Dilated cardiomyopathy

Last updated: November 01, 2022

Dilated cardiomyopathy

ER Nursing Week 2

ER Nursing Week 2

Heart failure: Clinical
Cardiac work
Frank-Starling relationship
Atrial fibrillation
Regulation of pulmonary blood flow
Respiratory alkalosis
Respiratory system anatomy and physiology
Respiratory acidosis
Metabolic and respiratory alkalosis: Clinical
Acute respiratory distress syndrome: Clinical
Respiratory distress syndrome: Pathology review
Upper respiratory tract infection
Acute respiratory distress syndrome
Metabolic and respiratory acidosis: Clinical
Ventilation
Lung cancer
Standards of care for COVID-19 patients
Cardiovascular system anatomy and physiology
Introduction to the cardiovascular system
Control of blood flow circulation
Coronary circulation
Aortic valve disease
Resistance to blood flow
Heart failure
Heart failure: Pathology review
Normal heart sounds
Heart blocks: Pathology review
Abnormal heart sounds
Valvular heart disease: Clinical
Cardiac conduction system
Anatomy of the heart
Valvular heart disease: Pathology review
Rheumatic heart disease
Anatomy clinical correlates: Heart
Left-sided heart failure: Nursing process (ADPIE)
Post-COVID syndrome: Heart, lungs and clotting
Pericardial disease: Pathology review
Tuberculosis: Pathology review
Myocarditis
Dilated cardiomyopathy
Coronary artery disease: Pathology review
Myocardial infarction
ECG cardiac infarction and ischemia
Knowledge Shot: Is Santa Claus at risk of a heart attack
Coronary artery disease: Clinical
Pericarditis and pericardial effusion
Ischemia
Excitability and refractory periods
Antiplatelet medications
Non-corticosteroid immunosuppressants and immunotherapies
Aortic dissection
Aortic aneurysms and dissections: Clinical
Coronary steal syndrome
Venous thromboembolism: Clinical
Pericardial disease: Clinical
Carbon dioxide transport in blood
Zones of pulmonary blood flow
Hypertension: Clinical
Tricuspid valve disease
Sympatholytics: Alpha-2 agonists
Calcium channel blockers
Hypoplastic left heart syndrome
Positive inotropic medications
Familial hypercholesterolemia
Hyperlipidemia
Hypoxia
Laryngitis
Bacterial epiglottitis
Wolff-Parkinson-White syndrome
Atrioventricular nodal reentrant tachycardia (AVNRT)
Marfan syndrome
Brugada syndrome
Action potentials in pacemaker cells
Cardiomyopathies: Clinical
Long QT syndrome and Torsade de pointes
Atrioventricular block
Infective endocarditis: Clinical
Bundle branch block
Peripheral artery disease
Arterial disease
Peripheral vascular disease: Clinical
Cardiac tamponade
Cardiac contractility
ECG cardiac hypertrophy and enlargement
Aortic dissections and aneurysms: Pathology review
Deep vein thrombosis and pulmonary embolism: Pathology review
Pulmonary embolism
Stable angina
Angina pectoris
Prinzmetal angina
Ludwig angina
Unstable angina
Aneurysms
Pleural effusion
Obstructive lung diseases: Pathology review
Pneumonia: Clinical
Emphysema
Imaging features of COVID-19 (LifeBridge Health)

Transcript

Watch video only

Cardiomyopathy translates to “heart muscle disease,” so cardiomyopathy is a broad term used to describe a variety of issues that result from disease of the myocardium, or heart muscle.

When cardiomyopathy develops as a way to compensate for some other underlying disease, such as hypertension or valve diseases, it’s called secondary cardiomyopathy. When it develops all by itself, it’s called primary cardiomyopathy.

Now, the most common type is dilated cardiomyopathy, which can cause all four chambers of the heart to dilate, or get bigger. Specifically, new sarcomeres, or muscle units, in the walls are added in series, and the chambers grow larger, which leaves the walls relatively thin compared to the large chamber size, with less muscle to use for contraction.

In other words, they have really weak contractions, which means less blood is pumped out each contraction. This also means that there’s a lower stroke volume, and if the heart’s failing to pump out as much blood to both the body from the left ventricle, and the lungs from the right ventricle, patients develop biventricular congestive heart failure. Since contraction happens during systole, we say this is a type of systolic heart failure.

Also, when the chambers get larger, they tend to stretch out the valves that separate the atria and ventricles. When they are stretched, the valves can’t close all the way, so they start to regurgitate blood back into the atria. This is called mitral valve regurgitation on the left side, and tricuspid valve regurgitation on the right. Mitral valve regurgitation might be heard on auscultation as a holosystolic murmur, meaning that it happens throughout systole.

Additionally, you might also hear an S3 heart sound on auscultation, which is the result of blood rushing and slamming into the dilated ventricular wall during diastole.

Another complication can be arrhythmias, because stretching out the muscle walls can irritate the cells in the conduction system, which are within those walls. Sometimes, an X-ray can be helpful for a diagnosing dilated cardiomyopathy.

As far as causes go, primary dilated cardiomyopathy is most often idiopathic, meaning there isn’t a clearly identifiable cause. Some cases, however, can be traced back to specific genetic mutations or genetic conditions, such as Duchenne Muscular Dystrophy and hemochromatosis. Also, in some cases it can be caused by an infection, like coxsackievirus B, which causes myocarditis — inflammation of the heart muscle — or Chagas disease, a protozoal infection.

Sources

  1. "Robbins Basic Pathology" Elsevier (2017)
  2. "Harrison's Principles of Internal Medicine, Twentieth Edition (Vol.1 & Vol.2)" McGraw-Hill Education / Medical (2018)
  3. "Pathophysiology of Disease: An Introduction to Clinical Medicine 8E" McGraw-Hill Education / Medical (2018)
  4. "The Diagnosis and Evaluation of Dilated Cardiomyopathy" Journal of the American College of Cardiology (2016)
  5. "Idiopathic Dilated Cardiomyopathy" New England Journal of Medicine (1994)
  6. "Dilated cardiomyopathy" Nature Reviews Disease Primers (2019)