HF Guideline Slide 2006

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    ACC Heart Failure GuidelinesSlide Deck

    Based on the ACC/AHA 2005 Guideline Update

    for the Diagnosis and Management of

    Chronic Heart Failure in the Adult

    January 2006

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    Supported by Medtronic, Inc.

    Medtronic, Inc. was not involved in the development of this

    slide deck and in no way influenced its contents.

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    William T. Abraham, MD, FACC, FAHA

    Marshall H. Chin, MD, MPH, FACP

    Arthur M. Feldman, MD, PhD, FACC,

    FAHA

    Gary S. Francis, MD, FACC, FAHA

    Theodore G. Ganiats, MD

    Mariell Jessup, MD, FACC, FAHA

    Marvin A. Konstam, MD, FACC

    Sharon Ann Hunt, MD, FACC, FAHA, Chair

    Donna M. Mancini, MD

    Keith Michl, MD, FACP

    John A. Oates, MD, FAHA

    Peter S. Rahko, MD, FACC, FAHA

    Marc A. Silver, MD, FACC, FAHA

    Lynne Warner Stevenson, MD, FACC,

    FAHA

    Clyde W. Yancy, MD, FACC, FAHA

    ACC/AHA 2005 Guideline Update for the

    Management of Patients With Chronic Heart

    Failure in the AdultWriting Committee Members

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    Class IBenefit >>> Risk

    Procedure/ TreatmentSHOULD be

    performed/administered

    Class IIaBenefit >> RiskAdditional studies withfocused objectivesneeded

    IT IS REASONABLE toperform

    procedure/administertreatment

    Class IIbBenefit RiskAdditional studies withbroad objectivesneeded; Additionalregistry data would behelpful

    Procedure/TreatmentMAY BE CONSIDERED

    Class IIIRisk BenefitNo additional studiesneeded

    Procedure/Treatmentshould NOT beperformed/administered

    SINCE IT IS NOTHELPFUL AND MAY BEHARMFUL

    shouldis recommendedis indicatedis useful/effective/beneficial

    is reasonablecan be useful/effective/beneficialis probably recommendedor indicated

    may/might be consideredmay/might be reasonableusefulness/effectiveness isunknown /unclear/uncertainor not well established

    is not recommendedis not indicatedshould notis notuseful/effective/beneficialmay be harmful

    Applying Classification of

    Recommendations and Level of Evidence

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    Level A

    Multiple (3-5)population riskstrataevaluated

    Generalconsistency ofdirection andmagnitude ofeffect

    Class I

    Recommen-dation thatprocedure ortreatment isuseful/effective Sufficientevidence frommultiplerandomizedtrials or meta-analyses

    Class IIa

    Recommen-dation in favorof treatment orprocedurebeing useful/effective Someconflictingevidence frommultiplerandomizedtrials or meta-

    analyses

    Class IIb

    Recommen-dationsusefulness/efficacy lesswellestablished Greaterconflictingevidence frommultiplerandomizedtrials or meta-

    analyses

    Class III

    Recommen-dation thatprocedure ortreatment notuseful/effectiveand may beharmful Sufficientevidence frommultiplerandomizedtrials or meta-

    analyses

    Applying Classification of

    Recommendations and Level of Evidence

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    Level B

    Limited (2-3)population riskstrataevaluated

    Class I

    Recommen-dation thatprocedure ortreatment isuseful/effectiv

    e Limitedevidence fromsinglerandomizedtrial or non-randomized

    studies

    Class IIa

    Recommen-dation in favorof treatment orprocedurebeing useful/

    effective Someconflictingevidence fromsinglerandomizedtrial or non-

    randomizedstudies

    Class IIb

    Recommen-dationsusefulness/efficacy lesswell established

    Greaterconflictingevidence fromsinglerandomized trialor non-randomized

    studies

    Class III

    Recommen-dation thatprocedure ortreatment notuseful/effective

    and may beharmful Limitedevidence fromsinglerandomized trialor non-

    randomizedstudies

    Applying Classification of

    Recommendations and Level of Evidence

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    Applying Classification of

    Recommendations and Level of Evidence

    Level C

    Very limited (1-2) populationrisk strataevaluated

    Class I

    Recommen-dation thatprocedure ortreatment is

    useful/effective Only expertopinion, casestudies, orstandard-of-care

    Class IIa

    Recommen-dation in favorof treatment orprocedure

    beinguseful/effective Only divergingexpert opinion,case studies, orstandard-of-care

    Class IIb

    Recommen-dationsusefulness/efficacy less

    well established Only divergingexpert opinion,case studies, orstandard-of-care

    Class III

    Recommend-ation thatprocedure ortreatment not

    useful/effectiveand may beharmful Only expertopinion, casestudies, orstandard-of-care

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    Heart Failure is a Major and Growing Public

    Health Problem in the U.S.

    y Approximately 5 million patients in this country have

    HF

    y Over 550,000 patients are diagnosed with HF for the

    first time each year

    y Primary reason for 12 to 15 million office visits and

    6.5 million hospital days each year

    y In 2001, nearly 53,000 patients died of HF as a

    primary cause

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    Heart Failure is Primarily a

    Condition of the Elderly

    y The incidence of HF approaches 10 per 1000

    population after age 65

    y HF is the most common Medicare diagnosis-

    related group

    y More dollars are spent for the diagnosis and

    treatment of HF than any other diagnosis by

    Medicare

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    Guideline Scope

    Document focuses on :

    y

    Prevention of HFy Diagnosis and management of

    chronic HF in the adult

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    Definition of Heart Failure

    HF is a complex clinical syndrome that can

    result from any structural or functionalcardiac disorder that impairs the ability of

    the ventricle to fill with or eject blood.

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    Heart Failure vs. Congestive Heart Failure

    Because not all patients have volume overload at

    the time of initial or subsequent evaluation, theterm heart failure is preferred over the older

    term congestive heart failure.

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    Causes of HF in Western World

    For a substantial proportion of patients,

    causes are:

    1. Coronary artery disease

    2. Hypertension

    3. Dilated cardiomyopathy

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    Stages of Heart Failure

    At Riskfor Heart Failure:

    STAGE A High risk for developing HF

    STAGE B Asymptomatic LV dysfunction

    Heart Failure:

    STAGE C Past or current symptoms of HF

    STAGE D End-stage HF

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    Stages of Heart Failure

    Designed to emphasize preventability of HF

    Designed to recognize the progressive

    nature of LV dysfunction

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    Stages of Heart Failure

    COMPLEMENT, DO NOT REPLACE NYHA

    CLASSES

    NYHA Classes - shift back/forth in individualpatient (in response to Rx and/or progression of

    disease)

    Stages - progress in one direction due to cardiac

    remodeling

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    Stage A

    Patients at High Risk for

    Developing Heart Failure

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    Stage A Therapy

    Recommended Therapies to Reduce Risk Include: Treating known risk factors (hypertension, diabetes, etc.)

    with therapy consistent with contemporary guidelines

    Avoiding behaviors increasing risk (i.e., smoking

    excessive consumption of alcohol, illicit drug use)

    Periodic evaluation for signs and symptoms of HF Ventricular rate control or sinus rhythm restoration

    Noninvasive evaluation of LV function

    Drug therapy

    Angiotensin Converting Enzyme Inhibitors (ACEI)

    Angiotensin Receptor Blockers (ARBs)

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    Stage A Therapy

    In patients at high risk for developing HF,

    systolic and diastolic hypertension should be

    controlled in accordance with contemporaryguidelines.

    In patients at high risk for developing HF, lipid

    disorders should be treated in accordance

    with contemporary guidelines.

    Using Therapy Consistent withContemporary Guidelines

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

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    Stage A Therapy

    In patients at high risk for developing HF who

    have known atherosclerotic vascular disease,healthcare providers should follow current

    guidelines for secondary prevention.

    For patients with diabetes mellitus (who are all

    at high risk for developing HF), blood sugarshould be controlled in accordance with

    contemporary guidelines.

    Using Therapy Consistent withContemporary Guidelines

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

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    Stage A Therapy

    Thyroid disorders should be treated in

    accordance with contemporary guidelines inpatients at high risk for developing HF.

    Using Therapy Consistent withContemporary Guidelines

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

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    Stage A Therapy

    Patients at high risk for developing HF should

    be counseled to avoid behaviors that may

    increase the risk of HF (e.g., smoking,excessive alcohol consumption, and illicit

    drug use).

    Avoiding Behaviors ThatIncrease Risk

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

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    Stage A Therapy

    Healthcare providers should perform periodic

    evaluation for signs and symptoms of HF inpatients at high risk for developing HF.

    Periodic Evaluation forSigns and Symptoms

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

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    Stage A Therapy

    Ventricular rate should be controlled or sinus

    rhythm restored in patients with

    supraventricular tachyarrhythmias who are at

    high risk for developing HF.

    Ventricular Rate Control or SinusRhythm Restoration

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIa IIbIIa IIb IIIIIb IIIIII

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    Stage A Therapy

    Healthcare providers should perform a

    noninvasive evaluation of LV function (i.e.,

    LVEF) in patients with a strong family history

    of cardiomyopathy or in those receiving

    cardiotoxic interventions.

    Noninvasive Evaluation ofLV Function

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

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    Stage A Therapy

    ACEI can be useful to prevent HF in patients at

    high risk for developing HF who have a history of

    atherosclerotic vascular disease, diabetesmellitus, or hypertension with associated

    cardiovascular risk factors.

    Angiotensin Converting EnzymeInhibitors (ACEI)

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

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    Stage A Therapy

    ARBs can be useful to prevent HF in patients

    at high risk for developing HF who have a

    history of atherosclerotic vascular disease,diabetes mellitus, or hypertension with

    associated cardiovascular risk factors.

    Angiotension Receptor Blockers(ARBs)

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

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    Stage A Therapy

    Routine use of nutritional supplements solely

    to prevent the development of structural heart

    disease should not be recommended forpatients at high risk for developing HF.

    Therapies NOT Recommended

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

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    Stage B

    Patients with Asymptomatic

    LV Dysfunction

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    Stage B Therapy

    Recommended Therapies:

    General Measures as advised for Stage A

    Drug therapy for all patients

    ACEI or ARBs

    Beta-BlockersICDs in appropriate patients

    Coronary revascularization in appropriate patients

    Valve replacement or repair in appropriate patients

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    Stage B Therapy

    All Class I recommendations for Stage A

    should apply to patients with cardiac

    structural abnormalities who have notdeveloped HF. (Levels ofEvidence: A, B, and

    C as appropriate)

    Patients who have not developed HF

    symptoms should be treated according tocontemporary guidelines after an acute MI.

    General Measures

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

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    Stage B Therapy

    Beta-blockers and ACEIs should be used in all

    patients with a recent or remote history of MI

    regardless of EF or presence of HF.

    ACEI should be used in patients with a reduced EF

    and no symptoms of HF, even if they have not

    experienced MI.

    ACEI or ARBs can be beneficial in patients with

    hypertension and LVH and no symptoms of HF.

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    Angiotensin Converting EnzymeInhibitors (ACEI)

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    Stage B Therapy

    An ARB should be administered to post-MI patients

    without HF who are intolerant of ACEIs and have a

    low LVEF.

    ACEIs or ARBs can be beneficial in patients with

    hypertension and LVH and no symptoms of HF.

    ARBs can be beneficial in patients with low EF and

    no symptoms of HF who are intolerant of ACEIs.

    Angiotensin Receptor Blockers(ARBs)

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

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    Stage B Therapy

    Beta-blockers and ACEIs should be used in all

    patients with a recent or remote history of MI

    regardless of EF or presence of HF.

    Beta-blockers are indicated in all patients

    without a history of MI who have a reduced

    LVEF with no HF symptoms.

    Beta-Blockers

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

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    Stage B Therapy

    Placement of an ICD is reasonable in patients with

    ischemic cardiomyopathy who are at least 40 days

    post-MI, have an LVEF of 30% or less, are NYHA

    functional class I on chronic optimal medical therapy,and have reasonable expectation of survival with a

    good functional status for more than 1 year.

    Placement of an ICD might be considered in patients

    without HF who have nonischemic cardiomyopathy

    and an LVEF less than or equal to 30% who are inNYHA functional class I with chronic optimal medical

    therapy and have a reasonable expectation of survival

    with good functional status for more than 1 year.

    Internal Cardioverter Defibrillator (ICD)

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

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    Stage B Therapy

    Coronary revascularization should be

    recommended in appropriate patients

    without symptoms of HF in accordancewith contemporary guidelines (see

    ACC/AHA Guidelines for the Management

    of Patients With Chronic Stable Angina).

    Coronary Revascularization

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

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    Stage B Therapy

    Valve replacement or repair should be

    recommended for patients with

    hemodynamically significant valvularstenosis or regurgitation and no

    symptoms of HF in accordance with

    contemporary guidelines.

    Valve Replacement/Repair

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

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    Stage B Therapy

    Digoxin should not be used in patients with low EF,

    sinus rhythm, and no history of HF symptoms,

    because in this population, the risk of harm is not

    balanced by any known benefit.

    Use of nutritional supplements to treat structural

    heart disease or to prevent the development of

    symptoms of HF is not recommended.

    Calcium channel blockers with negative inotropiceffects may be harmful in asymptomatic patients

    with low LVEF and no symptoms of HF after MI.

    Therapies NOT Recommended

    III IIaIIaIIa

    IIbIIbIIb

    IIIIIIIII

    III IIaIIaIIa

    IIbIIbIIb

    IIIIIIIII

    III IIaIIaIIa

    IIbIIbIIb

    IIIIIIIII

    IIaIIaIIa

    IIbIIbIIb

    IIIIIIIII

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

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    Stage C

    Patients with Past or CurrentSymptoms of Heart Failure

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    Recommended Therapies:General measures as advised for Stages A and B

    Drug therapy for all patients

    Diuretics for fluid retention

    ACEI

    Beta-blockersDrug therapy for selected patients

    Aldosterone Antagonists

    ARBs

    Digitalis

    Hydralazine/nitratesICDs in appropriate patients

    Cardiac resynchronization in appropriate patients

    Exercise Testing and Training

    Stage C Therapy(Reduced LVEF with Symptoms)

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    Measures listed as Class I recommendations for

    patients in stages A and B are also appropriate for

    patients in Stage C. (Levels ofEvidence: A, B, and C as

    appropriate)

    Drugs known to adversely affect the clinical status of

    patients with current or prior symptoms of HF and

    reduced LVEF should be avoided or withdrawn

    whenever possible (e.g., nonsteroidal anti-inflammatory

    drugs, most antiarrhythmic drugs, and most calciumchannel blocking drugs).

    General Measures

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    Stage C Therapy(Reduced LVEF with Symptoms)

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    Diuretics and salt restriction are indicated in

    patients with current or prior symptoms of HF

    and reduced LVEF who have evidence of fluidretention.

    Diuretics

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    Stage C Therapy(Reduced LVEF with Symptoms)

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    ACEIs are recommended for all patients with

    current or prior symptoms of HF and reducedLVEF, unless contraindicated.

    Routine combined use of an ACEI, ARB, and

    aldosterone antagonist is not recommended forpatients with current or prior symptoms of HF

    and reduced LVEF.

    Angiotensin Enzyme ConvertingInhibitors (ACEIs)

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    Stage C Therapy(Reduced LVEF with Symptoms)

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

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    ARBs approved for the treatment of HF are

    recommended in patients with current or prior

    symptoms of HF and reduced LVEF who are ACEI-

    intolerant (see full text guidelines for informationregarding patients with angioedema).

    ARBs are reasonable to use as alternatives to ACEIs

    as first-line therapy for patients with mild to

    moderate HF and reduced LVEF, especially for

    patients already taking ARBs for other indications.

    Angiotensin Receptor Blockers (ARBs)

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    Stage C Therapy(Reduced LVEF with Symptoms)

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    The addition of an ARB may be considered in

    persistently symptomatic patients with reduced

    LVEF who are already being treated with

    conventional therapy.

    Routine combined use of an ACEI, ARB, and

    aldosterone antagonist is not recommended for

    patientswith current or prior symptoms of HF and

    reduced LVEF.

    ARBs (contd)

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    Stage C Therapy(Reduced LVEF with Symptoms)

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

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    Addition of an aldosterone antagonist is recommended in

    selected patients with moderately severe to severe

    symptoms of HF and reduced LVEF who can be

    carefully monitored for preserved renal function and

    normal potassium concentration. Creatinine should be

    less than or equal to 2.5 mg/dL in men or less than orequal to 2.0 mg/dL in women and potassium should be

    less than 5.0 mEq/L. Under circumstances where

    monitoring for hyperkalemia or renal dysfunction is not

    anticipated to be feasible, the risks may outweigh the

    benefits of aldosterone antagonists.

    Routine combined use of an ACEI, ARB, and aldosterone

    antagonist is not recommended for patients with current

    or prior symptoms of HF and reduced LVEF.

    Aldosterone Antagonists

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    Stage C Therapy(Reduced LVEF with Symptoms)

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    Beta-blockers (using 1 of the 3 proven to reduce

    mortality, i.e., bisoprolol, carvedilol, and sustained

    release metoprolol succinate) are recommended forall stable patients with current or prior symptoms of

    HF and reduced LVEF, unless contraindicated.

    Beta-Blockers

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    Stage C Therapy(Reduced LVEF with Symptoms)

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    Digitalis can be beneficial in patients with

    current or prior symptoms of HF and reduced

    LVEF to decrease hospitalizations for HF.

    Digitalis

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    Stage C Therapy(Reduced LVEF with Symptoms)

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    The addition of a combination of hydralazine and a

    nitrate is reasonable for patients with reduced

    LVEF who are already taking an ACEI and beta-

    blocker for symptomatic HF and who have

    persistent symptoms.

    A combination of hydralazine and a nitrate might be

    reasonable in patients with current or priorsymptoms of HF and reduced LVEF who cannot be

    given an ACEI or ARB because of drug intolerance,

    hypotension, or renal insufficiency.

    Hydralazine and Isosorbide Dinitrate

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    Stage C Therapy(Reduced LVEF with Symptoms)

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    An ICD is recommended as secondary prevention to

    prolong survival in patients with current or prior

    symptoms of HF and reduced LVEF who have a history of

    cardiac arrest, ventricular fibrillation, or hemodynamically

    destabilizing ventricular tachycardia.

    ICD therapy is recommended for primary prevention to

    reduce total mortality by a reduction in sudden cardiac

    death in patients with ischemic heart disease who are at

    least 40 days post-MI, have an LVEF less than or equal to

    30%, with NYHA functional class II or III symptoms while

    undergoing chronic optimal medical therapy, and have

    reasonable expectation of survival with a good functional

    status for more than 1 year.

    Implantable Cardioverter-Defibrillators (ICDs)

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    Stage C Therapy(Reduced LVEF with Symptoms)

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    ICD therapy is recommended for primary prevention to

    reduce total mortality by a reduction in sudden cardiac

    death in patients with nonischemic cardiomyopathy who

    have an LVEF less than or equal to 30%, with NYHA

    functional class II or III symptoms while undergoingchronic optimal medical therapy, and who have

    reasonable expectation of survival with a good functional

    status for more than 1 year.

    Placement of an ICD is reasonable in patients with LVEF

    of 30% to 35% of any origin with NYHA functional class IIor III symptoms who are taking chronic optimal medical

    therapy and who have reasonable expectation of survival

    with good functional status of more than 1 year.

    ICDs (contd)III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    Stage C Therapy(Reduced LVEF with Symptoms)

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    Patients with LVEF less than or equal to 35%, sinus

    rhythm, and NYHA functional class III or ambulatory

    class IV symptoms despite recommended, optimalmedical therapy and who have cardiac

    dyssynchrony, which is currently defined as a QRS

    duration greater than 120 ms, should receive cardiac

    resynchronization therapy unless contraindicated.

    Cardiac Resynchronization

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    Stage C Therapy(Reduced LVEF with Symptoms)

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    Maximal exercise testing with or without

    measurement of respiratory gas exchange is

    recommended to facilitate prescription of an

    appropriate exercise program for patientspresenting with HF.

    Exercise training is beneficial as an adjunctive

    approach to improve clinical status in ambulatory

    patients with current or prior symptoms of HF andreduced LVEF.

    Exercise Testing and Training

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    Stage C Therapy(Reduced LVEF with Symptoms)

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    Unproven/Not RecommendedDrugs and Interventions for HF

    Nutritional Supplements

    Hormonal Therapies Intermittent Intravenous

    Positive Inotropic Therapy

    Stage C Therapy(Reduced LVEF with Symptoms)

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    Long-term use of an infusion of a positive inotropic

    drug may be harmful and is not recommended for

    patients with current or prior symptoms of HF and

    reduced LVEF, except as palliation for patients withend-stage disease who cannot be stabilized with

    standard medical treatment (see recommendations

    for Stage D).

    Use of nutritional supplements as treatment for HF

    is not indicated in patients with current or priorsymptoms of HF and reduced LVEF.

    Unproven/Not Recommended Drugs and Interventions

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    Stage C Therapy(Reduced LVEF with Symptoms)

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    Calcium channel blocking drugs are not indicated as

    routine treatment for HF in patients with current or

    prior symptoms of HF and reduced LVEF.

    Hormonal therapies other than to replete

    deficiencies are not recommended and may be

    harmful to patients with current or prior symptoms

    of HF and reduced LVEF.

    Routine combined use of an ACEI, ARB, andaldosterone antagonist is not recommended for

    patientswith current or prior symptoms of HF and

    reduced LVEF.

    Unproven/Not Recommended Drugs and Interventions

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    Stage C Therapy(Reduced LVEF with Symptoms)

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    Recommended Therapies for Routine Use:Treating known risk factor (hypertension) with therapy

    consistent with contemporary guidelines

    Ventricular rate control for all patients

    Drugs for all patients -

    DiureticsDrugs for appropriate patients

    ACEI

    ARBs

    Beta-Blockers

    DigitalisCoronary revascularization in selected patients

    Restoration/maintenance of sinus rhythm in

    appropriate patients

    Stage C Therapy(Normal LVEF with Symptoms)

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    Differential Diagnosis in Patient with HF and

    Normal LVEF with Symptoms

    Incorrect diagnosis of HF

    Inaccurate measurement ofLVEF

    Primary valvular disease

    Restrictive (infiltrative)

    cardiomyopathies Amyloidosis, sarcoidosis,

    hemochromatosis

    Pericardial constriction

    Episodic or reversible LVsystolic dysfunction

    Severe hypertension,myocardial ischemia

    HF associated with highmetabolic demand (high-output states)

    Anemia, thyrotoxicosis,arteriovenous fistulae

    Chronic pulmonarydisease with right HF

    Pulmonary hypertensionassociated withpulmonary vasculardisorders

    Atrial myxoma

    Diastolic dysfunction ofuncertain origin

    Obesity

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    Physicians should control systolic and

    diastolic hypertension in patients with HF andnormal LVEF, in accordance with published

    guidelines.

    Treating known risk factors -Hypertension

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    Stage C Therapy(Normal LVEF with Symptoms)

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    Physicians should control ventricular rate in

    patients with HF and normal LVEF and atrial

    fibrillation.

    Ventricular Rate Control

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    Stage C Therapy(Normal LVEF with Symptoms)

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    Physicians should use diuretics to control

    pulmonary congestion and peripheral edema in

    patients with HF and normal LVEF.

    Diuretics

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    Stage C Therapy(Normal LVEF with Symptoms)

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    Coronary revascularization is reasonable in

    patients with HF and normal LVEF and

    coronary artery disease in whom symptomaticor demonstrable myocardial ischemia is

    judged to be having an adverse effect on

    cardiac function.

    Coronary Revascularization

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    Stage C Therapy(Normal LVEF with Symptoms)

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    Restoration and maintenance of sinus rhythm

    in patients with atrial fibrillation and HF and

    normal LVEF might be useful to improve

    symptoms.

    Restoration/Maintenanceof Sinus Rhythm

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    Stage C Therapy(Normal LVEF with Symptoms)

    S C

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    The use of beta-adrenergic blocking agents, ACEIs,

    ARBs, or calcium antagonists in patients with HF

    and normal LVEF and controlled hypertension mightbe effective to minimize symptoms of HF.

    Angiotensin Enzyme ConvertingInhibitors (ACEIs)

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    Stage C Therapy(Normal LVEF with Symptoms)

    St C Th

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    The use of beta-adrenergic blocking agents, ACEIs,

    ARBs, or calcium antagonists in patients with HF

    and normal LVEF and controlled hypertension mightbe effective to minimize symptoms of HF.

    Angiotensin Receptor Blockers (ARBs)

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    Stage C Therapy(Normal LVEF with Symptoms)

    St C Th

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    The use of beta-adrenergic blocking agents, ACEIs,

    ARBs, or calcium antagonists in patients with HF

    and normal LVEF and controlled hypertension mightbe effective to minimize symptoms of HF.

    Beta-Blockers

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    Stage C Therapy(Normal LVEF with Symptoms)

    St C Th

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    The usefulness of digitalis to minimize

    symptoms of HF in patients with HF and normal

    LVEF is not well established.

    Digitalis

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    Stage C Therapy(Normal LVEF with Symptoms)

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    Stage D

    Patients with Refractory End-Stage HF

    St D Th

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    Stage D Therapy

    Recommended Therapies Include:Control of fluid retention

    Referral to a HF program for appropriate pts

    Discussion of options for end-of-life care

    Informing re: option to inactivate defibrillator

    Device use in appropriate patientsSurgical therapy

    Cardiac transplantation

    Mitral valve repair or replacement

    Other

    Drug Therapy Positive inotrope infusion as palliation

    in appropriate patients

    St D Th

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    Stage D Therapy

    Meticulous identification and control of fluid

    retention is recommended in patients with

    refractory end-stage HF.

    Control of FluidRetention

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    St D Th

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    Stage D Therapy

    Referral of patients with refractory end-stage

    HF to an HF program with expertise in the

    management of refractory HF is useful.

    Referral to an HF Program

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    Stage D Therapy

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    Stage D Therapy

    Options for end-of-life care should be

    discussed with the patient and family when

    severe symptoms in patients with refractory

    end-stage HF persist despite application of all

    recommended therapies.

    Discussion of Options forEnd-of-Life Care

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    Stage D Therapy

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    Stage D Therapy

    Patients with refractory end-stage HF and

    implantable defibrillators should receive

    information about the option to inactivate

    defibrillation.

    Inform on option toinactivate defibrillation

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    Stage D Therapy

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    Stage D Therapy

    Referral for cardiac transplantation in

    potentially eligible patients is recommended for

    patients with refractory end-stage HF.

    The effectiveness of mitral valve repair or

    replacement is not established for severe

    secondary mitral regurgitation in refractory

    end-stage HF.

    Surgical Therapy

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    Stage D Therapy

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    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    Stage D Therapy

    Consideration of an LV assist device as

    permanentordestination therapy is

    reasonable in highly selected patients with

    refractory end-stage HF and an estimated1-year mortality over 50% with medical therapy.

    Pulmonary artery catheter placement may be

    reasonable to guide therapy in patients with

    refractory end-stage HF and persistently severesymptoms.

    Device Use

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    Stage D Therapy

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    Stage D Therapy

    Continuous intravenous infusion of a positive

    inotropic agent may be considered for

    palliation of symptoms in patients with

    refractory end-stage HF.

    Routine intermittent infusions of positive

    inotropic agents are not recommended for

    patients with refractory end-stage HF.

    Medical TherapyIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    Stage D Therapy

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    Stage D Therapy

    Partial left ventriculectomy is not

    recommended inpatients with nonischemic

    cardiomyopathy and refractory end-stage HF.

    Routine intermittent infusions of positive

    inotropic agents are not recommended for

    patients with refractory end-stage HF.

    Therapies NOT Recommended

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII

    III IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIII IIaIIaIIa IIbIIbIIb IIIIIIIIIIIaIIaIIa IIbIIbIIb IIIIIIIII