Pulmonologists, Primary Care Physicians, Radiologists, Nurse Practitioners, Nurses, Pharmacists, Physician Assistants, Respiratory Therapists, Managed Care Associates
Idiopathic Pulmonary Fibrosis
1. | Distinguish IPF from other forms of interstitial lung disease and other respiratory disorders | 2. | Delineate updated and evolving guideline recommendations for the treatment of patients with IPF, including those with concomitant comorbidities |
3. | Identify key diagnostic criteria and methods to accurately diagnose IPF and initiate prompt disease intervention | 4. | Distinguish current and emerging data on pharmacologic therapies for IPF and their potential role in delaying disease progression and improving patient management |
5. | Identify and mitigate patient and clinician attitudes and behaviors that create barriers to diagnostic and therapeutic concordance to overcome therapeutic inertia and appropriately assimilate new knowledge into clinical practice. |
1. | Distinguish IPF from other forms of interstitial lung disease and other respiratory disorders |
2. | Delineate updated and evolving guideline recommendations for the treatment of patients with IPF, including those with concomitant comorbidities |
3. | Identify key diagnostic criteria and methods to accurately diagnose IPF and initiate prompt disease intervention |
4. | Distinguish current and emerging data on pharmacologic therapies for IPF and their potential role in delaying disease progression and improving patient management |
5. | Identify and mitigate patient and clinician attitudes and behaviors that create barriers to diagnostic and therapeutic concordance to overcome therapeutic inertia and appropriately assimilate new knowledge into clinical practice. |
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