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Perioperative Management of Cardiac
patients With Coronary Stents
Lecturer Of Anesthesiology And Intensive Care
, Al-Azhar University
pediatric cardiac anesthesiologist
Ali_m7areak@yahoo.com
ALI AHMED MAHAREAK, MD
Coronary Artery Disease
 Myocardial ischemia results from the reduction of
coronary blood flow to an extent that leads to
decrease in oxygen supply to myocardial tissue
 prolonged & irreversible ischemia myocardial cell
death & necrosis ---this is defined as
myocardial infarction
 Leading cause of death
 Caused by buildup of plaque
Risk factors
 Age
 Gender
 Genes
 High blood pressure (hypertension)
 High blood cholesterol
 Smoking
 Obesity
 Physical inactivity
 Diabetes
 Stress
Major Risk Factors:
The Big Three
• Hypertension
• High cholesterol
• Cigarette smoking
All three increase risk
factor eight times
AND…. we should add LACK OF EXERCISE
Major Risk Factors
Major Risk Factors
Biochemical Changes in Acute Myocardial Infarction
(mechanism of release of myocardial markers)
ischemia to myocardial muscles (with low O2 supply)
anaerobic glycolysis
increased accumulation of Lactate
decrease in pH
activate lysosomal enzymes
disintegration of myocardial proteins
cell death & necrosis
release of intracellular
contents to blood
BIOCHEMICAL
MARKERS
clinical manifestations
(chest pain)
ECG
changes
Pathophysiology of Coronary Artery Disease
Chest pain
Diagnosis for Coronary Artery Disease
Symptoms
Symptoms ECG TESTS
• Chest pain
• Fatigue
• Shortness of
breath
• Weakness
•S-T segment elevation
•S-T segment depression
•Hyper-acute T-waves
•T-wave inversion
•Pathological Q-waves
•Left bundle branch block
•Cardiac enzymes
•Echocardiography
•Exercise Stress Test
•Nuclear Stress Test
•CT Scan
•Coronary Angiograph
ECG TESTS
Horizontal ST depression
ST-Segment Elevation
Hyperacute T waves
Inferior T-wave inversion
Non-ST Elevation Infarction
ST depression & T-wave inversion
The ECG changes seen with a non-ST elevation infarction are:
Before injury Normal ECG
ST depression & T-wave inversion
ST returns to baseline, but T-wave
inversion persists
Ischemia
Infarction
Fibrosis
Non-ST Elevation Infarction
Note the ST
depression and
T-wave inversion
in leads V2-V6.
Cardiac enzymes
ECHOCARDIOGRAPHY
ECHOCARDIOGRAPHY
Treatment Options for Coronary
Artery Disease
Medications
Balloon
angioplasty
Coronary
stenting
CABG
What is a Stent
 A small, mesh-like device
made of metal
 Acts as a support in keeping
the vessel open
 Stent helps to improve blood
flow to the heart muscle and
reduce the pain of angina
Scope of the Problem
 In the US over 600,000 percutaneous
coronary interventions (PCI) are done every
year
 The majority of PCIs involve drug eluting stent
placement
 About 5% of patients undergoing PCI will need
non-cardiac surgery within 1 year
 Roughly 1% of elective non-cardiac surgery
pts. had PCI in the preceding year
What Problems are There?
Increased risk of myocardial infarction
Risk of stent thrombosis
Increased risk of bleeding due to DAPT
Bare metal stents:
 Traditional method
 May have an increased rate of re-narrowing due to
growth of scar tissue in the stent, a condition called
Restenosis.
Drug-eluting stents:
 Combat Restenosis
 Controlled release of medicine into tissue
 Drug limits overgrowth of natural tissue
Types of Stent
Limitations of Stents
Stent Thrombosis
• Formed the concept of DAPT
Durability – (Restenosis)
• Neointimal hyperplasia got worse
• Restenosis rates were 20-30%
• Small Vessels, Diabetics, diffuse disease all had
even higher restenosis rates
Coronary Restenosis
•30-40%
Balloon
angioplasty
•20-30%BMS
•4-5%DES
Why Cardiologists Love PCI & DES
PCI reduces mortality and morbidity in acute
coronary syndromes
PCI is effective in controlling anginal symptoms
Patient recovery time is short
Long term durability is very good
Limitations of Drug eluting stents
• Increased, but later, stent thrombosis in DES
• Late (>30 days)
• Very Late (>1 year)
• Inhibition of neo-intimal growth also inhibits
endothelial formation inside the stent
• Long term (12 month) Plavix is recommended
Bleeding Stent Thrombosis
Balance
Stent Thrombosis
 Stent thrombosis
– Acute –first 24 hours
– Sub-acute – first month
– Late – first year
– Very late - > 1 year
 Stent thrombosis is a serious adverse event, commonly
associated with MI and even sudden cardiac death
 STH is associated with up to 70% rate of MI and 20%
mortality
 Overall stent thrombosis rate is 1-2 % in first year
Stent Thrombosis
High risk
<1 month after PCI with BMS
<6 months after PCI with DES
<12 months after complex PCI with DES (long
stents, multiple
stents, overlapping, small vessels,
bifurcations, left main, last remaining vessel)
Dual Anti-Platelet Therapy (DAPT)
 Stent implantation is a thrombogenic
procedure.
DAPT is the cornerstone of oral antiplatelet therapy for
the prevention of stent thrombosis
Aspirin irreversibly inhibits platelet cyclooxygenase
(COX-1)
The thienopyridines [e.g., clopidogrel (Plavix®)]
irreversibly bind to the platelet P2Y12 receptor and
inhibit ADP - mediated platelet activation and
aggregation
Dual Anti-Platelet Therapy (DAPT)
Aspirin and a P2Y12 inhibitor
Duration:
 2 weeks following PCI
 6 weeks following bare metal stent
 12 months following DES
 12 months following MI
Continuation of aspirin indefinitely
Risk of thrombosis is increased more than 14 folds and 1-year
mortality is increased 10 folds if DAPT is stopped prematurely
Stent Thrombosis
Surgery
During surgery there is a hypercoagulable
state induced:
oIncreased inflammation and platelet
activation
oincreased catecholamine release
odecreased fibrinolysis
Bleeding Risk During Surgery
Aspirin alone 2.5% to 20%
DAPT 30% to 50%
Intracranial procedures
Spine
Major vascular
fatal bleeding
No increased risk of bleeding-related mortality except
during intracranial, spine and vascular surgeries
Bleeding
ASPIRIN 2.5% to 20%
DAPT 30% to 50%
Mortality in brain, spine and
vascular surgeries only
Balance
Stent Thrombosis
 Overall rate is 1-2 % in first year
 Premature stopping 14 folds
 70% rate of MI and 20%
mortality
Surgical Risk and Timing
• Non cardiac surgery done less than 6 weeks
after PCI has the highest mortality
• The single biggest predictor of stent
thrombosis is discontinuation of anti-platelet
therapy
Surgical Risk and Timing
Bare Metal Stent:
• Risk of death, MI and stent thrombosis is
increased 5% to 30% if surgery is performed
within 6 weeks of placement.
• Emergency surgery triples the risk of adverse
events compared with elective surgery.
Surgical Risk and Timing
Drug-Eluting Stent:
 Risk of major adverse cardiac events is very
significant if antiplatelet therapy is
discontinued and noncardiac surgery
performed within 1 year.
 Emergency surgery is associated with a 3.5-
fold increase in adverse events compared with
elective surgery
Strategies for Peri-op Management of DES
ELECTIVE SURGERY
 Elective surgery should be delayed at least until
12 months post DES
 Plavix- if stopped - 5 to 7 days pre-op, continue
aspirin if at all possible
 Resume Plavix with 300 or 600mg loading dose
Strategy for Peri-op Management of DES
ELECTIVE SURGERY
 Perioperative Monitoring: Urgent cardiac evaluation should be
performed if perioperative angina occurs.
Anesthetic Technique: Neuraxial blockade is avoided patients
undergoing DAPT.
 Platelets: can be administered for bleeding
 Availability of Interventional Cardiology: Patients should
be triaged to an interventional cardiologist within 90 minutes of
a diagnosis or suspicion of acute MI or acute stent thrombosis
Strategy for Peri-op Management of DES
 “Bridging Therapy” with GP IIb/IIIa inhibitor
 Stop Plavix 5-7 days pre-op
 Admit 2-3 days pre-op and start IIb/IIIa
 Continue aspirin throughout if possible
 Restart Plavix as soon as possible post-op
Strategies for Peri-op Management of DES
URGENT SURGERY
Urgent-Emergent surgeries have 4-fold
higher mortality
Strategy for Peri-op Management of DES
URGENT SURGERY
• Continue DAPT if possible - stent thrombosis risk is
high
• Closed/confined space – intracranial, spinal medullary,
posterior chamber ophthalmic surgeries will need
DAPT discontinued
• If P2Y12 inhibitor stopped, try to maintain aspirin
• Restart the P2Y12 inhibitor post surgery (within 24
hours if possible, with 300mg bolus).
Strategies for Peri-op Management of DES
Post Op issues
• Resumption of DAPT as soon as possible
• Using bolus dose of P2Y12 inhibitor
• Intensive post–op monitoring if off DAPT
• Prompt evaluation and intervention for stent
thrombosis or any bleeding
Strategies for Peri-op Management of DES
Post-op Stent Thrombosis
• Usually presents as ST elevation MI
• Fibrinolytic therapy is contraindicated
• Primary PCI is the treatment of choice
Pharmacologic Management
β-Blockers:
 Currently, the only class I recommendation is to
continue them in patients who are already
receiving them.
Other patients who may benefit from β-blockers
include:
 undergoing vascular surgery
 Patients have multiple cardiac risk factors
 Patients show reversible cardiac ischemia on preoperative testing
Pharmacologic Management
 α2-Agonists: have analgesic, sedative, and
sympatholytic effects and may be useful
 Nitrovasodilators
 Statin therapy: may be beneficial if started
1 to 4 weeks before high-risk surgery.
 Hyperglycemia: must be controlled (180
mg/dl).
 Anxiety must be treated
Intraoperative Management
Goals:
• to prevent myocardial ischemia by optimizing
myocardial oxygen supply and reducing myocardial
oxygen demand
• keep the heart rate and blood pressure within 20%
of the normal awake value
• to monitor for and treat ischemia
Maintenance of the balance between myocardial oxygen
supply and demand is more important than the specific
anesthetic technique or drugs selected to produce
anesthesia and muscle relaxation
DECREASED OXYGEN DELIVERY
 Decreased coronary blood flow
 Tachycardia
 Diastolic hypotension
 Hypocapnia
 Coronary artery spasm
 Decreased oxygen content
 Anemia
 Arterial hypoxemia
 Shift of the oxyhemoglobin dissociation curve to
the left
INCREASED OXYGEN REQUIREMENTS
 Sympathetic nervous system stimulation
 Tachycardia
 Hypertension
 Increased myocardial contractility
 Increased afterload
 Increased preload
Approach to the Management of Patients with
Previous PCI Who Require Noncardiac Surgery
Balloon
angioplasty
Bare-metal
stent
Drug-eluting
stent
Delay for elective or
nonurgent surgery
<14 days
Proceed to the
operation room
with aspirin
Delay for elective or
Nonurgent surgery
>30- 45 days <30- 45 days
Proceed to the
operating room
with aspirin
>365 days
Previous PCI
Time since
PCI
<365 days
>14 days
Treatment for Patients Requiring PCI
Who Need Subsequent Surgery
Balloon
angioplasty
Bare-metal
stent
Drug-eluting
stent
14-29 days 30-365 days >365 days
Bleeding risk of surgery
Timing of surgery
Acute MI, H risk ACS
Stent & continue
dual antiplatelet
therapy
low
Not low
Stents mahareak

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Stents mahareak

  • 1. Perioperative Management of Cardiac patients With Coronary Stents Lecturer Of Anesthesiology And Intensive Care , Al-Azhar University pediatric cardiac anesthesiologist Ali_m7areak@yahoo.com ALI AHMED MAHAREAK, MD
  • 2. Coronary Artery Disease  Myocardial ischemia results from the reduction of coronary blood flow to an extent that leads to decrease in oxygen supply to myocardial tissue  prolonged & irreversible ischemia myocardial cell death & necrosis ---this is defined as myocardial infarction  Leading cause of death  Caused by buildup of plaque
  • 3. Risk factors  Age  Gender  Genes  High blood pressure (hypertension)  High blood cholesterol  Smoking  Obesity  Physical inactivity  Diabetes  Stress
  • 4. Major Risk Factors: The Big Three • Hypertension • High cholesterol • Cigarette smoking All three increase risk factor eight times AND…. we should add LACK OF EXERCISE
  • 7. Biochemical Changes in Acute Myocardial Infarction (mechanism of release of myocardial markers) ischemia to myocardial muscles (with low O2 supply) anaerobic glycolysis increased accumulation of Lactate decrease in pH activate lysosomal enzymes disintegration of myocardial proteins cell death & necrosis release of intracellular contents to blood BIOCHEMICAL MARKERS clinical manifestations (chest pain) ECG changes
  • 8. Pathophysiology of Coronary Artery Disease Chest pain
  • 9. Diagnosis for Coronary Artery Disease Symptoms Symptoms ECG TESTS • Chest pain • Fatigue • Shortness of breath • Weakness •S-T segment elevation •S-T segment depression •Hyper-acute T-waves •T-wave inversion •Pathological Q-waves •Left bundle branch block •Cardiac enzymes •Echocardiography •Exercise Stress Test •Nuclear Stress Test •CT Scan •Coronary Angiograph ECG TESTS
  • 14. Non-ST Elevation Infarction ST depression & T-wave inversion The ECG changes seen with a non-ST elevation infarction are: Before injury Normal ECG ST depression & T-wave inversion ST returns to baseline, but T-wave inversion persists Ischemia Infarction Fibrosis
  • 15. Non-ST Elevation Infarction Note the ST depression and T-wave inversion in leads V2-V6.
  • 19. Treatment Options for Coronary Artery Disease Medications Balloon angioplasty Coronary stenting CABG
  • 20. What is a Stent  A small, mesh-like device made of metal  Acts as a support in keeping the vessel open  Stent helps to improve blood flow to the heart muscle and reduce the pain of angina
  • 21. Scope of the Problem  In the US over 600,000 percutaneous coronary interventions (PCI) are done every year  The majority of PCIs involve drug eluting stent placement  About 5% of patients undergoing PCI will need non-cardiac surgery within 1 year  Roughly 1% of elective non-cardiac surgery pts. had PCI in the preceding year
  • 22. What Problems are There? Increased risk of myocardial infarction Risk of stent thrombosis Increased risk of bleeding due to DAPT
  • 23. Bare metal stents:  Traditional method  May have an increased rate of re-narrowing due to growth of scar tissue in the stent, a condition called Restenosis. Drug-eluting stents:  Combat Restenosis  Controlled release of medicine into tissue  Drug limits overgrowth of natural tissue Types of Stent
  • 24.
  • 25. Limitations of Stents Stent Thrombosis • Formed the concept of DAPT Durability – (Restenosis) • Neointimal hyperplasia got worse • Restenosis rates were 20-30% • Small Vessels, Diabetics, diffuse disease all had even higher restenosis rates
  • 27. Why Cardiologists Love PCI & DES PCI reduces mortality and morbidity in acute coronary syndromes PCI is effective in controlling anginal symptoms Patient recovery time is short Long term durability is very good
  • 28. Limitations of Drug eluting stents • Increased, but later, stent thrombosis in DES • Late (>30 days) • Very Late (>1 year) • Inhibition of neo-intimal growth also inhibits endothelial formation inside the stent • Long term (12 month) Plavix is recommended
  • 30. Stent Thrombosis  Stent thrombosis – Acute –first 24 hours – Sub-acute – first month – Late – first year – Very late - > 1 year  Stent thrombosis is a serious adverse event, commonly associated with MI and even sudden cardiac death  STH is associated with up to 70% rate of MI and 20% mortality  Overall stent thrombosis rate is 1-2 % in first year
  • 31. Stent Thrombosis High risk <1 month after PCI with BMS <6 months after PCI with DES <12 months after complex PCI with DES (long stents, multiple stents, overlapping, small vessels, bifurcations, left main, last remaining vessel)
  • 32. Dual Anti-Platelet Therapy (DAPT)  Stent implantation is a thrombogenic procedure. DAPT is the cornerstone of oral antiplatelet therapy for the prevention of stent thrombosis Aspirin irreversibly inhibits platelet cyclooxygenase (COX-1) The thienopyridines [e.g., clopidogrel (Plavix®)] irreversibly bind to the platelet P2Y12 receptor and inhibit ADP - mediated platelet activation and aggregation
  • 33. Dual Anti-Platelet Therapy (DAPT) Aspirin and a P2Y12 inhibitor Duration:  2 weeks following PCI  6 weeks following bare metal stent  12 months following DES  12 months following MI Continuation of aspirin indefinitely Risk of thrombosis is increased more than 14 folds and 1-year mortality is increased 10 folds if DAPT is stopped prematurely
  • 34. Stent Thrombosis Surgery During surgery there is a hypercoagulable state induced: oIncreased inflammation and platelet activation oincreased catecholamine release odecreased fibrinolysis
  • 35. Bleeding Risk During Surgery Aspirin alone 2.5% to 20% DAPT 30% to 50% Intracranial procedures Spine Major vascular fatal bleeding No increased risk of bleeding-related mortality except during intracranial, spine and vascular surgeries
  • 36. Bleeding ASPIRIN 2.5% to 20% DAPT 30% to 50% Mortality in brain, spine and vascular surgeries only Balance Stent Thrombosis  Overall rate is 1-2 % in first year  Premature stopping 14 folds  70% rate of MI and 20% mortality
  • 37. Surgical Risk and Timing • Non cardiac surgery done less than 6 weeks after PCI has the highest mortality • The single biggest predictor of stent thrombosis is discontinuation of anti-platelet therapy
  • 38. Surgical Risk and Timing Bare Metal Stent: • Risk of death, MI and stent thrombosis is increased 5% to 30% if surgery is performed within 6 weeks of placement. • Emergency surgery triples the risk of adverse events compared with elective surgery.
  • 39. Surgical Risk and Timing Drug-Eluting Stent:  Risk of major adverse cardiac events is very significant if antiplatelet therapy is discontinued and noncardiac surgery performed within 1 year.  Emergency surgery is associated with a 3.5- fold increase in adverse events compared with elective surgery
  • 40. Strategies for Peri-op Management of DES ELECTIVE SURGERY  Elective surgery should be delayed at least until 12 months post DES  Plavix- if stopped - 5 to 7 days pre-op, continue aspirin if at all possible  Resume Plavix with 300 or 600mg loading dose
  • 41. Strategy for Peri-op Management of DES ELECTIVE SURGERY  Perioperative Monitoring: Urgent cardiac evaluation should be performed if perioperative angina occurs. Anesthetic Technique: Neuraxial blockade is avoided patients undergoing DAPT.  Platelets: can be administered for bleeding  Availability of Interventional Cardiology: Patients should be triaged to an interventional cardiologist within 90 minutes of a diagnosis or suspicion of acute MI or acute stent thrombosis
  • 42. Strategy for Peri-op Management of DES  “Bridging Therapy” with GP IIb/IIIa inhibitor  Stop Plavix 5-7 days pre-op  Admit 2-3 days pre-op and start IIb/IIIa  Continue aspirin throughout if possible  Restart Plavix as soon as possible post-op
  • 43. Strategies for Peri-op Management of DES URGENT SURGERY Urgent-Emergent surgeries have 4-fold higher mortality
  • 44. Strategy for Peri-op Management of DES URGENT SURGERY • Continue DAPT if possible - stent thrombosis risk is high • Closed/confined space – intracranial, spinal medullary, posterior chamber ophthalmic surgeries will need DAPT discontinued • If P2Y12 inhibitor stopped, try to maintain aspirin • Restart the P2Y12 inhibitor post surgery (within 24 hours if possible, with 300mg bolus).
  • 45. Strategies for Peri-op Management of DES Post Op issues • Resumption of DAPT as soon as possible • Using bolus dose of P2Y12 inhibitor • Intensive post–op monitoring if off DAPT • Prompt evaluation and intervention for stent thrombosis or any bleeding
  • 46. Strategies for Peri-op Management of DES Post-op Stent Thrombosis • Usually presents as ST elevation MI • Fibrinolytic therapy is contraindicated • Primary PCI is the treatment of choice
  • 47. Pharmacologic Management β-Blockers:  Currently, the only class I recommendation is to continue them in patients who are already receiving them. Other patients who may benefit from β-blockers include:  undergoing vascular surgery  Patients have multiple cardiac risk factors  Patients show reversible cardiac ischemia on preoperative testing
  • 48. Pharmacologic Management  α2-Agonists: have analgesic, sedative, and sympatholytic effects and may be useful  Nitrovasodilators  Statin therapy: may be beneficial if started 1 to 4 weeks before high-risk surgery.  Hyperglycemia: must be controlled (180 mg/dl).  Anxiety must be treated
  • 49. Intraoperative Management Goals: • to prevent myocardial ischemia by optimizing myocardial oxygen supply and reducing myocardial oxygen demand • keep the heart rate and blood pressure within 20% of the normal awake value • to monitor for and treat ischemia Maintenance of the balance between myocardial oxygen supply and demand is more important than the specific anesthetic technique or drugs selected to produce anesthesia and muscle relaxation
  • 50. DECREASED OXYGEN DELIVERY  Decreased coronary blood flow  Tachycardia  Diastolic hypotension  Hypocapnia  Coronary artery spasm  Decreased oxygen content  Anemia  Arterial hypoxemia  Shift of the oxyhemoglobin dissociation curve to the left
  • 51. INCREASED OXYGEN REQUIREMENTS  Sympathetic nervous system stimulation  Tachycardia  Hypertension  Increased myocardial contractility  Increased afterload  Increased preload
  • 52. Approach to the Management of Patients with Previous PCI Who Require Noncardiac Surgery Balloon angioplasty Bare-metal stent Drug-eluting stent Delay for elective or nonurgent surgery <14 days Proceed to the operation room with aspirin Delay for elective or Nonurgent surgery >30- 45 days <30- 45 days Proceed to the operating room with aspirin >365 days Previous PCI Time since PCI <365 days >14 days
  • 53. Treatment for Patients Requiring PCI Who Need Subsequent Surgery Balloon angioplasty Bare-metal stent Drug-eluting stent 14-29 days 30-365 days >365 days Bleeding risk of surgery Timing of surgery Acute MI, H risk ACS Stent & continue dual antiplatelet therapy low Not low