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Acute and chronic heart failure (ESC guidline)
1.
2. 2016 ESC guidelines
for the diagnosis and treatment of acute
and chronic heart failure
PRESENTED BY
DR. MD. ROKUN UDDIN
MD (CARDIOLOGY)-3RD PART STUDENT
DEPT. OF CARDIOLOGY, SSMC & MH
3.
4. What is Heart Failure?
HF is a clinical syndrome characterized by
typical symptoms (e.g. breathlessness, ankle
swelling and fatigue) that may be accompanied
by signs (e.g. elevated jugular venous pressure,
pulmonary crackles and peripheral oedema)
caused by a structural and/or functional cardiac
abnormality, resulting in a reduced cardiac
output and/or elevated intracardiac pressures at
rest or during stress.
5. HFrEF HFmrEF HFpEF
Symptoms±Signs Symptoms±Signs Symptoms±Signs
LVEF <40% LVEF 40-49% LVEF ≥50%
1. Elevated levels of
natriuretic peptides
2. At least one
a.structural heart
disease(LVH and/or
LAE)
b.diastolic dysfunction
1. Elevated levels of
natriuretic peptides
2. At least one
a.structural heart
disease(LVH and/or
LAE)
b.diastolic dysfunction
14. ECG
provide information on aetiology (e.g.
myocardial infarction.
HF is unlikely in patients presenting with a
completely normal ECG (sensitivity 89%).
the routine use of an ECG is mainly
recommended to rule out HF.
15. Chest X-ray
show pulmonary venous congestion or
oedema in a patient with HF,
probably most useful in identifying an
alternative diagosis
16. Natriuretic peptides (NPs)
Patients with normal plasma NP concentrations
are unlikely to have HF.
Upper limit of normal:
Non acute setting
BNP is 35 pg/mL and NT-proBNP is 125 pg/mL
Acute setting
BNP 100 pg/mL, NT-proBNP 300 pg/ml
17. Transthoracic echo
myocardial structure and function
diagnosis of either HFrEF, HFmrEF or HFpEF
identify patients who would be suitable for
pharmacological and device (ICD, CRT)
assessment of valve disease, right ventricular
function and pulmonary arterial pressure
identify those suitable for correction of valve disease
assessment of structure and function in subjects
exposed to treatment (chemotheraphy).
18. Transthoracic echo-cont.
measurement of LVEF, the modified biplane
Simpson’s rule is recommended
The Teichholz and Quinones methods as well as a
measurement of fractional shortening, are not
recommended, particularly with regional LV
dysfunction and/or LV remodelling.
19. Transoesophageal echo.
valve disease
suspected aortic dissection
suspected endocarditis or congenital heart
disease
ruling out intracavitary thrombi in AF patients
20. Coronary angiography
recommended in patients with HF who suffer from
angina pectoris recalcitrant to medical therapy
patients with a history of symptomatic ventricular
arrhythmia or aborted cardiac arrest
patients with HF and intermediate to high pre-test
probability of CAD
presence of ischaemia in non-invasive stress tests
21. Cardiac magnetic resonance
(CMR)
assessment of myocardial structure and function
subjects with poor acoustic window and with
complex congenital heart diseases.
suspected myocarditis, amyloidosis, sarcoidosis,
Chagas disease, haemochromatosis
22. Single-photon emission CT (SPECT)
&Positron emission tomography (PET):
used to assess ischaemia and viability
23. Recommendations to prevent or delay the
development of overt heart failure
Treatment of hypertension (class 1)
Treatment with statins (class 1)
smoking cessation and alcohol intake reduction
(class 1)
ACE-I is recommended in patients with asymptomatic
LV systolic dysfunction and with/without history of MI
(class 1)
ACE-I should be considered in patients with stable
CAD even if they do not have LV systolic dysfunction
(class IIa)
24. Beta-blocker is recommended in patients with
asymptomatic LV systolic dysfunction and a
history of myocardial infarction (class1)
Treating other risk factors of HF (e.g. obesity, DM)
(class IIa)
ICD in recommended patient (class 1)
25. Algorithm for the diagnosis of heart
failure in the non-acute setting
36. Treatments recommended in
all symptomatic patients with HFrEF
ACEi
Beta-Blocker
Mineralocorticoid receptor antagonist
37. Treatments recommended in selected
symptomatic patients with HFrEF
Diuretics
Angiotensin receptor neprolysin inhibitor(ARNI)
If-chennel inhibitor- Ivabradine
ARB
Combination of Hydralazine and Isosorbde dinitrate
38. Treatments with less certain benefits in
symptomatic patients with HFrEF
Digoxin
N-3 polyunsaturated fatty acids
Treatments not recommended(unproven benefit)
Statins
Oral anticoagulants and antiplatelate.
Renin inhibitors
39. Treatments not recommended (believed to
cause harm) in symptomatic patients with
HFrEF
Calcium chennel blocker-Diltiazem and Verapamil )
There is only evidence on safety for amlodipine
40. Practical guidance on the use of
ACEi or ARB with HFrEF
WHY?
To improve symptoms and exercise capacity, reduce the risk of
HF hospitalization and increase survival.
IN WHOM AND WHEN?
indications:
1. Potentially all patients with HF and an LVEF <40%.
2. First-line treatment (along with a beta-blockers and an MRA)
with NYHA Class II–IV, start as early as possible.
3.ACEI also benefit asymptomatic HF (NYHA I)
41. Contra-indications:
1. History of angioedema
2. Known bilateral renal artery stenosis.
3. Pregnancy/risk of pregnancy.
4.Known allergic reaction/adverse reaction
43. WHERE?
In the community in stable patients.
In patients hospitalized with worsening HF – after
stabilizing, relieving congestion, and, if possible,
restoring ‘euvolaemia’ (but ideally before
discharge).
44. HOW TO USE ACEi ?
Check renal function and electrolytes.
Start with a low dose
Double the dose at not less than 2-week intervals in
the community. More rapid dose up-titration in hospital
or closely monitored pt.
Aim for target dose or the highest tolerated dose
45. Monitor blood chemistry 4 monthly thereafter.
It is very rarely necessary to stop an ACE-I (or ARB),
and clinical deterioration is likely if treatment is
withdrawn.
47. PROBLEM SOLVING (pt. With ACEi)
Asymptomatic low blood pressure:
Does not usually require any change in therapy.
Symptomatic hypotension:
Reconsider need for nitrates, calcium-channel
blockers and other vasodilators and reduce dose/stop,
if possible.
If no signs or symptoms of congestion, consider
reducing diuretic dose.
48. Cough:
ACE-I-induced cough does not always require
treatment discontinuation.
When a troublesome cough does develop
substitution of an ARB is recommended.
49. Worsening renal function and hyperkalaemia (pt
with ACEi with HF):
creatinine of up to 50% above baseline
or 3 mg/dL
Or eGFR <25 mL/min/1.73 m2,
whichever is the smaller, is acceptable.
potassium upto ≤5.5 mmol/L is acceptable.
if no signs of congestion, reducing the dose of diuretic.
50. If greater rise
the dose of the ACE-I (or ARB) should be halved
ACE-I (or ARB) should be stopped
If potassium rises to >5.5 mmol/L or
creatinine increases by >100% or 3.5 mg/dL or
eGFR <20 mL/min/1.73 m2,
and specialist advice sought.
51. Practical guidance on the use of
β-blocker with HFrEF
WHY?
To improve symptoms, reduce the risk of HF hospitalization and
increase survival.
IN WHOM AND WHEN?
Indications:
1. Potentially all patients with stable mild or moderate systolic
HF (LVEF <40%) (NYHA Class II-III).
2. Pts. With severe HF also benefit but treatment with caution
3. First-line treatment, along with an ACE-I and an MRA, in
patients with stabilized HF; start as early as possible in the
course of disease.
52. Contra-indications of β-blocker :
1. Second- or third-degree AV block
2. Critical limb ischaemia.
3. Asthma (relative contra-indication): if cardio-
selective beta-blockers are indicated, asthma is not
necessarily an absolute contra-indication
COPD is not a contra-indication
54. HOW TO USE BETA-BLOCKER?
Start with a low dose in a stable condition (see Table
7.2).
Double the dose at not less than 2-week intervals
Aim for target dose or the highest tolerated dose
(remember: some beta-blocker is better than no beta-
blocker).
Monitor heart rate, blood pressure, and clinical status
(symptoms, signs–especially signs of congestion,
body weight).
55. PROBLEM SOLVING
Worsening symptoms or signs (dyspnoea, fatigue,
oedema):
If increasing congestion, increase dose of diuretic or
halve dose of beta-blocker
If marked fatigue (bradycardia) halve dose of beta-
blocker (rarely necessary)
If serious deterioration, halve dose of beta-blocker or
stop this treatment (rarely necessary)
56. Asymptomatic low blood pressure:
Does not usually require any change in therapy
Low heart rate:
If <50 bpm and worsening symptoms, halve dose of
beta-blocker, or, if severe deterioration, stop beta-
blocker (rarely necessary).
Review need for other heart rate-slowing drugs
(digoxin, amiodarone, diltiazem, or verapamil)
57. Practical guidance on the use
of MRA with HFrEF
WHY?
To improve symptoms, reduce the risk of HF
hospitalization and increase survival.
Indications:
Potentially all patients with persisting symptoms
(NYHA Class II–IV) and an LVEF ≤35% despite
treatment with an ACE-I (or ARB) and a beta-blocker
58. WHICH MRA AND WHAT DOSE?
Eplerenone: starting dose 25 mg o.d., target dose 50
mg o.d.
Spironolactone: starting dose 25 mg o.d., target dose
50 mg o.d.
59. HOW TO USE?
Consider dose up-titration after 4–8 weeks.
halve dose
If K+ rises above 5.5 mmol/L or creatinine rises to 2.5 mg/dL or
eGFR <30 mL/min/1.73 m2, and monitor blood chemistry
closely.
stop MRA immediately
If K+ rises to >6.0 mmol/L or creatinine to >3.5 mg/dL) eGFR
<20 mL/min/1.73 m2, and seek specialist advice.
60. Practical guidance on the use
of Diuretics with HFrEF
WHY?
To relieve breathlessness and oedema in patients with
symptoms and signs of congestion.
Indications:
Potentially all patients with symptoms and signs of congestion,
irrespective of LVEF.
always be used in combination with an ACE-I (or ARB), a beta-
blocker, and an MRA in patients with HFrEF (unless contra-
indicated)
Thaizde diuretics can be used in patients with preserved renal
function and mild symptoms of congestion
62. Contra-indications:
Not indicated if the patient has never had symptoms or signs of
congestion.
Known allergic reaction
HOW TO USE?
Start with a low dose
Use minimum dose necessary to maintain euvolaemia
Dose may need to be increased or decreased according to the
patient’s volume status
64. Implantable cardioverter-defibrillator (ICD)
(Recommendations)
Primary prevention
An ICD is recommended
o to reduce the risk of sudden death and all-cause mortality
o in patients with symptomatic HF (NYHA Class II–III), and
o an LVEF ≤35% despite ≥3 months of OMT,
o provided they are expected to survive substantially longer
than one year with good functional status, and they have:
1. IHD (unless they have had an MI in the prior 40 days
2. DCM.
65. Secondary prevention
An ICD is recommended to reduce the risk of sudden
death and all-cause mortality in patients who have
recovered from a ventricular arrhythmia causing
haemodynamic instability,
and who are expected to survive for >1 year with
good functional status
66. Recommendations for cardiac resynchronization
therapy(CRT) implantation
CRT is recommended for symptomatic patients
With HF in sinus rhythm with a QRS duration ≥150
msec/130–149 msec and LBBB QRS morphology and
with LVEF ≤35% despite OMT
in order to improve symptoms and reduce morbidity
and mortality. (Class I)
Editor's Notes
significant LV dysfunction may be present without
cardiomegaly on the chest X-ray
Clinical profiles of patients with acute heart failure based on the presence/absence of congestion and/or hypoperfusion
(remember: some ACE-I (or ARB) is better than no ACE-I).
Ideally, specialist advice should be sought before treatment discontinuation
Drug interactions to look out for:
K+ supplements/ K+-sparing diuretics, e.g. amiloride and).
MRAs. Renin inhibitors NSAIDs, Trimethoprim/trimethoprim-sulfamethoxazole
Dizziness/light headedness is common and often improves with time–patients should be reassured.
If these measures do not solve problem, seek specialist advice
common with HF, may have smoking-related lung disease.
also a symptom of pulmonary oedema, which should be excluded when a new worsening cough develops.
Some rise in urea (BUN), creatinine, and potassium is to be expected, no action is necessary.
consider stopping concomitant nephrotoxic drugs (e.g. NSAIDsd) and other potassium supplements or
Cautions/seek specialist advice:
1. Severe (NYHA Class IV) HF.
2. Current or recent (<4 weeks) exacerbation of HF, heart block, or heart rate <50 bpm.
3. If persisting signs of congestion, hypotension (systolic <90 mmHg), raised jugular venous pressure, ascites, marked peripheral oedema - try to relieve congestion ,achieve ‘euvolaemia’ before starting a beta-blocker.
. Drug interactions to look out for (because of risk of bradycardia/atrioventricular block):
Verapamil, diltiazem (should be discontinued).
Digoxin. Amiodarone. Ivabradine.
ADVICE TO PATIENT
Symptomatic improvement may develop slowly after starting treatment, sometimes taking 3–6 months or longer.
Temporary symptomatic deterioration may occur during initiation or up-titration phase; in the long term beta-blockers improve well-being.
Check renal function and electrolytes (particularly K+).
Start with a low dose (see above).
Start with a low dose, but an effective dose for a patient to achieving positive diuresis with a simultaneous reduction of body weight by 0.75–1,0 kg per day