Look at the quality of that evidence and recommendations for drug Tx! 😃💊
Beta-blockers:
- start low, go slow
- ALWAYS titrate 📈for maximum benefit
- intolerance likely to resolve with time ⏲️
MRAs:
- minimal impact on BP
- watch that K! (Include dietary advice 🥗)
ARNI (Sacubitril/Valsartan):
- Going direct to ARNI is well tolerated
- STOP🛑ACEi 36 hours to reduce risk of angioedema
- Lowest dose drops BP the most, so there is more scope for titration than you may think 💊📈
SGLT2 inhibitors:
- Quick benefit (2-4 weeks)
- How do they work in HF?!?! (Let's be honest we still don't really know!🤔 But we do know they work!)
- Ideal across any clinical presentation of HF
- Watch out for adverse effects
- Renal function will drop - don't STOP the SGLT2
So which drug when?? 💊⏲️
Current problem, not practical, too slow
Old vs new ESC Guidelines:
Starting to think about horizontal initiation. Currently lacking evidence in this area.
How do we speed up titration and what is the best order of drug initiation in HF?
From trial modelling these regimens came out top:
Note different order to reduce CV death vs reducing CV death and HF hospitalisation
Is this the future of HF treatment pathways? 🤔
Hospitalisation is an opportunity to give HFrEF drugs. EMPULSE and SOLOIST and now DELIVER showed safety in hospitalised patients
Don't forget individual patients need individualised pathways. One size won't fit all. Trials are needed in this area to determine best sequence
Last but not least, HFpEF and HFmrEF:
ESC recommend 'concomitant implementation' of the four pillars
⬆️💊Uptitration should be according to pt phenotype rather than target doses
• • •
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Let's start with the headline, drum roll please 🥁... Dapagliflozin in HFmrEF and HFpEF DELIVER Trial results
1. Background💔
HFpEF pts represent approx 50% of all people with HF
Currently limited Tx options in this group
Uncertainty remains re:
- People in highest part of EF range, ?attenuation of Tx effect
- People initiated on Tx during/soon after hospitalisation
- EF improved to >40%
2. Trial design, Endpoints and Flow
Note: either ambulatory or hospitalised patients
6236 patients. 3131 received dapagliflozin. Across 20 countries 🗺️
Follow up - 2.3 years
Equal drop out and incomplete follow up in Tx and in placebo arms