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IPF Reprint Compendium

FOR HEALTHCARE PROFESSIONALS MAKING POPULATION-BASED DECISIONS. Here you will find information about Idiopathic Pulmonary Fibrosis (IPF), a rare and serious lung disease. To learn more about IPF, click on the About IPF tab above, or click here. To access IPF-related reprints, click on the Access IPF Reprints tab above, or click here. Meltzer EB, Noble PW. Idiopathic pulmonary fibrosis. Orphanet J Rare Dis. 2008;3:8. 2.

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IPF Reprint Compendium | ipfreprintcompendium.com Reviews
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FOR HEALTHCARE PROFESSIONALS MAKING POPULATION-BASED DECISIONS. Here you will find information about Idiopathic Pulmonary Fibrosis (IPF), a rare and serious lung disease. To learn more about IPF, click on the About IPF tab above, or click here. To access IPF-related reprints, click on the Access IPF Reprints tab above, or click here. Meltzer EB, Noble PW. Idiopathic pulmonary fibrosis. Orphanet J Rare Dis. 2008;3:8. 2.
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IPF Reprint Compendium | ipfreprintcompendium.com Reviews

https://ipfreprintcompendium.com

FOR HEALTHCARE PROFESSIONALS MAKING POPULATION-BASED DECISIONS. Here you will find information about Idiopathic Pulmonary Fibrosis (IPF), a rare and serious lung disease. To learn more about IPF, click on the About IPF tab above, or click here. To access IPF-related reprints, click on the Access IPF Reprints tab above, or click here. Meltzer EB, Noble PW. Idiopathic pulmonary fibrosis. Orphanet J Rare Dis. 2008;3:8. 2.

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1

IPF Reprint Compendium

http://www.ipfreprintcompendium.com/popcalc.html

FOR HEALTHCARE PROFESSIONALS MAKING POPULATION-BASED DECISIONS. The IPF Population Calculator is a tool designed to estimate the number of members in your health plan population who may have IPF. To use the tool, first enter the size of the adult population in your health plan (age ≥18 years). Then enter the age distribution of adult members. Click CALCULATE to see the estimated number of members in your health plan who may have IPF. Enter the age distribution of ADULT members in your health plan.

2

IPF Reprint Compendium

http://www.ipfreprintcompendium.com/access.html

FOR HEALTHCARE PROFESSIONALS MAKING POPULATION-BASED DECISIONS. To access a brief summary of a reprint below, click the VIEW SUMMARY button beneath the description. Within the summary section, click the VIEW ARTICLE button to read the reprint. There is an option to save one copy of the reprint, or to print it, for personal use. Olson AL, Swigris JJ. Idiopathic pulmonary fibrosis: diagnosis and epidemiology. Clin Chest Med.

3

IPF Reprint Compendium

http://www.ipfreprintcompendium.com/about.html

FOR HEALTHCARE PROFESSIONALS MAKING POPULATION-BASED DECISIONS. IPF is a rare and serious lung disease. Categorized as a restrictive lung disease within the interstitial lung disease (ILD) class. Up to 132,000 people affected in the United States. Poor prognosis with a low 5-year survival rate, between 20% to 40%, which is worse than many forms of cancer. Median survival time is estimated to be 2 to 3 years from diagnosis. In addition to supportive therapies,. Learn more about IPF:. New IPF cases are dia...

4

IPF Reprint Compendium

http://www.ipfreprintcompendium.com/index.html

FOR HEALTHCARE PROFESSIONALS MAKING POPULATION-BASED DECISIONS. Information and resources to help you manage your idiopathic pulmonary fibrosis (IPF) population. Discover key information, including the burden of IPF on healthcare systems, the clinical course of IPF, and the impact of acute IPF exacerbations. Estimate the number of members in your health plan population who may have IPF in just 3 simple steps. In addition to supportive therapies,* there are FDA-approved medications to treat IPF.

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IPF Reprint Compendium

FOR HEALTHCARE PROFESSIONALS MAKING POPULATION-BASED DECISIONS. Here you will find information about Idiopathic Pulmonary Fibrosis (IPF), a rare and serious lung disease. To learn more about IPF, click on the About IPF tab above, or click here. To access IPF-related reprints, click on the Access IPF Reprints tab above, or click here. Meltzer EB, Noble PW. Idiopathic pulmonary fibrosis. Orphanet J Rare Dis. 2008;3:8. 2.

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