Congestive heart failure implantation of intracardiac defibrillator: Difference between revisions

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*Implantation of an [[ICD]] for primary prevention of sudden death should be considered for patients with [[LVEF]] ≤ 35% who are in [[New york heart association functional classification|NYHA functional class II or III]].
*Implantation of an [[ICD]] for primary prevention of sudden death should be considered for patients with [[LVEF]] ≤ 35% who are in [[New york heart association functional classification|NYHA functional class II or III]].


*[[ICD]] implantation is not appropriate or beneficial for patients in [[New york heart association functional classification|NYHA class IV]] (severely debilitated).  
*[[ICD]] implantation is not appropriate or beneficial for patients in [[New york heart association functional classification|NYHA class IV]] (severely debilitated). In post-[[MI]] patients, implantation of an [[ICD]] should be performed no earlier than 40 days post-MI in patients with persistent moderate or severe [[left ventricular systolic dysfunction]]: [[LVEF]] ≤ 30% for asymptomatic ([[New york heart association functional classification|NYHA class I]]) patients or [[LVEF]] ≤ 35% for symptomatic ([[New york heart association functional classification|NYHA class II or III]]) patients.
:*In post-[[MI]] patients, implantation of an [[ICD]] should be performed no earlier than 40 days post-MI in patients with persistent moderate or severe [[left ventricular systolic dysfunction]]:  
::*[[LVEF]] ≤ 30% for asymptomatic ([[New york heart association functional classification|NYHA class I]]) patients or [[LVEF]] ≤ 35% for symptomatic ([[New york heart association functional classification|NYHA class II or III]]) patients.


*[[ICD]] implantation has NOT been demonstrated to prolong life in patients who are severely symptomatic or otherwise profoundly debilitated ([[New york heart association functional classification|NYHA class IV]]).
*[[ICD]] implantation has NOT been demonstrated to prolong life in patients who are severely symptomatic or otherwise profoundly debilitated ([[New york heart association functional classification|NYHA class IV]]).

Revision as of 03:02, 4 April 2012

Congestive Heart Failure Microchapters

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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 implantation of intracardiac defibrillator On the Web

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Editor(s)-In-Chief: James Chang, M.D., Cardiovascular Division Beth Israel Deaconess Medical Center, Boston MA, Harvard Medical School [1] and C. Michael Gibson, M.S., M.D. [2], Cardiovascular Division Beth Israel Deaconess Medical Center, Boston MA, Harvard Medical School

Overview

  • 50% of heart failure patients die of sudden cardiac death.
  • ICDs are indicated for patients with previous myocardial infarction and LVEF <30%, sustained ventricular tachycardia, inducible ventricular tachycardia.
  • Morbidity/mortality benefit of ICD placement vs. anti-arrhythmic drug therapy is controversial.

Indications for an Intracardiac Defibrillator

1. The left ventricular ejection fraction (LVEF) is ≤ 35%

and

2. NYHA class II/III

OR

1. The left ventricular ejection fraction (LVEF) is ≤ 30%

and

2. There is a prior history of myocardial infarction (MI)

Background

  • ICD implantation has NOT been demonstrated to prolong life in patients who are severely symptomatic or otherwise profoundly debilitated (NYHA class IV).

References


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