Perioperative management of
antithrombotic therapy
Ext. Phatcharapol Udomluck
Medical student
Naresuan university
Antithrombotic therapy
• Long-term anticoagulation therapy for the
prevention of thromboembolism due to
– Atrial fibrillation
– Placement of a mechanical heart-valve prosthesis
– Venous thromboembolism
• Dual antiplatelet therapy (combination
treatment with aspirin and a thienopyridine)
after the placement of a coronary-artery stent
has dramatically increased
Perioperative management of
antithrombotic therapy
Goal
• Prevent thromboembolic (TE) events
– Arterial TE : Prosthetic valve thrombosis (5.9-64.7%) ,
Cardioembolic stroke (fatality 4.2-14.9)
– Venous TE : DVT, PE (fatality 26.4)
• Reduced major hemorrhage in the
periprocedural period
http://www.drtedwilliams.net/
Dr Ted Williams, PharmD education (2009)
ASSESSMENT OF THROMBOTIC RISK
• Valvular atrial fibrillation
– Severe valvular heart disease (mechanical valvular
prosthesis or mitral-valve repair) : high risk for TE
• non-valvular atrial fibrillation
– The CHA 2 DS 2 -VASc score
( Prior MI, PAD, Aortic plaque )
ASSESSMENT OF THROMBOTIC RISK
• Mechanical heart valves and venous thromboembolism
ASSESSMENT OF THROMBOTIC RISK
Cancer
– Increased risk of periprocedural thrombosis
• Cancer-specific prothrombotic activity, hormonal
therapy, angiogenesis inhibitors, radiotherapy, and
the presence of indwelling central venous catheters
– Increased risk of bleeding
• Prophylactic agents for the prevention of venous
thromboembolism, chemotherapy-related hepatic and
renal dysfunction and thrombocytopenia
ASSESSMENT OF THROMBOTIC RISK
Coronary stents
• Some patients with coronary stents may require
dual antiplatelet therapy
• Premature discontinuation of antiplatelet therapy
in anticipation of invasive procedure may lead to
stent thrombosis and precipitation of myocardial
infarction
• Rate of 50% or higher
Coronary stent
Bare-metal stent
• Risk of thrombosis is
highest within 6 Wks
after placement of stent
• Dual antiplatelet
required
– ASA(165-325 mg/day) : 1 mo
– Clopidogrel : at least 1 mo
and Up to 12 mo
Drug-eluting stent
• Risk of thrombosis is
highest within 3-6 mo
after placement of stent
• Dual antiplatelet
required
– ASA(165-325 mg/day)
• Sirolimus 3 mo
• Paclitaxel 6 mo
– Clopidogrel : at least 12 mo
Assessment of
Periprocedural bleeding risk
• Major bleeding depends on procedure
– High-risk : Major bleed
• intracranial, intraspinal, intraocular, retroperitoneal, int
rathoracic, or pericardial bleeding
• Additional Risk factors
– Residual effects of antithrombotic agents
– Active cancer
– Chemotherapy
– History of bleeding
– Reinitiation of antithrombotic therapy within 24 hours
after the procedure
HAS-BLED risk score
• SBP > 160 mmHg
• Chronic dialysis or renal transplantation or serum
creatinine ≥ 200 mmol/L
• Chronic hepatic disease (e.g. Cirrhosis) or
biochemical evidence of significant hepatic
derangement
• Previous bleeding history and/or predisposition to
bleeding, e.g. Bleeding diathesis, anaemia
• Concomitant use of drugs, such as antiplatelet
agents, NSAIDs
Low – intermediate (HAS-BLED 0-2)
High risk (HAS-BLED score >= 3)
Bridging anticoagulant therapy
Assessment tool for identifying patient-specific and surgical risk factors for patients on
anticoagulation therapy who are undergoing elective surgery
JAFFER A K Cleveland Clinic Journal of Medicine
2009;76:S37-S44
©2009 by Cleveland Clinic
Low risk  Stop anticoagulant but not start bridging anticoagulant
Recommend for Warfarin use
• Stop oral anticoagulant 5 day before invasive procedure
– Keep INR <1.5
• If follow up INR > 1.5 in 1-2 day before invasive procedure
– Vitamin K 1-2 mg
• If Continue Warfarin : Keep INR approximately 2.5
• Urgent operative procedure
– Oral or IV Vitamin K 2.5-5.0 mg
• Emergency operative procedure
– FFP + Low dose (IV or Oral) Vitamin K
• Mechanical heart valve
– Only use FFP ( NOT use Vitamin K  “Warfarin resistance”)
Bridging anticoagulant
• Recommend for Moderate to High risk TE
– Start when INR <2
– Therapeutic dose SC LMWH or IV UFH
– If GFR < 30  IV UFH is preferred
• Stop bridging before invasive procedure
– Therapeutic SC LMWH or SC UFH : 12-24 hr before
procedure (Use half dose in Morning last dose)
– IV UFH : 4-6 hr before procedure
• Half life 60 – 90 min , Dissipate after discont. 3 – 4 hr
After procedure : Start Oral anticoagulant when keep
desired INR level for 3 day
Y. Chintammit : Update in internal medicine
2009 : 343 – 349
SC
IV UFH : Keep aPTT 1.5 – 2 x control
Y. Chintammit : Update in internal medicine
2009 : 343 – 349
Reversal of anticoagulant
Reversible anticoagulant agent
• Warfarin
– Vitamin K and Fresh frozen plasma
– Prothrombin complex concentrates preferred in …
• CHF, Valvular heart disease, Renal failure
• Volume overload from Large volume infusion of FFP
• Heparin
– Protamine can reverse the action
• UFH : Completely reversal
• LMWH : Partial reversal
2011 Clinical Practice Guide on Anticoagulant Dosing and
Management of Anticoagulant-Associated Bleeding Complications in Adults
2011 Clinical Practice Guide on Anticoagulant Dosing and
Management of Anticoagulant-Associated Bleeding Complications in Adults
Reversal warfarin
• ACCP (2008) guidelines recommends
• Oral doses of vitamin K
– 1-2.5 mg for an INR between 5 and 9
– 2.5-5 mg for INR ≥ 9, no significant bleeding
– 10 mg for serious bleeding and elevated INR
2011 Clinical Practice Guide on Anticoagulant Dosing and
Management of Anticoagulant-Associated Bleeding Complications in Adults
* heparin-induced
thrombocytopenia
Reversal of anticoagulant
Nonreverssible anticoagulant agent
– Reliable reversibility has not been proved
• Direct factor Xa inhibitors (Rivaroxaban)
– Prothrombin complex concentrates (contain factor
II, VII, IX, X and protein C ,S)
• Direct thrombin inhibitor (Dabigatan)
– Life-threatening bleeding that cannot be managed with
supportive care and local hemostatic measures
– Hemodialysis or charcoal hemoperfusion can be
considered
Perioperative management of
antiplatelet therapy
Antiplatelet
• Antiplatelet drugs (irreversible)
– ASA, clopidogrel, ticlopidine, and prasugrel
– For each day after interruption 10% to 14% of
normal platelet function is restored; later, it takes
7 to 10 days for an entire platelet pool to be
replenished
Antiplatelet
• Antiplatelet drugs (reversible)
– Dipyridamole, Cilostazol, and NSAIDs
• Dipyridamole, a pyridopyrimidine derivative with
antiplatelet and vasodilator properties, has a half-life of 10 h
• Cilostazol, a phosphodiesterase inhibitor with anti-platelet
and vasodilator properties, has a half-life of 10 h
• NSAID have half-lives that vary from
– 2 to 6 h (ibuprofen, ketoprofen, indomethacin)
– to 7 to 15 h (celecoxib, naproxen, difl unisal)
– to . 20 h (meloxicam, nabumetone, piroxicam)
Antiplatelet
• Patients who were receiving a VKA and ASA
typically resumed ASA at the same time as the
VKA, which was within 24 h after surgery
Schematic of different therapeutic options for inhibition of platelet P2Y12 receptor.
Ferreiro J L , and Angiolillo D J Circ Cardiovasc Interv
2012;5:433-445
Copyright © American Heart Association
Assessment
• Optimal preoperative management of patients with
coronary artery stents depends on many factors
• Relative risks and benefits of stopping versus
continuing antiplatelet therapy
– Identification of patients at high risk for a perioperative
event after cessation of antiplatelet therapy
– Identifi cation of patients at high risk of bleeding
• The risk of perioperative bleeding increases when two
or more antiplatelet agents are used
Recommendation of ACCP 2012
Minor surgery
• In patients who are receiving ASA for the
secondary prevention of cardiovascular
disease and are having minor dental or
dermatologic procedures or cataract surgery
– suggest continuing ASA around the time of the
procedure instead of stopping ASA 7 to 10 days
before the procedure
Non-cardiac surgery
• In patients at moderate to high risk for
cardiovascular events
– suggest continuing ASA around the time of surgery
instead of stopping ASA 7 to 10 days before surgery
(Grade 2C)
• In patients at low risk for cardiovascular events
– suggest stopping ASA 7 to 10 days before surgery instead
of continuation of ASA (Grade 2C)
CABG surgery
• suggest continuing ASA around the time of surgery
instead of stopping ASA 7 to 10 days before surgery
(Grade 2C)
• In patients who are receiving dual antiplatelet drug
therapy and require CABG surgery
– suggest continuing ASA around the time of surgery and
stopping clopidogrel/prasugrel 5 days before surgery
instead of continuing dual antiplatelet therapy around
the time of surgery (Grade 2C)
Patients with Coronary Stents
having Surgery
• Surgery for at least 6 weeks after placement bare-metal stent
• Surgery for at least 6 months after placement drug-eluting
stent instead of undertaking surgery within these time
periods (Grade 1C)
• In patients who require surgery within 6 weeks of placement
of a bare-metal stent or within 6 months of placement of a
drug-eluting stent
– suggest continuing dual antiplatelet therapy around the time of
surgery instead of stopping dual antiplatelet therapy 7 to 10
days before surgery (Grade 2C)
Resumption of antiplatelet
• Clopidogrel administered at maintenance doses has a
delayed onset of action, and treatment can therefore
be reinitiated within 24 hours after the procedure
• Treatment with other antiplatelet agents, including
aspirin, can be reinitiated within 24 hours
• Caution when reinitiating treatment with prasugrel or
ticagrelor because of
– their rapid onset of action, potent antiplatelet
inhibition, and the lack of agents to reverse their effects
Canadian Cardiovascular Society (CCS)
class of angina
• Class I – Angina only during strenuous or prolonged
physical activity
• Class II – Slight limitation, with angina only during
vigorous physical activity
• Class III – Symptoms with everyday living
activities, i.e., moderate limitation
• Class IV – Inability to perform any activity without
angina or angina at rest, i.e., severe limitation
GRACE
Killip class
• I: no clinical signs of heart failure
• II: crackles, S3 gallop and elevated jugular venous
pressure
• III: frank pulmonary oedema
• IV: cardiogenic shock - hypotension (systolic < 90
mmHg) and evidence of peripheral vasoconstriction
(oliguria, cyanosis, sweating)
perioperativemanagementofantithrombotictherapy-130707120103-phpapp02.pdf

perioperativemanagementofantithrombotictherapy-130707120103-phpapp02.pdf

  • 1.
    Perioperative management of antithrombotictherapy Ext. Phatcharapol Udomluck Medical student Naresuan university
  • 2.
    Antithrombotic therapy • Long-termanticoagulation therapy for the prevention of thromboembolism due to – Atrial fibrillation – Placement of a mechanical heart-valve prosthesis – Venous thromboembolism • Dual antiplatelet therapy (combination treatment with aspirin and a thienopyridine) after the placement of a coronary-artery stent has dramatically increased
  • 3.
    Perioperative management of antithrombotictherapy Goal • Prevent thromboembolic (TE) events – Arterial TE : Prosthetic valve thrombosis (5.9-64.7%) , Cardioembolic stroke (fatality 4.2-14.9) – Venous TE : DVT, PE (fatality 26.4) • Reduced major hemorrhage in the periprocedural period
  • 4.
  • 5.
    ASSESSMENT OF THROMBOTICRISK • Valvular atrial fibrillation – Severe valvular heart disease (mechanical valvular prosthesis or mitral-valve repair) : high risk for TE • non-valvular atrial fibrillation – The CHA 2 DS 2 -VASc score
  • 6.
    ( Prior MI,PAD, Aortic plaque )
  • 9.
    ASSESSMENT OF THROMBOTICRISK • Mechanical heart valves and venous thromboembolism
  • 10.
    ASSESSMENT OF THROMBOTICRISK Cancer – Increased risk of periprocedural thrombosis • Cancer-specific prothrombotic activity, hormonal therapy, angiogenesis inhibitors, radiotherapy, and the presence of indwelling central venous catheters – Increased risk of bleeding • Prophylactic agents for the prevention of venous thromboembolism, chemotherapy-related hepatic and renal dysfunction and thrombocytopenia
  • 11.
    ASSESSMENT OF THROMBOTICRISK Coronary stents • Some patients with coronary stents may require dual antiplatelet therapy • Premature discontinuation of antiplatelet therapy in anticipation of invasive procedure may lead to stent thrombosis and precipitation of myocardial infarction • Rate of 50% or higher
  • 12.
    Coronary stent Bare-metal stent •Risk of thrombosis is highest within 6 Wks after placement of stent • Dual antiplatelet required – ASA(165-325 mg/day) : 1 mo – Clopidogrel : at least 1 mo and Up to 12 mo Drug-eluting stent • Risk of thrombosis is highest within 3-6 mo after placement of stent • Dual antiplatelet required – ASA(165-325 mg/day) • Sirolimus 3 mo • Paclitaxel 6 mo – Clopidogrel : at least 12 mo
  • 13.
    Assessment of Periprocedural bleedingrisk • Major bleeding depends on procedure – High-risk : Major bleed • intracranial, intraspinal, intraocular, retroperitoneal, int rathoracic, or pericardial bleeding • Additional Risk factors – Residual effects of antithrombotic agents – Active cancer – Chemotherapy – History of bleeding – Reinitiation of antithrombotic therapy within 24 hours after the procedure
  • 15.
    HAS-BLED risk score •SBP > 160 mmHg • Chronic dialysis or renal transplantation or serum creatinine ≥ 200 mmol/L • Chronic hepatic disease (e.g. Cirrhosis) or biochemical evidence of significant hepatic derangement • Previous bleeding history and/or predisposition to bleeding, e.g. Bleeding diathesis, anaemia • Concomitant use of drugs, such as antiplatelet agents, NSAIDs
  • 16.
    Low – intermediate(HAS-BLED 0-2)
  • 17.
  • 20.
  • 21.
    Assessment tool foridentifying patient-specific and surgical risk factors for patients on anticoagulation therapy who are undergoing elective surgery JAFFER A K Cleveland Clinic Journal of Medicine 2009;76:S37-S44 ©2009 by Cleveland Clinic
  • 22.
    Low risk Stop anticoagulant but not start bridging anticoagulant
  • 23.
    Recommend for Warfarinuse • Stop oral anticoagulant 5 day before invasive procedure – Keep INR <1.5 • If follow up INR > 1.5 in 1-2 day before invasive procedure – Vitamin K 1-2 mg • If Continue Warfarin : Keep INR approximately 2.5 • Urgent operative procedure – Oral or IV Vitamin K 2.5-5.0 mg • Emergency operative procedure – FFP + Low dose (IV or Oral) Vitamin K • Mechanical heart valve – Only use FFP ( NOT use Vitamin K  “Warfarin resistance”)
  • 24.
    Bridging anticoagulant • Recommendfor Moderate to High risk TE – Start when INR <2 – Therapeutic dose SC LMWH or IV UFH – If GFR < 30  IV UFH is preferred • Stop bridging before invasive procedure – Therapeutic SC LMWH or SC UFH : 12-24 hr before procedure (Use half dose in Morning last dose) – IV UFH : 4-6 hr before procedure • Half life 60 – 90 min , Dissipate after discont. 3 – 4 hr
  • 25.
    After procedure :Start Oral anticoagulant when keep desired INR level for 3 day Y. Chintammit : Update in internal medicine 2009 : 343 – 349
  • 26.
    SC IV UFH :Keep aPTT 1.5 – 2 x control Y. Chintammit : Update in internal medicine 2009 : 343 – 349
  • 29.
    Reversal of anticoagulant Reversibleanticoagulant agent • Warfarin – Vitamin K and Fresh frozen plasma – Prothrombin complex concentrates preferred in … • CHF, Valvular heart disease, Renal failure • Volume overload from Large volume infusion of FFP • Heparin – Protamine can reverse the action • UFH : Completely reversal • LMWH : Partial reversal
  • 30.
    2011 Clinical PracticeGuide on Anticoagulant Dosing and Management of Anticoagulant-Associated Bleeding Complications in Adults
  • 31.
    2011 Clinical PracticeGuide on Anticoagulant Dosing and Management of Anticoagulant-Associated Bleeding Complications in Adults
  • 32.
    Reversal warfarin • ACCP(2008) guidelines recommends • Oral doses of vitamin K – 1-2.5 mg for an INR between 5 and 9 – 2.5-5 mg for INR ≥ 9, no significant bleeding – 10 mg for serious bleeding and elevated INR
  • 33.
    2011 Clinical PracticeGuide on Anticoagulant Dosing and Management of Anticoagulant-Associated Bleeding Complications in Adults * heparin-induced thrombocytopenia
  • 34.
    Reversal of anticoagulant Nonreverssibleanticoagulant agent – Reliable reversibility has not been proved • Direct factor Xa inhibitors (Rivaroxaban) – Prothrombin complex concentrates (contain factor II, VII, IX, X and protein C ,S) • Direct thrombin inhibitor (Dabigatan) – Life-threatening bleeding that cannot be managed with supportive care and local hemostatic measures – Hemodialysis or charcoal hemoperfusion can be considered
  • 35.
  • 36.
    Antiplatelet • Antiplatelet drugs(irreversible) – ASA, clopidogrel, ticlopidine, and prasugrel – For each day after interruption 10% to 14% of normal platelet function is restored; later, it takes 7 to 10 days for an entire platelet pool to be replenished
  • 37.
    Antiplatelet • Antiplatelet drugs(reversible) – Dipyridamole, Cilostazol, and NSAIDs • Dipyridamole, a pyridopyrimidine derivative with antiplatelet and vasodilator properties, has a half-life of 10 h • Cilostazol, a phosphodiesterase inhibitor with anti-platelet and vasodilator properties, has a half-life of 10 h • NSAID have half-lives that vary from – 2 to 6 h (ibuprofen, ketoprofen, indomethacin) – to 7 to 15 h (celecoxib, naproxen, difl unisal) – to . 20 h (meloxicam, nabumetone, piroxicam)
  • 38.
    Antiplatelet • Patients whowere receiving a VKA and ASA typically resumed ASA at the same time as the VKA, which was within 24 h after surgery
  • 40.
    Schematic of differenttherapeutic options for inhibition of platelet P2Y12 receptor. Ferreiro J L , and Angiolillo D J Circ Cardiovasc Interv 2012;5:433-445 Copyright © American Heart Association
  • 41.
    Assessment • Optimal preoperativemanagement of patients with coronary artery stents depends on many factors • Relative risks and benefits of stopping versus continuing antiplatelet therapy – Identification of patients at high risk for a perioperative event after cessation of antiplatelet therapy – Identifi cation of patients at high risk of bleeding • The risk of perioperative bleeding increases when two or more antiplatelet agents are used
  • 42.
  • 43.
    Minor surgery • Inpatients who are receiving ASA for the secondary prevention of cardiovascular disease and are having minor dental or dermatologic procedures or cataract surgery – suggest continuing ASA around the time of the procedure instead of stopping ASA 7 to 10 days before the procedure
  • 44.
    Non-cardiac surgery • Inpatients at moderate to high risk for cardiovascular events – suggest continuing ASA around the time of surgery instead of stopping ASA 7 to 10 days before surgery (Grade 2C) • In patients at low risk for cardiovascular events – suggest stopping ASA 7 to 10 days before surgery instead of continuation of ASA (Grade 2C)
  • 45.
    CABG surgery • suggestcontinuing ASA around the time of surgery instead of stopping ASA 7 to 10 days before surgery (Grade 2C) • In patients who are receiving dual antiplatelet drug therapy and require CABG surgery – suggest continuing ASA around the time of surgery and stopping clopidogrel/prasugrel 5 days before surgery instead of continuing dual antiplatelet therapy around the time of surgery (Grade 2C)
  • 46.
    Patients with CoronaryStents having Surgery • Surgery for at least 6 weeks after placement bare-metal stent • Surgery for at least 6 months after placement drug-eluting stent instead of undertaking surgery within these time periods (Grade 1C) • In patients who require surgery within 6 weeks of placement of a bare-metal stent or within 6 months of placement of a drug-eluting stent – suggest continuing dual antiplatelet therapy around the time of surgery instead of stopping dual antiplatelet therapy 7 to 10 days before surgery (Grade 2C)
  • 47.
    Resumption of antiplatelet •Clopidogrel administered at maintenance doses has a delayed onset of action, and treatment can therefore be reinitiated within 24 hours after the procedure • Treatment with other antiplatelet agents, including aspirin, can be reinitiated within 24 hours • Caution when reinitiating treatment with prasugrel or ticagrelor because of – their rapid onset of action, potent antiplatelet inhibition, and the lack of agents to reverse their effects
  • 51.
    Canadian Cardiovascular Society(CCS) class of angina • Class I – Angina only during strenuous or prolonged physical activity • Class II – Slight limitation, with angina only during vigorous physical activity • Class III – Symptoms with everyday living activities, i.e., moderate limitation • Class IV – Inability to perform any activity without angina or angina at rest, i.e., severe limitation
  • 53.
  • 54.
    Killip class • I:no clinical signs of heart failure • II: crackles, S3 gallop and elevated jugular venous pressure • III: frank pulmonary oedema • IV: cardiogenic shock - hypotension (systolic < 90 mmHg) and evidence of peripheral vasoconstriction (oliguria, cyanosis, sweating)