Let's start with a poll followed by a #tweetorial on direct oral anticoagulants. First things first, which is your go-to choice of #DOAC ? (COI: none):
2/ These agents work "directly" to anti-coagulate and since they are hardly "new' anymore the term #NOAC has become obsolete. Dabigatran is a direct thrombin inhibitor (factor IIa), whereas the others are factor Xa inhibitors (note the Xa in their names)
3/ In general they share many characteristics such as a quick onset of action, shorter half-lives, potential for drug-drug interactions (CYP3A4 & P-gp) and renal elimination (except apixaban) when compared with warfarin
4/ In terms of efficacy many studies have shown that DOACs as a class are equal to or better than warfarin to prevent ischemic stroke and systemic embolism for patients with non-valvular AF, venous thromboembolism (VTE) and even cancer related VTE
5/ Another added advantage is the reduction in major bleeding such as intracranial hemorrhage or gastrointestinal bleeding
6/ How about reversal agents? One drawback initially for #DOACs was a lack of specific antidotes but lately drugs such as idarucizumab for dabigatran reversal, and with andexanet alfa/ciraparantag in the pipeline things will change
7/ So the question remains: are all #DOACs equal, or are some more equal than others?
8/ At least from the #gitwitter perspective, the latest evidence would suggest that apixaban has the most favourable profile from the #GIB perspective: from an excellent retrospective propensity matched study by @NeenaSAbrahamMD & Co in @AGA_Gastro
9/ Another piece in @Gut_BMJ showed that apixaban was found to be the safest drug, with reduced risks of major, intracranial, and gastrointestinal bleeding compared with warfarin
10/ Last but not least a paper just out recently by @CUHKMedicine in @Gut_BMJ that explored #DOAC and the risk of post-polypectomy bleeding #PPB showing that apixaban was associated with a ⬇ risk of #PPB and thromboembolism, particularly in the elderly and patients with R polyps
11/ An additional footnote is that the original trials of apixaban do include a substantial number of patients with moderate renal impairment down to 30 mL/min and they didn't just extrapolate from pre-clinical data
easter eggs: notable mention for dabigatran. As a pro-drug with low bioavailability the unabsorbed drug may be converted to active dabigatran in the distal bowel and then excreted in the feces. ?cause of GIB and the mucosal injuries per @lean_stein
1/
Sharing of measures observed at my institution in #HongKong currently in place for #COVID19 and some personal practice I have adopted, not exhaustive:
2/ Departmental 1. Cut all elective cases (only GI bleeds, cholangitis, OJ left; cancer cases reviewed case-by-case) 2. FTOCC +ve should be deferred if possible 3. Full PPE (hair net, face shield/goggles, N95, gowns, gloves etc) as appropriate per local guidance
3/ 4. Extended use of N95, but not reuse (changing is protecting patients more than healthcare staff; if you take it off you shouldn't put the same one back on) 5. Scopes done by senior/independent endoscopists; no more training to reduce staff risk exposure and preserve PPE