HF TTT
HF TTT
There are three major goals of treatment for patients with HFrEF: 1) reduction in mortality, 2) prevention of recurrent hospi‐
talizations due to worsening HF, and 3) improvement in clinical status, functional capacity and quality of life (QOL).
Modulation of the renin-angiotensin-aldosterone (RAAS) and sympathetic nervous systems (SNS) with angiotensin-convert‐
ing enzyme inhibitors (ACE-I) or an angiotensin receptor-neprilysin inhibitor (ARNI), beta-blockers, and mineralocorticoid re‐
ceptor antagon ists (MRA) has been shown to improve survival, reduce the risk of HF hospitalizations and reduce symptoms,
in patients with HFrEF. These drugs serve as the foundations of pharmacotherapy for patients with HFrEF. The triad of an
ACE-I/ARNI, a beta-blocker and an MRA is recommended as cornerstone therapy for these patients, unless the drugs are
contraindicated or not tolerated. They should be uptitrated to the doses used in the clinical trials (or to maximally tolerated
doses if that is not possible). This guideline still recommends the use of ARNI as a replacement for ACE-I in suitable pa‐
tients who remain symptomatic on ACE-I, beta-blocker and MRA therapies, however, an ARNI may be considered as a first-
line therapy instead of an ACE-I.
The SGLT2 inhibitors dapagliflozin and empagliflozin, added to therapy with ACE-I/ARNI/beta-blocker/MRA reduced the risk
of CV death and worsening HF in patients with HFrEF. Unless contraindicated or not tolerated, dapagliflozin or empagliflozin
are recommended for all patients with HFrEF already treated with an ACE-I/ARNI, a beta-blocker and an MRA, regardless of
whether they have diabetes or not.
Figure 2 depicts the algorithm for the treatment strateg y, including drugs and devices in patients with HFrEF, for Class I indi‐
cations for the reduction of mortality (either all cause or CV). The recommendations for each treatment are summarized be‐
low.
Figure 2 Therapeutic algorithm of Class I Therapy Indications for a patient with heart failure with reduced ejection fraction
ACE-I = angiotensin-converting enzyme inhibitor; ARNI = angiotensin receptor-neprilysin inhibitor; CRT-D = cardiac resynchronization
therapy with defibrillator; CRT-P = cardiac resynchronization therapy pacemaker; ICD = implantable cardioverter-defibrillator; HFrEF =
heart failure with reduced ejection fraction; MRA = mineralocorticoid receptor antagonist; QRS = Q, R, and S waves of an ECG; SR =
sinus rhythm.
a
As a replacement for ACE-I.
b
Where appropriate.
Pharmacological treatments indicated in patients with (NYHA class II-IV) heart failure with reduced ejection fraction (LVEF
≤40%)
ACE-I = angiotensin-converting enzyme inhibitor; HF = heart failure; HFrEF = heart failure with reduced ejection fraction; LVEF = left
ventricular ejection fraction; MRA = mineralocorticoid receptor antagonist; NYHA = New York Heart Association. aClass of
recommendation. bLevel of evidence.
Other pharmacological treatments indicated in selected patients with NYHA class II-IV heart failure with reduced ejection
fraction (LVEF ≤40%)
Loop diuretics
ARB
If-channel inhibitor
Solub
le guanylate cyclase stimulator
Digoxin
ACE-I = angiotensin-converting enzyme inhibitor; ARB = angiotensin-receptor blocker; ARNI = angiotensin receptor-neprilysin inhibitor;
CV = cardiovascular; HF = heart failure; HFrEF = heart failure with reduced ejection fraction; LVEF = left ventricular ejection fraction;
MRA = mineralocorticoid receptor antagonist; NYHA = New York Heart Association; SR = sinus rhythm.
a
Class of recommendation. bLevel of evidence.
c
The ARBs with evidence in HFrEF are candesartan, losartan and valsartan.
In addition to the general therapies considered in Section Cardiac rhythm management for heart failure with reduced
ejection fraction, other therapies are appropriate to consider in selected patients. These are covered in detail in later sec‐
tions. Some of the main ones (i.e. those with Class I and IIa Mortality/Hospitalization indications) are depicted in Figure 3.
Figure 3 Strategic phenotypic overview of the management of heart failure with reduced ejection fraction