Hypertrophic Obstructive Cardiomyopathy: Understanding The ICD-10 Code

What is Hypertrophic Obstructive Cardiomyopathy (ICD-10 code I42.1)?

Hypertrophic obstructive cardiomyopathy (HOCM) is a genetic heart condition characterized by abnormal thickening of the heart muscle, most commonly affecting the left ventricle. This thickening can obstruct the flow of blood out of the heart, leading to symptoms such as chest pain, shortness of breath, and fatigue. HOCM is classified under ICD-10 code I42.1, which is used to document and track cases of this specific type of cardiomyopathy.

Code Information

The ICD-10 code I42.1 is used to indicate a diagnosis of hypertrophic obstructive cardiomyopathy in medical records and billing systems. This code helps healthcare providers accurately document and track cases of HOCM, allowing for appropriate treatment and management of the condition.

Diagnostic Related Groups (MS-DRG)

Hypertrophic cardiomyopathy - Diagnosis and treatment - Mayo Clinic
Hypertrophic cardiomyopathy – Diagnosis and treatment – Mayo Clinic

Patients diagnosed with hypertrophic obstructive cardiomyopathy may be assigned to specific Diagnostic Related Groups (DRGs) for billing and reimbursement purposes. The most common MS-DRG associated with HOCM is 308 – Cardiac Arrhythmia and Conduction Disorders with Major Complications or Comorbidities.

Convert to ICD-9 Code

Prior to the adoption of the ICD-10 code set, hypertrophic obstructive cardiomyopathy was classified under the ICD-9 code 425.1. Healthcare providers and coders may need to convert old ICD-9 codes to the current ICD-10 code I42.1 for accurate documentation and billing.

Code History

Hypertrophic Cardiomyopathy (HCM) - Australian Genetic Heart
Hypertrophic Cardiomyopathy (HCM) – Australian Genetic Heart

The ICD-10 code I42.1 for hypertrophic obstructive cardiomyopathy was introduced as part of the 10th revision of the International Classification of Diseases by the World Health Organization. This code has been in use since October 1, 2015, and is the standard code used for documenting cases of HOCM in medical records.

Approximate Synonyms

Other terms and phrases that may be used interchangeably with hypertrophic obstructive cardiomyopathy include idiopathic hypertrophic subaortic stenosis, asymmetric septal hypertrophy, and familial hypertrophic cardiomyopathy. These synonyms are often used in medical literature and discussions about the condition.

Clinical Information

Diagnosis and Management of Hypertrophic Cardiomyopathy - American
Diagnosis and Management of Hypertrophic Cardiomyopathy – American

Hypertrophic obstructive cardiomyopathy is a complex and often progressive condition that can lead to serious complications such as heart failure, arrhythmias, and sudden cardiac death. Treatment for HOCM typically focuses on managing symptoms, improving heart function, and reducing the risk of complications.

Causes

Hypertrophic obstructive cardiomyopathy is primarily caused by genetic mutations that affect the structure and function of the heart muscle. These mutations can lead to abnormal thickening of the heart walls and impaired blood flow, increasing the risk of symptoms and complications associated with HOCM.

Symptoms

Common symptoms of hypertrophic obstructive cardiomyopathy include chest pain or discomfort, shortness of breath, fatigue, dizziness, fainting spells, and heart palpitations. These symptoms may vary in severity and can worsen over time as the condition progresses.

Diagnosis

Diagnosing hypertrophic obstructive cardiomyopathy typically involves a thorough medical history, physical exam, imaging tests such as echocardiography, and genetic testing to identify specific mutations associated with HOCM. Additional tests may be needed to assess heart function and rule out other potential causes of symptoms.

Treatment

Treatment for hypertrophic obstructive cardiomyopathy focuses on managing symptoms, improving heart function, and reducing the risk of complications. This may include medications to control blood pressure and heart rate, surgical procedures to remove excess heart muscle, or implantation of devices such as pacemakers or defibrillators.

Conclusion

In conclusion, hypertrophic obstructive cardiomyopathy is a genetic heart condition characterized by abnormal thickening of the heart muscle, leading to symptoms such as chest pain, shortness of breath, and fatigue. Proper diagnosis and management of HOCM are essential to reduce the risk of complications and improve quality of life for affected individuals.

FAQs

Can hypertrophic obstructive cardiomyopathy be cured?While there is no cure for HOCM, treatment can help manage symptoms and reduce the risk of complications

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