Heart Failure Rev UKRIDA

Embed Size (px)

Citation preview

  • 8/13/2019 Heart Failure Rev UKRIDA

    1/65

    DR. Med. Dr. Tike Ha ri Prati kto, SpJP, FIHA,FICA

  • 8/13/2019 Heart Failure Rev UKRIDA

    2/65

    The situation when the heart is incapable of maintaining a cardiac

    output adequate to accommodate metabolic requirements and the

    venous return. (E. Braunwald)

    The inability of the heart to pump blood forward at a sufficient rate to

    meet the metabolic demands of the body (forward failure), or the

    ability to do so only if the cardiac filling pressure are abnormally high

    (backward failure), or both. (Pathophysiology of Heart Disease 4 thed,

    Liily, Leonard S)

    DEFINITION

  • 8/13/2019 Heart Failure Rev UKRIDA

    3/65

    Heart Failure is a clinical syndrome in which patients have the following

    features :

    DEFINITION

    Symptoms typical of HF

    (breathlessness at rest or on exercise, fatigue, tiredness, ankle swelling

    And

    Signs typical of HF

    (tachycardia, tachypnoea, pulmonary rales, pleural effusion, raisedjugular venous pressure, peripheral oedema, hepatomegaly)

    And

    Objective evidence of a structural or functional abnormality of the heartat rest (cardiomegaly, third heart soud, cardiac murmurs, abnormality onthe echocardiogram, raised natriuretic peptide concentration)

  • 8/13/2019 Heart Failure Rev UKRIDA

    4/65

    Symptoms

  • 8/13/2019 Heart Failure Rev UKRIDA

    5/65

    ACC/AHA A New Approach To The

    Classification of HF

    2009 Focused Update: ACCF/AHA Guidelines for the Diagnosis and Management of Heart Failure in Adults

    Stage AAt high risk of HF but

    without structural heartdisease or symptoms of

    HF

    Stage Bstructural heart disease

    but withoutsigns/symptoms of HF

    Stage CStructural heart disease

    with prior or currentsymptoms of HF

    Stage DRefractory HF requiring

    specializedinterventions

    e.g. patient with-Hypertension-Atherosclerosisdisease-Diabetes

    -Obesity-Metabolic syndr-Using cardiotoxin-with Familialhistory

    e.g. patient with-Previous MI-LV remodeling:including LVH, lowEF-Asymptomaticvalvular disease

    e.g. patient with-Known structuralheart disease-Shortness ofbreath and fatigue,reduced exercisetolerance

    e.g. patient with-Who have markedsymptoms at restdespite maximalmedical therapy(recurrentlyhospitalized/cannot be safelydischarged fromhospital withoutspecializedinterventionStructural heart

    diseaseDevelopment of HF

    symptoms

    Refractory symptomsof HF at rest

    At Risk For Heart Failure Heart Failure

  • 8/13/2019 Heart Failure Rev UKRIDA

    6/65

    Determinant of ventricular function

    STROKEVOLUME

    PRELOAD

    CONTRACTILITY

    CARDIAC OUTPUT

    HEARTRATE

    - Synergistic LV contraction- LV wall integrity- Valvular competence

    AFTERLOAD

  • 8/13/2019 Heart Failure Rev UKRIDA

    7/65

    The goal of treatment : relieve symptoms and signs

    prevent hospital admission

    improve survival

    Treatment strategy for the use of drugs in patients with HR-REF

    Three neurohumoral antagonist

    ACE inhibitor (or Angiotensin Receptor Blocker (ARB))

    Beta-blocker

    MRA (Mineralocorticoid Receptor Blocker)

    The aforementioned drugs commonly used in conjunction witha diuretic given to relieve the symptoms and signs ofcongestion

    TREATMENT

  • 8/13/2019 Heart Failure Rev UKRIDA

    8/65

    Evaluation of acutely decompensatedchronic HF

  • 8/13/2019 Heart Failure Rev UKRIDA

    9/65

  • 8/13/2019 Heart Failure Rev UKRIDA

    10/65

  • 8/13/2019 Heart Failure Rev UKRIDA

    11/65

  • 8/13/2019 Heart Failure Rev UKRIDA

    12/65

  • 8/13/2019 Heart Failure Rev UKRIDA

    13/65

  • 8/13/2019 Heart Failure Rev UKRIDA

    14/65

  • 8/13/2019 Heart Failure Rev UKRIDA

    15/65

  • 8/13/2019 Heart Failure Rev UKRIDA

    16/65

    THANK YOU

  • 8/13/2019 Heart Failure Rev UKRIDA

    17/65

    Diagnosis of heart failure

    The diagnosis of HF-REF requiresthree conditions to be satisfied :

    Symptoms typical of HF

    Signs typical of HF

    Reduced LVEF

    The diagnosis of HF-PEF requiresfor conditions to be satisfied :

    Symptoms typical of HF

    Signs typical of HF

    Normal or only mildly reduced

    LVEF and LV not dilated

    Relevant structural heart disease(LV hypertrophy/LA

    enlargement) and/or diastolicdysfunctions

  • 8/13/2019 Heart Failure Rev UKRIDA

    18/65

  • 8/13/2019 Heart Failure Rev UKRIDA

    19/65

  • 8/13/2019 Heart Failure Rev UKRIDA

    20/65

    Patients who should get ACEI

    LVEF 40%, irrespective of symptoms

    Initiation of an ACEI :

    Check renal function and serum electrolytes

    Consider dose up-titration after 2-4 weeks

    Do not increase dose if worsening renal function or hyperkalaemia

    It is common to up-titrate slowly but more rapid titration is possiblein closely monitored patients

    ACE inhibitors

  • 8/13/2019 Heart Failure Rev UKRIDA

    21/65

    Starting dose (mg) Target dose (mg)

    ACE Inhibitors

    Captopril 6.25 mg t.i.d 50 t.i.d

    Enalapril 2.5 b.i.d 10-20 b.i.d

    Lisinopril 2.5- 5 o.d 20-35 o.d

    Ramipril 2.5 o.d 5 o.d

    Trandolapril 0.5 o.d 4 o.d

    ACE Inhibitors (Dosage)

  • 8/13/2019 Heart Failure Rev UKRIDA

    22/65

  • 8/13/2019 Heart Failure Rev UKRIDA

    23/65

    Patients who should get an ARB

    LVEF 40% and either

    As an alternative in patients with mild to severe symptoms (NYHA fc II-IV) whoare intolerant of an ACEI

    Or in patients with persistent symptoms (NYHA fc IV) despite treatment withan ACEI and beta blocker

    Initiation of an ARB

    Check renal function and serum electrolytes Consider dose up-titration after 2-4 weeks

    Do not increase dose if worsening renal function or hyperkalaemia

    It is common to up-titrate slowly but more rapid titration is possible in closelymonitored patients

    ARBs

  • 8/13/2019 Heart Failure Rev UKRIDA

    24/65

    ARBs (dosage)

    Starting dose (mg) Target dose (mg)

    ARB

    Candesartan 4 or 8 mg o.d 32 o.d

    Valsartan 40 b.i.d 160 b.i.d

    Losartan 50 o.d 150 o.d

  • 8/13/2019 Heart Failure Rev UKRIDA

    25/65

    Patients who should get a beta-blocker LVEF 40%

    Mild to severe symptoms (NYHA fc II-IV)

    Optimal dose level of an ACEI or/and ARB

    Patients should be clinically stable(e.g. no recent change in dose of diuretic)

    Initiation of a beta-blocker

    Beta-blocker may be initiated prior to hospital discharge in recently

    decompensated patients with caution

    Visits every 2-4 weeks to up-titrate the dose of beta-blocker (slower dose up-titration may be needed in some patients). Do not increase dose if signs ofworsening HF, symptomatic hypotension (e.g. dizziness) or excessivebradycardia (pulse rate

  • 8/13/2019 Heart Failure Rev UKRIDA

    26/65

    Beta-blockers (dosage)

    Starting dose (mg) Target dose (mg)

    Beta blockers

    Bisoprolol 1.25 mg o.d 10 o.d

    Carvedilol 3.125 b.i.d 25-50 b.i.d

    Metoprolol (CR/XL) 12.5/25 o.d 200 o.d

    Nebivolol 1.25 o.d 1o.d

  • 8/13/2019 Heart Failure Rev UKRIDA

    27/65

    Patients who should get an MRA

    LVEF 35%

    Moderate to severe symptoms (NYHA fc II-IV)

    Optimal dose of beta-blocker and an ACEI or an ARB (but not an ACEI and

    an ARB)

    Initiation of spironolactone (eplerenone)

    Check renal function and serum electrolytes

    Consider up-titration after 4-8 weeks. Do not increase dose if worseningrenal function or hyperkalaemia

    Mineralocorticoid receptor antagonist(MRA)

  • 8/13/2019 Heart Failure Rev UKRIDA

    28/65

    Diuretics and MRAs (dosage)

  • 8/13/2019 Heart Failure Rev UKRIDA

    29/65

    Potential adverse effect Hyperkalemia

    K > 5.5 halve dose

    K > 6.0stop

    Worsening renal function

    Cr > 220 umol/L (~2.5 mg/dl) halve dose

    Cr > 310 umol (~3.5 mg/dl)stop

    Breast tenderness and/ enlargement

    Switch from spironolactone to eplerenone

    MRA (potential adverse effects)

  • 8/13/2019 Heart Failure Rev UKRIDA

    30/65

    Ivabradine is a drug that inhibits the I fchannel in the sinusnode. Its only known pharmacological effect is to slowheart rate in patients in sinus rhythm (it does not slow theventricular rate in AF)

    Patients who should get an Ivabradine

    Mild to severe symptoms (NYHA fc II-IV)

    Sinus rhythm with a rate 70 bpm

    LVEF 35%

    Ivabradine

  • 8/13/2019 Heart Failure Rev UKRIDA

    31/65

    In patients in sinus rhythm with symptomatic HF andLVEF 40%, this treatment improve patient well-beingand reduce hospital admission for worsening HF

    Patients in AF with ventricular rate at rest >80, and at

    exercise >110-120 beat/minute should get digoxin

    In patients with sinus rhythm and left ventricularsystolic dysfunction (LVEF 40%) receiving optimaldoses of diuretic, ACEI or/and ARB, beta-blocker and

    aldosterone antagonist if indicated, who aresymptomatic, digoxin may be considered)

    Digoxin

  • 8/13/2019 Heart Failure Rev UKRIDA

    32/65

    Patients who should get H-ISDN

    An alternative to an ACEI/ARB where both of the latter are not tolerated

    As add-on, therapy to an ACEI if ARB or aldosterone antagonist is nottolerated or if significant symptoms persist despite therapy with an ACEI,ARB, beta-blocker, and aldosterone antagonist

    Initiation of H-ISDN

    Consider dose up-titration after 2-4 weeks. Do not increase dose withsymptomatic hypotension

    Hydralazine and ISDN

  • 8/13/2019 Heart Failure Rev UKRIDA

    33/65

  • 8/13/2019 Heart Failure Rev UKRIDA

    34/65

    A h th i b d di d t i t i l

  • 8/13/2019 Heart Failure Rev UKRIDA

    35/65

    Atrial Fibrillation

    The most common arrhythmia in HF

    increases the risk of thrombo-embolic complications (particularly stroke)and may lead to worsening of symptoms

    The following issues need to be considered in patients with HF and AF,especially a first episode of AF or paroxysmal AF:

    Identification of correctable causes (e.g. hyperthyroidism, electrolytedisorders, uncontrolled hypertension, mitral valve disease).

    Identification of potential precipitating factors (e.g. recent surgery, chest

    infection or exacerbation of chronic pulmonary disease/asthma, acutemyocardial ischaemia, alcohol binge) as this may determine whether arhythm-control strategy is preferred to a rate-control strategy.

    Assessment for thromboembolism prophylaxis.

    Arrhythmia, bradycardia, and atrioventricular

    block in patients with heart failure with reduced EFand heart failure with preserved EF

  • 8/13/2019 Heart Failure Rev UKRIDA

    36/65

  • 8/13/2019 Heart Failure Rev UKRIDA

    37/65

    Atrial Fibrillation

    Thrombo-embolism prophylaxis

  • 8/13/2019 Heart Failure Rev UKRIDA

    38/65

  • 8/13/2019 Heart Failure Rev UKRIDA

    39/65

    Ventricular arrhythmia in HF

  • 8/13/2019 Heart Failure Rev UKRIDA

    40/65

  • 8/13/2019 Heart Failure Rev UKRIDA

    41/65

  • 8/13/2019 Heart Failure Rev UKRIDA

    42/65

    Chronic obstructive pulmonary disease and Asthma

    may cause diagnostic difficulties, especially in HF-PEF

    Beta-blockers are contraindicated in asthma but not in

    COPDselective beta-1 adrenoceptor antagonist (i.e.bisoprolol, metoprolol succinate, or nebivolol) Preferred

    Oral corticosteroids cause sodium and water retentionworsening of HF

  • 8/13/2019 Heart Failure Rev UKRIDA

    43/65

    Diabetes Melitus

    Associated with poorer functional status and worse prognosis

    Prevented by treatment with ARBs and possibly ACE inhibitors.

    Beta-blockers are NOTcontraindicated in diabetes and are aseffective in improving outcome in diabetic patients as in non-diabetic individuals

    Thiazolidinediones (glitazones)sodium and water retention andincreased risk of worsening HF and hospitalization

    Metformin is NOTrecommended in patients with severe RENAL

    or HEPATIC IMPAIRMENT

    HYPERTENSION

  • 8/13/2019 Heart Failure Rev UKRIDA

    44/65

    HYPERTENSION

  • 8/13/2019 Heart Failure Rev UKRIDA

    45/65

    Acute Heart Failure

  • 8/13/2019 Heart Failure Rev UKRIDA

    46/65

    Defined as the rapid onset of, or change in,symptoms and signs of HF. It may occur withor without previous cardiac disease.

    ESC guidelines for the Diagnosis & Treatment of Acute and Chronic Heart Failure 2012

  • 8/13/2019 Heart Failure Rev UKRIDA

    47/65

  • 8/13/2019 Heart Failure Rev UKRIDA

    48/65

    Precipitants and causes

  • 8/13/2019 Heart Failure Rev UKRIDA

    49/65

    Clinical classification

    Worsening or decompensated chronic HF There is usually a history of progressive worsening of known chronic HF

    on treatment and evidence of systemic and pulmonary congestion

    Pulmonary oedema

    Present with severe respiratory distress, tachypnoea and orthopnoeawith rales over on lung fields. Artery O2 saturation is usually

  • 8/13/2019 Heart Failure Rev UKRIDA

    50/65

  • 8/13/2019 Heart Failure Rev UKRIDA

    51/65

  • 8/13/2019 Heart Failure Rev UKRIDA

    52/65

  • 8/13/2019 Heart Failure Rev UKRIDA

    53/65

    Oxygen

    Given to treat hypoxemia (SpO2

  • 8/13/2019 Heart Failure Rev UKRIDA

    54/65

    Vasodilators

  • 8/13/2019 Heart Failure Rev UKRIDA

    55/65

    Positive Inotropes or vasopressors or both

  • 8/13/2019 Heart Failure Rev UKRIDA

    56/65

  • 8/13/2019 Heart Failure Rev UKRIDA

    57/65

  • 8/13/2019 Heart Failure Rev UKRIDA

    58/65

  • 8/13/2019 Heart Failure Rev UKRIDA

    59/65

    Goals of treatment in acute heart

  • 8/13/2019 Heart Failure Rev UKRIDA

    60/65

    Immediate (ED/ICU/ICCU) Treat symptoms

    Restore oxygenation

    Improve haemodynamics and organ

    perfusion Limit cardiac and renal damage

    Prevent thrombo-embolism

    Minimize ICU length of stay

    Goals of treatment in acute heartfailure

  • 8/13/2019 Heart Failure Rev UKRIDA

    61/65

    Most of the knowledge about the epidemiology, riskfactors,prognosis, treatment, and prevention of HF is based onNorth American and European studies

    EPIDEMIOLOGY

    (ESC Guidelines for the Diagnosis andTreatment of Acute and Chronic Heart

    Failure ,2008)

    ACC/AHA Guidelines for the

    Evaluation and Management of Chronic Heart Failure

    in the Adult 2001

    Europe

    The prevalence of symptomatic HFrange from 2-3%

    Prevalence in 70- to 80-year-oldpeople is between 10 and 20%.

    15 million HF pts in 900 million totalpopulation

    Overall 50% of patients are dead at 4

    years. Forty per cent of patientsadmitted to hospital with HF aredead or readmitted within 1 year

    USA

    Nearly 5 million HF pts. 500,000 pts are HF for the 1st time

    each year.

    Last 10 yearsnumber ofhospitalizations has increased.

    Nearly 300,000 patients die of HFeach year.

    Terminology related to the time-course

  • 8/13/2019 Heart Failure Rev UKRIDA

    62/65

    A patient who/whose Never exhibited the typical signs or symptoms of HFasymptomatic LV

    systolic dysfunction

    Have had HFchronic HF

    Chronic stable HF conditions deteriorates

    decompensated Chronic stable HF resolves from acute conditioncompensated

    HFs condition presents acutelyNew (de novo) HF

    Terminology related to the time courseof heart failure

  • 8/13/2019 Heart Failure Rev UKRIDA

    63/65

  • 8/13/2019 Heart Failure Rev UKRIDA

    64/65

    Suspected Heart Failure

    Acute onset

    ECGChest x-ray

    Echocardiography BNP/NT-pro BNP

    ECG normaland

    NT-proBNP

  • 8/13/2019 Heart Failure Rev UKRIDA

    65/65

    Starting dose (mg) Target dose (mg)

    MRA

    Eplerenone 25 mg o.d 50 o.d

    Spironolactone 25 o.d 25-50 o.d