Faculty Presentations
| Jeremy Vandiver, Pharm.D, BCPS |
Fig. 01 -
Title Slide
Fig. 02 -
Learning Objectives
Fig. 03 -
Oral Anticoagulants
Fig. 04 -
Adoption of DOACs
Fig. 05 -
Parenteral Anticoagulants
Fig. 06 -
Coagulation Cascade
Fig. 07 -
Site of Action
Fig. 08 -
Monitoring Methods
Fig. 09 -
Factor X Assays
Fig. 10 -
Chromogenetic
Fig. 11 -
Monitoring
Fig. 12 -
Unfractionated Heparin
Fig. 13 -
Methods of Monitoring
Fig. 14 -
aPTT
Fig. 15 -
Disadvantages
Fig. 16 -
Therapeutic Range
Fig. 17 -
Advantages
Fig. 18 -
Advantages (Cont.)
Fig. 19 -
Progression
Fig. 20 -
Anti-Xa vs. aPTT
Fig. 21 -
Practical Issues
Fig. 22 -
Full-dose UFH
Fig. 23 -
Baseline Monitoring
Fig. 24 -
Prophylactic UFH Monitoring
Fig. 25 -
Low-molecular Weight Heparins
Fig. 26 -
LMWH Anti-Xa Monitoring
Fig. 27 -
Direct Oral Anticoagulants
Fig. 28 -
Advantages of DOACs
Fig. 29 -
Disadvantages of DOACs
Fig. 30 -
Monitoring Effects
Fig. 31 -
Dabigatran
Fig. 32 -
Dabigatran Example
Fig. 33 -
Factor Xa Inhibitor
Fig. 34 -
Rivaroxaban Monitoring
Fig. 35 -
Rivaroxaban Example
Fig. 36 -
Apixaban Monitoring Example
Fig. 37 -
Monitoring of Anticoagulants 1
Fig. 38 -
Monitoring of Anticoagulants 2
Fig. 39 -
Monitoring of Anticoagulants 3
Fig. 40 -
Conclusions
Fig. 41 -
Conclusions (Cont.)
Fig. 42 -
Thank You
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Six (6) provocative statements concerning clinical treatment of IBD. Each statement is presented as 5 steps:Step 1: the statement & introduction, + 5 possible opinions of that statement -- please choose one
Step 2: a graph of an international survey’s opinions of that statement
Step 3: a literature review for that statement
Step 4: a graph comparing the faculty's vs an international survey’s opinions, + faculty discussion
Step 5: a brief faculty summary, plus the list of references.
Please click on any Statement or any Step tab to read this publication in the order you prefer.