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Dr. Mohammad Ashraful AminDr. Mohammad Ashraful Amin
Cardiology deptCardiology dept
Presentation onPresentation on
Pulmonary embolismPulmonary embolism
managementmanagement
TopicsTopics
 •• IntroductionIntroduction
 •• Diagnostic approachDiagnostic approach
 •• Treatment optionsTreatment options
 •• Special circumstances: Pregnant patientSpecial circumstances: Pregnant patient
 •• PreventionPrevention
IntroductionIntroduction
 •• Pulmonary embolism (PE) is aPulmonary embolism (PE) is a
medical emergencymedical emergency
 where pulmonary artery or its brancheswhere pulmonary artery or its branches
are blockedare blocked
 with embolic substances most commonlywith embolic substances most commonly
blood clotsblood clots
 •• Most cases are not life threatening.Most cases are not life threatening.
Types of PETypes of PE
 •• Massive PE: Acute PE with obstructive shockMassive PE: Acute PE with obstructive shock
or SBPor SBP
<90 mmHg<90 mmHg
 •• Sub-massive PE: Acute PE without systemicSub-massive PE: Acute PE without systemic
hypotension (SBP ≥90 mm Hg) but with either RVhypotension (SBP ≥90 mm Hg) but with either RV
dysfunction or myocardial necrosisdysfunction or myocardial necrosis
 •• Non-massive or low risk PE: None of theNon-massive or low risk PE: None of the
aboveabove
 severe featuressevere features..
PathophysiologyPathophysiology
 Deep vein thrombosis from large veinDeep vein thrombosis from large vein
commonly abovecommonly above
 the knee → Inferior vena cava → Rightthe knee → Inferior vena cava → Right
atrium →atrium →
 Right ventricle → Pulmonary artery → PERight ventricle → Pulmonary artery → PE
 Ventilation perfusion mismatch →Ventilation perfusion mismatch →
HypoxemiaHypoxemia
 ↓↓Venous return → Right heart failure →Venous return → Right heart failure →
ShockShock
DiagnosisDiagnosis
 •• Risk stratificationRisk stratification
 •• Clinical examinationClinical examination
 •• Bed side testsBed side tests
 •• Laboratory testsLaboratory tests
 •• Imaging techniquesImaging techniques
Risk factorsRisk factors
 •• Alteration of blood flow:Alteration of blood flow:
 –– Prolonged immobilization,Prolonged immobilization,
 –– Obesity,Obesity,
 –– Pregnancy,Pregnancy,
 –– CancerCancer
 Factors in blood vessel wall:Factors in blood vessel wall:
a.a. –– Surgery,Surgery,
b.b. –– Catheterisation.Catheterisation.
c.c. –– TraumaTrauma
Hypercoagulable states:Hypercoagulable states:
 –– Estrogen containing OCP,Estrogen containing OCP,
 –– Genetic thrombophilia (Factor V LeidenGenetic thrombophilia (Factor V Leiden
deficiency, Protein C anddeficiency, Protein C and
 Protein S deficiency, antithrombinProtein S deficiency, antithrombin
deficiency etc.),deficiency etc.),
 –– Acquired thrombophilia (antiphospholipidAcquired thrombophilia (antiphospholipid
syndrome, nephroticsyndrome, nephrotic
 syndrome, paroxysmal nocturnalsyndrome, paroxysmal nocturnal
hemoglobinuria)hemoglobinuria)
Risk stratificationRisk stratification
 Clinical judgmentClinical judgment
 •• Wells score for PEWells score for PE
 •• Modified Geneva score for PEModified Geneva score for PE
Wells score for PEWells score for PE
Modified Geneva score forModified Geneva score for
PEPE
Clinical Presentation:Clinical Presentation:
SymptomsSymptoms
 •• Chest pain: Sharp, pleuritic in nature, noChest pain: Sharp, pleuritic in nature, no
radiation,radiation,
 aggravated by coughing and deep breathaggravated by coughing and deep breath
 •• HaemoptysisHaemoptysis
 •• Shortness of breathShortness of breath
 •• CollapseCollapse
 •• PalpitationsPalpitations
 •• Sudden death: 15% of sudden death dueSudden death: 15% of sudden death due
to PEto PE
Clinical Presentation:Clinical Presentation:
SignsSigns
 Dyspnoea, cyanosis, paleDyspnoea, cyanosis, pale
 •• TachypneaTachypnea
 •• TachycardiaTachycardia
 •• HypoxiaHypoxia
 •• HypotensionHypotension
 •• Pulmonary hypertensionPulmonary hypertension
Chest examinationChest examination
 •• May be normalMay be normal
 •• Friction rubFriction rub
 •• Features of pleural effusionFeatures of pleural effusion
 •• Raised JVPRaised JVP
InvestigationsInvestigations
 •• Bed side tests: ECG, ABGBed side tests: ECG, ABG
 •• Blood tests: D-dimer, FBC,Blood tests: D-dimer, FBC,
Troponin, UECTroponin, UEC
 •• Imaging techniques: Ultrasound/Imaging techniques: Ultrasound/
Doppler scan,Doppler scan,
 Chest xray, CTPA, V/Q scan,Chest xray, CTPA, V/Q scan,
EchocardiogramEchocardiogram
ABG findings in PEABG findings in PE
 pH= ↑pH= ↑
 •• PaO2= ↓PaO2= ↓
 •• PaCO2= ↓PaCO2= ↓
 •• HCO3= NormalHCO3= Normal
 •• Aa gradient= LargeAa gradient= Large
 Aa gradient= PAO2- PaO2Aa gradient= PAO2- PaO2
Chest xrayChest xray
 Mostly normal findingsMostly normal findings
 •• Done to exclude other pathologyDone to exclude other pathology
 •• Plural effusionPlural effusion
•• Specific signs:Specific signs:
 - Hampton’s hump- Hampton’s hump
 - Westermark sign- Westermark sign
 Hampton's humpHampton's hump, also called , also called HamptonHampton
humphump, is a radiologic sign which consists, is a radiologic sign which consists
of a shallow wedge-shaped opacity in theof a shallow wedge-shaped opacity in the
periphery of the lung with its base againstperiphery of the lung with its base against
the pleural surface. the pleural surface. 
Hampton’s humpHampton’s hump
Westermark signWestermark sign
   the the Westermark signWestermark sign  is a  is a signsign that that
represents a focus of represents a focus of oligemiaoligemia
 (hypovolemia) (leading to collapse of (hypovolemia) (leading to collapse of
vessel) seen distal to a vessel) seen distal to a 
pulmonary embolismpulmonary embolism (PE) (PE)
Westermark signWestermark sign
ECG findings in PEECG findings in PE
 •• Normal sinus rhythmNormal sinus rhythm
 •• Sinus tachycardiaSinus tachycardia
 •• Tall peaked T waves in V1- V4Tall peaked T waves in V1- V4
 •• S1Q3T3 pattern: Not specific. Can beS1Q3T3 pattern: Not specific. Can be
seen in any Cor pulmonale syndromeseen in any Cor pulmonale syndrome
 •• RBBBRBBB
S1Q3T3 pattern ECGS1Q3T3 pattern ECG
D-dimer in PED-dimer in PE
 D-dimer is a type of Fibrin degradationD-dimer is a type of Fibrin degradation
productproduct
 •• Can be raised due to a number ofCan be raised due to a number of
reasonsreasons
 •• Negative D-dimer rules out PE/DVT inNegative D-dimer rules out PE/DVT in
98% cases98% cases
 •• False positive D-dimer:False positive D-dimer: infection,infection,
pregnancy, renalpregnancy, renal failure, post-operativefailure, post-operative
Echocardiogram in PEEchocardiogram in PE
CTPACTPA
 Indications:Indications:
 - Suspected PE- Suspected PE
 Contra-indications:Contra-indications:
 - Renal failure- Renal failure
 - Pregnancy- Pregnancy
 - Allergy to radio-contrast- Allergy to radio-contrast
 Procedure:Procedure:
 - Radioactive iodine administered IV- Radioactive iodine administered IV
 - CT scan performed- CT scan performed
Ventilation-perfusion scanVentilation-perfusion scan
 Indications:Indications:
 - Renal failure- Renal failure
 - Pregnancy- Pregnancy
 Procedure:Procedure:
 - Ventilation scan with Xenon inhalation- Ventilation scan with Xenon inhalation
 - Perfusion scan with Tc99m labelled radioactive- Perfusion scan with Tc99m labelled radioactive
dye infusiondye infusion
 - Scan V/Q- Scan V/Q
 - Result: unmatched V/Q- Result: unmatched V/Q
Ventilation-perfusion scanVentilation-perfusion scan
Pulmonary angiogramPulmonary angiogram
 Gold standard test for PEGold standard test for PE
•• Procedure:Procedure:
 –– Catheter inserted to right ventricleCatheter inserted to right ventricle
 –– Radio opaque dye injectedRadio opaque dye injected
 –– Imaging technique used to identify theImaging technique used to identify the
clotclot
Treatment optionsTreatment options
 Symptomatic treatment:Symptomatic treatment:
 –– ABCD approachABCD approach
 –– OxygenOxygen
 –– AnalgesiaAnalgesia
 •• Anticoagulation:Anticoagulation:
 –– IV HeparinIV Heparin
 –– S/C LMWH eg Enoxaparine, DalteparineS/C LMWH eg Enoxaparine, Dalteparine
 –– Oral WarfarinOral Warfarin
 •• IVC filter: If there is contra-indications forIVC filter: If there is contra-indications for
anti-coagulationanti-coagulation
 •• Thrombolysis: tPA eg Alteplase, TenectaplaseThrombolysis: tPA eg Alteplase, Tenectaplase
 •• Surgical procedures: Pulmonary embolectomySurgical procedures: Pulmonary embolectomy
Treatment optionsTreatment options
 Massive PE:Massive PE:
Thrombolysis/embolectomyThrombolysis/embolectomy
 •• Sub-massive PE: StronglySub-massive PE: Strongly
considerconsider
 thrombolysis/embolectomy but need tothrombolysis/embolectomy but need to
balance risk of bleedingbalance risk of bleeding
 •• Non-massive PE: AnticoagulationNon-massive PE: Anticoagulation
ThrombolysisThrombolysis
 Indications:Indications:
 –– Massive PEMassive PE
 –– Sub-massive PE where risk of bleeding lowSub-massive PE where risk of bleeding low
 •• Contraindications:Contraindications:
 –– Bleeding, recent stroke, HI, current GI bleeding,Bleeding, recent stroke, HI, current GI bleeding,
 bleeding PUD, surgery within 7 daybleeding PUD, surgery within 7 day
Drugs:Drugs:
Lytic agent Dose regimen
Streptokinase Loading dose:250000UIV
Continuous infusion:100000 U/h For
24hrs
Uroklinase Loading dose:2000U/Ib IV over 10min
Continuous infusion :2000 U/Ib/H for
12-24h
Alteplase (Tpa) Loading dose:None
Continous infusion :100mg over 2h
Reteplase 1.Bolus: 10U IV
2.Bolus :10U IV after 30min
AnticoagulationAnticoagulation
 IV Heparin:IV Heparin:
80 units/kg bolus followed by 18 units/kg infusion80 units/kg bolus followed by 18 units/kg infusion
 •• Monitor APTT 60-90 secMonitor APTT 60-90 sec
•• Side effects:Side effects:
 –– HITS (Heparin induced thrombocytopeniaHITS (Heparin induced thrombocytopenia
syndrome):syndrome):
paradoxical hypercoagulable state leads to clotsparadoxical hypercoagulable state leads to clots
 –– BleedingBleeding
AnticoagulationAnticoagulation
 Low molecular weight Heparin (LMWH)Low molecular weight Heparin (LMWH)
 Enoxaprin (Clexane): S/CEnoxaprin (Clexane): S/C
 - 1.5mg/kg/24 hours Or 1mg/kg/12 hours- 1.5mg/kg/24 hours Or 1mg/kg/12 hours
 - 1 mg/kg/24 hours in renal impairment- 1 mg/kg/24 hours in renal impairment
 Duration: 6 to 9 monthsDuration: 6 to 9 months
 Side effect: Low HITSSide effect: Low HITS
AnticoagulationAnticoagulation
 Vitamin K antagonistVitamin K antagonist
 •• Warfarin:Warfarin:
5mg PO initial dose5mg PO initial dose
Check regular INR 2-3Check regular INR 2-3
Side effects:Side effects:
 –– BleedingBleeding
 –– Unusual bruisesUnusual bruises
IVC filterIVC filter
 Indications:Indications:
 - DVT with massive pulmonary embolus- DVT with massive pulmonary embolus
 - Recurrent PE not treatable with- Recurrent PE not treatable with
anticoagulationanticoagulation
 - Absolute contra-indications for anti-- Absolute contra-indications for anti-
coagulationcoagulation
 - Trauma patients- Trauma patients
PE in PregnancyPE in Pregnancy
 All three components of Virchow’s triadAll three components of Virchow’s triad
are affected duringare affected during
 pregnancypregnancy
 •• D-dimer has high negative predictiveD-dimer has high negative predictive
value. False positivevalue. False positive
 result is commonresult is common
 •• V/Q scan is preferred techniqueV/Q scan is preferred technique
 •• CTPA can be done if VQ is inconclusiveCTPA can be done if VQ is inconclusive
 •• Preferred treatment option: LMWHPreferred treatment option: LMWH
 •• Warfarin is contraindicatedWarfarin is contraindicated
Prevention of PEPrevention of PE
 Control of obesityControl of obesity
 •• Stop smokingStop smoking
 •• StockingsStockings
 •• Heparin: 5000 units/day IVHeparin: 5000 units/day IV
 •• Enoxaprin: 40 mg/day S/CEnoxaprin: 40 mg/day S/C
And finally…And finally…
 PE is often over-diagnosed;PE is often over-diagnosed;
 PE is often under-diagnosed;PE is often under-diagnosed;
 The over- or under-diagnosis of PE resultsThe over- or under-diagnosis of PE results
in increasedin increased
 cost, morbidity, mortality and medico-legalcost, morbidity, mortality and medico-legal
risks.risks.
Pulmonary embolism managenent

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Pulmonary embolism managenent

  • 1. Dr. Mohammad Ashraful AminDr. Mohammad Ashraful Amin Cardiology deptCardiology dept Presentation onPresentation on Pulmonary embolismPulmonary embolism managementmanagement
  • 2. TopicsTopics  •• IntroductionIntroduction  •• Diagnostic approachDiagnostic approach  •• Treatment optionsTreatment options  •• Special circumstances: Pregnant patientSpecial circumstances: Pregnant patient  •• PreventionPrevention
  • 3. IntroductionIntroduction  •• Pulmonary embolism (PE) is aPulmonary embolism (PE) is a medical emergencymedical emergency  where pulmonary artery or its brancheswhere pulmonary artery or its branches are blockedare blocked  with embolic substances most commonlywith embolic substances most commonly blood clotsblood clots  •• Most cases are not life threatening.Most cases are not life threatening.
  • 4. Types of PETypes of PE  •• Massive PE: Acute PE with obstructive shockMassive PE: Acute PE with obstructive shock or SBPor SBP <90 mmHg<90 mmHg  •• Sub-massive PE: Acute PE without systemicSub-massive PE: Acute PE without systemic hypotension (SBP ≥90 mm Hg) but with either RVhypotension (SBP ≥90 mm Hg) but with either RV dysfunction or myocardial necrosisdysfunction or myocardial necrosis  •• Non-massive or low risk PE: None of theNon-massive or low risk PE: None of the aboveabove  severe featuressevere features..
  • 5. PathophysiologyPathophysiology  Deep vein thrombosis from large veinDeep vein thrombosis from large vein commonly abovecommonly above  the knee → Inferior vena cava → Rightthe knee → Inferior vena cava → Right atrium →atrium →  Right ventricle → Pulmonary artery → PERight ventricle → Pulmonary artery → PE  Ventilation perfusion mismatch →Ventilation perfusion mismatch → HypoxemiaHypoxemia  ↓↓Venous return → Right heart failure →Venous return → Right heart failure → ShockShock
  • 6.
  • 7. DiagnosisDiagnosis  •• Risk stratificationRisk stratification  •• Clinical examinationClinical examination  •• Bed side testsBed side tests  •• Laboratory testsLaboratory tests  •• Imaging techniquesImaging techniques
  • 8. Risk factorsRisk factors  •• Alteration of blood flow:Alteration of blood flow:  –– Prolonged immobilization,Prolonged immobilization,  –– Obesity,Obesity,  –– Pregnancy,Pregnancy,  –– CancerCancer
  • 9.  Factors in blood vessel wall:Factors in blood vessel wall: a.a. –– Surgery,Surgery, b.b. –– Catheterisation.Catheterisation. c.c. –– TraumaTrauma
  • 10. Hypercoagulable states:Hypercoagulable states:  –– Estrogen containing OCP,Estrogen containing OCP,  –– Genetic thrombophilia (Factor V LeidenGenetic thrombophilia (Factor V Leiden deficiency, Protein C anddeficiency, Protein C and  Protein S deficiency, antithrombinProtein S deficiency, antithrombin deficiency etc.),deficiency etc.),  –– Acquired thrombophilia (antiphospholipidAcquired thrombophilia (antiphospholipid syndrome, nephroticsyndrome, nephrotic  syndrome, paroxysmal nocturnalsyndrome, paroxysmal nocturnal hemoglobinuria)hemoglobinuria)
  • 11. Risk stratificationRisk stratification  Clinical judgmentClinical judgment  •• Wells score for PEWells score for PE  •• Modified Geneva score for PEModified Geneva score for PE
  • 12. Wells score for PEWells score for PE
  • 13. Modified Geneva score forModified Geneva score for PEPE
  • 14. Clinical Presentation:Clinical Presentation: SymptomsSymptoms  •• Chest pain: Sharp, pleuritic in nature, noChest pain: Sharp, pleuritic in nature, no radiation,radiation,  aggravated by coughing and deep breathaggravated by coughing and deep breath  •• HaemoptysisHaemoptysis  •• Shortness of breathShortness of breath  •• CollapseCollapse  •• PalpitationsPalpitations  •• Sudden death: 15% of sudden death dueSudden death: 15% of sudden death due to PEto PE
  • 15. Clinical Presentation:Clinical Presentation: SignsSigns  Dyspnoea, cyanosis, paleDyspnoea, cyanosis, pale  •• TachypneaTachypnea  •• TachycardiaTachycardia  •• HypoxiaHypoxia  •• HypotensionHypotension  •• Pulmonary hypertensionPulmonary hypertension
  • 16. Chest examinationChest examination  •• May be normalMay be normal  •• Friction rubFriction rub  •• Features of pleural effusionFeatures of pleural effusion  •• Raised JVPRaised JVP
  • 17. InvestigationsInvestigations  •• Bed side tests: ECG, ABGBed side tests: ECG, ABG  •• Blood tests: D-dimer, FBC,Blood tests: D-dimer, FBC, Troponin, UECTroponin, UEC  •• Imaging techniques: Ultrasound/Imaging techniques: Ultrasound/ Doppler scan,Doppler scan,  Chest xray, CTPA, V/Q scan,Chest xray, CTPA, V/Q scan, EchocardiogramEchocardiogram
  • 18. ABG findings in PEABG findings in PE  pH= ↑pH= ↑  •• PaO2= ↓PaO2= ↓  •• PaCO2= ↓PaCO2= ↓  •• HCO3= NormalHCO3= Normal  •• Aa gradient= LargeAa gradient= Large  Aa gradient= PAO2- PaO2Aa gradient= PAO2- PaO2
  • 19. Chest xrayChest xray  Mostly normal findingsMostly normal findings  •• Done to exclude other pathologyDone to exclude other pathology  •• Plural effusionPlural effusion •• Specific signs:Specific signs:  - Hampton’s hump- Hampton’s hump  - Westermark sign- Westermark sign
  • 20.  Hampton's humpHampton's hump, also called , also called HamptonHampton humphump, is a radiologic sign which consists, is a radiologic sign which consists of a shallow wedge-shaped opacity in theof a shallow wedge-shaped opacity in the periphery of the lung with its base againstperiphery of the lung with its base against the pleural surface. the pleural surface. 
  • 22. Westermark signWestermark sign    the the Westermark signWestermark sign  is a  is a signsign that that represents a focus of represents a focus of oligemiaoligemia  (hypovolemia) (leading to collapse of (hypovolemia) (leading to collapse of vessel) seen distal to a vessel) seen distal to a  pulmonary embolismpulmonary embolism (PE) (PE)
  • 24. ECG findings in PEECG findings in PE  •• Normal sinus rhythmNormal sinus rhythm  •• Sinus tachycardiaSinus tachycardia  •• Tall peaked T waves in V1- V4Tall peaked T waves in V1- V4  •• S1Q3T3 pattern: Not specific. Can beS1Q3T3 pattern: Not specific. Can be seen in any Cor pulmonale syndromeseen in any Cor pulmonale syndrome  •• RBBBRBBB
  • 26. D-dimer in PED-dimer in PE  D-dimer is a type of Fibrin degradationD-dimer is a type of Fibrin degradation productproduct  •• Can be raised due to a number ofCan be raised due to a number of reasonsreasons  •• Negative D-dimer rules out PE/DVT inNegative D-dimer rules out PE/DVT in 98% cases98% cases  •• False positive D-dimer:False positive D-dimer: infection,infection, pregnancy, renalpregnancy, renal failure, post-operativefailure, post-operative
  • 28. CTPACTPA  Indications:Indications:  - Suspected PE- Suspected PE  Contra-indications:Contra-indications:  - Renal failure- Renal failure  - Pregnancy- Pregnancy  - Allergy to radio-contrast- Allergy to radio-contrast  Procedure:Procedure:  - Radioactive iodine administered IV- Radioactive iodine administered IV  - CT scan performed- CT scan performed
  • 29.
  • 30. Ventilation-perfusion scanVentilation-perfusion scan  Indications:Indications:  - Renal failure- Renal failure  - Pregnancy- Pregnancy  Procedure:Procedure:  - Ventilation scan with Xenon inhalation- Ventilation scan with Xenon inhalation  - Perfusion scan with Tc99m labelled radioactive- Perfusion scan with Tc99m labelled radioactive dye infusiondye infusion  - Scan V/Q- Scan V/Q  - Result: unmatched V/Q- Result: unmatched V/Q
  • 31.
  • 33.
  • 34. Pulmonary angiogramPulmonary angiogram  Gold standard test for PEGold standard test for PE •• Procedure:Procedure:  –– Catheter inserted to right ventricleCatheter inserted to right ventricle  –– Radio opaque dye injectedRadio opaque dye injected  –– Imaging technique used to identify theImaging technique used to identify the clotclot
  • 35. Treatment optionsTreatment options  Symptomatic treatment:Symptomatic treatment:  –– ABCD approachABCD approach  –– OxygenOxygen  –– AnalgesiaAnalgesia  •• Anticoagulation:Anticoagulation:  –– IV HeparinIV Heparin  –– S/C LMWH eg Enoxaparine, DalteparineS/C LMWH eg Enoxaparine, Dalteparine  –– Oral WarfarinOral Warfarin  •• IVC filter: If there is contra-indications forIVC filter: If there is contra-indications for anti-coagulationanti-coagulation  •• Thrombolysis: tPA eg Alteplase, TenectaplaseThrombolysis: tPA eg Alteplase, Tenectaplase  •• Surgical procedures: Pulmonary embolectomySurgical procedures: Pulmonary embolectomy
  • 36. Treatment optionsTreatment options  Massive PE:Massive PE: Thrombolysis/embolectomyThrombolysis/embolectomy  •• Sub-massive PE: StronglySub-massive PE: Strongly considerconsider  thrombolysis/embolectomy but need tothrombolysis/embolectomy but need to balance risk of bleedingbalance risk of bleeding  •• Non-massive PE: AnticoagulationNon-massive PE: Anticoagulation
  • 37.
  • 38. ThrombolysisThrombolysis  Indications:Indications:  –– Massive PEMassive PE  –– Sub-massive PE where risk of bleeding lowSub-massive PE where risk of bleeding low  •• Contraindications:Contraindications:  –– Bleeding, recent stroke, HI, current GI bleeding,Bleeding, recent stroke, HI, current GI bleeding,  bleeding PUD, surgery within 7 daybleeding PUD, surgery within 7 day
  • 39. Drugs:Drugs: Lytic agent Dose regimen Streptokinase Loading dose:250000UIV Continuous infusion:100000 U/h For 24hrs Uroklinase Loading dose:2000U/Ib IV over 10min Continuous infusion :2000 U/Ib/H for 12-24h Alteplase (Tpa) Loading dose:None Continous infusion :100mg over 2h Reteplase 1.Bolus: 10U IV 2.Bolus :10U IV after 30min
  • 40. AnticoagulationAnticoagulation  IV Heparin:IV Heparin: 80 units/kg bolus followed by 18 units/kg infusion80 units/kg bolus followed by 18 units/kg infusion  •• Monitor APTT 60-90 secMonitor APTT 60-90 sec •• Side effects:Side effects:  –– HITS (Heparin induced thrombocytopeniaHITS (Heparin induced thrombocytopenia syndrome):syndrome): paradoxical hypercoagulable state leads to clotsparadoxical hypercoagulable state leads to clots  –– BleedingBleeding
  • 41. AnticoagulationAnticoagulation  Low molecular weight Heparin (LMWH)Low molecular weight Heparin (LMWH)  Enoxaprin (Clexane): S/CEnoxaprin (Clexane): S/C  - 1.5mg/kg/24 hours Or 1mg/kg/12 hours- 1.5mg/kg/24 hours Or 1mg/kg/12 hours  - 1 mg/kg/24 hours in renal impairment- 1 mg/kg/24 hours in renal impairment  Duration: 6 to 9 monthsDuration: 6 to 9 months  Side effect: Low HITSSide effect: Low HITS
  • 42. AnticoagulationAnticoagulation  Vitamin K antagonistVitamin K antagonist  •• Warfarin:Warfarin: 5mg PO initial dose5mg PO initial dose Check regular INR 2-3Check regular INR 2-3 Side effects:Side effects:  –– BleedingBleeding  –– Unusual bruisesUnusual bruises
  • 43. IVC filterIVC filter  Indications:Indications:  - DVT with massive pulmonary embolus- DVT with massive pulmonary embolus  - Recurrent PE not treatable with- Recurrent PE not treatable with anticoagulationanticoagulation  - Absolute contra-indications for anti-- Absolute contra-indications for anti- coagulationcoagulation  - Trauma patients- Trauma patients
  • 44.
  • 45. PE in PregnancyPE in Pregnancy  All three components of Virchow’s triadAll three components of Virchow’s triad are affected duringare affected during  pregnancypregnancy  •• D-dimer has high negative predictiveD-dimer has high negative predictive value. False positivevalue. False positive  result is commonresult is common  •• V/Q scan is preferred techniqueV/Q scan is preferred technique  •• CTPA can be done if VQ is inconclusiveCTPA can be done if VQ is inconclusive  •• Preferred treatment option: LMWHPreferred treatment option: LMWH  •• Warfarin is contraindicatedWarfarin is contraindicated
  • 46. Prevention of PEPrevention of PE  Control of obesityControl of obesity  •• Stop smokingStop smoking  •• StockingsStockings  •• Heparin: 5000 units/day IVHeparin: 5000 units/day IV  •• Enoxaprin: 40 mg/day S/CEnoxaprin: 40 mg/day S/C
  • 47. And finally…And finally…  PE is often over-diagnosed;PE is often over-diagnosed;  PE is often under-diagnosed;PE is often under-diagnosed;  The over- or under-diagnosis of PE resultsThe over- or under-diagnosis of PE results in increasedin increased  cost, morbidity, mortality and medico-legalcost, morbidity, mortality and medico-legal risks.risks.