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MDCT and Pulmonary Embolism
Heber MacMahon
The University of Chicago
Department of Radiology
https://tinyurl.com/hmpe17
Disclosures
• Consultant for Riverain Medical
• Minor stockholder in Hologic, Inc.
• Consultant for GE Healthcare
• Research Support from Philips Healthcare
• License and royalty fees from University of Chicago
(UC Tech)
https://tinyurl.com/hmpe17
Pulmonary Embolism
 Risk Factors & pre-test probability
 CXR findings
 CT technique
 Dx on contrast and non-contrast CT scans
 Acute vs Chronic PE
 Non thrombotic PE
https://tinyurl.com/hmpe17
Pulmonary Embolism
 500,000 episodes of PE / yr in USA
 12 – 64% ICU patients at autopsy
 Contributing cause of death in 10-15% ICU pts
 Clinical diagnosis difficult
https://tinyurl.com/hmpe17
Risk Factors for PE
Strong Risk Factors
 Lower limb Fx, Hip or Knee Replacement
 Major Trauma
 MI in previous 3 mos.
 Spinal Cord Injury
 Previous VTE
2014 ESC Guidelines on the diagnosis and management of acute pulmonary
embolism; Task Force for the Diagnosis and Management of Acute Pulmonary
Embolism of the European Society of Cardiology (ESC)
European Heart Journal (2014) 35, 3033–3080
https://tinyurl.com/hmpe17
Moderate Risk Factors
 CHF
 Infection
 Cancer
 Postpartum
 Oral contraceptives
 Autoimmune disease
 Blood transfusions
Risk Factors for PE
Weak Risk Factors
 Bed rest > 3 days
 Travel of 4 hr or more in the past month
 Pregnancy
 Obesity
 Advanced age
Risk Factors for PE
Most Common Symptoms of PE
Unexplained:
 Dyspnea (50%) – Esp. sudden onset
 Pleuritic pain (39%)
 Substernal (15%)
 Hemoptysis (8%)
 Syncope/near syncope (6%)
More specific
Clinical Signs in PE
 Hypoxemia (70%)
 Tachypnea/dyspnea (90%)
 Tachycardia (40%)
 Arrythmia
 Wheezing
 Hemoptysis
 Fever (but < 39.5C)
 Signs of DVT
Simplified Wells Criteria (>2: PE likely)
 History of DVT or PE — 1 point
 Tachycardia (heart rate > 100) — 1 point
 Immobilization (≥ 3d)/surgery in previous four
weeks — 1 point
 Hemoptysis — 1 point
 Malignancy (with treatment within 6 months)
or palliative — 1 point
 Clinically suspected DVT — 1 point
 Alternative diagnosis is less likely than PE —
3.0 points
D-dimer for PE
 Cut-off value: 500 ug/L
 Negative predictive value: 98-99%
 Positive predictive value: 27-29%
 False positives associated with:
 female sex; increasing age; black (vs. white) race;
cocaine use; immobility; hemoptysis; hemodialysis;
active malignancy; rheumatoid arthritis; lupus; sickle
cell disease; prior venous thromboembolism (VTE; not
under treatment); pregnancy and postpartum state;
and abdominal, chest, orthopedic, or other surgery.
Multiple PEs with infarcts
76 y/o with pleuritic chest pain
Multiple Emboli with Small Infarcts
CXR in PE
 CXR often normal
 Focal subpleural rounded opacity, esp. CP angles
 Westermark Sign : Peripheral oligemia, caused
by chronic embolism, but often with
superimposed new acute episode
Westermark Sign
Large PE causing asymmetric pulmonary edema
CXR in PE
 CXR often normal
 Focal subpleural rounded opacity, esp. CP angles
 Westermark Sign : Peripheral oligemia, caused
by chronic embolism, but often with
superimposed new acute episode
 Fleischner Sign : Enlargement and sharp
definition of central PA
Fleischner Sign
CXR in PE
 CXR often normal
 Focal subpleural rounded opacity, esp. CP angles
 Westermark Sign : Peripheral oligemia, caused
by chronic embolism, but often with
superimposed new acute episode
 Fleischner Sign : Enlargement and sharp
definition of central PA
 Bibasilar atelectasis, subpleural opacity,
effusions, suggestive in previously healthy
individual
Unexplained Basilar Subsegmental Atelectasis
V/Q Scan accuracy for PE
V/Q Scan Results PE Prevalence
Normal or low probability
+ low clinical suspicion 4%
High probability
+ high clinical suspicion 96%
 Still a reasonable test for young women with
low PE probability and normal CXR.
or
 Patients with contraindication to IV contrast
Pulmonary C.T. Angiography
 Rapid contrast infusion (3-6 cc/sec)
 Antecubital fossa vein
 1 – 1.5 mm collimation
 Shallow breath hold
 Fixed delay, bolus tracking, timing bolus
Test bolus vs Bolus Tracking
• Test bolus: Visual estimation by tech of
optimal contrast timing.
• Makes cursor placement less critical.
• Subjective judgement
• Bolus Tracking: Automatic trigger for scan
based on bolus arrival
• Cursor placement critical
• Adds several seconds to scan delay
Test Bolus. Cursor on PA
Normal Circulation Time
Abnormal Test Bolus – Slow Circulation
Main Contrast Bolus – Slow Circulation
Test Bolus using Descending Aorta
Non-Diagnostic CTA
 Bolus Timing
 Motion artifact
 Poor contrast enhancement
- Flow obstruction
- Deep inspiration > dilution
- Contrast timing error
 Beam hardening and noise –obesity
Dilution by unopacified IVC inflow
“Relax, take in a small breath and hold it”
PE CT Results over 12 months at U Chicago
Saddle EmbolusSaddle and Subsegmental Emboli
“Very small PE of uncertain chronicity and clinical significance”
PA diameter Septal deviation
Clinical Significance and Prognosis in Acute PE
PE-related mortality predictors
 Age above 60 years
 RV/LV area >1 (odds ratio 8.6)
 RV/LV diameter >1.5 (odds ratio 48.8,P<0.001)
 Timing bolus upslope time > 6 seconds (odds ratio
23.3), 50% downslope time >6 seconds (odds ratio
20)
 Embolus load score >15 (odds ratio 25)
 Li C, Lin CT, Kligerman SJ, Hong SN, White CS. JTI 2014
Pulmonary Infarct - Hampton’s Hump
 Only 15% cause true
infarction
 Most in lower lobes
 Usually multiple
Pulmonary Infarct
Pulmonary Infarct
• Sharply defined consolidation
• Central lucency
• Absence of air bronchogram
Pulmonary Infarcts
Likelihood Ratios:
23.0 for central lucencies
2.9 for vessel sign
(enlarged vessel at apex)
0.2 for air bronchograms
Revel et al. Radiology: Volume 244: Number 3 September 2007
PE with HemorrhageR flank pain. Acute PE
Breast cancer patient with lung nodule
Acute PE
Resolving Infarct
Evolving Infarct – Melting Ice cube Sign
Incidental RUL Nodule
6 months3 weeks
BaselineBaseline
3-4-03 3 months
Evolving Infarct: “Melting Ice Cube Sign”
60 y/o male with hemoptysis
60 y/o male with hemoptysis
60 y/o male with hemoptysis
Non-Contrast Scan
Non-Contrast Scan
Saddle Embolus on Non- Enhanced CT Scan
Chronic PE
Chronic PE
Chronic PE
 Recanalized, organized or calcified thrombus
Arterial Web
12-02 1-03Embolus > Web
2 yrs later- arterial web
12-04
Chronic PE
 Recanalized, organized or calcified thrombus
 Intraluminal webs or bands
 Pulmonary hypertension
Chronic PE
Chronic and Acute PE
Chronic PE – Mosaic Perfusion
Chronic PE – Decreased perfusion & bronchiectasis
Enlarged Bronchial Collaterals in Chronic PE
Enlarged Bronchial Collaterals in Chronic PE
Chronic PE
 Recanalized, organized, calcified thrombus
 Intraluminal webs or bands
 Pulmonary hypertension
 Mosaic perfusion
 Collateral vascularization
CTA for PE: Common Pitfalls
 Failure to use proper window & level
Narrow window settingStandard ST Window
CTA for PE: Common Pitfalls
 Failure to use correct window &level
 Use of lung (sharp) algorithm
Lung Standard
Effect of lung filter
ECG Gated Cardiac Scan
CTA for PE: Common Pitfalls
 Failure to optimize window level/width
 Use of lung reconstruction filter
 Vascular bifurcations (false positives)
5 mm
1mm
CTA for PE: Common Pitfalls
 Failure to optimize window level/width
 Use of lung reconstruction algorithm
 Vascular bifurcations (false positives)
 Motion/averaging artifact (false positive or
negative)
Motion with Density Averaging
Density Averaging : Crossing Bronchus
Decreased flow with Incomplete Opacification
CTA for PE: Common Pitfalls
 Failure to use workstation (window/level)
 Use of lung reconstruction algorithm
 Vascular bifurcations (false positives)
 Motion/averaging artifact (false positive or
negative)
 Bronchiectasis
Bronchiectasis
Postpneumonectomy. R/O PE
 Occurs in up to 12% of cases
 Likelihood related to length of arterial stump
 May propagate or resolve
 Benign course without treatment
Arterial Stump Thrombus
 Post-op Lobectomy or Pneumonectomy thrombosis
in situ
Non- embolic thrombus &
Non-thrombotic emboli
51 y/o woman with severe SOB
Uterine Leiomyosarcoma
 Post-op Lobectomy or Pneumonectomy thrombosis
in situ
 Tumor Embolism
 Tumor embolism from remote solid tumors (breast, lung,
stomach)
 Propagation of tumor via IVC (renal, hepatic, uterine)
 Primary arterial sarcomas
Non- embolic thrombus &
Non-thrombotic emboli
Asymptomatic Patient
Asymptomatic Patient
Polymethymethacrylate Cement Embolism
Polymethymethacrylate cement embolism
• 4-23% of procedures
• <1% symptomatic
Polymethymethacrylate Cement Embolism
 Post-op Lobectomy or Pneumonectomy thrombosis
in situ
 Tumor Embolism
 Tumor embolism from remote solid tumors (breast, lung,
stomach)
 Propagation of tumor via IVC (renal, hepatic, uterine)
 Primary arterial sarcomas
 Foreign material (Surgical cement, filter fragments,
Needle fragments)
Non- embolic thrombus &
Non-thrombotic emboli
Take Home Points
 CTA is the preferred diagnostic test for PE except
in young patients with low clinical probability.
 PE can often be recognized on CXRs and non
contrast CT scans
 Technique is important; use high injection rate
with saline chaser, thin sections, and small
inspiration.
 Use bolus time to aorta to estimate timing
 Significance of isolated subsegmental emboli is
uncertain
https://tinyurl.com/hmpe17
https://tinyurl.com/hmpe17

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Mac mahon venice pe pdf

  • 1. MDCT and Pulmonary Embolism Heber MacMahon The University of Chicago Department of Radiology https://tinyurl.com/hmpe17
  • 2. Disclosures • Consultant for Riverain Medical • Minor stockholder in Hologic, Inc. • Consultant for GE Healthcare • Research Support from Philips Healthcare • License and royalty fees from University of Chicago (UC Tech) https://tinyurl.com/hmpe17
  • 3. Pulmonary Embolism  Risk Factors & pre-test probability  CXR findings  CT technique  Dx on contrast and non-contrast CT scans  Acute vs Chronic PE  Non thrombotic PE https://tinyurl.com/hmpe17
  • 4. Pulmonary Embolism  500,000 episodes of PE / yr in USA  12 – 64% ICU patients at autopsy  Contributing cause of death in 10-15% ICU pts  Clinical diagnosis difficult https://tinyurl.com/hmpe17
  • 5. Risk Factors for PE Strong Risk Factors  Lower limb Fx, Hip or Knee Replacement  Major Trauma  MI in previous 3 mos.  Spinal Cord Injury  Previous VTE 2014 ESC Guidelines on the diagnosis and management of acute pulmonary embolism; Task Force for the Diagnosis and Management of Acute Pulmonary Embolism of the European Society of Cardiology (ESC) European Heart Journal (2014) 35, 3033–3080 https://tinyurl.com/hmpe17
  • 6. Moderate Risk Factors  CHF  Infection  Cancer  Postpartum  Oral contraceptives  Autoimmune disease  Blood transfusions Risk Factors for PE
  • 7. Weak Risk Factors  Bed rest > 3 days  Travel of 4 hr or more in the past month  Pregnancy  Obesity  Advanced age Risk Factors for PE
  • 8. Most Common Symptoms of PE Unexplained:  Dyspnea (50%) – Esp. sudden onset  Pleuritic pain (39%)  Substernal (15%)  Hemoptysis (8%)  Syncope/near syncope (6%) More specific
  • 9. Clinical Signs in PE  Hypoxemia (70%)  Tachypnea/dyspnea (90%)  Tachycardia (40%)  Arrythmia  Wheezing  Hemoptysis  Fever (but < 39.5C)  Signs of DVT
  • 10. Simplified Wells Criteria (>2: PE likely)  History of DVT or PE — 1 point  Tachycardia (heart rate > 100) — 1 point  Immobilization (≥ 3d)/surgery in previous four weeks — 1 point  Hemoptysis — 1 point  Malignancy (with treatment within 6 months) or palliative — 1 point  Clinically suspected DVT — 1 point  Alternative diagnosis is less likely than PE — 3.0 points
  • 11. D-dimer for PE  Cut-off value: 500 ug/L  Negative predictive value: 98-99%  Positive predictive value: 27-29%  False positives associated with:  female sex; increasing age; black (vs. white) race; cocaine use; immobility; hemoptysis; hemodialysis; active malignancy; rheumatoid arthritis; lupus; sickle cell disease; prior venous thromboembolism (VTE; not under treatment); pregnancy and postpartum state; and abdominal, chest, orthopedic, or other surgery.
  • 12. Multiple PEs with infarcts
  • 13. 76 y/o with pleuritic chest pain
  • 14. Multiple Emboli with Small Infarcts
  • 15. CXR in PE  CXR often normal  Focal subpleural rounded opacity, esp. CP angles  Westermark Sign : Peripheral oligemia, caused by chronic embolism, but often with superimposed new acute episode
  • 17. Large PE causing asymmetric pulmonary edema
  • 18. CXR in PE  CXR often normal  Focal subpleural rounded opacity, esp. CP angles  Westermark Sign : Peripheral oligemia, caused by chronic embolism, but often with superimposed new acute episode  Fleischner Sign : Enlargement and sharp definition of central PA
  • 20. CXR in PE  CXR often normal  Focal subpleural rounded opacity, esp. CP angles  Westermark Sign : Peripheral oligemia, caused by chronic embolism, but often with superimposed new acute episode  Fleischner Sign : Enlargement and sharp definition of central PA  Bibasilar atelectasis, subpleural opacity, effusions, suggestive in previously healthy individual
  • 22. V/Q Scan accuracy for PE V/Q Scan Results PE Prevalence Normal or low probability + low clinical suspicion 4% High probability + high clinical suspicion 96%  Still a reasonable test for young women with low PE probability and normal CXR. or  Patients with contraindication to IV contrast
  • 23. Pulmonary C.T. Angiography  Rapid contrast infusion (3-6 cc/sec)  Antecubital fossa vein  1 – 1.5 mm collimation  Shallow breath hold  Fixed delay, bolus tracking, timing bolus
  • 24. Test bolus vs Bolus Tracking • Test bolus: Visual estimation by tech of optimal contrast timing. • Makes cursor placement less critical. • Subjective judgement • Bolus Tracking: Automatic trigger for scan based on bolus arrival • Cursor placement critical • Adds several seconds to scan delay
  • 27. Abnormal Test Bolus – Slow Circulation
  • 28. Main Contrast Bolus – Slow Circulation
  • 29. Test Bolus using Descending Aorta
  • 30. Non-Diagnostic CTA  Bolus Timing  Motion artifact  Poor contrast enhancement - Flow obstruction - Deep inspiration > dilution - Contrast timing error  Beam hardening and noise –obesity
  • 31. Dilution by unopacified IVC inflow “Relax, take in a small breath and hold it”
  • 32. PE CT Results over 12 months at U Chicago
  • 33. Saddle EmbolusSaddle and Subsegmental Emboli
  • 34. “Very small PE of uncertain chronicity and clinical significance”
  • 35. PA diameter Septal deviation Clinical Significance and Prognosis in Acute PE
  • 36. PE-related mortality predictors  Age above 60 years  RV/LV area >1 (odds ratio 8.6)  RV/LV diameter >1.5 (odds ratio 48.8,P<0.001)  Timing bolus upslope time > 6 seconds (odds ratio 23.3), 50% downslope time >6 seconds (odds ratio 20)  Embolus load score >15 (odds ratio 25)  Li C, Lin CT, Kligerman SJ, Hong SN, White CS. JTI 2014
  • 37. Pulmonary Infarct - Hampton’s Hump
  • 38.  Only 15% cause true infarction  Most in lower lobes  Usually multiple Pulmonary Infarct
  • 39. Pulmonary Infarct • Sharply defined consolidation • Central lucency • Absence of air bronchogram
  • 40. Pulmonary Infarcts Likelihood Ratios: 23.0 for central lucencies 2.9 for vessel sign (enlarged vessel at apex) 0.2 for air bronchograms Revel et al. Radiology: Volume 244: Number 3 September 2007
  • 41. PE with HemorrhageR flank pain. Acute PE
  • 42. Breast cancer patient with lung nodule
  • 44. Evolving Infarct – Melting Ice cube Sign Incidental RUL Nodule
  • 45. 6 months3 weeks BaselineBaseline 3-4-03 3 months Evolving Infarct: “Melting Ice Cube Sign”
  • 46. 60 y/o male with hemoptysis
  • 47. 60 y/o male with hemoptysis
  • 48. 60 y/o male with hemoptysis
  • 51. Saddle Embolus on Non- Enhanced CT Scan
  • 54. Chronic PE  Recanalized, organized or calcified thrombus
  • 57. 2 yrs later- arterial web 12-04
  • 58. Chronic PE  Recanalized, organized or calcified thrombus  Intraluminal webs or bands  Pulmonary hypertension
  • 61. Chronic PE – Mosaic Perfusion
  • 62. Chronic PE – Decreased perfusion & bronchiectasis
  • 65. Chronic PE  Recanalized, organized, calcified thrombus  Intraluminal webs or bands  Pulmonary hypertension  Mosaic perfusion  Collateral vascularization
  • 66. CTA for PE: Common Pitfalls  Failure to use proper window & level
  • 68. CTA for PE: Common Pitfalls  Failure to use correct window &level  Use of lung (sharp) algorithm
  • 69. Lung Standard Effect of lung filter
  • 71. CTA for PE: Common Pitfalls  Failure to optimize window level/width  Use of lung reconstruction filter  Vascular bifurcations (false positives)
  • 72.
  • 74. CTA for PE: Common Pitfalls  Failure to optimize window level/width  Use of lung reconstruction algorithm  Vascular bifurcations (false positives)  Motion/averaging artifact (false positive or negative)
  • 75. Motion with Density Averaging
  • 76. Density Averaging : Crossing Bronchus
  • 77. Decreased flow with Incomplete Opacification
  • 78. CTA for PE: Common Pitfalls  Failure to use workstation (window/level)  Use of lung reconstruction algorithm  Vascular bifurcations (false positives)  Motion/averaging artifact (false positive or negative)  Bronchiectasis
  • 79.
  • 82.  Occurs in up to 12% of cases  Likelihood related to length of arterial stump  May propagate or resolve  Benign course without treatment Arterial Stump Thrombus
  • 83.  Post-op Lobectomy or Pneumonectomy thrombosis in situ Non- embolic thrombus & Non-thrombotic emboli
  • 84. 51 y/o woman with severe SOB
  • 86.  Post-op Lobectomy or Pneumonectomy thrombosis in situ  Tumor Embolism  Tumor embolism from remote solid tumors (breast, lung, stomach)  Propagation of tumor via IVC (renal, hepatic, uterine)  Primary arterial sarcomas Non- embolic thrombus & Non-thrombotic emboli
  • 90. Polymethymethacrylate cement embolism • 4-23% of procedures • <1% symptomatic Polymethymethacrylate Cement Embolism
  • 91.  Post-op Lobectomy or Pneumonectomy thrombosis in situ  Tumor Embolism  Tumor embolism from remote solid tumors (breast, lung, stomach)  Propagation of tumor via IVC (renal, hepatic, uterine)  Primary arterial sarcomas  Foreign material (Surgical cement, filter fragments, Needle fragments) Non- embolic thrombus & Non-thrombotic emboli
  • 92. Take Home Points  CTA is the preferred diagnostic test for PE except in young patients with low clinical probability.  PE can often be recognized on CXRs and non contrast CT scans  Technique is important; use high injection rate with saline chaser, thin sections, and small inspiration.  Use bolus time to aorta to estimate timing  Significance of isolated subsegmental emboli is uncertain https://tinyurl.com/hmpe17