2012 ICD-9-CM Diagnosis Code 425.8. Cardiomyopathy in other diseases classified elsewhere. Short description: Cardiomyopath in oth dis. ICD-9-CM 425.8 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 425.8 should only be used for claims with a date of service on or before September 30, 2015.
ICD-9-CM 425.8 is one of thousands of ICD-9-CM codes used in healthcare. Although ICD-9-CM and CPT codes are largely numeric, they differ in that CPT codes describe medical procedures and services.
Cardiomyopathies are classified according to their predominant pathophysiological features (dilated cardiomyopathy; hypertrophic cardiomyopathy; restrictive cardiomyopathy) or their etiological/pathological factors (cardiomyopathy, alcoholic; endocardial fibroelastosis). Cardiomyopathy refers to diseases of the heart muscle.
I42. 9 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2022 edition of ICD-10-CM I42.
Cardiomyopathy (kahr-dee-o-my-OP-uh-thee) is a disease of the heart muscle that makes it harder for the heart to pump blood to the rest of the body. Cardiomyopathy can lead to heart failure. The main types of cardiomyopathy include dilated, hypertrophic and restrictive cardiomyopathy.
The main types of cardiomyopathy are: Dilated cardiomyopathy. Hypertrophic cardiomyopathy. Restrictive cardiomyopathy.
Primary cardiomyopathies consist of disorders namely or predominantly confined to the heart muscle, which have genetic, nongenetic, or acquired causes. Secondary cardiomyopathies are disorders that have myocardial damage as a result of systemic or multi-organ disease[1].
Coding for Cardiomyopathy in ICD-10-CM I42. 9, Cardiomyopathy, unspecified (includes cardiomyopathy [primary] [secondary] NOS).
Heart failure can occur when the heart muscle is weak (systolic failure) or when it is stiff and unable to relax normally (diastolic failure). Cardiomyopathy, which means “disease of the heart muscle,” is one of many causes of heart failure.
Hypertrophic cardiomyopathy is thought to be the most common inherited or genetic heart disease. While this type of cardiomyopathy occurs at many ages, in children and young adults with this condition there may be no symptoms, yet they are at high risk of sudden cardiac death.
Signs and symptoms of cardiomyopathy include:Shortness of breath or trouble breathing, especially with physical exertion.Fatigue.Swelling in the ankles, feet, legs, abdomen and veins in the neck.Dizziness.Lightheadedness.Fainting during physical activity.Arrhythmias (abnormal heartbeats)More items...•
This can lead to heart failure, heart valve disease, blood clots and other heart conditions. Ischemic cardiomyopathy is a type of dilated cardiomyopathy. Non-ischemic cardiomyopathy are forms of cardiomyopathy not related to coronary artery disease. Find out more about all types of cardiomyopathy.
There are four stages of heart failure, named A, B, C and D.Heart Failure Stage A. Pre-heart failure, which means that you are at high risk of developing heart failure.Heart Failure Stage B. ... Heart Failure Stage C. ... Heart Failure Stage D.
0 - Dilated cardiomyopathy is a sample topic from the ICD-10-CM. To view other topics, please log in or purchase a subscription. ICD-10-CM 2022 Coding Guide™ from Unbound Medicine.
Myocarditis is, by definition, an inflammatory disorder, while dilated cardiomyopathy (DCM) is, in most cases, idiopathic. However, accumulating data has revealed an important inflammatory component in the pathogenesis of DCM, and there is growing evidence that myocarditis and DCM are closely related.
425.8 is a legacy non-billable code used to specify a medical diagnosis of cardiomyopathy in other diseases classified elsewhere. This code was replaced on September 30, 2015 by its ICD-10 equivalent.
The GEMs are the raw material from which providers, health information vendors and payers can derive specific applied mappings to meet their needs.