GP IIB/IIIA Inhibitor Use During GP IIB/IIIA Inhibitor Use During - - PowerPoint PPT Presentation

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GP IIB/IIIA Inhibitor Use During GP IIB/IIIA Inhibitor Use During - - PowerPoint PPT Presentation

GP IIB/IIIA Inhibitor Use During GP IIB/IIIA Inhibitor Use During Endovascular Intervention Endovascular Intervention Jay S. Yadav M.D. Director, Vascular Intervention Dept of Cardiovascular Medicine The Cleveland Clinic Foundation Name: Jay


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GP IIB/IIIA Inhibitor Use During GP IIB/IIIA Inhibitor Use During Endovascular Intervention Endovascular Intervention

Jay S. Yadav M.D.

Director, Vascular Intervention Dept of Cardiovascular Medicine The Cleveland Clinic Foundation

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Nothing to Disclose Related to this Presentation Nothing to Disclose Related to this Presentation Name: Jay Yadav, M.D.

Jay Yadav, M.D.

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GP IIb/IIIa Receptor Blockade in GP IIb/IIIa Receptor Blockade in Peripheral Vascular Intervention: Rationale Peripheral Vascular Intervention: Rationale

◆ Underlying pathophysiology of PVD is atherosclerosis ◆ Plaque rupture (spontaneous or due to vascular intervention) is a

potent stimulus for platelet activation and aggregation

◆ Coagulation system is activated by vessel damage and activated

platelets generate thrombin

◆ Diabetes incidence high in patients with PVD ◆ GP IIb/IIIa inhibitors not associated with increased incidence of ICH

(unlike fibrinolytics)

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GP IIB/IIIA Inhibitor Use GP IIB/IIIA Inhibitor Use During Endovascular During Endovascular Intervention Intervention

◆ Safety ◆ Benefit ◆ Cost

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Acute Coronary Acute Coronary Syndromes Syndromes

ejt 029–144

The “Hot” Vessel The “Hot” Vessel Microvascular Microvascular Obstruction Obstruction

1000x 1000x 5x 5x

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SLIDE 6

Topol EJ. Circulation. 1998;97:211-218.

Intracerebral Hemorrhage Rates in GP Intracerebral Hemorrhage Rates in GP IIb/IIIa Receptor Inhibitor Coronary IIb/IIIa Receptor Inhibitor Coronary Intervention Trials Intervention Trials

Trial Placebo (%) Inhibitor (%)

EPIC 0.3 0.3 IMPACT 0.1 0.1 RESTORE 0.2 0.1 CAPTURE 0.0 0.0 EPILOG 0.0 0.1 Pooled 0.1 0.1

N

2,099 4,010 2,139 1,265 2,792 12,305

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Abciximab in Carotid Stenting Abciximab in Carotid Stenting

Kapadia et al , Stroke 2001, 32: 2328-32 Kapadia et al , Stroke 2001, 32: 2328-32

Control group Control group

ASA + ADP antagonist ASA + ADP antagonist

Abciximab group Abciximab group

ASA + ADP antagonist ASA + ADP antagonist + + Abciximab (0.25 mg/kg bolus Abciximab (0.25 mg/kg bolus ± 0.125 mcg/kg/min for 12 0.125 mcg/kg/min for 12 hrs) hrs)

151 patients 151 patients 159 procedures 159 procedures 128 patients 128 patients 134 procedures 134 procedures 23 patients 23 patients 25 procedures 25 procedures

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Procedural Events Procedural Events

Control Abciximab (n=25) (n=134) Minor strokes 1 (0.8%) Major strokes 1 (4%) Retinal infarct 1 (0.8%) ICH 1 (4%) MI Death 1 (4%) Total events 2 (8%) 2 (1.6%)

p=0.05

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30 Day Follow-up: New Events 30 Day Follow-up: New Events

Control Abciximab (n=25) (n=134) Minor strokes Major strokes ICH 1 (0.8%) MI Death 2 (8%) 5 (3.7%) Total events 2 (8%) 6 (4.5%)

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All events: 30 days All events: 30 days

8% 2.3% 8% 3.7%

Events (%) Events (%)

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Severe Aortic Arch Tortuosity with MCA Severe Aortic Arch Tortuosity with MCA embolization embolization

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PLAQUE PROTRUSION PLAQUE PROTRUSION THROUGH STENT STRUTS THROUGH STENT STRUTS

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Dethrombosis of Left Anterior Dethrombosis of Left Anterior Descending Coronary Artery with Descending Coronary Artery with Abciximab Abciximab

Initial Angiogram Angiogram Post Abciximab Bolus

Adapted with permission from Rerkpattanapipat P et al. Circulation. 1999;99:2965.

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Combination Therapy in PVD Combination Therapy in PVD

Low Dose Retavase

Full Dose ReoPro

Low Dose, Weight-Adjusted Heparin

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“White” Thrombus “Red” Thrombus

Fibrinolytic ineffective Fibrinolytic ineffective Antiplatelet effective Antiplatelet effective Fibrinolytic effective Fibrinolytic effective Antiplatelet effective Antiplatelet effective Platelet-Rich Thrombus Platelet/Fibrin Thrombus

Platelet Thrombus vs Stabilized Clot

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Abciximab + Urokinase in Peripheral Abciximab + Urokinase in Peripheral Arterial Thrombolysis Arterial Thrombolysis

Tepe G et al. Am J Roentgenol. 1999;172:1343-1346.

Baseline After 1 Hour of Treatment

Digital subtraction angiogram of a right common iliac artery occlusion

Tepe et al

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Abciximab + Reteplase in Abciximab + Reteplase in Chronic SFA Occlusion Chronic SFA Occlusion

Katzen B. Presented at the 11th Annual Symposium of Transcatheter Cardiovascular Therapeutics; September 22, 1999; Washington, DC.

Katzen

Baseline After 2 hours After At 6.5 hours After lysis 6 hours and stent (palpable pulse)

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Major Bleeding at Discharge/Day 7 by Abciximab

Note: No incidence of intracranial hemorrhage

  • r stroke among the subjects in the study.

50 9 25 15 33 8 33 20 25 50 75 100

0.1 U/hr 0.2 U/hr 0.5 U/hr 1.0 U/hr Combined

Percentage of Patie Reteplase Reteplase + abciximab

P=NS P=NS

N 6 6 N 6 6 12 12 12 12 12 14 12 14 12 6 12 6 36 38 36 38

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Patency on 20-hour Angiogram

33 42 100 40 49 67 64 62 80 66 20 40 60 80 100 120 0.1 U/hr 0.2 U/hr 0.5 U/hr 1.0 U/hr Combined Percentage of Patie Reteplase Reteplase + abciximab

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Distal Embolization Distal Embolization (Sufficient to Require Intervention) (Sufficient to Require Intervention)

090302.1 Smith.ppt - On-

67 25 33 31 7 17 5 25 50 75 100 0.1 U/hr 0.2 U/hr 0.5 U/hr 1.0 U/hr Combined Percentage of Patie Reteplase Reteplase + abciximab

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Case Examples of GP IIB/IIIA Use

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RICA PRE POST LICA PRE POST

Bilateral Carotid Dissection with Acute Stroke Bilateral Carotid Dissection with Acute Stroke

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Middle Cerebral Artrery Middle Cerebral Artrery Intervention Intervention

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Symptomatic Pt with Single Vertebral Symptomatic Pt with Single Vertebral Supplying Entire Brain Supplying Entire Brain

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◆ 83 y.o. woman ◆ IRDM x 30 yrs ◆ PMHx: ◆ Left CEA ◆ S/p CABG ◆ Renal artery disease ◆ Aug 01: right femoral-

anterior tibial bypass for claudication

◆ Jan 02: bypass

thrombectomy for acute leg ischemia

◆ Apr 02: Non-healing ulcer,

gangrenous toe, redo femoral-AT bypass

◆ May 02: graft occlusion by

U/S

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◆ 64 yo Sx Rica ◆ Severe ankylosing spondylitis-

◆ Cannot move neck in any plane ◆ Cervical and thoracic spine anteriorly

flexed at 45 degrees

◆ Chronic renal insuffic – Cr 4.2 ◆ Gadolinium

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Case 1 Case 1

◆ 59 yo Male w HTN, ↑Chol, Cigs

undergoing L Heart Cath

◆ Immediately upon withdrawal of

Pigtail Catheter from LV developed Neurological Sx

◆ Global Aphasia ◆ R Hemianopsia ◆ Flacid R Hemiparesis ◆ NIHSS=22

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Angiogram Angiogram

◆ Acute Cutoff of L

MCA Trunk

  • Few Pial Collaterals

from ACA to MCA

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Endovascular Approach Endovascular Approach

◆ 4500U IA Heparin

  • 2.3F Microcatheter advanced into MCA over

0.014” Soft Hydrophilic Wire

  • 6F MPA1 Guide Inserted into L ICA over 0.035”

Glide Wire

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Endovascular Approach Endovascular Approach

◆ Wire Advanced

Through Thrombus for More Support

  • Results in Thrombus

Migration into MCA Superior Division

  • 21 min after onset
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Endovascular Approach Endovascular Approach

◆ Microcatheter is Placed

Within Thrombus in Superior Division

  • 1 U Retevase Infused over

1 min

  • Repeat Angiogram after 5

min Unchanged

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Endovascular Approach Endovascular Approach

◆ Reopro 1mg Injected

Into Thrombus

  • Five min Later Partial

Recannalization of Superior Division

  • Persistent Slow Flow in

Distal Branches of Inferior Division and Proximal Superior Division

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SLIDE 38

Endovascular Approach Endovascular Approach

◆ Retevase 1U followed

by Reopro 5mg (1/4 Bolus) Injected into Sup Division

  • 10 min Later Nearly Complete

Flow Except for One Distal Branch Occlusion

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Outcome Outcome

◆ Speech and R Arm

Movement Began To Return on the “Table”

  • Final Angiogram at 75

min After Onset is Normal

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Outcome Outcome

◆ By Next AM

NIHSS=1

◆ CT Normal ◆ D/C Day 2- Normal

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CONCLUSIONS – Carotid CONCLUSIONS – Carotid Use Use

◆ GP IIb/IIIa antagonists are safe in carotid

stenting

◆ Role with Emboli prevention devices is not

clear

◆ Acute stroke / carotid thrombosis

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Conclusions –Carotid Use Conclusions –Carotid Use

◆ May Reduce Post Procedure

Embolization from Plaque Protruding through Stent Struts

◆ Careful Dosing/Monitoring Critical:

◆ 50 u/kg heparin, ACT, PAU ◆ Heparin and ACT correlates of ICH

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General Suggestions for General Suggestions for 2b3a in Endovascular 2b3a in Endovascular Cases Cases

◆ High Risk for Acute/Sub-acute

Thrombosis

◆ Consequence of AT/SAT Catastrophic ◆ High Risk of Embolization during or

immediately Post-Procedure And

◆ No Adventitial Wire Perforation

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CONCLUSIONS CONCLUSIONS

◆ Below the Knee ◆ Combination with Lytics ◆ Inability to Stent ◆ Acute Thrombosis ◆ Active Embolizers – Shaggy Aorta