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dilated cardiomyopathy 1EE
ICD-10 Codes
Related ICD-10:
Description
Dilated Cardiomyopathy: A Heart Muscle Disease
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, causing them to grow larger than usual.
- Causes: DCM can occur at any age but is more common in adults younger than 50 [3]. The exact cause of DCM is often unknown, but it may be related to genetic factors, viral infections, or other underlying conditions.
- Symptoms: People with DCM may experience symptoms such as shortness of breath, fatigue, swelling in the legs and feet, and chest pain [2].
- Characteristics: The left ventricle (bottom chamber) is often affected first, leading to a decrease in its ability to contract and pump blood effectively. This can cause the heart to work harder, leading to further enlargement and dysfunction [5].
Key Facts
- DCM is a progressive disease that can lead to heart failure if left untreated.
- It is essential to seek medical attention if symptoms persist or worsen over time.
- Treatment options for DCM may include medications, lifestyle changes, and in some cases, heart transplantation.
References: [1] - Not provided (initial query) [2] - Feb 27, 2024 [3] - May 28, 2024 [5] - Sep 24, 2024
Additional Characteristics
- Dilated cardiomyopathy
- A 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, causing them to grow larger than usual
- A progressive disease that can lead to heart failure if left untreated
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 reduced ability to pump blood effectively [1].
- Chest pain or pressure: This symptom may be more pronounced with exercise and is a common sign of dilated cardiomyopathy [4].
Other symptoms that may be present include:
- Cough
- Fatigue (unusual tiredness)
- Irregular or rapid pulse
- Loss of appetite
It's essential to note that these symptoms can vary in severity and may not always be present. If you're experiencing any of these symptoms, it's 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
- Shortness of breath
- Chest pain or pressure
- Swelling (edema)
- Irregular or rapid pulse
- cough
- loss of appetite
- fatigue
Diagnostic Tests
Diagnostic Tests for Dilated Cardiomyopathy 1EE
Dilated cardiomyopathy 1EE (DCM 1EE) is a genetic form of heart disease, and its diagnosis involves various tests to confirm the condition. Here are some diagnostic tests used to diagnose DCM 1EE:
- Sequence analysis of the entire coding region: This test is used to identify mutations in the genes associated with DCM 1EE (CROG Dilated cardiomyopathy 1EE) [1].
- Next-Generation Sequencing (NGS)/Massively Parallel Sequencing (MPS): This test is also used to sequence the entire coding region of the genes associated with DCM 1EE, providing a comprehensive view of the genetic mutations [2].
- Clinical Molecular Genetics test: This test is specifically designed for diagnosing DCM 1EE and involves sequencing analysis of the entire coding region [3].
These diagnostic tests are essential in confirming the diagnosis of DCM 1EE and can help guide treatment decisions. It's worth noting that a molecular diagnosis is required before proceeding with genetic testing, as stated in clinical guidelines [4].
Additional Tests to Consider
In some cases, additional tests may be recommended to further evaluate the condition or to rule out other potential causes. These may include:
- Electrocardiogram (ECG): An ECG can help identify any abnormalities in heart rhythm or electrical activity.
- Echocardiogram: This test uses sound waves to create images of the heart, helping to assess its structure and function.
It's essential to consult with a healthcare professional for medical advice and treatment. They will be able to guide you through the diagnostic process and recommend the most appropriate tests based on your individual needs [5].
References
[1] Clinical resource with information about Dilated cardiomyopathy 1E and its clinical features, SCN5A, available genetic tests ... CROGDilated cardiomyopathy 1EE. [2] Clinical Molecular Genetics test for Dilated cardiomyopathy 1EE and using Sequence analysis of the entire coding region, Next-Generation (NGS)/Massively ... [3] Apr 1, 2017 — Familial dilated cardiomyopathy is a genetic form of heart disease. Explore symptoms, inheritance, genetics of this condition. [4] The patient is not eligible if they have a molecular diagnosis for their condition. - Genetic testing should continue according to routine local practice for ... [5] Jun 14, 2024 — Supplementary test information for Dilated Cardiomyopathy Panel, Sequencing such as test interpretation, additional tests to consider, ...
Additional Diagnostic Tests
- Electrocardiogram (ECG)
- Sequence analysis of the entire coding region
- Echocardiogram
- Clinical Molecular Genetics test
- Massively Parallel Sequencing (MPS)
Treatment
Treatment Options for Dilated Cardiomyopathy
Dilated cardiomyopathy is a condition where the heart becomes weakened and unable to pump blood effectively. Fortunately, there are several treatment options available to manage this condition.
Medications
Several medications can help improve heart function in patients with dilated cardiomyopathy:
- ACE inhibitors: These medications can help reduce the strain on the heart by relaxing blood vessels and improving blood flow. (Source: [2])
- Aldosterone antagonists: These medications can also help reduce fluid buildup in the body, which can put additional strain on the heart. (Source: [2])
- Beta-blockers: Beta-blockers, such as carvedilol, bisoprolol, and metoprolol CR/XL, can improve heart function by reducing the heart's workload. (Sources: [3], [5])
- Digoxin: In some cases, digoxin may be prescribed to help improve the heart's ability to pump blood in patients with reduced ejection fraction heart failure. (Source: [7])
Other Treatment Options
In addition to medications, other treatment options may include:
- Lifestyle modifications: Making healthy lifestyle choices, such as a balanced diet and regular exercise, can help manage symptoms of dilated cardiomyopathy.
- Cardiac rehabilitation: A cardiac rehabilitation program can help patients with dilated cardiomyopathy recover from heart failure and improve their overall health.
References
[1] Context result 2 [2] Context result 4 [3] Context result 3 [5] Context result 5 [7] Context result 7
💊 Drug information is sourced from ChEBI (Chemical Entities of Biological Interest) database. Always consult with a healthcare professional before starting any medication. Click on any medication name for detailed information.
Differential Diagnosis
Differential Diagnosis of Dilated Cardiomyopathy
Dilated cardiomyopathy (DCM) is a condition where the heart's ability to pump blood is impaired due to a weakening of the heart muscle. When diagnosing DCM, it's essential to consider other conditions that may cause similar symptoms. Here are some differential diagnoses for DCM:
- Acute coronary syndrome: This refers to a range of conditions caused by reduced blood flow to the heart, including heart attacks and unstable angina [1].
- Acute pericarditis: Inflammation of the sac surrounding the heart (pericardium) can cause symptoms similar to DCM, such as chest pain and shortness of breath [2].
- Beriberi: A disease caused by a thiamine (vitamin B1) deficiency that can lead to heart failure and other systemic problems [1].
- Amphetamine toxicity: Long-term use or overdose of amphetamines can cause cardiac damage, including cardiomyopathy [3].
- Coronary artery disease: Narrowing or blockage of the arteries supplying blood to the heart can lead to impaired heart function [4].
- Hypertension: High blood pressure can put additional strain on the heart, leading to DCM in some cases [5].
- Diabetes: Long-standing diabetes can cause damage to the heart muscle and impair its pumping ability [6].
Other conditions that may mimic DCM symptoms
- Infections: Certain infections, such as HIV or Lyme disease, can affect the heart and lead to symptoms similar to DCM [7].
- Autoimmune diseases: Conditions like polymyositis can cause inflammation in various parts of the body, including the heart [8].
- Alcohol abuse: Chronic alcohol consumption can damage the heart muscle and impair its function [9].
References
[1] Context 1: Sep 24, 2024 [2] Context 5: Dec 29, 2019 [3] Context 6: May 28, 2024 [4] Context 7: Jan 24, 2024 [5] Context 8: by P Rubis · Cited by 19 — [6] Context 9: by M Weigner · Cited by 19 — [7] Context 3: by A Ferreira · 2023 · Cited by 13 — [8] Context 4: Nov 4, 2015 [9] Context 2: by P Rubis · Cited by 19 —
Additional Information
- rdf-schema#domain
- https://w3id.org/def/predibionto#has_symptom_4807
- owl#annotatedSource
- t370538
- oboInOwl#hasOBONamespace
- disease_ontology
- oboInOwl#hasDbXref
- MIM:613252
- oboInOwl#id
- DOID:0110453
- core#notation
- DOID:0110453
- IAO_0000115
- A dilated cardiomyopathy that has_material_basis_in mutation in the MYH6 gene on chromosome 14q11.2.
- oboInOwl#hasExactSynonym
- CMD1EE
- rdf-schema#label
- dilated cardiomyopathy 1EE
- rdf-schema#subClassOf
- t370524
- RO_0004019
- http://purl.obolibrary.org/obo/SO_0000704
- relatedICD
- http://example.org/icd10/I42.0
- 22-rdf-syntax-ns#type
- http://www.w3.org/2002/07/owl#Class
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