1/ #HFpEF treatment algorithm #tweetorial. This is the algorithm I currently use to treat HFpEF based on evidence we have thus far and my anecdotal experience treating patients over the past 16 years in the @NMCardioVasc HFpEF Clinic.
3/ Step 1: Start by confirming the #HFpEF diagnosis. In equivocal cases, remember to use provocative testing, preferably exercise testing! ncbi.nlm.nih.gov/pmc/articles/P…
4/ Step 2: Once the diagnosis of HFpEF is made based on elevated LV filling pressures at rest or with exercise in the setting of an LVEF ≥50%, first evaluate for masqueraders…
5/ …if you take care of patients with HFpEF, you need to know your zebras!
6/ Step 3: Start with an SGLT2i in all pts but use with caution in pts with exercise-induced LA hypertension (EILAH) because they have normal filling pressures at rest. See our recent paper on EILAH in @JACCJournals: sciencedirect.com/science/articl…
7/ Step 4: Is volume overload present? If so, start diuretics, with preferential up-front use of an MRA (e.g., spironolactone) and loop diuretics as needed (but minimize loop diuretic dose once euvolemic)
8/ Step 5: Treat comorbidities…
9/ Step 6: Start ARNI (sacubitril/valsartan) if not yet started for high BP if the patient is (1) still symptomatic, (2) LVEF <55-60% or frequent HF hospitalizations or +residual congestion, and (3) systolic BP >110 mmHg, and up-titrate as tolerated
10/ Step 7: Ask 6 key questions in all patients: (1) Is the pt on an SGLT2i? If not, why not? (2) Is the pt on an MRA? If not, why not? (3) Is the pt on an ARNI? If not, why not? (4) Is the patient on K+? If yes, replace with (or up-titrate) MRA if possible
11/ Step 7 (continued): (5) Is the patient on a nitrate or pulmonary vasodilator? Discontinue if possible (6) Is the patient on a beta-blocker? Wean off unless using for AF, angina, or MI, or other non-HFpEF indication
12/ Step 8a: Implement HF education in all patients (daily weights, BP, and HR; establish “dry weight” for volume overloaded pts to guide diuretic dosing [esp loop diuretics])
13/ Step 8b: Educate pts on an exercise training regimen that combines aerobic training + resistance training (maintaining muscle mass and reducing risk for worsening frailty is critical!). Phase 3 cardiac rehab or Rx pulmonary rehab in pts with concomitant pulmonary disease
14/ Step 9: For persistent symptoms and/or HF hospitalizations ➡️ HF clinic referral, reevaluate for HFpEF masqueraders, check for worsening comorbidities, if persistent fluid overload Rx HCTZ, use implantable PA monitoring, and evaluate for chronotropic incompetence
15/ Step 10: ENROLL IN A HFpEF CLINICAL TRIAL!
16/ Additional tip #1: In patients with persistent fluid overload on SGLT2i, MRA, and loop diuretic, avoid metolazone! Low-dose HCTZ typically works because of the benefit of sequential nephron blockade...
17/ ...The distal convoluted tubule is amped up if already on SGLT2i, MRA, and loop diuretic, so just a little bit of HCTZ (e.g., 12.5 mg qd) can result in significant diuresis. What if eGFR is very low? No problem, if still making urine, HCTZ will still usually work in HF pts.
18/ Additional tip #2: Which exercise training regimen do you prescribe? I try to mimic what’s been done in trials of exercise in HFpEF patients… ahajournals.org/doi/10.1161/CI…
19/ Additional tip #4: Pathophys often changes in HFpEF pts as they have events (e.g., hospitalization; changes in lifestyle, diet, environment; new meds started for other conditions; new-onset comorbidities or cardiac conditions). Don’t get complacent when caring for HFpEF pts!
20/ Additional tip #5: When caring for HFpEF pts, we often become the coordinator of care ➡️ need to treat the WHOLE patient in order to make them feel better. Provide a multi-disciplinary Rx plan.
21/ Additional tip #6: Avoid polypharmacy, use combo meds when possible (many are generic), and watch out for adverse effects of non-cardiac medications that may exacerbate HFpEF.
22/ Finally… there are many patients with HFpEF that need our help. Please consider starting a dedicated HFpEF program at your institution if you don’t have one already. This paper explains how to do it 😊… link.springer.com/article/10.100…
23/ Caveats (the fine print): SGLT2i should be considered in all patients except those with type 1 diabetes, orthostatic hypotension, eGFR <20-25, or very frequent yeast infections (or history of severe GU infections).
24/ Caveats (cont’d): Yeast infections are readily treatable, usually not a reason to permanently stop SGLT2i. Instruct pts to hold SGLT2i therapy for a few days on “sick days” (GI illness, dehydration, active infections). High HgbA1c not a contraindication to SGLT2i.
25/ Caveats (cont’d): MRA should be considered in all pts except those with K+ >5.0 or eGFR <30. Replace K+ supplementation with MRA whenever possible. Re-check K+ and renal function 1 week and 1 month after initiation, and q3-6 months thereafter.
26/ Caveats (cont’d): ARNI most effective if EF <55-60% or frequent HF hosp (congested phenotype); avoid in pts with history of angioedema, low BP, orthostatic hypotension, restrictive cardiomyopathy, pulmonary arterial hypertension, constrictive pericarditis, cardiac amyloidosis
27/ Caveats (cont’d): AF patients often have low stroke volume and inability to augment stroke volume during exertion due to LA dysfunction. Avoid excessive rate control in these patients.
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1/ Grant-writing tips. This #tweetorial mainly applies to @NIH grants (particularly R01s) but some stuff may be applicable to other types of grants and funding agencies. Based on my experience writing grants for 20 yrs +lots of cringe-worthy missteps and rejections along the way!
2/ Where do you begin? Part 1: pick scientific topics that you love thinking about and reading about. Start building a story. Publish 4-5 papers on your topic (1st or last author) to establish yourself. Make sure you're senior author on a few papers (shows independence)
3/ Where do you begin? Part 2: Think big, come up with a “zero-to-one” idea. Don't be incremental. If you had $100M to solve your scientific problem, what would you do? Write down all your ideas ➡️ narrow idea to $10M project ➡️ narrow further to a $2M ($500K x 4 yrs for an R01).
#HFpEF pearl of the day: Eval of filling pressures is critical for HFpEF management. Use entire echo and integrate info for filling pressures assessment: E, E/A, decel time, pulm vein flow, LA volume, LA strain, PASP, PR end-diastolic gradient, IVC, hepatic vein, tricuspid E/e'.
⬆️E, ⬇️DT, ⬆️E/A, and D-dominant pulm vein flow (in older pts); ⬆️E/e’, ⬆️LA volume (esp. ⬆️LA min volume), ⬇️LA reservoir strain; ⬆️PASP, ⬆️PREDP gradient (in absence of PAH); ⬆️tricuspid E/e’ > 6, ⬆️size ⬇️collapsibility of IVC, hep. vein flow reversal all = ⬆️filling pressures
Alternatively, continuous flow by 2D doppler into RA (in RV inflow views) or continuous forward flow on hepatic vein tracing can be helpful signs of normal RA pressure.
#HFpEF pearl of the day: Once the Dx of HFpEF is made, the 1st step is looking for and Rx'ing congestion, then Rx'ing comorbidities, and then exercise/weight loss program. I use sequential nephron blockade to minimize loop diuretic dose, always try to use MRAs when possible.
#HFpEF pearl of the day: speckle-tracking strain bullseye map of the LV can help determine etiology of HFpEF. Here's an example: 58-year-old man with HTN, CKD presents with SOB, leg swelling, elevated JVP. Echo shows normal LVEF.
What did his ECG show?
The answer is deep T wave inversions due to apical HCM.
#HFpEF pearl of the day: Always look at echo LVOT VTI when eval. HFpEF pts. Normal 18-22 cm at HR 60-100. ⬆️LVOT VTI: look for NASH, anemia, cirrhosis, AVMs, etc. If ⬇️LVOT VTI: infiltrative/restrictive CM, constriction, LA failure, PAH, RV failure, obstructive lung dz, MS, etc.
If ⬆️LVOT, measure volumes/dimensions of all 4 cardiac chambers to look for enlargement. Case: 31 yo woman previously healthy presents with dyspnea, leg swelling, BNP 166 pg/ml. Training for a marathon. Urine pregnancy test negative.
Echo shows normal LVEF (65%). E/e’ = 6. Lateral e’ velocity = 15 cm/s. LV dilated (LVEDVI = 85 ml/m2) and LA dilated (LA volume index = 50 ml/m2). ⬆️LVOT VTI = 30 cm.
#HFpEF pearl of the day: In HFpEF pts with #CardioMEMS devices, bike stress echo + continuous CardioMEMS PA pressure recording can help evaluate underlying pathophysiologic abnormalities.
Case: 71 yo woman w/apical HCM, AF s/p ablation, pacemaker, HTN, CKD with cardiorenal syndrome and PH-HFpEF presents with worsening overload. Echo shows preserved LVEF with apical HCM, PASP 85 mmHg, RAP 15 mmHg, RVOT PW notching consistent with ⬆️PVR.