Billable Medical Code for Primary Pulmonary Hypertension Diagnosis Code for Reimbursement Claim: ICD-9-CM 416.0. Code will be replaced by October 2015 and relabeled as ICD-10-CM 416.0. The Short Description Is: Prim pulm hypertension. Known As
Billable Medical Code for Other Chronic Pulmonary Heart Diseases Diagnosis Code for Reimbursement Claim: ICD-9-CM 416.8. Code will be replaced by October 2015 and relabeled as ICD-10-CM 416.8. The Short Description Is: Chr pulmon heart dis NEC. Known As
2015 ICD-9-CM Diagnosis Code 416.0 Primary pulmonary hypertension 2015 Billable Thru Sept 30/2015 Non-Billable On/After Oct 1/2015 ICD-9-CM 416.0 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 416.0 should only be used for claims with a date of service on or before September 30, 2015.
ICD-9 Code 416.0 Primary pulmonary hypertension. ICD-9 Index; Chapter: 390–459; Section: 415-417; Block: 416 Chronic pulmonary heart disease; 416.0 - Prim pulm hypertension
Pulmonary hypertension is also known as drug-induced pulmonary hypertension, facultative pulmonary hypertension with shunt at atrial level, high altitude pulmonary hypertension, post-arteritic pulmonary hypertension, post-capillary pulmonary hypertension, pulmonary arterial hypertension, pulmonary capillary hemangiomatosis, pulmonary HTN, pulmonary HTN arterial, pulmonary HTN secondary, pulmonary hypertension, pulmonary hypertension associated with chronic underventilation, pulmonary hypertension secondary to raised pulmonary vascular resistance, pulmonary hypertension with extreme obesity, pulmonary hypertension with occult mitral stenosis, pulmonary hypertensive arterial disease, pulmonary veno-occlusive disease, right heart failure due to pulmonary HTN, right heart failure due to pulmonary hypertension, secondary pulmonary HTN, secondary pulmonary hypertension, secondary pulmonary hypertension (HTN), and thromboembolic pulmonary hypertension.
Pulmonary hypertension is a type of high blood pressure which affects the arteries in the right side of the heart and the lungs. This occurs when arteries and capillaries in the lungs become blacked or destroyed, making it difficult for blood to flow properly.
Group 1: Pulmonary arterial hypertension: This is the most recognized category of pulmonary hypertension. This type includes both primary and secondary causes. This can be idiopathic (cause unknown) or due to a variety of other conditions/factors.
Group 5: Other secondary pulmonary hypertension: This would include causes such as polycythemia vera, essential thrombocytopenia, sarcoidosis, vasculitis, thyroid or glycogen storage disease, kidney disease, anything that presses on the pulmonary artery (like a tumor) or multifactorial.
As stated above, there is no cure for the disease pulmonary hypertension. But medication/treatment can lessen the symptoms and improve quality of life. Here are a few life style changes that can improve the symptoms: Record your weight. If there is a rapid weight gain it may be a sign of worsening.
Some forms of pulmonary hypertension are not curable but there are medications that can help lessen the symptoms and improve quality of life. Pulmonary hypertension is different than systemic high blood pressure/hypertension. Pulmonary blood pressure reflects the pressure the heart exerts to pump blood from the heart through the lung arteries.
Group 1 – Pulmonary Arterial Hypertension (PAH) – PAH refers to high pressure in the vessels caused by obstruction in the small arteries in the lungs, for a variety of reasons. These include “idiopathic” (no identifiable cause or underlying contributing condition); drug-related, HIV infection; connective tissue/autoimmune disorders ...
Pulmonary hypertension (PH) refers to high blood pressure in the blood vessels leading from the heart to the lungs (pulmonary arteries). When the blood pressure in the pulmonary arteries gets too high, the arteries in the lungs narrow (or constrict), reducing blood flow through the lungs and causing low levels of oxygen in the blood.
The changes in the pulmonary arteries that lead to PH can be caused by several factors such as lung ...
In some cases, physicians may also order additional tests like – Computerized tomography (CT) scan, Magnetic resonance imaging (MRI), Polysomnogram, Ventilation/perfusion (V/Q) scan, Pulmonary function test, Open-lung biopsy and genetic tests to check the condition of the lungs and pulmonary arteries. There is no exact treatment for pulmonary ...
Cardiologists and other clinicians need to know the specific medical codes to report the diagnosis of PH and the treatment services they provide for it, as well as the payer reimbursement guidelines for this condition.
Billing and coding tasks for pulmonary hypertension can become much easier with the support of a reliable and experienced medical billing company. Pulmonary hypertension can occur among people of all age groups and its incidence increases with age. However, this condition happens to be more common among women in the age group of 35- 60 years.