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dilated cardiomyopathy 1K
ICD-10 Codes
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Description
What is Dilated Cardiomyopathy?
Dilated cardiomyopathy (DCM) is a type of heart muscle disease that affects the heart's ability to pump blood effectively. It is characterized by the thinning and stretching of the heart chambers, particularly the left ventricle.
- The condition causes the heart muscle to become weakened and enlarged, leading to reduced cardiac function [1].
- DCM often starts in the left ventricle, which is responsible for pumping oxygenated blood throughout the body [5].
- As a result, the heart cannot pump enough blood to meet the body's needs, leading to symptoms such as shortness of breath, fatigue, and swelling in the legs and feet [2].
Causes and Risk Factors
While the exact cause of DCM is often unknown, several factors can contribute to its development:
- Genetics: Family history plays a significant role in the development of DCM [7].
- Viral infections: Certain viral infections, such as myocarditis, can lead to DCM [6].
- Other medical conditions: Conditions like diabetes, high blood pressure, and thyroid disorders can increase the risk of developing DCM [8].
Symptoms and Diagnosis
Common symptoms of dilated cardiomyopathy include:
- Shortness of breath
- Fatigue
- Swelling in the legs and feet
- Chest pain or discomfort
Diagnosis is typically made through a combination of physical examination, medical history, and diagnostic tests such as echocardiography, electrocardiogram (ECG), and cardiac catheterization [3].
Treatment and Prognosis
While there is no cure for DCM, treatment options can help manage symptoms and improve quality of life:
- Medications: Diuretics, ACE inhibitors, and beta blockers may be prescribed to alleviate symptoms and slow disease progression [4].
- Lifestyle modifications: Maintaining a healthy diet, exercising regularly, and quitting smoking can also contribute to better outcomes.
Prognosis varies depending on the severity of the condition and individual factors. However, with proper treatment and management, many people with DCM can lead active and fulfilling lives.
References:
[1] Feb 27, 2024 [2] May 28, 2024 [3] Sep 24, 2024 [4] by HP Schultheiss · 2019 · Cited by 633 [5] Dilated cardiomyopathy is an issue with your heart muscle stretching out and becoming larger than usual. It starts in your heart's main pumping chamber (left ventricle) [4] [6] A cardiomyopathy is a primary disorder of the heart muscle (see also Overview of Cardiomyopathies). Dilated cardiomyopathy can develop at any age but is more common in adults younger than 50 [8] [7] by HP Schultheiss · 2019 · Cited by 633 [8] A cardiomyopathy is a primary disorder of the heart muscle (see also Overview of Cardiomyopathies). Dilated cardiomyopathy can develop at any age but is more common in adults younger than 50 [8]
Additional Characteristics
- Dilated cardiomyopathy
- Thinning and stretching of the heart chambers
- Heart muscle disease
- Weakening and enlargement of the heart muscle
- Reduced cardiac function
- Symptoms: shortness of breath, fatigue, swelling in the legs and feet
Signs and Symptoms
Common Signs and Symptoms of Dilated Cardiomyopathy
Dilated cardiomyopathy is a condition where the heart's ability to pump blood is weakened, leading to various symptoms. Here are some common signs and symptoms associated with this condition:
- Shortness of breath: This is one of the most common symptoms of dilated cardiomyopathy, especially when exerting oneself or lying down [3].
- Fatigue: Patients often experience unusual tiredness due to the heart's inability to pump enough blood [2].
- Swelling (edema): Fluid buildup in the legs, ankles, feet, and abdomen can occur due to the heart's failure to efficiently pump blood [1].
- Chest pain or pressure: This symptom may be more pronounced with exercise [4].
Other possible symptoms include:
- Dizziness or lightheadedness
- Fainting
- Irregular or rapid pulse
- Loss of appetite
It is essential to note that these symptoms can vary in severity and may not be present in all patients. If you are experiencing any of these symptoms, it is crucial to consult a healthcare professional for proper diagnosis and treatment.
References: [1] - Symptoms · Fatigue · Shortness of breath (dyspnea) during activity or while lying down · Reduced ability to exercise · Swelling (edema) in the legs, ankles, feet or ... [2] - What are the symptoms? · Chest pain · Cough and congestion · Dizziness or lightheadedness · Fainting · Fatigue (unusual tiredness) · Palpitations or fluttering in ... [3] - What are the symptoms of dilated cardiomyopathy? · Shortness of breath with exertion (may progress to shortness of breath when at rest) · Shortness of breath when ... [4] - Feb 27, 2024 — Symptoms · Chest pain or pressure (more likely with exercise) · Cough · Fatigue, weakness, faintness · Irregular or rapid pulse · Loss of appetite ...
Additional Symptoms
- Fainting
- Shortness of breath
- Chest pain or pressure
- Swelling (edema)
- Dizziness or lightheadedness
- Irregular or rapid pulse
- loss of appetite
- fatigue
Diagnostic Tests
Diagnostic Tests for Dilated Cardiomyopathy
Dilated cardiomyopathy (DCM) can be diagnosed using various tests and examinations. Here are some of the common diagnostic tests used to diagnose DCM:
- Echocardiography: This is a non-invasive test that uses sound waves to create images of the heart. It provides information on the size, shape, and function of the heart's chambers and valves [1]. Echocardiography is often considered the first-line imaging test in the assessment of patients with DCM [2].
- Electrocardiogram (ECG): This quick and painless test measures the electrical activity of the heart. It can help identify abnormal heart rhythms, which are common in people with DCM [8].
- Chest X-ray: A chest x-ray can show an enlarged heart or fluid buildup in the lungs, which can be indicative of DCM [3].
- Cardiac MRI: This test uses magnetic fields and radio waves to create detailed images of the heart. It can help diagnose DCM and assess its severity [4].
- Endomyocardial biopsy (selected cases): In some cases, a biopsy may be performed to examine tissue samples from the heart muscle for signs of inflammation or scarring.
- Testing for cause: Depending on the suspected underlying cause of DCM, additional tests such as blood work or genetic testing may be ordered.
It's worth noting that a diagnosis of DCM is often made based on a combination of these tests and clinical evaluation. A healthcare professional will consider the results of these tests along with symptoms and medical history to make an accurate diagnosis [6].
References: [1] T Mathew (2017) - Echocardiography in dilated cardiomyopathy [2] T Mathew (2017) - First-line imaging test for DCM [3] Context result 3 - Chest x-ray findings in DCM [4] A Ferreira (2023) - Cardiac MRI in DCM diagnosis [5] P Rubis (no year) - Criteria for dilated cardiomyopathy [6] AG Japp (2016) - Clinical screening and testing for DCM [7] Context result 9 - Common diagnostic tests for DCM
Additional Diagnostic Tests
- Electrocardiogram (ECG)
- Chest X-ray
- Echocardiography
- Cardiac MRI
- Endomyocardial biopsy (selected cases)
Treatment
Treatment Options for Dilated Cardiomyopathy
Dilated cardiomyopathy (DCM) is a progressive heart disorder that requires effective management to improve symptoms, prevent further damage, and enhance quality of life. Medications play a crucial role in the treatment of DCM.
Commonly Prescribed Medications
- ACE Inhibitors: These medications reduce the heart's workload by blocking the effects of angiotensin II, a potent vasoconstrictor. ACE inhibitors have been shown to improve symptoms and slow disease progression [3].
- Beta Blockers: Beta blockers, such as carvedilol, can improve ventricular remodeling, cardiac function, and clinical efficacy in patients with DCM [6]. They work by reducing the heart's workload and improving its pumping efficiency.
- Digoxin: Digoxin is a digitalis glycoside that can help improve the heart's ability to pump blood in patients with reduced ejection fraction heart failure [8].
- Angiotensin-Converting Enzyme (ACE) Inhibitors or Angiotensin II Receptor Blockers (ARBs): These medications reduce the heart's workload by blocking the effects of angiotensin II, a potent vasoconstrictor.
- Other Medications: Other medications, such as diuretics and vasodilators, may be prescribed to manage symptoms and improve quality of life.
Medication Classes Used in DCM Treatment
- Beta blockers: 59% (male), 40% (female), 52% (all) [10]
- ACE inhibitors or ARBs: 47% (male), 36% (female), 43% (all) [10]
Importance of Medication Adherence
Adhering to medication regimens is crucial in managing DCM. Studies have shown that patients who adhere to their medication regimens experience improved symptoms, reduced hospitalizations, and better quality of life.
References:
[3] Treatment of dilated cardiomyopathy (DCM) requires effective management to improve symptoms, prevent further damage, and enhance quality of life. [6] Beta blockers can improve ventricular remodeling, cardiac function, and clinical efficacy in patients with DCM. [8] Digoxin is a digitalis glycoside that can help improve the heart's ability to pump blood in patients with reduced ejection fraction heart failure. [10] Medication classes used in DCM treatment include beta blockers, ACE inhibitors or ARBs, and other medications.
Recommended Medications
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Differential Diagnosis
Differential Diagnosis of Dilated Cardiomyopathy
Dilated cardiomyopathy (DCM) is a progressive disease of the heart muscle that can be challenging to diagnose, as it shares similar symptoms with other cardiac conditions. Therefore, it's essential to consider a comprehensive differential diagnosis to exclude other possible causes of left ventricular dysfunction.
Common Causes of Left Ventricular Dysfunction
- Coronary Artery Disease: This is one of the most frequent causes of left ventricular dysfunction and should be excluded in the differential diagnosis of DCM.
- Hypertrophic Cardiomyopathy: A genetic disorder that affects the heart muscle, leading to thickening of the heart walls. It can cause similar symptoms to DCM.
- Left Ventricular Noncompaction: A rare condition characterized by a thinning and dilatation of the left ventricle.
- Toxic Cardiomyopathy: Certain toxins, such as heavy metals or alcohol, can damage the heart muscle and lead to DCM-like symptoms.
Other Conditions to Consider
- Acute Coronary Syndrome: A condition that occurs when the blood flow to the heart is suddenly blocked, leading to a heart attack.
- High Blood Pressure: Uncontrolled high blood pressure can put additional strain on the heart, potentially leading to DCM.
- Diabetes: This condition can cause damage to the blood vessels and nerves that control the heart, increasing the risk of DCM.
- Thyroid Disease: An underactive or overactive thyroid gland can affect the heart's function and lead to DCM-like symptoms.
- Viral Infections: Certain viral infections, such as HIV or Lyme disease, can damage the heart muscle and lead to DCM.
- Autoimmune Diseases: Conditions like polymyositis can cause inflammation in the heart muscle, leading to DCM-like symptoms.
Key Points
- A comprehensive differential diagnosis is crucial to exclude other possible causes of left ventricular dysfunction.
- Common causes of left ventricular dysfunction include coronary artery disease, hypertrophic cardiomyopathy, and left ventricular noncompaction.
- Other conditions that should be considered in the differential diagnosis of DCM include acute coronary syndrome, high blood pressure, diabetes, thyroid disease, viral infections, and autoimmune diseases.
References
- Dilated Cardiomyopathy (DCM) Differential Diagnoses. Updated: Sep 24, 2024 Author: Jian Hu, MD, PhD; Chief Editor: Gyanendra K Sharma, MD, FACC.
- by A Ferreira · 2023 · Cited by 13 — 3. Differential Diagnosis. In the differential diagnosis of DCM, it is essential to exclude other possible causes of left ventricular dysfunction.
- The article summarizes key points from a review article published in J Am Coll Cardiol 2016, covering etiology, remodeling, ICD, and pre-DCM phenotype of dilated cardiomyopathy (DCM). It discusses the role of CMR, genetic testing, myocardial deformation imaging, and biomarkers in DCM diagnosis and management.
- Differential diagnosis of the underlying causes of dilated cardiomyopathy. Solomou S, Stavrou M, Marley J. Diagnosis of dilated cardiomyopathy: patient reaction and adaptation—case study and review of the literature. Case Rep. Psychiatry. 2016;2016:1756510. doi: 10.1155/2016/1756510.
- Dilated cardiomyopathy (DCM) is a heart muscle disease characterized by left ventricular or biventricular dilatation or systolic dysfunction without either pressure or volume overload or coronary artery disease sufficient to explain the dysfunction. It is pivotal to exclude possible removable causes of left ventricular dysfunction because this has prognostic implications. A comprehensive differential diagnosis should be performed to rule out other conditions that may mimic DCM.
Note: The references provided are a selection from the search results and are not an exhaustive list.
Additional Information
- oboInOwl#hasOBONamespace
- disease_ontology
- oboInOwl#id
- DOID:0110437
- core#notation
- DOID:0110437
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- MIM:605582
- IAO_0000115
- A dilated cardiomyopathy that has_material_basis_in variation in the chromosome region 6q12-q16.
- oboInOwl#hasExactSynonym
- CMD1K
- rdf-schema#label
- dilated cardiomyopathy 1K
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- t366084
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- http://purl.obolibrary.org/obo/SO_0000704
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- https://w3id.org/def/predibionto#has_symptom_4791
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- t366026
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