MANAGEMENT PLAN FOLLOWING INITIATION OF DIRECT ORAL ANTICOAGULANTS (DOACs) APIXABAN/DABIGATRAN/EDOXABAN/RIVAROXABAN
CONSIDERATIONS AT TIME OF INITIATION Confirm appropriateness of therapy Obtain baseline labs (CBC/LFTs/SCr) and calculate creatinine clearance (CrCl) using Cockcroft-Gault Conduct medication review to assess potential for drug interactions (see https://depts.washington.edu/anticoag) Review indication for therapy and provide education to patient, supplemented by written materials
Apixaban for treatment of VTE: DOAC MONIITORING CHECKLIST change dose from 10mg bid (for 1 week ) to 5mg bid 1 1 Week Follow-Up FOR EACH FOLLOWUP VISIT
Adherence (including Rx refills) Is patient experiencing Yes Take with food and full glass dyspepsia? of water Thromboembolic events Consider PPI or H2 blocker Bleeding events/risk factors Is patient experiencing Yes other adverse side effects? Treat any modifiable factors Adverse effects and/or consider switching to No another agent Medication review for potentially interacting drugs At 3 weeks Rivaroxaban for including ASA and NSAIDs (see treatment of VTE: change dose from https://depts.washington.edu/ 15mg bid (for 3 anticoag) weeks) to 20mg qday Reassessment of appropriate- ness and duration of therapy At 3 Months
Repeat CBC
Repeat SCR/Calculate CrCl Any sign of medication
1 intolerance? Clinical judgment should be used to At 6 months determine frequency of monitoring based on patient’s overall health, compliance, and risk factors
Continuing Follow-up After 1st 6 Months
1. CrCl > 60 m/min: Checklist once yearly Any concerns? including annual LFTs
2. CrCl < 60 ml, age> 75, wt < 60kg or medically fragile: Checklist q6months and No Yes annual LFTs Continue routine scheduled Reassess risk vs benefit follow-up Adjust dose or switch to another anticoagulant Increase frequency of monitoring for patients with renal or hepatic impairment or at risk for worsening renal or hepatic function
UW Medicine Anticoagulation Services June 2015