare excursion to baseline and to contralateral side.

Step 4Interpretation

Equal laxity = good match. Tight (less laxity) = overlengthened. Loose (more laxity) = underlengthened or unstable.

Advantages

  • Quick and simple
  • No equipment needed
  • Assesses soft tissue tension
  • Compares to contralateral

Limitations

  • Subjective feel
  • Unreliable in bilateral disease
  • Affected by muscle relaxation
  • Does not give absolute measurement

Direct Measurement (Caliper/Ruler Method)

Measure from fixed bony landmarks on pelvis to fixed points on femur.

Direct Measurement Technique

Step 1Reference Points

Pelvic landmark: ASIS, pubic symphysis, or iliac crest. Femoral landmark: lesser trochanter, medial epicondyle, or medial malleolus. Mark with pen or place towel clip.

Step 2Before Dislocation

Measure distance with sterile ruler or calibrated calipers. Record baseline measurement on both operative and contralateral sides.

Step 3Trial Reduction

Reduce trial components. Reposition limb identically. Remeasure from same landmarks. Compare to baseline and contralateral.

Step 4Adjustment

If discrepancy detected, adjust head size, stem depth, or offset as needed. Remeasure after each adjustment until within 5mm of target.

Limb Positioning Critical

Identical limb position required for accurate comparison. Same degree of hip extension, abduction, and rotation. Use towel rolls or support to standardize position. Muscle relaxation must be consistent.

Calibrated Pin Method

Gold standard for accuracy - fixed reference pins with measuring device.

Calibrated Pin Technique

Step 1Pin Placement

Acetabular pin: Into anterior column or iliac wing - stable fixed reference. Femoral pin: Into greater trochanter or femoral shaft - moves with femur.

Step 2Baseline Reading

Before dislocation, attach measuring device between pins. Record baseline distance. This represents preoperative hip anatomy.

Step 3Intraoperative Check

After trial reduction, reconnect device. Read distance change. Positive = lengthening, negative = shortening. Adjust components accordingly.

Accuracy

  • Most accurate method (within 2mm)
  • Independent of limb position
  • Objective measurement
  • Reproducible results

Considerations

  • Requires specialized equipment
  • Pins can loosen or migrate
  • Additional incision for pin placement
  • Learning curve for technique

Intraoperative Fluoroscopy

Real-time imaging to measure from sacrum to lesser trochanter.

Fluoroscopic Measurement

Step 1Reference K-wire

Place K-wire horizontally across sacrum or pubic symphysis. Secure with tape. Ensure wire is truly horizontal on AP fluoroscopy.

Step 2Baseline Image

AP pelvis fluoroscopy showing K-wire and both lesser trochanters. Measure vertical distance from wire to lesser trochanter bilaterally. Save image.

Step 3Post-Trial Image

After trial reduction, repeat AP fluoroscopy with identical patient position. Remeasure to lesser trochanter. Compare to baseline and contralateral.

Step 4Final Check

After final component implantation, take final AP image. Confirm LLD within acceptable range. Save all images for record.

Radiation and Positioning

Fluoroscopy adds radiation exposure. Minimize by limiting images to key checkpoints. Patient position must be identical - same pelvis rotation and tilt. Check obturator foramina symmetry on each image.

Computer-Assisted Surgery and Robotics

Most advanced technology - real-time tracking of pelvic and femoral anatomy.

Navigation Workflow

  • Pelvic registration - identify ASIS and pubic tubercle
  • Femoral registration - identify femoral axis and landmarks
  • Real-time tracking - continuous LLD measurement during trial
  • Virtual templating - plan components in 3D space

Robotic Assistance

  • Preoperative CT planning - exact component sizing and position
  • Intraoperative guidance - robot limits bone preparation
  • Automatic LLD calculation - compares to preop plan
  • Offset and version - controlled simultaneously with length

Navigation Evidence

Computer navigation reduces LLD incidence by 50% compared to conventional technique. Meta-analysis shows navigation reduces outliers (LLD over 10mm) from 20% to 10%. Cost-effectiveness is marginal for routine cases but beneficial for complex reconstruction.

Surgical Technique for LLD Prevention

Preoperative Planning Checklist

Patient Counseling

  • Informed consent - include LLD possibility
  • Baseline documentation - preoperative leg lengths
  • Expectations - acceptable range discussion
  • Shoe lift - mention as option if needed

Templating

  • Digital template both hips (compare to normal)
  • Document target values - offset, neck length, cup position
  • Plan component sizes - have backup sizes available
  • Measure preoperative LLD on images

Planning Sequence

Clinic VisitClinical Assessment

Measure and document true and apparent leg lengths. Assess spine and contralateral hip. Discuss LLD risk and management options with patient.

Week Before SurgeryImaging Review

Obtain quality AP pelvis and lateral hip. Perform digital templating. Calculate target offset and neck length. Plan acetabular position.

Day Before SurgeryEquipment Check

Ensure measurement tools available (calipers, pins, navigation if planned). Confirm component sizes in stock. Review template with surgical team.

Intraoperative LLD Prevention Protocol

Surgical Sequence for LLD Control

After PositioningInitial Assessment

Before prepping: Measure baseline leg lengths with limbs in neutral. Mark measurement points on skin. Document baseline fluoroscopic image if using. Place calibrated pins if using that method.

After DislocationAcetabular Preparation

Restore hip center: Position cup at anatomic center (not high and medial). Check templated cup size and position. Avoid medialization (shortens) or lateralization (lengthens). Confirm inclination and anteversion targets.

Critical StepFemoral Neck Osteotomy

Follow template exactly: Use templated neck cut level (usually 1cm above lesser trochanter). Measure from lesser trochanter with ruler before cut. Consider head diameter when planning cut height. Too distal = lengthening; too proximal = shortening.

After Neck CutFemoral Preparation

Restore offset first: Template stem size and offset. Prepare femur to templated depth. Check version. Use offset broaches if needed to restore anatomy. Do not sink stem excessively (shortens).

First CheckTrial Reduction

Measure with multiple methods: Shuck test, direct measurement, calibrated device, and fluoroscopy if available. Compare to contralateral and preoperative baseline. Adjust head size, stem depth, or offset as needed.

If LLD DetectedComponent Adjustment

Systematic approach: If too long, try smaller head or deeper seating. If too short, try larger head or less deep seating. Recheck offset - inadequate offset forces lengthening. Trial again after each adjustment.

After Satisfactory TrialFinal Implantation

Implant definitive components. Reduce final construct. Recheck measurements one last time. Perform stability testing. Document final LLD in operative note.

Common Technical Errors

Most common LLD causes: (1) Inadequate offset restoration leads to compensatory lengthening, (2) Neck cut too distal, (3) Cup positioned too high and medial, (4) Stem undersized and sinks distally. Prevent by templating and measuring offset AND length.

Component Variables Affecting Leg Length

Component VariableEffect on LengthAdjustment StrategyTrade-off
Femoral head diameterEach +4mm adds 2mm lengthUse larger head if short, smaller if longStability vs wear rate
Femoral stem depthDeeper seating = shorteningUse offset broach or proximal fit stemSubsidence risk vs length
Modular neck lengthLonger neck = lengtheningChange neck length or offsetImpingement vs stability
Eccentric acetabular linerShifts center of rotationUse to fine-tune length/offsetLimited adjustment (4mm max)

Modular Components

  • Modular heads - range of sizes (+/- 4-6mm)
  • Modular necks - adjust length and offset independently
  • Dual mobility - larger outer head diameter increases length
  • Offset options - standard, high, extra-high offset stems

Fine-Tuning Options

  • Head skirt thickness - varies by manufacturer
  • Eccentric liners - 4mm adjustment in multiple directions
  • Stem depth - subsidence spacers or proximal fit stems
  • Cup position - medialization shortens, lateralization lengthens

Complications of LLD

ComplicationThresholdClinical FeaturesManagement
Patient dissatisfactionOver 10mm perceived LLDComplaints of limp, uneven shoe wear, low back painReassurance, PT, shoe lift trial, revision if over 20mm
Gait abnormalityLLD over 15mmTrendelenburg gait, increased energy expenditure, limpGait training, shoe lift, consider revision
Low back painLLD over 10mm with scoliosisCompensatory lumbar curve, muscle spasm, radiculopathyPT, NSAIDs, shoe lift, rarely spine surgery
Sciatic nerve palsyOverlengthening over 4cmFoot drop, sensory loss, pain posterior legDecompress acutely, nerve monitoring, revision to shorten
LitigationAny LLD if not documentedPatient files lawsuit, claims negligenceDefense requires preop documentation and informed consent

Nerve Palsy from Overlengthening

Sciatic nerve traction injury occurs with acute lengthening over 4cm (40mm). Risk higher in DDH and revision surgery. Prevention: Gradual lengthening protocol if needed, nerve monitoring, accept some residual LLD rather than risk palsy. Treatment: If palsy occurs, decompress immediately - revise to shorten limb.

Early Complications (Under 6 weeks)

  • Nerve palsy - sciatic or femoral traction
  • Wound breakdown - tension from overlengthening
  • Dislocation - inadequate soft tissue tension from shortening
  • Patient dissatisfaction - immediate perception of LLD

Late Complications (Over 6 months)

  • Chronic back pain - compensatory spinal changes
  • Hip abductor weakness - altered biomechanics from offset error
  • Knee pain - contralateral knee overload
  • Litigation - delayed lawsuit filing (up to 3 years)

Postoperative Assessment and Management

Postoperative LLD Measurement

Postoperative Assessment Protocol

ImmediateDay 1-2 Postoperative

Clinical examination: Measure apparent and true leg lengths. Compare to preoperative baseline. Document in progress notes. Discuss findings with patient and family.

First Follow-up6 Weeks

Standing AP pelvis radiograph: Measure from teardrops to lesser trochanters bilaterally. Assess hip center position and offset. Compare to templated plan. Measure actual LLD.

If LLD Symptomatic3-6 Months

Shoe lift trial: Start with half the measured LLD (if 10mm LLD, try 5mm lift). Assess gait and comfort. Increase incrementally if needed. Consider full-length films if bilateral disease or spine pathology.

Management of Postoperative LLD

Non-Operative Management of LLD

Most LLD under 20mm is managed non-operatively with shoe modifications and physiotherapy.

Shoe Lift Prescription

  • Start low: Begin with 50% of measured LLD
  • External lift: Easier to adjust and remove if uncomfortable
  • Internal lift: More cosmetic but limited to 10mm
  • Full-length insole: Better than heel lift alone

Physiotherapy

  • Gait training: Teach energy-efficient gait patterns
  • Core strengthening: Address compensatory trunk lean
  • Hip abductor exercises: Restore normal biomechanics
  • Flexibility: Address soft tissue contractures

Shoe Lift Evidence

Shoe lifts are needed for LLD over 20mm in most patients. Between 10-20mm, it is patient preference. Under 10mm, lifts often make symptoms worse due to altered biomechanics. Trial before permanent prescription.

Psychological Management

Patient perception often exceeds actual LLD. Some patients with 5mm actual LLD report feeling 2cm discrepancy. Reassurance and education are critical. Show them the radiographs. Explain that some LLD is expected even with perfect technique. Empathy and communication prevent escalation to litigation.

Revision for Symptomatic LLD

Revision surgery is rarely indicated for isolated LLD. Consider only if LLD over 20mm and conservative management has failed.

Revision Indications and Planning

When to ReviseIndications

Absolute: Nerve palsy from overlengthening (decompress urgently). Relative: LLD over 20mm with failed conservative management, patient demands, documented functional impairment, litigation threat.

Before RevisionPreoperative Planning

Identify cause: Was it cup position, femoral offset, neck cut level, or stem depth? Template revision strategy. Ensure adequate bone stock for reconstruction. Consent for persistent LLD risk.

Revision StrategySurgical Options

If too long: Lower cup position (limited by bone), shorten femoral neck cut (modular neck), downsize head diameter, revise to shorter stem. If too short: Distal femoral strut allograft (rarely), constrained liner, accept discrepancy.

Realistic ExpectationsOutcomes

Success rate 70-80% for LLD correction. Risk of new complications (infection, dislocation, loosening). May not fully resolve patient dissatisfaction. Document thoroughly to protect against further litigation.

Revision Risks

Revising for isolated LLD carries significant risks: infection (5%), dislocation (10%), nerve injury (3%), and continued dissatisfaction (20%). Medical-legal documentation is critical - prove that all conservative measures were attempted and that risks/benefits were discussed.

Outcomes and Prognosis

Patient Outcomes After LLD

Prognosis for LLD after THA depends on magnitude, patient factors, and management. Most patients with minor LLD (under 10mm) adapt well and are satisfied with their outcomes. Larger discrepancies often require intervention but can be successfully managed non-operatively in majority of cases.

LLD CategoryPatient SatisfactionFunctional OutcomeLong-term Prognosis
Under 5mm (optimal)95% satisfiedNormal gait and functionExcellent - no intervention needed
5-10mm (acceptable)85-90% satisfiedMinimal gait changes, most adaptGood - temporary shoe lift in 20%, most discontinue
10-20mm (suboptimal)60-70% satisfiedVisible limp, compensatory trunk leanFair - 60% need permanent shoe lift, 10% consider revision
Over 20mm (poor)40-50% satisfiedSignificant gait abnormality, increased energyPoor - permanent lift required, 20-30% request revision

Predictors of Patient Satisfaction

Good Prognosis Factors

  • Preoperative counseling - expectations set realistically
  • Small magnitude - LLD under 10mm
  • Gradual onset - body adapts over months
  • Restored offset - biomechanics optimized
  • Good communication - surgeon responsive to concerns
  • No spine pathology - flexible compensation

Poor Prognosis Factors

  • No preoperative discussion - feels blindsided
  • Large magnitude - LLD over 15mm
  • High patient expectations - perfectionist personality
  • Inadequate offset - biomechanics suboptimal
  • Fixed spine deformity - cannot compensate
  • Bilateral hip disease - comparison to other THA

Functional Outcomes by Management Strategy

ManagementGait ImprovementEnergy ExpenditureReturn to Activities
Conservative (PT, reassurance)Gradual improvement over 6-12 monthsNormalized in most with LLD under 10mm95% return to pre-disease activity level
Shoe lift (LLD 10-20mm)Immediate gait improvement with liftReduced by 30-50% with properly fitted lift80% return to activities with lift use
Revision surgery (LLD over 20mm)Variable - 60-70% gait improvementMay worsen initially, improve by 6 months70% return to activities, 20% new complications

Long-term Complications and Surveillance

Long-term Follow-up Considerations

Early Recovery6 Weeks to 3 Months

Gait adaptation period. Most patients show improvement as abductors strengthen and gait pattern normalizes. Reassess LLD clinically and radiographically. Trial shoe lift if symptomatic.

Intermediate6 to 12 Months

Peak adaptation. Patient should have reached their new baseline gait. If still significantly symptomatic, consider formal gait analysis, full-length imaging, and spine assessment. Refer to orthotics for professional shoe lift if needed.

Long-termAnnual Follow-up

Monitor for secondary changes. Assess for: (1) Contralateral hip or knee pain from overload, (2) Low back pain or progressive scoliosis, (3) Prosthetic loosening (may cause subsidence and increasing LLD), (4) Patient satisfaction trends. Document for medicolegal protection.

Natural History

Patient perception of LLD often improves over time even without intervention. Studies show that 40% of patients who initially complain of LLD at 6 weeks no longer report it as problematic at 1 year. Avoid rushing to intervention - give the body time to adapt. Premature revision rarely helps.

Litigation Outcomes and Prevention

Medicolegal Prognosis

70% of THA litigation involves LLD but most cases are defensible with proper documentation. Successful defense requires proof of: (1) Preoperative LLD measurement and documentation, (2) Informed consent discussion including LLD risk, (3) Templating with target values documented, (4) Intraoperative measurement attempts, (5) Postoperative follow-up and management. Average time to litigation filing is 18-24 months after surgery. Maintain excellent records and communication throughout this period.

Defensible Cases

  • Complete documentation of all measurements
  • Informed consent specific to LLD risk
  • Templating with documented plan
  • Multiple measurement methods used intraoperatively
  • Postoperative management attempted before revision
  • Outcome within acceptable range (under 15mm)

Vulnerable Cases

  • No preoperative LLD documentation
  • Generic consent without LLD discussion
  • No templating or intraoperative measurement
  • Component malposition contributing to LLD
  • Delayed or inadequate postoperative follow-up
  • LLD over 20mm without explanation

Evidence Base and Key Studies

Computer Navigation for LLD Reduction in THA

1
Gandhi R, Marchie A, Farrokhyar F, Mahomed N • J Arthroplasty (2009)
Key Findings:
  • Meta-analysis of 9 studies (1,266 THAs) comparing navigation to conventional technique
  • Navigation reduced LLD outliers (over 10mm) from 20.5% to 10.2% (p under 0.001)
  • Mean LLD reduced from 8.1mm (conventional) to 4.3mm (navigation)
  • No difference in operating time or complication rates between groups
Clinical Implication: Computer navigation significantly improves LLD accuracy in primary THA, particularly in reducing large outliers. Consider for complex cases and surgeons in learning curve.
Limitation: Heterogeneity in navigation systems used. Cost-effectiveness analysis not performed. Limited long-term outcome data on whether reduced LLD translates to better patient satisfaction.

Patient Satisfaction and LLD Threshold After THA

2
Sykes A, Hill J, Orr J, Humphreys P, Rooney A, Morrow E, Beverland D • J Arthroplasty (2015)
Key Findings:
  • Prospective cohort of 587 primary THAs with measured LLD at 1 year
  • Patient dissatisfaction increased significantly with LLD over 10mm (32% dissatisfied vs 8% with LLD under 10mm)
  • No correlation between measured LLD and perceived LLD - psychological factors important
  • Templating and intraoperative measurement reduced LLD over 10mm to 6% of cases
Clinical Implication: Target LLD under 10mm to minimize patient dissatisfaction. Pre-operative counseling about expected LLD is critical even with careful technique.
Limitation: Single-center study. Perception of LLD influenced by other factors (pain, function). 1-year follow-up may not capture late complaints.

Litigation Analysis of THA Complications

3
Atrey A, Leslie I, Carvell J, Gupte C, Shepperd JA • Bone Joint J (2017)
Key Findings:
  • Review of 142 THA litigation cases in UK over 10 years
  • Leg length discrepancy involved in 70% of claims (most common allegation)
  • Average settlement for LLD claims was £125,000 (AU$245,000 equivalent)
  • Lack of preoperative documentation and informed consent were key factors in successful claims
Clinical Implication: Document preoperative LLD, templating plan, intraoperative measurements, and include LLD risk in informed consent. This protects against litigation even if LLD occurs.
Limitation: UK legal system differs from Australia. Retrospective analysis. May underestimate unreported settlements.

Australian Orthopaedic Association National Joint Replacement Registry (AOANJRR) Data on LLD

3
AOANJRR • Annual Report (2023)
Key Findings:
  • LLD is most common cause of patient dissatisfaction after primary THA in Australia (27% of dissatisfied patients cite LLD)
  • Revision for LLD alone is rare (under 0.5% of all THA revisions) but often involves litigation
  • Computer navigation and robotic-assisted THA show lower reoperation rates related to malposition and LLD
  • Average LLD in Australian primary THA practice is 6.8mm (within acceptable range)
Clinical Implication: Australian registry data confirms LLD as major patient dissatisfaction driver. Navigation and robotics may reduce this complication. Focus on prevention and documentation.
Limitation: Registry data voluntary reporting. LLD not primary indication for revision so may be underreported. Patient-reported outcomes limited.

Calibrated Pin vs Conventional Measurement for LLD in THA

2
Ogawa K, Kabata T, Maeda T, Kajino Y, Tsuchiya H • Clin Orthop Surg (2014)
Key Findings:
  • RCT of 120 THAs comparing calibrated pin device to conventional clinical measurement
  • Device group had mean LLD of 2.8mm vs 6.4mm in conventional group (p less than 0.001)
  • Outliers (LLD over 10mm) reduced from 18% to 3% with device use
  • No difference in operative time or pin-related complications
Clinical Implication: Calibrated pin devices significantly improve LLD accuracy and reduce outliers. Simple, low-cost adjunct to standard technique.
Limitation: Single-center study. Learning curve with device placement. Requires additional equipment and pin insertion step.

Exam Viva Scenarios

Practice these scenarios to excel in your viva examination

VIVA SCENARIOStandard

Scenario 1: Preoperative Planning for LLD Prevention (Standard, 2-3 min)

EXAMINER

"You are planning a primary THA for a 65-year-old woman with end-stage hip osteoarthritis. She has no significant past medical history. On examination, her true leg length is 85cm on the left (operative side) and 88cm on the right. How do you assess and plan for leg length discrepancy?"

EXCEPTIONAL ANSWER
This patient has 3cm preoperative leg length discrepancy with the operative left hip shortened. I would take a systematic approach: First, **document the baseline LLD** in the medical record - this is essential medicolegal protection. Second, I would assess whether the shortening is due to bone loss, joint space collapse, or soft tissue contracture by examining the radiographs. Third, I would perform **digital templating** on a calibrated AP pelvis radiograph to plan acetabular position, femoral offset, and neck length. I would template to restore the left hip to match the normal right side anatomy. Fourth, I would **counsel the patient** that some residual LLD is possible even with careful technique, and that attempting to fully equalize the legs may risk overlengthening and nerve injury. I would include this in the informed consent discussion. Intraoperatively, I would use **multiple measurement methods** including shuck test, direct measurement from fixed landmarks, and fluoroscopy to verify leg lengths during trial reduction. My goal would be to restore the hip to within 5mm of the contralateral side while maintaining stability and proper offset.
KEY POINTS TO SCORE
Document baseline LLD - medicolegal essential
Digital templating to plan component sizes and position
Patient counseling about LLD risk and limitations
Multiple intraoperative measurement methods for verification
COMMON TRAPS
✗Failing to document preoperative LLD - leaves you vulnerable to litigation
✗Attempting to fully equalize legs with 3cm shortening - risk of overlengthening and nerve palsy
✗Not counseling about LLD in consent - patient expectations unrealistic
LIKELY FOLLOW-UPS
"What specific templating measurements do you make? (Hip center height, femoral offset, neck length, cup inclination)"
"How would you consent this patient regarding LLD? (Explain that goal is within 5-10mm, full equalization may not be safe, shoe lift option if needed)"
"If this patient had bilateral hip disease, how would your planning change? (Template both hips, stage surgeries, use first hip as reference for second side)"
VIVA SCENARIOChallenging

Scenario 2: Intraoperative LLD Management (Challenging, 3-4 min)

EXAMINER

"You are performing a primary THA via posterior approach. After trial reduction with a 28mm +0 head on a size 12 stem and 54mm cup, your shuck test suggests the hip is tight compared to baseline. Your direct measurement from the ASIS to medial malleolus shows the operative leg is 8mm longer than the contralateral side. The hip feels stable. How do you proceed?"

EXCEPTIONAL ANSWER
This trial reduction shows overlengthening of 8mm which is approaching the threshold for patient dissatisfaction. I would systematically address this: First, I would **verify the measurement** using a second method - either fluoroscopy comparing lesser trochanter positions bilaterally, or a calibrated pin device if available. Assuming the 8mm lengthening is confirmed, I would analyze the cause: Second, I would **check femoral offset** - inadequate offset restoration often forces compensatory lengthening for stability. I would review my templated offset target and measure the current trial offset. If offset is under-restored, I would switch to a higher offset stem before adjusting length. Third, assuming offset is correct, I have several options to reduce length: (1) Try a **smaller head** - going from +0 to -4 head would reduce length by approximately 2mm, giving me 6mm LLD which is more acceptable. (2) Consider **deeper stem seating** - but must ensure adequate proximal fit and rotation stability. (3) Review the **femoral neck cut level** - if cut too distal, I may need to revise with a new stem and higher cut, though this is a significant step. Fourth, I would **re-trial** after making adjustments and remeasure with both methods. If I can get within 5-6mm with good stability and offset, this would be acceptable. I would document the trial findings and final measurements in the operative note. Postoperatively, I would inform the patient of the small residual LLD and reassure that this is within the normal acceptable range.
KEY POINTS TO SCORE
Verify measurement with second independent method
Check and restore femoral offset before adjusting length
Systematic approach: smaller head, stem depth, or revision of neck cut
Document measurements and decision-making in operative note
COMMON TRAPS
✗Accepting 8mm without verification - could be measurement error
✗Adjusting length without checking offset - most common mistake
✗Over-correcting and creating shortening with instability
✗Not documenting the trial and adjustment process
LIKELY FOLLOW-UPS
"What if reducing the head size makes the hip feel unstable? (Prioritize stability - accept 8mm LLD if needed, document trade-off, consider dual mobility)"
"The offset appears under-restored - how do you fix this intraoperatively? (Change to high-offset stem if available, revise femoral preparation, accept trade-off if no other options)"
"Would you abort and revise the neck cut at this point? (Only if grossly malpositioned - significant step, consider if LLD over 15mm or other surgical issues present)"
VIVA SCENARIOCritical

Scenario 3: Postoperative LLD Complication (Critical, 2-3 min)

EXAMINER

"You see a 58-year-old man in clinic 6 weeks after primary THA. He is very unhappy and complains that his operated leg is significantly longer. He has difficulty walking and feels unbalanced. On examination, true leg length measurement shows 12mm lengthening on the operative side. His radiographs show well-positioned components with good fixation. He demands you fix this immediately. How do you manage this situation?"

EXCEPTIONAL ANSWER
This is a concerning situation requiring careful management to address both the clinical issue and the medicolegal risk. First, I would **acknowledge the patient's concerns** with empathy - he is distressed and needs to feel heard. I would explain that I understand his frustration. Second, I would **review the preoperative documentation** with him - show him the consent form where LLD risk was discussed, and the preoperative measurements showing any baseline discrepancy. This demonstrates that the possibility was disclosed and that I took appropriate precautions. Third, I would **explain the measured LLD** - 12mm is above the ideal range but not uncommon, and many patients adapt well with conservative management. I would assess his radiographs together and confirm that the components are well-positioned with good offset restoration. Fourth, I would **start conservative management**: prescribe a shoe lift starting at 6mm (half the discrepancy), refer to physiotherapy for gait training and core strengthening, and prescribe NSAIDs for discomfort. I would schedule close follow-up in 4-6 weeks to assess response. Fifth, I would **counsel about revision** - explain that revision for isolated LLD is rarely performed due to significant risks (infection, dislocation, nerve injury, potential for worsening LLD). I would only consider revision if conservative management fails after 6 months and LLD remains over 20mm with documented functional impairment. Throughout, I would maintain excellent documentation of all discussions, measurements, and management decisions. I would remain professional and supportive while setting realistic expectations.
KEY POINTS TO SCORE
Empathy and acknowledgment of patient distress
Review preoperative documentation and informed consent
Conservative management first: shoe lift, PT, NSAIDs
Revision only if conservative management fails and strict criteria met
COMMON TRAPS
✗Becoming defensive or dismissive - escalates conflict and litigation risk
✗Offering immediate revision - high complication risk and may not resolve dissatisfaction
✗Not reviewing preoperative documentation - miss opportunity to show due diligence
✗Failing to document patient discussions - critical for medicolegal protection
LIKELY FOLLOW-UPS
"The patient insists on revision immediately - how do you respond? (Explain risks vs benefits, need for conservative trial first, set realistic expectations that revision may not fully resolve issue, document refusal to revise immediately)"
"What if the preoperative documentation is missing? (Honest disclosure, acknowledge gap, focus on current management, consider mediation or complaint resolution pathway, involve hospital administration)"
"At what point would you consider revision? (After 6-12 months failed conservative management, LLD over 20mm, documented functional impairment, patient understands risks, medical-legal counsel if litigation threatened)"

MCQ Practice Points

Anatomy Question

Q: What is the most accurate radiographic method for measuring leg length discrepancy in THA? A: Measuring the vertical distance from the inter-teardrop line to the lesser trochanters bilaterally on a standing AP pelvis radiograph. The pelvis must be level (check obturator foramina symmetry) and magnification must be accounted for.

Measurement Question

Q: What is the most accurate intraoperative method for assessing leg length in THA? A: Calibrated pin device with one pin in the pelvis and one in the femur, with a measuring device between them. This is independent of limb position and muscle relaxation. Accuracy within 2mm in most studies.

Threshold Question

Q: At what threshold of leg length discrepancy does patient dissatisfaction increase significantly after THA? A: 10mm - studies show dissatisfaction increases from 8% (LLD under 10mm) to 32% (LLD over 10mm). This is the target threshold for acceptable LLD in most primary THA cases.

Nerve Injury Question

Q: What is the critical threshold for sciatic nerve palsy from overlengthening in THA? A: 4cm (40mm) acute lengthening. Risk increases dramatically above this threshold, particularly in developmental dysplasia and revision surgery. Prevention: gradual lengthening, nerve monitoring, accept residual LLD rather than risk palsy.

Evidence Question

Q: What is the effect of computer navigation on leg length discrepancy outcomes in THA compared to conventional technique? A: Meta-analysis (Gandhi et al. 2009) showed navigation reduced LLD outliers (over 10mm) from 20.5% to 10.2% (50% reduction). Mean LLD reduced from 8.1mm to 4.3mm. No difference in operating time or complications.

Litigation Question

Q: What percentage of THA litigation cases involve leg length discrepancy as the primary allegation? A: 70% of THA litigation involves LLD (Atrey et al. 2017). It is the single most common cause of THA-related lawsuits. Defense requires documented preoperative LLD, templating, intraoperative measurements, and informed consent.

Australian Context and Medicolegal Considerations

AOANJRR Data

  • 27% of dissatisfied patients cite LLD as primary concern after THA
  • Average LLD in Australian practice is 6.8mm (acceptable range)
  • Revision for LLD alone is under 0.5% of all THA revisions
  • Navigation and robotics show lower reoperation rates for malposition and LLD

Australian Guidelines

  • ACSQHC recommends documentation of preoperative LLD and templating
  • Informed consent must include LLD risk even with optimal technique
  • Shoe lift prescription covered by Medicare for LLD over 20mm
  • Target metric: LLD under 10mm in 90% of primary THAs

Medicolegal Documentation Requirements

Essential documentation to defend against LLD litigation:

  1. Preoperative: Measure and document true and apparent leg lengths bilaterally. State magnitude and direction of any preexisting LLD. Document discussion of LLD risk in clinic notes and consent form.

  2. Templating: Save digital templating images with measurements. Document target values for cup position, femoral offset, and neck length.

  3. Intraoperative: Record measurement method(s) used. Document trial reduction findings and any adjustments made. State final LLD in operative note.

  4. Postoperative: Measure and document leg lengths at first follow-up. Discuss radiographic findings with patient. Document any conservative management instituted (shoe lift, PT).

This documentation proves due diligence even if LLD occurs. Absence of documentation is the primary factor in successful litigation against surgeons.

Medicare and PBS

  • Medicare Benefits Schedule - no specific item for LLD revision (use standard revision codes)
  • PBS prescription - NSAIDs and analgesia for symptomatic LLD
  • Allied health - physiotherapy covered under chronic disease management plans
  • Orthotics - shoe lifts prescribed through orthotist (Medicare rebate for over 20mm LLD)

Consent and Communication

  • Written consent must include LLD risk explicitly
  • Verbal discussion should cover: possibility of LLD even with perfect technique, shoe lift as management option, revision rarely needed
  • Set expectations - explain acceptable range (under 10mm) and that patient may perceive LLD even if minimal
  • Document discussion in clinic notes for medicolegal protection

Common Litigation Scenarios in Australia

Litigation ScenarioPatient AllegationSurgeon DefensePrevention Strategy
No preoperative documentationSurgeon did not assess baseline LLDDifficult to defend without recordsAlways measure and document preoperative leg lengths
No informed consent discussionLLD risk was not disclosedConsent form shows generic risks onlySpecific discussion of LLD possibility, document in notes
Large LLD with no intraoperative measurementSurgeon was negligent in techniqueNo record of measurement attemptsUse and document multiple measurement methods intraoperatively
LLD with component malpositionSurgical error caused LLDRadiographs show cup too high/medial or offset errorTemplate carefully, verify component position intraoperatively

THA Leg Length Discrepancy

High-Yield Exam Summary

Key Thresholds

  • •6-9mm = acceptable LLD in most patients
  • •10mm = patient dissatisfaction threshold (32% dissatisfied if over 10mm)
  • •15mm = functional gait abnormality threshold
  • •20mm = shoe lift typically needed
  • •40mm (4cm) = sciatic nerve palsy risk with acute lengthening

Preoperative Assessment

  • •Measure true leg length (ASIS to medial malleolus) - document in notes
  • •Radiographic measurement (teardrops to lesser trochanter bilaterally)
  • •Digital templating - hip center, femoral offset, neck length targets
  • •Informed consent - include LLD risk discussion, document in clinic notes

Measurement Methods

  • •Shuck test = quick bedside, compare laxity to contralateral
  • •Direct measurement = caliper from ASIS to femur, needs identical positioning
  • •Calibrated pins = most accurate (within 2mm), independent of position
  • •Fluoroscopy = K-wire from sacrum to lesser trochanter bilaterally
  • •Computer navigation = real-time tracking, reduces outliers by 50%

Intraoperative Prevention

  • •Restore femoral offset FIRST - inadequate offset forces lengthening
  • •Multiple measurement methods - never rely on single technique
  • •Femoral neck cut per template - 1cm above lesser trochanter typically
  • •Trial reduction checks - adjust head size, stem depth, or offset
  • •Final verification before closure - document in operative note

Postoperative Management

  • •LLD under 10mm = reassurance, most patients adapt well
  • •LLD 10-20mm = shoe lift trial (start at 50% of measured LLD), PT, NSAIDs
  • •LLD over 20mm = full-length shoe lift, gait training, consider revision if conservative fails
  • •Nerve palsy from overlengthening = urgent revision to decompress and shorten

Medicolegal Essentials

  • •70% of THA litigation involves LLD - highest risk complication
  • •Document preoperative LLD, templating, intraoperative measurements, consent
  • •Average settlement AU$150,000-250,000 for successful LLD claims
  • •Defense requires proof of due diligence - documentation is key
  • •Navigation/robotics reduces LLD outliers and may reduce litigation risk
Quick Stats
Reading Time164 min
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