Update on Direct Oral AntiCoagulants (DOACs)
Updated guidelines for Direct Oral AntiCoagulants (DOACs) perioperative use recommend 24-96 hour preoperative interruption based on patient factors and bleeding risk. Bridging with LMWH is discouraged due to increased bleeding risk, with DOACs resuming post-op within 24-72 hours.
Area of Science:
- Cardiology
- Pharmacology
- Anesthesiology
Background:
- Current recommendations for perioperative management of Direct Oral AntiCoagulants (DOACs) require updating.
- Individual patient characteristics, renal/hepatic function, and surgery-specific bleeding risk influence DOAC interruption duration.
- The risk of neurologic deficits necessitates conservative interruption intervals for neuraxial anesthesia.
Purpose of the Study:
- To provide updated recommendations for the perioperative management of DOACs.
- To clarify the role of bridging therapy and drug interactions.
- To address medication adherence in long-term DOAC use.
Main Methods:
- Review of pharmacokinetic profiles of DOACs.
- Analysis of bleeding and thromboembolic risks associated with different interruption and bridging strategies.
- Evaluation of drug-drug interactions and medication adherence data.
Main Results:
- A preoperative interruption of 24-96 hours is recommended, individualized by patient factors and bleeding risk.
- Preoperative bridging with LMWH should be omitted due to increased bleeding risk without altering thromboembolic risk.
- Postoperative reinstitution of DOACs within 24-72 hours is advised, with LMWH considered for high-risk patients.
- Drug interactions require careful management using specialized resources.
- Long-term DOAC adherence presents challenges, with persistence being a key factor for treatment success.
Conclusions:
- Updated perioperative DOAC management strategies are crucial for patient safety.
- Individualized patient assessment is paramount for determining optimal interruption and resumption timing.
- Addressing drug interactions and improving medication adherence are essential for effective long-term DOAC therapy.
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