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When do you usually screen for PPF (eg, PFTs, HRCT)?

When I recognize signs of an ILD from the clinical assessment

When the patient reports symptoms of an ILD

When I recognize that the patient is at high risk of developing ILD through assessment of risk factors (eg, demographics, disease manifestations, and antibody profiles)

I do not screen for ILD/PPF

When do you initiate antifibrotic treatment in PPF patients?

Immediately upon detection of first signs of progression regardless of the underlying disease and existing treatment

When pulmonary symptoms worsen

When immunosuppressants/disease-modifying antirheumatic drugs (DMARDs)/corticosteroids fail

I do not consider nor initiate antifibrotic treatment

I refer patients to a pulmonologist when I believe antifibrotic treatment is necessary

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Japan real world evidence supports sequential treatment with the use of upfront 2nd generation TKI

12/04/2024 | Author: Boehringer Ingelheim

Document ID: PC-MY-102820

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