Congestive heart failure Management of Acute heart failure: Difference between revisions

Jump to navigation Jump to search
 
(3 intermediate revisions by the same user not shown)
Line 111: Line 111:


===Beta Blockers===
===Beta Blockers===
====Discontinuation====
While [[beta blockers]] may play a role in the management of chronic heart failure, '''beta blockade should not be initiated during acute decompensated heart failure'''.
While [[beta blockers]] may play a role in the management of chronic heart failure, '''beta blockade should not be initiated during acute decompensated heart failure'''.


Regarding whether patients already on [[beta-blocker]]s should have these medications stopped when they have acute heart failure:
Regarding whether patients already on [[beta-blocker]]s should have these medications stopped when they have acute heart failure, the [[adrenergic receptor]] profile of concomittent inotropes may affect decisions:
* [[alpha-1 adrenergic receptor | α<sub>1</sub> adrenergic receptor]]'s vasoconstriction
* [[beta receptor | β<sub>1</sub> adrenergic receptor]]s cardiac-stimulating (chronotropic and inotropic) effect
:


* If the patient is chronically administered a [[beta blocker]], the [[beta blocker]] can be continued in the absence of [[hypotension]].If the patient becomes hemodynamically unstable, the beta blocker dosing can be reduced.  If inotropic agents are required, then the beta blocker should be discontinued.   
If the patient is chronically administered a [[beta blocker]], the [[beta blocker]] can be continued in the absence of [[hypotension]]. If the patient becomes hemodynamically unstable, the beta blocker dosing can be reduced.  If inotropic agents are required, then the beta blocker should be discontinued.   
* Gattis in 2003,
* The Gattis [[cohort study]] in 2003.
* In the OPTIMIZE-HF [[cohort study]] by Fonarow in 2004, which was restricted to patients "eligible for beta-blockers at discharge," was associated with adjusted higher mortality<ref name="pmid18617067">{{cite journal| author=Fonarow GC, Abraham WT, Albert NM, Stough WG, Gheorghiade M, Greenberg BH | display-authors=etal| title=Influence of beta-blocker continuation or withdrawal on outcomes in patients hospitalized with heart failure: findings from the OPTIMIZE-HF program. | journal=J Am Coll Cardiol | year= 2008 | volume= 52 | issue= 3 | pages= 190-9 | pmid=18617067 | doi=10.1016/j.jacc.2008.03.048 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=18617067  }} </ref>.
* In the OPTIMIZE-HF [[cohort study]] by Fonarow in 2004, which was restricted to patients "eligible for beta-blockers at discharge," was associated with adjusted higher mortality<ref name="pmid18617067">{{cite journal| author=Fonarow GC, Abraham WT, Albert NM, Stough WG, Gheorghiade M, Greenberg BH | display-authors=etal| title=Influence of beta-blocker continuation or withdrawal on outcomes in patients hospitalized with heart failure: findings from the OPTIMIZE-HF program. | journal=J Am Coll Cardiol | year= 2008 | volume= 52 | issue= 3 | pages= 190-9 | pmid=18617067 | doi=10.1016/j.jacc.2008.03.048 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=18617067  }} </ref>.
* In the ESCAPE [[cohort study]] by Butler in 2006, withdrawal of [[beta blockers]] was associated with adjusted higher mortality.<ref name="pmid16781374">{{cite journal |author=Butler J, Young JB, Abraham WT, Bourge RC, Adams KF, Clare R, O'Connor C |title=Beta-blocker use and outcomes among hospitalized heart failure patients |journal=[[Journal of the American College of Cardiology]] |volume=47 |issue=12 |pages=2462–9 |year=2006 |month=June |pmid=16781374 |doi=10.1016/j.jacc.2006.03.030 |url=http://linkinghub.elsevier.com/retrieve/pii/S0735-1097(06)00861-8 |accessdate=2013-04-30}}</ref>
* In the ESCAPE [[cohort study]] by Butler in 2006, withdrawal of [[beta blockers]] was associated with adjusted higher mortality.<ref name="pmid16781374">{{cite journal |author=Butler J, Young JB, Abraham WT, Bourge RC, Adams KF, Clare R, O'Connor C |title=Beta-blocker use and outcomes among hospitalized heart failure patients |journal=[[Journal of the American College of Cardiology]] |volume=47 |issue=12 |pages=2462–9 |year=2006 |month=June |pmid=16781374 |doi=10.1016/j.jacc.2006.03.030 |url=http://linkinghub.elsevier.com/retrieve/pii/S0735-1097(06)00861-8 |accessdate=2013-04-30}}</ref>
* by Orso in 2009,
* The Orso [[cohort study]] in 2009.
* The B-CONVINCED [[randomized controlled trial]] by Jondeau in 2009 found no differences in outcomes during the hospitalization, but the patients randomized to stay on beta-blockers were more likely to be taking [[beta-blocker]]s at 3 months (90% vs. 76%)<ref name="pmid19717851">{{cite journal| author=Jondeau G, Neuder Y, Eicher JC, Jourdain P, Fauveau E, Galinier M | display-authors=etal| title=B-CONVINCED: Beta-blocker CONtinuation Vs. INterruption in patients with Congestive heart failure hospitalizED for a decompensation episode. | journal=Eur Heart J | year= 2009 | volume= 30 | issue= 18 | pages= 2186-92 | pmid=19717851 | doi=10.1093/eurheartj/ehp323 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=19717851  }} </ref>.
* The B-CONVINCED [[randomized controlled trial]] by Jondeau in 2009 found no differences in outcomes during the hospitalization, but the patients randomized to stay on beta-blockers were more likely to be taking [[beta-blocker]]s at 3 months (90% vs. 76%)<ref name="pmid19717851">{{cite journal| author=Jondeau G, Neuder Y, Eicher JC, Jourdain P, Fauveau E, Galinier M | display-authors=etal| title=B-CONVINCED: Beta-blocker CONtinuation Vs. INterruption in patients with Congestive heart failure hospitalizED for a decompensation episode. | journal=Eur Heart J | year= 2009 | volume= 30 | issue= 18 | pages= 2186-92 | pmid=19717851 | doi=10.1093/eurheartj/ehp323 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=19717851  }} </ref>.
* In the retrospective, observational [[cohort study | cohort analysis]] of the SURVIVE Trial studying patients requiring [[inotrope]]s by Böhm in 2011, patients remaining on beta-blockers had lower adjusted mortality at 30 and 180 days<ref name="pmid21283007">{{cite journal| author=Böhm M, Link A, Cai D, Nieminen MS, Filippatos GS, Salem R | display-authors=etal| title=Beneficial association of β-blocker therapy on recovery from severe acute heart failure treatment: data from the Survival of Patients With Acute Heart Failure in Need of Intravenous Inotropic Support trial. | journal=Crit Care Med | year= 2011 | volume= 39 | issue= 5 | pages= 940-4 | pmid=21283007 | doi=10.1097/CCM.0b013e31820a91ed | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21283007  }} </ref>.  
* In the retrospective, observational [[cohort study | cohort analysis]] of the SURVIVE Trial studying patients requiring [[inotrope]]s by Böhm in 2011, patients remaining on beta-blockers had lower adjusted mortality at 30 and 180 days<ref name="pmid21283007">{{cite journal| author=Böhm M, Link A, Cai D, Nieminen MS, Filippatos GS, Salem R | display-authors=etal| title=Beneficial association of β-blocker therapy on recovery from severe acute heart failure treatment: data from the Survival of Patients With Acute Heart Failure in Need of Intravenous Inotropic Support trial. | journal=Crit Care Med | year= 2011 | volume= 39 | issue= 5 | pages= 940-4 | pmid=21283007 | doi=10.1097/CCM.0b013e31820a91ed | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21283007  }} </ref>.  


The Prins [[systematic review]] in 2015 of five [[cohort study | cohort studies]] and the B-CONVINCED [[randomized clinical trial]]<ref name="pmid19717851">{{cite journal| author=Jondeau G, Neuder Y, Eicher JC, Jourdain P, Fauveau E, Galinier M | display-authors=etal| title=B-CONVINCED: Beta-blocker CONtinuation Vs. INterruption in patients with Congestive heart failure hospitalizED for a decompensation episode. | journal=Eur Heart J | year= 2009 | volume= 30 | issue= 18 | pages= 2186-92 | pmid=19717851 | doi=10.1093/eurheartj/ehp323 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=19717851  }} </ref> found:
The Prins [[systematic review]] in 2015 of five [[cohort study | cohort studies]] and the B-CONVINCED [[randomized clinical trial]]<ref name="pmid19717851">{{cite journal| author=Jondeau G, Neuder Y, Eicher JC, Jourdain P, Fauveau E, Galinier M | display-authors=etal| title=B-CONVINCED: Beta-blocker CONtinuation Vs. INterruption in patients with Congestive heart failure hospitalizED for a decompensation episode. | journal=Eur Heart J | year= 2009 | volume= 30 | issue= 18 | pages= 2186-92 | pmid=19717851 | doi=10.1093/eurheartj/ehp323 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=19717851  }} </ref> found benefit and included:* In the OPTIMIZE-HF [[cohort study]] by Fonarow in 2004
* The B-CONVINCED [[randomized controlled trial]] by Jondeau in 2009
* The B-CONVINCED [[randomized controlled trial]] by Jondeau in 2009
* In Böhm's retrospective, observational [[cohort study | cohort analysis]] of the SURVIVE Trial,
* In Böhm's retrospective, observational [[cohort study | cohort analysis]] of the SURVIVE Trial in 2011


More recent studies than the Prins [[systematic review]] include:
Studies either more recent or missed<ref name="pmid25044535"/> by Prins [[systematic review]] include:
* The [[cohort study | cohort]], non-randomized analysis of the SENIORS trial by Montero-Perez-Barquero in 2014 found insignificantly reduced hospital mortality with the vasodilating [[beta-1]] selective [[beta-blocker]] nebivolol<ref name="pmid25044535">{{cite journal| author=Montero-Perez-Barquero M, Flather M, Roughton M, Coats A, Böhm M, Van Veldhuisen DJ | display-authors=etal| title=Influence of systolic blood pressure on clinical outcomes in elderly heart failure patients treated with nebivolol: data from the SENIORS trial. | journal=Eur J Heart Fail | year= 2014 | volume= 16 | issue= 9 | pages= 1009-15 | pmid=25044535 | doi=10.1002/ejhf.136 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25044535  }} </ref>.
* The GULF-CARE group's [[cohort study]] by Abi Khalil in 2017 found reduced hospital mortality, but no benefit at 3 and 12 months<ref name="pmid28694343">{{cite journal| author=Abi Khalil C, Sulaiman K, Mahfoud Z, Singh R, Asaad N, AlHabib KF | display-authors=etal| title=Non-withdrawal of beta blockers in acute decompensated chronic and de novo heart failure with reduced ejection fraction in a prospective multicentre study of patients with acute heart failure in the Middle East. | journal=BMJ Open | year= 2017 | volume= 7 | issue= 7 | pages= e014915 | pmid=28694343 | doi=10.1136/bmjopen-2016-014915 | pmc=5734353 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=28694343  }} </ref>
* The GULF-CARE group's [[cohort study]] by Abi Khalil in 2017 found reduced hospital mortality, but no benefit at 3 and 12 months<ref name="pmid28694343">{{cite journal| author=Abi Khalil C, Sulaiman K, Mahfoud Z, Singh R, Asaad N, AlHabib KF | display-authors=etal| title=Non-withdrawal of beta blockers in acute decompensated chronic and de novo heart failure with reduced ejection fraction in a prospective multicentre study of patients with acute heart failure in the Middle East. | journal=BMJ Open | year= 2017 | volume= 7 | issue= 7 | pages= e014915 | pmid=28694343 | doi=10.1136/bmjopen-2016-014915 | pmc=5734353 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=28694343  }} </ref>
* The KCHF [[cohort study]] by Tamaki in 2021 found reduced hospital mortality with more benefit with higher doses of [[beta-blocker]]s<ref name="pmid34180244">{{cite journal| author=Tamaki Y, Yaku H, Morimoto T, Inuzuka Y, Ozasa N, Yamamoto E | display-authors=etal| title=Lower In-Hospital Mortality With Beta-Blocker Use at Admission in Patients With Acute Decompensated Heart Failure. | journal=J Am Heart Assoc | year= 2021 | volume= 10 | issue= 13 | pages= e020012 | pmid=34180244 | doi=10.1161/JAHA.120.020012 | pmc=8403288 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=34180244  }} </ref>
* The Loma Linda [[cohort study]] by Ryu in 2022 of patients<ref name="pmid36412905">{{cite journal| author=Ryu R, Hauschild C, Bahjri K, Tran H| title=The Usage of Concomitant Beta-Blockers with Vasopressors and Inotropes in Cardiogenic Shock. | journal=Med Sci (Basel) | year= 2022 | volume= 10 | issue= 4 | pages=  | pmid=36412905 | doi=10.3390/medsci10040064 | pmc=9680500 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=36412905  }} </ref>
====Up titration====
Beta-blocker therapy can be up-titrated either guideline-directed medical therapy (GDMT)<ref name="pmid36356631">{{cite journal| author=Mebazaa A, Davison B, Chioncel O, Cohen-Solal A, Diaz R, Filippatos G | display-authors=etal| title=Safety, tolerability and efficacy of up-titration of guideline-directed medical therapies for acute heart failure (STRONG-HF): a multinational, open-label, randomised, trial. | journal=Lancet | year= 2022 | volume= 400 | issue= 10367 | pages= 1938-1952 | pmid=36356631 | doi=10.1016/S0140-6736(22)02076-1 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=36356631  }}  [https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=&cmd=prlinks&id=36877970 Review in: Ann Intern Med. 2023 Mar;176(3):JC31] </ref> or NT-proBNP-guided therapy intensification<ref name="pmid28829876">{{cite journal| author=Felker GM, Anstrom KJ, Adams KF, Ezekowitz JA, Fiuzat M, Houston-Miller N | display-authors=etal| title=Effect of Natriuretic Peptide-Guided Therapy on Hospitalization or Cardiovascular Mortality in High-Risk Patients With Heart Failure and Reduced Ejection Fraction: A Randomized Clinical Trial. | journal=JAMA | year= 2017 | volume= 318 | issue= 8 | pages= 713-720 | pmid=28829876 | doi=10.1001/jama.2017.10565 | pmc=5605776 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=28829876  }} </ref><ref name="pmid32319999">{{cite journal| author=Fiuzat M, Ezekowitz J, Alemayehu W, Westerhout CM, Sbolli M, Cani D | display-authors=etal| title=Assessment of Limitations to Optimization of Guideline-Directed Medical Therapy in Heart Failure From the GUIDE-IT Trial: A Secondary Analysis of a Randomized Clinical Trial. | journal=JAMA Cardiol | year= 2020 | volume= 5 | issue= 7 | pages= 757-764 | pmid=32319999 | doi=10.1001/jamacardio.2020.0640 | pmc=7177636 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=32319999  }} </ref>. GDMT may lead to higher doses and better outcomes<ref name="pmid36356631"/>.


===Aldosterone Antagonism===
===Aldosterone Antagonism===

Latest revision as of 18:24, 30 April 2023



Resident
Survival
Guide
Congestive Heart Failure Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Systolic Dysfunction
Diastolic Dysfunction
HFpEF
HFrEF

Causes

Differentiating Congestive heart failure from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

Clinical Assessment

History and Symptoms

Physical Examination

Laboratory Findings

Electrocardiogram

Chest X Ray

Cardiac MRI

Echocardiography

Exercise Stress Test

Myocardial Viability Studies

Cardiac Catheterization

Other Imaging Studies

Other Diagnostic Studies

Treatment

Invasive Hemodynamic Monitoring

Medical Therapy:

Summary
Acute Pharmacotherapy
Chronic Pharmacotherapy in HFpEF
Chronic Pharmacotherapy in HFrEF
Diuretics
ACE Inhibitors
Angiotensin receptor blockers
Aldosterone Antagonists
Beta Blockers
Ca Channel Blockers
Nitrates
Hydralazine
Positive Inotropics
Anticoagulants
Angiotensin Receptor-Neprilysin Inhibitor
Antiarrhythmic Drugs
Nutritional Supplements
Hormonal Therapies
Drugs to Avoid
Drug Interactions
Treatment of underlying causes
Associated conditions

Exercise Training

Surgical Therapy:

Biventricular Pacing or Cardiac Resynchronization Therapy (CRT)
Implantation of Intracardiac Defibrillator
Ultrafiltration
Cardiac Surgery
Left Ventricular Assist Devices (LVADs)
Cardiac Transplantation

ACC/AHA Guideline Recommendations

Initial and Serial Evaluation of the HF Patient
Hospitalized Patient
Patients With a Prior MI
Sudden Cardiac Death Prevention
Surgical/Percutaneous/Transcather Interventional Treatments of HF
Patients at high risk for developing heart failure (Stage A)
Patients with cardiac structural abnormalities or remodeling who have not developed heart failure symptoms (Stage B)
Patients with current or prior symptoms of heart failure (Stage C)
Patients with refractory end-stage heart failure (Stage D)
Coordinating Care for Patients With Chronic HF
Quality Metrics/Performance Measures

Implementation of Practice Guidelines

Congestive heart failure end-of-life considerations

Specific Groups:

Special Populations
Patients who have concomitant disorders
Obstructive Sleep Apnea in the Patient with CHF
NSTEMI with Heart Failure and Cardiogenic Shock

Congestive heart failure Management of Acute heart failure On the Web

Most recent articles

Most cited articles

Review articles

CME Programs

Powerpoint slides

Images

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

FDA on Congestive heart failure Management of Acute heart failure

CDC on Congestive heart failure Management of Acute heart failure

Congestive heart failure Management of Acute heart failure in the news

Blogs on Congestive heart failure Management of Acute heart failure

Directions to Hospitals Treating Congestive heart failure Management of Acute heart failure

Risk calculators and risk factors for Congestive heart failure Management of Acute heart failure

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Synonyms and keywords: Acute decompensated heart failure; ADHF; flash pulmonary edema

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 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 inhibtors,beta blockers and digoxin).

General Recommendations

Hospitalization

Hospitalization is required for the management of the patient with ADHF with the following signs, symptoms and laboratory abnormalities: [1]

Telemetry and Monitoring

The patient should be admitted to a level of care that allows for constant electrocardiographic monitoring given the risk of arrhythmias and frequent vital signs.

  • The heart rhythm and oxygen saturation should be monitored continuously.
  • Is and Os (intake and output) should be monitored carefully. A daily target should be established (for example the patient should be one liter negative for the day) and diuretic dosing should be adjusted to achieve this target.
  • Daily weights should be obtained using the same scale at the same time of the day, usually before the patient has eaten, and after they have first voided in the morning. Often times Is and Os measurements will underestimate insensible losses that occur through the lungs.
  • The BUN and creatinine, serum 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) should be monitored daily. Potassium and magnesium should be repeated as needed following diuresis.
  • If the patient is hyponatremic this does not suggest an inadequate intake of salt, but excess free water ingestion and retention. In these patients, access to free water should be restricted to <2 li/day if the Na is < 130 meq/li, and < 1 li/day or more if the Na is < 125 meq/li. It should be borne in mind that juices are essentially free water with sugar. In the hyponatremia patient, drips should not be in D5W. Patients with congestive heart failure should be on a <2 g per day sodium diet.

Oxygen

Oxygen improves the patient's status if hypoxemia is present, and the goal is to keep the oxygen saturation above 90%. Continuous positive airway pressure may be applied using a face mask; this has been shown to improve symptoms more quickly than oxygen therapy alone,[2] and has been shown to reduce the risk of death.[3][4] Severe respiratory failure requires treatment with endotracheal intubation and mechanical ventilation.

Management Considerations

The patient's therapy must be tailored to:

  • Whether the patient has acute diastolic or systolic heart failure
  • The patient's intravascular volume status
  • The patient's hemodynamic status
  • The precipitant of the decompensation

Systolic Versus Diastolic Heart Failure

The management of the patient with acute decompensated heart failure depends upon whether the patient has acute decompensated systolic heart failure or acute decompensated diastolic heart failure. Both forms of acute decompensated heart failure are treated with oxygen and vasodilator therapy and diuresis. Importantly, inotropic agents that increase contractility are not indicated in the patient with acute decompensated diastolic heart failure while they are 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.

Intravascular Volume Status

The aggressiveness of diuresis depends upon the patient's volume status. If the patient is total body and intravascular volume overloaded in normotensive, then diuresis alone should be undertaken. If the patient is volume overloaded but hypotensive, then inotropes must be administered in addition to diuretics. Vasodilators cannot be administered to these patients.

Identification of and Treatment of Underlying Cause of Decompensation

Identification of and treatment of precipitants of acute decompensation is a mainstay of therapy. Please see the accompanying chapters for detailed management strategies.

  • Hypertension: Vasodilators should be administered
  • Acute coronary syndrome: Antiplatelets, antithrombin, vasodilators, PCI, intra-aortic balloon pump placement should be used to reverse myocardial ischemia
  • Valvular heart disease: For mitral regurgitation vasodilator therapy should be administered, for mitral stenosis heart rate slowed to prolonged left ventricular filling, for aortic stenosis either balloon vavlotomy, TAVR or valve replacement may be necessary
  • Atrial fibrillation can cause acute decompensation of heart failure due to an increase in heart rate and oxygen demands, and conversely acute decompensation of heart failure can precipitate atrial fibrillation due to left atrial dilation and increased wall stress. Thus, atrial fibrillation and acute decompensated heart failure are often intimately related, and the successful management of atrial fibrillation is often critical to the success of reversing the acute decompensation.
In the patient with acute decompensated heart failure, rate control of atrial fibrillation is the mainstay of arrhythmia therapy. Obviously agents that have a negative inotropic effect such as beta blockers and non-dihydropyridine calcium channel blockers are relatively contraindicated in the management of acute decompensated systolic heart failure. Intravenous diltiazem does not have a negative inotropic effect and is often used for rate control. Short acting esmolol is sometimes used. Digoxin has a very narrow therapeutic/toxic window, it's onset of action is relatively delayed, and it is often not used.
If a patient is in cardiogenic shock, then cardioversion can be considered in the patient with atrial fibrillation, however in the absence of severe hemodynamic compromise it should be noted that atrial fibrillation will often recur in this setting. Thus, cardioversion is not particularly helpful in the absence of profound hemodynamic compromise. Cardioversion can also be undertaken if new onset atrial fibrillation is the clear precipitant of the hemodynamic decompensation. If the patient is going to be cardioverted, unfractionated heparin should be administered.
  • Ventricular Arrhythmias: The development of either ventricular tachycardia or ventricular fibrillation are life-threatening complications and must be treated promptly with the cardioversion. Many antiarrhythmic's can be pro-arrhythmic in the patient with heart failure and are contraindicated. Amiodarone is the antiarrhythmic of choice for the management of ventricular arrhythmias in the patient with heart failure. Underlying precipitants of ventricular arrhythmias such as hypokalemia and hypomagnesemia should be corrected. It should also be noted that inotropic agents can be proarrhythmic, and for this reason as low a dose as possible should be used, and they should be tapered as soon as possible.

Specific Therapies

Diuretics

  • Usually, but not always, patients with decompensated systolic heart failure are total body and intravascular volume overload and intravenous diuretics are often required in the acute setting. Even in the absence of volume overload (decompensation due to hypertension or valvular heart disease) diuresis may help the symptoms of congestive heart failure because "dry lungs work better than wet lungs". These drugs also cause venodilation in the lung vasculature that also relieves shortness of breath. While contractility of the heart increases with increasing volumes, this relationship is not preserved past a certain volume. By reducing volume overload, these drugs optimize the heart's contractility (they keep the patient from falling off the end of the Starling curve). Reducing the heart's volume also reduces functional mitral regurgitation and tricuspid regurgitation.
  • Diuretics reduce preload and reduce intravascular volume.
  • Intravenous preparations are preferred because of more predictable absorption. When a patient is extremely fluid overloaded, they can develop intestinal edema as well, which can affect enteral absorption of medications.
  • The traditional starting dose of Lasix or furosemide is 40 mg intravenously. If this does not work, the dose is doubled. There is insufficient data to suggest a Lasix drip is superior to boluses of Lasix.[5] A useful rule of thumb is that the IV dose should be 2.5 times the usual oral dose based upon the trend for superiority of high doses over low doses in the DOSE trial [6]. Usually an effect is seen in 30 minutes.
  • Torsemide is another alternative and it's dose is 10 to 20 mg intravenously.
  • If high doses of furosemide are inadequate, boluses or continuous infusions of bumetanide (1 mg intravenously) may be preferred.
  • These loop diuretics may be combined with thiazide diuretics such as oral metolazone, hydrochlorothiazide (25 to 50 mg twice daily) or intravenous chlorothiazide (500 to 1000 mg/day) for a synergistic effect.
  • Hypotension may result from diuresis if mobilization of fluid from the extra vascular space does not keep pace with fluid leaving the intravascular space through diuresis. Patients with diastolic dysfunction and restrictive physiology are also prone to hypotension due to reductions in preload.
  • Typically the BUN and Cr will rise during diuresis (hopefully the Cr only slightly). If the rise in creatinine is minimal, and the patient remains fluid overloaded, then diuresis can continue with careful attention to the renal function. If the creatinine rises significantly before the patient is euvolemic, this suggests that there is reduced perfusion to the kidney, and this is associated with a poorer prognosis. If the creatinine rises significantly, other nephrotoxic drugs should be discontinued, and the dosing of the diuretic may need to be reduced. Despite a rise in the creatinine, continued diuresis is sometimes required if severe pulmonary edema persists and consideration should be given to the addition of an inotropic agent.
  • If further efforts to induce diuresis are failing and the patient remains volume overloaded, then ultrafiltration or dialysis should be considered.
  • In patients who have sustained a myocardial infarction and have heart failure, an aldosterone antagonist such as spironolactone or eplerenone can be added instead of a thiazide diuretic. Given the risk of hyperkalemia these agent should only be added if the renal function and serum potassium can be carefully monitored.

Vasodilator Therapy

In the absence of hypotension, the intravenous administration of vasodilators such as nitroglycerin, nitroprusside and nesiritide can reduce both preload and afterload and can rapidly improve symptoms. These benefits are observed when the drugs are administered in addition to diuretics or when there is a poor response to diuretics.

Nitroglycerin

  • Nitroglycerine reduces afterload and reduces preload. Nitroglycerine is helpful in improving symptoms of dyspnea. At higher doses, nitroglycerin also reduces afterload.
  • Unfortunately tolerance or tachyphylaxis can develop within hours of continuous administration of high-dose nitroglycerin.
  • The initial dose of intravenous nitroglycerin is 5 to 10 µg per minute and this dose is increased every 3-5 minutes in 5 to 10 µg increments to a maximum dose of 10 to to 200 µg per minute.

Nitroprusside

Inotropic Therapy

  • Ionotropes may be administered if the cardiac output and the systolic blood pressure are low, if there is evidence of end organ hypoperfusion (e.g. a rising creatinine), and if there is evidence of elevated filling pressures (an elevated pulmonary capillary wedge pressure or an elevated jugular venous pressure) which limit diuresis and/or vasodilator therapy.
  • Milrinone increases contractility and reduces afterload
  • Dobutamine increases contractility in reduces afterload
  • Dopamine increases blood pressure and increases renal perfusion at low doses
  • There is ongoing concern that inotropes, by increasing heart rate and contractility, may damage hibernating but viable myocardium. These agents are also proarrhythmic. Consistent with these concerns, the randomized OPTIME-CHF trial demonstrated that randomization to Milrinone versus placebo was associated with an increased incidence of hypotension, atrial arrhythmias as well as a non-significant increase in mortality.
  • In so far as Milrinone does not exert its effects through beta receptors, it may be more effective in those patients on a beta blocker.
  • The starting dose of dobutamine is 2.5 µg/kg/min and the dosing can be gradually titrated up to 15 µg/kg/min.
  • The loading dose of Milrinone is 50 µg/kg over 10 minutes. The initial maintenance dose is 0.375 µg/kg/min and the maximum dose is 0.750 µg/kg/min.

Vasopressor Support

Prophylaxis for Venous Thromboembolism

In the absence of contraindications, either low-dose unfractionated heparin, fondaparinux or a low molecular weight heparin are recommended as DVT prophylaxis in the patient with acute decompensated heart failure.

ACE Inhibition

Continuation of Chronic ACE Inhibition

Initiation of Acute ACE Inhibition

Beta Blockers

Discontinuation

While beta blockers may play a role in the management of chronic heart failure, beta blockade should not be initiated during acute decompensated heart failure.

Regarding whether patients already on beta-blockers should have these medications stopped when they have acute heart failure, the adrenergic receptor profile of concomittent inotropes may affect decisions:

If the patient is chronically administered a beta blocker, the beta blocker can be continued in the absence of hypotension. If the patient becomes hemodynamically unstable, the beta blocker dosing can be reduced. If inotropic agents are required, then the beta blocker should be discontinued.

  • The Gattis cohort study in 2003.
  • In the OPTIMIZE-HF cohort study by Fonarow in 2004, which was restricted to patients "eligible for beta-blockers at discharge," was associated with adjusted higher mortality[8].
  • In the ESCAPE cohort study by Butler in 2006, withdrawal of beta blockers was associated with adjusted higher mortality.[9]
  • The Orso cohort study in 2009.
  • The B-CONVINCED randomized controlled trial by Jondeau in 2009 found no differences in outcomes during the hospitalization, but the patients randomized to stay on beta-blockers were more likely to be taking beta-blockers at 3 months (90% vs. 76%)[10].
  • In the retrospective, observational cohort analysis of the SURVIVE Trial studying patients requiring inotropes by Böhm in 2011, patients remaining on beta-blockers had lower adjusted mortality at 30 and 180 days[11].

The Prins systematic review in 2015 of five cohort studies and the B-CONVINCED randomized clinical trial[10] found benefit and included:* In the OPTIMIZE-HF cohort study by Fonarow in 2004

Studies either more recent or missed[12] by Prins systematic review include:

  • The cohort, non-randomized analysis of the SENIORS trial by Montero-Perez-Barquero in 2014 found insignificantly reduced hospital mortality with the vasodilating beta-1 selective beta-blocker nebivolol[12].
  • The GULF-CARE group's cohort study by Abi Khalil in 2017 found reduced hospital mortality, but no benefit at 3 and 12 months[13]
  • The KCHF cohort study by Tamaki in 2021 found reduced hospital mortality with more benefit with higher doses of beta-blockers[14]
  • The Loma Linda cohort study by Ryu in 2022 of patients[15]

Up titration

Beta-blocker therapy can be up-titrated either guideline-directed medical therapy (GDMT)[16] or NT-proBNP-guided therapy intensification[17][18]. GDMT may lead to higher doses and better outcomes[16].

Aldosterone Antagonism

  • If the patient is chronically being administered an aldosterone antagonist prior to the episode of decompensated congestive heart failure, the agent may be continued in the absence of hypotension, hyperkalemia, and impaired renal function.
  • If the patient meets the criteria for initiation of an aldosterone antagonist for the management of chronic heart failure, this can be initiated prior to hospital discharge.

Morphine

  • Morphine reduces preload, reduces catecholamines, and reduces the stimulation by stretch receptors in the lung thereby improving symptoms of dyspnea.
  • Nonrandomized observational studies have demonstrated that in the setting of acute decompensated heart failure morphine is associated with an increase in-hospital mortality, increased mechanical ventilation and longer hospital admissions despite adjustment of covariates in multivariate models.
  • Given the potential hazard identified in these non-randomized observational studies, morphine administration is generally not recommended in the setting of acute decompensated heart failure.

Contraindicated medications

Congestive heart failure is considered an absolute contraindication to the use of the following medications:

References

  1. 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 (2010). "HFSA 2010 Comprehensive Heart Failure Practice Guideline". Journal of Cardiac Failure. 16 (6): e1–194. doi:10.1016/j.cardfail.2010.04.004. PMID 20610207. Retrieved 2013-04-29. Unknown parameter |month= ignored (help)
  2. Gray A, Goodacre S, Newby DE, Masson M, Sampson F, Nicholl J (2008). "Noninvasive ventilation in acute cardiogenic pulmonary edema". N. Engl. J. Med. 359 (2): 142–51. doi:10.1056/NEJMoa0707992. PMID 18614781. Unknown parameter |month= ignored (help)
  3. Peter JV, Moran JL, Phillips-Hughes J, Graham P, Bersten AD (2006). "Effect of non-invasive positive pressure ventilation (NIPPV) on mortality in patients with acute cardiogenic pulmonary oedema: a meta-analysis". Lancet. 367 (9517): 1155–63. doi:10.1016/S0140-6736(06)68506-1. PMID 16616558. Unknown parameter |month= ignored (help)
  4. Weng CL; Zhao YT; Liu QH; et al. (2010). "Meta-analysis: Noninvasive ventilation in acute cardiogenic pulmonary edema". Ann. Intern. Med. 152 (9): 590–600. doi:10.1059/0003-4819-152-9-201005040-00009. PMID 20439577. Unknown parameter |month= ignored (help); Unknown parameter |author-separator= ignored (help)
  5. Salvador DR, Rey NR, Ramos GC, Punzalan FE (2005). "Continuous infusion versus bolus injection of loop diuretics in congestive heart failure". Cochrane Database of Systematic Reviews (Online) (3): CD003178. doi:10.1002/14651858.CD003178.pub3. PMID 16034890. Retrieved 2013-04-30.
  6. 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 (2011). "Diuretic strategies in patients with acute decompensated heart failure". The New England Journal of Medicine. 364 (9): 797–805. doi:10.1056/NEJMoa1005419. PMC 3412356. PMID 21366472. Retrieved 2013-04-30. Unknown parameter |month= ignored (help)
  7. Sigurdsson A, Swedberg K (1994). "Left ventricular remodelling, neurohormonal activation and early treatment with enalapril (CONSENSUS II) following myocardial infarction". European Heart Journal. 15 Suppl B: 14–9, discussion 26–30. PMID 8076657. Retrieved 2013-04-30. Unknown parameter |month= ignored (help)
  8. Fonarow GC, Abraham WT, Albert NM, Stough WG, Gheorghiade M, Greenberg BH; et al. (2008). "Influence of beta-blocker continuation or withdrawal on outcomes in patients hospitalized with heart failure: findings from the OPTIMIZE-HF program". J Am Coll Cardiol. 52 (3): 190–9. doi:10.1016/j.jacc.2008.03.048. PMID 18617067.
  9. Butler J, Young JB, Abraham WT, Bourge RC, Adams KF, Clare R, O'Connor C (2006). "Beta-blocker use and outcomes among hospitalized heart failure patients". Journal of the American College of Cardiology. 47 (12): 2462–9. doi:10.1016/j.jacc.2006.03.030. PMID 16781374. Retrieved 2013-04-30. Unknown parameter |month= ignored (help)
  10. 10.0 10.1 Jondeau G, Neuder Y, Eicher JC, Jourdain P, Fauveau E, Galinier M; et al. (2009). "B-CONVINCED: Beta-blocker CONtinuation Vs. INterruption in patients with Congestive heart failure hospitalizED for a decompensation episode". Eur Heart J. 30 (18): 2186–92. doi:10.1093/eurheartj/ehp323. PMID 19717851.
  11. Böhm M, Link A, Cai D, Nieminen MS, Filippatos GS, Salem R; et al. (2011). "Beneficial association of β-blocker therapy on recovery from severe acute heart failure treatment: data from the Survival of Patients With Acute Heart Failure in Need of Intravenous Inotropic Support trial". Crit Care Med. 39 (5): 940–4. doi:10.1097/CCM.0b013e31820a91ed. PMID 21283007.
  12. 12.0 12.1 Montero-Perez-Barquero M, Flather M, Roughton M, Coats A, Böhm M, Van Veldhuisen DJ; et al. (2014). "Influence of systolic blood pressure on clinical outcomes in elderly heart failure patients treated with nebivolol: data from the SENIORS trial". Eur J Heart Fail. 16 (9): 1009–15. doi:10.1002/ejhf.136. PMID 25044535.
  13. Abi Khalil C, Sulaiman K, Mahfoud Z, Singh R, Asaad N, AlHabib KF; et al. (2017). "Non-withdrawal of beta blockers in acute decompensated chronic and de novo heart failure with reduced ejection fraction in a prospective multicentre study of patients with acute heart failure in the Middle East". BMJ Open. 7 (7): e014915. doi:10.1136/bmjopen-2016-014915. PMC 5734353. PMID 28694343.
  14. Tamaki Y, Yaku H, Morimoto T, Inuzuka Y, Ozasa N, Yamamoto E; et al. (2021). "Lower In-Hospital Mortality With Beta-Blocker Use at Admission in Patients With Acute Decompensated Heart Failure". J Am Heart Assoc. 10 (13): e020012. doi:10.1161/JAHA.120.020012. PMC 8403288 Check |pmc= value (help). PMID 34180244 Check |pmid= value (help).
  15. Ryu R, Hauschild C, Bahjri K, Tran H (2022). "The Usage of Concomitant Beta-Blockers with Vasopressors and Inotropes in Cardiogenic Shock". Med Sci (Basel). 10 (4). doi:10.3390/medsci10040064. PMC 9680500 Check |pmc= value (help). PMID 36412905 Check |pmid= value (help).
  16. 16.0 16.1 Mebazaa A, Davison B, Chioncel O, Cohen-Solal A, Diaz R, Filippatos G; et al. (2022). "Safety, tolerability and efficacy of up-titration of guideline-directed medical therapies for acute heart failure (STRONG-HF): a multinational, open-label, randomised, trial". Lancet. 400 (10367): 1938–1952. doi:10.1016/S0140-6736(22)02076-1. PMID 36356631 Check |pmid= value (help). Review in: Ann Intern Med. 2023 Mar;176(3):JC31
  17. Felker GM, Anstrom KJ, Adams KF, Ezekowitz JA, Fiuzat M, Houston-Miller N; et al. (2017). "Effect of Natriuretic Peptide-Guided Therapy on Hospitalization or Cardiovascular Mortality in High-Risk Patients With Heart Failure and Reduced Ejection Fraction: A Randomized Clinical Trial". JAMA. 318 (8): 713–720. doi:10.1001/jama.2017.10565. PMC 5605776. PMID 28829876.
  18. Fiuzat M, Ezekowitz J, Alemayehu W, Westerhout CM, Sbolli M, Cani D; et al. (2020). "Assessment of Limitations to Optimization of Guideline-Directed Medical Therapy in Heart Failure From the GUIDE-IT Trial: A Secondary Analysis of a Randomized Clinical Trial". JAMA Cardiol. 5 (7): 757–764. doi:10.1001/jamacardio.2020.0640. PMC 7177636 Check |pmc= value (help). PMID 32319999 Check |pmid= value (help).

Template:WikiDoc Sources