Heart failure resident survival guide: Difference between revisions

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'''For acute heart failure prevention resident survival guide click [[Acute heart failure prevention resident survival guide|here]].'''
'''For acute heart failure prevention click [[Acute heart failure prevention|here]].'''


{{CMG}}; {{AE}} {{MS}}; {{AO}}
{{CMG}}; {{AE}} {{MS}}; {{AO}}; {{Rim}}


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! style="font-size: 80%; padding: 0 5px; background: #DCDCDC" align=left | Treatment
! style="font-size: 80%; padding: 0 5px; background: #DCDCDC" align=left | Treatment
:[[Acute heart failure resident survival guide#Treatment|Stage C]]
[[Heart failure resident survival guide#Prevention of Heart Failure in Stage A and B|Stage A and B]]<br>
:[[Chronic heart failure resident survival guide|Stage D]]
[[Heart failure resident survival guide#Treatment of Heart Failure in Stage C and D|Stage C and D]]<br>
:[[Acute heart failure resident survival guide#Diuretic Therapy|Diuretic Therapy]]
[[Heart failure resident survival guide#Diuretic Therapy Details|Diuretic Therapy]]<br>
:[[Acute heart failure resident survival guide#Medications|Medications]]
[[Heart failure resident survival guide#Medications|Medication Dosages]]
|-
|-
! style="font-size: 80%; padding: 0 5px; background: #DCDCDC" align=left | Prevention
! style="font-size: 80%; padding: 0 5px; background: #DCDCDC" align=left | [[Heart failure resident survival guide#Do's|Do's]]
:[[Acute heart failure resident survival guide#Prevention of Heart Failure|Stage A & B]]
|-
|-
! style="font-size: 80%; padding: 0 5px; background: #DCDCDC" align=left | [[Acute 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]]
|-
! style="font-size: 80%; padding: 0 5px; background: #DCDCDC" align=left | [[Acute heart failure resident survival guide#Don'ts|Don'ts]]
|}
|}


==Overview==
==Overview==
Acute heart failure can occur in the setting of a new onset heart failure or worsening of an existing chronic heart failure (also known as [[acute decompensated heart failure]], [[flash pulmonary edema]], [[ADHF]]).  ADHF presents with acute shortness of breath due to the development of [[pulmonary edema]] (the rapid accumulation of fluid in the lung).  Other signs and symptoms of ADHF include [[hypotension]] with impaired and organ perfusion manifested by [[worsening renal function]], altered mentation and [[cold clammy extremities]].  ADHF is associated with a poor prognosis if not treated aggressively.  Like chronic heart failure therapy, the goal is to improve symptoms but unlike chronic therapy the other goals are to improve oxygenation and hemodynamic stability.  The mainstays of the acute medical treatment in acute decompensated [[congestive heart failure]] include [[oxygen]] to improve [[hypoxia]], [[diuresis]] to reduce both [[preload]] and intravascular volume and vasodilators to reduce [[afterload]].  Some of the mainstays of [[chronic heart failure]] therapy are not initiated acutely ([[ACE inhibitors]], [[beta blockers]] and [[digoxin]]).
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==
===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>


===Based on the Severity of Congestive Heart Failure===
{| style="cellpadding=0; cellspacing= 0; width: 800px;"
The New York Heart Association (NYHA) assessment of heart failure severity is often used to guide treatment:
|-
{|class="wikitable"
| 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'''
! NYHA<br> classification!! Description
|-
|-
| '''I'''|| No limitation of physical activity. Ordinary physical activity does not cause symptoms of heart failure (HF)
| 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'''
|-
|-
| '''II'''|| 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 |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 | -
|-
|-
| '''III'''|| 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 |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
|-
|-
| '''IV'''|| 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 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
''NYHA - New York Heart Association''
 
===Based on the Stage of Heart Failure===
{|class="wikitable"
! ACCF/AHA Stages !! Description
|-
|-
| '''A'''|| 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 |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
|-
|-
| '''B'''|| Structural heart disease but without signs or 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
|-
|-
| '''C'''|| Structural heart disease with prior or current 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
|-
|-
| '''D'''|| Refractory HF requiring specialized interventions
|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
|}
|}
''ACCF - American College of Cardiology Foundation; AHA - American Heart Association''


===Based on Left Ventricular Ejection Fraction (LVEF)===
===Classification by Other Factors===
* [[Diastolic dysfunction|Heart failure with preserved ejection fraction]] (HFpEF) or [[diastolic heart failure]]: [[ejection fraction]] ≥ 50%
====Left Ventricular Ejection Fraction (LVEF)====
* [[Systolic dysfunction|Heart failure with reduced ejection fraction]] (HFrEF) or [[Systolic dysfunction|systolic heart failure]]: [[ejection fraction]] 40%
* [[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==
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==FIRE: Focused Initial Rapid Evaluation==
==FIRE: Focused Initial Rapid Evaluation==
A Focused Initial Rapid Evaluation (FIRE) should be performed to identify patients in need of immediate intervention.<br>
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%">Boxes in red signify that an urgent management is needed.</span>


<span style="font-size:85%">'''Abbreviations:'''
<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]];
'''MAP:''' [[Mean arterial pressure]];
'''NYHA:''' New York Heart Association;
'''Na:''' [[Sodium]];
'''SBP:''' [[Systolic blood pressure]]
'''NSAID:''' [[Non steroidal anti-inflammatory drug]];
'''SBP:''' [[Systolic blood pressure]];
'''S3:''' [[Third heart sound]];
</span>
</span>
<br>
<br>
{{familytree/start}}
{{familytree/start}}
{{familytree | | | A01 | | A01=<div style="float: left; text-align: left; width: 20em; padding:1em;">  '''Identify cardinal findings that increase the pretest probability of acute heart failure'''<br>
{{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>
❑ Past medical history of [[heart failure]] <br>
❑ History of [[orthopnea]] and [[paroxysmal nocturnal dyspnea]]<br>
❑ History of [[orthopnea]] and [[paroxysmal nocturnal dyspnea]]<br>
❑ [[Dyspnea]]<br>
❑ [[Chest pain]] <br>
❑ Pulmonary [[crepitations]]/[[rales]]/[[crackles]]<br>
❑ Pulmonary [[crepitations]]/[[rales]]/[[crackles]]<br>
❑ [[Cool extremities]]<br>
❑ [[Pedal edema|Peripheral edema]] <br>
❑ [[Heart sounds#Third heart sound S3|Third heart sound (S3)]]</div>}}
❑ [[Heart sounds#Third heart sound S3|Third heart sound (S3)]]</div>}}
{{familytree | | | |!| |}}
{{familytree | | | |!| |}}
{{familytree | | | W01 | |W01=<div style="float: left; text-align: left; width: 25em; padding:1em;">'''Does the patient have any of the following findings that require urgent management?'''<br>
{{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>
❑ [[Hypotension]] ([[SBP]] < 90 mmHg or drop in [[MAP]] >30 mmHg)<br>
❑ Severe decompendated HF:
❑ [[Altered mental status]]<br>
:❑ [[Hypotension]] ([[SBP]] < 90 mmHg or drop in [[MAP]] >30 mmHg) and/or [[cardiogenic shock]]<br>
❑ [[Cool extremities|Cold and clammy extremities]]<br>
:❑ [[Altered mental status]]<br>
❑ [[Oliguria|Urine output <0.5mL/kg/hr]]<br>
:❑ [[Cool extremities|Cold and clammy extremities]]<br>
❑ [[Metabolic acidosis]] </div>}}
:❑ [[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 | |,|-|^|-|.| |}}
{{familytree | B01 | | B02 | |B01=<div style=" background: #FA8072"> {{fontcolor|#F8F8FF|Yes}}</div> |B02='''No'''}}
{{familytree | B01 | | B02 | |B01=<div style=" background: #FA8072"> {{fontcolor|#F8F8FF|Yes}}</div> |B02='''No'''}}
{{familytree | |!| | | |!| | |}}
{{familytree | |!| | | |!| | |}}
{{familytree | C01 | | C02 | |C01=<div style=" background: #FA8072; color: #F8F8FF;; text-align: left; width: 25em; padding:1em;">'''Treat cardiogenic shock'''<br>
{{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>
❑ Admit to intensive care unit (ICU) or coronary care unit (CCU) for closer monitoring<br>
|C02=<div style="float: left; text-align: center; width: 25em;">[[Heart failure resident survival guide#Complete Diagnostic Approach|Proceed to complete diagnostic approach]]</div> }}
❑ Initiate [[oxygen|<span style="color:white;">oxygen</span>]] therapy for patients with oxygen saturation <90% or PaO2 <60 mmHg (8.0 kPa)<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><br>
{{familytree | |!| | | | | | |}}
:❑ Non-rebreather face masks<br>
{{familytree |boxstyle=background: #FA8072; color: #F8F8FF;  | D01 | | | | | |D01= <div style="float: left; text-align: left; width: 45em; padding:1em;">
:❑ [[Positive airway pressure|<span style="color:white;">Continuous positive airway pressure (CPAP)</span>]] or noninvasive positive pressure ventilation (NPPV) if oxygen saturation cannot be maintained by the use face masks<br>
'''Initial stabilization:''' <br>
:Mechanical ventilation (PEEP) usually when CPAP or NPPV fails<br>
Assess the airway <br>
❑ For [[SBP|<span style="color:white;">SBP </span>]] 85 - 100 mm Hg <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>
:❑ Consider [[dobutamine|<span style="color:white;">dobutamine at 2.5 to 5 mcg/kg/min</span>]] or [[milrinone|<span style="color:white;">milrinone at 0.125 to 0.75 mcg/kg/min</span>]]<br>
Monitor [[heart rate|<span style="color:white;">heart rate</span>]] and [[blood pressure|<span style="color:white;">blood pressure</span>]] continuously<br>
❑ For [[SBP|<span style="color:white;">SBP </span>]] < 85 mm Hg<br>
❑ Monitor oxygen saturation continuously<br>
:Consider [[dopamine|<span style="color:white;">dopamine at 5 to 10 mcg/kg/min</span>]] and [[norepinephrine|<span style="color:white;">norepinephrine at 0.2–1.0 mcg/kg/min</span>]]<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>
❑ Consider [[Intra-aortic balloon pump|<span style="color:white;">intra-aortic balloon pump</span>]], if [[hypotension|<span style="color:white;">hypotension</span>]] persists<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>
Consider [[Ventricular assist device|<span style="color:white;">left ventricular assist devices in severe cases</span>]]<br>
Secure intravenous access with 18 gauge cannula <br>
[[Cardiogenic shock resident survival guide|<span style="color:white;">Click here for cardiogenic shock resident survival guide</span>]]</div>|C02=<div style="float: left; text-align: left; width: 18em; padding:1em;">'''Does the patient have severe symptoms of heart failure?'''<br>
❑ Monitor fluid intake and urine output carefully (guide the adjustment of the diuretics dose)  <br><br>
❑ '''NYHA class III'''<br>
 
:Marked limitation of physical activity<br>
'''Assess congestion and perfusion:'''<br>
:Comfortable at rest, but less than ordinary activity causes symptoms of HF<br>
'''''Congestion at rest''''' (dry vs. wet)<br>
❑ '''NYHA class IV'''<br>
''"Wet" suggested by orthopnea, ↑JVP, rales, S3, pedal edema''<br>
:❑ Unable to carry on any physical activity without symptoms of HF, or symptoms of HF at rest
'''''Low perfusion at rest (warm vs. cold)'''''<br>
</div> }}
''"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>
{{familytree | | | |,|-|^|-|.| |}}
The patient is:<br>
{{familytree | | | D01 | | D02 | |D01=<div style=" background: #FA8072; color: #F8F8FF;"> {{fontcolor|#F8F8FF|Yes}}</div> |D02='''No'''}}
Warm and dry, OR <br>
{{familytree | | | |!| | | |!| | | |}}
Warm and wet, OR <br>
{{familytree | | | E01 | | E02 |E01=<div style=" background: #FA8072; color: #F8F8FF;; text-align: left; width: 25em; padding:1em;">'''<span style="color:white;">Urgent treatment</span>'''<br>
Cold and dry, OR <br>
❑ [[Acute heart failure resident survival guide#Diuretic Therapy Details|<span style="color:white;">Diuretic therapy (click for details)</span>]]<br>
❑ Cold and wet <br><br>
❑ <span style="color:white;">Administer</span> [[oxygen|<span style="color:white;">oxygen (as noted above)</span>]]<br>
 
<span style="color:white;">Administer IV</span> [[Vasodilators|<span style="color:white;">vasodilators</span>]] e.g.,[[nitroglycerin|<span style="color:white;">nitroglycerin at 5 to 10 mcg/min, increase dose by 5-10mcg/min <br>every 3-5 mins as tolerated.  Max of 400mcg/min</span>]] '''OR''' [[nesiritide|<span style="color:white;">nesiritide at 2 mcg/kg bolus; then 0.01 mcg/kg/minute continuous infusion.  Max of 0.03 mcg/kg/minute</span>]]<br></div>|E02=<div style="float: left; text-align: left; width: 15em; padding:1em;"> '''[[Acute heart failure resident survival guide#Complete Diagnostic Approach|Continue with the complete diagnostic approach below]]''' </div>}}
'''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}}
{{familytree/end}}


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<span style="font-size:85%">'''Abbreviations:'''
<span style="font-size:85%">'''Abbreviations:'''
'''ANA:''' [[Antinuclear antibody]];
'''ARDS:''' [[Acute respiratory distress syndrome]];
'''ARDS:''' [[Acute respiratory distress syndrome]];
'''BNP:''' [[B-type natriuretic peptide]];
'''BNP:''' [[B-type natriuretic peptide]];
Line 158: Line 254:
'''CBC:''' [[Complete blood count]];
'''CBC:''' [[Complete blood count]];
'''CCB:''' [[Calcium channel blocker]];
'''CCB:''' [[Calcium channel blocker]];
'''CHF:''' [[Congestive heart failure]];
'''CT:''' [[Computed tomography]];
'''CT:''' [[Computed tomography]];
'''CXR:''' [[Chest X-ray]];
'''CXR:''' [[Chest X-ray]];
'''DM:''' [[Diabetes mellitus]];
'''DM:''' [[Diabetes mellitus]];
'''EKG:''' [[Electrocardiogram]];
'''ECG:''' [[Electrocardiogram]];
'''GDMT:''' Guideline-directed medical therapy;
'''JVP:''' [[Jugular venous pressure]];
'''HF:''' [[Heart failure]];
'''HTN:''' [[Hypertension]];
'''HTN:''' [[Hypertension]];
'''LVEF:''' [[Left ventricular ejection fraction]];
'''LVEF:''' [[Left ventricular ejection fraction]];
Line 168: Line 266:
'''MI:''' [[Myocardial infarction]];
'''MI:''' [[Myocardial infarction]];
'''MRI:''' [[Magnetic resonance imaging]];
'''MRI:''' [[Magnetic resonance imaging]];
'''NT-pro BNP:''' N-terminal pro-brain natriuretic peptide;
'''NT-pro BNP:''' [[N-terminal pro-brain natriuretic peptide]];
'''OCPs:''' [[Oral contraceptive pill]]s;
'''OCPs:''' [[Oral contraceptive pill]]s;
'''PAWP:''' [[Pulmonary capillary wedge pressure|Pulmonary artery wedge pressure]];
'''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]]
'''TSH:''' [[Thyroid stimulating hormone]]
</span>
</span>
<br>
<br>


{{familytree/start}}
{{familytree/start}}
{{familytree | | | | | | | | A01 | | |A01=<div style="float: left; text-align: left; width: 20em; padding:1em;"> '''Characterize the symptoms:'''<br>
{{familytree | | | | | | | | A01 | | |A01=<div style="float: left; text-align: left; width: 30em; padding:1em;"> '''Characterize the symptoms:'''<br>
''Symptoms of fluid accumulation''<br>
''Symptoms of left-sided fluid accumulation:''<br>
❑ [[Dyspnea]]<br>
❑ [[Dyspnea]]<br>
:❑ At rest<br>
:❑ At rest<br>
Line 185: Line 285:
❑ [[Orthopnea]]<br>
❑ [[Orthopnea]]<br>
❑ [[Cough]]<br>
❑ [[Cough]]<br>
''Symptoms of right-sided fluid accumulation:''<br>
❑ [[Peripheral edema]]<br>
❑ [[Peripheral edema]]<br>
❑ [[Ascites]]<br>
❑ Right upper quadrant abdominal discomfort<br>
''Symptoms of reduced cardiac output''<br>
❑ [[Bloating]]<br>
❑ [[Satiety]]<br>
''Symptoms of reduced cardiac output:''<br>
❑ [[Fatigue]]<br>
❑ [[Fatigue]]<br>
❑ [[Exercise intolerance]]<br>
❑ [[Oliguria]]<br>
❑ [[Oliguria]]<br>
❑ [[Dizziness]]<br>
❑ [[Dizziness]]<br>
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❑ [[Altered mental status]]<br>
❑ [[Altered mental status]]<br>
❑ [[Cyanosis]]<br>
❑ [[Cyanosis]]<br>
❑ [[Anorexia]]<br>
❑ [[Abdominal pain]] (suggestive of [[mesenteric ischemia]])<br>
❑ [[Abdominal pain]] (suggestive of [[mesenteric ischemia]])<br>
''Symptoms suggestive of precipitating events''<br>
''Symptoms suggestive of precipitating events:''<br>
❑ [[Chest pain]] (if [[Coronary heart disease|myocardial ischemia]] is present)<br>
❑ [[Chest pain]] (suggestive of [[coronary heart disease|myocardial ischemia]])<br>
❑ [[Palpitations]] (suggestive of [[arrhythmia]]s)<br>
❑ [[Palpitations]] (suggestive of [[arrhythmia]]s)<br>
❑ [[Fever]] (suggestive of [[sepsis]])<br>
❑ [[Fever]] (suggestive of [[infection]])<br>
''Nonspecific symptoms''<br>
''Nonspecific symptoms:''<br>
❑ [[Anorexia]]<br>
❑ [[Bloating]]<br>
❑ [[Nausea]]<br>
❑ [[Nausea]]<br>
❑ [[Weight loss]]<br>
❑ [[Weight loss]]<br>
Line 228: Line 331:
❑ '''Family history'''<br>
❑ '''Family history'''<br>
:❑ History of [[dilated cardiomyopathy]]<br>
:❑ History of [[dilated cardiomyopathy]]<br>
❑ [[Radiation]] to the chest</div>}}
:❑ [[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 | | | | | | | | |!| | | | |}}
{{familytree | | | | | | | | B01 | | | |B01=<div style="float: left; text-align: left; width: 25em; padding:1em;"> '''Examine the patient:'''<br>
{{familytree | | | | | | | | B01 | | | |B01=<div style="float: left; text-align: left; width: 25em; padding:1em;"> '''Examine the patient:'''<br>
Line 234: Line 344:
❑ Ill-looking<br>
❑ Ill-looking<br>
❑ In respiratory distress<br>
❑ In respiratory distress<br>
Usually in upright sitting position<br>
In upright sitting position<br>


'''Vitals:'''<br>
'''Vitals:'''<br>
Line 241: Line 351:
❑ [[Pulse]]<br>
❑ [[Pulse]]<br>
:❑ [[Tachycardia]]<br>
:❑ [[Tachycardia]]<br>
:❑ [[Pulse pressure#Narrowed Pulse Pressure causes|Narrow pulse pressure]] (<25 mmHg)<br>
:❑ [[Pulse pressure#Narrowed Pulse Pressure causes|Narrow pulse pressure]] (<25% of SBP)<br>
❑ [[Blood pressure]]<br>
❑ [[Blood pressure]]<br>
:❑ [[Hypotension]] (suggestive of circulatory collapse)<br>
:❑ [[Hypotension]] (suggestive of circulatory collapse)<br>
:❑ [[Hypertension]]  <br>
:❑ [[Hypertension]]  <br>
❑ [[Respiration]]<br>   
❑ [[Respiration]]<br>   
:❑ [[Tachypnea]] (commonest symptom)<br>
:❑ [[Tachypnea]] (most common symptom)<br>
❑ [[Pulse oximetry]] assure sat is > 90%<br>
❑ [[Pulse oximetry]] (maintain oxygen sat ≥ 94% unless COPD)<br>


'''Weight:'''<br>
'''Weight:'''<br>
❑ Subtract 'dry weight' from current weight to quantitate extent of volume overload and [[edema]]<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>
'''Skin'''<br>
❑ [[Cool extremities|Cool and clammy]], in hypoperfusion or [[cardiogenic shock]]<br>
❑ [[Cool extremities|Cool and clammy]] (suggestive of hypoperfusion)<br>
❑ [[Cyanosis]], in severe [[hypoxemia]]<br>
❑ [[Cyanosis]] (suggestive of severe [[hypoxemia]])<br>
❑ [[Anasarca]]<br>
❑ [[Anasarca]]<br>
❑ [[Jaundice]] (suggestive of liver dysfunction secondary to right-sided fluid overload)<br>
'''Neck examination:'''<br>
'''Neck examination:'''<br>
❑ [[Jugular vein distention]] is often present<br>
❑ [[Jugular vein distention]] (suggestive of right-sided fluid overload)<br>
❑ Positive [[hepatojugular reflux]] (suggestive of right-sided fluid overload)<br>


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


'''Cardiovascular examination'''<br>
'''Cardiovascular examination'''<br>
Line 269: Line 384:
❑ [[Parasternal heave]] (suggestive of elevated right ventricular pressure)<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>
❑ [[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>
❑ New or changed [[murmur]] (suggestive of an underlying [[valvular heart disease]]s)<br>
:❑ [[Mitral regurgitation]] - [[Systolic heart murmur#Holosystolic (pansystolic)|Holosystolic murmur]]<br>
:❑ [[Mitral regurgitation]] - [[Systolic heart murmur#Holosystolic (pansystolic)|Holosystolic murmur]]<br>
Line 275: Line 393:


'''Abdominal examination'''<br>
'''Abdominal examination'''<br>
The following suggest volume overload and / or poor forward cardiac output:<br>
The following findings suggest volume overload and / or poor forward cardiac output:<br>
❑ [[Hepatojugular reflux]]<br>
❑ [[Hepatojugular reflux]]<br>
❑ [[Hepatomegaly]]<br>
❑ [[Hepatomegaly]]<br>
Line 285: Line 403:
'''Neurological examination'''<br>
'''Neurological examination'''<br>
❑ [[Altered mental status]]<br>
❑ [[Altered mental status]]<br>
❑ [[Syncope]] (suggestive of [[aortic stenosis]] or [[pulmonary embolism]])</div>}}
❑ [[Syncope]] (suggestive of [[aortic stenosis]] or [[pulmonary embolism]])
-----
'''Determine status of congestion and perfusion based on physical exam:'''<br>
''Congestion at rest (dry vs. wet)'' <br>
:"Wet" suggested by orthopnea, ↑JVP, positive hepatojugular reflux, abnormal valsalva response, rales, dullness upon percussion in bases, S3, peripheral edema, hepatomegaly, ascites, jaundice <br>
''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 | | | | | | | | |!| | | | | |}}
{{familytree | | | | | | | | D01 | | | |D01=<div style="float: left; text-align: left; width: 25em; padding:1em;">'''Order tests''': <br>
{{familytree | | | | | | | | D01 | | | |D01=<div style="float: left; text-align: left; width: 25em; padding:1em;">'''Order tests''': <br>
Line 292: Line 422:
:❑ [[Troponin]]
:❑ [[Troponin]]
::❑ Elevated in [[myocardial ischemia]] and acute cardiogenic pulmonary edema, particularly if [[creatinine clearance|creatinine clearance (CrCl)]] is reduced<br>
::❑ 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>
::❑ [[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>
:❑ [[Electrolytes]]<br>
::❑ Dilutional [[hyponatremia]] (with the presence of edema)
::❑ [[Sodium]]: [[hyponatremia]] may occur due to fluid overlaod
:❑ [[calcium|Serum calcium]]<br>
:❑ [[calcium|Serum calcium]]<br>
:❑ [[Magnesium|Serum magnesium]] which can be lowered by [[diuresis]]<br>
:❑ [[Magnesium|Serum magnesium]] can be lowered by [[diuresis]]<br>
:❑ [[Serum bicarbonate]] to monitor [[contraction alkalosis]] with [[diuresis]]
:❑ [[Serum bicarbonate]]: to monitor [[contraction alkalosis]] with [[diuresis]]
:❑ [[BUN]], [[creatinine]] may be elevated due to poor renal perfusion<br>
:❑ [[BUN]], [[creatinine]]: may be elevated due to poor renal perfusion<br>
:❑ [[Urinalysis]] <br>
:❑ [[Urinalysis]] <br>
:❑ [[Blood sugar|Fasting blood sugar]]<br>
:❑ [[Blood sugar|Fasting blood sugar]]<br>
:❑ [[Lipid profile|Fasting lipid profile]]<br>
:❑ [[Lipid profile|Fasting lipid profile]]<br>
:❑ [[Liver function tests]]<br>
:❑ [[Liver function tests]]: can be elevated secondary to peripheral hypoperfusion<br>
:❑ [[Thyroid-stimulating hormone|TSH]]<br>
:❑ [[Thyroid-stimulating hormone|TSH]]<br>
❑ [[B-type natriuretic peptide|BNP]] or NT-pro BNP (if diagnosis is uncertain)<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>
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>
:❑ [[B-type natriuretic peptide|BNP]] ≤ 100 pg/mL, or<br>
:❑ NT-pro BNP ≤ 300 pg/mL <br>
:❑ [[NT-pro BNP]] ≤ 300 pg/mL <br>
❑ [[Chest X-ray]] ([[ACC AHA guidelines classification scheme|Class I, level of evidence C]])<br>
❑ [[Chest X-ray]] ([[ACC AHA guidelines classification scheme|Class I, level of evidence C]])<br>
:❑ [[Cardiomegaly]] ([[cardiothoracic ratio]] >50%)<br>
:❑ [[Cardiomegaly]] ([[cardiothoracic ratio]] >50%)<br>
Line 315: Line 445:
:❑ [[Congestive heart failure chest x ray#Cephalization|Cephalization]]
:❑ [[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>
[[Image:Pulmonary edema.gif|center|200px|thumb|Chest X-ray findings in a patient with acute heart failure ]]<br>
❑ [[EKG]]<br>
❑ [[ECG]] (to help identify the cause of heart failure)<br>
:❑ [[Low QRS voltage]] due to electrically inert [[myocardium]]<br>
:❑ [[Low QRS voltage]] (suggestive of infiltrative or [[dilated cardiomyopathy]])<br>
:❑ [[Arrhythmia]] (usually [[atrial fibrillation]] which carries a poor prognosis and requires slowing to improve filling & [[cardiac output]])<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>
:❑ [[Poor R wave progression]] (suggestive of a prior [[MI]])<br>
:❑ [[Left ventricular hypertrophy]] (consistent with a history of [[hypertension]])<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 bundle branch block]] ([[LBBB]]) due to prior [[MI]], may result in dysynchrony)<br>
:❑ [[Left atrial enlargement]]<br> due to [[valvular disease]] or [[hypertension]]<br>
:❑ [[Left atrial enlargement]] (due to [[valvular disease]] or [[hypertension]])<br>
:❑ Non-specific [[ST segment]] and [[T wave]] changes may suggest [[ischemia]]<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]])
❑ 2-D [[echocardiography]] with Doppler <br> ([[ACC AHA guidelines classification scheme|Class I, level of evidence C]])
:❑ Assess ventricular size, function, wall thickness, wall motion, and valve function<br>
:❑ Assess chambers size, wall thickness, wall motion, and valve function<br>
:❑ Assess [[ejection fraction]]
❑ [[Cardiac radionuclide imaging|Radionuclide ventriculography]] or [[MRI]]<br>
❑ [[Cardiac radionuclide imaging|Radionuclide ventriculography]] or [[MRI]]<br>
:❑ To assess [[LVEF]] and volume when [[echocardiography]] is inadequate<br>
:❑ To assess [[LVEF]] and volume when [[echocardiography]] is inadequate<br>
:❑ To assess myocardial infiltrative processes or scar burden ([[MRI]])<br>
:❑ To assess myocardial infiltrative processes or scar burden ([[MRI]])<br>
❑ [[Coronary angiography]] (in settings of ischemia)<br>
❑ [[Coronary angiography]] looking for CAD<br>
❑ [[Right heart catheterization|Pulmonary artery catheterization]] in [[respiratory distress]] or [[shock]] or to definitively assess volume status and tailor therapy<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>
'''Order additional tests to rule out other etiologies:'''<br>
❑ [[Antinuclear antibodies|ANA]], [[rheumatoid factor]] (for rheumatologic diseases)<br>
❑ [[Antinuclear antibodies|ANA]] and [[rheumatoid factor]] (for rheumatologic diseases)<br>
❑ Diagnostic tests for [[hemochromatosis]], [[pheochromocytoma]]<br>
❑ Diagnostic tests for [[hemochromatosis]] and [[pheochromocytoma]]<br>
❑ [[Endomyocardial biopsy]] (when [[myocarditis]] is suspected)
❑ [[Endomyocardial biopsy]] (when [[myocarditis]] is suspected)
</div>}}
</div>}}
Line 342: Line 477:
<tr class="v-firstrow"><th>Alternative diagnoses</th><th>Features</th></tr>
<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> [[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> [[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> [[Pneumonia]]</td><td>❑ [[Fever]], [[cough]], [[sputum]]<br>❑ [[Pneumonia chest x ray|Consolidation]] on [[chest X-ray]]</td></tr>
Line 350: Line 486:
</div>}}
</div>}}
{{familytree | | | | | | |,|-|^|-|.| | | | | |}}
{{familytree | | | | | | |,|-|^|-|.| | | | | |}}
{{familytree | | | | | | X01 | | X02 | | | |X01=<div style="float: left; text-align: left; width: 15em; padding:1em;">'''[[Acute heart failure resident survival guide#Prevention of Heart Failure|Stage C]]''' <br> <br>
{{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>
❑ '''Patients with structural heart disease'''<br>
This refers to patients with the following:<br>
This refers to patients with the following:<br>
Line 357: Line 493:
:❑ Asymptomatic [[valvular disease]]<br><br>'''AND'''<br>
:❑ Asymptomatic [[valvular disease]]<br><br>'''AND'''<br>
❑ '''Signs or symptoms of heart failure'''<br><br>
❑ '''Signs or symptoms of heart failure'''<br><br>
''LV remodeling refers to the changes in size, shape and function of the heart resulting from cardiac load or injury''</div>
''<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: 15em; padding:1em;">'''[[Acute heart failure resident survival guide#Prevention of Heart Failure|Stage D]]''' <br> <br>
|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>
❑ '''Refractory heart failure'''<br>
:❑ Marked symptoms at rest<br>
:❑ Marked symptoms at rest<br>
Line 364: Line 500:
{{familytree/end}}
{{familytree/end}}


==Treatment==
==Prevention of Heart Failure in Stage A and B==
{{familytree/start}}
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>
{{familytree | | | | | | | | C01 | | | | | |C01=<div style="float: left; text-align: left; width: 25em; padding:1em;">'''Initial stabilization:'''<br>
 
----
<span style="font-size:85%">'''Abbreviations:'''
❑ Assess the [[airway]] <br>
'''ACE I:''' [[Angiotensin converting enzyme inhibitor]];
❑ Position the patient upright at an angle of 45 degrees<BR>
'''ACS:''' [[Acute coronary syndrome]];
❑ Check [[pulse oximetry]] <br>
'''CVD:''' [[Cardiovascular disease]];
❑ If [[hypoxemia]] is present (Sa02 < 90% or Pa02 <60 mmHg)
'''DM:''' [[Diabetes mellitus]];
:❑ Give [[oxygen]] by:<br>
'''EF:''' [[Ejection fraction]];
::❑ Non-rebreather face masks <br>
'''HF:''' [[Heart failure]];
::❑ [[Positive airway pressure|Continuous positive airway pressure]]<br>
'''HTN:''' [[Hypertension]];
:❑ Avoid [[morphine|IV morphine]] - may increase mortality / duration of intubation, generally not advisable, may relieve refractory symptoms though<br>
'''ICD:''' [[Implantable cardioverter defibrillator]];
❑ Ensure continuous cardiac monitoring<br>
'''MI:''' [[Myocardial infarction]];
❑ Secure intravenous access with 18 gauge canula <br>
'''PAD:''' [[Peripheral artery disease]]
❑ Monitor vitals signs <br>
</span>
❑ Monitor fluid intake and urine output
 
</div>}}
{{Family tree/start}}
{{familytree | | | | | | | | |!| | | |}}
{{Family tree | | | A01 | | | | | | | | | | A01= <div style="float: left; text-align: left; width: 25em; padding:1em;">'''What is the stage of heart failure (HF)?''' </div>}}
{{familytree | | | | | | | | E01 | | | |E01=<div style="float: left; text-align: left; width: 25em; padding:1em;">'''Consider admission if the following is present:'''<ref name="pmid20610207">{{cite journal |author=Lindenfeld J, Albert NM, Boehmer JP, Collins SP, Ezekowitz JA, Givertz MM, Katz SD, Klapholz M, Moser DK, Rogers JG, Starling RC, Stevenson WG, Tang WH, Teerlink JR, Walsh MN |title=HFSA 2010 Comprehensive Heart Failure Practice Guideline |journal=[[Journal of Cardiac Failure]] |volume=16 |issue=6 |pages=e1–194 |year=2010 |month=June |pmid=20610207 |doi=10.1016/j.cardfail.2010.04.004 |url=http://linkinghub.elsevier.com/retrieve/pii/S1071-9164(10)00173-9 |accessdate=2013-04-29}}</ref><br>
{{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>}}
❑ [[Hypotension]] and/or [[cardiogenic shock]]  <br>
{{Family tree | |!| | | |!| | | | | }}
❑ Poor end-organ perfusion - [[worsening renal function]], [[cold clammy extremities]], [[altered mental status]] <br>
{{Family tree | C01 | | C02 | | | | C01=<div style="float: left; text-align: left; width: 25em; padding:1em;">
❑ [[Hypoxemia]] - Sa02 ↓90%<br>
❑ Encourage healthy lifestyle and exercise <br>
❑ [[Atrial fibrillation]] with a rapid ventricular response resulting in [[hypotension]]<br>
Treat [[hypertension]] ( I-A) <br>
Presence of an [[acute coronary syndrome]]</div>}}
❑ Treat [[dyslipidemia]] (I-A) <br>
{{familytree | | | | | | | | |!| | | | |}}
Control [[obesity]] (I-C) <br>
{{familytree | | | | | | | | H01 | |H01=<div style="float: left; text-align: left; width: 25em; padding:1em;">'''Treat precipitating causes/co-morbidities'''<br> <span style="font-size:100%;color:red">Click for detailed management</span><br>
❑ Treat [[DM]] (I-C) <br>
----
❑ Avoid tobacco (I-C) <br>
[[Aortic regurgitation resident survival guide|Acute aortic]]/[[Mitral regurgitation resident survival guide|mitral regurgitation]]<br>
❑ Avoid cardiotoxic agents (I-C) <br>
❑ [[STEMI resident survival guide|Acute coronary syndrome]] <br>
❑ Administer [[ACE-I]] if [[HTN]], [[DM]], [[CVD]], [[PAD]] <br> </div>
[[Anemia resident survival guide|Anemia]]<br>
| C02=<div style="float: left; text-align: left; width: 25em; padding:1em;">
❑ [[Aortic dissection resident survival guide|Aortic dissection]]<br>
Encourage healthy lifestyle and exercise <br>
❑ [[Atrial fibrillation resident survival guide|Atrial fibrillation]]<br>
Treat [[hypertension]] (I-A) <br>
❑ [[Hypertensive crisis resident survival guide|Hypertensive crisis]]<br>
Treat [[dyslipidemia]] (I-A) <br>
❑ [[Acute kidney failure resident survival guide|Renal failure]] <br>
Control [[obesity]] (I-C) <br>
[[Sepsis resident survival guide|Sepsis]]</div>}}
Treat [[DM]] (I-C) <br>
{{familytree | | | | | | | | |!| | | | | | | |}}
Avoid tobacco (I-C) <br>
{{familytree | | | | | | | | I01 | | | | | | | |I01=<div style="float: left; text-align: left; width: 25em; padding:1em;">'''Assess hemodynamic and volume status'''<ref name="pmid12767667">{{cite journal| author=Nohria A, Tsang SW, Fang JC, Lewis EF, Jarcho JA, Mudge GH et al.| title=Clinical assessment identifies hemodynamic profiles that predict outcomes in patients admitted with heart failure. | journal=J Am Coll Cardiol | year= 2003 | volume= 41 | issue= 10 | pages= 1797-804 | pmid=12767667 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=12767667  }} </ref><br>
❑ Avoid cardiotoxic agents (I-C)</div>}}
❑ [[Congestion|Congestion at rest]] ('''dry vs. wet''')<br> "Wet" suggested by [[orthopnea]], ↑[[JVP]], [[rales]], [[Heart sounds#Third heart sound S3|S3]], [[pedal edema]]
{{Family tree | | | | | |!| | | | | }}
<br>
{{Family tree | | | | | D01 | | | | D01=<div style="float: left; text-align: left; width: 25em; padding:1em;">
❑ Low perfusion at rest ('''warm vs. cold''')<br> "Cold" suggested by [[Pulse pressure|narrow pulse pressure]], [[cool extremities]], [[hypotension]]</div>}}
'''Consider additional measures in selected patients:'''
{{familytree | |,|-|-|-|v|-|-|^|-|-|v|-|-|-|.| | |}}
❑ 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>
{{familytree | J01 | | J02 | | | | J03 |~| J04 | | |J01=<div style="float: left; text-align: left; width: 10em; padding:1em;">'''Warm & Dry'''<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 outpatient treatment<br>❑ Dietary sodium restriction (2-3 g daily)<br>❑ [[Smoking cessation]]<br>❑ [[Alcohol]] abstinence (≤2 standard drinks per day for men; ≤1 for women)<br>❑ Encourage exercise/physical activity<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>}}
'''Although [[ACE inhibitors]] and [[beta blockers]] should not be administered to patients with [[acute decompensated heart failure]], if the patient is compensated in the outpatient setting then administer:<br> ❑ [[ACE inhibitors]] or ([[ARBs]]) if LVEF is ≤ 40%<br>❑ [[Beta blockers]]'''<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><br></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)


J02=<div style="float: left; text-align: left; width: 10em; padding:1em;">'''Warm & Wet''' <br>
'''''Mechanical circulatory support (MCS)'''''
----
* Temporary [[MCS]] in [[HFrEF]] awaiting definitive therapy or resolution of acute precipitating event (I-B)
[[Acute heart failure resident survival guide#Diuretic Therapy Details|Diuretic therapy]]<br>
* Temporary [[MCS]] [[HFrEF]] with severe hemodynamic compromise, as a bridge therapy to recovery or decision (I-B)
❑ Treat co-morbidities [[HTN]], [[DM]], [[CAD]], [[AF]]</div>|
* 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)


J03=<div style="float: left; text-align: left; width: 10em; padding:1em;">'''Cold & Wet'''<br>
'''''Cardiac transplantation'''''
----
* Refractory to medical therapy, device, and surgery (I-C) </div>}}
❑ CCU admission<br>
{{Family tree/end}}
❑ Invasive hemodynamic monitoring (arterial line, consider pulmonary catheter if volume status unclear)<br>
❑ Intravenous inotropic drugs (e.g., [[dobutamine]])<br>❑ [[Acute heart failure resident survival guide#Diuretic Therapy Details|Diuretic therapy]] while monitoring [[blood pressure]]<br>❑ IV vasodilators</div>|J04=<div style="float: left; text-align: left; width: 10em; padding:1em;">'''Cold & Dry'''<br>
----
❑ CCU admission <br>
❑ Intravenous inotropic drugs (e.g., [[dobutamine]])<br>
❑ '''Persistent organ hypoperfusion''' (e.g., low urine output or persistent low SBP<85)<br>
:❑ [[Norepinephrine]] 0.2–1.0 mcg/kg/min, titrate to maintain a blood pressure of </div>}}
{{familytree | | | | | |!| | | | | |!| | | |!| | | | |}}
{{familytree | | | | | |`|-|-|v|-|-|^|-|-|-|'| | |}}
{{familytree | | | | | | | | X01 | | |X01=<div style="float: left; text-align: left; width: 25em; padding:1em;">'''Indications for [[implantable cardioverter defibrillator]] (ICD)'''<br>
----
❑ As primary prevention of sudden cardiac death in: <br>
:❑ Post [[MI]] with LVEF ≤ 35%, NYHA II or III on chronic GDMT ([[ACC AHA guidelines classification scheme|Class I, level of evidence A]])<br>
:❑ Post [[MI]] with LVEF ≤ 30%, NYHA I on chronic GDMT ([[ACC AHA guidelines classification scheme|Class I, level of evidence B]])<br>
:❑ Nonischemic dilated cardiomyopathy with LVEF ≤ 35% and NYHA II or III <br>
'''Contraindications'''<br>
❑ No reasonable expectation of survival with an acceptable functional status for at least 1 year<br>
❑ Incessant [[ventriculat tachycardia]] or [[ventricular fibrillation]]<br>
❑ Significant psychiatric illnesses that may be aggravated by device or that may preclude follow-up<br>
❑ NYHA class IV patients with drug-refractory congestive heart failure who are not candidates for cardiac transplantation or [[cardiac resynchronization therapy]]<br>
❑ [[Ventricular tachycardia]] due to completely reversible disorder in the absence of structural heart disease (e.g., electrolyte imbalance, drugs, or trauma) <br></div>}}
{{familytree | | | | | | | | |!| |}}
{{familytree | | | | | | | | K01 | | | |K01=<div style="float: left; text-align: left; width: 25em; padding:1em;">'''General measures'''<br>
----
❑ [[Low sodium diet]] <br>
❑ Monitor blood pressure, congestion, oxygenation<br>
❑ Daily weights using same scale after 1st void at same time of day<br>
❑ Intake and output charts<br>
❑ Convert all IV diuretic to oral forms in anticipation of discharge<br>
❑ '''Continue or initiate'''<br>
:❑ [[ACE inhibitors]]<br>
:❑ [[Beta blockers]]<br>
:❑ [[Omega-3 fatty acid]]<ref name="pmid18757090">{{cite journal| author=Gissi-HF Investigators. Tavazzi L, Maggioni AP, Marchioli R, Barlera S, Franzosi MG et al.| title=Effect of n-3 polyunsaturated fatty acids 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= 1223-30 | pmid=18757090 | doi=10.1016/S0140-6736(08)61239-8 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=18757090  }}  [http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=19172716 Review in: Ann Intern Med. 2009 Jan 20;150(2):JC1-11] </ref><br>
❑ Daily serum [[electrolytes]], [[urea]] & [[creatinine]]<br>
❑ [[DVT prophylaxis]]<br>
❑ [[Influenza]] & [[Streptococcus pneumoniae|pneumococcal]] vaccination <br>
❑ Encourage [[physical activity]] in stable patients</div>}}
{{familytree | | | | | | | | |!| | | | | | |}}
{{familytree | | | | | | | | L01 | | | |L01=<div style="float: left; text-align: left; width: 20em; padding:1em;">'''Discharge and follow-Up'''<br>
----
❑ Patient and family education<br>
❑ Prior to discharge, '''ensure''':<br>
:❑ Low salt diet<br>
:❑ Oral medication plan is stable for 24 hours<br>
:❑ No IV [[vasodilator]] or inotropic drugs for 24 hours<br>
:❑ Weighing scale is present in patient's home<br>
:❑ [[Smoking cessation]] counseling <br>
:❑ Follow-up clinic visit scheduled within 7 to 10 days
:❑ Ambulation prior to discharge to assess functional capacity<br>
❑ Telephone follow-up call usually 3 days post discharge <br>
❑ Potassium monitoring and repletion<br>
Click here for the detailed management of [[Hyperkalemia resident survival guide|hyperkalemia]] and [[Hypokalemia resident survival guide|hypokalemia]]</div>}}
{{familytree/end}}


====Diuretic Therapy Details====
{{familytree/start}}
{{familytree | | | A01 | |A01='''Evidence of volume overload'''}}
{{familytree | | | |!| |}}
{{familytree | | | B01 | |B01=<div style="float: left; text-align: left; width: 20em; padding:1em;">
❑ [[Low sodium diet]] (<2 g daily)<br>
❑ Free water restriction to <2 L/day if the Na is < 130 meq/L, and < 1 L/day or more if the Na is < 125 meq/L<br>
❑ Initiate IV [[diuretics]] due to poor absorption from gut<br>
:❑ [[Frusemide]] 40 mg, or
:❑ [[Torsemide]] 20 mg, or
:❑ [[Bumetanide]] 1 mg<br>
'''Contraindications to IV Diuresis'''<br>
❑ [[Hypotension]] and [[cardiogenic shock]]<br><br>
'''Note''' - Give a higher dose of IV diuretic in patients chronically on diuretic therapy (e.g., 2.5x their maintenance dose)
</div>}}
{{familytree | | | |!| | | |}}
{{familytree | | | C01 | |C01='''Symptomatic improvement?'''}}
{{familytree | |,|-|^|-|.| | |}}
{{familytree | D01 | | D02 | |D01=Yes|D02=No}}
{{familytree | |!| | | |!| | |}}
{{familytree | E01 | | E02 | |E01=Maintain current IV diuretic dose|E02=Double IV [[diuretic]] dose <br>and titrate according to patient's response <br>or when the maximum dose is reached}}
{{familytree | |!| | | |!| | |}}
{{familytree | |!| | | F01 | |F01='''No symptomatic improvement'''}}
{{familytree | |!| |,|-|^|-|.| | |}}
{{familytree | |!| G01 | | G02 | |G01=<div style="float: left; text-align: left; width: 20em; padding:1em;">'''Add'''<br>
❑ Another diuretic e.g., IV [[chlorothiazide]] or oral [[metolazone]]<br>'''or'''<br>
❑ An aldosterone antagonist e.g., [[spironolactone]] or [[eplerenone]], in post [[ST elevation myocardial infarction|MI]] patients<br>
'''Indications:'''<br>
❑ Cr ≤ 2.5 mg/dL in men or ≤ 2.0 mg/dL in women<br>
❑ Estimated [[glomerular filtration rate]] >30 mL/min/1.73 m2<br>
❑ [[Potassium|Serum potassium]] ≤ 5.0 mEq/L <br>
❑ NYHA class II–IV HF with LVEF ≤ 35%<br>
<span style="font-size:100%;color:red"> K<sup>+</sup>- sparing diuretic e.g [[amiloride]] or [[triamterene]] should not be administered with aldosterone antagonist given the risk of [[hyperkalemia]]</span><br></div>
|G02=<div style="float: left; text-align: left; width: 20em; padding:1em;">'''Adjuvants to diuretics'''<br>
----
❑ Low dose [[dopamine]] to preserve renal function and [[renal blood flow]]<br>
❑ IV [[nitroprusside]], [[nitroglycerin]], or [[nesiritide]] for hemodynamically stable patients to relieve [[dyspnea]]<br>
❑ Vasopressin antagonists (e.g. [[tolvaptan]]; start with 15mg orally daily) <ref name="pmid15113814">{{cite journal| author=Gheorghiade M, Gattis WA, O'Connor CM, Adams KF, Elkayam U, Barbagelata A et al.| title=Effects of tolvaptan, a vasopressin antagonist, in patients hospitalized with worsening heart failure: a randomized controlled trial. | journal=JAMA | year= 2004 | volume= 291 | issue= 16 | pages= 1963-71 | pmid=15113814 | doi=10.1001/jama.291.16.1963 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=15113814  }} </ref> <ref name="pmid11705818">{{cite journal| author=Udelson JE, Smith WB, Hendrix GH, Painchaud CA, Ghazzi M, Thomas I et al.| title=Acute hemodynamic effects of conivaptan, a dual V(1A) and V(2) vasopressin receptor antagonist, in patients with advanced heart failure. | journal=Circulation | year= 2001 | volume= 104 | issue= 20 | pages= 2417-23 | pmid=11705818 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11705818  }} </ref></div>}}
{{familytree | |!| |`|-|v|-|'| |}}
{{familytree | |!| | | H01 | | |H01=No symptomatic improvement<br>('''refractory edema''')}}
{{familytree | |!| | | |!| |}}
{{familytree | |!| | | I01 | |I01=[[Ultrafiltration]] or [[dialysis]]}}
{{familytree | |`|-|v|-|'| |}}
{{familytree | | | J01 | |J01=<div style="float: left; text-align: left; width: 25em; padding:1em;">'''General measures'''<br>
----
❑ Monitor BP, volume status, congestion<br>❑ Daily weights<br>❑ Intake and output charts<br>
❑ Convert all IV diuretic to oral<br>❑ Daily serum [[electrolytes]], [[urea]] & [[creatinine]]<br>❑ [[DVT prophylaxis]]</div>}}
{{familytree/end}}


==Primary Prevention==
{{familytree/start}}
{{familytree | | | | | A00 | | A00=<div style="float: left; text-align: left; width: 25em; padding:1em;">'''Does the patient have stage A or stage B of heart failure according to the [[Acute heart failure resident survival guide#Classification|ACCF/AHA staging system]]?'''</div>}}
{{familytree | |,|-|-|-|+|-|-|-|.| | | | }}
{{familytree | A01 | | A02 | | A03 | |A01=<div style="float: left; text-align: left; width: 20em; padding:1em;">'''Yes, the patient has stage A'''
----
Therapeutic goals:<br>
❑ Promote healthy lifestyle<br>
❑ Prevent CAD and comorbidities<br>
❑ Prevent LV structural abnormalities</div>|A02=<div style="float: left; text-align: left; width: 20em; padding:1em;">'''Yes, the patient has stage B'''
----
Therapeutic goal:
❑ Prevent symptoms of heart failure</div>
|A03=<div style="float: left; text-align: left; width: 20em; padding:1em;">'''No, the patient does not belong to any of the stages'''
----
No preventive therapy is needed</div>}}
{{familytree | |!| | | |!| |}}
{{familytree | B01 | | B02 | | |B01=<div style="float: left; text-align: left; width: 20em; padding:1em;">
❑ Control HTN and lipid disorders<br>
:❑ [[ACE inhibitors]] or ([[ARBs]]) in patients with vascular disease or DM<br>
:❑ [[Statins]]<br>
❑ Minimize risk factors
:❑ Dietary sodium restriction (2-3 g daily)<br>
:❑ [[Smoking cessation]]<br>
:❑ Alcohol abstinence (≤2 standard drinks per day for men; ≤1 for women)<br>
:❑ Encourage exercise/physical activity</div>|B02=<div style="float: left; text-align: left; width: 20em; padding:1em;">
❑ Administer [[ACE inhibitors]] or ([[ARBs]]) in patients with:<br>
:❑ Prior [[MI]] and LVEF ≤40% to prevent heart failure ([[ACC AHA guidelines classification scheme|Class I, level of evidence A]])<br>'''OR'''
:❑ LVEF ≤40% ([[ACC AHA guidelines classification scheme|Class I, level of evidence A]])<br>
❑ Administer [[beta blockers]] in patients with:<br>
:❑ Prior [[MI]] and LVEF ≤ 40% to prevent heart failure ([[ACC AHA guidelines classification scheme|Class I, level of evidence B]])<br>
:❑ LVEF ≤ 40% to prevent heart failure ([[ACC AHA guidelines classification scheme|Class I, level of evidence C]])<br>
❑ [[Statins]]<br>
:❑ Patients with MI ([[ACC AHA guidelines classification scheme|Class I, level of evidence A]])<br>
❑ Implantable cardioverter defibrillator (ICD) to prevent sudden death in: <br>
:❑ Asymptomatic ischemic cardiomyopathy ([[ACC AHA guidelines classification scheme|Class IIa, level of evidence B]])<br>
::❑ ≥ 40 day post-[[MI]]<br>
::❑ LVEF ≤ 30%<br>
::❑ On GDMT<br>
❑<span style="font-size:100%;color:red"> The use of CCBs e.g., verapamil and diltiazem in patients with LVEF ≤ 30%</span></div>}}
{{familytree/end}}


====Medications====
====Medications====
Line 571: Line 674:
! Maximum daily dose
! Maximum daily dose
|-
|-
| [[Loop diuretics]]||[[Furosemide]] ||20 to 40 mg once or twice <br>In HF patients on loop diuretic, the initial IV dose should <br>be greater or equal to their chronic oral daily dose.<ref name="pmid21366472">{{cite journal |author=Felker GM, Lee KL, Bull DA, Redfield MM, Stevenson LW, Goldsmith SR, LeWinter MM, Deswal A, Rouleau JL, Ofili EO, Anstrom KJ, Hernandez AF, McNulty SE, Velazquez EJ, Kfoury AG, Chen HH, Givertz MM, Semigran MJ, Bart BA, Mascette AM, Braunwald E, O'Connor CM |title=Diuretic strategies in patients with acute decompensated heart failure |journal=[[The New England Journal of Medicine]] |volume=364 |issue=9 |pages=797–805 |year=2011 |month=March |pmid=21366472 |pmc=3412356 |doi=10.1056/NEJMoa1005419 |url=http://www.nejm.org/doi/abs/10.1056/NEJMoa1005419?url_ver=Z39.88-2003&rfr_id=ori:rid:crossref.org&rfr_dat=cr_pub%3dwww.ncbi.nlm.nih.gov |accessdate=2013-04-30}}</ref>|| 600 mg
| [[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]] || 0.5 to 1.0 mg once or twice || 10 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]]|| 10 to 20 mg once|| 200 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]] || 250 to 500 mg once or twice|| 1000 mg
| [[Thiazide diuretics]] || [[Chlorothiazide]] <br> ''(duration of action: 6 to 12 h)''|| PO: 250 to 500 mg once or twice|| 1000 mg
|-
|-
|  || [[Hydrochlorothiazide]] || 25 mg once or twice|| 200 mg
|  || [[Hydrochlorothiazide]] <br> ''(duration of action: 6 to 12 h)''|| PO: 25 mg once or twice|| 200 mg
|-
|-
|  || [[Metolazone]] || 2.5 mg once|| 20 mg
|  || [[Metolazone]] <br> ''(duration of action: 12 to 24 h)''|| PO: 2.5 mg once|| 20 mg
|-
|-
| K<sup>+</sup>- sparing diuretic|| [[Amiloride]] || 5 mg once|| 20 mg
| K<sup>+</sup>- sparing diuretic|| [[Amiloride]] <br> ''(duration of action: 24 h)''|| PO: 5 mg once|| 20 mg
|-
|-
|  || [[Spironolactone]] || 12.5 to 25.0 mg once|| 50 mg
|  || [[Spironolactone]] <br> ''(duration of action: 1 to 3 h)''|| PO: 12.5 to 25.0 mg once|| 50 mg
|-
|-
| || [[Triamterene]] || 50 to 75 mg twice|| 200 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
| [[ACE inhibitors]] || [[Enalapril]] || 2.5 mg twice|| 10 to 20 mg twice
Line 597: Line 706:
| [[ARBs]] || [[Candesartan]] || 4 to 8 mg once|| 32 mg once
| [[ARBs]] || [[Candesartan]] || 4 to 8 mg once|| 32 mg once
|-
|-
|  || [[Losartan]] || 25 to 50 mg once, 50 to 150 mg once
|  || [[Losartan]] || 25 to 50 mg once || 50 to 150 mg once
|-
|-
|  || [[Valsartan]] || 20 to 40 mg twice|| 160 mg twice
|  || [[Valsartan]] || 20 to 40 mg twice|| 160 mg twice
Line 605: Line 714:
|  || [[Carvedilol]] || 3.125 mg twice|| 50 mg twice
|  || [[Carvedilol]] || 3.125 mg twice|| 50 mg twice
|-
|-
|  || [[Metoprolol succinate]] || 12.5 to 25.0 mg once|| 200 mg once
|  || [[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
| [[Aldosterone antagonists]]|| [[Spironolactone]] || 12.5 to 25.0 mg once|| 25 mg once or twice
Line 611: Line 722:
|  || [[Eplerenone]] || 25 mg once|| 50 mg once
|  || [[Eplerenone]] || 25 mg once|| 50 mg once
|-
|-
| Inotropes || [[Dopamine]] || 5 to 10 mcg/kg/min||
| Inotropes || [[Dopamine]] || 5 to 10 mcg/kg/min, OR <br> 10 to 15 mcg/kg/min||
|-
|-
|  || [[Dobutamine]] || 2.5 to 5 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||
|  || [[Milrinone]] || 0.125 to 0.75 mcg/kg/min||
Line 623: Line 734:
|  || [[Nesiritide]] || 2 mcg/kg bolus; then 0.01 mcg/kg/minute continuous infusion|| Max of 0.03 mcg/kg/minute
|  || [[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, <br>75 mg hydralazine/40 mg isosorbide dinitrate 3 times daily
| [[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, 300 mg daily in divided doses<br>[[Isosorbide dinitrate]]: 20 to 30 mg 3 or 4 times daily|| 120 mg daily in divided doses
| ||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]] ||  || 0.125 to 0.25 mg daily. There is no need for a loading dose in CHF.<br> Drugs that increase the concentration of digoxin include [[amiodarone]], [[quinidine]] and [[verapamil]]||
| [[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==
* 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.
===Acute Decompensated Heart Failure===
* Order an [[echocardiogram]] as soon as possible in the absence of a recent one or if the patient's clinical status is deteriorating.
* Differentiate systolic and diastolic heart failure among patients with ADHF in order to guide therapy:
* [[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 & 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>
** [[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 inhibitor]]s 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:
** [[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
 
* [[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>
* [[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.
* 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 .<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>
===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==
* 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>
* 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 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 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 dysfunction 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 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.
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