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Interstitial Lung Disease Evaluation 2

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Version:

2

Program ID:

8306

Developer:

e-MedTools
All programs by this developer

Downloads:

23

License:

Shareware

Cost:

$150.00 US

Operating Systems:

Windows 95 Windows 98 Windows Me Windows NT 4 Windows 2000 Windows XP Windows 2003 Server Windows Vista

Size:

353K

Release Status:

new

Last Updated:

2007-04-29

File Cart Rating:

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Publisher's description of Interstitial Lung Disease Evaluation

Interstitial Lung Disease Evaluation iconMedicalTemplates has developed a interstitial lung disease evaluation medical note template. This template is suitable for any health care provider who may evaluate a patient with interstitial lung disease.
Interstitial Lung Disease (ILD) is a diverse group of more than 200 diseases that cause progressive fibrosis (scarring) of lung tissue, which leads to chronic, progressive breathlessness and respiratory failure. The Pulmonary Fibrosis Foundation (www.pulmonaryfibrosis.org) estimates that more than 200,000 Americans have ILD, and nearly 40,000 Americans die each year from ILD.

ILD includes idiopathic pulmonary fibrosis (IPF), sarcoidosis, hypersensitivity pneumonitis, Nonspecific Interstitial Pneumonitis (NSIP), Desquamative
Interstitial Pneumonitis (DIP), Cryptogenic Organizing Pneumonia (COP, aka BOOP), medication induced lung disease, post-radiation fibrosis, and many other diseases.

The primary symptoms of ILD are nonspecific, such as non-productive cough and progressive breathlessness. These symptoms are seen in many other medical conditions such as asthma, heart failure, or chronic obstructive pulmonary disease (COPD). The lack of specificity of the presenting symptoms makes the identification of ILD challenging, particularly in individuals with known heart or lung disease. Early and accurate diagnosis of ILD is essential so that treatment options can be considered before extensive and permanent damage occurs, resulting in disabling breathlessness. While there is currently no proven, FDA-approved treatment for idiopathic pulmonary fibrosis, many forms of interstitial lung disease can be treated, if detected early in the disease process. Thus, having a low threshold for suspecting interstitial disease, and assessing a patient?s risk of developing pulmonary fibrosis by obtaining important historical information is critical to early diagnosis.


Keywords: interstital lung disease, pulmonary fibrosis, medical template, medical office notes

Recent Changes: Not Established

Install Support: Install and Uninstall

Supported Languages: English

Additional Requirements: Adobe Reader

PAD file URL: http://www.e-medtools.com/ildeval.xml



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