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Heart Failure

Definition

A complex clinical syndrome with symptoms and signs that result from any structural or functional impairment of ventricular filling or ejection of blood

Causes

  • IHD, MI, valvular heart disease (VHD)
  • hypertension
  • Others
    • familial,genetic, RV pacing, peripartum or stress-induced cardiomyopathies
    • amyloidosis
    • cardiotoxicity with cancer or other treatments
    • substance abuse - alcohol, cocaine, or methamphetamine
    • tachycardia, myocarditis, autoimmune causes, sarcoidosis,
    • iron overload, including haemochromatosis
    • thyroid disease and other endocrine metabolic and nutritional causes

Symptoms

  • breathlessness - many other causes of SOB though
  • leg swelling
  • orthopnoea
  • bendopnoea

New York Heart Failure Classification
I - cardiac disease but no symptoms or limitation of daily activities
II - mild symptoms and slight limitation to ordinary activity
III - significant limitation due to symptoms. Comfortable only at rest
IV - severe limitation and symptoms at rest

Signs

  • raised JVP
  • a square-wave response to the Valsalva manoeuvre
  • pitting oedema of legs
  • fine crep's on chest auscultation - beware other causes

Investigations

  • FBC, U&E's (Ca++, Mg++), LFTs, Glu, TSH
  • fasting lipid profile
  • Fe studies (serum iron, ferritin, transferrin saturation)
  • urinalysis
  • ECG and ECHO

Management

Treatment of HF is dependent on classification:

Goal of Heart Failure Mx. The 4 pillar approach:

  1. ACEi or ARB or ARNi
  2. a β-blocker
  3. an MRA
  4. SLGT2i

To prescribe a combination of all at low initial doses and titrate to target/max tolerated doses (with doubling of doses), one at a time.

  • double the dose of each, one at a time, every 2–4/52(except MRAs; up-titrated in 4–8/52), or as tolerated.
  • add the next drug before reaching target or maximum tolerated dose, eg, if the patient is euvolaemic, a heart failure beta blocker may be started before achieving target or maximum tolerated dose of an ACE inhibitor.
  • clinical and lab review every 1–2/52 after each medicine initiation and dose increase.

ACE inhibitors (ACEi)

Medications

ACEi initial target
enalapril 2.5mg OD 20mg OD
lisinopril 2.5mg OD 50mg OD
perindopril 2.5mg OD 10mg OD
ramipril 2.5mg bd 5mg bd
Angiotensin Receptor Blockers (ARB)
ARB initial target
candesartan 4mg OD 32mg OD
irbesartan 75mg OD 300mg OD
losartan 25mg OD 100mg OD
valsartan 40mg bd 160mg bd
olmesartan 10mg OD 40mg OD
Heart β-blockers
β blockers initial target
bisoprolol 1.25mg OD 10mg OD
carvedilol 3.125mg bd 50mg bd
nebivolol 1.25mg OD 10mg OD
Aldosterone Receptor Antagonists (MRA)
MRA initial target
spironolactone 25mg OD 50mg OD
eplerenone 25mg OD 50mg OD
Other
other initial target
ivabradine 5mg bd 7.5mg bd

  • beware of stopping diuretics in HF when renal function worsens. Diuretics are NOT the cause of reduced renal function in HF and NOT associated with increased mortality in this setting.
  • diuretics are NOT intrinsically nephrotoxic
  • caution needs to be exercised in monitoring electrolyte changes - patients with HF commonly have a degree of renal failure and, combined with other cardiac medications, are at risk of BRASH syndrome.
Diuretic type example electrolyte side effect
Loop diuretics furosemide
bumetanide
low K, low Ca
high Na
Thiazides
& thiazide like
bendroflumathiazide
indapamide
metolazone
low Na/K/Mg
high Urate/Glu
hypochloraemic metabolic alkalosis
Potassium sparing:
aldosterone antagonist
spironolactone
eplerenone
low Na
High K
Potassium sparing:
aldosterone independent
amiloride
triamterene
low Na
high K
metab acidosis
SGLT2 inhibitors dapagliflozin not directly

Subcutaneous furosemide infusion is effective when oral agents are not appropriate or suitable. The use of an elastomeric pump can simplify this. Setup guide using Braun elastomeric pumps

Author: Dr Dylan Jenkins, Oct 2023
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