Dilated cardiomyopathy resident survival guide: Difference between revisions

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! style="font-size: 80%; padding: 0 5px; background: #DCDCDC" align=left | [[{{PAGENAME}}#Complete Diagnostic Approach|Diagnosis]]
! style="font-size: 80%; padding: 0 5px; background: #DCDCDC" align=left | [[{{PAGENAME}}#Complete Diagnostic Approach|Diagnosis]]
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! style="font-size: 80%; padding: 0 5px; background: #DCDCDC" align=left | [[{{PAGENAME}}#Treatment|Treatment]]
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! style="font-size: 80%; padding: 0 5px; background: #DCDCDC" align=left | [[{{PAGENAME}}#Do's|Do's]]
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==Overview==
==Overview==
Dilated cardiomyopathy (DCM) relates to a group of heterogeneous myocardial disorders and is characterized by dilatation and impaired contraction and systolic function of the left or both ventricles. Atrial and/or ventricular arrhythmias can occcur, and there is a risk for sudden death. <ref name="pmid7459150">{{cite journal| author=| title=Report of the WHO/ISFC task force on the definition and classification of cardiomyopathies. | journal=Br Heart J | year= 1980 | volume= 44 | issue= 6 | pages= 672-3 | pmid=7459150 | doi= | pmc=PMC482464 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=7459150  }} </ref> The weight of the heart is increased but the maximal thicknesses of the left ventricular free wall and septum are usually normal as a result of the abnormally dilated chambers.<ref name="pmid3521345">{{cite journal| author=Tazelaar HD, Billingham ME| title=Leukocytic infiltrates in idiopathic dilated cardiomyopathy. A source of confusion with active myocarditis. | journal=Am J Surg Pathol | year= 1986 | volume= 10 | issue= 6 | pages= 405-12 | pmid=3521345 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=3521345  }} </ref>
[[Dilated cardiomyopathy]] (DCM) relates to a group of heterogeneous myocardial disorders and is characterized by dilatation and impaired contraction and systolic function of the left or both ventricles. Atrial and/or ventricular [[arrhythmia]]s can occcur, and there is a risk for sudden death. <ref name="pmid7459150">{{cite journal| author=| title=Report of the WHO/ISFC task force on the definition and classification of cardiomyopathies. | journal=Br Heart J | year= 1980 | volume= 44 | issue= 6 | pages= 672-3 | pmid=7459150 | doi= | pmc=PMC482464 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=7459150  }} </ref> The weight of the heart assessed by the MRI and echocardiogram is increased but the maximal thicknesses of the left ventricular free wall and septum are usually normal as a result of the abnormally dilated chambers.<ref name="pmid3521345">{{cite journal| author=Tazelaar HD, Billingham ME| title=Leukocytic infiltrates in idiopathic dilated cardiomyopathy. A source of confusion with active myocarditis. | journal=Am J Surg Pathol | year= 1986 | volume= 10 | issue= 6 | pages= 405-12 | pmid=3521345 | doi= | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=3521345  }} </ref> [[Dilated cardiomyopathy]] is treated the same way that congestive [[Chronic heart failure resident survival guide#Treatment|heart failure]] is.
 
==Causes==
==Causes==
Life-threatening causes include conditions which may result in death or permanent disability within 24 hours if left untreated.<ref name="pmid10760308">{{cite journal| author=Felker GM, Thompson RE, Hare JM, Hruban RH, Clemetson DE, Howard DL et al.| title=Underlying causes and long-term survival in patients with initially unexplained cardiomyopathy. | journal=N Engl J Med | year= 2000 | volume= 342 | issue= 15 | pages= 1077-84 | pmid=10760308 | doi=10.1056/NEJM200004133421502 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=10760308  }} </ref>
Life-threatening causes include conditions which may result in death or permanent disability within 24 hours if left untreated.<ref name="pmid10760308">{{cite journal| author=Felker GM, Thompson RE, Hare JM, Hruban RH, Clemetson DE, Howard DL et al.| title=Underlying causes and long-term survival in patients with initially unexplained cardiomyopathy. | journal=N Engl J Med | year= 2000 | volume= 342 | issue= 15 | pages= 1077-84 | pmid=10760308 | doi=10.1056/NEJM200004133421502 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=10760308  }} </ref>
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:*[[Doxorubicin]]
:*[[Doxorubicin]]
:*Other  
:*Other  
==FIRE: Focused Initial Rapid Evaluation==
A Focused Initial Rapid Evaluation (FIRE) should be performed to identify patients with signs and symptoms of severe acute decompensated heart failure who require immediate intervention.<ref name="pmid23741057">{{cite journal| author=Yancy CW, Jessup M, Bozkurt B, Butler J, Casey DE, Drazner MH et al.| title=2013 ACCF/AHA guideline for the management of heart failure: executive summary: a report of the American College of Cardiology Foundation/American Heart Association Task Force on practice guidelines. | journal=Circulation | year= 2013 | volume= 128 | issue= 16 | pages= 1810-52 | pmid=23741057 | doi=10.1161/CIR.0b013e31829e8807 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23741057  }} </ref><br>
<span style="font-size:85%">Boxes in red signify that an urgent management is needed.</span>
<span style="font-size:85%">'''Abbreviations:'''
'''BU:''' [[Blood urea nitrogen]];
'''COPD:''' [[Chronic obstructive pulmonary disease]];
'''D5W:''' 5% dextrose solution in water ;
'''HF:''' [[Heart failure]];
'''IV:''' [[Intravenous]];
'''MAP:''' [[Mean arterial pressure]];
'''Na:''' [[Sodium]];
'''NSAID:''' [[Non steroidal anti-inflammatory drug]];
'''SBP:''' [[Systolic blood pressure]];
'''S3:''' [[Third heart sound]];
</span>
<br>
{{familytree/start}}
{{familytree | | | A01 | | A01=<div style="float: left; text-align: left; width: 35em; padding:2em;">  '''Identify cardinal findings that increase the pretest probability of acute decompensated heart failure'''<br>
❑ [[Dyspnea]]<br>
❑ [[Cool extremities]]<br>
❑ [[Pedal edema|Peripheral edema]] <br>
❑ [[Decreased urine output]] <br>
❑ Past medical history of [[heart failure]] <br>
❑ History of [[orthopnea]] and [[paroxysmal nocturnal dyspnea]]<br>
❑ Pulmonary [[crepitations]]/[[rales]]/[[crackles]]<br>
❑ [[Heart sounds#Third heart sound S3|Third heart sound (S3)]]</div>}}
{{familytree | | | |!| |}}
{{familytree | | | W01 | |W01=<div style="float: left; text-align: left; width: 35em; padding:1em;">'''Does the patient have any of the following findings that require hospitalization and urgent management?'''<br>
❑ Severe decompendated HF:
:❑ [[Hypotension]] (either [[SBP]] < 90 mmHg or drop in [[MAP]] >30 mmHg) and/or [[cardiogenic shock]]<br>
:❑ [[Altered mental status]]<br>
:❑ [[Cool extremities|Cold and clammy extremities]]<br>
:❑ [[Oliguria|Urine output <0.5mL/kg/hr]]<br>
❑ [[Dyspnea]] at rest manifested by [[tachypnea]] or oxygen saturation <90% <br>
❑ [[Atrial fibrillation]] with a rapid ventricular response resulting in [[hypotension]]<br>
❑ [[Acute coronary syndrome]]<br>
:❑ '''[[Chest pain]] or [[chest discomfort]]''' <br>
::❑ Sudden onset
::❑ Sensation of heaviness, tightness, pressure, or squeezing
::❑ Duration> 20 minutes <br>
::❑ Radiation to the left arm, jaw, neck, right arm, back or [[epigastrium]]
::❑ No relief with medications<br>
::❑ No relief with rest <br>
::❑ Worse with time <br>
::❑ Worse with exertion<br>
:❑ [[Palpitations]]
:❑ [[Nausea]]
:❑ [[Vomiting]]
:❑ [[Sweating]]</div>}}
{{familytree | |,|-|^|-|.| |}}
{{familytree | B01 | | B02 | |B01=<div style=" background: #FA8072"> {{fontcolor|#F8F8FF|Yes}}</div> |B02='''No'''}}
{{familytree | |!| | | |!| | |}}
{{familytree | C01 | | C02 | |C01=<div style=" background: #FA8072"> {{fontcolor|#F8F8FF|Admit to a level of care that allows for constant ECG monitoring}}</div>
|C02=[[Dilated cardiomyopathy resident survival guide#Complete Diagnostic Approach|Proceed to complete diagnostic approach]] }}
{{familytree | |!| | | | | | |}}
{{familytree |boxstyle=background: #FA8072; color: #F8F8FF;  | D01 | | | | | |D01= <div style="float: left; text-align: left; width: 25em;">
'''Airway Stabilization''' <br>
❑ Position the patient upright at an angle of 45 degrees, with legs dangling off the bedside (decrease [[preload|<span style="color:white;">preload</span>]])<br>
❑ Monitor oxygen saturation continuously<br>
❑ If [[hypoxemia|<span style="color:white;">hypoxemia</span>]] is present (Sa02 < 90% or Pa02 <60 mmHg), administer oxygen with/without [[noninvasive ventilation|<span style="color:white;">noninvasive ventilation</span>]] <br>
:❑ Non-rebreather face mask with delivery of high flow oxygen
:❑ Consider non-invasive positive pressure ventilation (NPPV) for patients with no contraindication
<sup><span style="color:black">NPPV is contraindicated in cardiorespiratory arrest, glasgow coma scale < 10 or no patient cooperation, severe upper GI bleeding, hemodynamic instability, facial injury, upper airway obstruction, or high aspiration risk</span></sup><br>
❑ Titrate oxygen delivery to maintain SpO2 >90%<br>
:SPO2 in patients with COPD should not exceed 92-94%<br><br>
</div>}}
{{familytree | |!| | | | | | |}}
{{familytree |boxstyle=background: #FA8072; color: #F8F8FF; | Z01 | | | | | |Z01=<div style="float: left; text-align: left; width: 25em;">'''Assess Congestion and Perfusion'''<br>
'''Congestion at rest''' (dry vs. wet)<br>
''"Wet" suggested by orthopnea, ↑JVP, rales, S3, pedal edema''<br>
'''Low perfusion at rest''' (warm vs. cold)<br>
''"Cold" suggested by narrow [[pulse pressure|<span style="color:white;">pulse pressure</span>]], [[cool extremities|<span style="color:white;">cool extremities</span>]], [[hypotension|<span style="color:white;">hypotension</span>]]'' <br>
The patient is:<br>
❑ Warm and dry, OR <br>
❑ Warm and wet, OR <br>
❑ Cold and dry, OR <br>
❑ Cold and wet </div>}}
{{familytree | |!| | | | | | |}}
{{familytree |boxstyle=background: #FA8072; color: #F8F8FF; | Y01 | | | | | |Y01=<div style="float: left; text-align: left; width: 25em;">'''Identify Precipitating Factors and Treat Accordingly''' <br>
''Click on the precipitating factor for more details on the management'' <br>
❑ [[Acute coronary syndrome|<span style="color:white;">Acute coronary syndrome</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></div>}}
{{familytree | |!| | | | | | |}}
{{familytree |boxstyle=background: #FA8072; color: #F8F8FF; | X01 | | | | | |X01=<div style="float: left; text-align: left; width: 25em;">'''Manage the Patient's Acute Symptoms'''<br>
<u>'''Chest Pain'''</u><br>
❑ Administer [[morphine|<span style="color:white;">morphine</span>]] IV to reduce symptom severity.<br>
:❑ Initial dose 4-8 mg
:❑ 2-8 mg every 5 to 15 minutes, as needed<br><br>
'''<u>Relieve Congestiona and Improve Volume Status</u>''' <br>
'''''Initial Diuresis''''' <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>]]: Rule of thumb: Administer IV dose with total daily dose = 2.5 x usual daily PO dose<br>
:❑ Generally, administer IV furosemide bolus dose 40 mg IV for patients with normal renal function.
:❑ 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 (most common), '''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
:❑ Evaluate adequacy of diuresis. For furosemide, adequate diuresis is defined as urine output > 1L/2hours following IV administration.
:❑ If not adequate, increase furosemide IV dose to 80 mg. Re-evaluate diuresis adequacy in the following 2 hours post-administration.
:❑ Titrate dose until adequate diuresis is achieved. Once achieved, administer the dose at a twice daily rate.
:❑ Perform serial assessment of fluid input 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>
❑ Maintain a low sodium diet (<2 g daily)<br><br>
❑ In case of persistent symptoms:
:❑ Add a second [[diuretics|<span style="color:white;">diuretics</span>]], such as [[thiazide|<span style="color:white;">thiazide</span>]] (preferably metolazone) (I-B) <br>
:❑ Metolazone PO dose: 2.5 - 10 mg once daily (there is no IV preparation for metolazone)
:❑ Reassess diuresis adequacy several hours (2 to 9) following metolazone administration.
❑ 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><br>
'''''Maintenance of Diuresis'''''<br>
❑ Consider continuous infusion of furosemide following bolus administration. Infusion dose and rate vary according to the patient's creatinine clearance:
:❑ CrCl > 75 ml/min: Administer furosemide infusion 100 mg loading dose with an initial infusion rate of 10 mg/hour. Maximum daily infusion rate is 240-360 mg/hour in non-elderly adults (170 mg/hour in elderly).
:❑ CrCl= 25-75 ml/min: Administer furosemide infusion 100-200 mg loading dose with an initial infusion rate of 10-20 mg/hour. Maximum daily infusion rate is 240-360 mg/hour in non-elderly adults (170 mg/hour in elderly).
:❑ CrCl < 25 ml/min: Administer furosemide infusion 200 mg loading dose with an initial infusion rate of 20-40 mg/hour. Maximum daily infusion rate is 240-360 mg/hour in non-elderly adults (170 mg/hour in elderly).
❑ Monitor urine output to achieve goal urine output > 100 mL/hour.<br><br>
'''<u>Administer Venodilators</u>'''<br>
❑ Consider administration of 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>
:''Do not administer [[vasodilator|<span style="color:white;">vesodilators</span>]] among patients with [[hypotension|<span style="color:white;">hypotension</span>]].''<br><br>
'''<u>Manage Low Perfusion / Low Output</u>'''<br>
❑ Administer IV [[Inotrope|<span style="color:white;">inotropic agents</span>]]
:Administer inotropic agents temporarily to patients with reduced LVEF and reduced peripheral perfusion/end-organ damage to maintain systemic tissue perfusion until either acute factors are resolved or the patient receives definitive therapy (e.g. revascularization or heart transplant)<br>
:❑ Dobutamine: IV initial dose 0.5 to 1 microgram/kg/minute followed by maintenance dose of 2 to 20 microgram/kg/min (maximum dose 40 microgram/kg/min).
❑ Monitor vital signs continuously during administration of inotropic agents<br>
❑ Monitor for worsening tachyarrhythmia or worsening hypotension, which requires discontinuation of inotropic agents<br><br>
'''<u>Consider Invasive Hemodynamic Monitoring</u>'''<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>]]</div>}}
{{familytree | |!| | | | | | |}}
{{familytree |boxstyle=background: #FA8072; color: #F8F8FF; | V01 | | | | | |V01=<div style="float: left; text-align: left; width: 25em;">'''Hospital Care'''<br>
'''<u>Administer Thromboprophylaxis</u>'''<br>
❑ [[Anticoagulation|<span style="color:white;">Anticoagulation</span>]] in the absence of contraindications (I-B)<br><br>
'''<u>Hold Home Administered Chronic Medical Therapy</u>'''<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 ACEI/ARBs during an acute decompensation<br>
❑ DO NOT INITIATE BETA BLOCKER during an acute decompensation; initiate beta blockers at a low dose in stable patients following optimization of volume status and D/C of IV diuretics and inotropes (I-B) <br><br>
'''<u>Monitor Laboratory Tests</u>''' <br>
❑ [[BUN|<span style="color:white;">BUN</span>]] daily <br>
❑ [[Creatinine|<span style="color:white;">Creatinine</span>]] daily <br>
❑ [[Electrolytes|<span style="color:white;">Electrolytes</span>]] daily</div>}}
{{familytree | |!| | | | | | |}}
{{familytree | Q01 | | | | | |Q01=[[Dilated cardiomyopathy resident survival guide#Complete Diagnostic Approach|Proceed to complete diagnostic approach]]}}
{{familytree/end}}


==Complete Diagnostic Approach==
==Complete Diagnostic Approach==
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{{familytree | | | | | | | | |!| | | | | | |}}
{{familytree | | | | | | | | |!| | | | | | |}}
{{familytree | | | | | | | | C01 | |C01=<div style="text-align: left;"><b><u>History and symptoms:</u></b><br>
{{familytree | | | | | | | | C01 | |C01=<div style="text-align: left;"><b><u>History and symptoms:</u></b><br>
❑&nbsp;&nbsp;Hints for etiology (family history, and others)<br>
❑&nbsp;&nbsp;Hints for etiology (at least 3 generations of family history, and others)<br>
❑&nbsp;&nbsp;Duration and onset of illness<br>
❑&nbsp;&nbsp;Duration and onset of illness<br>
❑&nbsp;&nbsp;Severity and triggers of dyspnea and fatigue, presence of chest pain, exercise capacity, physical activity, sexual activity (NYHA?)<br>
❑&nbsp;&nbsp;Severity and triggers of dyspnea and fatigue, presence of chest pain, exercise capacity, physical activity, sexual activity (NYHA?)<br>
❑&nbsp;&nbsp;Weight loss/weight gain (cachexia/volume overload?)<br>
❑&nbsp;&nbsp;Weight loss/weight gain ([[cachexia]]/volume overload?)<br>
❑&nbsp;&nbsp;Palpitations/(pre)syncope/ICD shocks(adverse prognosis)<br>
❑&nbsp;&nbsp;Palpitations/(pre)[[syncope]]/ICD shocks(adverse prognosis)<br>
❑&nbsp;&nbsp;Symptoms of transient ischemic attack or thromboembolism (anticoagulation necessary?)<br>
❑&nbsp;&nbsp;Symptoms of [[transient ischemic attack]] or [[thromboembolism]] (anticoagulation necessary?)<br>
❑&nbsp;&nbsp;Presence of peripheral edema or ascites (volume overload?)<br>
❑&nbsp;&nbsp;Presence of peripheral edema or [[ascites]] (volume overload?)<br>
❑&nbsp;&nbsp;Problems with breathing at night/ sleep<br>
❑&nbsp;&nbsp;Problems with breathing at night/ sleep<br>
❑&nbsp;&nbsp;Medical history:
❑&nbsp;&nbsp;Medical history:
:❑&nbsp;&nbsp;Prior hospitalizations for HF (adverse prognosis?)
:❑&nbsp;&nbsp;Prior hospitalizations for [[HF]] (adverse prognosis?)
:❑&nbsp;&nbsp;Discontinuation of medications (reasons?)
:❑&nbsp;&nbsp;Discontinuation of medications (reasons?)
:❑&nbsp;&nbsp;Medications that may exacerbate HF<br>
:❑&nbsp;&nbsp;Medications that may exacerbate [[HF]]<br>
❑&nbsp;&nbsp;Diet (restriction of sodium and fluid intake?)</div>}}
❑&nbsp;&nbsp;Diet (restriction of sodium and fluid intake?)</div>}}
{{familytree | | | | | | | | |!| | | | | | |}}
{{familytree | | | | | | | | D01 | |D01=<div style="text-align: left;"><b><u>Physical examination:</u></b><br>
{{familytree | | | | | | | | D01 | |D01=<div style="text-align: left;"><b><u>Physical examination:</u></b><br>
❑&nbsp;&nbsp;Vital signs:
❑&nbsp;&nbsp;Vital signs:
Line 68: Line 250:
:❑&nbsp;&nbsp;Peripheral edema
:❑&nbsp;&nbsp;Peripheral edema
❑&nbsp;&nbsp;Heart:
❑&nbsp;&nbsp;Heart:
:❑&nbsp;&nbsp;Extra heart sounds and murmurs (associated with adverse prognosis, valvular heart disease?)
:❑&nbsp;&nbsp;Extra heart sounds and murmurs (S4; S3 associated with adverse prognosis, [[valvular heart disease]]?)
:❑&nbsp;&nbsp;[[Carvallo's sign]] (augmented murmurs of TR on inspiration) is frequently absent
:❑&nbsp;&nbsp;Orthostatic changes in blood pressure and heart rate (volume status/vasodilation?)
:❑&nbsp;&nbsp;Orthostatic changes in blood pressure and heart rate (volume status/vasodilation?)
:❑&nbsp;&nbsp;Jugular venous pressure at rest and following abdominal compression (to identify congestion)
:❑&nbsp;&nbsp;Jugular venous pressure at rest and following abdominal compression (to identify congestion)
:❑&nbsp;&nbsp;± Prominent V wave with brisk Y descent (suggestive of tricuspid regurgitation)
:❑&nbsp;&nbsp;Size and location of point of maximal impulse (ventricular enlargement?)
:❑&nbsp;&nbsp;Size and location of point of maximal impulse (ventricular enlargement?)
:❑&nbsp;&nbsp;Right ventricular heave (right ventricular dysfunction and/or pulmonary hypertension?)
:❑&nbsp;&nbsp;Right ventricular heave (right ventricular dysfunction and/or pulmonary hypertension?)
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:❑&nbsp;&nbsp;Pleural effusion
:❑&nbsp;&nbsp;Pleural effusion
❑&nbsp;&nbsp;Abdomen:
❑&nbsp;&nbsp;Abdomen:
:❑&nbsp;&nbsp;Hepatomegaly and/or ascites (volume overload)
:❑&nbsp;&nbsp;[[Hepatomegaly]] and/or [[ascites]] (volume overload)
❑&nbsp;&nbsp;Extremities:
❑&nbsp;&nbsp;Extremities:
:❑&nbsp;&nbsp;Temperature of lower extremities</div>}}
:❑&nbsp;&nbsp;Temperature of lower extremities</div>}}
{{familytree | | | | | | | | |!| | | | | | |}}
{{familytree | | | | | | | | E01 | |E01=<div style="text-align: left;"><b><u>Laboratory findings:</u></b><br>
{{familytree | | | | | | | | E01 | |E01=<div style="text-align: left;"><b><u>Laboratory findings:</u></b><br>
❑&nbsp;&nbsp;Complete blood count<br>
❑&nbsp;&nbsp;Complete blood count<br>
Line 93: Line 279:
:❑&nbsp;&nbsp;Consider Screening for [[hemochromatosis]], [[HIV]], [[rheumatologic diseases]], [[amyloidosis]], or [[pheochromocytoma]]<br>
:❑&nbsp;&nbsp;Consider Screening for [[hemochromatosis]], [[HIV]], [[rheumatologic diseases]], [[amyloidosis]], or [[pheochromocytoma]]<br>
:❑&nbsp;&nbsp;Urinalysis</div>}}
:❑&nbsp;&nbsp;Urinalysis</div>}}
{{familytree | | | | | | | | |!| | | | | | |}}
{{familytree | | | | | | | | F01 | |F01=<div style="text-align: left;"><b><u>Imaging and additional tests:</u></b><br>
{{familytree | | | | | | | | F01 | |F01=<div style="text-align: left;"><b><u>Imaging and additional tests:</u></b><br>
❑&nbsp;&nbsp;<b>Noninvasive imaging:</b>
❑&nbsp;&nbsp;<b>Noninvasive imaging:</b>
:❑&nbsp;&nbsp;<u>ECG</u>
:❑&nbsp;&nbsp;<u>ECG</u>: nonspecific repolarization or conduction abnormalities, poor R wave progression, and LVH
:❑&nbsp;&nbsp;<u>Chest x-ray</u> (heart size, pulmonary congestion and alternative cardiac, pulmonary, and other diseases?)
:❑&nbsp;&nbsp;<u>Chest x-ray</u>: cardiomegaly, pulmonary venous redistribution, and pulmonary congestion
:❑&nbsp;&nbsp;<u>2-dimensional echocardiogram with Doppler</u> (ventricular function, size, wall thickness, wall motion, and valve function?)
:❑&nbsp;&nbsp;<u>2-dimensional echocardiogram with Doppler</u> (ventricular function, size, wall thickness, wall motion, and valve function?)
::❑&nbsp;&nbsp;Repeat measurement of EF and severity of structural remodeling (after significant change in clinical status, after clinical event, after treatment or if candidates for device therapy)
::❑&nbsp;&nbsp;Repeat measurement of EF and severity of structural remodeling (after significant change in clinical status, after clinical event, after treatment or if candidates for device therapy)
Line 114: Line 301:
:::❑&nbsp;&nbsp;If parenteral vasoactive agents are required
:::❑&nbsp;&nbsp;If parenteral vasoactive agents are required
:::❑&nbsp;&nbsp;If consideration for MCS or transplantation
:::❑&nbsp;&nbsp;If consideration for MCS or transplantation
:::❑&nbsp;&nbsp;If ischemia contributes to HF coronary arteriography for patients who are eligible for revascularization
:::❑&nbsp;&nbsp;If ischemia contributes to [[HF]] coronary arteriography for patients who are eligible for revascularization
:❑&nbsp;&nbsp;<u>Endomyocardial biopsy:</u>
:❑&nbsp;&nbsp;<u>Endomyocardial biopsy:</u>
::❑&nbsp;&nbsp;Consider if a specific diagnosis is suspected that would influence therapy
::❑&nbsp;&nbsp;Consider if a specific diagnosis is suspected that would influence therapy
::❑&nbsp;&nbsp;Consider if rapidly progressive clinical HF or worsening ventricular dysfunction that persists despite appropriate medical therapy
::❑&nbsp;&nbsp;Consider if rapidly progressive clinical [[HF]] or worsening ventricular dysfunction that persists despite appropriate medical therapy
::❑&nbsp;&nbsp;Consider if suspicion of an acute cardiac rejection status after heart transplantation or a myocardial infiltrative processes
::❑&nbsp;&nbsp;Consider if suspicion of an acute cardiac rejection status after heart transplantation or a myocardial infiltrative processes
:❑&nbsp;&nbsp;<u>Coronary angiography:</u>
:❑&nbsp;&nbsp;<u>Coronary angiography:</u>
::❑&nbsp;&nbsp;Consider for patients with HF and angina, or without angina but with LV dysfunction
::❑&nbsp;&nbsp;Consider for patients with [[HF]] and angina, or without angina but with LV dysfunction
::❑&nbsp;&nbsp;In patients with known CAD and angina or with significant ischemia diagnosed by ECG or noninvasive testing and impaired ventricular function
::❑&nbsp;&nbsp;In patients with known [[CAD]] and angina or with significant ischemia diagnosed by ECG or noninvasive testing and impaired ventricular function
::❑&nbsp;&nbsp;CAD should be considered as a potential etiology of impaired LV function and should be excluded wherever possible among those without prior diagnosis</div>}}
::❑&nbsp;&nbsp;[[CAD]] should be considered as a potential etiology of impaired LV function and should be excluded wherever possible among those without prior diagnosis</div>}}
{{familytree | | | | | | | | |!| | | | | | |}}  
{{familytree | | | | | | | | |!| | | | | | |}}  
{{familytree | | | | | | | | G01 | |G01=<div style="text-align: left;"><b>Examples for specific findings for [[dilated cardiomyopathy]]:</b>
{{familytree | | | | | | | | G01 | |G01=<div style="text-align: left;"><b>Examples for specific findings for [[dilated cardiomyopathy]]:</b>
❑&nbsp;&nbsp;Echo (dilated left and/or right ventricle, global hypokinesis with left ventricular ejection fraction under 40%
❑&nbsp;&nbsp;Echo (dilated left and/or right ventricle, global hypokinesis with left ventricular ejection fraction under 40%<br>
❑&nbsp;&nbsp;no specific cause identified
❑&nbsp;&nbsp;no specific cause identified
❑&nbsp;&nbsp;coronary angiography shows no severe disease</div>}}
❑&nbsp;&nbsp;coronary angiography shows no severe disease</div>}}
Line 133: Line 320:
<b>Or conduction abnormalities?</b><br>
<b>Or conduction abnormalities?</b><br>
<b>And/or suspected [[myocarditis?]]</b></div>}}
<b>And/or suspected [[myocarditis?]]</b></div>}}
{{familytree | | | | |,|-|-|-|^|-|-|-|-|.| | | }}
{{familytree | | | | |,|-|-|-|^|-|-|-|-|-|-|-|.| | | }}
{{familytree | | | B01 | | | | | | | | B02 | | |B01=<b>Yes</b>|B02=<b>No</b>}}
{{familytree | | | B01 | | | | | | | | | | | B02 | | |B01=<b>Yes</b>|B02=<b>No</b>}}
{{familytree | | | |!| | | | | | | | | |!| }}
{{familytree | | | |!| | | | | | | | | | | | |!| }}
{{familytree | | | I01 | | | | | | | | I02 | | |I01=<b>Consider endomyocardial biopsy</b>|I02=<b>Treat with conventional [[heart failure]] medications</b>}}{{familytree | | | | | | | | | | | | | |!| }}
{{familytree | | | I01 | | | | | | | | | | | I02 | | |I01=<b>Consider endomyocardial biopsy</b>|I02=<b>Treat with conventional [[heart failure]] medications</b>}}
{{familytree | | | | | | | | | | | | | J01 | | |J01=<b>Clinical improvement after 1 week?</b>}}
{{familytree | | | | | | | | | | | | | | | | |!| |}}
{{familytree | | | | | | | | | |,|-|-|-|^|-|-|-|.}}
{{familytree | | | | | | | | | | | | | | | | J01 | | |J01=<b>Clinical improvement after 1 week?</b>}}
{{familytree | | | | | | | | | K01 | | | | | | K02 |K01=<b>Yes</b>|K02=<b>No</b>}}
{{familytree | | | | | | | | | | | | | |,|-|-|^|-|-|.| |}}
{{familytree | | | | | | | | | |!| | | | | | | |!| | |}}
{{familytree | | | | | | | | | | | | | K01 | | | | K02 | |K01=<b>Yes</b>|K02=<b>No</b>}}
{{familytree | | | | | | | | | L01 | | | | | | L02| | |L01=<b>Continue conventional [[heart failure]] treatment</b>|L02=<b>Consider endomyocardial biopsy</b>}}
{{familytree | | | | | | | | | | | | | |!| | | | | |!| | |}}
{{familytree | | | | | | | | | | | | | L01 | | | | L02| | |L01=<b>Continue conventional [[Chronic heart failure resident survival guide#Treatment|heart failure]] treatment</b>|L02=<b>Consider endomyocardial biopsy</b>}}
{{familytree/end}}
{{familytree/end}}
The timing of endomyocardial biopsyis if patients fail to improve on medical therapy is controversial. <ref name="pmid10760308">{{cite journal| author=Felker GM, Thompson RE, Hare JM, Hruban RH, Clemetson DE, Howard DL et al.| title=Underlying causes and long-term survival in patients with initially unexplained cardiomyopathy. | journal=N Engl J Med | year= 2000 | volume= 342 | issue= 15 | pages= 1077-84 | pmid=10760308 | doi=10.1056/NEJM200004133421502 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=10760308  }} </ref>
==Treatment==
<div class="mw-collapsible mw-collapsed">
shown
<div class="mw-collapsible-content">
hidden
</div></div>


==Do's==
==Do's==
 
* The initial diagnostic approach should aim to identify potentially reversible causes of left ventricular dysfunction. Pertinent history includes alcohol consumption, recent viral illness, coronary risk factors, and family history.


==Dont's==
==Dont's==
❑&nbsp;&nbsp;Endomyocardial biopsy should not be performed in the routine evaluation of patients with HF<ref name="YancyJessup2013">{{cite journal|last1=Yancy|first1=C. W.|last2=Jessup|first2=M.|last3=Bozkurt|first3=B.|last4=Butler|first4=J.|last5=Casey|first5=D. E.|last6=Drazner|first6=M. H.|last7=Fonarow|first7=G. C.|last8=Geraci|first8=S. A.|last9=Horwich|first9=T.|last10=Januzzi|first10=J. L.|last11=Johnson|first11=M. R.|last12=Kasper|first12=E. K.|last13=Levy|first13=W. C.|last14=Masoudi|first14=F. A.|last15=McBride|first15=P. E.|last16=McMurray|first16=J. J. V.|last17=Mitchell|first17=J. E.|last18=Peterson|first18=P. N.|last19=Riegel|first19=B.|last20=Sam|first20=F.|last21=Stevenson|first21=L. W.|last22=Tang|first22=W. H. W.|last23=Tsai|first23=E. J.|last24=Wilkoff|first24=B. L.|title=2013 ACCF/AHA Guideline for the Management of Heart Failure: A Report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines|journal=Circulation|volume=128|issue=16|year=2013|pages=e240–e327|issn=0009-7322|doi=10.1161/CIR.0b013e31829e8776}}</ref>
* Endomyocardial biopsy should not be performed in the routine evaluation of patients with HF.<ref name="YancyJessup2013">{{cite journal|last1=Yancy|first1=C. W.|last2=Jessup|first2=M.|last3=Bozkurt|first3=B.|last4=Butler|first4=J.|last5=Casey|first5=D. E.|last6=Drazner|first6=M. H.|last7=Fonarow|first7=G. C.|last8=Geraci|first8=S. A.|last9=Horwich|first9=T.|last10=Januzzi|first10=J. L.|last11=Johnson|first11=M. R.|last12=Kasper|first12=E. K.|last13=Levy|first13=W. C.|last14=Masoudi|first14=F. A.|last15=McBride|first15=P. E.|last16=McMurray|first16=J. J. V.|last17=Mitchell|first17=J. E.|last18=Peterson|first18=P. N.|last19=Riegel|first19=B.|last20=Sam|first20=F.|last21=Stevenson|first21=L. W.|last22=Tang|first22=W. H. W.|last23=Tsai|first23=E. J.|last24=Wilkoff|first24=B. L.|title=2013 ACCF/AHA Guideline for the Management of Heart Failure: A Report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines|journal=Circulation|volume=128|issue=16|year=2013|pages=e240–e327|issn=0009-7322|doi=10.1161/CIR.0b013e31829e8776}}</ref> Optimal timing of endomyocardial biopsy for patients unresponsive to medical therapy remains unclear.<ref name="pmid10760308">{{cite journal| author=Felker GM, Thompson RE, Hare JM, Hruban RH, Clemetson DE, Howard DL et al.| title=Underlying causes and long-term survival in patients with initially unexplained cardiomyopathy. | journal=N Engl J Med | year= 2000 | volume= 342 | issue= 15 | pages= 1077-84 | pmid=10760308 | doi=10.1056/NEJM200004133421502 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=10760308  }} </ref>
* Nondihydropyridine calcium channel blockers with negative inotropic effects may be harmful in asymptomatic patients with low LVEF and no symptoms of [[HF]] after [[MI]].<ref name="pmid23741058">{{cite journal| author=WRITING COMMITTEE MEMBERS. Yancy CW, Jessup M, Bozkurt B, Butler J, Casey DE et al.| title=2013 ACCF/AHA guideline for the management of heart failure: 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= e240-327 | pmid=23741058 | doi=10.1161/CIR.0b013e31829e8776 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23741058  }} </ref>


==References==
==References==
Line 168: Line 345:
[[Category:Cardiology]]
[[Category:Cardiology]]
[[Category:Emergency medicine]]
[[Category:Emergency medicine]]
[[Category:Primary care]]

Latest revision as of 21:23, 29 July 2020

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Steven Bellm, M.D. [2]

Dilated cardiomyopathy resident survival guide Microchapters
Overview
Causes
Diagnosis
Do's
Dont's

Overview

Dilated cardiomyopathy (DCM) relates to a group of heterogeneous myocardial disorders and is characterized by dilatation and impaired contraction and systolic function of the left or both ventricles. Atrial and/or ventricular arrhythmias can occcur, and there is a risk for sudden death. [1] The weight of the heart assessed by the MRI and echocardiogram is increased but the maximal thicknesses of the left ventricular free wall and septum are usually normal as a result of the abnormally dilated chambers.[2] Dilated cardiomyopathy is treated the same way that congestive heart failure is.

Causes

Life-threatening causes include conditions which may result in death or permanent disability within 24 hours if left untreated.[3]

  • Life-threatening causes:
  • Common causes:

FIRE: Focused Initial Rapid Evaluation

A Focused Initial Rapid Evaluation (FIRE) should be performed to identify patients with signs and symptoms of severe acute decompensated heart failure who require immediate intervention.[4]

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 (either 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

Chest pain or chest discomfort
❑ Sudden onset
❑ Sensation of heaviness, tightness, pressure, or squeezing
❑ Duration> 20 minutes
❑ Radiation to the left arm, jaw, neck, right arm, back or epigastrium
❑ No relief with medications
❑ No relief with rest
❑ Worse with time
❑ Worse with exertion
Palpitations
Nausea
Vomiting
Sweating
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Yes
 
No
 
 
 
 
 
 
 
 
 
 
 
Admit to a level of care that allows for constant ECG monitoring
 
Proceed to complete diagnostic approach
 
 
 
 
 
 
 
 
 
 

Airway Stabilization
❑ Position the patient upright at an angle of 45 degrees, with legs dangling off the bedside (decrease preload)
❑ Monitor oxygen saturation continuously
❑ If hypoxemia is present (Sa02 < 90% or Pa02 <60 mmHg), administer oxygen with/without noninvasive ventilation

❑ Non-rebreather face mask with delivery of high flow oxygen
❑ Consider non-invasive positive pressure ventilation (NPPV) for patients with no contraindication

NPPV is contraindicated in cardiorespiratory arrest, glasgow coma scale < 10 or no patient cooperation, severe upper GI bleeding, hemodynamic instability, facial injury, upper airway obstruction, or high aspiration risk

❑ Titrate oxygen delivery to maintain SpO2 >90%

SPO2 in patients with COPD should not exceed 92-94%

 
 
 
 
 
 
 
 
 
 
 
 
 
 
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 Factors and Treat Accordingly

Click on the precipitating factor for more details on the management
Acute coronary syndrome
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
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Manage the Patient's Acute Symptoms

Chest Pain
❑ Administer morphine IV to reduce symptom severity.

❑ Initial dose 4-8 mg
❑ 2-8 mg every 5 to 15 minutes, as needed

Relieve Congestiona and Improve Volume Status
Initial Diuresis
❑ Administer IV loop diuretics as intermittent boluses or continuous infusion (I-B)

❑ If patient is already on loop diuretics: Rule of thumb: Administer IV dose with total daily dose = 2.5 x usual daily PO dose
❑ Generally, administer IV furosemide bolus dose 40 mg IV for patients with normal renal function.
❑ If patient is not already on loop diuretics, administer IV starting dose:
Furosemide 20 to 40 mg (most common), OR
Torsemide 5 to 10 mg, OR
Bumetanide 0.5 to 1 mg
❑ Evaluate adequacy of diuresis. For furosemide, adequate diuresis is defined as urine output > 1L/2hours following IV administration.
❑ If not adequate, increase furosemide IV dose to 80 mg. Re-evaluate diuresis adequacy in the following 2 hours post-administration.
❑ Titrate dose until adequate diuresis is achieved. Once achieved, administer the dose at a twice daily rate.
❑ Perform serial assessment of fluid input 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)

❑ Maintain a low sodium diet (<2 g daily)

❑ In case of persistent symptoms:

❑ Add a second diuretics, such as thiazide (preferably metolazone) (I-B)
❑ Metolazone PO dose: 2.5 - 10 mg once daily (there is no IV preparation for metolazone)
❑ Reassess diuresis adequacy several hours (2 to 9) following metolazone administration.

❑ 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

Maintenance of Diuresis
❑ Consider continuous infusion of furosemide following bolus administration. Infusion dose and rate vary according to the patient's creatinine clearance:

❑ CrCl > 75 ml/min: Administer furosemide infusion 100 mg loading dose with an initial infusion rate of 10 mg/hour. Maximum daily infusion rate is 240-360 mg/hour in non-elderly adults (170 mg/hour in elderly).
❑ CrCl= 25-75 ml/min: Administer furosemide infusion 100-200 mg loading dose with an initial infusion rate of 10-20 mg/hour. Maximum daily infusion rate is 240-360 mg/hour in non-elderly adults (170 mg/hour in elderly).
❑ CrCl < 25 ml/min: Administer furosemide infusion 200 mg loading dose with an initial infusion rate of 20-40 mg/hour. Maximum daily infusion rate is 240-360 mg/hour in non-elderly adults (170 mg/hour in elderly).

❑ Monitor urine output to achieve goal urine output > 100 mL/hour.

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

Do not administer vesodilators among patients with hypotension.

Manage Low Perfusion / Low Output
❑ Administer IV inotropic agents

Administer inotropic agents temporarily to patients with reduced LVEF and reduced peripheral perfusion/end-organ damage to maintain systemic tissue perfusion until either acute factors are resolved or the patient receives definitive therapy (e.g. revascularization or heart transplant)
❑ Dobutamine: IV initial dose 0.5 to 1 microgram/kg/minute followed by maintenance dose of 2 to 20 microgram/kg/min (maximum dose 40 microgram/kg/min).

❑ Monitor vital signs continuously during administration of inotropic agents
❑ Monitor for worsening tachyarrhythmia or worsening hypotension, which requires discontinuation of inotropic agents

Consider 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
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Hospital Care

Administer Thromboprophylaxis
Anticoagulation in the absence of contraindications (I-B)

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

Monitor Laboratory Tests
BUN daily
Creatinine daily

Electrolytes daily
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Proceed to complete diagnostic approach
 
 
 
 
 

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.[5]

 
 
 
 
 
 
 
Symptoms of heart failure
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
History and symptoms:

❑  Hints for etiology (at least 3 generations of family history, and others)
❑  Duration and onset of illness
❑  Severity and triggers of dyspnea and fatigue, presence of chest pain, exercise capacity, physical activity, sexual activity (NYHA?)
❑  Weight loss/weight gain (cachexia/volume overload?)
❑  Palpitations/(pre)syncope/ICD shocks(adverse prognosis)
❑  Symptoms of transient ischemic attack or thromboembolism (anticoagulation necessary?)
❑  Presence of peripheral edema or ascites (volume overload?)
❑  Problems with breathing at night/ sleep
❑  Medical history:

❑  Prior hospitalizations for HF (adverse prognosis?)
❑  Discontinuation of medications (reasons?)
❑  Medications that may exacerbate HF
❑  Diet (restriction of sodium and fluid intake?)
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Physical examination:

❑  Vital signs:

❑  Pulse (strength and regularity?)
❑  Blood pressure (supine and upright) to reflect adequacy of cardiac output
❑  Respiratory rate

❑  General appearance:

❑  BMI(weight loss/weight gain)
❑  Peripheral edema

❑  Heart:

❑  Extra heart sounds and murmurs (S4; S3 associated with adverse prognosis, valvular heart disease?)
❑  Carvallo's sign (augmented murmurs of TR on inspiration) is frequently absent
❑  Orthostatic changes in blood pressure and heart rate (volume status/vasodilation?)
❑  Jugular venous pressure at rest and following abdominal compression (to identify congestion)
❑  ± Prominent V wave with brisk Y descent (suggestive of tricuspid regurgitation)
❑  Size and location of point of maximal impulse (ventricular enlargement?)
❑  Right ventricular heave (right ventricular dysfunction and/or pulmonary hypertension?)

❑  Lungs:

❑  Rales
❑  Pleural effusion

❑  Abdomen:

❑  Hepatomegaly and/or ascites (volume overload)

❑  Extremities:

❑  Temperature of lower extremities
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Laboratory findings:

❑  Complete blood count
❑  Chemistry:

❑  Troponin, BNP or NT-proBNP
❑  Serum electrolytes (including calcium and magnesium)
❑  Blood urea nitrogen
❑  Serum creatinine
❑  Glucose
❑  Fasting lipid profile
❑  Liver function tests
❑  Thyroid-stimulating hormone
❑  Consider Screening for hemochromatosis, HIV, rheumatologic diseases, amyloidosis, or pheochromocytoma
❑  Urinalysis
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Imaging and additional tests:

❑  Noninvasive imaging:

❑  ECG: nonspecific repolarization or conduction abnormalities, poor R wave progression, and LVH
❑  Chest x-ray: cardiomegaly, pulmonary venous redistribution, and pulmonary congestion
❑  2-dimensional echocardiogram with Doppler (ventricular function, size, wall thickness, wall motion, and valve function?)
❑  Repeat measurement of EF and severity of structural remodeling (after significant change in clinical status, after clinical event, after treatment or if candidates for device therapy)
❑  Cardiac-MRI (ventricular size, wall/muscle thickness, valves, pericardium, wall motion, etc.)
❑  Consider check for myocardial ischemia and viability for patients with known CAD and no angina
❑  Viability assessment when planning revascularization in HF patients with CAD
❑  Radionuclide ventriculography or magnetic resonance imaging can be useful to assess LVEF and volume when echocardiography is inadequate
❑  Consider magnetic resonance imaging when assessing myocardial infiltrative processes or scar burden

❑  Invasive imaging: Consider invasive Imaging only in specific cases.

❑  Invasive hemodynamic monitoring with a pulmonary artery catheter to guide therapy in patients with respiratory distress or clinical evidence of impaired perfusion if the adequacy or excess of intracardiac filling pressures cannot be determined from clinical assessment
❑  Careful consideration of invasive hemodynamic monitoring for patients:
❑  With persistent symptoms despite empiric adjustment of standard therapies
❑  If fluid status, perfusion, or systemic or pulmonary vascular resistance is uncertain
❑  Systolic pressure remains low, or is associated with symptoms, despite initial therapy
❑  If renal function is worsening with therapy
❑  If parenteral vasoactive agents are required
❑  If consideration for MCS or transplantation
❑  If ischemia contributes to HF coronary arteriography for patients who are eligible for revascularization
❑  Endomyocardial biopsy:
❑  Consider if a specific diagnosis is suspected that would influence therapy
❑  Consider if rapidly progressive clinical HF or worsening ventricular dysfunction that persists despite appropriate medical therapy
❑  Consider if suspicion of an acute cardiac rejection status after heart transplantation or a myocardial infiltrative processes
❑  Coronary angiography:
❑  Consider for patients with HF and angina, or without angina but with LV dysfunction
❑  In patients with known CAD and angina or with significant ischemia diagnosed by ECG or noninvasive testing and impaired ventricular function
❑  CAD should be considered as a potential etiology of impaired LV function and should be excluded wherever possible among those without prior diagnosis
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Examples for specific findings for dilated cardiomyopathy:

❑  Echo (dilated left and/or right ventricle, global hypokinesis with left ventricular ejection fraction under 40%
❑  no specific cause identified

❑  coronary angiography shows no severe disease
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Rapidly progressive symptoms (within 1 month)?

And/or new ventricular tachycardia?
Or conduction abnormalities?

And/or suspected myocarditis?
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Yes
 
 
 
 
 
 
 
 
 
 
No
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Consider endomyocardial biopsy
 
 
 
 
 
 
 
 
 
 
Treat with conventional heart failure medications
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Clinical improvement after 1 week?
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Yes
 
 
 
No
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Continue conventional heart failure treatment
 
 
 
Consider endomyocardial biopsy
 
 

Do's

  • The initial diagnostic approach should aim to identify potentially reversible causes of left ventricular dysfunction. Pertinent history includes alcohol consumption, recent viral illness, coronary risk factors, and family history.

Dont's

  • Endomyocardial biopsy should not be performed in the routine evaluation of patients with HF.[5] Optimal timing of endomyocardial biopsy for patients unresponsive to medical therapy remains unclear.[3]
  • Nondihydropyridine calcium channel blockers with negative inotropic effects may be harmful in asymptomatic patients with low LVEF and no symptoms of HF after MI.[6]

References

  1. "Report of the WHO/ISFC task force on the definition and classification of cardiomyopathies". Br Heart J. 44 (6): 672–3. 1980. PMC 482464. PMID 7459150.
  2. Tazelaar HD, Billingham ME (1986). "Leukocytic infiltrates in idiopathic dilated cardiomyopathy. A source of confusion with active myocarditis". Am J Surg Pathol. 10 (6): 405–12. PMID 3521345.
  3. 3.0 3.1 Felker GM, Thompson RE, Hare JM, Hruban RH, Clemetson DE, Howard DL; et al. (2000). "Underlying causes and long-term survival in patients with initially unexplained cardiomyopathy". N Engl J Med. 342 (15): 1077–84. doi:10.1056/NEJM200004133421502. PMID 10760308.
  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.
  5. 5.0 5.1 Yancy, C. W.; Jessup, M.; Bozkurt, B.; Butler, J.; Casey, D. E.; Drazner, M. H.; Fonarow, G. C.; Geraci, S. A.; Horwich, T.; Januzzi, J. L.; Johnson, M. R.; Kasper, E. K.; Levy, W. C.; Masoudi, F. A.; McBride, P. E.; McMurray, J. J. V.; Mitchell, J. E.; Peterson, P. N.; Riegel, B.; Sam, F.; Stevenson, L. W.; Tang, W. H. W.; Tsai, E. J.; Wilkoff, B. L. (2013). "2013 ACCF/AHA Guideline for the Management of Heart Failure: A Report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines". Circulation. 128 (16): e240–e327. doi:10.1161/CIR.0b013e31829e8776. ISSN 0009-7322.
  6. WRITING COMMITTEE MEMBERS. Yancy CW, Jessup M, Bozkurt B, Butler J, Casey DE; et al. (2013). "2013 ACCF/AHA guideline for the management of heart failure: a report of the American College of Cardiology Foundation/American Heart Association Task Force on practice guidelines". Circulation. 128 (16): e240–327. doi:10.1161/CIR.0b013e31829e8776. PMID 23741058.