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Bone Scintigraphy: Three-Phase Interpretation

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Bone Scintigraphy: Three-Phase Interpretation

Comprehensive guide to bone scintigraphy interpretation including three-phase technique, common patterns, and clinical applications in orthopaedics for fellowship exam preparation.

High Yield
complete
Updated: 2026-01-16
High Yield Overview

Bone Scintigraphy: Three-Phase Interpretation

—Tracer
99Tc-m MDP/HDP
—Delayed Phase Timing
3-4hours post-injection
—Sensitivity
90%Greater than for bone pathology
99Half-life Tc-m
6hours

Three-Phase Bone Scan Patterns

All 3 phases positive: Osteomyelitis, tumour, fracture (acute)

Phase 1 & 2 positive, Phase 3 negative: Cellulitis, soft tissue infection

Phase 3 only positive: Degenerative, chronic fracture, bone island

Key: Osteomyelitis is three-phase positive with focal uptake in all phases

Critical Must-Knows

  • Three phases: Flow, Blood pool, Delayed
  • Tc-99m MDP uptake reflects osteoblastic activity
  • High sensitivity, low specificity
  • Three-phase positive in all phases = osteomyelitis or tumour
  • Delayed phase only positive = degenerative, stress fracture

Examiner's Pearls

  • "
    Superscan: diffuse increased uptake, no kidney visualisation (metastases, metabolic)
  • "
    Cold lesion: photopenic area suggests avascular, aggressive, or metal artefact
  • "
    Flare phenomenon: increased uptake after treatment = healing response
  • "
    Shin splints vs stress fracture: linear vs focal uptake
  • "
    SPECT-CT improves specificity significantly

Exam Warning

Bone scan interpretation is commonly tested. You must know the three phases and their timing, understand what causes increased vs decreased uptake, and recognise classic patterns (superscan, three-phase positive). Remember: bone scan shows osteoblastic activity, not malignancy per se.

Normal whole-body bone scan showing anterior view
Click to expand
Whole-body bone scan (delayed phase, anterior view) demonstrating normal physiological tracer distribution. Tc-99m MDP uptake is visible in the skull (calvarium), spine (vertebral bodies), ribs, sternum, pelvis (including bilateral acetabulum and sacroiliac joints), and proximal femora. Normal bone scans show symmetric uptake with physiologically increased activity at sites of high bone turnover (growth plates in children, joints). The kidneys and bladder may also be visualised as the tracer is renally excreted. This baseline knowledge of normal appearances is essential for recognising pathological focal or diffuse abnormalities.Credit: Kieran Maher via Wikimedia - Public Domain

Radiopharmaceutical and Mechanism

Bone Scan Radiopharmaceuticals

AgentMechanismNotes
Tc-99m MDPBinds to hydroxyapatite via chemisorptionMost commonly used
Tc-99m HDPSimilar to MDP, slightly different biodistributionAlternative agent
Tc-99m HMDPSimilar propertiesRegional availability varies

Uptake Mechanism

Tc-99m diphosphonates bind to the calcium hydroxyapatite matrix of bone. Uptake is increased wherever there is: increased blood flow (delivery), increased osteoblastic activity (bone turnover), or exposed hydroxyapatite crystal surface. This is why bone scans detect metabolic bone activity, not cancer cells directly.
Mnemonic

BLOOD and BONEBone Scan Uptake Factors

B
B = Blood flow (delivery to bone)
L
L = Local bone metabolism
O
O = Osteoblast activity
O
O = Osteoid formation
D
D = Degree of mineralisation

Memory Hook:Purely lytic lesions (myeloma, some metastases) may be cold or normal because there's no osteoblastic response

Three-Phase Technique

Three-Phase Bone Scan Protocol

PhaseTimingWhat It ShowsImage Type
Phase 1: Flow (angiogram)0-60 secondsArterial blood flow to regionDynamic 2-5 sec frames
Phase 2: Blood pool (soft tissue)2-5 minutesRegional hyperaemia, soft tissue activityStatic image
Phase 3: Delayed (bone)3-4 hoursBone uptake, osteoblastic activityWhole body + spot views

Three-Phase Scan Interpretation

PatternPhase 1Phase 2Phase 3Likely Diagnosis
Classic osteomyelitisPositivePositivePositive (focal)Osteomyelitis
CellulitisPositivePositiveNegativeSoft tissue infection only
Degenerative/chronicNegativeNegativePositiveOA, old fracture, bone island
Acute fracturePositivePositivePositiveRecent fracture
Stress fracture±±Positive (focal)Stress fracture
RSD/CRPSPositivePositivePositive (regional)Complex regional pain syndrome

Osteomyelitis Evaluation

Three-phase positive with focal bone uptake in all phases is sensitive (greater than 90%) for osteomyelitis but not specific. In diabetic foot or post-surgical bone, specificity drops significantly. Consider labelled WBC scan for better specificity.

Prosthetic Joint Assessment

Bone scan remains positive for 1-2 years after arthroplasty (normal healing). Cannot reliably distinguish infection from aseptic loosening. Use combined WBC/marrow scan for prosthetic joint infection.

Common Patterns and Findings

Superscan Definition

Diffusely increased skeletal uptake with absent or faint kidney visualisation. Causes: diffuse metastatic disease (prostate, breast), metabolic bone disease (hyperparathyroidism, osteomalacia, Paget's). The kidneys are not seen because all tracer is taken up by bone. Look for heterogeneous uptake pattern to distinguish metastases from metabolic.

Causes of Photopenic (Cold) Lesions

CauseMechanismExamples
AvascularNo blood flow to deliver tracerAVN (early), bone infarct
Aggressive tumourDestruction outpaces osteoblast responseMyeloma, anaplastic mets
Metal artefactAttenuation of photonsProstheses, plates
Prior radiationDecreased bone metabolismRadiation field
Lytic mets without responseNo osteoblastic activityRenal cell, thyroid mets

Bone Scan in Fractures

TypeAppearanceTiming
Acute fracture (less than 1 week)Three-phase positive, linear uptakePositive within 24-72 hours
Subacute fracturePhase 3 positive, phases 1/2 normalisingWeeks to months
Stress fractureFocal intense uptake (phase 3)May be positive before X-ray
Shin splintsLinear longitudinal uptake, less intensePeriostitis pattern
Healing fractureGradually decreasing uptakeMay take 1-2 years to normalise
Non-unionPersistent focal uptake at fracture siteBeyond expected healing time

Clinical Applications

Bone Scan Indications in Orthopaedics

IndicationRoleLimitations
Occult fractureHigh sensitivity, whole body coverageLow specificity, limited anatomic detail
Stress fracturePositive before X-raySPECT or MRI for precise localisation
Metastatic surveyWhole body screeningFalse negatives in purely lytic disease
OsteomyelitisSensitive screeningLow specificity in diabetic foot, hardware
Bone pain evaluationLocalise source when unclearNon-specific findings common
Paget's diseaseExtent of disease, activityCannot assess complications
Loosening vs infectionLimited roleWBC scan more specific for infection

Bone Scan vs MRI

Bone scan: Whole body, very sensitive, low anatomic detail, low specificity. MRI: Limited coverage, very sensitive, excellent anatomic detail, better specificity. Use bone scan for whole body screening (metastases, multifocal disease) and MRI for regional assessment with anatomic detail needed.

SPECT and SPECT-CT

SPECT vs Planar Bone Scan

FeaturePlanarSPECTSPECT-CT
Acquisition2D projection3D tomographic3D + anatomic CT
Lesion localisationLimitedGoodExcellent
SensitivityGoodImproved 20-50%Improved 20-50%
SpecificityLowModerateSignificantly improved
Anatomic detailPoorPoorExcellent (CT)
Scan timeShorterLongerLonger

SPECT-CT Advantages

Hybrid SPECT-CT combines functional bone scan information with CT anatomic detail. Significantly improves specificity by allowing precise anatomic localisation of uptake. Particularly useful for: spine (differentiating facet vs disc vs pars), foot (tarsal coalition, OCD), and equivocal findings on planar imaging.

Exam Viva Scenarios

Practice these scenarios to excel in your viva examination

VIVA SCENARIOStandard

EXAMINER

"A 65-year-old man with prostate cancer and new back pain is referred for bone scan staging. The scan shows diffusely increased skeletal uptake with poor kidney visualisation."

EXCEPTIONAL ANSWER
This pattern is called a 'superscan' - characterised by diffusely increased skeletal uptake with absent or faint renal visualisation. The kidneys are not seen because essentially all tracer is taken up by bone. In this patient with prostate cancer, the most likely cause is diffuse skeletal metastatic disease. However, the differential includes: (1) Diffuse metastases (prostate, breast most common), (2) Metabolic bone disease - hyperparathyroidism, osteomalacia, renal osteodystrophy. To differentiate, I would look for heterogeneous uptake pattern (favours metastases) versus uniform uptake (favours metabolic). Correlate with PSA level, calcium, PTH, and vitamin D. Plain radiographs may show blastic metastases.
KEY POINTS TO SCORE
Superscan: diffuse uptake, no kidney visualisation
Differential: diffuse metastases vs metabolic bone disease
Heterogeneous uptake favours metastases
Correlate with biochemistry (Ca, PTH, PSA)
Prostate mets are typically blastic
COMMON TRAPS
✗Assuming superscan always means metastases
✗Not considering metabolic causes
✗Missing heterogeneity that suggests metastases
VIVA SCENARIOStandard

EXAMINER

"A 12-year-old presents with ankle pain after a twisting injury. X-rays are normal. The sports medicine physician orders a three-phase bone scan."

EXCEPTIONAL ANSWER
A three-phase bone scan has: Phase 1 (flow/angiogram, 0-60 seconds) showing arterial blood flow, Phase 2 (blood pool, 2-5 minutes) showing soft tissue hyperaemia, and Phase 3 (delayed, 3-4 hours) showing bone uptake. For a stress fracture, I would expect: Phases 1 and 2 may be mildly positive or negative, Phase 3 positive with focal intense uptake at the fracture site. For osteomyelitis, I would expect: All three phases positive with focal bone uptake. The key difference is that stress fractures typically have less prominent early phases compared to osteomyelitis. However, bone scan cannot reliably differentiate acute fracture from osteomyelitis - clinical correlation and potentially MRI would be needed.
KEY POINTS TO SCORE
Phase 1: Flow (0-60 sec)
Phase 2: Blood pool (2-5 min)
Phase 3: Delayed bone (3-4 hours)
Stress fracture: Phase 3 positive, early phases ±
Osteomyelitis: All three phases positive
COMMON TRAPS
✗Not knowing phase timing
✗Expecting bone scan to definitively diagnose osteomyelitis
✗Forgetting clinical correlation is essential
VIVA SCENARIOStandard

EXAMINER

"A patient with a painful total hip replacement has a bone scan showing increased uptake around the prosthesis 3 years post-operatively."

EXCEPTIONAL ANSWER
Bone scan interpretation around arthroplasty is challenging. Normal healing causes increased uptake for 1-2 years post-surgery, so uptake at 3 years is abnormal. However, bone scan cannot reliably differentiate aseptic loosening from prosthetic joint infection - both cause increased uptake. The scan has low specificity in this setting. For improved specificity, I would recommend combined labelled white cell scan and sulphur colloid marrow scan. In infection, WBC uptake occurs WITHOUT corresponding marrow uptake (spatial mismatch). In normal post-operative change or aseptic loosening, WBC and marrow uptake are matched. This combined technique has greater than 90% accuracy for prosthetic joint infection.
KEY POINTS TO SCORE
Normal post-arthroplasty uptake persists 1-2 years
Uptake at 3 years is abnormal
Bone scan cannot differentiate infection from aseptic loosening
Combined WBC/marrow scan is gold standard for PJI
Mismatch (WBC without marrow) = infection
COMMON TRAPS
✗Using bone scan alone to diagnose PJI
✗Not knowing about combined WBC/marrow technique
✗Expecting bone scan to be specific for infection

Bone Scan Interpretation Quick Reference

High-Yield Exam Summary

Three-Phase Timing

  • •Phase 1 (Flow): 0-60 seconds
  • •Phase 2 (Blood pool): 2-5 minutes
  • •Phase 3 (Delayed): 3-4 hours

Three-Phase Patterns

  • •All phases +: Osteomyelitis, acute fracture, tumour
  • •Phases 1-2 +, Phase 3 -: Cellulitis
  • •Phase 3 only +: Degenerative, chronic fracture
  • •CRPS: Regional pattern, all phases +

Superscan Causes

  • •Diffuse metastases (prostate, breast)
  • •Metabolic bone disease
  • •Kidneys not visualised
  • •Heterogeneous = metastases

Cold Lesion Causes

  • •Avascular (AVN, infarct)
  • •Aggressive tumour (myeloma)
  • •Metal artefact
  • •Prior radiation
Quick Stats
Reading Time35 min
Related Topics

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Labelled White Cell Scanning for Infection