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Published on: February 26, 2013
Cardiac implantable electronic device surgery with interruption of warfarin forgoing post-operative bridging therapy
Andrew Kei-Yan Ng1, Pauline Yeung Ng2,3, Eva Wai-Ying Tam4
1Cardiac Medical Unit, Grantham Hospital, 125 Wong Chuk Hang Road, Hong Kong SAR, China. drandrewkyng@gmail.com.
Insights
Interrupting warfarin without heparin bridging for cardiac device surgery is safe, showing low risks of blood clots and acceptable bleeding. Further research is needed to confirm the best anticoagulation strategy.
Area of Science:
- Cardiology
- Electrophysiology
- Anticoagulation Management
Background:
- Current guidelines recommend continuing warfarin or using heparin bridging for patients undergoing cardiac implantable electronic device (CIED) surgery.
- Interruption of warfarin without post-operative bridging is a potential alternative, but data is limited.
Purpose of the Study:
- To evaluate the safety and feasibility of interrupting warfarin therapy without post-operative bridging in patients undergoing CIED surgery.
Main Methods:
- A single-arm observational study of adult patients who had warfarin interrupted without bridging therapy for CIED surgery between 2010 and 2019.
- Primary outcome: composite of all-cause mortality, arterial or venous thromboembolic events.
- Secondary outcomes: device-pocket hematoma and procedural complications.
Main Results:
- In 411 patients (257 with mechanical heart valves), the primary outcome occurred in 1.2% within 30 days (0.7% mortality, 0.2% TIA, 0.2% non-CNS embolism).
- Clinically significant hematomas occurred in 5.8% of patients, with 3.7% requiring further anticoagulation interruption and 1.5% needing clot evacuation.
- Other procedural complications and bleeding events were infrequent (<1%).
Conclusions:
- Warfarin interruption without post-operative bridging for CIED surgery demonstrated low thromboembolic risk and acceptable bleeding risk.
- Randomized controlled trials are necessary to establish optimal anticoagulation management strategies for these patients.
Background:
For patients taking warfarin and undergoing pacemaker or implantable cardioverter-defibrillator surgery, clinical evidence and guidelines support continuation of warfarin therapy, as opposed to interruption of warfarin therapy with heparin bridging. Interruption of warfarin without post-operative bridging therapy may be a feasible alternative but data is sparse.
Methods:
This is a single-arm observational study including adults who had interruption of warfarin therapy without post-operative bridging therapy for cardiac implantable electronic device (CIED) surgery performed between 2010 and 2019 in a tertiary referral hospital. The primary outcome was a composite of all-cause mortality, arterial or venous thromboembolic events. The secondary outcomes were clinically significant device-pocket hematoma and other procedural complications.
Results:
Of the 411 patients analysed including 257 patients (62.5%) who had mechanical heart valves, the primary outcome developed in 5 (1.2%) patients within 30 days after surgery, including death in 3 (0.7%) patients, transient ischemic attack in 1 (0.2%) patient and non-CNS embolism in 1 (0.2%) patient. Clinically significant hematomas occurred in 24 (5.8%) patients, including 15 (3.7%) requiring additional interruption of anti-coagulation and 6 (1.5%) requiring clot evacuation. Other procedural complications and bleeding events were rare (< 1%).
Conclusions:
Warfarin interruption without post-operative bridging therapy for CIED surgery was associated with low thromboembolic risks and acceptable bleeding risk. Randomized controlled trials are required to formulate an optimal approach to anti-coagulation management.
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