Pulmonary Arterial Hypertension (PAH) Enrollment Form 2025

Get Form
Pulmonary Arterial Hypertension (PAH) Enrollment Form Preview on Page 1

Here's how it works

01. Edit your form online
Type text, add images, blackout confidential details, add comments, highlights and more.
02. Sign it in a few clicks
Draw your signature, type it, upload its image, or use your mobile device as a signature pad.
03. Share your form with others
Send it via email, link, or fax. You can also download it, export it or print it out.

How to use or fill out Pulmonary Arterial Hypertension (PAH) Enrollment Form with DocHub

Form edit decoration
9.5
Ease of Setup
DocHub User Ratings on G2
9.0
Ease of Use
DocHub User Ratings on G2
  1. Click ‘Get Form’ to open the Pulmonary Arterial Hypertension (PAH) Enrollment Form in our editor.
  2. Begin by filling out the 'Patient Information' section. Enter the patient's name, date of birth, and contact details including primary and alternate phone numbers.
  3. Next, move to the 'Prescription Information' section. Input the prescriber’s name, state license number, DEA number, and relevant medication details including dosage and directions.
  4. Complete the 'Insurance Information' section by providing a copy of insurance cards if available. This ensures that all necessary coverage details are included.
  5. In the 'Diagnosis and Clinical Information' section, specify the diagnosis codes (ICD-9/ICD-10) and any additional clinical information required for processing.
  6. Finally, review all entered information for accuracy before submitting. Use our platform's features to save or share your completed form easily.

Start using our platform today to streamline your PAH Enrollment Form process for free!

be ready to get more

Complete this form in 5 minutes or less

Get form

Got questions?

We have answers to the most popular questions from our customers. If you can't find an answer to your question, please contact us.
Contact us

If you regularly work with documents stored in your Google Drive, DocHub is an excellent solution for you to easily and quickly fill out, modify, and approve them. This editor integrates well with Google apps, so you can export your Pulmonary Arterial Hypertension (PAH) Enrollment Form from your Google Drive to the editor without downloading and re-uploading it. Right-click on your document, select Open With → DocHub PDF Sign and Edit. In our editor, add and assign Signature Fields for all parties involved, then click on the Menu option above → Send → choose how you want to share your form.

You can find the latest and most relevant version of the Pulmonary Arterial Hypertension (PAH) Enrollment Form in our DocHub forms library. Browse it by categories or utilize the search field to locate the exact template that fits your case. You may open this form for editing once you find it.

Pulmonary Hypertension Life Expectancy Overall, average survival rates were about: 86% at 1 year. 67% at 3 years. 54% at 5 years.
Pulmonary hypertension is a type of high blood pressure that affects the arteries in the lungs and the right side of the heart. In one form of pulmonary hypertension, called pulmonary arterial hypertension (PAH), blood vessels in the lungs are narrowed, blocked or destroyed.
Pulmonary hypertension, defined as a mean pulmonary arterial pressure greater than 25 mm Hg at rest or greater than 30 mm Hg during exercise, is often characterized by a progressive and sustained increase in pulmonary vascular resistance that eventually may lead to right ventricular failure.
be ready to get more

Complete this form in 5 minutes or less

Get form

People also ask

Pulmonary arterial hypertension (PAH) is one form of a broader condition known as pulmonary hypertension, which is high blood pressure in the lungs. In PAH, this increased pressure in the vessels is caused by obstruction in the small arteries in the lung for a variety of reasons.
Treatments for pulmonary hypertension anticoagulant medicines such as warfarin to help prevent blood clots. diuretics (water tablets) to remove excess fluid from the body caused by heart failure. home oxygen therapy this involves inhaling air that contains a higher concentration of oxygen than normal.
Key Messages. For people with Functional Class (FC) II or III pulmonary arterial hypertension (PAH), all single-drug therapies appear similarly effective at preventing the disease from worsening. Sildenafil or tadalafil generally provide the best value, so these are preferred first-line treatments for most patients.
WHO Classification of Pulmonary Hypertension Subtypes Pulmonary arterial hypertension (PAH) Pulmonary hypertension due to left heart disease. Pulmonary hypertension due to lung diseases and/or hypoxia. Chronic thromboembolic pulmonary hypertension (CTEPH) Pulmonary hypertension with unclear multifactorial mechanisms.
Regardless of why you have chronic pulmonary hypertension, the Social Security Administration should find you eligible for Social Security disability benefits if you can document that you have a mean pulmonary artery pressure equal to or greater than 40 mm Hg as determined by cardiac catheterization when you are

Related links