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VASCULAR PLUGS: CURRENT USE
SHORT SEMINAR
Satyam Rajvanshi
INTRODUCTION
• Embolization is defined as the "therapeutic
introduction of various substances into the
circulation to occlude vessels, either to arrest or
prevent active hemorrhage; to devitalize a structure,
tumor, or organ by occluding its blood supply; or to
reduce blood flow to an arteriovenous
malformation."
Stedman T. Stedman's Medical Dictionary. 27th ed. Lippincott Williams & Wilkins. 2000.
• Endovascular embolization, or embolotherapy, is
performed by interventional cardiologists or
interventional radiologists
Embolization therapeutic goals:
• An adjunctive goal (preoperative, adjunct to
chemotherapy or radiation therapy)
• A curative goal (aneurysms, arteriovenous fistulae
[AVFs], arteriovenous malformations [AVMs], and
traumatic bleeding)
Medical conditions treated by using embolotherapy can
be grouped as follows:
• Vascular anomalies (eg, AVM, AVF, venous
malformation [VM], lymphatic malformation [LM],
and hemangioma)
• Hemorrhage (eg, pseudoaneurysms, GI tract, pelvic,
posttraumatic, epistaxis, and hemoptysis bleeding)
• Other conditions (eg, tumors, varicoceles, organ
ablation, BPF)
EMBOLIZATION MATERIALS AND
SUBSTANCES
• Permanent vessel occlusion
– Particulate material
• Polyvinyl alcohol
• Gelatin-acrylic microspheres
– Sclerosing agents
• Alcohols
– Glue
• Cyanoacrylate
• Sodium Tetradecyl Sulfate
– Metallic
• Coils
• Vascular Plugs
• Temporary occlusion
– Gelfoam
VASCULAR PLUGS
VASCULAR PLUG
• Self-expandable devices made of nitinol wire
mesh (or other material) which can be
cylinderized into a sheath and deployed
precisely at embolization targets
Vascular plug vs. Coil
• Speed: Reduction in procedure times
• Radiation Exposure: Reduction in radiation times
• Cost-effectiveness: Reduction in procedural costs
– specially in large vessels
• Efficiency: Reduction in materials used,
uncommon recanalisation or persistent flow,
device embolisation rare
• Precision: Recapturable and redeployable for
precise placement
• Amplatzer vascular plugs
• Cera vascular plugs
• Medusa vascular plug
• Microvascular plug
AMPLATZER VASCULAR PLUG
• Manufactured by St. Jude Medical (USA)
• First approved by USFDA on May 3, 2004, for
peripheral vascular embolizations
• 1st study reporting successful use of the AVP was
published in 2004
Hijazi ZM (2004) New device for percutaneous closure of aortopulmonary collaterals.
Catheter Cardiovasc Interv 63(4): 482–485
• Designed as a permanent occluding flexible
cylindrical device derived as a modification of the
family of Amplatz septal occluders and Amplatzer
Duct Occluder
• Excellent alternative to coils or detachable balloons
in the embolization of medium to large vessels with
high flow - otherwise require multiple coils
• All AVP models - 2 basic components: a vascular plug
and a delivery wire
• Plugs built with nitinol braids, self-expanding
radiopaque platinum marker bands at both ends
that allow for high visibility under fluoroscopy
Stainless-steel screw on one of the platinum
marker bands attaches to a delivery cable
• Ability to recapture and reposition the device as
needed
• After satisfactory positioning, counterclockwise
rotation of connecting cable releases device
• Single model has evolved into 4 models
• For use in various types of anatomy,
hemodynamics, and lesion entities
• AVP I and II – USFDA approved 2004, 2007
• AVP III – 2008 CE marked but not available in
US
• AVP 4 – USFDA approved 2012
AVP or AVP I
Single lobar plug
Guide 5-8 Fr
Sheath 4-6 Fr
Diameter 4-16 mm
Increments 2 mm
Length 7-8 mm
Lesion with short landing
zone requiring high
radial force to secure
AVP
Select a device with a diameter approximately 30-50% larger
than the vessel diameter at the occlusion site
AVP II
Multi (6)-layered Tri-lobar
plug with increased
length
Guide 5-9 Fr
Sheath 4-7 Fr
Diameter 3-22 mm
Increments 2 mm
Length 6-18 mm
Rapid occlusion
Used when Variable landing
zone – can be shortened
by compression
Minimises migration and
recanalization
Select a device with a diameter approximately 30-50% larger
than the vessel diameter at the occlusion site
Large Left Segmental Pulmonary Artery Pseudoaneurysm
AVP 4
Multi (4)-layered Bi-lobar
plug with small profile,
more flexible delivery
wire
Simple delivery - 0.038”
guidewire compatible
diagnostic catheter
(Guide/Sheath not
required)
Diameter 4-8 mm
Increments 1 mm
Length 10-13.5 mm
Small, tortuous vessel
Rapid occlusion
Select a device with a diameter approximately 30-50% larger
than the vessel diameter at the occlusion site
AVP 4 completely occluding coronary fistula originating from
proximal RCA draining into the right upper lung field
AVP III
Oblong plug with 2
extended rims
Guide 6-9 Fr
Sheath 4-7 Fr
Diameter 4-14 mm (Long Axis)
Increments 2 mm (Long Axis)
Length 2-5 mm (Short Axis)
Fastest occlusion of all AVPs
Enhanced stability in high
flow states
Niche device for suitable
anatomy
Like ASD occluder stretched sideways!
Amplatzer Vascular Plug III 12/5 device implant in aortic position. A: in systole, the device does not interfere
with the prosthesis. B: in diastole, the device does interfere with the prosthesis. C: an Amplatzer Duct
Occluder 12/10 device implant that does not interfere in systole. D: or in diastole
CERA VASCULAR PLUG SYSTEM
• Manufactured by Lifetech Scientific Corp., China
• Single lobe device coated with Titanium Nitride –
prevent thrombosis and improves endothelialisation
• PTFE coated – shorter occlusion time
Single lobed, PTFE covered
Guide 4-9 Fr
Diameter 4-24 mm
Increments 2 mm
Length 7-14 mm
Rapid occlusion due to PTFE
MEDUSA VASCULAR PLUG
• Manufactured by Endoshape, USA
• USFDA approved in Nov,2013
• Constructed from multiple 0.018” polymer coils
• Highly trackable in tortuous anatomy
MEDUSA VASCULAR PLUG
• Manufactured by Endoshape, USA
• USFDA approved in Nov,2013
• Constructed from multiple 0.018” polymer coils
• Highly trackable in tortuous anatomy
• Better Imaging - Minimal metal content reduces
artifacts; follow up can be with a CT/MRI versus an
angiogram
MICROVASCULAR PLUG
• Manufactured originally by Covidien, USA
• Covidien later bought by Medtronic, USA
• MVP plug - The first plug deliverable through a
micro catheter
• Enables super-selective embolization of distal
vessels
• PTFE coated Nitinol design – rapid occlusion
• Length 12 mm
• Diameter 5.3 mm and 6.5 mm
• 3 mm MVP™ plug: recommended delivery through .021"
micro catheter2
• 5 mm MVP™ plug: recommended delivery through .027"
micro catheter
APPLICATIONS
VASCULAR
• ARTERIAL: Parent artery occlusion
– Internal iliac
– Carotid
– Vertebral
– Renal
– Gastroduodenal
– Aberrant right subclavian artery
– Popliteal artery aneurysm
– Hepatic artery pseudoaneurysm
– Hepatic cavernous hemangioma
VASCULAR
• VENOUS
– Portal Vein –Preoperative embolization of tumor
side portal vein stimulates contralateral liver
lobular hypertrophy - improves resection rate
– Gastric varix in conjunction with a TIPS
– Varicocele embolization for infertility
– Ovarian vein embolization for female pelvic
congestion syndrome
– Saphenous vein graft aneurysm
– Large inferior vena cava aneurysm
ABNORMAL VASCULAR CONNECTIONS
• CONGENITAL
– Pulmonary AVMs; renal AVMs; Hepatic AVMs
– PDA
– PDV – intrahepatic portosystemic shunt
– Splenorenal shunt
– Spontaneous mesocaval shunt in SMA
– Scimitar vein to left atrium
– Congenital coronary artery fistula
ABNORMAL VASCULAR CONNECTIONS
• ACQUIRED
– HD-AVF
– TIPS
– Blalock-Taussig shunt
– Traumatic arteriovenous fistula
CARDIAC
• Paravalvular leak closure
– Mechanical MV/AV
– TAVI
• PDA
• LAA
MICROVASCULAR PLUGS
• Hepatic artery skeletonisation – before
radioembolisation/chemoembolisation of tumor
• Gastroduodenal artery - during radioembolization
• Recanalized pulmonary arteriovenous
malformation previously coil embolised
• Splenic artery hemorrhage secondary to tumoral
erosion
• Lower gastrointestinal hemorrhage
• Temporary vessel occlusion by undeployed MVP
plug - Whenever only temporary occlusion of a
critical vessel is desired - during complex vascular
procedures; or Radio/chemo embolisation
NON-VASCULAR
• EXTRA VASCULAR
– Bronchopleural fistula!
– Vesicovaginal fistula!
– Intraperitoneal bile leak!
CONCLUSION
• Vascular plugs as occlusion devices are valuable in
managing a wide variety of disease processes
• Easy to use, can be precisely deployed in the target
vessel, high resistance to migration, low recanalization
rate
• Vessel size, high-flow status, and coagulopathy can
prolong the occlusion time. The addition of coils,
gelfoams as an adjunct can achieve rapid and reliable
occlusion with minimal cost
• Continued evolution in product design has improved
occlusion properties and decreased device profile –
alongwith interventionalist’s innovative usage – has
truly widened the spectrum of clinical indications for
these versatile devices
CARDIOLOGY IS NOTHING BUT
‘JUGAAD’ WITH EXPERTISE
- Dr. Ranjeet Nath
Use of Vascular plugs in cardiovascular medicine

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Use of Vascular plugs in cardiovascular medicine

  • 1. VASCULAR PLUGS: CURRENT USE SHORT SEMINAR Satyam Rajvanshi
  • 3. • Embolization is defined as the "therapeutic introduction of various substances into the circulation to occlude vessels, either to arrest or prevent active hemorrhage; to devitalize a structure, tumor, or organ by occluding its blood supply; or to reduce blood flow to an arteriovenous malformation." Stedman T. Stedman's Medical Dictionary. 27th ed. Lippincott Williams & Wilkins. 2000.
  • 4. • Endovascular embolization, or embolotherapy, is performed by interventional cardiologists or interventional radiologists
  • 5. Embolization therapeutic goals: • An adjunctive goal (preoperative, adjunct to chemotherapy or radiation therapy) • A curative goal (aneurysms, arteriovenous fistulae [AVFs], arteriovenous malformations [AVMs], and traumatic bleeding)
  • 6. Medical conditions treated by using embolotherapy can be grouped as follows: • Vascular anomalies (eg, AVM, AVF, venous malformation [VM], lymphatic malformation [LM], and hemangioma) • Hemorrhage (eg, pseudoaneurysms, GI tract, pelvic, posttraumatic, epistaxis, and hemoptysis bleeding) • Other conditions (eg, tumors, varicoceles, organ ablation, BPF)
  • 8. • Permanent vessel occlusion – Particulate material • Polyvinyl alcohol • Gelatin-acrylic microspheres – Sclerosing agents • Alcohols – Glue • Cyanoacrylate • Sodium Tetradecyl Sulfate – Metallic • Coils • Vascular Plugs • Temporary occlusion – Gelfoam
  • 10. VASCULAR PLUG • Self-expandable devices made of nitinol wire mesh (or other material) which can be cylinderized into a sheath and deployed precisely at embolization targets
  • 11. Vascular plug vs. Coil • Speed: Reduction in procedure times • Radiation Exposure: Reduction in radiation times • Cost-effectiveness: Reduction in procedural costs – specially in large vessels • Efficiency: Reduction in materials used, uncommon recanalisation or persistent flow, device embolisation rare • Precision: Recapturable and redeployable for precise placement
  • 12. • Amplatzer vascular plugs • Cera vascular plugs • Medusa vascular plug • Microvascular plug
  • 13. AMPLATZER VASCULAR PLUG • Manufactured by St. Jude Medical (USA) • First approved by USFDA on May 3, 2004, for peripheral vascular embolizations • 1st study reporting successful use of the AVP was published in 2004 Hijazi ZM (2004) New device for percutaneous closure of aortopulmonary collaterals. Catheter Cardiovasc Interv 63(4): 482–485
  • 14. • Designed as a permanent occluding flexible cylindrical device derived as a modification of the family of Amplatz septal occluders and Amplatzer Duct Occluder • Excellent alternative to coils or detachable balloons in the embolization of medium to large vessels with high flow - otherwise require multiple coils
  • 15. • All AVP models - 2 basic components: a vascular plug and a delivery wire • Plugs built with nitinol braids, self-expanding radiopaque platinum marker bands at both ends that allow for high visibility under fluoroscopy Stainless-steel screw on one of the platinum marker bands attaches to a delivery cable • Ability to recapture and reposition the device as needed • After satisfactory positioning, counterclockwise rotation of connecting cable releases device
  • 16.
  • 17. • Single model has evolved into 4 models • For use in various types of anatomy, hemodynamics, and lesion entities • AVP I and II – USFDA approved 2004, 2007 • AVP III – 2008 CE marked but not available in US • AVP 4 – USFDA approved 2012
  • 18. AVP or AVP I Single lobar plug Guide 5-8 Fr Sheath 4-6 Fr Diameter 4-16 mm Increments 2 mm Length 7-8 mm Lesion with short landing zone requiring high radial force to secure AVP
  • 19. Select a device with a diameter approximately 30-50% larger than the vessel diameter at the occlusion site
  • 20.
  • 21.
  • 22.
  • 23. AVP II Multi (6)-layered Tri-lobar plug with increased length Guide 5-9 Fr Sheath 4-7 Fr Diameter 3-22 mm Increments 2 mm Length 6-18 mm Rapid occlusion Used when Variable landing zone – can be shortened by compression Minimises migration and recanalization
  • 24. Select a device with a diameter approximately 30-50% larger than the vessel diameter at the occlusion site
  • 25. Large Left Segmental Pulmonary Artery Pseudoaneurysm
  • 26. AVP 4 Multi (4)-layered Bi-lobar plug with small profile, more flexible delivery wire Simple delivery - 0.038” guidewire compatible diagnostic catheter (Guide/Sheath not required) Diameter 4-8 mm Increments 1 mm Length 10-13.5 mm Small, tortuous vessel Rapid occlusion
  • 27. Select a device with a diameter approximately 30-50% larger than the vessel diameter at the occlusion site
  • 28. AVP 4 completely occluding coronary fistula originating from proximal RCA draining into the right upper lung field
  • 29. AVP III Oblong plug with 2 extended rims Guide 6-9 Fr Sheath 4-7 Fr Diameter 4-14 mm (Long Axis) Increments 2 mm (Long Axis) Length 2-5 mm (Short Axis) Fastest occlusion of all AVPs Enhanced stability in high flow states Niche device for suitable anatomy Like ASD occluder stretched sideways!
  • 30. Amplatzer Vascular Plug III 12/5 device implant in aortic position. A: in systole, the device does not interfere with the prosthesis. B: in diastole, the device does interfere with the prosthesis. C: an Amplatzer Duct Occluder 12/10 device implant that does not interfere in systole. D: or in diastole
  • 31. CERA VASCULAR PLUG SYSTEM • Manufactured by Lifetech Scientific Corp., China • Single lobe device coated with Titanium Nitride – prevent thrombosis and improves endothelialisation • PTFE coated – shorter occlusion time
  • 32. Single lobed, PTFE covered Guide 4-9 Fr Diameter 4-24 mm Increments 2 mm Length 7-14 mm Rapid occlusion due to PTFE
  • 33. MEDUSA VASCULAR PLUG • Manufactured by Endoshape, USA • USFDA approved in Nov,2013 • Constructed from multiple 0.018” polymer coils • Highly trackable in tortuous anatomy
  • 34. MEDUSA VASCULAR PLUG • Manufactured by Endoshape, USA • USFDA approved in Nov,2013 • Constructed from multiple 0.018” polymer coils • Highly trackable in tortuous anatomy • Better Imaging - Minimal metal content reduces artifacts; follow up can be with a CT/MRI versus an angiogram
  • 35.
  • 36.
  • 37. MICROVASCULAR PLUG • Manufactured originally by Covidien, USA • Covidien later bought by Medtronic, USA • MVP plug - The first plug deliverable through a micro catheter • Enables super-selective embolization of distal vessels • PTFE coated Nitinol design – rapid occlusion
  • 38. • Length 12 mm • Diameter 5.3 mm and 6.5 mm • 3 mm MVP™ plug: recommended delivery through .021" micro catheter2 • 5 mm MVP™ plug: recommended delivery through .027" micro catheter
  • 40.
  • 41. VASCULAR • ARTERIAL: Parent artery occlusion – Internal iliac – Carotid – Vertebral – Renal – Gastroduodenal – Aberrant right subclavian artery – Popliteal artery aneurysm – Hepatic artery pseudoaneurysm – Hepatic cavernous hemangioma
  • 42. VASCULAR • VENOUS – Portal Vein –Preoperative embolization of tumor side portal vein stimulates contralateral liver lobular hypertrophy - improves resection rate – Gastric varix in conjunction with a TIPS – Varicocele embolization for infertility – Ovarian vein embolization for female pelvic congestion syndrome – Saphenous vein graft aneurysm – Large inferior vena cava aneurysm
  • 43. ABNORMAL VASCULAR CONNECTIONS • CONGENITAL – Pulmonary AVMs; renal AVMs; Hepatic AVMs – PDA – PDV – intrahepatic portosystemic shunt – Splenorenal shunt – Spontaneous mesocaval shunt in SMA – Scimitar vein to left atrium – Congenital coronary artery fistula
  • 44. ABNORMAL VASCULAR CONNECTIONS • ACQUIRED – HD-AVF – TIPS – Blalock-Taussig shunt – Traumatic arteriovenous fistula
  • 45. CARDIAC • Paravalvular leak closure – Mechanical MV/AV – TAVI • PDA • LAA
  • 46. MICROVASCULAR PLUGS • Hepatic artery skeletonisation – before radioembolisation/chemoembolisation of tumor • Gastroduodenal artery - during radioembolization • Recanalized pulmonary arteriovenous malformation previously coil embolised • Splenic artery hemorrhage secondary to tumoral erosion • Lower gastrointestinal hemorrhage • Temporary vessel occlusion by undeployed MVP plug - Whenever only temporary occlusion of a critical vessel is desired - during complex vascular procedures; or Radio/chemo embolisation
  • 47. NON-VASCULAR • EXTRA VASCULAR – Bronchopleural fistula! – Vesicovaginal fistula! – Intraperitoneal bile leak!
  • 48. CONCLUSION • Vascular plugs as occlusion devices are valuable in managing a wide variety of disease processes • Easy to use, can be precisely deployed in the target vessel, high resistance to migration, low recanalization rate • Vessel size, high-flow status, and coagulopathy can prolong the occlusion time. The addition of coils, gelfoams as an adjunct can achieve rapid and reliable occlusion with minimal cost • Continued evolution in product design has improved occlusion properties and decreased device profile – alongwith interventionalist’s innovative usage – has truly widened the spectrum of clinical indications for these versatile devices
  • 49. CARDIOLOGY IS NOTHING BUT ‘JUGAAD’ WITH EXPERTISE - Dr. Ranjeet Nath