When to stop and start Direct Oral Anticoagulants (DOACs) before and after left heart catheterization with or without Percutaneous Coronary Intervention (PCI)?

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Last updated: November 20, 2025View editorial policy

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DOAC Management for Left Heart Catheterization ± PCI

Direct Answer

For elective left heart catheterization with or without PCI, hold DOACs for 24 hours (transradial) or 48 hours (transfemoral) in patients with normal renal function (CrCl ≥30 mL/min), and resume within 24 hours post-procedure once hemostasis is achieved; for emergency procedures (STEMI or high-risk NSTEMI), stop the DOAC immediately and proceed without delay. 1


Pre-Procedure Management: When to STOP DOACs

Emergency Procedures (STEMI or High-Risk NSTEMI)

  • Stop anticoagulation immediately and proceed to catheterization without delay 1
  • Do not wait for DOAC levels to decline 1
  • Activated clotting time (ACT) is not a reliable indicator of anticoagulation status in DOAC patients 1
  • Consider reversal agents (idarucizumab for dabigatran, andexanet alfa for factor Xa inhibitors) only in life-threatening bleeding scenarios 2

Elective or Urgent Procedures (Can Be Safely Deferred)

The 2020 ACC Expert Consensus provides the most comprehensive, kidney function-based approach for DOAC interruption 1:

Apixaban:

  • Transradial approach: Hold 24 hours if CrCl ≥30 mL/min; 36 hours if CrCl 15-29 mL/min 1
  • Transfemoral approach: Hold 48 hours if CrCl ≥30 mL/min; 72 hours if CrCl <29 mL/min 1

Rivaroxaban:

  • Transradial approach: Hold 24 hours if CrCl ≥30 mL/min; 36 hours if CrCl 15-29 mL/min 1
  • Transfemoral approach: Hold 48 hours if CrCl ≥30 mL/min; 72 hours if CrCl <29 mL/min 1

Edoxaban:

  • Transradial approach: Hold 24 hours if CrCl ≥30 mL/min; 36 hours if CrCl 15-29 mL/min 1
  • Transfemoral approach: Hold 48 hours if CrCl ≥30 mL/min; 72 hours if CrCl <29 mL/min 1

Dabigatran (requires longer interruption due to renal elimination):

  • Transradial approach: Hold 24 hours if CrCl ≥80 mL/min; 36 hours if CrCl 50-79 mL/min; 48 hours if CrCl 30-49 mL/min; 72 hours if CrCl 15-29 mL/min 1
  • Transfemoral approach: Hold 48 hours if CrCl >80 mL/min; 72 hours if CrCl 50-79 mL/min; 96 hours if CrCl 30-49 mL/min; 120 hours if CrCl 15-29 mL/min 1

Key Considerations for Pre-Procedure Planning

  • Always assess recent creatinine clearance using the Cockcroft-Gault formula before determining hold duration 1, 3
  • Do NOT use heparin bridging - this increases bleeding risk without reducing thrombotic events 1, 3, 4, 5
  • For diagnostic catheterization only (no PCI planned), the same interruption guidelines apply 1
  • Radial access is strongly preferred when feasible to minimize bleeding risk 1, 6

Intra-Procedure Management

Anticoagulation During the Procedure

  • Use standard intraprocedural anticoagulation (unfractionated heparin 70 IU/kg, LMWH, or bivalirudin) per local practice 1, 7
  • Target ACT or aPTT levels according to standard clinical practice 1
  • Bivalirudin may be preferred due to its very short half-life 1

Access Site Strategy

  • Strongly prefer transradial access to minimize bleeding complications, particularly in patients who were recently on anticoagulation 1, 6
  • Use vascular closure devices for transfemoral access when radial is not feasible 1
  • Crossover to femoral access may be necessary in 5-10% of radial cases 1

Post-Procedure Management: When to RESTART DOACs

Timing of Resumption

Resume DOACs within 24 hours after uncomplicated catheterization/PCI once adequate hemostasis is confirmed 1, 8. The ACC guidelines provide specific timing 1:

  • As early as 6 hours post-procedure if hemostasis is secure and no bleeding complications 1, 3
  • Most commonly the evening of the procedure day for once-daily evening dosing 1
  • Next morning for once-daily morning dosing 1
  • Evening of procedure day for twice-daily regimens 1

Pre-Restart Assessment Checklist

Before restarting anticoagulation, evaluate 1, 8:

  • Access site hemostasis - this is the primary consideration 1, 8
  • History of recent bleeding 1
  • Body habitus (obese patients with transfemoral access require extra caution) 1
  • Platelet abnormalities (qualitative or quantitative) 1
  • Post-procedure renal function (may require dose adjustment) 1

Dosing Considerations Post-PCI

  • For atrial fibrillation patients on rivaroxaban: Use 15 mg daily (not 20 mg) if CrCl >50 mL/min while on dual antiplatelet therapy, then increase to 20 mg daily once antiplatelet therapy is stopped 1
  • For all other DOACs: Use FDA-approved doses appropriate for the indication 1
  • Reassess renal function post-procedure as it may have changed, requiring dose adjustment 1

Delayed Resumption Scenarios

Delay DOAC resumption to 24-48 hours post-procedure if: 3

  • Ongoing bleeding or surgical contraindication exists 1
  • High bleeding risk procedure was performed 3
  • Inadequate hemostasis at access site 1, 8
  • Start venous thromboprophylaxis (mechanical or pharmacologic) during the delay period based on thrombotic risk 1

Special Considerations and Common Pitfalls

What NOT to Do

  • Do NOT bridge with heparin - this significantly increases bleeding without reducing thrombotic events 1, 3, 4, 5
  • Do NOT assume 24 hours is sufficient for all patients - renal function and access site dictate timing 1, 3
  • Do NOT use ACT to guide anticoagulation in DOAC patients - it is unreliable 1
  • Do NOT routinely measure DOAC levels before elective procedures 4, 5
  • Do NOT switch from DOAC to warfarin peri-procedurally - this increases bleeding and thrombotic risk 1

When DOAC Level Testing May Be Useful

  • Emergency or urgent procedures (<24 hours) where DOAC levels may still be elevated 5, 2
  • Severe renal impairment (CrCl <15 mL/min) where clearance is unpredictable 1
  • Consideration of reversal agents in urgent/emergent settings 5, 2
  • DOAC levels >50 ng/mL may be considered clinically relevant and necessitate reversal before urgent procedures 2

Antiplatelet Therapy Coordination

  • Continue aspirin throughout the peri-procedural period 8
  • Administer P2Y12 inhibitor loading dose (clopidogrel 600 mg preferred) if not already on therapy 1, 8
  • Post-PCI, follow standard dual antiplatelet therapy duration based on stent type and clinical scenario 1

Fully Anticoagulated Patients (Uninterrupted DOAC)

  • While the 2018 EHRA guidelines suggest DOACs should be discontinued before catheterization 1, a small study demonstrated that transradial diagnostic catheterization can be safely performed in fully anticoagulated patients (INR 2.5 ± 0.5) with no access site complications 6
  • However, this approach is NOT standard practice and most guidelines recommend interruption as outlined above 1
  • If PCI is performed without DOAC interruption, periprocedural anticoagulation dosing remains uncertain 1

Algorithm Summary

Step 1: Assess Urgency

  • Emergency (STEMI/high-risk NSTEMI) → Stop DOAC, proceed immediately 1
  • Elective/urgent (can defer) → Calculate CrCl, determine hold duration 1

Step 2: Determine Hold Duration (Elective/Urgent)

  • Transradial: 24 hours (most DOACs, CrCl ≥30) 1
  • Transfemoral: 48 hours (most DOACs, CrCl ≥30) 1
  • Adjust for renal function and specific DOAC (dabigatran requires longer) 1

Step 3: Perform Procedure

  • Use standard intraprocedural anticoagulation 1
  • Prefer radial access 1, 6

Step 4: Assess for Restart

  • Check access site hemostasis 1, 8
  • Evaluate bleeding risk factors 1
  • Reassess renal function 1

Step 5: Resume DOAC

  • Typical: 6-24 hours post-procedure 1, 8
  • Delayed: 24-48 hours if high bleeding risk 3
  • Adjust dose for renal function 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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