Boston Scientific Corporation · NYSE:BSX

Boston Scientific — Technical Presentation (2006)

23 slides from Boston Scientific's technical presentation, Nov 19, 2006

  1. Slide 1: Arteriovenous Malformations

    Arteriovenous Malformations Stanley E. Crawford Symposium 2006 Alan B. Lumsden, MD FACS Professor and Chief Division of Vascular Surgery & Endovascular Therapy Michael E. DeBakey Department of Surgery Baylor College of Medicine

  2. Slide 2: Vascular Lesion Treatment: Arteriovenous Malformation (AVM)

    Vascular Lesion Treatment Arteriovenous Malformation (AVM) • Definition - Congenital lesion • Abnormal arteriovenous communications • Feeding arteries • Nidus • Outflow veins • Symptoms • Significant shunting / CV compromise • Pain, neuromuscular dysfunction, tissue ulceration • Hemorrhage

  3. Slide 3: Treatment

    Treatment • Absolute indications • Hemorrhage • Ischemia (steal) • Refractory ulceration • Congestive heart failure • Relative indications • Disabling pain • Claudication • Functional impairment

  4. Slide 4: Treatment

    Treatment • Conservative • Stockings • Limb elevation • Surgery • 10% lesions • Best after embolization • 100% success when amenable for resection

  5. Slide 5: Vascular Lesion Treatment: AVM Embolization

    Vascular Lesion Treatment AVM Embolization • Effective therapy • Destruction of the nidus • Procedural requirements • Superselective access to feeding artery • Injection non-resorbable embolic agent into the nidus • Contour® PVA Particles / Contour SETM Microspheres • Absolute ethanol • n-BCA • .018

  6. Slide 6: Present Understanding of Important Phases of Vascular Development

    Present Understanding of Important Phases of Vascular Development Embryology • Stage I Undifferentiated: primitive blood lakes, capillary networks, no veins or arteries • Stage II Retiform: Capillaries form large plexiform structures • Stage III Maturation: Mature vascular channels

  7. Slide 7: Summary of the Most Important Factors Known to be Involved in Vascular Development

    Summary of the Most Important Factors Known to be Involved in Vascular Development* Protein/Molecule/Re ceptor Function Deficient Mice/Other Animals FGF Participation in angioblast differentiation from mesoderm No overt abnormalities (formation of "blood islands") VEGF-R2 (Flk-1) EC birth, migration

  8. Slide 8: MRI Classification

    MRI Classification Low-Flow Anomalies High-Flow Anomalies T1-weighted image 1. Increased signal intensity when compared 1. Signal voids with fat and skeletal muscle 2. Small amounts of tissue matrix T2-weighted image 1. Decreased signal intensity when compared 1. Signal voids with fat 2. Small amoun

  9. Slide 9: What do we really need to know?

    What do we really need to know? • Location: • subcutaneous • deep to fascia • both • Proximity to major structures • sciatic nerve • rectum • Localized or diffuse • Arterial or venous • relative contribution

  10. Slide 10: towel roll

    Boston, Seientific

  11. Slide 11: head rectus femoris foot

    head foot rectus femoris femoral nerve branches tensor fascia lata

  12. Slide 12: venous connection

    Boston cientific dh -vehous.. mm connection —> | re Sit

  13. Slide 13: joint capsule femur

    joint capsule femur

  14. Slide 14: Boston,

    Boston, Scientific

  15. Slide 15: Treatment

    Treatment Embolization • Multiple sessions • Long-term commitment • Usually under general anesthesia

  16. Slide 16: Steps For Safe Embolization

    Steps For Safe Embolization • Good preliminary angiography • Think about collateral pathways • Use shortest straightest approach, especially when coils used • Stable catheter position and verify: • Wire if using coils • Contrast if soluble agent • Use non-heparinized saline to flush and dilute contr

  17. Slide 17: Vascular Lesion Treatment: AVM Embolization Hazards

    Vascular Lesion Treatment AVM Embolization Hazards • Non-Target Distal embolic embolization • Venous outflow vessels pulmonary circulation • Potentially fatal PE (Pulmonary Embolism) • Prevention • Proper sizing of PVA microspheres / particles • Impact within the nidus • Careful injection of liquid

  18. Slide 18: Non-Resorbable Embolic Agents: Liquid Embolic Agent

    Non-Resorbable Embolic Agents: Liquid Embolic Agent n-Butyl Cyanoacrylate (n-BCA) • Description • Tissue adhesive or “glue” • Treatment of cerebral AVMs • Mechanism of action • Polymerization upon contact with ionic fluids • Formation of a solid cast within the vessel • Vessel occlusion • Technique

  19. Slide 19: AVM dorsum left hand

    • AVM dorsum left hand • Draining vein punctured • Tourniquet above arterial pressure • 2.5cc absolute ETOH via 3Fr catheter

  20. Slide 20: Radial Head AVM

    •Radial Head AVM, multiple vessels feeding venous component. •Catheter inserted into draining vein. •Absolute alcohol injected in 4 stages. •Venogram at 6 months - ablation of veins

  21. Slide 21: Conclusion: AVM Treatment

    Conclusion: AVM Treatment 1. These patients lack a home 2. Vascular Surgeons see most of AVM,s 3. No single therapeutic option 4. Need broad oversight 5. Emerging advanced endovascular skills in vascular surgery community 6. Rapid growth of excellent imaging 7. MEN -1 of vascular surgery: patient fo

  22. Slide 22: Contour PVA Particles Instructions for Use

    Contour PVA Particles Instructions for Use: Refer to the operator's manual for complete instructions for use. Indications Contour Emboli are used for the embolization of hyper vascular tumors and arteriovenous malformations. Contraindications Patient intolerance to temporary occlusion procedures. Va

  23. Slide 23: Contour SE Microspheres Instructions for Use

    Contour SE Microspheres Instructions for Use: Refer to the operator's manual for complete instructions for use. Indications Contour SE Microspheres may be used for the embolization of hypervascular tumors and arteriovenous malformations (AVMs). Contraindications Patient intolerance to occlusion proc

Boston Scientific — Technical Presentation (2006) on 6ix