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Acute Pulmonary Embolism By  Medhat  A.  Soliman   Prof. of Pulmonary & Critical Care Medicine Cairo University [email_address]
Severity of  acute  obstruction pre-existing  chronic  cor pulmonale Co-morbidity Adverse outcome  Pathophysiology of Pulmonary Embolism
Venous Thromboembolism  Importance of Right Ventricular Dysfunction PA pressure   RV afterload   RV wall stress   O 2  demand   RV dilation  RV dysfunction RV ischemia RV perfusion   RV ejection   Septal shift LV preload   LV ejection   Hypotension / Shock
* RVPO: right ventricular pressure overload In-Hospital Mortality  Venous Thromboembolism   Continuum of RV Dysfunction W Kasper. J Am Coll Cardiol 1997;30:1165-1171  Massive PE
Respiratory Effects ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
2006 2007 Clinical probability Guidelines
State-of-the-art Three scoring systems have been tested prospectively and validated in large scale clinical trials: ,[object Object],[object Object],[object Object],Clinical probability
n=1239, mostly outpatients Wells’ score 28% intermediate high low 78% 3% 28% 78% 3% State-of-the-art Clinical probability Low < 2 Intermediate 2 to 6 High > 6 Signs and symptoms of DVT 3.0 Heart rate > 100 1.5 Immobilization or surgery 1.5 Previous DVT or PE 1.5 Hemoptysis 1.5 Malignancy 1.5 PE as or more likely than an alternative diagnosis  3.0
low Geneva score n=986, only outpatients intermediate high 10% 81% 38% State-of-the-art Clinical probability Recent surgery 2 Previous PE or DVT 2 Older age 2 Hypocapnia 2 Hypoxemia 2 Tachycardia 2 Platelike atelectasis 2 Hemidiaphragm elevation 2 Low ≤   4 Intermediate 5 to 8 High ≥   9
Pisa score n=750, mostly inpatients 3% 97% 41% intermediate high low State-of-the-art Clinical probability High One or more of three symptoms   (sudden onset dyspnea, chest pain, fainting) ,   not explained, and one or more of three chest x-ray findings   (amputation of hilar artery, focal oligemia, pleural-based consolidation) Interme-diate One or more of the above symptoms, alone or with   EKG findings   of acute right ventricular overload Low None of the above symptoms is present or an  alternative diagnosis that may account for their presence is identified
2006 2007 Guidelines Diagnostic strategies
2006 2007 D-dimer Diagnostic strategies
D-dimer in suspected PE di Nisio et al, JTH 2007;5: 296-304 SimpliRed (40) Whole-blood assay VIDAS (40) ELFA STA-lia test (25) Tinaquant (12) Latex quantitative Nycocard (23) Instantia (13) Membrane ELISA Asserachrome (24) Microplate ELISA (number of studies) Type of D-dimer 82 (59-93) 96 (93-98) 94 (83-98) 92 (75-98) 88 (68-96) 86 (59-96) 94 (83-98) Sn, % Deep vein thrombosis 72 (56-84) 44 (36-52) 46 (28-64) 53 (32-73) 50 (31-68) 65 (43-81) 47 (29-65) Sp, % 86  (43-97) 97  (91-99) 96  (80-99) 94  (71-99) 91  (64-98) 89  (54-98) 96   (80-99) Sn, % Pulmonary embolism 70 (44-87) 41 (26-57) 43 (20-68) 50 (23-76) 47 (23-72) 62 (33-84) 44 (21-69) Sp, %
D-dimer in suspected PE di Nisio et al, JTH 2007;5: 296-304 100 90 80 70 60 50 40 30 20 10 0 100 90 80 70 60 50 40 30 20 10 0 ELFA Latex quantitative Microplate ELISA Membrane ELISA Latex semiquantitative Whole-blood Latex qualitative Sensitivity, % Specificity, %
D-dimer in suspected PE ,[object Object],[object Object],[object Object],[object Object],[object Object]
2006 2007 Guidelines Diagnostic strategies
Imaging – Modalities until ~1992 ~1998 ~2000 Scinti CT MSCT MIPS , Perfusion-Imaging MRI Angio SPECT
Spiral CT
CT in suspected PE: a story of evolution 2-slice  CT 199 2 2 x 2.7 mm 25 sec Courtesy of Emmanuel Coche 4-slice CT 1998 4 x 1 mm 25 sec 64 - slice 2004 64 x 0.625 mm 4 sec 16-slice CT 2002 16 x 0.75 mm 10 sec
MDCT: visualization of peripheral arteries Coche E et al.  Eur Radiol 2003;13:815-22.  Ghaye et al.  Radiology 2001;219:629-36. 96% of subsegmental arteries  and 54% of sub-subsegmental arteries are identified on multislice CT (4 rows of detectors) Courtesy of Emmanuel Coche
LR Goodman, University of Wisconsin CT angiography Pulmonary embolism
LR Goodman, University of Wisconsin CT angiography Pulmonary embolism
LR Goodman, University of Wisconsin CT angiography Pulmonary embolism
Multidetector-Row CT:  Superior Resolution and Sensitivity
CT angiography Pulmonary embolism
Chest radiography Pulmonary embolism Miniati et al. AJRCCM 1999
Westermark’s sign (1938) Fleischner’s sign (1962)   Hampton’s sign (1940) At least one of these findings was identified in  75%  of 202 patients with  proven PE  PISA-PED  Am J Respir Crit Care Med   1999 chest radiography Clinical probability
2006 2007 Guidelines Diagnostic strategies
 
Chest radiography Pulmonary embolism
Chest radiography Pulmonary embolism
Q scan Chest radiography Pulmonary embolism
Comparison between MD-CTPA  and perfusion lung scan
PE ruled out PE ruled out Comparison between MD-CTPA  and perfusion lung scan
PE ruled out PE ruled out PE confirmed PE confirmed Comparison between MD-CTPA  and perfusion lung scan
Role of V/Q scan in PE diagnosis ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Advantages of CT for PE: summary ,[object Object],[object Object],[object Object],[object Object]
Clinical probability of PE assessment Implicit or prediction rule Validated algorithm for diagnosing PE based on CT <  500 µg/L No Rx Low or intermediate ELISA D-dimer No PE V/Q scan? CT venography? Angiography? Lower limb US? Helical CT PE Rx High No PE No Rx PE Rx > 500 µg/L Helical CT ?
Conclusions ,[object Object],[object Object],[object Object],[object Object],[object Object]
Initial Therapy for  APE ,[object Object],[object Object],[object Object],[object Object]
 
 
Hirsh, J. et al. Chest 2008;133:141S-159S Inactivation of clotting enzymes by heparin
 
 
Subcutaneous UFH ,[object Object],[object Object]
Hirsh, J. et al. Chest 2008;133:141S-159S Molecular weight distributions of LMWHs and heparin
LMWH Prepared from animal gut mucosa; contains heparin sulfate (84%), dermatan sulfate (12%), and chondroitin sulfate (4%) NV Organon/Oss, Netherlands Danaparoid sodium (Orgaran) Nitrous acid depolymerization Knoll/Markham, Ont Reviparin (Clivarine) Enzymatic depolymerization with heparinaze Leo Laboratories/Dublin, Ireland Tinzaparin (Innohep) Peroxidative depolymerization Wyeth-Ayerst/Philadelphia, PA Ardeparin (Normiflo) Nitrous acid depolymerization Pharmacia/Peakack, NJ Dalteparin (Fragmin) Benzylation followed by alkaline depolymerization Aventis/Collegeville, PA Enoxaparin sodium (Lovenox/Clexane) Nitrous acid depolymerization Sanofi/Gentilly, France Nadroparin calcium (Fraxiparin) Method of Preparation Manufacturer/Location Agents
4.1Initial anticoagulation in VTE ,[object Object],[object Object],[object Object],[object Object],Item 1 Item 2 Item 3 Item 4 Item 5 Item 6 Item 7 Item 8 Item 9 598,1,2,1,0,1,1,1,1,1,1,1,1,0 HR Büller 7th ACCP Conference Chest 2004; 126: 401S-428S
[object Object],[object Object],[object Object],[object Object],LMWH versus UFH in the treatment of acute venous thromboembolism
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],LMWH versus   UFH
Similar efficacy Superior safety  Out of hospital  Cost-effective Easier to use  Less thrombocytopenia No laboratory monitoring LMWH drug of choice in the treatment of venous thromboembolism
[object Object],[object Object],[object Object],[object Object],[object Object],New drugs for the Treatment of DVT and PE
Pentasaccharides tailor made OCH 3 OCH 3 Fondaparinux ( Arixtra ®  ) MOST LIKE NATURAL Once-a-day (1987) Org31550 MORE POTENT A new binding site discovered Idraparinux,  SanOrg34006   SIMPLIFIED (1992) Once-a-week
Specific inhibition of factor Xa via ATIII Fondaparinux Idraparinux DX9065a BAY59-7939 LY-51,7717 BMS-562247 Mechanism of Action: 1 AT pentasacharides 3 AT Xa IIa II Fibrinogen Fibrin  clot Extrinsic  pathway Intrinsic pathway Xa AT 2
Fondaparinux Idraparinux ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Conclusions ,[object Object],[object Object],[object Object]
Anticoagulation for Treatment of PE ACCP Guidelines 8 th  Ed; 2008 ,[object Object],[object Object],[object Object],[object Object]
Anticoagulation for Treatment of VT and PE (cont.) ,[object Object],[object Object],[object Object],[object Object]
 
Initial therapy for APE ,[object Object],[object Object],[object Object],[object Object]
Retrievable Vena cavafilter(ALN ) for secondary prevention of VTE  Mismetti et al Chest 2007; 131: 223-9 ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Initial therapy for APE ,[object Object],[object Object],[object Object],[object Object]
Severity of pulmonary embolism Clinical Massive Non-massive Different management strategies Thrombolysis Heparins
Shock SBP<90 mmHg :  Miller index/angio/sCT/autopsy :  Swan-Ganz, Echo-Doppler Anatomic Hemodynamic Clinical Massive Non-massive Classification of severity of pulmonary embolism ESC Task Force 2000 Syncope HR/SBP > 1
NP Fam. N Engl J Med 2002; Vol. 347, No. 15 Massive PE With Haemodynamic Instability   Rationale For Thrombolysis
Size/morphology of PE thrombi Saddle PE – no influence on outcome Pruszczyk et al., Heart 2002 Mobile PE – better outcome on th-lysis Podbregar et al., Chest 2002
Acute PE: Approved thrombolytic regimens Accelerated regimen:  0.6 mg/kg over 15 min 100 mg over 2 h rtPA Accelerated regimen:  3 million IU over 2 h 4,400 IU/kg as a loading dose over 10 min, followed by 4,400 IU/Kg/h over 12-24 h Urokinase Accelerated regimen:  1.5 million IU over 2 h 250,000 IU as a loading dose over 30 min, followed by 100,000 IU/h over 12-24 h Streptokinas e
THROMBOLYTIC THERAPY in the treatment of acute PE ,[object Object],[object Object],7th   ACCP Conference on Antithrombotic and Thrombolytic therapy( CHEST 2004,)
Severity of pulmonary embolism RV hypokinesis (Echo) Hemodynamic Clinical Massive Non-massive submassive ESC Task Force 2000
submassive TH-lysis ?  SBP<90mmHg Shock,  ECHO/CT High PASP ? RV dilatation ? RV domination ? IVC distension ?  RV hypokinesis ? pressure overload reversible (?) RV failure subjective assessment
RV RV D /LV D   < 0.9: good prognosis RV D /LV D  >0.9 :   high death risk 4 retrospective studies; 692 patients Venous Thromboembolism  Risk Stratification: Multidetector-CT
Risk Stratification of PE  Contemporary Algorithm for PE Severity PE confirmed,  stable  patient Troponin (or BNP) testing Imaging of RV (Echo, CT) Low risk (non-massive PE) Intermediate risk (submassive PE) Biomarker test  negative  AND  RV normal Either biomarker  positive  OR   RV abnormal Biomarker test  positive AND  RV abnormal
Risk Stratification of PE  Therapeutic Implications High-Risk PE Shock, CPR Low Risk Patient normotensive Anticoagulation LMWH►VKA Thrombolysis Surgery / Intervention Intermediate Risk normotensive, echo+, biomarker+ ? 5% 85% 10%
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Initial therapy for PE ,[object Object],[object Object],[object Object]
Massive PE With Haemodynamic Instability   Surgical Embolectomy L Aklog. In: Management of Pulmonary Embolism. Humana Press 2007
Massive PE With Haemodynamic Instability   Catheter-Based Procedures N Kucher. In: Management of Pulmonary Embolism. Humana Press 2007 AngioJet Xpeedior, Possis, MN Aspirex, Straub, CH
[object Object],[object Object],[object Object],[object Object],Pulmonary embolectomy  for the initial treatment of PE
488 patients underwent thrombolysis 40 (8.2%) did  not  respond within 36 h (persistent “clinical instability” + RV dysfunction) Repeat Thrombolysis (n=26) Uneventful in-hospital  course in 31% (mortality, 38%)  A prospective single-centre registry N Meneveau. Chest 2006;129:1043-1050 Surgical Embolectomy (n=14) Uneventful in-hospital  course in 79% (mortality, 7%) P=0.004 Massive PE With Haemodynamic Instability   Embolectomy After Failed Thrombolysis
 
Prognostic Parameters for Acute PE ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]

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Pulmonary Embolism

  • 1. Acute Pulmonary Embolism By Medhat A. Soliman Prof. of Pulmonary & Critical Care Medicine Cairo University [email_address]
  • 2. Severity of acute obstruction pre-existing chronic cor pulmonale Co-morbidity Adverse outcome Pathophysiology of Pulmonary Embolism
  • 3. Venous Thromboembolism Importance of Right Ventricular Dysfunction PA pressure  RV afterload  RV wall stress  O 2 demand  RV dilation RV dysfunction RV ischemia RV perfusion  RV ejection  Septal shift LV preload  LV ejection  Hypotension / Shock
  • 4. * RVPO: right ventricular pressure overload In-Hospital Mortality Venous Thromboembolism Continuum of RV Dysfunction W Kasper. J Am Coll Cardiol 1997;30:1165-1171 Massive PE
  • 5.
  • 6. 2006 2007 Clinical probability Guidelines
  • 7.
  • 8. n=1239, mostly outpatients Wells’ score 28% intermediate high low 78% 3% 28% 78% 3% State-of-the-art Clinical probability Low < 2 Intermediate 2 to 6 High > 6 Signs and symptoms of DVT 3.0 Heart rate > 100 1.5 Immobilization or surgery 1.5 Previous DVT or PE 1.5 Hemoptysis 1.5 Malignancy 1.5 PE as or more likely than an alternative diagnosis 3.0
  • 9. low Geneva score n=986, only outpatients intermediate high 10% 81% 38% State-of-the-art Clinical probability Recent surgery 2 Previous PE or DVT 2 Older age 2 Hypocapnia 2 Hypoxemia 2 Tachycardia 2 Platelike atelectasis 2 Hemidiaphragm elevation 2 Low ≤ 4 Intermediate 5 to 8 High ≥ 9
  • 10. Pisa score n=750, mostly inpatients 3% 97% 41% intermediate high low State-of-the-art Clinical probability High One or more of three symptoms (sudden onset dyspnea, chest pain, fainting) , not explained, and one or more of three chest x-ray findings (amputation of hilar artery, focal oligemia, pleural-based consolidation) Interme-diate One or more of the above symptoms, alone or with EKG findings of acute right ventricular overload Low None of the above symptoms is present or an alternative diagnosis that may account for their presence is identified
  • 11. 2006 2007 Guidelines Diagnostic strategies
  • 12. 2006 2007 D-dimer Diagnostic strategies
  • 13. D-dimer in suspected PE di Nisio et al, JTH 2007;5: 296-304 SimpliRed (40) Whole-blood assay VIDAS (40) ELFA STA-lia test (25) Tinaquant (12) Latex quantitative Nycocard (23) Instantia (13) Membrane ELISA Asserachrome (24) Microplate ELISA (number of studies) Type of D-dimer 82 (59-93) 96 (93-98) 94 (83-98) 92 (75-98) 88 (68-96) 86 (59-96) 94 (83-98) Sn, % Deep vein thrombosis 72 (56-84) 44 (36-52) 46 (28-64) 53 (32-73) 50 (31-68) 65 (43-81) 47 (29-65) Sp, % 86 (43-97) 97 (91-99) 96 (80-99) 94 (71-99) 91 (64-98) 89 (54-98) 96 (80-99) Sn, % Pulmonary embolism 70 (44-87) 41 (26-57) 43 (20-68) 50 (23-76) 47 (23-72) 62 (33-84) 44 (21-69) Sp, %
  • 14. D-dimer in suspected PE di Nisio et al, JTH 2007;5: 296-304 100 90 80 70 60 50 40 30 20 10 0 100 90 80 70 60 50 40 30 20 10 0 ELFA Latex quantitative Microplate ELISA Membrane ELISA Latex semiquantitative Whole-blood Latex qualitative Sensitivity, % Specificity, %
  • 15.
  • 16. 2006 2007 Guidelines Diagnostic strategies
  • 17. Imaging – Modalities until ~1992 ~1998 ~2000 Scinti CT MSCT MIPS , Perfusion-Imaging MRI Angio SPECT
  • 19. CT in suspected PE: a story of evolution 2-slice CT 199 2 2 x 2.7 mm 25 sec Courtesy of Emmanuel Coche 4-slice CT 1998 4 x 1 mm 25 sec 64 - slice 2004 64 x 0.625 mm 4 sec 16-slice CT 2002 16 x 0.75 mm 10 sec
  • 20. MDCT: visualization of peripheral arteries Coche E et al. Eur Radiol 2003;13:815-22. Ghaye et al. Radiology 2001;219:629-36. 96% of subsegmental arteries and 54% of sub-subsegmental arteries are identified on multislice CT (4 rows of detectors) Courtesy of Emmanuel Coche
  • 21. LR Goodman, University of Wisconsin CT angiography Pulmonary embolism
  • 22. LR Goodman, University of Wisconsin CT angiography Pulmonary embolism
  • 23. LR Goodman, University of Wisconsin CT angiography Pulmonary embolism
  • 24. Multidetector-Row CT: Superior Resolution and Sensitivity
  • 26. Chest radiography Pulmonary embolism Miniati et al. AJRCCM 1999
  • 27. Westermark’s sign (1938) Fleischner’s sign (1962) Hampton’s sign (1940) At least one of these findings was identified in 75% of 202 patients with proven PE PISA-PED Am J Respir Crit Care Med 1999 chest radiography Clinical probability
  • 28. 2006 2007 Guidelines Diagnostic strategies
  • 29.  
  • 32. Q scan Chest radiography Pulmonary embolism
  • 33. Comparison between MD-CTPA and perfusion lung scan
  • 34. PE ruled out PE ruled out Comparison between MD-CTPA and perfusion lung scan
  • 35. PE ruled out PE ruled out PE confirmed PE confirmed Comparison between MD-CTPA and perfusion lung scan
  • 36.
  • 37.
  • 38. Clinical probability of PE assessment Implicit or prediction rule Validated algorithm for diagnosing PE based on CT < 500 µg/L No Rx Low or intermediate ELISA D-dimer No PE V/Q scan? CT venography? Angiography? Lower limb US? Helical CT PE Rx High No PE No Rx PE Rx > 500 µg/L Helical CT ?
  • 39.
  • 40.
  • 41.  
  • 42.  
  • 43. Hirsh, J. et al. Chest 2008;133:141S-159S Inactivation of clotting enzymes by heparin
  • 44.  
  • 45.  
  • 46.
  • 47. Hirsh, J. et al. Chest 2008;133:141S-159S Molecular weight distributions of LMWHs and heparin
  • 48. LMWH Prepared from animal gut mucosa; contains heparin sulfate (84%), dermatan sulfate (12%), and chondroitin sulfate (4%) NV Organon/Oss, Netherlands Danaparoid sodium (Orgaran) Nitrous acid depolymerization Knoll/Markham, Ont Reviparin (Clivarine) Enzymatic depolymerization with heparinaze Leo Laboratories/Dublin, Ireland Tinzaparin (Innohep) Peroxidative depolymerization Wyeth-Ayerst/Philadelphia, PA Ardeparin (Normiflo) Nitrous acid depolymerization Pharmacia/Peakack, NJ Dalteparin (Fragmin) Benzylation followed by alkaline depolymerization Aventis/Collegeville, PA Enoxaparin sodium (Lovenox/Clexane) Nitrous acid depolymerization Sanofi/Gentilly, France Nadroparin calcium (Fraxiparin) Method of Preparation Manufacturer/Location Agents
  • 49.
  • 50.
  • 51.
  • 52. Similar efficacy Superior safety Out of hospital Cost-effective Easier to use Less thrombocytopenia No laboratory monitoring LMWH drug of choice in the treatment of venous thromboembolism
  • 53.
  • 54. Pentasaccharides tailor made OCH 3 OCH 3 Fondaparinux ( Arixtra ® ) MOST LIKE NATURAL Once-a-day (1987) Org31550 MORE POTENT A new binding site discovered Idraparinux, SanOrg34006 SIMPLIFIED (1992) Once-a-week
  • 55. Specific inhibition of factor Xa via ATIII Fondaparinux Idraparinux DX9065a BAY59-7939 LY-51,7717 BMS-562247 Mechanism of Action: 1 AT pentasacharides 3 AT Xa IIa II Fibrinogen Fibrin clot Extrinsic pathway Intrinsic pathway Xa AT 2
  • 56.
  • 57.
  • 58.
  • 59.
  • 60.  
  • 61.
  • 62.
  • 63.
  • 64. Severity of pulmonary embolism Clinical Massive Non-massive Different management strategies Thrombolysis Heparins
  • 65. Shock SBP<90 mmHg : Miller index/angio/sCT/autopsy : Swan-Ganz, Echo-Doppler Anatomic Hemodynamic Clinical Massive Non-massive Classification of severity of pulmonary embolism ESC Task Force 2000 Syncope HR/SBP > 1
  • 66. NP Fam. N Engl J Med 2002; Vol. 347, No. 15 Massive PE With Haemodynamic Instability Rationale For Thrombolysis
  • 67. Size/morphology of PE thrombi Saddle PE – no influence on outcome Pruszczyk et al., Heart 2002 Mobile PE – better outcome on th-lysis Podbregar et al., Chest 2002
  • 68. Acute PE: Approved thrombolytic regimens Accelerated regimen: 0.6 mg/kg over 15 min 100 mg over 2 h rtPA Accelerated regimen: 3 million IU over 2 h 4,400 IU/kg as a loading dose over 10 min, followed by 4,400 IU/Kg/h over 12-24 h Urokinase Accelerated regimen: 1.5 million IU over 2 h 250,000 IU as a loading dose over 30 min, followed by 100,000 IU/h over 12-24 h Streptokinas e
  • 69.
  • 70. Severity of pulmonary embolism RV hypokinesis (Echo) Hemodynamic Clinical Massive Non-massive submassive ESC Task Force 2000
  • 71. submassive TH-lysis ? SBP<90mmHg Shock, ECHO/CT High PASP ? RV dilatation ? RV domination ? IVC distension ? RV hypokinesis ? pressure overload reversible (?) RV failure subjective assessment
  • 72. RV RV D /LV D < 0.9: good prognosis RV D /LV D >0.9 : high death risk 4 retrospective studies; 692 patients Venous Thromboembolism Risk Stratification: Multidetector-CT
  • 73. Risk Stratification of PE Contemporary Algorithm for PE Severity PE confirmed, stable patient Troponin (or BNP) testing Imaging of RV (Echo, CT) Low risk (non-massive PE) Intermediate risk (submassive PE) Biomarker test negative AND RV normal Either biomarker positive OR RV abnormal Biomarker test positive AND RV abnormal
  • 74. Risk Stratification of PE Therapeutic Implications High-Risk PE Shock, CPR Low Risk Patient normotensive Anticoagulation LMWH►VKA Thrombolysis Surgery / Intervention Intermediate Risk normotensive, echo+, biomarker+ ? 5% 85% 10%
  • 75.
  • 76.
  • 77. Massive PE With Haemodynamic Instability Surgical Embolectomy L Aklog. In: Management of Pulmonary Embolism. Humana Press 2007
  • 78. Massive PE With Haemodynamic Instability Catheter-Based Procedures N Kucher. In: Management of Pulmonary Embolism. Humana Press 2007 AngioJet Xpeedior, Possis, MN Aspirex, Straub, CH
  • 79.
  • 80. 488 patients underwent thrombolysis 40 (8.2%) did not respond within 36 h (persistent “clinical instability” + RV dysfunction) Repeat Thrombolysis (n=26) Uneventful in-hospital course in 31% (mortality, 38%) A prospective single-centre registry N Meneveau. Chest 2006;129:1043-1050 Surgical Embolectomy (n=14) Uneventful in-hospital course in 79% (mortality, 7%) P=0.004 Massive PE With Haemodynamic Instability Embolectomy After Failed Thrombolysis
  • 81.  
  • 82.