Clopidogrel Should Be Held for 5 Days Before PEG Placement
Yes, clopidogrel (Plavix) should be discontinued 5 days before PEG placement when the procedure can be safely delayed, as recommended by the FDA drug label and multiple cardiology guidelines. 1
Primary Recommendation
The FDA-approved drug label for clopidogrel explicitly states: "When possible, interrupt therapy with clopidogrel for five days prior to such surgery" for procedures with a major risk of bleeding. 1 This 5-day window allows for dissipation of the antiplatelet effect, as clopidogrel irreversibly inhibits platelet aggregation for the lifetime of the platelet (7-10 days). 1
Supporting Guideline Evidence
Multiple ACC/AHA guidelines consistently recommend the 5-day discontinuation period:
For STEMI patients requiring CABG: Clopidogrel should be withheld for at least 5 days (and preferably 7 days) unless the urgency for revascularization outweighs the bleeding risks. 2
For UA/NSTEMI patients: When CABG is planned and can be delayed, discontinue clopidogrel at least 5 days before surgery to allow for dissipation of the antiplatelet effect. 2
For general surgical procedures: The standard recommendation across cardiology guidelines is 5 days discontinuation for elective procedures with significant bleeding risk. 3
Critical Risk-Benefit Assessment
However, this recommendation must be balanced against cardiovascular risk. The decision to hold clopidogrel depends on:
High-Risk Cardiovascular Scenarios (Consider NOT Holding):
- Recent coronary stent placement (especially <12 months for drug-eluting stents, <6 weeks for bare-metal stents) 3
- Recent acute coronary syndrome (<12 months) 2
- History of stent thrombosis with prior clopidogrel discontinuation 3
In these high-risk patients, abrupt discontinuation dramatically increases the risk of stent thrombosis, myocardial infarction, and death. 3, 4 For such patients, either:
- Postpone the PEG placement beyond the critical stent period, or
- Perform the procedure on clopidogrel after cardiology consultation, or
- Consider bridging with short-acting antiplatelet agents (though evidence is limited) 5
Lower-Risk Cardiovascular Scenarios (Safe to Hold):
- Stable cardiovascular disease >12 months post-ACS or revascularization 6
- Peripheral arterial disease without recent events 6
- Secondary stroke prevention (>90 days post-event) 6
Evidence Specific to PEG Procedures
Importantly, a retrospective study of 990 PEG placements found no association between periprocedural clopidogrel use and post-PEG bleeding (adjusted analysis showed no increased bleeding risk). 7 This suggests that the bleeding risk with PEG may be lower than with major surgical procedures like CABG. However, this was a single-center retrospective study with limited statistical power. 7
Interestingly, the same study found that serotonin reuptake inhibitors (SRIs) administered within 24 hours before PEG were associated with significantly higher odds of bleeding (adjusted OR 4.1,95% CI 1.1-13.4, P=0.04), while aspirin at any dose showed no association. 7
Practical Algorithm for PEG Placement
Assess cardiovascular risk:
If safe to hold:
If unsafe to hold:
Common Pitfalls to Avoid
Never abruptly discontinue clopidogrel in patients with recent coronary stents without cardiology consultation - this is the leading cause of stent thrombosis with potentially fatal consequences. 3, 4
Do not confuse prasugrel with clopidogrel - prasugrel requires 7 days discontinuation, not 5 days. 2
Do not hold aspirin - aspirin should be continued throughout the perioperative period in most patients, as it does not significantly increase bleeding risk for PEG procedures. 3, 7
Screen for SRI use - serotonin reuptake inhibitors pose a greater bleeding risk than clopidogrel for PEG procedures and should be held if possible. 7