Anticoagulated Patients Requiring ICD or Pacemaker

Key Points

  • Peri-operative procedural planning of anti-platelet and anticoagulant therapy for device patients is required to minimise the risk of both bleeding and stroke

  • Warfarin can usually be continued with careful INR monitoring

  • DOAC therapy may need to be discontinued for a short duration as per guidance

Version:2.0
Date Issued:01/05/2025
Review Date:01/05/2028
Key words:Antiplatelets, Anticoagulation, ICD, CRT, Pacemaker

This is a controlled document. If you are using a printed copy, check it against the guidelines site to ensure you are using the latest edition. Print copies must be destroyed after use.

Abbreviations

ACSAcute Coronary Syndrome
CrClCreatinine Clearance
CRTCardiac Resynchronization Therapy
DAPTDual Antiplatelet Therapy
DOACDirect Oral Anticoagulant
ESCEuropean Society of Cardiology
ICDImplantable Cardioverter Defibrillator
LMWHLow Molecular Weight Heparin

Guideline rationale

Each year, an estimated 1.25 million pacemakers and 410,000 implantable cardioverter–defibrillators (ICDs) are implanted worldwide. Between 14 and 35% of patients receiving these devices require long-term oral anticoagulation therapy, and their periprocedural treatment presents a dilemma to physicians. This is particularly true for the subset of patients at moderate-to-high risk (≥5% per year) for thromboembolic events. The risk of pocket haematoma is as high using a bridging heparin protocol. Pocket haematoma is associated with increased risk of device related infection. Temporary cessation of anticoagulation may be associated with increased risk of stroke in high risk patients.

Pre-Procedure

Aspirin - continue if indicated

Clopidogrel- continue if indicated

Dual antiplatelet therapy (any combination) – continue if indicated; review with operating consultant if more than 12 months since coronary intervention/ACS

LMWH/Heparin- Stop ≥ 24 hours pre-procedure

Warfarin – Continue, if clinically indicated, aiming for INR 2-2.5

An INR of 2.5-3.5 may be acceptable to selected operators and should be discussed

Check INR 2-5 days pre-procedure and dose accordingly

Warfarin + single-antiplatelet- continue if clinically indicated

Warfarin + DAPT – discuss strategy with operating consultant

DOAC (as per ESC guidance 2018)

Dabigatran*Apixaban/Rivaroxaban/Edoxaban *
CrCl ≥ 80mL/min - Stop ≥ 24 hours
CrCl 50–80mL/min - Stop ≥ 36 hours
CrCl 30–49mL/min - Stop ≥48 hours
CrCl ≥ 30mL/min - Stop ≥ 24 hours
CrCl 15–30 mL/min - Stop ≥ 36 hours

*Emergency/urgent device procedures can be performed on DOAC after discussion with operator.

Post Procedure

  1. Warfarin dosing and testing, as per pre-procedure, to be resumed same day

  2. Avoid re-loading Warfarin unless clinically indicated

  3. Restart DOAC ≥ 24 hours post-procedure unless clinical concerns

  4. Restart prophylactic LMWH/heparin ≥ 24hour post-procedure

  5. Avoid high (treatment) dose LMWH/heparin post-procedure unless clinically appropriate. Ideally establish DOAC post-procedure as above or perform on/initiate warfarin to reduce bleeding complications

  6. Patient should be counselled to monitor for signs of bleeding at insertion site and to seek medical attention if this occurs.

  7. Inform anticoagulant clinic as appropriate.

References

Airaksinen KE., Korkeila P., Lund J., Ylitalo A., Karjalainen P., Virtanen V., et al. (2013) 'Safety of pacemaker and implantable cardioverter-defibrillator implantation during uninterrupted warfarin treatment--the FinPAC study', Int J Cardiol, 168(4), pp. 3679-82. Available at: https://doi.org/10.1016/j.ijcard.2013.06.022

Birnie DH., Healey JS., Wells GA., Verma A., Tang AS., Krahn AD., et al. (2013) 'Pacemaker or defibrillator surgery without interruption of anticoagulation', N Engl J Med., 368(22). pp. 2084-93. Available at: https://doi.org/10.1056/NEJMoa1302946

Birnie DH., Healey JS., Wells GA., Ayala-Paredes F., Coutu B., Sumner GL., et al. (2018) 'Continued vs. interrupted direct oral anticoagulants at the time of device surgery, in patients with moderate to high risk of arterial thrombo-embolic events (BRUISE CONTROL-2)', Eur Heart J., 39(44), pp. 3973-3979. Available at: https://doi.org/10.1093/eurheartj/ehy413

Full version control record

Version:2.0
Guidelines Leads:Dr Paresh Mehta, Consultant Cardiologist
Contributors:Dr Andrew Cox, Consultant Cardiologist
Dr Navin Chandra, Consultant Cardiologist
Dr Sofia Metaxa, Consultant Cardiologist
Dr Vinod Achan, Consultant Cardiologist
Dr Matt Faircloth, Consultant Cardiologist
Dr Mark Norman, Consultant Cardiologist
Dr Peter Clarkson, Consultant Cardiologist
Chief of Service:Dr Peter Clarkson, CoS for Cardiology
Library check completed:30/09/2024
Ratified at:Cross-site Cardiology Clinical Governance 29/04/2025
Date Issued:01/05/2025
Review Date:01/05/2028
Pharmaceutical dosing advice and formulary compliance checked by:Preya Fakira, Lead Cardiology Pharmacist (WPH) 6/3/25
Key words:Antiplatelets, Anticoagulation, ICD, CRT, Pacemaker

This guideline has been registered with the Trust. However, clinical guidelines are guidelines only. The interpretation and application of clinical guidelines will remain the responsibility of the individual clinician. If in doubt, contact a senior colleague or expert. Caution is advised when using guidelines after the review date.

This guideline is for use in Frimley Health NHS Foundation Trust hospitals only. Any use outside this location will not be supported by the Trust and will be at the risk of the individual using it.

Version History

VersionDateGuideline Lead(s)StatusComment
1.0April 2022Dr Paresh Mehta, Consultant CardiologistFinal
2.0April 2025Dr Paresh Mehta, Consultant CardiologistFinalFull review