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{{CMG}}; {{AE}} {{MS}}
'''For acute heart failure prevention click [[Acute heart failure prevention|here]].'''


==Definition==
{{CMG}}; {{AE}} {{MS}}; {{AO}}; {{Rim}}
Heart failure is a complex syndrome whereby there is inadequate output of the [[heart]] to meet the metabolic demands of the body. Abnormal function of different anatomic parts of the heart cause heart failure including the [[pericardium]], the [[myocardium]], the [[endocardium]], the [[heart valves]] and the [[great vessels]]. Symptoms of heart failure are due to a lack of both forward blood flow to the body, and backward flow into the lungs. Heart failure is a clinical syndrome characterized by symptoms of [[dyspnea]], [[edema]] and [[fatigue]] and signs such as [[rales]] on physical examination.
 
{| class="infobox" style="margin: 0 0 0 0; border: 0; float: right; width: 100px; background: #A8A8A8; position: fixed; top: 250px; right: 21px; border-radius: 0 0 10px 10px;" cellpadding="0" cellspacing="0";
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! style="padding: 0 5px; font-size: 85%; background: #A8A8A8" align=center| {{fontcolor|#2B3B44|Acute Heart Failure Resident Survival Guide Microchapters}}
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! style="font-size: 80%; padding: 0 5px; background: #DCDCDC" align=left | [[Acute heart failure resident survival guide#Overview|Overview]]
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! style="font-size: 80%; padding: 0 5px; background: #DCDCDC" align=left | [[Acute heart failure resident survival guide#Classification|Classification]]
|-
! style="font-size: 80%; padding: 0 5px; background: #DCDCDC" align=left | [[Acute heart failure resident survival guide#Causes|Causes]]
|-
! style="font-size: 80%; padding: 0 5px; background: #DCDCDC" align=left | [[Acute heart failure resident survival guide#FIRE: Focused Initial Rapid Evaluation|FIRE]]
|-
! style="font-size: 80%; padding: 0 5px; background: #DCDCDC" align=left | [[Acute heart failure resident survival guide#Complete Diagnostic Approach|Diagnosis]]
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! style="font-size: 80%; padding: 0 5px; background: #DCDCDC" align=left | Treatment
[[Heart failure resident survival guide#Prevention of Heart Failure in Stage A and B|Stage A and B]]<br>
[[Heart failure resident survival guide#Treatment of Heart Failure in Stage C and D|Stage C and D]]<br>
[[Heart failure resident survival guide#Diuretic Therapy Details|Diuretic Therapy]]<br>
[[Heart failure resident survival guide#Medications|Medication Dosages]]
|-
! style="font-size: 80%; padding: 0 5px; background: #DCDCDC" align=left | [[Heart failure resident survival guide#Do's|Do's]]
|-
! style="font-size: 80%; padding: 0 5px; background: #DCDCDC" align=left | [[Heart failure resident survival guide#Don'ts|Don'ts]]
|}
 
==Overview==
Heart failure is a complex syndrome characterized by inadequate blood ejection or impaired ventricular filling, leading to the inability of the heart to pump blood to meet the metabolic demands of the body. Heart failure is a clinical syndrome for which the diagnosis relies mainly on symptoms and physical examination findings.  The main symptoms and signs of heart failure are [[dyspnea]], volume overload (leading to [[pulmonary edema]] and/or [[peripheral edema]]), [[fatigue]], and [[exercise intolerance]].  Acute decompensated heart failure (ADHF) is a life-threatening condition that can occur in the setting of a new onset heart failure or worsening of an existing chronic heart failure.  Symptoms of ADHF may include [[dyspnea]] secondary to [[pulmonary edema]], [[peripheral edema]], [[hypotension]], and impaired end organ perfusion that can manifest by [[worsening renal function]], [[altered mental status]], and [[cold clammy extremities]].  The mainstays of treatment of ADHF are 1) [[oxygen therapy]] to improve [[hypoxia]], 2) [[diuresis]] to reduce both [[preload]] and intravascular volume, and 3) vasodilators to reduce [[afterload]]. The goals of treatment for chronic heart failure are to relieve symptoms, decrease hospitalization rate, and decrease morbidity and mortality. Treatment of heart failure includes identification and management of precipitating factors, lifestyle changes, pharmacological therapy, and devices.
 
==Classification==
===Classification by Severity of Congestive Heart Failure===
Shown below is a table comparing American College of Cardiology Foundation/American Heart Association (ACCF/AHA) stages to New York Heart Association (NYHA) classification of severity of heart failure.<ref name="pmid23741057">{{cite journal| author=Yancy CW, Jessup M, Bozkurt B, Butler J, Casey DE, Drazner MH et al.| title=2013 ACCF/AHA guideline for the management of heart failure: executive summary: a report of the American College of Cardiology Foundation/American Heart Association Task Force on practice guidelines. | journal=Circulation | year= 2013 | volume= 128 | issue= 16 | pages= 1810-52 | pmid=23741057 | doi=10.1161/CIR.0b013e31829e8807 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23741057  }} </ref>
 
{| style="cellpadding=0; cellspacing= 0; width: 800px;"
|-
| style="padding: 0 5px; font-size: 100%; background: #4682B4; color: #FFFFFF;" align=center colspan="2"| '''ACCF/AHA Stages''' || style="padding: 0 5px; font-size: 100%; background: #4682B4; color: #FFFFFF;" align=center colspan="2" colspan="2"|'''New York Heart Association (NYHA) Classification'''
|-
| style="padding: 0 5px; font-size: 100%; background: #F5F5F5" align=center |'''Stage''' || style="padding: 0 5px; font-size: 100%; background: #F5F5F5" align=center |'''Interpretation'''|| style="padding: 0 5px; font-size: 100%; background: #F5F5F5" align=center |'''Class'''|| style="padding: 0 5px; font-size: 100%; background: #F5F5F5" align=center |'''Interpretation'''
|-
|style="font-size: 100; padding: 0 5px; background: #B8B8B8" align=left |A ||  style="font-size: 100; padding: 0 5px; background: #B8B8B8" align=left |At high risk for heart failure (HF) but without structural heart disease or symptoms of HF || style="font-size: 100; padding: 0 5px; background: #B8B8B8" align=left | - || style="font-size: 100; padding: 0 5px; background: #B8B8B8" align=left | -
|-
|style="font-size: 100; padding: 0 5px; background: #B8B8B8" align=left |B ||  style="font-size: 100; padding: 0 5px; background: #B8B8B8" align=left |Structural heart disease but without signs or symptoms of HF ||style="font-size: 100; padding: 0 5px; background: #B8B8B8" align=left |I ||style="font-size: 100; padding: 0 5px; background: #B8B8B8" align=left |No limitation of physical activity. Ordinary physical activity does not cause symptoms of HF
|-
|style="font-size: 100; padding: 0 5px; background: #B8B8B8" align=left rowspan="4"|C || style="font-size: 100; padding: 0 5px; background: #B8B8B8" align=left rowspan="4"| Structural heart disease with prior or current symptoms of HF
| style="font-size: 100; padding: 0 5px; background: #B8B8B8" align=left |I ||style="font-size: 100; padding: 0 5px; background: #B8B8B8" align=left |No limitation of physical activity. Ordinary physical activity does not cause symptoms of HF
|-
| style="font-size: 100; padding: 0 5px; background: #B8B8B8" align=left |II ||style="font-size: 100; padding: 0 5px; background: #B8B8B8" align=left |Slight limitation of physical activity. Comfortable at rest, but ordinary physical activity results in symptoms of HF
|-
| style="font-size: 100; padding: 0 5px; background: #B8B8B8" align=left |III ||style="font-size: 100; padding: 0 5px; background: #B8B8B8" align=left |Marked limitation of physical activity. Comfortable at rest, but less than ordinary activity causes symptoms of HF
|-
| style="font-size: 100; padding: 0 5px; background: #B8B8B8" align=left |IV ||style="font-size: 100; padding: 0 5px; background: #B8B8B8" align=left |Unable to carry on any physical activity without symptoms of HF, or symptoms of HF at rest
|-
|style="font-size: 100; padding: 0 5px; background: #B8B8B8" align=left |D ||  style="font-size: 100; padding: 0 5px; background: #B8B8B8" align=left |Refractory HF requiring specialized interventions|| style="font-size: 100; padding: 0 5px; background: #B8B8B8" align=left |IV ||style="font-size: 100; padding: 0 5px; background: #B8B8B8" align=left |Unable to carry on any physical activity without symptoms of HF, or symptoms of HF at rest
|}
 
===Classification by Other Factors===
====Left Ventricular Ejection Fraction (LVEF)====
* [[Systolic dysfunction|Heart failure with reduced ejection fraction]] (HFrEF) or [[Systolic dysfunction|systolic heart failure]]: [[ejection fraction]] (EF) ≤40%
* [[Diastolic dysfunction|Heart failure with preserved ejection fraction]] (HFpEF) or [[diastolic heart failure]]: [[EF]] ≥50%
** Borderline HFpEF: EF between 41 to 49%
** Improved HFpEF: EF >40% following a HFrEF
 
====Cardiac Output====
* Low cardiac output
* High stroke volume with/without cardiac output
 
====Left vs. Right Sided====
* Left sided: [[Pulmonary edema]]
* Right sided: [[Peripheral edema]], [[elevated jugular venous pressure]], [[hepatomegaly]]
 
====Backwards vs. Forward====
* Backwards: Congestion, elevated filling pressure
* Forwards: Low systemic perfusion


==Causes==
==Causes==
===Life Threatening Causes===
===Life Threatening Causes===
Acute decompensated heart failure is a life-threatening condition and must be treated as such irrespective of the causes.  Life-threatening conditions  can result in death or permanent disability within 24 hours if left untreated.
[[Congestive heart failure|Acute decompensated heart failure]] is life threatening and should be treated as such irrespective of the underlying cause.
* [[Accelerated hypertension]]
===Common Causes===
* [[Acute coronary syndrome]]
* [[Acute kidney injury]]
* [[Acute kidney injury]]
* [[Acute myocardial ischemia]]
* [[Myocarditis|Acute severe myocarditis]]
* Acute or progressive valvular disease (e.g. acute [[mitral regurgitation]])
* [[Cardiac arrhythmias]]
* [[Endocarditis|Acute or subacute valve disease endocarditis]]
* [[Cardiomyopathy]]
* [[Aortic dissection]]
* [[Cardiotoxicity|Cardiotoxic agents]] - [[alcohol]], [[cocaine]]
* Cardiac arrhythmias, specially [[ventricular arrhythmias]]
* Decompensation of an underlying [[chronic heart failure]]
* Cardiotoxic agents (e.g. [[alcohol]], [[cocaine]], and certain [[chemotherapy]] drugs)
* [[Hypertensive emergency|Hypertensive crisis]]
* Diabetic emergencies (e.g. [[ketoacidosis]])
* [[Myopericarditis]]
* [[Pulmonary embolus]]
* [[Pulmonary embolus]]
* Severe [[anemia]] (e.g. acute [[hemolysis]] or [[blood loss]])
* [[Sepsis|Systemic Inflammatory response syndrome]]
* [[Sepsis|Systemic Inflammatory response syndrome]]
* [[Thyrotoxicosis]]
* [[Valvular heart disease]]
 
Click '''[[Congestive heart failure causes|here]]''' for the complete list of causes.
 
==FIRE: Focused Initial Rapid Evaluation==
A Focused Initial Rapid Evaluation (FIRE) should be performed to identify patients of severe acute decompensated heart failure in need of immediate intervention.<ref name="pmid23741057">{{cite journal| author=Yancy CW, Jessup M, Bozkurt B, Butler J, Casey DE, Drazner MH et al.| title=2013 ACCF/AHA guideline for the management of heart failure: executive summary: a report of the American College of Cardiology Foundation/American Heart Association Task Force on practice guidelines. | journal=Circulation | year= 2013 | volume= 128 | issue= 16 | pages= 1810-52 | pmid=23741057 | doi=10.1161/CIR.0b013e31829e8807 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23741057  }} </ref><br>
 
<span style="font-size:85%">Boxes in red signify that an urgent management is needed.</span>
 
<span style="font-size:85%">'''Abbreviations:'''
'''BU:''' [[Blood urea nitrogen]];
'''COPD:''' [[Chronic obstructive pulmonary disease]];
'''D5W:''' 5% dextrose solution in water ;
'''HF:''' [[Heart failure]];
'''IV:''' [[Intravenous]];
'''MAP:''' [[Mean arterial pressure]];
'''Na:''' [[Sodium]];
'''NSAID:''' [[Non steroidal anti-inflammatory drug]];
'''SBP:''' [[Systolic blood pressure]];
'''S3:''' [[Third heart sound]];
</span>
<br>
{{familytree/start}}
{{familytree | | | A01 | | A01=<div style="float: left; text-align: left; width: 35em; padding:1em;">  '''Identify cardinal findings that increase the pretest probability of acute decompensated heart failure'''<br>
❑ [[Dyspnea]]<br>
❑ [[Cool extremities]]<br>
❑ [[Pedal edema|Peripheral edema]] <br>
❑ [[Decreased urine output]] <br>
❑ Past medical history of [[heart failure]] <br>
❑ History of [[orthopnea]] and [[paroxysmal nocturnal dyspnea]]<br>
❑ Pulmonary [[crepitations]]/[[rales]]/[[crackles]]<br>
❑ [[Heart sounds#Third heart sound S3|Third heart sound (S3)]]</div>}}
{{familytree | | | |!| |}}
{{familytree | | | W01 | |W01=<div style="float: left; text-align: left; width: 35em; padding:1em;">'''Does the patient have any of the following findings that require hospitalization and urgent management?'''<br>
❑ Severe decompendated HF:
:❑ [[Hypotension]] ([[SBP]] < 90 mmHg or drop in [[MAP]] >30 mmHg) and/or [[cardiogenic shock]]<br>
:❑ [[Altered mental status]]<br>
:❑ [[Cool extremities|Cold and clammy extremities]]<br>
:❑ [[Oliguria|Urine output <0.5mL/kg/hr]]<br>
❑ [[Dyspnea]] at rest manifested by [[tachypnea]] or oxygen saturation <90% <br>
❑ [[Atrial fibrillation]] with a rapid ventricular response resulting in [[hypotension]]
❑ [[Acute coronary syndrome]] </div>}}
{{familytree | |,|-|^|-|.| |}}
{{familytree | B01 | | B02 | |B01=<div style=" background: #FA8072"> {{fontcolor|#F8F8FF|Yes}}</div> |B02='''No'''}}
{{familytree | |!| | | |!| | |}}
{{familytree | C01 | | C02 | |C01=<div style=" background: #FA8072"> {{fontcolor|#F8F8FF|Admit to to a level of care that allows for constant ECG monitoring given the risk of arrhythmia }}</div>
|C02=<div style="float: left; text-align: center; width: 25em;">[[Heart failure resident survival guide#Complete Diagnostic Approach|Proceed to complete diagnostic approach]]</div> }}
{{familytree | |!| | | | | | |}}
{{familytree |boxstyle=background: #FA8072; color: #F8F8FF;  | D01 | | | | | |D01= <div style="float: left; text-align: left; width: 45em; padding:1em;">
'''Initial stabilization:''' <br>
❑ Assess the airway <br>
❑ Position the patient upright at an angle of 45 degrees, with legs dangling off the bedside (decrease [[preload|<span style="color:white;">preload</span>]])<br>
❑ Monitor [[heart rate|<span style="color:white;">heart rate</span>]] and [[blood pressure|<span style="color:white;">blood pressure</span>]] continuously<br>
❑ Monitor oxygen saturation continuously<br>
❑ If [[hypoxemia|<span style="color:white;">hypoxemia</span>]] is present (Sa02 < 90% or Pa02 <60 mmHg), administer oxygen with/without [[noninvasive ventilation|<span style="color:white;">noninvasive ventilation</span>]] <br>
❑ [[Morphine|<span style="color:white;">Morphine</span>]] to decrease symptoms and [[afterload|<span style="color:white;">Afterload</span>]] (avoid IV [[morphine|<span style="color:white;">morphine</span>]], may increase mortality / duration of [[intubation|<span style="color:white;">intubation</span>]], generally not advisable, may relieve refractory symptoms) <br>
❑ Secure intravenous access with 18 gauge cannula <br>
❑ Monitor fluid intake and urine output carefully (guide the adjustment of the diuretics dose)  <br><br>
 
'''Assess congestion and perfusion:'''<br>
'''''Congestion at rest''''' (dry vs. wet)<br>
''"Wet" suggested by orthopnea, ↑JVP, rales, S3, pedal edema''<br>
'''''Low perfusion at rest (warm vs. cold)'''''<br>
''"Cold" suggested by narrow [[pulse pressure|<span style="color:white;">pulse pressure</span>]], [[cool extremities|<span style="color:white;">cool extremities</span>]], [[hypotension|<span style="color:white;">hypotension</span>]]'' <br>
The patient is:<br>
❑ Warm and dry, OR <br>
❑ Warm and wet, OR <br>
❑ Cold and dry, OR <br>
❑ Cold and wet <br><br>
 
'''Identify precipitating factor and treat accordingly:''' <br>
''Click on the precipitating factor for more details on the management'' <br>
❑ [[Myocardial infarction|<span style="color:white;">Myocardial infarction</span>]] <br>
❑ [[Myocarditis|<span style="color:white;">Myocarditis</span>]] <br>
❑ [[Renal failure|<span style="color:white;">Renal failure</span>]] <br>
❑ [[Hypertensive crisis|<span style="color:white;">Hypertensive crisis</span>]] <br>
❑ Non adherence to medications <br>
❑ Worsening [[aortic stenosis|<span style="color:white;">Aortic stenosis</span>]] <br>
❑ Drugs ([[NSAIDS|<span style="color:white;">NSAIDS</span>]], [[thiazides|<span style="color:white;">thiazides</span>]], [[calcium channel blocker|<span style="color:white;">calcium channel blocker</span>]], [[beta blockers|<span style="color:white;">beta blockers</span>]]) <br>
❑ Toxins ([[alcohol|<span style="color:white;">alcohol</span>]], [[anthracycline|<span style="color:white;">anthracyclines</span>]]) <br>
❑ [[Atrial fibrillation|<span style="color:white;">Atrial fibrillation</span>]] <br>
: ''Rate control of [[atrial fibrillation|<span style="color:white;">atrial fibrillation</span>]] is the mainstay of [[arrhythmia|<span style="color:white;">arrhythmia</span>]] therapy. Avoid the use of drugs with negative [[inotropic|<span style="color:white;">inotropic</span>]] effects such as [[beta blocker|<span style="color:white;">beta blockers</span>]] and [[non-dihydropyridine calcium channel blocker|<span style="color:white;">non-dihydropyridine calcium channel blockers</span>]] e.g., [[verapamil|<span style="color:white;">verapamil</span>]] in the treatment of acute decompensated [[systolic heart failure|<span style="color:white;">systolic heart failure</span>]]''
: ''Consider [[cardioversion|<span style="color:white;">cardioversion</span>]] if the patient is in [[cardiogenic shock|<span style="color:white;">cardiogenic shock</span>]] or if new onset [[atrial fibrillation|<span style="color:white;">atrial fibrillation</span>]] is the clear precipitant of the hemodynamic decompensation''
❑ [[COPD|<span style="color:white;">COPD</span>]] <br>
❑ [[Pulmonary embolism|<span style="color:white;">Pulmonary embolism</span>]] <br>
❑ [[Anemia|<span style="color:white;">Anemia</span>]] <br>
❑ [[Thyroid|<span style="color:white;">Thyroid</span>]] abnormalities <br>
❑ Systemic [[infection|<span style="color:white;">infection</span>]] <br><br>
 
'''Treat congestion and optimize volume status:''' <br>
'''''Diuretics''''' <br>
❑ Administer IV [[loop diuretics|<span style="color:white;">loop diuretics</span>]] as intermittent boluses or continuous infusion (I-B)<br>
:❑ If patient is already on [[loop diuretics|<span style="color:white;">loop diuretics</span>]]: IV dose ≥ home PO dose (I-B); rule of thumb: IV dose = 2.5x equivalent oral daily dose<br>
:❑ If patient is not already on [[loop diuretics|<span style="color:white;">loop diuretics</span>]], administer IV starting dose:
:: [[Furosemide|<span style="color:white;">Furosemide</span>]] 20 to 40 mg, '''OR'''
:: [[Torsemide|<span style="color:white;">Torsemide</span>]] 5 to 10 mg, '''OR'''
:: [[Bumetanide|<span style="color:white;">Bumetanide</span>]] 0.5 to 1 mg
:❑ Adjust dose according to volume status (I-B) <br>
:❑ Perform serial assessment of fluid intake and output, [[vital signs|<span style="color:white;">vital signs</span>]], daily body weight (measured every day, with the same scale, at the same time, after first void) and symptoms <br>
:❑ Order daily [[electrolytes|<span style="color:white;">electrolytes</span>]], [[BUN|<span style="color:white;">BUN</span>]], [[creatinine|<span style="color:white;">creatinine</span>]] (I-C) <br>
❑ Low sodium diet (<2 g daily)<br>
❑ In case of persistent symptoms:
:❑ Increase dose of IV [[loop diuretics|<span style="color:white;">loop diuretics</span>]] (I-B)- double dose at 2 hour interval up to maximal daily dose
:: [[Furosemide|<span style="color:white;">Furosemide</span>]] maximal dose: 40 to 80 mg
:: [[Torsemide|<span style="color:white;">Torsemide</span>]] maximal dose: 20 to 40 mg
:: [[Bumetanide|<span style="color:white;">Bumetanide</span>]] maximal dose: 1 to 2 mg
:'''OR'''
:❑ Add a second [[diuretics|<span style="color:white;">diuretics</span>]], such as [[thiazide|<span style="color:white;">thiazide</span>]] (I-B) <br>
❑ Consider low dose [[dopamine|<span style="color:white;">dopamine</span>]] infusion for improved diuresis and renal blood flow (IIb-B) <br>
❑ Consider [[renal replacement therapy|<span style="color:white;">renal replacement therapy</span>]]/[[ultrafiltration|<span style="color:white;">ultrafiltration</span>]] in obvious volume overload (IIb-B) refractory to higher dose/combination of IV diuretics <br>
 
'''''Venodilators'''''<br>
❑ Consider IV [[nitroglycerin|<span style="color:white;">nitroglycerin</span>]], [[nitroprusside|<span style="color:white;">nitroprusside</span>]], or [[nesiritide|<span style="color:white;">nesiritide</span>]] as add-on to diuretics to relieve [[dyspnea|<span style="color:white;">dyspnes</span>]] (IIb-A) <br><br>
:''Do not administer [[vasodilator|<span style="color:white;">vesodilators</span>]] among patients with [[hypotension|<span style="color:white;">hypotension</span>]].''
 
'''Treat low perfusion:'''<br>
❑ [[Inotrope|<span style="color:white;">Inotropes</span>]] (click her for details)<br><br>
:''If the total body and intravascular volumes are overloaded and the patient is normotensive, then [[diuresis|<span style="color:white;">diuresis</span>]] alone should be undertaken. If the patient is volume overloaded but [[hypotensive|<span style="color:white;">hypotensive</span>]], then [[inotrope|<span style="color:white;">inotropes</span>]] must be administered in addition to [[diuretics|<span style="color:white;">diuretics</span>]].''
 
'''Invasive hemodynamic monitoring:'''<br><br>
❑ Consider [[Right heart catheterization|<span style="color:white;">pulmonary artery catheterization</span>]] in case of failure to respond to medical therapy, [[respiratory distress|<span style="color:white;">respiratory distress</span>]], [[shock|<span style="color:white;">shock</span>]], uncertainty regarding volume status, or increase in [[creatinine|<span style="color:white;">creatinine</span>]]; assess the following parameters:<br>
:❑ [[PCWP|<span style="color:white;">PCWP</span>]]
:❑ [[Cardiac output|<span style="color:white;">Cardiac output</span>]]
:❑ [[Systemic vascular resistance|<span style="color:white;">Systemic vascular resistance</span>]]
 
'''VTE prevention:''' <br>
❑ [[Anticoagulation|<span style="color:white;">Anticoagulation</span>]] in the absence of contraindications (I-B)<br><br>
 
'''Chronic medical therapy:''' <br>
❑ Chronic [[ACE inhibitor|<span style="color:white;">ACE inhibitor</span>]]: Hold if patient is hemodynamically unstable <br>
❑ Chronic [[beta blocker|<span style="color:white;">beta blocker</span>]]:
: Hold if patient is hemodynamically unstable and/or in need or [[inotrope|<span style="color:white;">inotropes</span>]]
: Decrease dose by ≥ half if patient is in moderate [[heart failure|<span style="color:white;">heart failure</span>]]
❑ DO NOT INITIATE ACE INHIBITORS during an acute decompensation<br>
❑ DO NOT INITIATE BETA BLOCKER during an acute decompensation; initiate beat blockers at a low dose in stable patients following optimization of volume status and D/C IV diuretics and inotropes (I-B) <br><br>
 
'''Monitor laboratory tests:''' <br>
❑ [[BUN|<span style="color:white;">BUN</span>]] <br>
❑ [[Creatinine|<span style="color:white;">Creatinine</span>]] <br>
❑ [[Sodium|<span style="color:white;">Sodium</span>]] (to detect [[hyponatremia|<span style="color:white;">hyponatremia</span>]] which carries a poor prognosis), [[chloride|<span style="color:white;">chloride</span>]], [[bicarbonate|<span style="color:white;">bicarbonate</span>]] (to detect [[contraction alkalosis|<span style="color:white;">contraction alkalosis</span>]]) and serum potassium (to detect [[hypokalemia|<span style="color:white;">hypokalemia</span>]] as a result of diuresis and which can precipitate [[arrhythmia|<span style="color:white;">arrhythmias</span>]]), [[potassium|<span style="color:white;">potassium</span>]], [[magnesium|<span style="color:white;">magnesium</span>]] <br>
 
'''Management of hyponatremia:''' <br>
❑ Water restriction <br>
:❑ <2 L/day if the Na is < 130 meq/L
:❑ < 1 L/day or more if the Na is < 125 meq/L
: ''Keep in min that juices are essentially free water with sugar.''
: ''In the [[hyponatremia|<span style="color:white;">hyponatremia</span>]] patient, drips should not be in D5W.''
❑ Optimization of chronic home medications <br>
❑ Persistent [[hyponatremia|<span style="color:white;">hyponatremia</span>]] and risk of cognitive impairment: vasopressin antagonist for short term (hypervolemic) </div>}}
{{familytree/end}}
 
==Complete Diagnostic Approach==
A complete diagnostic approach should be carried out after a focused initial rapid evaluation is conducted and following initiation of any urgent intervention.<ref name="pmid23741057">{{cite journal| author=Yancy CW, Jessup M, Bozkurt B, Butler J, Casey DE, Drazner MH et al.| title=2013 ACCF/AHA guideline for the management of heart failure: executive summary: a report of the American College of Cardiology Foundation/American Heart Association Task Force on practice guidelines. | journal=Circulation | year= 2013 | volume= 128 | issue= 16 | pages= 1810-52 | pmid=23741057 | doi=10.1161/CIR.0b013e31829e8807 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23741057  }} </ref><ref name="pmid19358937">{{cite journal| author=Hunt SA, Abraham WT, Chin MH, Feldman AM, Francis GS, Ganiats TG et al.| title=2009 Focused update incorporated into the ACC/AHA 2005 Guidelines for the Diagnosis and Management of Heart Failure in Adults A Report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines Developed in Collaboration With the International Society for Heart and Lung Transplantation. | journal=J Am Coll Cardiol | year= 2009 | volume= 53 | issue= 15 | pages= e1-e90 | pmid=19358937 | doi=10.1016/j.jacc.2008.11.013 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=19358937  }} </ref>
 
<span style="font-size:85%">'''Abbreviations:'''
'''ANA:''' [[Antinuclear antibody]];
'''ARDS:''' [[Acute respiratory distress syndrome]];
'''BNP:''' [[B-type natriuretic peptide]];
'''BUN:''' [[Blood urea nitrogen]];
'''CAD:''' [[Coronary artery disease]];
'''CBC:''' [[Complete blood count]];
'''CCB:''' [[Calcium channel blocker]];
'''CHF:''' [[Congestive heart failure]];
'''CT:''' [[Computed tomography]];
'''CXR:''' [[Chest X-ray]];
'''DM:''' [[Diabetes mellitus]];
'''ECG:''' [[Electrocardiogram]];
'''JVP:''' [[Jugular venous pressure]];
'''HF:''' [[Heart failure]];
'''HTN:''' [[Hypertension]];
'''LVEF:''' [[Left ventricular ejection fraction]];
'''LVH:''' [[Left ventricular hypertrophy]];
'''MI:''' [[Myocardial infarction]];
'''MRI:''' [[Magnetic resonance imaging]];
'''NT-pro BNP:''' [[N-terminal pro-brain natriuretic peptide]];
'''OCPs:''' [[Oral contraceptive pill]]s;
'''PAWP:''' [[Pulmonary capillary wedge pressure|Pulmonary artery wedge pressure]];
'''SBP:''' [[Systolic blood pressure]];
'''S1:''' [[First heart sound]];
'''S3:''' [[Third heart sound]];
'''TSH:''' [[Thyroid stimulating hormone]]
</span>
<br>
 
{{familytree/start}}
{{familytree | | | | | | | | A01 | | |A01=<div style="float: left; text-align: left; width: 30em; padding:1em;"> '''Characterize the symptoms:'''<br>
''Symptoms of left-sided fluid accumulation:''<br>
❑ [[Dyspnea]]<br>
:❑ At rest<br>
:❑ Exertional<br>
❑ [[Paroxysmal nocturnal dyspnea]]<br>
❑ [[Orthopnea]]<br>
❑ [[Cough]]<br>
''Symptoms of right-sided fluid accumulation:''<br>
❑ [[Peripheral edema]]<br>
❑ Right upper quadrant abdominal discomfort<br>
❑ [[Bloating]]<br>
❑ [[Satiety]]<br>
''Symptoms of reduced cardiac output:''<br>
❑ [[Fatigue]]<br>
❑ [[Exercise intolerance]]<br>
❑ [[Oliguria]]<br>
❑ [[Dizziness]]<br>
❑ [[Syncope]]<br>
❑ [[Altered mental status]]<br>
❑ [[Cyanosis]]<br>
❑ [[Anorexia]]<br>
❑ [[Abdominal pain]] (suggestive of [[mesenteric ischemia]])<br>
''Symptoms suggestive of precipitating events:''<br>
❑ [[Chest pain]] (suggestive of [[coronary heart disease|myocardial ischemia]])<br>
❑ [[Palpitations]] (suggestive of [[arrhythmia]]s)<br>
❑ [[Fever]] (suggestive of [[infection]])<br>
''Nonspecific symptoms:''<br>
❑ [[Nausea]]<br>
❑ [[Weight loss]]<br>
----
'''Obtain a detailed history:'''<br>
❑ '''Past medical history'''<br>
:❑ [[Atrial fibrillation]]<br>
:❑ [[Cardiomyopathy]]<br>
:❑ [[Diabetes mellitus]]<br>
:❑ [[Hypertension]]<br>
:❑ [[Myocarditis]]<br>
:❑ [[myocardial infarction|Previous myocardial infarction]]<br>
:❑ [[Congestive heart failure|Prior heart failure]]<br>
:❑ [[Sleep apnea]]<br>
:❑ [[Thyroid disease]]<br>
:❑ [[Valvular heart disease]]<br>
❑ '''Medication history'''<br>
:❑ Noncompliance with previously prescribed medications for [[heart failure]]<br>
:❑ Intake of the following drugs:<br>
::❑ [[Alcohol]]<br>
::❑ [[Beta blockers]]<br>
::❑ [[Calcium channel blockers]] like [[verapamil]] which can exacerbate CHF or [[diltiazem]] which can cause [[peripheral edema]]<br>
::❑ [[Chemotherapy]] drugs - [[anthracyclines]]<br>
::❑ [[NSAID]]s which should not be given in CHF<br>
::❑ [[Thiazolidinedione]]<br>
❑ '''Family history'''<br>
:❑ History of [[dilated cardiomyopathy]]<br>
:❑ [[Radiation]] to the chest
----
'''Determine the [[Heart failure resident survival guide#Classification by Severity of Congestive Heart Failure|NYHA classification]] based on symptoms:''' <br>
❑ Class I (no symptoms) <br>
❑ Class II (symptoms with ordinary activities) <br>
❑ Class III (symptoms upon minimal activity) <br>
❑ Class IV (symptoms at rest)
</div>}}
{{familytree | | | | | | | | |!| | | | |}}
{{familytree | | | | | | | | B01 | | | |B01=<div style="float: left; text-align: left; width: 25em; padding:1em;"> '''Examine the patient:'''<br>
'''General appearance:'''<br>
❑ Ill-looking<br>
❑ In respiratory distress<br>
❑ In upright sitting position<br>
 
'''Vitals:'''<br>
❑ [[Temperature]]<br>
:❑ [[Fever]] (suggestive of underlying [[infection]])<br>
❑ [[Pulse]]<br>
:❑ [[Tachycardia]]<br>
:❑ [[Pulse pressure#Narrowed Pulse Pressure causes|Narrow pulse pressure]] (<25% of SBP)<br>
❑ [[Blood pressure]]<br>
:❑ [[Hypotension]] (suggestive of circulatory collapse)<br>
:❑ [[Hypertension]]  <br>
❑ [[Respiration]]<br> 
:❑ [[Tachypnea]] (most common symptom)<br>
❑ [[Pulse oximetry]] (maintain oxygen sat ≥ 94% unless COPD)<br>
 
'''Weight:'''<br>
❑ Measure weight daily at the same time after the first void<br>
❑ Subtract 'dry weight' from current weight to estimate extent of volume overload and [[edema]]<br>
 
'''Skin'''<br>
❑ [[Cool extremities|Cool and clammy]] (suggestive of hypoperfusion)<br>
❑ [[Cyanosis]] (suggestive of severe [[hypoxemia]])<br>
❑ [[Anasarca]]<br>
❑ [[Jaundice]] (suggestive of liver dysfunction secondary to right-sided fluid overload)<br>


===Common Causes===
'''Neck examination:'''<br>
❑ [[Jugular vein distention]] (suggestive of right-sided fluid overload)<br>
❑ Positive [[hepatojugular reflux]] (suggestive of right-sided fluid overload)<br>


* [[Accelerated hypertension]]
'''Respiratory examination'''<br>
* [[Acute kidney injury]]
[[Tachypnea]]<br>
* [[Acute myocardial ischemia]]
[[Wheeze]]<br>
* Acute or progressive valvular disease (e.g. acute [[mitral regurgitation]])
❑ Dullness at lung bases (suggestive of [[pleural effusion]], may be present in chronic HF secondary to lymphatic compensation)<br>
* [[Cardiac arrhythmias]]
[[Crackles]]/[[crepitations]]/[[rales]] (suggestive of [[pleural effusion]])<br>
*  Excessive [[alcohol]] or illicit drug use  (e.g. [[cocaine]])
[[Cheyne-stokes respiration]]<br>
* [[Myocardial ischemia]] (e.g. [[AF]])
* [[Pulmonary embolus]]
* [[Sepsis|Systemic Inflammatory response syndrome]]


==Management==
'''Cardiovascular examination'''<br>
❑ Displaced [[apex beat]] (suggestive of enlarged [[left ventricle]])<br>
❑ [[Parasternal heave]] (suggestive of elevated right ventricular pressure)<br>
❑ [[Heart sounds#Third heart sound S3|S3]] (typical) or [[Heart sounds#Fourth heart sound S4|S4]] or both<br>
❑ Soft S1 <br>
❑ Pulsus alternans <br>
❑ [[S4]] (suggestive of [[diastolic]] dysfunction) <br>
❑ New or changed [[murmur]] (suggestive of an underlying [[valvular heart disease]]s)<br>
:❑ [[Mitral regurgitation]] - [[Systolic heart murmur#Holosystolic (pansystolic)|Holosystolic murmur]]<br>
:❑ [[Aortic regurgitation]] - [[Diastolic heart murmur#Individual murmurs|Decrescendo diastolic murmur]]<br>
:❑ [[Aortic stenosis]] - Crescendo-decrescendo systolic ejection murmur with ejection click<br>


*Figure 1: Approach to patients presenting with acutely decompensated [[HF]].
'''Abdominal examination'''<br>
The following findings suggest volume overload and / or poor forward cardiac output:<br>
[[Hepatojugular reflux]]<br>
❑ [[Hepatomegaly]]<br>
❑ [[Ascites]]<br>


{{familytree/start |summary=Acute HF Algorithm.}}
'''Extremity examination'''<br>
{{familytree | | | | | | | | | A01 | | | | | |A01=* Focused history (e.g. [[dyspnea]], <BR> [[orthopnea]], [[edema]],<br>altered mentation<BR> Hx of [[HF]], Hx of drug abuse)<br>* [[Vital signs]] <br>* Physical exam [e.g. assess volume status (e.g. rales, edema, JVD) and perfusion (e.g. narrow pulse pressure, cold extremities) ]<br>* Initial labs to include <BR> [[B-type natriuretic peptide|BNP]] and [[troponin|troponins]]<br> * [[Congestive heart failure electrocardiogram|EKG]]<br> *[[Congestive heart failure chest x ray|Chest X-ray]]<ref name="pmid16476871">{{cite journal| author=Januzzi JL, Sakhuja R, O'donoghue M, Baggish AL, Anwaruddin S, Chae CU et al.| title=Utility of amino-terminal pro-brain natriuretic peptide testing for prediction of 1-year mortality in patients with dyspnea treated in the emergency department. | journal=Arch Intern Med | year= 2006 |volume= 166 | issue= 3 | pages= 315-20 | pmid=16476871 | doi=10.1001/archinte.166.3.315 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16476871  }} </ref><ref name="pmid11216950">{{cite journal| author=Dao Q, Krishnaswamy P, Kazanegra R, Harrison A, Amirnovin R, Lenert L et al.| title=Utility of B-type natriuretic peptide in the diagnosis of congestive heart failure in an urgent-care setting. | journal=J Am Coll Cardiol | year= 2001 | volume= 37 | issue= 2 | pages= 379-85 | pmid=11216950 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11216950  }} </ref><ref name="pmid14960741">{{cite journal| author=Mueller C, Scholer A, Laule-Kilian K, Martina B, Schindler C, Buser P et al.| title=Use of B-type natriuretic peptide in the evaluation and management of acute dyspnea. | journal=N Engl J Med | year= 2004 |volume= 350 | issue= 7 | pages= 647-54 | pmid=14960741 | doi=10.1056/NEJMoa031681 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=14960741  }}  [http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=15341455 Review in: ACP J Club. 2004 Sep-Oct;141(2):35] </ref><ref name="pmid16860029">{{cite journal| author=van Kimmenade RR, Pinto YM, Bayes-Genis A, Lainchbury JG, Richards AM, Januzzi JL| title=Usefulness of intermediate amino-terminal pro-brain natriuretic peptide concentrations for diagnosis and prognosis of acute heart failure. | journal=Am J Cardiol | year= 2006 | volume= 98 | issue= 3 | pages= 386-90 | pmid=16860029 |doi=10.1016/j.amjcard.2006.02.043 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16860029  }} </ref><ref name="pmid15451800">{{cite journal| author=Bettencourt P, Azevedo A, Pimenta J, Friões F, Ferreira S, Ferreira A| title=N-terminal-pro-brain natriuretic peptide predicts outcome after hospital discharge in heart failure patients. |journal=Circulation | year= 2004 | volume= 110 | issue= 15 | pages= 2168-74 | pmid=15451800 | doi=10.1161/01.CIR.0000144310.04433.BE | pmc= |url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=15451800  }} </ref><ref name="pmid22665814">{{cite journal| author=Lee DS, Stitt A, Austin PC, Stukel TA, Schull MJ, Chong A et al.| title=Prediction of heart failure mortality in emergent care: a cohort study. | journal=Ann Intern Med | year= 2012 | volume= 156 | issue= 11 | pages= 767-75, W-261, W-262 | pmid=22665814 |doi=10.7326/0003-4819-156-11-201206050-00003 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22665814  }} </ref>}}
[[Pedal edema]]<br>
{{familytree | | | | | | | | | |!| | | | | |}}
{{familytree | | | | | | | | | A01 | | | | | |A01=*Non-invasive monitoring (SaO2, BP, temperature)+ Oxygen therapy}}
{{familytree | | |,|-|-|-|-|-|-|+|-|-|-|-|-|-|-|.}}
{{familytree | | B01 | | | | | B02 | | | | | B03 |B01=Patient is in [[shock]] or [[respiratory failure]]; <br>Address emergently <BR> (e.g. intubate, IV inotropes (e.g.dobutamine 2-20mcg/kg/min IV), ICU)|B02=Hemodynamically stable acute [[HF]]<br> (Data exist to support early and aggressive treatment in the first 6–12 hrs may result in more favorable outcomes) <ref name="pmid18158472">{{cite journal |author=Mebazaa A, Gheorghiade M, Piña IL, Harjola VP, Hollenberg SM, Follath F, Rhodes A, Plaisance P, Roland E, Nieminen M, Komajda M, Parkhomenko A, Masip J, Zannad F, Filippatos G |title=Practical recommendations for prehospital and early in-hospital management of patients presenting with acute heart failure syndromes |journal=[[Critical Care Medicine]] |volume=36|issue=1 Suppl |pages=S129–39 |year=2008 |month=January |pmid=18158472 |doi=10.1097/01.CCM.0000296274.51933.4C|url=http://meta.wkhealth.com/pt/pt-core/template-journal/lwwgateway/media/landingpage.htm?issn=0090-3493&volume=36&issue=1&spage=S129 |accessdate=2012-04-06}}</ref>|B03=Accelerated [[HTN]];<br> IV vasoactive therapy (e.g. IV Enalaprilat 0.625-1.25mg or IV NTG drip 5mcg/min)<ref name="pmid17643575">{{cite journal |author=Costanzo MR, Johannes RS, Pine M, Gupta V, Saltzberg M, Hay J, Yancy CW, Fonarow GC |title=The safety of intravenous diuretics alone versus diuretics plus parenteral vasoactive therapies in hospitalized patients with acutely decompensated heart failure: a propensity score and instrumental variable analysis using the Acutely Decompensated Heart Failure National Registry (ADHERE) database |journal=[[American Heart Journal]] |volume=154 |issue=2 |pages=267–77|year=2007 |month=August |pmid=17643575 |doi=10.1016/j.ahj.2007.04.033 |url=http://linkinghub.elsevier.com/retrieve/pii/S0002-8703(07)00357-2|accessdate=2012-04-06}}</ref><ref name="pmid18158472">{{cite journal |author=Mebazaa A, Gheorghiade M, Piña IL, Harjola VP, Hollenberg SM, Follath F, Rhodes A, Plaisance P, Roland E, Nieminen M, Komajda M, Parkhomenko A, Masip J, Zannad F, Filippatos G |title=Practical recommendations for prehospital and early in-hospital management of patients presenting with acute heart failure syndromes |journal=[[Critical Care Medicine]] |volume=36|issue=1 Suppl |pages=S129–39 |year=2008 |month=January |pmid=18158472 |doi=10.1097/01.CCM.0000296274.51933.4C|url=http://meta.wkhealth.com/pt/pt-core/template-journal/lwwgateway/media/landingpage.htm?issn=0090-3493&volume=36&issue=1&spage=S129 |accessdate=2012-04-06}}</ref><ref name="pmid17408803">{{cite journal |author=Silvers SM, Howell JM, Kosowsky JM, Rokos IC, Jagoda AS |title=Clinical policy: Critical issues in the evaluation and management of adult patients presenting to the emergency department with acute heart failure syndromes |journal=[[Annals of Emergency Medicine]] |volume=49 |issue=5 |pages=627–69 |year=2007 |month=May |pmid=17408803 |doi=10.1016/j.annemergmed.2006.10.024|url=http://linkinghub.elsevier.com/retrieve/pii/S0196-0644(06)02461-9 |accessdate=2012-04-06}}</ref>}}
{{familytree | | | | | | | | | |!| | | | | | | | }}
{{familytree | |,|-|-|-|v|-|-|-|+|-|-|-|v|-|-|-|.| | }}
{{familytree | |!| | | |!| | | |!| | | |!| | | |!| | | }}
{{familytree | C01 | | C02 | | C03 | | C04 | | |C05 |C01=[[Acute myocardial ischemia]]|C02=[[Atrial fibrillation]]|C03=No precipitating factors identified|C04= Renal injury|C05=Other etiologies (e.g. sepsis or pulmonary embolus)}}
{{familytree | |!| | | |!| | | |!| | | |!| | | |!| }}
{{familytree | D01 | | D02 | | |!| | |D04| | |D05 |D01=[[Nitrates]], [[beta blockers]],[[anticoagulation]], [[antiplatelets]] (e.g. aspirin 325mg stat+clopidogrel 300mg stat)<br>Urgent [[revascularization]]<br>Refer to [[Acute coronary syndrome resident survival guide]]
|D02=Beta blockers; anticoagulation<ref name="pmid21870978">{{cite journal| author=Granger CB, Alexander JH, McMurray JJ, Lopes RD, Hylek EM, Hanna M et al.| title=Apixaban versus warfarin in patients with atrial fibrillation. | journal=N Engl J Med | year= 2011 | volume= 365 | issue= 11 | pages= 981-92 | pmid=21870978 | doi=10.1056/NEJMoa1107039 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21870978  }}  [http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22250164 Review in: Ann Intern Med. 2012 Jan 17;156(2):JC1-2, JC1-3] </ref><ref name="pmid21830957">{{cite journal| author=Patel MR, Mahaffey KW, Garg J, Pan G, Singer DE, Hacke W et al.| title=Rivaroxaban versus warfarin in nonvalvular atrial fibrillation. | journal=N Engl J Med | year= 2011 | volume= 365 | issue= 10 | pages= 883-91 | pmid=21830957 | doi=10.1056/NEJMoa1009638 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21830957  }}  [http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22345038 Review in: Evid Based Med. 2012 Oct;17(5):148-9] [http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22250165 Review in: Ann Intern Med. 2012 Jan 17;156(2):JC1-2, JC1-3] </ref> (e.g. enoxaparin 1mg/kg sc stat)<br>Refer to [[atrial fibrillation resident survival guide]]|D04=Hydral-nitrates<ref>Carson P, Ziesche S, Johnson G, et al., for the Vasodilator-Heart Failure Trial Study Group. Racial differences in response to therapy for heart failure: analysis of the vasodilator-heart failure trials. J Card Fail. 1999;5:178–87.</ref><ref>Cohn JN. The Vasodilator-Heart Failure Trials (V-HeFT). Mechanistic data from the VA Cooperative Studies. Introduction. Circulation. 1993; 87:VI1–4.</ref><ref>Carson P, Ziesche S, Johnson G, et al., for the Vasodilator-Heart Failure Trial Study Group. Racial differences in response to therapy for heart failure: analysis of the vasodilator-heart failure trials. J Card Fail.


1999;5:178–87.</ref><ref>Cohn JN, Archibald DG, Ziesche S, et al. Effect of vasodilator therapy on mortality in chronic congestive heart failure. Results of a Veterans Administration Cooperative Study. N Engl J Med. 1986;314:1547–52.</ref><ref>Loeb HS, Johnson G, Henrick A, et al., for the V-HeFT VA Cooperative Studies Group. Effect of enalapril, hydralazine plus isosorbide dinitrate, and prazosin on hospitalization in patients with chronic congestive heart failure. Circulation. 1993;87:VI78–87.</ref>  
'''Neurological examination'''<br>
<br>Avoid combining ACEIs, ARBs, aldosterone blockers|D05=Refer to resident survival guide for [[Sepsis resident survival guide|sepsis]] or [[pulmonary embolism resident survival guide|pulmonary embolus]] or otherwise.}}
❑ [[Altered mental status]]<br>
{{familytree | | | | | | | | | |!| | | | | | | | | }}
❑ [[Syncope]] (suggestive of [[aortic stenosis]] or [[pulmonary embolism]])
{{familytree | |,|-|-|-|v|-|-|-|+|-|-|-|-|-|-|-|.| | }}
-----
{{familytree | |!| | | |!| | | |!| | | | | | | |!| | | }}
'''Determine status of congestion and perfusion based on physical exam:'''<br>
{{familytree | E01 | | E02 | | E03 | | | | | |E04 |E01=Presence of congestion<br>Poor perfusion<br>(i.e. wet&cold)|E02=NO congestion<br>Poor perfusion<br>(i.e. dry&cold)|E03=Presence of congestion<br>Normal perfusion <br>(i.e. wet&warm)|E04=NO congestion<br>Normal perfusion <br>(i.e. dry&warm)}}
''Congestion at rest (dry vs. wet)'' <br>
{{familytree | |!| | | |!| | | |!| | | | | | ||!| | | }}
:"Wet" suggested by orthopnea, ↑JVP, positive hepatojugular reflux, abnormal valsalva response, rales, dullness upon percussion in bases, S3, peripheral edema, hepatomegaly, ascites, jaundice <br>
{{familytree | F01 | | F02 | | F03 | | | | | |F04 |F01=* Rapid intervention<br>* [[Loop diuretics]] (e.g. furosemide 0.1mg/kg IV once, then double dose Q2h as needed) <br>* Consider invasive hemodynamic monitoring (Central or arterial line)<br>* Intravenous inotropic drugs (e.g.dobutamine 2-20mcg/kg/min IV)|F02=* Hydralazine+nitrate [[Bp]] permitting<br>* Intravenous inotropic drugs (e.g.dobutamine 2-20mcg/kg/min IV)|F03=Salt restriction<br> * Continue [[GDMT]]<br> * Early [[loop diuretics]]<ref name="pmid18158472">{{cite journal |author=Mebazaa A, Gheorghiade M, Piña IL, Harjola VP, Hollenberg SM, Follath F, Rhodes A, Plaisance P, Roland E, Nieminen M, Komajda M, Parkhomenko A, Masip J, Zannad F, Filippatos G |title=Practical recommendations for prehospital and early in-hospital management of patients presenting with acute heart failure syndromes |journal=[[Critical Care Medicine]] |volume=36 |issue=1 Suppl |pages=S129–39 |year=2008 |month=January |pmid=18158472 |doi=10.1097/01.CCM.0000296274.51933.4C |url=http://meta.wkhealth.com/pt/pt-core/template-journal/lwwgateway/media/landingpage.htm?issn=0090-3493&volume=36&issue=1&spage=S129 |accessdate=2012-04-06}}</ref><ref name="pmid17643575">{{cite journal |author=Costanzo MR, Johannes RS, Pine M, Gupta V, Saltzberg M, Hay J, Yancy CW, Fonarow GC |title=The safety of intravenous diuretics alone versus diuretics plus parenteral vasoactive therapies in hospitalized patients with acutely decompensated heart failure: a propensity score and instrumental variable analysis using the Acutely Decompensated Heart Failure National Registry (ADHERE) database |journal=[[American Heart Journal]] |volume=154 |issue=2 |pages=267–77 |year=2007 |month=August |pmid=17643575 |doi=10.1016/j.ahj.2007.04.033 |url=http://linkinghub.elsevier.com/retrieve/pii/S0002-8703(07)00357-2 |accessdate=2012-04-06}}</ref><ref name="pmid17408803">{{cite journal |author=Silvers SM, Howell JM, Kosowsky JM, Rokos IC, Jagoda AS |title=Clinical policy: Critical issues in the evaluation and management of adult patients presenting to the emergency department with acute heart failure syndromes |journal=[[Annals of Emergency Medicine]] |volume=49 |issue=5 |pages=627–69 |year=2007 |month=May |pmid=17408803 |doi=10.1016/j.annemergmed.2006.10.024 |url=http://linkinghub.elsevier.com/retrieve/pii/S0196-0644(06)02461-9 |accessdate=2012-04-06}}</ref><br>* Consider ultrafiltration for refractory congestion<ref name="pmid17291932">{{cite journal |author=Costanzo MR, Guglin ME, Saltzberg MT, Jessup ML, Bart BA, Teerlink JR, Jaski BE, Fang JC, Feller ED, Haas GJ, Anderson AS, Schollmeyer MP, Sobotka PA |title=Ultrafiltration versus intravenous diuretics for patients hospitalized for acute decompensated heart failure |journal=[[Journal of the American College of Cardiology]] |volume=49 |issue=6 |pages=675–83 |year=2007 |month=February |pmid=17291932 |doi=10.1016/j.jacc.2006.07.073 |url=http://linkinghub.elsevier.com/retrieve/pii/S0735-1097(06)02889-0 |accessdate=2012-04-06}}</ref>|F04=* Continue [[GDMT]]<ref>pmid17581778">{{cite journal |author=Metra M, Torp-Pedersen C, Cleland JG, Di Lenarda A, Komajda M, Remme WJ, Dei Cas L, Spark P, Swedberg K, Poole-Wilson PA |title=Should beta-blocker therapy be reduced or withdrawn after an episode of decompensated heart failure? Results from COMET |journal=[[European Journal of Heart Failure]] |volume=9 |issue=9 |pages=901–9 |year=2007 |month=September |pmid=17581778|doi=10.1016/j.ejheart.2007.05.011 |url=http://eurjhf.oxfordjournals.org/cgi/pmidlookup?view=long&pmid=17581778 |accessdate=2012-04-06}}</ref><ref name="pmid18617067">{{cite journal |author=Fonarow GC, Abraham WT, Albert NM, Stough WG, Gheorghiade M, Greenberg BH, O'Connor CM, Sun JL, Yancy CW, Young JB|title=Influence of beta-blocker continuation or withdrawal on outcomes in patients hospitalized with heart failure: findings from the OPTIMIZE-HF program|journal=[[Journal of the American College of Cardiology]] |volume=52 |issue=3 |pages=190–9 |year=2008 |month=July |pmid=18617067 |doi=10.1016/j.jacc.2008.03.048|url=http://linkinghub.elsevier.com/retrieve/pii/S0735-1097(08)01503-9 |accessdate=2012-04-06}}</ref><ref name="pmid16781374">{{cite journal| author=Butler J, Young JB, Abraham WT, Bourge RC, Adams KF, Clare R et al.| title=Beta-blocker use and outcomes among hospitalized heart failure patients. | journal=J Am Coll Cardiol | year= 2006 |volume= 47 | issue= 12 | pages= 2462-9 | pmid=16781374 | doi=10.1016/j.jacc.2006.03.030 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16781374  }} </ref> <br>* Continue evidence-based [[beta-blockers]] ( i.e., bisoprolol, carvedilol, and sustained release metoprolol succinate)<ref name="pmid17581778">{{cite journal |author=Metra M, Torp-Pedersen C, Cleland JG, Di Lenarda A, Komajda M, Remme WJ, Dei Cas L, Spark P, Swedberg K, Poole-Wilson PA |title=Should beta-blocker therapy be reduced or withdrawn after an episode of decompensated heart failure? Results from COMET |journal=[[European Journal of Heart Failure]] |volume=9 |issue=9 |pages=901–9 |year=2007 |month=September |pmid=17581778 |doi=10.1016/j.ejheart.2007.05.011 |url=http://eurjhf.oxfordjournals.org/cgi/pmidlookup?view=long&pmid=17581778 |accessdate=2012-04-06}}</ref>}}
''Low perfusion at rest (warm vs. cold)'' <br>
:"Cold" suggested by narrow pulse pressure, cool extremities, hypotension, soft S1, pulsus alternans, decreased urinary output <br>
The patient is: <br>
❑ Warm and dry, OR <br>
❑ Warm and wet, OR <br>
❑ Cold and dry, OR <br>
❑ Cold and wet
</div>}}
{{familytree | | | | | | | | |!| | | | | |}}
{{familytree | | | | | | | | D01 | | | |D01=<div style="float: left; text-align: left; width: 25em; padding:1em;">'''Order tests''': <br>
'''Routine''' ([[ACC AHA guidelines classification scheme|Class I, level of evidence C]])<br>
:❑ [[Complete blood count|CBC]] (rule out [[anemia]])  <br>
:❑ [[Troponin]]
::❑ Elevated in [[myocardial ischemia]] and acute cardiogenic pulmonary edema, particularly if [[creatinine clearance|creatinine clearance (CrCl)]] is reduced<br>
::❑ [[Troponin|Troponin T]] ≥ 0.1 ng/mL (associated with poor survival)<ref name="Perna-2002">{{Cite journal  | last1 = Perna | first1 = ER. | last2 = Macín | first2 = SM. | last3 = Parras | first3 = JI. | last4 = Pantich | first4 = R. | last5 = Farías | first5 = EF. | last6 = Badaracco | first6 = JR. | last7 = Jantus | first7 = E. | last8 = Medina | first8 = F. | last9 = Brizuela | first9 = M. | title = Cardiac troponin T levels are associated with poor short- and long-term prognosis in patients with acute cardiogenic pulmonary edema. | journal = Am Heart J | volume = 143 | issue = 5 | pages = 814-20 | month = May | year = 2002 | doi =  | PMID = 12040342 }}</ref>
:❑ [[Electrolytes]]<br>
::❑ [[Sodium]]: [[hyponatremia]] may occur due to fluid overlaod
:❑ [[calcium|Serum calcium]]<br>
:❑ [[Magnesium|Serum magnesium]] can be lowered by [[diuresis]]<br>
:❑ [[Serum bicarbonate]]: to monitor [[contraction alkalosis]] with [[diuresis]]
:❑ [[BUN]], [[creatinine]]: may be elevated due to poor renal perfusion<br>
:❑ [[Urinalysis]] <br>
:❑ [[Blood sugar|Fasting blood sugar]]<br>
:❑ [[Lipid profile|Fasting lipid profile]]<br>
:❑ [[Liver function tests]]: can be elevated secondary to peripheral hypoperfusion<br>
:❑ [[Thyroid-stimulating hormone|TSH]]<br>
❑ [[B-type natriuretic peptide|BNP]] or NT-pro BNP (if diagnosis is uncertain)<br>
Heart failure is unlikely if:<ref name="pmid22611136">{{cite journal| author=McMurray JJ, Adamopoulos S, Anker SD, Auricchio A, Böhm M, Dickstein K et al.| title=ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure 2012: The Task Force for the Diagnosis and Treatment of Acute and Chronic Heart Failure 2012 of the European Society of Cardiology. Developed in collaboration with the Heart Failure Association (HFA) of the ESC. | journal=Eur Heart J | year= 2012 | volume= 33 | issue= 14 | pages= 1787-847 | pmid=22611136 | doi=10.1093/eurheartj/ehs104 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22611136  }} </ref><ref name="pmid16638247">{{cite journal| author=Fuat A, Murphy JJ, Hungin AP, Curry J, Mehrzad AA, Hetherington A et al.| title=The diagnostic accuracy and utility of a B-type natriuretic peptide test in a community population of patients with suspected heart failure. | journal=Br J Gen Pract | year= 2006 | volume= 56 | issue= 526 | pages= 327-33 | pmid=16638247 | doi= | pmc=PMC1837840 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16638247  }} </ref> <br>
:❑ [[B-type natriuretic peptide|BNP]] ≤ 100 pg/mL, or<br>
:❑ [[NT-pro BNP]] ≤ 300 pg/mL <br>
❑ [[Chest X-ray]] ([[ACC AHA guidelines classification scheme|Class I, level of evidence C]])<br>
:❑ [[Cardiomegaly]] ([[cardiothoracic ratio]] >50%)<br>
:❑ Cardiogenic [[pulmonary edema]]<br>
:❑ [[Kerley B lines]]<br>
:❑ [[Peribronchial cuffing]]<br>
:❑ [[Congestive heart failure chest x ray#Cephalization|Cephalization]]
[[Image:Pulmonary edema.gif|center|200px|thumb|Chest X-ray findings in a patient with acute heart failure ]]<br>
[[ECG]] (to help identify the cause of heart failure)<br>
:❑ [[Low QRS voltage]] (suggestive of infiltrative or [[dilated cardiomyopathy]])<br>
:❑ [[Arrhythmia]] ([[atrial fibrillation]] carries a poor prognosis and requires slowing of the heart rate to improve filling & [[cardiac output]])<br>
:❑ [[Poor R wave progression]] (suggestive of a prior [[MI]])<br>
:❑ [[Left ventricular hypertrophy]] (consistent with a history of [[hypertension]])<br>
:❑ [[Left bundle branch block]] ([[LBBB]]) due to prior [[MI]], may result in dysynchrony)<br>
:❑ [[Left atrial enlargement]] (due to [[valvular disease]] or [[hypertension]])<br>
:❑ Non-specific [[ST segment]] and [[T wave]] changes may suggest [[ischemia]]<br>
❑ 2-D [[echocardiography]] with Doppler <br> ([[ACC AHA guidelines classification scheme|Class I, level of evidence C]])
:❑ Assess chambers size, wall thickness, wall motion, and valve function<br>
:❑ Assess [[ejection fraction]]
❑ [[Cardiac radionuclide imaging|Radionuclide ventriculography]] or [[MRI]]<br>
:❑ To assess [[LVEF]] and volume when [[echocardiography]] is inadequate<br>
:❑ To assess myocardial infiltrative processes or scar burden ([[MRI]])<br>
❑ [[Coronary angiography]] looking for CAD<br>
❑ Comprehensive metabolic panel if no evidence of CAD on coronary angiography <br>
❑ Consider [[Right heart catheterization|pulmonary artery catheterization]] in case of failure to respond to medical therapy, [[respiratory distress]], [[shock]], uncertainty regarding volume status, or increase in creatinine; assess the following parameters:<br>
:❑ [[PCWP]]
:❑ [[Cardiac output]]
:❑ [[Systemic vascular resistance]]
----
'''Order additional tests to rule out other etiologies:'''<br>
❑ [[Antinuclear antibodies|ANA]] and [[rheumatoid factor]] (for rheumatologic diseases)<br>
❑ Diagnostic tests for [[hemochromatosis]] and [[pheochromocytoma]]<br>
❑ [[Endomyocardial biopsy]] (when [[myocarditis]] is suspected)
</div>}}
{{familytree | | | | | | | | |!| |}}
{{familytree | | | | | | | | W01 | |W01=<div style="float: left; text-align: left; width: 25em; padding:1em;">'''Consider alternative diagnoses:'''<br>
----
<table class="wikitable">
<tr class="v-firstrow"><th>Alternative diagnoses</th><th>Features</th></tr>
<tr><td> [[Asthma|Acute asthma]]</td><td>❑ [[Wheeze]]<br>❑ Reversal of symptoms following<br> administration of [[bronchodilator]]s</td></tr>
<tr><td> [[COPD]]</td><td>❑ Increased [[cough]]<br>❑ Increased [[dyspnea]]<br>❑ Increased [[sputum]] production </td></tr>
<tr><td> [[Acute respiratory distress syndrome|ARDS]]</td><td>❑ Severe [[hypoxia]]<br>❑ Bilateral opacities on [[chest X-ray]]<br>❑ [[Pulmonary capillary wedge pressure|PCWP]] < 15 mmHg</td></tr>
<tr><td> [[Pneumonia]]</td><td>❑ [[Fever]], [[cough]], [[sputum]]<br>❑ [[Pneumonia chest x ray|Consolidation]] on [[chest X-ray]]</td></tr>
<tr><td> [[Pulmonary embolism]]</td><td>❑ [[Pleurisy|Pleuritic chest pain]], [[cough]], [[Heart sounds#Fourth heart sound S4|S4]]<br>❑ Risk factors: trauma, immobilization, smoking, OCPs <br>❑ Clot in pulmonary artery on [[Pulmonary embolism CT pulmonary angiography|CT pulmonary angiography]] </td></tr>
</table></div>}}
{{familytree | | | | | | | | |!| | |}}
{{familytree | | | | | | | | Z01 | | |Z01=<div style="float: left; text-align: left; width: 25em; padding:1em;">'''Assess the stage of heart failure using the [[Acute heart failure resident survival guide#Classification|ACCF/AHA staging system]] to guide chronic therapy'''
</div>}}
{{familytree | | | | | | |,|-|^|-|.| | | | | |}}
{{familytree | | | | | | X01 | | X02 | | | |X01=<div style="float: left; text-align: left; width: 20em; padding:1em;">'''[[Acute heart failure resident survival guide#Prevention of Heart Failure|Stage C]]''' <br> <br>
❑ '''Patients with structural heart disease'''<br>
This refers to patients with the following:<br>
:❑ Previous [[MI]]<br>
:❑ LV remodeling* (including [[ LVH]] + low [[EF]])<br>
:❑ Asymptomatic [[valvular disease]]<br><br>'''AND'''<br>
❑ '''Signs or symptoms of heart failure'''<br><br>
''<sup>*</sup>LV remodeling refers to the changes in size, shape and function of the heart resulting from cardiac load or injury''</div>
|X02=<div style="float: left; text-align: left; width: 20em; padding:1em;">'''[[Acute heart failure resident survival guide#Prevention of Heart Failure|Stage D]]''' <br> <br>
❑ '''Refractory heart failure'''<br>
:❑ Marked symptoms at rest<br>
:❑ Recurrent hospitalizations</div>}}
{{familytree/end}}
{{familytree/end}}
==Prevention of Heart Failure in Stage A and B==
Shown below is an algorithm depicting the management of stage A and B heart failure.<ref name="pmid23741057">{{cite journal| author=Yancy CW, Jessup M, Bozkurt B, Butler J, Casey DE, Drazner MH et al.| title=2013 ACCF/AHA guideline for the management of heart failure: executive summary: a report of the American College of Cardiology Foundation/American Heart Association Task Force on practice guidelines. | journal=Circulation | year= 2013 | volume= 128 | issue= 16 | pages= 1810-52 | pmid=23741057 | doi=10.1161/CIR.0b013e31829e8807 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23741057  }} </ref>
<span style="font-size:85%">'''Abbreviations:'''
'''ACE I:''' [[Angiotensin converting enzyme inhibitor]];
'''ACS:''' [[Acute coronary syndrome]];
'''CVD:''' [[Cardiovascular disease]];
'''DM:''' [[Diabetes mellitus]];
'''EF:''' [[Ejection fraction]];
'''HF:''' [[Heart failure]];
'''HTN:''' [[Hypertension]];
'''ICD:''' [[Implantable cardioverter defibrillator]];
'''MI:''' [[Myocardial infarction]];
'''PAD:''' [[Peripheral artery disease]]
</span>
{{Family tree/start}}
{{Family tree | | | A01 | | | | | | | | | | A01= <div style="float: left; text-align: left; width: 25em; padding:1em;">'''What is the stage of heart failure (HF)?''' </div>}}
{{Family tree | |,|-|^|-|.| | }}
{{Family tree | B01 | | B02 | | B01= '''Stage A''' <br><div style="float: left; text-align: left; width: 25em; padding:1em;">''At high risk for HF but without structural heart disease or symptoms of HF'' </div>| B02= '''Stage B''' <br> <div style="float: left; text-align: left; width: 25em; padding:1em;">''Structural heart disease but without signs or symptoms of HF'' </div>}}
{{Family tree | |!| | | |!| | | | | }}
{{Family tree | C01 | | C02 | | | | C01=<div style="float: left; text-align: left; width: 25em; padding:1em;">
❑ Encourage healthy lifestyle and exercise <br>
❑ Treat [[hypertension]] ( I-A) <br>
❑ Treat [[dyslipidemia]] (I-A) <br>
❑ Control [[obesity]] (I-C) <br>
❑ Treat [[DM]] (I-C) <br>
❑ Avoid tobacco (I-C) <br>
❑ Avoid cardiotoxic agents (I-C) <br>
❑ Administer [[ACE-I]] if [[HTN]], [[DM]], [[CVD]], [[PAD]] <br> </div>
| C02=<div style="float: left; text-align: left; width: 25em; padding:1em;">
❑ Encourage healthy lifestyle and exercise <br>
❑ Treat [[hypertension]] (I-A) <br>
❑ Treat [[dyslipidemia]] (I-A) <br>
❑ Control [[obesity]] (I-C) <br>
❑ Treat [[DM]] (I-C) <br>
❑ Avoid tobacco (I-C) <br>
❑ Avoid cardiotoxic agents (I-C)</div>}}
{{Family tree | | | | | |!| | | | | }}
{{Family tree | | | | | D01 | | | | D01=<div style="float: left; text-align: left; width: 25em; padding:1em;">
'''Consider additional measures in selected patients:'''
❑ Administer [[ACE-I]] if history of [[MI]] or [[ACS]] and reduced [[EF]] to prevent symptoms and reduce mortality (I-A), in all decreased [[EF]] to prevent symptoms (I-A) <br>
❑ Administer [[beta-blocker]]s if history of [[MI]] or [[ACS]] and reduced [[EF]] to reduce mortality (I-B), in all reduced [[EF]] to prevent symptoms (I-C) <br>
❑ Administer [[statin]]s if history of [[MI]] or [[ACS]] to prevent symptoms (I-A) <br>
❑ Consider [[ICD]] placement to prevent sudden death if asymptomatic ischemic [[cardiomyopathy]], > 40 days post-MI, [[LVEF]] ≤30%, on adequate medical therapy, and good 1 year survival</div>}}
{{Family tree/end}}
==Treatment of Heart Failure in Stage C and D==
Shown below is an algorithm depicting the management of stage C and D heart failure.<ref name="pmid23741057">{{cite journal| author=Yancy CW, Jessup M, Bozkurt B, Butler J, Casey DE, Drazner MH et al.| title=2013 ACCF/AHA guideline for the management of heart failure: executive summary: a report of the American College of Cardiology Foundation/American Heart Association Task Force on practice guidelines. | journal=Circulation | year= 2013 | volume= 128 | issue= 16 | pages= 1810-52 | pmid=23741057 | doi=10.1161/CIR.0b013e31829e8807 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23741057  }} </ref>
<span style="font-size:85%">'''Abbreviations:'''
'''ACE I:''' [[Angiotensin converting enzyme inhibitor]];
'''ARB:''' [[Angiotensin II receptor blocker]];
'''ACS:''' [[Acute coronary syndrome]];
'''BID:''' Twice a day;
'''BNP:''' [[Brain natriuretic peptide]];
'''CRT:''' [[Cardiac resynchronization therapy]]
'''CVD:''' [[Cardiovascular disease]];
'''DM:''' [[Diabetes mellitus]];
'''EF:''' [[Ejection fraction]];
'''GDMT:''' Guideline determined medial therapy;
'''GFR:''' [[Glomerular filtration rate]];
'''HF:''' [[Heart failure]];
'''HFrEF:''' [[Heart failure reduced ejectoon fraction]];
'''HFpEF:''' [[Heart failure preserved ejection fraction]];
'''HTN:''' [[Hypertension]];
'''ICD:''' [[Implantable cardioverter defibrillator]];
'''LVEF:''' [[Left ventricular ejection fraction]];
'''MCS:''' [[Mechanical circulatory support]];
'''NYHA:''' [[New York Heart Association]];
'''MI:''' [[Myocardial infarction]];
'''PAD:''' [[Peripheral artery disease]];
'''TID:''' Three times a day
</span>
{{Family tree/start}}
{{Family tree | | | | | A01 | | | | | | | | | | A01= <div style="float: left; text-align: left; width: 25em; padding:1em;">'''What is the stage of heart failure (HF)?''' </div>}}
{{Family tree | |,|-|-|-|+|-|-|-|.| }}
{{Family tree | B01 | | B02 | | B03 | | | | B01= '''Stage C HFrEF'''<br><div style="float: left; text-align: left; width: 25em; padding:1em;">''Structural heart disease with prior or current symptoms of HF and reduced ejection fraction''</div>| B02= '''Stage C HFpEF''' <br> <div style="float: left; text-align: left; width: 25em; padding:1em;">''Structural heart disease with prior or current symptoms of HF and preserved ejection fraction'' </div>| B03= '''Stage D''' <br> <div style="float: left; text-align: left; width: 25em; padding:1em;">''Refractory HF requiring specialized interventions'' </div>}}
{{Family tree | |!| | | |!| | | |!| | | }}
{{Family tree | C01 | | C02 | | C03 | | C01= <div style="float: left; text-align: left; width: 25em; padding:1em;">
* Exercise training (I-A)
* Education for self-care (I-B)
* Sodium restriction if symptomatic (IIa-C)
* Cardiac rehabilitation in patients clinically stable (IIa-B)
* Treatment of [[HTN]], [[dyslipidemia]], [[obesity]], [[DM]]
* Avoid tobacco (I-C)
* Avoid cardiotoxic agents
'''''Medical therapy:'''''
* Control [[systolic]] and [[diastolic]] [[blood pressure]] (I-B)
* Oral [[diuretics]] to decrease symptoms of congestion (I-C)
: Starting dose:
:❑ [[Furosemide]] 20 to 40 mg, '''OR'''
:❑ [[Torsemide]] 10 to 20 mg, '''OR'''
:❑ [[Bumetanide]] 0.5 to 1 mg
: Monitor volume status and adjust dose
: No response: double oral diuretics dose rather than administer BID
: No or minimal response despite maximal diuretic dose: Administer diuretics BID or TID
* [[Coronary revascularization]] in symptomatic [[CAD]] (IIa-C)
* Treat concomitant [[AF]] (IIa-C)
* [[Beta blocker]], [[ACE-I]], [[ARB]] for [[hypertension]] (IIa-C)
* [[ARB]] to decrease hospitalization (IIb-B)
* [[Congestive heart failure angiotensin receptor-neprilysin inhibitor|ARNI]] to decrease morbidity and mortality (I-B) </div>
| C02= <div style="float: left; text-align: left; width: 25em; padding:1em;">
* Exercise training (I-A)
* Education for self-care (I-B)
* Sodium restriction if symptomatic (IIa-C)
* Cardiac rehabilitation in patients clinically stable (IIa-B)
* Treatment of [[HTN]], [[dyslipidemia]], [[obesity]], [[DM]]
* Avoid tobacco (I-C)
* Avoid cardiotoxic agents
'''''Routine drugs:'''''
* [[ACE-I]] or [[ARB]] (decrease mortality by 17%) (I-A)
* PLUS
* [[Beta blocker]]s (decrease mortality by 34%) (I-A)
** [[Bisoprolol]]
** [[Carvedilol]]
** Sustained release [[metoprolol succinate]]
PLUS
* [[Loop diuretics]] (for symptomatic volume overload; Class II-IV) (I-A)
: Starting dose:
:❑ [[Furosemide]] 20 to 40 mg, '''OR'''
:❑ [[Torsemide]] 10 to 20 mg, '''OR'''
:❑ [[Bumetanide]] 0.5 to 1 mg
: Monitor volume status and adjust dose
: No response: double oral diuretics dose rather than administer BID
: No or minimal response despite maximal diuretic dose: Administer [[diuretics]] BID or TID
PLUS
* [[Aldosterone antagonist]]
** NYHA class II with prior history of cardiovascular hospitalization or high [[BNP]] OR NYHA class III-IV, AND [[LVEF]] <=35%, AND estimated [[GFR]] >30 mL/min/1.73 m2, K+< 5 mEq/L (decrease mortality by 34%) (I-A)
** [[LVEF]] ≥40% AND symptoms of [[HF]] or [[DM]] (I-B)
'''''Add-on drugs in selected patients:'''''
* Persistent symptoms AND African American AND NYHA class III-IV  already on [[ACE-I]] and [[beta blocker]]s: [[Hydralazine nitrate]]  (decrease mortality by 43%) (I-A)
* Contraindications to [[ACE-I]] or [[ARB]] (IIa-B)
* [[Digitalis]]: to decrease hospitalizations (IIa-B)
* NYHA class II–IV symptoms and [[HFrEF]] or [[HFpEF]]: Omega-3 polyunsaturated fatty acid supplementation (IIa-B)</div>
| C03=<div style="float: left; text-align: left; width: 25em; padding:1em;">
'''''Fluid restriction:'''''
* Restriction to 1.5 to 2 L/d particularly in case of [[hyponatremia]] (IIa-C)
'''''Inotropes'''''
* Temporary [[inotrope]]s: in case of [[cardiogenic shock]] to maintain perfusion, awaiting definitive therapy or resolution of acute precipitating event (I-C), '''''OR'''''
* Continuous [[inotrope]]s:
:* Bridge therapy in stage D [[HF]] refractory to medical therapy and device therapy among patients eligible/awaiting [[MCS]] or [[heart transplant]] (IIa-B)
:* Short-term, continuous intravenous [[inotrope]]s to maintain perfusion among hospitalized, severe [[systolic dysfunction]], low [[blood pressure]] and significantly decreased [[cardiac output]] (IIb-B)
:* Long-term, continuous intravenous [[inotrope]]s for symptom control in select patients with stage D HF despite optimal GDMT and device therapy who are not eligible for either [[MCS]] or [[cardiac transplantation]] (IIb-B)
'''''Mechanical circulatory support (MCS)'''''
* Temporary [[MCS]] in [[HFrEF]] awaiting definitive therapy or resolution of acute precipitating event (I-B)
* Temporary [[MCS]] [[HFrEF]] with severe hemodynamic compromise, as a bridge therapy to recovery or decision (I-B)
* Durable [[MCS]] to prolong survival in selected patients ([[LVEF]] <25% and NYHA class III–IV functional status despite GDMT, including, when indicated, [[CRT]], with either high predicted 1- to 2-year mortality, or dependence on continuous parenteral [[inotropic]] support, multidisciplinary team) (I-B)
'''''Cardiac transplantation'''''
* Refractory to medical therapy, device, and surgery (I-C) </div>}}
{{Family tree/end}}
====Medications====
{| class="wikitable sortable"
! Drug Class
! Drug
! Daily dose
! Maximum daily dose
|-
| [[Loop diuretics]]||[[Furosemide]] <br> ''(duration of action: 6 to 8 h)'' ||PO dose for chronic heart failure: 20 to 40 mg once or twice<br>
IV dose for acute heart failure:
: Initial dose given slowly (1 to 2 minutes)<br>
:❑ If patient is already on loop diuretics: IV dose ≥ home PO dose (rule of thumb: IV dose = 2.5x equivalent oral daily dose)
:❑ If patient is not already on loop diuretics, administer IV starting dose of 20 to 40 mg
:Continuous IV infusion:
Initial IV bolus administered slowly over 1 to 2 minutes, then continuous IV infusion rate of 10-40 mg/h|| 600 mg
|-
|  || [[Bumetanide]] <br> ''(duration of action: 4 to 6 h)'' || PO dose for chronic heart failure: 0.5 to 1.0 mg once or twice || 10 mg
|-
|  || [[Torsemide]] <br> ''(duration of action: 12 to 16 h)''|| PO dose for chronic heart failure: 10 to 20 mg once|| 200 mg
|-
| [[Thiazide diuretics]] || [[Chlorothiazide]] <br> ''(duration of action: 6 to 12 h)''|| PO: 250 to 500 mg once or twice|| 1000 mg
|-
|  || [[Hydrochlorothiazide]] <br> ''(duration of action: 6 to 12 h)''|| PO: 25 mg once or twice|| 200 mg
|-
|  || [[Metolazone]] <br> ''(duration of action: 12 to 24 h)''|| PO: 2.5 mg once|| 20 mg
|-
| K<sup>+</sup>- sparing diuretic|| [[Amiloride]] <br> ''(duration of action: 24 h)''|| PO: 5 mg once|| 20 mg
|-
|  || [[Spironolactone]] <br> ''(duration of action: 1 to 3 h)''|| PO: 12.5 to 25.0 mg once|| 50 mg
|-
| || [[Triamterene]] <br> ''(duration of action: 7 to 9 h)''|| PO: 50 to 75 mg twice|| 200 mg
|-
| [[ACE inhibitors]] || [[Enalapril]] || 2.5 mg twice|| 10 to 20 mg twice
|-
|  || [[Lisinopril]] || 2.5 to 5 mg once|| 20 to 40 mg once
|-
|  || [[Ramipril]] ||1.25 to 2.5 mg once|| 10 mg once
|-
| [[ARBs]] || [[Candesartan]] || 4 to 8 mg once|| 32 mg once
|-
|  || [[Losartan]] || 25 to 50 mg once || 50 to 150 mg once
|-
|  || [[Valsartan]] || 20 to 40 mg twice|| 160 mg twice
|-
| [[Beta blockers]] || [[Bisoprolol]] || 1.25 mg once|| 10 mg once
|-
|  || [[Carvedilol]] || 3.125 mg twice|| 50 mg twice
|-
|  || [[Carvedilol CR]] || 10 mg once|| 80 mg once
|-
|  || [[Metoprolol succinate extended release]] || 12.5 to 25.0 mg once|| 200 mg once
|-
| [[Aldosterone antagonists]]|| [[Spironolactone]] || 12.5 to 25.0 mg once|| 25 mg once or twice
|-
|  || [[Eplerenone]] || 25 mg once|| 50 mg once
|-
| Inotropes || [[Dopamine]] || 5 to 10 mcg/kg/min, OR <br> 10 to 15 mcg/kg/min||
|-
|  || [[Dobutamine]] || 2.5 to 5 mcg/kg/min, OR <br> 5 to 20 mcg/kg/min||
|-
|  || [[Milrinone]] || 0.125 to 0.75 mcg/kg/min||
|-
| [[Vasodilators]] || [[Nitroglycerin]] || 5 to 10 mcg/min, increase dose by 5-10mcg/min <br>every 3-5 mins as tolerated||Max is 400mcg/min
|-
|  || [[Nitroprusside]] ||  5 to 10 mcg/min, increase dose by 5-10mcg/min <br>every 5 mins as tolerated||Max is 400mcg/min
|-
|  || [[Nesiritide]] || 2 mcg/kg bolus; then 0.01 mcg/kg/minute continuous infusion|| Max of 0.03 mcg/kg/minute
|-
| [[Hydralazine]] and [[isosorbide dinitrate]] ||Fixed-dose combination  || 37.5 mg hydralazine/20 mg isosorbide dinitrate 3 times daily || 75 mg hydralazine/40 mg isosorbide dinitrate 3 times daily
|-
| ||Individual doses||[[Hydralazine]]: 25 to 50 mg 3 or 4 times daily<br>[[Isosorbide dinitrate]]: 20 to 30 mg 3 or 4 times daily|| [[Hydralazine]]: 300 mg daily in divided doses <br> [[Isosorbide dinitrate]]: 120 mg daily in divided doses
|-
| [[Digoxin]] ||  ||
''Loading dose:'' PO- 10 to 15 mcg/kg (half the total loading dose initially, then 1/4<sup>th</sup> the loading dose every 6 to 8 hours two times), OR<br>
IV- 8 to 12 mcg/kg (half the total loading dose initially, then 1/4<sup>th</sup> the loading dose every 6 to 8 hours two times)<br>
''Maintenance dose:'' PO- 3.4 to 5.1 mcg/kg/day once daily, OR <br> IV- 2.4 to 3.6 mcg/kh/day once daily
<br> Drugs that increase the concentration of digoxin include [[amiodarone]], [[quinidine]] and [[verapamil]]||
|}


==Do's==
==Do's==
* Order an [[echocardiogram]] as soon as possible if no recent one available or if the patient's clinical status is deteriorating.
===Acute Decompensated Heart Failure===
* Digitalis decreases hospitalization but not mortality. It can be beneficial in symptomatic patients with low EF.<ref>The Captopril-Digoxin Multicenter Research Group. Comparative effects of therapy with captopril and digoxin in patients with mild to moderate heart failure. JAMA. 1988;259:539–44.</ref><ref>Dobbs SM, Kenyon WI, Dobbs RJ. Maintenance digoxin after an
* Differentiate systolic and diastolic heart failure among patients with ADHF in order to guide therapy:
episode of heart failure: placebo-controlled trial in outpatients. Br Med J. 1977;1:749–52</ref><ref>Lee DC, Johnson RA, Bingham JB, et al. Heart failure in outpatients: a randomized trial of digoxin versus placebo. N Engl J Med. 1982;306: 699–705.</ref><ref>Guyatt GH, Sullivan MJ, Fallen EL, et al. A controlled trial of digoxin in congestive heart failure. Am J Cardiol. 1988;61:371–5.</ref><ref>. DiBianco R, Shabetai R, Kostuk W, et al. A comparison of oral milrinone, digoxin, and their combination in the treatment of patients with chronic heart failure. N Engl J Med. 1989;320:677–83.</ref><ref>Uretsky BF, Young JB, Shahidi FE, et al., for the PROVED Investigative Group. Randomized study assessing the effect of digoxin withdrawal in patients with mild to moderate chronic congestive heart failure: results of the PROVED trial. J Am Coll Cardiol. 1993;22:955–62.</ref><ref>Packer M, Gheorghiade M, Young JB, et al. Withdrawal of digoxin from patients with chronic heart failure treated with angiotensin-convertingenzyme inhibitors. RADIANCE Study. N Engl J Med. 1993;329:1–7.</ref>
** [[Inotropic]] agents that increase contractility are not indicated as important for the patient with [[acute decompensated systolic heart failure]].
* Make sure your patient is on [[DVT]] prophylaxis unless contraindicated.<ref name="pmid12945875">{{cite journal| author=Alikhan R, Cohen AT, Combe S, Samama MM, Desjardins L, Eldor A et al.| title=Prevention of venous thromboembolism in medical patients with enoxaparin: a subgroup analysis of the MEDENOX study. | journal=Blood Coagul Fibrinolysis | year= 2003 | volume= 14 | issue= 4 | pages= 341-6 | pmid=12945875 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12945875  }} </ref><ref name="pmid22315257">{{cite journal| author=Guyatt GH, Akl EA, Crowther M, Gutterman DD, Schuünemann HJ, American College of Chest Physicians Antithrombotic Therapy and Prevention of Thrombosis Panel| title=Executive summary: Antithrombotic Therapy and Prevention of Thrombosis, 9th ed: American College of Chest Physicians Evidence-Based Clinical Practice Guidelines. | journal=Chest | year= 2012 | volume= 141 | issue= 2 Suppl | pages= 7S-47S | pmid=22315257 | doi=10.1378/chest.1412S3 | pmc=PMC3278060 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22315257  }} </ref>
** While [[beta blocker]] initiation is relatively contraindicated in acute decompensated systolic heart failure, control of [[tachycardia]] is very useful in the patient with [[diastolic heart failure]] to prolong left ventricular filling time.
* Make use of aldosterone receptor antagonists [or mineralocorticoid receptor antagonists] in patients with NYHA class II-IV and who have [[LVEF]] of 35% or less, unless contraindicated, to reduce morbidity and mortality. Patients with NYHA class II should have a history of prior cardiovascular hospitalization or elevated plasma natriuretic peptide levels to be considered for aldosterone receptor antagonists. Creatinine should be 2.5 mg/dL or less in men or 2.0 mg/dL or less in women (or estimated glomerular filtration rate >30 mL/min/1.73 m2), and potassium should be less than 5.0 mEq/L. Careful monitoring of potassium, renal function, and diuretic dosing should be performed at initiation and closely followed thereafter to minimize risk of hyperkalemia and renal insufficiency.<ref name="pmid10471456">{{cite journal| author=Pitt B, Zannad F, Remme WJ, Cody R, Castaigne A, Perez A et al.| title=The effect of spironolactone on morbidity and mortality in patients with severe heart failure. Randomized Aldactone Evaluation Study Investigators. | journal=N Engl J Med | year= 1999 | volume= 341 | issue= 10 | pages= 709-17 | pmid=10471456 | doi=10.1056/NEJM199909023411001 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=10471456  }} </ref><ref name="pmid21073363">{{cite journal| author=Zannad F, McMurray JJ, Krum H, van Veldhuisen DJ, Swedberg K, Shi H et al.| title=Eplerenone in patients with systolic heart failure and mild symptoms. | journal=N Engl J Med | year= 2011 | volume= 364 | issue= 1 | pages= 11-21 | pmid=21073363 | doi=10.1056/NEJMoa1009492 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21073363  }}  [http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21558564 Review in: Evid Based Med. 2011 Aug;16(4):121-2] [http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21814643 Review in: J Fam Pract. 2011 Aug;60(8):482-4] </ref><ref name="pmid21029826">{{cite journal| author=Vizzardi E, D'Aloia A, Giubbini R, Bordonali T, Bugatti S, Pezzali N et al.| title=Effect of spironolactone on left ventricular ejection fraction and volumes in patients with class I or II heart failure. | journal=Am J Cardiol | year= 2010 | volume= 106 | issue= 9 | pages= 1292-6 | pmid=21029826 | doi=10.1016/j.amjcard.2010.06.052 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21029826  }} </ref>
** While the initiation of [[ACE inhibitor]]s may not be recommended in acute decompensated systolic heart failure, ACE inhibition may be of benefit in acute decompensated diastolic heart failure.  
* Start [[hydralazine]] and [[nitrates|isosorbide dinitrate]] to reduce morbidity or mortality in patients with current or prior symptomatic [[systolic dysfunction|HFrEF]] who cannot be given an [[ACE inhibitor]] or [[ARB]] because of drug intolerance, hypotension, or renal insufficiency, unless contraindicated. This combination has proven beneficial in African American population as well. <ref>Carson P, Ziesche S, Johnson G, et al., for the Vasodilator-Heart Failure Trial Study Group. Racial differences in response to therapy for heart failure: analysis of the vasodilator-heart failure trials. J Card Fail. 1999;5:178–87.</ref><ref>Cohn JN. The Vasodilator-Heart Failure Trials (V-HeFT). Mechanistic data from the VA Cooperative Studies. Introduction. Circulation. 1993; 87:VI1–4.</ref><ref>Carson P, Ziesche S, Johnson G, et al., for the Vasodilator-Heart Failure Trial Study Group. Racial differences in response to therapy for heart failure: analysis of the vasodilator-heart failure trials. J Card Fail.
* Rely on the patient's volume status to guide the aggressiveness of diuresis in ADHF.
* Continue chronic medications during acute decompensation in the following conditions:
** [[ACE inhibitor]]: may be continued if the patient is hemodynamically stable without a rising [[creatinine]] or [[hyperkalemia]]
** [[Beta blocker]]: may be continued in the absence of [[hypotension]]
** [[Aldosterone antagonist]]: may be continued in the absence of [[hypotension]], [[hyperkalemia]], and impaired renal function


1999;5:178–87.</ref><ref>Cohn JN, Archibald DG, Ziesche S, et al. Effect of vasodilator therapy on mortality in chronic congestive heart failure. Results of a Veterans Administration Cooperative Study. N Engl J Med. 1986;314:1547–52.</ref><ref>Loeb HS, Johnson G, Henrick A, et al., for the V-HeFT VA Cooperative Studies Group. Effect of enalapril, hydralazine plus isosorbide dinitrate, and prazosin on hospitalization in patients with chronic congestive heart failure. Circulation. 1993;87:VI78–87.</ref>  
* [[Digoxin]] decreases hospitalization but not mortality in the RALES study. It can be used in CHF & afib to reduce the ventricular response. In the RALES study, a level of < 1 ng/ml was associated with efficacy. Levels > 1 ng/ml not associated with greater efficacy and associated with higher mortality. No need to load a CHF patient with dig. For majority of patients with normal Cr, a daily dose of 0.25 mg of digoxin is usually adequate.  In the older patient or in those patients with renal impairment, a dose of 0.125 mg per day may be adequate. Drugs that increase the concentration of digoxin include [[amiodarone]], [[quinidine]] and [[verapamil]]. <ref>The Captopril-Digoxin Multicenter Research Group. Comparative effects of therapy with captopril and digoxin in patients with mild to moderate heart failure. JAMA. 1988;259:539–44.</ref><ref>Dobbs SM, Kenyon WI, Dobbs RJ. Maintenance digoxin after an episode of heart failure: placebo-controlled trial in outpatients. Br Med J. 1977;1:749–52</ref><ref>Lee DC, Johnson RA, Bingham JB, et al. Heart failure in outpatients: a randomized trial of digoxin versus placebo. N Engl J Med. 1982;306: 699–705.</ref><ref>Guyatt GH, Sullivan MJ, Fallen EL, et al. A controlled trial of digoxin in congestive heart failure. Am J Cardiol. 1988;61:371–5.</ref><ref>. DiBianco R, Shabetai R, Kostuk W, et al. A comparison of oral milrinone, digoxin, and their combination in the treatment of patients with chronic heart failure. N Engl J Med. 1989;320:677–83.</ref><ref>Uretsky BF, Young JB, Shahidi FE, et al., for the PROVED Investigative Group. Randomized study assessing the effect of digoxin withdrawal in patients with mild to moderate chronic congestive heart failure: results of the PROVED trial. J Am Coll Cardiol. 1993;22:955–62.</ref><ref>Packer M, Gheorghiade M, Young JB, et al. Withdrawal of digoxin from patients with chronic heart failure treated with angiotensin-convertingenzyme inhibitors. RADIANCE Study. N Engl J Med. 1993;329:1–7.</ref>
* [[DVT prophylaxis]] unless contraindicated.<ref name="pmid12945875">{{cite journal| author=Alikhan R, Cohen AT, Combe S, Samama MM, Desjardins L, Eldor A et al.| title=Prevention of venous thromboembolism in medical patients with enoxaparin: a subgroup analysis of the MEDENOX study. | journal=Blood Coagul Fibrinolysis | year= 2003 | volume= 14 | issue= 4 | pages= 341-6 | pmid=12945875 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12945875  }} </ref><ref name="pmid22315257">{{cite journal| author=Guyatt GH, Akl EA, Crowther M, Gutterman DD, Schuünemann HJ, American College of Chest Physicians Antithrombotic Therapy and Prevention of Thrombosis Panel| title=Executive summary: Antithrombotic Therapy and Prevention of Thrombosis, 9th ed: American College of Chest Physicians Evidence-Based Clinical Practice Guidelines. | journal=Chest | year= 2012 | volume= 141 | issue= 2 Suppl | pages= 7S-47S | pmid=22315257 | doi=10.1378/chest.1412S3 | pmc=PMC3278060 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22315257  }} </ref>
* Consider adding another diuretic (e.g. metolazone or thiazides) for worsening congestion despite high doses of loop diuretics.<ref name="pmid3793436">{{cite journal| author=Grosskopf I, Rabinovitz M, Rosenfeld JB| title=Combination of furosemide and metolazone in the treatment of severe congestive heart failure. | journal=Isr J Med Sci | year= 1986 | volume= 22 | issue= 11 | pages= 787-90 | pmid=3793436 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=3793436  }} </ref><ref name="pmid16189620">{{cite journal| author=Rosenberg J, Gustafsson F, Galatius S, Hildebrandt PR| title=Combination therapy with metolazone and loop diuretics in outpatients with refractory heart failure: an observational study and review of the literature. | journal=Cardiovasc Drugs Ther | year= 2005 | volume= 19 | issue= 4 | pages= 301-6 | pmid=16189620 | doi=10.1007/s10557-005-3350-2 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16189620  }} </ref>
* Consider adding another diuretic (e.g. metolazone or thiazides) for worsening congestion despite high doses of loop diuretics.<ref name="pmid3793436">{{cite journal| author=Grosskopf I, Rabinovitz M, Rosenfeld JB| title=Combination of furosemide and metolazone in the treatment of severe congestive heart failure. | journal=Isr J Med Sci | year= 1986 | volume= 22 | issue= 11 | pages= 787-90 | pmid=3793436 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=3793436  }} </ref><ref name="pmid16189620">{{cite journal| author=Rosenberg J, Gustafsson F, Galatius S, Hildebrandt PR| title=Combination therapy with metolazone and loop diuretics in outpatients with refractory heart failure: an observational study and review of the literature. | journal=Cardiovasc Drugs Ther | year= 2005 | volume= 19 | issue= 4 | pages= 301-6 | pmid=16189620 | doi=10.1007/s10557-005-3350-2 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16189620  }} </ref>
*  Daily serum electrolytes, urea nitrogen, and creatinine concentrations should be measured during the use of IV diuretics or active titration of heart failure medications.
*  Daily serum electrolytes, urea nitrogen, and creatinine concentrations should be measured during the use of IV diuretics or active titration of heart failure medications.
* Use a combination of [[hydralazine]] and [[nitrates|isosorbide dinitrate]]. They have been proven to reduce morbidity or mortality in patients with current or prior symptomatic [[systolic dysfunction|HFrEF]] who cannot be given an [[ACE inhibitor]] or [[ARB]] because of drug intolerance, hypotension, or renal insufficiency, unless contraindicated.<ref>Carson P, Ziesche S, Johnson G, et al., for the Vasodilator-Heart Failure Trial Study Group. Racial differences in response to therapy for heart failure: analysis of the vasodilator-heart failure trials. J Card Fail. 1999;5:178–87.</ref><ref>Cohn JN. The Vasodilator-Heart Failure Trials (V-HeFT). Mechanistic data from the VA Cooperative Studies. Introduction. Circulation. 1993; 87:VI1–4.</ref><ref>Carson P, Ziesche S, Johnson G, et al., for the Vasodilator-Heart Failure Trial Study Group. Racial differences in response to therapy for heart failure: analysis of the vasodilator-heart failure trials. J Card Fail.
* Convert all IV diuretic to oral forms in anticipation of discharge.
 
1999;5:178–87.</ref><ref>Cohn JN, Archibald DG, Ziesche S, et al. Effect of vasodilator therapy on mortality in chronic congestive heart failure. Results of a Veterans Administration Cooperative Study. N Engl J Med. 1986;314:1547–52.</ref><ref>Loeb HS, Johnson G, Henrick A, et al., for the V-HeFT VA Cooperative Studies Group. Effect of enalapril, hydralazine plus isosorbide dinitrate, and prazosin on hospitalization in patients with chronic congestive heart failure. Circulation. 1993;87:VI78–87.</ref>
* Schedule an early follow-up visit (within 7 to 14 days) and early telephone follow-up (within 3 days) of hospital discharge .<ref name="pmid10618565">{{cite journal| author=Krumholz HM, Chen YT, Wang Y, Vaccarino V, Radford MJ, Horwitz RI| title=Predictors of readmission among elderly survivors of admission with heart failure. | journal=Am Heart J | year= 2000 | volume= 139 | issue= 1 Pt 1 | pages= 72-7 | pmid=10618565 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=10618565  }} </ref><ref name="pmid20442387">{{cite journal| author=Hernandez AF, Greiner MA, Fonarow GC, Hammill BG, Heidenreich PA, Yancy CW et al.| title=Relationship between early physician follow-up and 30-day readmission among Medicare beneficiaries hospitalized for heart failure. | journal=JAMA | year= 2010 | volume= 303 | issue= 17 | pages= 1716-22 | pmid=20442387 | doi=10.1001/jama.2010.533 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=20442387  }} </ref>
* Schedule an early follow-up visit (within 7 to 14 days) and early telephone follow-up (within 3 days) of hospital discharge .<ref name="pmid10618565">{{cite journal| author=Krumholz HM, Chen YT, Wang Y, Vaccarino V, Radford MJ, Horwitz RI| title=Predictors of readmission among elderly survivors of admission with heart failure. | journal=Am Heart J | year= 2000 | volume= 139 | issue= 1 Pt 1 | pages= 72-7 | pmid=10618565 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=10618565  }} </ref><ref name="pmid20442387">{{cite journal| author=Hernandez AF, Greiner MA, Fonarow GC, Hammill BG, Heidenreich PA, Yancy CW et al.| title=Relationship between early physician follow-up and 30-day readmission among Medicare beneficiaries hospitalized for heart failure. | journal=JAMA | year= 2010 | volume= 303 | issue= 17 | pages= 1716-22 | pmid=20442387 | doi=10.1001/jama.2010.533 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=20442387  }} </ref>


* Refer your [[HF]] patients to the local Multidisciplinary [[HF]] disease-management programs for those with high risk for hospital readmission, to facilitate the implementation of [[Congestive heart failure chronic pharmacotherapy|GDMT]], to address different barriers to behavioral change, and to reduce the risk of subsequent rehospitalization for [[HF]].<ref name="pmid15312864">{{cite journal| author=McAlister FA, Stewart S, Ferrua S, McMurray JJ| title=Multidisciplinary strategies for the management of heart failure patients at high risk for admission: a systematic review of randomized trials. | journal=J Am Coll Cardiol | year= 2004 | volume= 44 | issue= 4 | pages= 810-9 | pmid=15312864 | doi=10.1016/j.jacc.2004.05.055 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=15312864  }} </ref><ref name="pmid12816174">{{cite journal| author=Windham BG, Bennett RG, Gottlieb S| title=Care management interventions for older patients with congestive heart failure. | journal=Am J Manag Care | year= 2003 | volume= 9 | issue= 6 | pages= 447-59; quiz 460-1 | pmid=12816174 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12816174  }} </ref><ref name="pmid17200476">{{cite journal| author=Fonarow GC, Abraham WT, Albert NM, Stough WG, Gheorghiade M, Greenberg BH et al.| title=Association between performance measures and clinical outcomes for patients hospitalized with heart failure. | journal=JAMA | year= 2007 | volume= 297 | issue= 1 | pages= 61-70 | pmid=17200476 | doi=10.1001/jama.297.1.61 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=17200476</ref>
===Chronic Heart Failure===
* Guideline-directed medical therapy (GDMT) is a term which represents the optimal medical therapy in the management of [[heart failure]] as defined by ACCF/AHA.  These are primarily the '''class 1 recommendations'''.  It involves the use of [[ACE inhibitor]]s or ([[Angiotensin II receptor antagonist|ARBs]]), [[beta blocker]]s, [[aldosterone antagonist]]s, and [[hydralazine]]/[[Isosorbide dinitrate|nitrate]] medications.
* Order an [[echocardiogram]] as soon as possible in the absence of a recent one or if the patient's clinical status is deteriorating.


==Don'ts==
==Don'ts==
* If possible, don't order NSAIDs, most antiarrhythmic drugs or most calcium channel blockers as they can cause harm in acute decompensated [[HF]]. <ref>Heerdink ER, Leufkens HG, Herings RM, et al. NSAIDs associated with increased risk of congestive heart failure in elderly patients taking diuretics. Arch Intern Med. 1998;158:1108–12.</ref><ref>. Herchuelz A, Derenne F, Deger F, et al. Interaction between nonsteroidal anti-inflammatory drugs and loop diuretics: modulation by sodiumbalance. J Pharmacol Exp Ther. 1989;248:1175–81.</ref><ref>Gottlieb SS, Robinson S, Krichten CM, et al. Renal response to indomethacin in congestive heart failure secondary to ischemic or idiopathic dilated cardiomyopathy. Am J Cardiol. 1992;70:890–3</ref><ref>Bank AJ, Kubo SH, Rector TS, et al. Local forearm vasodilation with intra-arterial administration of enalaprilat in humans. Clin Pharmacol Ther. 1991;50:314–21.</ref><ref>The Cardiac Arrhythmia Suppression Trial (CAST) Investigators. Preliminary report: effect of encainide and flecainide on mortality in a randomized trial of arrhythmia suppression after myocardial infarction. N Engl J Med. 1989;321:406–12.</ref><ref>The Cardiac Arrhythmia Suppression Trial II Investigators. Effect of the antiarrhythmic agent moricizine on survival after myocardial infarction. N Engl J Med. 1992;327:227–33.</ref><ref>Pratt CM, Eaton T, Francis M, et al. The inverse relationship between baseline left ventricular ejection fraction and outcome of antiarrhythmic therapy: a dangerous imbalance in the risk-benefit ratio. Am Heart J. 1989;118:433–40.</ref>
* Avoid, if possible, [[NSAIDs]], [[Sympathomimetic amine|sympathomimetics]], [[tricyclic antidepressant]]s, class I and III antiarrhythmics (except [[amiodarone]]), and nondihydropyridine [[calcium channel blocker]]s ([[diltiazem]], [[verapamil]] as they can be harmful in acute decompensated [[HF]]. <ref>Heerdink ER, Leufkens HG, Herings RM, et al. NSAIDs associated with increased risk of congestive heart failure in elderly patients taking diuretics. Arch Intern Med. 1998;158:1108–12.</ref><ref>. Herchuelz A, Derenne F, Deger F, et al. Interaction between nonsteroidal anti-inflammatory drugs and loop diuretics: modulation by sodiumbalance. J Pharmacol Exp Ther. 1989;248:1175–81.</ref><ref>Gottlieb SS, Robinson S, Krichten CM, et al. Renal response to indomethacin in congestive heart failure secondary to ischemic or idiopathic dilated cardiomyopathy. Am J Cardiol. 1992;70:890–3</ref><ref>Bank AJ, Kubo SH, Rector TS, et al. Local forearm vasodilation with intra-arterial administration of enalaprilat in humans. Clin Pharmacol Ther. 1991;50:314–21.</ref><ref>The Cardiac Arrhythmia Suppression Trial (CAST) Investigators. Preliminary report: effect of encainide and flecainide on mortality in a randomized trial of arrhythmia suppression after myocardial infarction. N Engl J Med. 1989;321:406–12.</ref><ref>The Cardiac Arrhythmia Suppression Trial II Investigators. Effect of the antiarrhythmic agent moricizine on survival after myocardial infarction. N Engl J Med. 1992;327:227–33.</ref><ref>Pratt CM, Eaton T, Francis M, et al. The inverse relationship between baseline left ventricular ejection fraction and outcome of antiarrhythmic therapy: a dangerous imbalance in the risk-benefit ratio. Am Heart J. 1989;118:433–40.</ref>
* Don't Use parenteral [[Congestive heart failure positive inotropics|inotropes]] in [[normotensive]] patients with acute decompensated [[HF]] without evidence of decreased organ perfusion. <ref name="pmid11911756">{{cite journal |author=Cuffe MS, Califf RM, Adams KF, Benza R, Bourge R, Colucci WS, Massie BM, O'Connor CM, Pina I, Quigg R, Silver MA, Gheorghiade M |title=Short-term intravenous milrinone for acute exacerbation of chronic heart failure: a randomized controlled trial |journal=[[JAMA : the Journal of the American Medical Association]] |volume=287 |issue=12 |pages=1541–7 |year=2002 |month=March |pmid=11911756 |doi= |url=http://jama.ama-assn.org/cgi/pmidlookup?view=long&pmid=11911756 |accessdate=2012-04-06}}</ref>
* Don't administer parenteral [[Congestive heart failure positive inotropics|inotropes]] in normotensive patients with acute decompensated [[HF]] without evidence of decreased organ perfusion. <ref name="pmid11911756">{{cite journal |author=Cuffe MS, Califf RM, Adams KF, Benza R, Bourge R, Colucci WS, Massie BM, O'Connor CM, Pina I, Quigg R, Silver MA, Gheorghiade M |title=Short-term intravenous milrinone for acute exacerbation of chronic heart failure: a randomized controlled trial |journal=[[JAMA : the Journal of the American Medical Association]] |volume=287 |issue=12 |pages=1541–7 |year=2002 |month=March |pmid=11911756 |doi= |url=http://jama.ama-assn.org/cgi/pmidlookup?view=long&pmid=11911756 |accessdate=2012-04-06}}</ref>
* Don't combine an [[ACEI]], [[ARB]], and [[aldosterone antagonist]] in patients with [[systolic dysfunction|HFrEF]] unless otherwise indicated as this combination carries a risk of renal functions worsening and hyperkalemia.
* Don't combine an [[ACEI]], [[ARB]], and [[aldosterone antagonist]] in patients with [[systolic dysfunction|HFrEF]] unless otherwise indicated as this combination carries a risk of renal dysfunction and [[hyperkalemia]].
* Don't use [[aldosterone receptor antagonists]] in patients with [[hyperkalemia]] or renal insufficiency when serum creatinine is more than 2.5 mg/dL in men or more than 2.0 mg/dL in women (or estimated glomerular filtration rate <30 mL/min/1.73 m2), and/or potassium more than 5.0 mEq/L.<ref name="pmid15295047">{{cite journal| author=Juurlink DN, Mamdani MM, Lee DS, Kopp A, Austin PC, Laupacis A et al.| title=Rates of hyperkalemia after publication of the Randomized Aldactone Evaluation Study. | journal=N Engl J Med | year= 2004 | volume= 351 | issue= 6 | pages= 543-51 | pmid=15295047 | doi=10.1056/NEJMoa040135 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=15295047  }} </ref><ref name="pmid12535810">{{cite journal| author=Bozkurt B, Agoston I, Knowlton AA| title=Complications of inappropriate use of spironolactone in heart failure: when an old medicine spirals out of new guidelines. | journal=J Am Coll Cardiol | year= 2003 | volume= 41 | issue= 2 | pages= 211-4 | pmid=12535810 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12535810  }} </ref>
* Don't use [[aldosterone receptor antagonists]] in patients with [[hyperkalemia]] or renal insufficiency when serum creatinine is more than 2.5 mg/dL in men or more than 2.0 mg/dL in women (or estimated glomerular filtration rate <30 mL/min/1.73 m2), and/or potassium more than 5.0 mEq/L.<ref name="pmid15295047">{{cite journal| author=Juurlink DN, Mamdani MM, Lee DS, Kopp A, Austin PC, Laupacis A et al.| title=Rates of hyperkalemia after publication of the Randomized Aldactone Evaluation Study. | journal=N Engl J Med | year= 2004 | volume= 351 | issue= 6 | pages= 543-51 | pmid=15295047 | doi=10.1056/NEJMoa040135 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=15295047  }} </ref><ref name="pmid12535810">{{cite journal| author=Bozkurt B, Agoston I, Knowlton AA| title=Complications of inappropriate use of spironolactone in heart failure: when an old medicine spirals out of new guidelines. | journal=J Am Coll Cardiol | year= 2003 | volume= 41 | issue= 2 | pages= 211-4 | pmid=12535810 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12535810  }} </ref>
* Don't continue nutritional supplements with no proven benefit.
* Don't use [[statins]] routinely without other indications.<ref name="pmid14975476">{{cite journal| author=Horwich TB, MacLellan WR, Fonarow GC| title=Statin therapy is associated with improved survival in ischemic and non-ischemic heart failure. | journal=J Am Coll Cardiol | year= 2004 | volume= 43 | issue= 4 | pages= 642-8 | pmid=14975476 | doi=10.1016/j.jacc.2003.07.049 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=14975476  }} </ref><ref name="pmid18757089">{{cite journal| author=Gissi-HF Investigators. Tavazzi L, Maggioni AP, Marchioli R, Barlera S, Franzosi MG et al.| title=Effect of rosuvastatin in patients with chronic heart failure (the GISSI-HF trial): a randomised, double-blind, placebo-controlled trial. | journal=Lancet | year= 2008 | volume= 372 | issue= 9645 | pages= 1231-9 | pmid=18757089 | doi=10.1016/S0140-6736(08)61240-4 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=18757089  }} </ref>
* Don't use statins routinely without other indications.<ref name="pmid14975476">{{cite journal| author=Horwich TB, MacLellan WR, Fonarow GC| title=Statin therapy is associated with improved survival in ischemic and non-ischemic heart failure. | journal=J Am Coll Cardiol | year= 2004 | volume= 43 | issue= 4 | pages= 642-8 | pmid=14975476 | doi=10.1016/j.jacc.2003.07.049 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=14975476  }} </ref><ref name="pmid18757089">{{cite journal| author=Gissi-HF Investigators. Tavazzi L, Maggioni AP, Marchioli R, Barlera S, Franzosi MG et al.| title=Effect of rosuvastatin in patients with chronic heart failure (the GISSI-HF trial): a randomised, double-blind, placebo-controlled trial. | journal=Lancet | year= 2008 | volume= 372 | issue= 9645 | pages= 1231-9 | pmid=18757089 | doi=10.1016/S0140-6736(08)61240-4 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=18757089  }} </ref>
* Don't administer K+- sparing diuretic e.g amiloride or triamterene with aldosterone antagonist due to the elevated risk of hyperkalemia.


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Latest revision as of 14:36, 19 August 2020

For acute heart failure prevention click here.

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Mahmoud Sakr, M.D. [2]; Ayokunle Olubaniyi, M.B,B.S [3]; Rim Halaby, M.D. [4]

Acute Heart Failure Resident Survival Guide Microchapters
Overview
Classification
Causes
FIRE
Diagnosis
Treatment

Stage A and B
Stage C and D
Diuretic Therapy
Medication Dosages

Do's
Don'ts

Overview

Heart failure is a complex syndrome characterized by inadequate blood ejection or impaired ventricular filling, leading to the inability of the heart to pump blood to meet the metabolic demands of the body. Heart failure is a clinical syndrome for which the diagnosis relies mainly on symptoms and physical examination findings. The main symptoms and signs of heart failure are dyspnea, volume overload (leading to pulmonary edema and/or peripheral edema), fatigue, and exercise intolerance. Acute decompensated heart failure (ADHF) is a life-threatening condition that can occur in the setting of a new onset heart failure or worsening of an existing chronic heart failure. Symptoms of ADHF may include dyspnea secondary to pulmonary edema, peripheral edema, hypotension, and impaired end organ perfusion that can manifest by worsening renal function, altered mental status, and cold clammy extremities. The mainstays of treatment of ADHF are 1) oxygen therapy to improve hypoxia, 2) diuresis to reduce both preload and intravascular volume, and 3) vasodilators to reduce afterload. The goals of treatment for chronic heart failure are to relieve symptoms, decrease hospitalization rate, and decrease morbidity and mortality. Treatment of heart failure includes identification and management of precipitating factors, lifestyle changes, pharmacological therapy, and devices.

Classification

Classification by Severity of Congestive Heart Failure

Shown below is a table comparing American College of Cardiology Foundation/American Heart Association (ACCF/AHA) stages to New York Heart Association (NYHA) classification of severity of heart failure.[1]

ACCF/AHA Stages New York Heart Association (NYHA) Classification
Stage Interpretation Class Interpretation
A At high risk for heart failure (HF) but without structural heart disease or symptoms of HF - -
B Structural heart disease but without signs or symptoms of HF I No limitation of physical activity. Ordinary physical activity does not cause symptoms of HF
C Structural heart disease with prior or current symptoms of HF I No limitation of physical activity. Ordinary physical activity does not cause symptoms of HF
II Slight limitation of physical activity. Comfortable at rest, but ordinary physical activity results in symptoms of HF
III Marked limitation of physical activity. Comfortable at rest, but less than ordinary activity causes symptoms of HF
IV Unable to carry on any physical activity without symptoms of HF, or symptoms of HF at rest
D Refractory HF requiring specialized interventions IV Unable to carry on any physical activity without symptoms of HF, or symptoms of HF at rest

Classification by Other Factors

Left Ventricular Ejection Fraction (LVEF)

Cardiac Output

  • Low cardiac output
  • High stroke volume with/without cardiac output

Left vs. Right Sided

Backwards vs. Forward

  • Backwards: Congestion, elevated filling pressure
  • Forwards: Low systemic perfusion

Causes

Life Threatening Causes

Acute decompensated heart failure is life threatening and should be treated as such irrespective of the underlying cause.

Common Causes

Click here for the complete list of causes.

FIRE: Focused Initial Rapid Evaluation

A Focused Initial Rapid Evaluation (FIRE) should be performed to identify patients of severe acute decompensated heart failure in need of immediate intervention.[1]

Boxes in red signify that an urgent management is needed.

Abbreviations: BU: Blood urea nitrogen; COPD: Chronic obstructive pulmonary disease; D5W: 5% dextrose solution in water ; HF: Heart failure; IV: Intravenous; MAP: Mean arterial pressure; Na: Sodium; NSAID: Non steroidal anti-inflammatory drug; SBP: Systolic blood pressure; S3: Third heart sound;

 
 
Identify cardinal findings that increase the pretest probability of acute decompensated heart failure

Dyspnea
Cool extremities
Peripheral edema
Decreased urine output
❑ Past medical history of heart failure
❑ History of orthopnea and paroxysmal nocturnal dyspnea
❑ Pulmonary crepitations/rales/crackles

Third heart sound (S3)
 
 
 
 
 
 
 
 
 
Does the patient have any of the following findings that require hospitalization and urgent management?

❑ Severe decompendated HF:

Hypotension (SBP < 90 mmHg or drop in MAP >30 mmHg) and/or cardiogenic shock
Altered mental status
Cold and clammy extremities
Urine output <0.5mL/kg/hr

Dyspnea at rest manifested by tachypnea or oxygen saturation <90%
Atrial fibrillation with a rapid ventricular response resulting in hypotension

Acute coronary syndrome
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Yes
 
No
 
 
 
 
 
 
 
 
 
 
 
Admit to to a level of care that allows for constant ECG monitoring given the risk of arrhythmia
 
 
 
 
 
 
 
 
 
 
 

Initial stabilization:
❑ Assess the airway
❑ Position the patient upright at an angle of 45 degrees, with legs dangling off the bedside (decrease preload)
❑ Monitor heart rate and blood pressure continuously
❑ Monitor oxygen saturation continuously
❑ If hypoxemia is present (Sa02 < 90% or Pa02 <60 mmHg), administer oxygen with/without noninvasive ventilation
Morphine to decrease symptoms and Afterload (avoid IV morphine, may increase mortality / duration of intubation, generally not advisable, may relieve refractory symptoms)
❑ Secure intravenous access with 18 gauge cannula
❑ Monitor fluid intake and urine output carefully (guide the adjustment of the diuretics dose)

Assess congestion and perfusion:
Congestion at rest (dry vs. wet)
"Wet" suggested by orthopnea, ↑JVP, rales, S3, pedal edema
Low perfusion at rest (warm vs. cold)
"Cold" suggested by narrow pulse pressure, cool extremities, hypotension
The patient is:
❑ Warm and dry, OR
❑ Warm and wet, OR
❑ Cold and dry, OR
❑ Cold and wet

Identify precipitating factor and treat accordingly:
Click on the precipitating factor for more details on the management
Myocardial infarction
Myocarditis
Renal failure
Hypertensive crisis
❑ Non adherence to medications
❑ Worsening Aortic stenosis
❑ Drugs (NSAIDS, thiazides, calcium channel blocker, beta blockers)
❑ Toxins (alcohol, anthracyclines)
Atrial fibrillation

Rate control of atrial fibrillation is the mainstay of arrhythmia therapy. Avoid the use of drugs with negative inotropic effects such as beta blockers and non-dihydropyridine calcium channel blockers e.g., verapamil in the treatment of acute decompensated systolic heart failure
Consider cardioversion if the patient is in cardiogenic shock or if new onset atrial fibrillation is the clear precipitant of the hemodynamic decompensation

COPD
Pulmonary embolism
Anemia
Thyroid abnormalities
❑ Systemic infection

Treat congestion and optimize volume status:
Diuretics
❑ Administer IV loop diuretics as intermittent boluses or continuous infusion (I-B)

❑ If patient is already on loop diuretics: IV dose ≥ home PO dose (I-B); rule of thumb: IV dose = 2.5x equivalent oral daily dose
❑ If patient is not already on loop diuretics, administer IV starting dose:
Furosemide 20 to 40 mg, OR
Torsemide 5 to 10 mg, OR
Bumetanide 0.5 to 1 mg
❑ Adjust dose according to volume status (I-B)
❑ Perform serial assessment of fluid intake and output, vital signs, daily body weight (measured every day, with the same scale, at the same time, after first void) and symptoms
❑ Order daily electrolytes, BUN, creatinine (I-C)

❑ Low sodium diet (<2 g daily)
❑ In case of persistent symptoms:

❑ Increase dose of IV loop diuretics (I-B)- double dose at 2 hour interval up to maximal daily dose
Furosemide maximal dose: 40 to 80 mg
Torsemide maximal dose: 20 to 40 mg
Bumetanide maximal dose: 1 to 2 mg
OR
❑ Add a second diuretics, such as thiazide (I-B)

❑ Consider low dose dopamine infusion for improved diuresis and renal blood flow (IIb-B)
❑ Consider renal replacement therapy/ultrafiltration in obvious volume overload (IIb-B) refractory to higher dose/combination of IV diuretics

Venodilators
❑ Consider IV nitroglycerin, nitroprusside, or nesiritide as add-on to diuretics to relieve dyspnes (IIb-A)

Do not administer vesodilators among patients with hypotension.

Treat low perfusion:
Inotropes (click her for details)

If the total body and intravascular volumes are overloaded and the patient is normotensive, then diuresis alone should be undertaken. If the patient is volume overloaded but hypotensive, then inotropes must be administered in addition to diuretics.

Invasive hemodynamic monitoring:

❑ Consider pulmonary artery catheterization in case of failure to respond to medical therapy, respiratory distress, shock, uncertainty regarding volume status, or increase in creatinine; assess the following parameters:

PCWP
Cardiac output
Systemic vascular resistance

VTE prevention:
Anticoagulation in the absence of contraindications (I-B)

Chronic medical therapy:
❑ Chronic ACE inhibitor: Hold if patient is hemodynamically unstable
❑ Chronic beta blocker:

Hold if patient is hemodynamically unstable and/or in need or inotropes
Decrease dose by ≥ half if patient is in moderate heart failure

❑ DO NOT INITIATE ACE INHIBITORS during an acute decompensation
❑ DO NOT INITIATE BETA BLOCKER during an acute decompensation; initiate beat blockers at a low dose in stable patients following optimization of volume status and D/C IV diuretics and inotropes (I-B)

Monitor laboratory tests:
BUN
Creatinine
Sodium (to detect hyponatremia which carries a poor prognosis), chloride, bicarbonate (to detect contraction alkalosis) and serum potassium (to detect hypokalemia as a result of diuresis and which can precipitate arrhythmias), potassium, magnesium

Management of hyponatremia:
❑ Water restriction

❑ <2 L/day if the Na is < 130 meq/L
❑ < 1 L/day or more if the Na is < 125 meq/L
Keep in min that juices are essentially free water with sugar.
In the hyponatremia patient, drips should not be in D5W.

❑ Optimization of chronic home medications

❑ Persistent hyponatremia and risk of cognitive impairment: vasopressin antagonist for short term (hypervolemic)
 
 
 
 
 

Complete Diagnostic Approach

A complete diagnostic approach should be carried out after a focused initial rapid evaluation is conducted and following initiation of any urgent intervention.[1][2]

Abbreviations: ANA: Antinuclear antibody; ARDS: Acute respiratory distress syndrome; BNP: B-type natriuretic peptide; BUN: Blood urea nitrogen; CAD: Coronary artery disease; CBC: Complete blood count; CCB: Calcium channel blocker; CHF: Congestive heart failure; CT: Computed tomography; CXR: Chest X-ray; DM: Diabetes mellitus; ECG: Electrocardiogram; JVP: Jugular venous pressure; HF: Heart failure; HTN: Hypertension; LVEF: Left ventricular ejection fraction; LVH: Left ventricular hypertrophy; MI: Myocardial infarction; MRI: Magnetic resonance imaging; NT-pro BNP: N-terminal pro-brain natriuretic peptide; OCPs: Oral contraceptive pills; PAWP: Pulmonary artery wedge pressure; SBP: Systolic blood pressure; S1: First heart sound; S3: Third heart sound; TSH: Thyroid stimulating hormone

 
 
 
 
 
 
 
Characterize the symptoms:

Symptoms of left-sided fluid accumulation:
Dyspnea

❑ At rest
❑ Exertional

Paroxysmal nocturnal dyspnea
Orthopnea
Cough
Symptoms of right-sided fluid accumulation:
Peripheral edema
❑ Right upper quadrant abdominal discomfort
Bloating
Satiety
Symptoms of reduced cardiac output:
Fatigue
Exercise intolerance
Oliguria
Dizziness
Syncope
Altered mental status
Cyanosis
Anorexia
Abdominal pain (suggestive of mesenteric ischemia)
Symptoms suggestive of precipitating events:
Chest pain (suggestive of myocardial ischemia)
Palpitations (suggestive of arrhythmias)
Fever (suggestive of infection)
Nonspecific symptoms:
Nausea
Weight loss


Obtain a detailed history:
Past medical history

Atrial fibrillation
Cardiomyopathy
Diabetes mellitus
Hypertension
Myocarditis
Previous myocardial infarction
Prior heart failure
Sleep apnea
Thyroid disease
Valvular heart disease

Medication history

❑ Noncompliance with previously prescribed medications for heart failure
❑ Intake of the following drugs:
Alcohol
Beta blockers
Calcium channel blockers like verapamil which can exacerbate CHF or diltiazem which can cause peripheral edema
Chemotherapy drugs - anthracyclines
NSAIDs which should not be given in CHF
Thiazolidinedione

Family history

❑ History of dilated cardiomyopathy
Radiation to the chest

Determine the NYHA classification based on symptoms:
❑ Class I (no symptoms)
❑ Class II (symptoms with ordinary activities)
❑ Class III (symptoms upon minimal activity)
❑ Class IV (symptoms at rest)

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Examine the patient:

General appearance:
❑ Ill-looking
❑ In respiratory distress
❑ In upright sitting position

Vitals:
Temperature

Fever (suggestive of underlying infection)

Pulse

Tachycardia
Narrow pulse pressure (<25% of SBP)

Blood pressure

Hypotension (suggestive of circulatory collapse)
Hypertension

Respiration

Tachypnea (most common symptom)

Pulse oximetry (maintain oxygen sat ≥ 94% unless COPD)

Weight:
❑ Measure weight daily at the same time after the first void
❑ Subtract 'dry weight' from current weight to estimate extent of volume overload and edema

Skin
Cool and clammy (suggestive of hypoperfusion)
Cyanosis (suggestive of severe hypoxemia)
Anasarca
Jaundice (suggestive of liver dysfunction secondary to right-sided fluid overload)

Neck examination:
Jugular vein distention (suggestive of right-sided fluid overload)
❑ Positive hepatojugular reflux (suggestive of right-sided fluid overload)

Respiratory examination
Tachypnea
Wheeze
❑ Dullness at lung bases (suggestive of pleural effusion, may be present in chronic HF secondary to lymphatic compensation)
Crackles/crepitations/rales (suggestive of pleural effusion)
Cheyne-stokes respiration

Cardiovascular examination
❑ Displaced apex beat (suggestive of enlarged left ventricle)
Parasternal heave (suggestive of elevated right ventricular pressure)
S3 (typical) or S4 or both
❑ Soft S1
❑ Pulsus alternans
S4 (suggestive of diastolic dysfunction)
❑ New or changed murmur (suggestive of an underlying valvular heart diseases)

Mitral regurgitation - Holosystolic murmur
Aortic regurgitation - Decrescendo diastolic murmur
Aortic stenosis - Crescendo-decrescendo systolic ejection murmur with ejection click

Abdominal examination
The following findings suggest volume overload and / or poor forward cardiac output:
Hepatojugular reflux
Hepatomegaly
Ascites

Extremity examination
Pedal edema

Neurological examination
Altered mental status
Syncope (suggestive of aortic stenosis or pulmonary embolism)


Determine status of congestion and perfusion based on physical exam:
Congestion at rest (dry vs. wet)

"Wet" suggested by orthopnea, ↑JVP, positive hepatojugular reflux, abnormal valsalva response, rales, dullness upon percussion in bases, S3, peripheral edema, hepatomegaly, ascites, jaundice

Low perfusion at rest (warm vs. cold)

"Cold" suggested by narrow pulse pressure, cool extremities, hypotension, soft S1, pulsus alternans, decreased urinary output

The patient is:
❑ Warm and dry, OR
❑ Warm and wet, OR
❑ Cold and dry, OR
❑ Cold and wet

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Order tests:

Routine (Class I, level of evidence C)

CBC (rule out anemia)
Troponin
❑ Elevated in myocardial ischemia and acute cardiogenic pulmonary edema, particularly if creatinine clearance (CrCl) is reduced
Troponin T ≥ 0.1 ng/mL (associated with poor survival)[3]
Electrolytes
Sodium: hyponatremia may occur due to fluid overlaod
Serum calcium
Serum magnesium can be lowered by diuresis
Serum bicarbonate: to monitor contraction alkalosis with diuresis
BUN, creatinine: may be elevated due to poor renal perfusion
Urinalysis
Fasting blood sugar
Fasting lipid profile
Liver function tests: can be elevated secondary to peripheral hypoperfusion
TSH

BNP or NT-pro BNP (if diagnosis is uncertain)
Heart failure is unlikely if:[4][5]

BNP ≤ 100 pg/mL, or
NT-pro BNP ≤ 300 pg/mL

Chest X-ray (Class I, level of evidence C)

Cardiomegaly (cardiothoracic ratio >50%)
❑ Cardiogenic pulmonary edema
Kerley B lines
Peribronchial cuffing
Cephalization
Chest X-ray findings in a patient with acute heart failure

ECG (to help identify the cause of heart failure)

Low QRS voltage (suggestive of infiltrative or dilated cardiomyopathy)
Arrhythmia (atrial fibrillation carries a poor prognosis and requires slowing of the heart rate to improve filling & cardiac output)
Poor R wave progression (suggestive of a prior MI)
Left ventricular hypertrophy (consistent with a history of hypertension)
Left bundle branch block (LBBB) due to prior MI, may result in dysynchrony)
Left atrial enlargement (due to valvular disease or hypertension)
❑ Non-specific ST segment and T wave changes may suggest ischemia

❑ 2-D echocardiography with Doppler
(Class I, level of evidence C)

❑ Assess chambers size, wall thickness, wall motion, and valve function
❑ Assess ejection fraction

Radionuclide ventriculography or MRI

❑ To assess LVEF and volume when echocardiography is inadequate
❑ To assess myocardial infiltrative processes or scar burden (MRI)

Coronary angiography looking for CAD
❑ Comprehensive metabolic panel if no evidence of CAD on coronary angiography
❑ Consider pulmonary artery catheterization in case of failure to respond to medical therapy, respiratory distress, shock, uncertainty regarding volume status, or increase in creatinine; assess the following parameters:

PCWP
Cardiac output
Systemic vascular resistance

Order additional tests to rule out other etiologies:
ANA and rheumatoid factor (for rheumatologic diseases)
❑ Diagnostic tests for hemochromatosis and pheochromocytoma
Endomyocardial biopsy (when myocarditis is suspected)

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Consider alternative diagnoses:

Alternative diagnosesFeatures
Acute asthmaWheeze
❑ Reversal of symptoms following
administration of bronchodilators
COPD❑ Increased cough
❑ Increased dyspnea
❑ Increased sputum production
ARDS❑ Severe hypoxia
❑ Bilateral opacities on chest X-ray
PCWP < 15 mmHg
PneumoniaFever, cough, sputum
Consolidation on chest X-ray
Pulmonary embolismPleuritic chest pain, cough, S4
❑ Risk factors: trauma, immobilization, smoking, OCPs
❑ Clot in pulmonary artery on CT pulmonary angiography
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Assess the stage of heart failure using the ACCF/AHA staging system to guide chronic therapy
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Stage C

Patients with structural heart disease
This refers to patients with the following:

❑ Previous MI
❑ LV remodeling* (including LVH + low EF)
❑ Asymptomatic valvular disease

AND

Signs or symptoms of heart failure

*LV remodeling refers to the changes in size, shape and function of the heart resulting from cardiac load or injury
 
Stage D

Refractory heart failure

❑ Marked symptoms at rest
❑ Recurrent hospitalizations
 
 
 

Prevention of Heart Failure in Stage A and B

Shown below is an algorithm depicting the management of stage A and B heart failure.[1]

Abbreviations: ACE I: Angiotensin converting enzyme inhibitor; ACS: Acute coronary syndrome; CVD: Cardiovascular disease; DM: Diabetes mellitus; EF: Ejection fraction; HF: Heart failure; HTN: Hypertension; ICD: Implantable cardioverter defibrillator; MI: Myocardial infarction; PAD: Peripheral artery disease

 
 
What is the stage of heart failure (HF)?
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Stage A
At high risk for HF but without structural heart disease or symptoms of HF
 
Stage B
Structural heart disease but without signs or symptoms of HF
 
 
 
 
 
 
 
 
 
 
 
 
 
 

❑ Encourage healthy lifestyle and exercise
❑ Treat hypertension ( I-A)
❑ Treat dyslipidemia (I-A)
❑ Control obesity (I-C)
❑ Treat DM (I-C)
❑ Avoid tobacco (I-C)
❑ Avoid cardiotoxic agents (I-C)

❑ Administer ACE-I if HTN, DM, CVD, PAD
 

❑ Encourage healthy lifestyle and exercise
❑ Treat hypertension (I-A)
❑ Treat dyslipidemia (I-A)
❑ Control obesity (I-C)
❑ Treat DM (I-C)
❑ Avoid tobacco (I-C)

❑ Avoid cardiotoxic agents (I-C)
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Consider additional measures in selected patients: ❑ Administer ACE-I if history of MI or ACS and reduced EF to prevent symptoms and reduce mortality (I-A), in all decreased EF to prevent symptoms (I-A)
❑ Administer beta-blockers if history of MI or ACS and reduced EF to reduce mortality (I-B), in all reduced EF to prevent symptoms (I-C)
❑ Administer statins if history of MI or ACS to prevent symptoms (I-A)

❑ Consider ICD placement to prevent sudden death if asymptomatic ischemic cardiomyopathy, > 40 days post-MI, LVEF ≤30%, on adequate medical therapy, and good 1 year survival
 
 
 

Treatment of Heart Failure in Stage C and D

Shown below is an algorithm depicting the management of stage C and D heart failure.[1]

Abbreviations: ACE I: Angiotensin converting enzyme inhibitor; ARB: Angiotensin II receptor blocker; ACS: Acute coronary syndrome; BID: Twice a day; BNP: Brain natriuretic peptide; CRT: Cardiac resynchronization therapy CVD: Cardiovascular disease; DM: Diabetes mellitus; EF: Ejection fraction; GDMT: Guideline determined medial therapy; GFR: Glomerular filtration rate; HF: Heart failure; HFrEF: Heart failure reduced ejectoon fraction; HFpEF: Heart failure preserved ejection fraction; HTN: Hypertension; ICD: Implantable cardioverter defibrillator; LVEF: Left ventricular ejection fraction; MCS: Mechanical circulatory support; NYHA: New York Heart Association; MI: Myocardial infarction; PAD: Peripheral artery disease; TID: Three times a day

 
 
 
 
What is the stage of heart failure (HF)?
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Stage C HFrEF
Structural heart disease with prior or current symptoms of HF and reduced ejection fraction
 
Stage C HFpEF
Structural heart disease with prior or current symptoms of HF and preserved ejection fraction
 
Stage D
Refractory HF requiring specialized interventions
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
  • Exercise training (I-A)
  • Education for self-care (I-B)
  • Sodium restriction if symptomatic (IIa-C)
  • Cardiac rehabilitation in patients clinically stable (IIa-B)
  • Treatment of HTN, dyslipidemia, obesity, DM
  • Avoid tobacco (I-C)
  • Avoid cardiotoxic agents

Medical therapy:

Starting dose:
Furosemide 20 to 40 mg, OR
Torsemide 10 to 20 mg, OR
Bumetanide 0.5 to 1 mg
Monitor volume status and adjust dose
No response: double oral diuretics dose rather than administer BID
No or minimal response despite maximal diuretic dose: Administer diuretics BID or TID
 
  • Exercise training (I-A)
  • Education for self-care (I-B)
  • Sodium restriction if symptomatic (IIa-C)
  • Cardiac rehabilitation in patients clinically stable (IIa-B)
  • Treatment of HTN, dyslipidemia, obesity, DM
  • Avoid tobacco (I-C)
  • Avoid cardiotoxic agents

  • Routine drugs:

    PLUS

    Starting dose:
    Furosemide 20 to 40 mg, OR
    Torsemide 10 to 20 mg, OR
    Bumetanide 0.5 to 1 mg
    Monitor volume status and adjust dose
    No response: double oral diuretics dose rather than administer BID
    No or minimal response despite maximal diuretic dose: Administer diuretics BID or TID

    PLUS

    • Aldosterone antagonist
      • NYHA class II with prior history of cardiovascular hospitalization or high BNP OR NYHA class III-IV, AND LVEF <=35%, AND estimated GFR >30 mL/min/1.73 m2, K+< 5 mEq/L (decrease mortality by 34%) (I-A)
      • LVEF ≥40% AND symptoms of HF or DM (I-B)

    Add-on drugs in selected patients:

    • Persistent symptoms AND African American AND NYHA class III-IV already on ACE-I and beta blockers: Hydralazine nitrate (decrease mortality by 43%) (I-A)
    • Contraindications to ACE-I or ARB (IIa-B)
    • Digitalis: to decrease hospitalizations (IIa-B)
    • NYHA class II–IV symptoms and HFrEF or HFpEF: Omega-3 polyunsaturated fatty acid supplementation (IIa-B)
     

    Fluid restriction:

    • Restriction to 1.5 to 2 L/d particularly in case of hyponatremia (IIa-C)

    Inotropes

    • Temporary inotropes: in case of cardiogenic shock to maintain perfusion, awaiting definitive therapy or resolution of acute precipitating event (I-C), OR
    • Continuous inotropes:

    Mechanical circulatory support (MCS)

    • Temporary MCS in HFrEF awaiting definitive therapy or resolution of acute precipitating event (I-B)
    • Temporary MCS HFrEF with severe hemodynamic compromise, as a bridge therapy to recovery or decision (I-B)
    • Durable MCS to prolong survival in selected patients (LVEF <25% and NYHA class III–IV functional status despite GDMT, including, when indicated, CRT, with either high predicted 1- to 2-year mortality, or dependence on continuous parenteral inotropic support, multidisciplinary team) (I-B)

    Cardiac transplantation

    • Refractory to medical therapy, device, and surgery (I-C)
     


    Medications

    Drug Class Drug Daily dose Maximum daily dose
    Loop diuretics Furosemide
    (duration of action: 6 to 8 h)
    PO dose for chronic heart failure: 20 to 40 mg once or twice

    IV dose for acute heart failure:

    Initial dose given slowly (1 to 2 minutes)
    ❑ If patient is already on loop diuretics: IV dose ≥ home PO dose (rule of thumb: IV dose = 2.5x equivalent oral daily dose)
    ❑ If patient is not already on loop diuretics, administer IV starting dose of 20 to 40 mg
    Continuous IV infusion:

    Initial IV bolus administered slowly over 1 to 2 minutes, then continuous IV infusion rate of 10-40 mg/h|| 600 mg

    Bumetanide
    (duration of action: 4 to 6 h)
    PO dose for chronic heart failure: 0.5 to 1.0 mg once or twice 10 mg
    Torsemide
    (duration of action: 12 to 16 h)
    PO dose for chronic heart failure: 10 to 20 mg once 200 mg
    Thiazide diuretics Chlorothiazide
    (duration of action: 6 to 12 h)
    PO: 250 to 500 mg once or twice 1000 mg
    Hydrochlorothiazide
    (duration of action: 6 to 12 h)
    PO: 25 mg once or twice 200 mg
    Metolazone
    (duration of action: 12 to 24 h)
    PO: 2.5 mg once 20 mg
    K+- sparing diuretic Amiloride
    (duration of action: 24 h)
    PO: 5 mg once 20 mg
    Spironolactone
    (duration of action: 1 to 3 h)
    PO: 12.5 to 25.0 mg once 50 mg
    Triamterene
    (duration of action: 7 to 9 h)
    PO: 50 to 75 mg twice 200 mg
    ACE inhibitors Enalapril 2.5 mg twice 10 to 20 mg twice
    Lisinopril 2.5 to 5 mg once 20 to 40 mg once
    Ramipril 1.25 to 2.5 mg once 10 mg once
    ARBs Candesartan 4 to 8 mg once 32 mg once
    Losartan 25 to 50 mg once 50 to 150 mg once
    Valsartan 20 to 40 mg twice 160 mg twice
    Beta blockers Bisoprolol 1.25 mg once 10 mg once
    Carvedilol 3.125 mg twice 50 mg twice
    Carvedilol CR 10 mg once 80 mg once
    Metoprolol succinate extended release 12.5 to 25.0 mg once 200 mg once
    Aldosterone antagonists Spironolactone 12.5 to 25.0 mg once 25 mg once or twice
    Eplerenone 25 mg once 50 mg once
    Inotropes Dopamine 5 to 10 mcg/kg/min, OR
    10 to 15 mcg/kg/min
    Dobutamine 2.5 to 5 mcg/kg/min, OR
    5 to 20 mcg/kg/min
    Milrinone 0.125 to 0.75 mcg/kg/min
    Vasodilators Nitroglycerin 5 to 10 mcg/min, increase dose by 5-10mcg/min
    every 3-5 mins as tolerated
    Max is 400mcg/min
    Nitroprusside 5 to 10 mcg/min, increase dose by 5-10mcg/min
    every 5 mins as tolerated
    Max is 400mcg/min
    Nesiritide 2 mcg/kg bolus; then 0.01 mcg/kg/minute continuous infusion Max of 0.03 mcg/kg/minute
    Hydralazine and isosorbide dinitrate Fixed-dose combination 37.5 mg hydralazine/20 mg isosorbide dinitrate 3 times daily 75 mg hydralazine/40 mg isosorbide dinitrate 3 times daily
    Individual doses Hydralazine: 25 to 50 mg 3 or 4 times daily
    Isosorbide dinitrate: 20 to 30 mg 3 or 4 times daily
    Hydralazine: 300 mg daily in divided doses
    Isosorbide dinitrate: 120 mg daily in divided doses
    Digoxin

    Loading dose: PO- 10 to 15 mcg/kg (half the total loading dose initially, then 1/4th the loading dose every 6 to 8 hours two times), OR
    IV- 8 to 12 mcg/kg (half the total loading dose initially, then 1/4th the loading dose every 6 to 8 hours two times)
    Maintenance dose: PO- 3.4 to 5.1 mcg/kg/day once daily, OR
    IV- 2.4 to 3.6 mcg/kh/day once daily
    Drugs that increase the concentration of digoxin include amiodarone, quinidine and verapamil||

    Do's

    Acute Decompensated Heart Failure

    • Differentiate systolic and diastolic heart failure among patients with ADHF in order to guide therapy:
      • Inotropic agents that increase contractility are not indicated as important for the patient with acute decompensated systolic heart failure.
      • While beta blocker initiation is relatively contraindicated in acute decompensated systolic heart failure, control of tachycardia is very useful in the patient with diastolic heart failure to prolong left ventricular filling time.
      • While the initiation of ACE inhibitors may not be recommended in acute decompensated systolic heart failure, ACE inhibition may be of benefit in acute decompensated diastolic heart failure.
    • Rely on the patient's volume status to guide the aggressiveness of diuresis in ADHF.
    • Continue chronic medications during acute decompensation in the following conditions:
    • Digoxin decreases hospitalization but not mortality in the RALES study. It can be used in CHF & afib to reduce the ventricular response. In the RALES study, a level of < 1 ng/ml was associated with efficacy. Levels > 1 ng/ml not associated with greater efficacy and associated with higher mortality. No need to load a CHF patient with dig. For majority of patients with normal Cr, a daily dose of 0.25 mg of digoxin is usually adequate. In the older patient or in those patients with renal impairment, a dose of 0.125 mg per day may be adequate. Drugs that increase the concentration of digoxin include amiodarone, quinidine and verapamil. [6][7][8][9][10][11][12]
    • DVT prophylaxis unless contraindicated.[13][14]
    • Consider adding another diuretic (e.g. metolazone or thiazides) for worsening congestion despite high doses of loop diuretics.[15][16]
    • Daily serum electrolytes, urea nitrogen, and creatinine concentrations should be measured during the use of IV diuretics or active titration of heart failure medications.
    • Convert all IV diuretic to oral forms in anticipation of discharge.
    • Schedule an early follow-up visit (within 7 to 14 days) and early telephone follow-up (within 3 days) of hospital discharge .[17][18]

    Chronic Heart Failure

    Don'ts

    References

    1. 1.0 1.1 1.2 1.3 1.4 Yancy CW, Jessup M, Bozkurt B, Butler J, Casey DE, Drazner MH; et al. (2013). "2013 ACCF/AHA guideline for the management of heart failure: executive summary: a report of the American College of Cardiology Foundation/American Heart Association Task Force on practice guidelines". Circulation. 128 (16): 1810–52. doi:10.1161/CIR.0b013e31829e8807. PMID 23741057.
    2. Hunt SA, Abraham WT, Chin MH, Feldman AM, Francis GS, Ganiats TG; et al. (2009). "2009 Focused update incorporated into the ACC/AHA 2005 Guidelines for the Diagnosis and Management of Heart Failure in Adults A Report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines Developed in Collaboration With the International Society for Heart and Lung Transplantation". J Am Coll Cardiol. 53 (15): e1–e90. doi:10.1016/j.jacc.2008.11.013. PMID 19358937.
    3. Perna, ER.; Macín, SM.; Parras, JI.; Pantich, R.; Farías, EF.; Badaracco, JR.; Jantus, E.; Medina, F.; Brizuela, M. (2002). "Cardiac troponin T levels are associated with poor short- and long-term prognosis in patients with acute cardiogenic pulmonary edema". Am Heart J. 143 (5): 814–20. PMID 12040342. Unknown parameter |month= ignored (help)
    4. McMurray JJ, Adamopoulos S, Anker SD, Auricchio A, Böhm M, Dickstein K; et al. (2012). "ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure 2012: The Task Force for the Diagnosis and Treatment of Acute and Chronic Heart Failure 2012 of the European Society of Cardiology. Developed in collaboration with the Heart Failure Association (HFA) of the ESC". Eur Heart J. 33 (14): 1787–847. doi:10.1093/eurheartj/ehs104. PMID 22611136.
    5. Fuat A, Murphy JJ, Hungin AP, Curry J, Mehrzad AA, Hetherington A; et al. (2006). "The diagnostic accuracy and utility of a B-type natriuretic peptide test in a community population of patients with suspected heart failure". Br J Gen Pract. 56 (526): 327–33. PMC 1837840. PMID 16638247.
    6. The Captopril-Digoxin Multicenter Research Group. Comparative effects of therapy with captopril and digoxin in patients with mild to moderate heart failure. JAMA. 1988;259:539–44.
    7. Dobbs SM, Kenyon WI, Dobbs RJ. Maintenance digoxin after an episode of heart failure: placebo-controlled trial in outpatients. Br Med J. 1977;1:749–52
    8. Lee DC, Johnson RA, Bingham JB, et al. Heart failure in outpatients: a randomized trial of digoxin versus placebo. N Engl J Med. 1982;306: 699–705.
    9. Guyatt GH, Sullivan MJ, Fallen EL, et al. A controlled trial of digoxin in congestive heart failure. Am J Cardiol. 1988;61:371–5.
    10. . DiBianco R, Shabetai R, Kostuk W, et al. A comparison of oral milrinone, digoxin, and their combination in the treatment of patients with chronic heart failure. N Engl J Med. 1989;320:677–83.
    11. Uretsky BF, Young JB, Shahidi FE, et al., for the PROVED Investigative Group. Randomized study assessing the effect of digoxin withdrawal in patients with mild to moderate chronic congestive heart failure: results of the PROVED trial. J Am Coll Cardiol. 1993;22:955–62.
    12. Packer M, Gheorghiade M, Young JB, et al. Withdrawal of digoxin from patients with chronic heart failure treated with angiotensin-convertingenzyme inhibitors. RADIANCE Study. N Engl J Med. 1993;329:1–7.
    13. Alikhan R, Cohen AT, Combe S, Samama MM, Desjardins L, Eldor A; et al. (2003). "Prevention of venous thromboembolism in medical patients with enoxaparin: a subgroup analysis of the MEDENOX study". Blood Coagul Fibrinolysis. 14 (4): 341–6. PMID 12945875.
    14. Guyatt GH, Akl EA, Crowther M, Gutterman DD, Schuünemann HJ, American College of Chest Physicians Antithrombotic Therapy and Prevention of Thrombosis Panel (2012). "Executive summary: Antithrombotic Therapy and Prevention of Thrombosis, 9th ed: American College of Chest Physicians Evidence-Based Clinical Practice Guidelines". Chest. 141 (2 Suppl): 7S–47S. doi:10.1378/chest.1412S3. PMC 3278060. PMID 22315257.
    15. Grosskopf I, Rabinovitz M, Rosenfeld JB (1986). "Combination of furosemide and metolazone in the treatment of severe congestive heart failure". Isr J Med Sci. 22 (11): 787–90. PMID 3793436.
    16. Rosenberg J, Gustafsson F, Galatius S, Hildebrandt PR (2005). "Combination therapy with metolazone and loop diuretics in outpatients with refractory heart failure: an observational study and review of the literature". Cardiovasc Drugs Ther. 19 (4): 301–6. doi:10.1007/s10557-005-3350-2. PMID 16189620.
    17. Krumholz HM, Chen YT, Wang Y, Vaccarino V, Radford MJ, Horwitz RI (2000). "Predictors of readmission among elderly survivors of admission with heart failure". Am Heart J. 139 (1 Pt 1): 72–7. PMID 10618565.
    18. Hernandez AF, Greiner MA, Fonarow GC, Hammill BG, Heidenreich PA, Yancy CW; et al. (2010). "Relationship between early physician follow-up and 30-day readmission among Medicare beneficiaries hospitalized for heart failure". JAMA. 303 (17): 1716–22. doi:10.1001/jama.2010.533. PMID 20442387.
    19. Heerdink ER, Leufkens HG, Herings RM, et al. NSAIDs associated with increased risk of congestive heart failure in elderly patients taking diuretics. Arch Intern Med. 1998;158:1108–12.
    20. . Herchuelz A, Derenne F, Deger F, et al. Interaction between nonsteroidal anti-inflammatory drugs and loop diuretics: modulation by sodiumbalance. J Pharmacol Exp Ther. 1989;248:1175–81.
    21. Gottlieb SS, Robinson S, Krichten CM, et al. Renal response to indomethacin in congestive heart failure secondary to ischemic or idiopathic dilated cardiomyopathy. Am J Cardiol. 1992;70:890–3
    22. Bank AJ, Kubo SH, Rector TS, et al. Local forearm vasodilation with intra-arterial administration of enalaprilat in humans. Clin Pharmacol Ther. 1991;50:314–21.
    23. The Cardiac Arrhythmia Suppression Trial (CAST) Investigators. Preliminary report: effect of encainide and flecainide on mortality in a randomized trial of arrhythmia suppression after myocardial infarction. N Engl J Med. 1989;321:406–12.
    24. The Cardiac Arrhythmia Suppression Trial II Investigators. Effect of the antiarrhythmic agent moricizine on survival after myocardial infarction. N Engl J Med. 1992;327:227–33.
    25. Pratt CM, Eaton T, Francis M, et al. The inverse relationship between baseline left ventricular ejection fraction and outcome of antiarrhythmic therapy: a dangerous imbalance in the risk-benefit ratio. Am Heart J. 1989;118:433–40.
    26. Cuffe MS, Califf RM, Adams KF, Benza R, Bourge R, Colucci WS, Massie BM, O'Connor CM, Pina I, Quigg R, Silver MA, Gheorghiade M (2002). "Short-term intravenous milrinone for acute exacerbation of chronic heart failure: a randomized controlled trial". JAMA : the Journal of the American Medical Association. 287 (12): 1541–7. PMID 11911756. Retrieved 2012-04-06. Unknown parameter |month= ignored (help)
    27. Juurlink DN, Mamdani MM, Lee DS, Kopp A, Austin PC, Laupacis A; et al. (2004). "Rates of hyperkalemia after publication of the Randomized Aldactone Evaluation Study". N Engl J Med. 351 (6): 543–51. doi:10.1056/NEJMoa040135. PMID 15295047.
    28. Bozkurt B, Agoston I, Knowlton AA (2003). "Complications of inappropriate use of spironolactone in heart failure: when an old medicine spirals out of new guidelines". J Am Coll Cardiol. 41 (2): 211–4. PMID 12535810.
    29. Horwich TB, MacLellan WR, Fonarow GC (2004). "Statin therapy is associated with improved survival in ischemic and non-ischemic heart failure". J Am Coll Cardiol. 43 (4): 642–8. doi:10.1016/j.jacc.2003.07.049. PMID 14975476.
    30. Gissi-HF Investigators. Tavazzi L, Maggioni AP, Marchioli R, Barlera S, Franzosi MG; et al. (2008). "Effect of rosuvastatin in patients with chronic heart failure (the GISSI-HF trial): a randomised, double-blind, placebo-controlled trial". Lancet. 372 (9645): 1231–9. doi:10.1016/S0140-6736(08)61240-4. PMID 18757089.

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