What is the management of antiplatelet therapy, including aspirin and P2Y12 inhibitors (e.g. clopidogrel), in patients with a history of cardiovascular disease undergoing Endoscopic Ultrasonography Fine Needle Aspiration (EUS FNA) or Fine Needle Biopsy (FNB)?

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Last updated: January 10, 2026View editorial policy

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Management of Antiplatelet Therapy for EUS FNA/FNB

For patients undergoing EUS-FNA or EUS-FNB, discontinue P2Y12 inhibitors (clopidogrel, prasugrel, ticagrelor) 7 days before the procedure in patients at low thrombotic risk, while continuing aspirin if the patient is on dual antiplatelet therapy. 1

Risk Stratification of the Procedure

EUS with fine needle aspiration or biopsy is classified as a high-risk endoscopic procedure for bleeding complications. 1 This classification drives the management strategy for antithrombotic medications.

Management Based on Thrombotic Risk

Low Thrombotic Risk Patients

Low thrombotic risk includes:

  • Ischemic heart disease without coronary stent 1
  • Cerebrovascular disease 1
  • Peripheral vascular disease 1

For these patients:

  • Stop clopidogrel, prasugrel, or ticagrelor 7 days before the procedure 1
  • Continue aspirin if already prescribed (if on dual antiplatelet therapy) 1
  • Restart the P2Y12 inhibitor 1-2 days after the procedure if no bleeding complications 1

High Thrombotic Risk Patients

High thrombotic risk includes:

  • Drug-eluting coronary stent placed within 6-12 months 1
  • Bare metal coronary stent placed within 1 month 1
  • Recent acute coronary syndrome 1

For these patients:

  • Continue aspirin 1
  • Liaise with a consultant interventional cardiologist about the risk/benefit of discontinuing the P2Y12 receptor antagonist 1
  • Consider temporary cessation only after cardiology consultation 1
  • If the P2Y12 inhibitor must be stopped, restart preferably within 5 days after endoscopic hemostasis 1

Aspirin Monotherapy

For patients on aspirin alone:

  • Continue aspirin for secondary prevention (history of MI, stroke, or peripheral arterial disease) 1
  • Discontinue aspirin if prescribed for primary prevention only 1

The evidence shows aspirin continuation does not significantly increase bleeding risk during EUS-FNA. 1, 2 A prospective study found 0% bleeding events (0/26) in patients continuing aspirin/NSAIDs during EUS-FNA. 2

Evidence Quality and Nuances

The 2021 BSG/ESGE guidelines 1 represent the most recent and authoritative recommendations, updating the 2016 version 1 with stronger evidence (moderate quality) for the 7-day discontinuation period for P2Y12 inhibitors. The Asian guidelines 1 note that bleeding risk from EUS-FNA is approximately 1%, rising to 6% for pancreatic cystic lesions. 1

Important caveat: There is limited direct evidence on continuation of non-aspirin antiplatelet drugs during EUS-FNA. 1 However, retrospective studies show that even when clopidogrel is continued, bleeding events remain rare (0-1.6%). 3, 4, 5 One study found no severe bleeding events in patients continuing aspirin or cilostazol during EUS-FNA. 4

Post-Procedure Management

  • Resume discontinued antiplatelet therapy 1-3 days after the procedure depending on perceived hemorrhagic and thrombotic risks 1
  • For high-risk patients with coronary stents, prioritize earlier resumption (within 5 days maximum) 1
  • Advise patients of increased post-procedure hemorrhage risk compared to those not on antiplatelet agents 1

Common Pitfalls to Avoid

  • Never stop both antiplatelet agents in patients with recent coronary stents without cardiology consultation 1
  • Do not routinely stop aspirin in patients on secondary prevention unless the bleeding risk is prohibitive 1
  • Avoid delaying resumption of P2Y12 inhibitors beyond 5 days in high-risk patients, as this increases stent thrombosis risk 1
  • Do not assume all cardiovascular disease patients have the same thrombotic risk—timing of stent placement is critical 1

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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