How many days should Plavix (clopidogrel) be held prior to orthopedic surgery?

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Last updated: April 29, 2025View editorial policy

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From the Guidelines

Plavix (clopidogrel) should be held for 5-7 days prior to orthopedic surgery to reduce bleeding risk, as recommended by the most recent and highest quality study 1. The exact timing depends on the specific surgical procedure and the patient's individual risk factors for both bleeding and thrombosis.

  • For high-risk orthopedic procedures like joint replacements, 7 days is often recommended,
  • while for lower-risk procedures, 5 days may be sufficient. This waiting period allows platelet function to return to normal, as Plavix irreversibly inhibits platelet aggregation by blocking the P2Y12 receptor. The medication's antiplatelet effects last for the lifetime of the affected platelets (7-10 days), but since only a portion of circulating platelets are affected at any time, hemostatic function begins to recover after 5 days. Patients with coronary stents or high cardiovascular risk may require bridging therapy with shorter-acting antiplatelet agents during this perioperative period. Always consult with both the orthopedic surgeon and cardiologist before stopping Plavix, as the decision must balance bleeding risk against thrombotic risk, as suggested by 1 and 1.

Key Considerations

  • The patient's individual risk factors for bleeding and thrombosis should be taken into account when deciding on the timing of Plavix discontinuation.
  • The type of orthopedic surgery being performed also plays a role in determining the optimal timing for holding Plavix, with higher-risk procedures requiring a longer discontinuation period.
  • Bridging therapy with shorter-acting antiplatelet agents may be necessary for patients with high cardiovascular risk or coronary stents, as noted in 1.

Recommendations

  • Hold Plavix for 5-7 days prior to orthopedic surgery, as recommended by the most recent and highest quality study 1.
  • Consult with both the orthopedic surgeon and cardiologist before stopping Plavix to balance bleeding risk against thrombotic risk.
  • Consider bridging therapy with shorter-acting antiplatelet agents for patients with high cardiovascular risk or coronary stents.

From the FDA Drug Label

5.3 Discontinuation of Clopidogrel Discontinuation of clopidogrel increases the risk of cardiovascular events. If clopidogrel must be temporarily discontinued (e.g., to treat bleeding or for surgery with a major risk of bleeding), restart it as soon as possible. When possible, interrupt therapy with clopidogrel for five days prior to such surgery. Resume clopidogrel as soon as hemostasis is achieved.

The recommended duration to hold Plavix (clopidogrel) prior to orthopedic surgery is 5 days 2.

From the Research

Holding Plavix Prior to Orthopedic Surgery

  • The decision to hold Plavix (clopidogrel) prior to orthopedic surgery depends on various factors, including the type of surgery, patient's medical history, and risk of bleeding or thrombosis 3.
  • There is no clear consensus on the exact number of days to hold Plavix before orthopedic surgery, but studies suggest that the risk of bleeding is higher if the medication is continued perioperatively 4, 3.
  • One study found that patients who underwent nonelective orthopaedic surgery while taking Plavix had similar transfusion rates and complications compared to those not taking Plavix, even with a surgical delay of less than 5 days 5.
  • Another study recommended that efforts should be made to continue clopidogrel therapy through the perioperative period, taking precautions to minimize bleeding, and that antiplatelet therapy should be reinstated as soon as considered reasonable after surgery 3.
  • The American College of Cardiology and American Heart Association guidelines suggest that patients undergoing orthopedic surgery should have their antiplatelet therapy managed on an individual basis, taking into account the risk of bleeding and thrombosis 4.

Risks and Considerations

  • The risk of bleeding is a significant concern when continuing Plavix perioperatively, especially in patients undergoing major orthopedic surgery 6, 7.
  • The risk of thrombosis is also a concern when discontinuing Plavix, particularly in patients with a history of cardiovascular or cerebrovascular events 4, 3.
  • Patients with drug-eluting stents are at higher risk of stent thrombosis if clopidogrel is discontinued, and therefore, the decision to hold Plavix should be made on an individual basis 3.

Recommendations

  • Orthopedic surgeons should take a team approach to assess the individual risks for all patients and consider continuation of clopidogrel therapy perioperatively where possible 3.
  • The decision to hold Plavix should be based on the patient's medical history, type of surgery, and risk of bleeding or thrombosis, and should be made in consultation with the patient's cardiologist or primary care physician 4, 3.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Clopidogrel dilemma for orthopaedic surgeons.

ANZ journal of surgery, 2011

Research

Aspirin, clopidogrel, and the surgeon.

Advances in surgery, 2014

Research

The ''critical thrombosis period'' in major orthopedic surgery: when to start and when to stop prophylaxis.

Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis, 2010

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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