Pulmonary Arterial Hypertension (PAH) Enrollment Form: Fill out & sign online

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 edit Pulmonary Arterial Hypertension (PAH) Enrollment Form in PDF format online

Ease of Setup

DocHub User Ratings on G2

Ease of Use

DocHub User Ratings on G2

Working on paperwork with our extensive and user-friendly PDF editor is easy. Follow the instructions below to fill out Pulmonary Arterial Hypertension (PAH) Enrollment Form online easily and quickly:

Log in to your account. Log in with your email and password or register a free account to test the service prior to upgrading the subscription.
Upload a document. Drag and drop the file from your device or add it from other services, like Google Drive, OneDrive, Dropbox, or an external link.
Edit Pulmonary Arterial Hypertension (PAH) Enrollment Form. Effortlessly add and highlight text, insert pictures, checkmarks, and symbols, drop new fillable areas, and rearrange or remove pages from your paperwork.
Get the Pulmonary Arterial Hypertension (PAH) Enrollment Form completed. Download your updated document, export it to the cloud, print it from the editor, or share it with other participants via a Shareable link or as an email attachment.

Benefit from DocHub, one of the most easy-to-use editors to promptly manage your paperwork online!

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

What is the life expectancy of someone with PAH?

Pulmonary Hypertension Life Expectancy Overall, average survival rates were about: 86% at 1 year. 67% at 3 years. 54% at 5 years.

Is PAH the same as pulmonary hypertension?

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.

What is the criteria for PAH?

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.

What is the difference between pulmonary hypertension and PAH?

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.

What is the best treatment for pulmonary hypertension?

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.

What is the first line treatment for PAH?

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.

What are the 5 types of pulmonary hypertension?

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.

Is PAH considered a disability?

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

Get the up-to-date Pulmonary Arterial Hypertension (PAH) Enrollment Form 2024 now