Perioperative Management of Antiplatelet Therapy 04july2021

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PERIOPERATIVE MANAGEMENT

OF ANTIPLATELET THERAPY

OBJECTIVE:
To provide guidance to clinicians, based on the Canadian Cardiovascular Society recommendations,
for the perioperative management of patients on antiplatelet therapy who require non-cardiac or
cardiac surgery.

BACKGROUND:
Antiplatelet drugs are commonly used in the primary and secondary prevention of cardiovascular
disease. Patients receiving antiplatelet therapy have a broad range of cardiovascular risk depending
on the clinical indication for treatment.

With over 200 million noncardiac surgical procedures performed worldwide each year, clinicians face
unique challenges regarding the perioperative management of patients with coronary artery disease
who are receiving acetylsalicylic acid (ASA) alone; clopidogrel alone; or any combination of ASA and a
P2Y12 inhibitor (clopidogrel, prasugrel, ticagrelor). Clinicians must balance the risks of major adverse
cardiovascular events associated with interrupting these therapies against the risk of bleeding from
continuing these therapies in the perioperative period. Additionally, other factors including the
pharmacokinetic actions of antiplatelet drugs and the optimal timing of surgery in patients with
coronary stenting must be considered. The latter group of patients requires special consideration due
to the increased risks and significant mortality of stent thrombosis.

RISK STRATIFICATION FOR PERIOPERATIVE THROMBOSIS AND BLEEDING


Risk stratification for thrombosis and bleeding is largely empiric in patients who are receiving
antiplatelet therapy. Patients considered at highest risk for cardiovascular events in the perioperative
period include those with recently (i.e. within one year) implanted bare metal stents (BMS) or drug-
eluting stents (DES), recent myocardial infarction (MI), those with carotid ulcerating plaque and
stroke or aortic ulcerating plaque and systemic embolism. Patients at low risk for perioperative
cardiovascular events are those taking antiplatelet therapy for primary prevention of MI, limb
ischemia or stroke (although this is rarely indicated). Clinicians must balance these risks against the
associated risks of perioperative bleeding (listed in Table 1).

DIAGNOSTIC TESTING, ARTHROCENTESIS, AND MINOR DENTAL, SKIN AND EYE PROCEDURES
Patients undergoing arthrocentesis, minor dental (extraction, root canal), eye (cataract) or skin
(biopsy, skin cancer excision) procedures, as well as low bleeding risk diagnostic procedures, can
continue ASA without interruption. Less is known about the safety of continuing P2Y12 inhibitors
(clopidogrel, ticagrelor, prasugrel) around minor procedures when taken as monotherapy. It is
reasonable to discontinue them for a short period (3-4 days) before the procedure. If patients are also

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taking ASA (dual antiplatelet therapy), the P2Y12 should be discontinued prior to surgery (clopidogrel
and ticagrelor for 5-7 days, prasugrel for 7-10 days) while ASA is continued.

Patients having a diagnostic test associated with a higher risk for bleeding should be managed like
higher risk surgeries, as outlined below.

MANAGEMENT OF PATIENTS WITHOUT CORONARY STENTS UNDERGOING ELECTIVE OR NON-URGENT


NONCARDIAC SURGERY
The Perioperative Ischemic Evaluation (POISE) 2 trial is the only randomized trial in noncardiac
surgery to assess perioperative antiplatelet drug management. It demonstrated that continuing ASA
did not have an effect on the incidence of major adverse cardiovascular events or mortality but
increased the risk of major bleeding. Only 4% of patients in this study had a coronary stent and it
excluded patients who underwent carotid endarterectomy, received a BMS in the 6 weeks before
surgery, or a DES in the 12 months before surgery.

Initiating ASA before surgery to reduce perioperative cardiovascular events is not recommended.

ASA should be discontinued 5-7 days prior to elective or non-urgent non-cardiac surgery except in
patients undergoing carotid endarterectomy or with recent coronary artery stenting (see below for
approach). Perioperative ASA continuation might also be reasonable for some surgical interventions
to prevent local thrombosis (e.g. lower extremity bypass or arterial aneurysm repair).

In patients with an indication for chronic ASA, this medication should be resumed when the risk of
bleeding related to surgery has passed, usually between 8-10 days after major noncardiac surgery or
after venous thromboembolism prophylaxis has stopped.

MANAGEMENT OF PATIENTS WITH CORONARY STENTS UNDERGOING ELECTIVE OR NON-URGENT


NONCARDIAC SURGERY
A sub-study of the POISE-2 trial involving 470 patients with previous percutaneous coronary
intervention (PCI) and cardiac stents revealed that for every 1000 patients with prior PCI,
perioperative ASA will prevent 59 myocardial infarctions but cause 8 major bleeds. It is, therefore,
viewed that in patients with prior PCI undergoing noncardiac surgery, perioperative ASA may be more
likely to benefit than harm patients.

Clinicians must consider the timing of surgery and perioperative dual antiplatelet (DAPT)
management in patients being treated with DAPT after PCI with a BMS or DES.

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Timing of Non-cardiac
Perioperative Antiplatelet Management
Surgery
PCI Patients with a Recommended to delay ASA should be continued perioperatively.
Bare Metal Stent surgery for at least 1 month Clopidogrel and ticagrelor should be
after PCI withheld 5-7 days preoperatively, and
prasugrel 7-10 days preoperatively
P2Y12 inhibitor should be restarted as
soon as it is deemed safe by the surgeon

PCI Patients with a Recommended to delay ASA should be continued perioperatively.


Drug Eluting Stent surgery for at least 3 Clopidogrel and ticagrelor should be
months after PCI. If semi- withheld 5-7 days preoperatively, and
urgent surgery is required, prasugrel 7-10 days preoperatively
surgery should be delayed
at least 1 month after PCI P2Y12 inhibitor should be restarted as
with a DES. soon as it is deemed safe by the surgeon

MANAGEMENT OF PATIENTS REQUIRING ELECTIVE OR SEMI-URGENT CABG AFTER ACUTE CORONARY


SYNDROME (ACS)
Coronary artery bypass grafting is associated with a high risk of bleeding with potentially significant
consequences (i.e. cardiac tamponade, death). An interdisciplinary assessment of the risks of
coronary thrombotic complications and risk of perioperative bleeding should be performed with the
surgeon, interventional cardiologist, attending physician / cardiologist and the patient.

Treatment Semi-urgent CABG Elective CABG


ASA ASA should be continued in all patients with ACS who require CABG
Ticagrelor Suggested to discontinue a minimum of 48-72 Recommended to be
hours prior to surgery to minimize the risk of discontinued ideally 5 days
bleeding. prior to surgery.
Clopidogrel Suggested to discontinue a minimum of 48-72 Recommended to be
hours prior to surgery to minimize the risk of discontinued ideally 5 days
bleeding. prior to surgery.
Prasugrel Suggested to discontinue a minimum of 5 days Recommended to be
prior to surgery to minimize the risk of discontinued ideally 7 days
bleeding. prior to surgery.

Table 1: Risk of Perioperative Bleeding

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OTHER RELEVANT THROMBOSIS CANADA CLINICAL GUIDES

• Acetylsalicylic Acid (ASA®)


• Clopidogrel (Plavix®)
• Prasugrel (Effient®)
• Ticagrelor (Brilinta®)

REFERENCES
Devereaux PJ, et al. Aspirin in patients undergoing noncardiac surgery. New Engl J Med 2014; 370:
1494-1503.

Graham M et al. Aspirin in patients with previous percutaneous coronary intervention undergoing
noncardiac surgery. Ann Intern Med 2018;168(4):237-244.

Mehta SR, et al. 2018 Canadian Cardiovascular Society/Canadian Association of Interventional


Cardiology focused update of the Guidelines for the Use of Antiplatelet Therapy. Can J Cardiol
2018;34(3):214-233.

Date of Version: 04July2021

Please note that the information contained herein is not to be interpreted as an alternative to medical advice
from your doctor or other professional healthcare provider. If you have any specific questions about any

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medical matter, you should consult your doctor or other professional healthcare providers, and as such you
should never delay seeking medical advice, disregard medical advice or discontinue medical treatment because
of the information contained herein.

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