Evidence checklist
Pulmonary Fibrosis (Interstitial Lung Disease)
Evidence strength
Mark what you already have below and your evidence strength appears here.
Specialist opinion
Highest value0 of 5 collectedHRCT is essential for diagnosing pulmonary fibrosis, demonstrating honeycombing, traction bronchiectasis, reticular changes, and subpleural basal predominance characteristic of UIP/IPF or other fibrotic patterns.
Not marked
Comprehensive pulmonary function testing showing restrictive ventilatory defect (reduced FVC and TLC) and impaired gas exchange (reduced DLCO). The most impaired value drives the VA rating.
Not marked
Serial diffusion capacity results over time demonstrating progressive decline in gas exchange, a key prognostic marker in pulmonary fibrosis that supports the severity of the claim.
Not marked
A medical opinion connecting your pulmonary fibrosis to in-service toxic exposures (burn pits, asbestos, chemical agents, radiation) or a service-connected condition such as sarcoidosis or connective tissue disease.
Not marked
A specialist evaluation confirming the fibrosis type (IPF, NSIP, COP, etc.) and documenting severity, prognosis, and treatment plan. Multidisciplinary team diagnosis is the standard of care.
Not marked
Treatment records
0 of 1 collectedRecords documenting antifibrotic therapy (nintedanib, pirfenidone), supplemental oxygen requirements at rest or exertion, pulmonary rehabilitation, and any lung transplant evaluation.
Not marked
Lay statements
0 of 1 collectedA written statement from someone who can describe observable symptoms and how your condition affects daily life.
Not marked
Benefits questionnaire
0 of 1 collectedStandardized form capturing PFT values, DLCO, oxygen requirements, and functional impact of pulmonary fibrosis.
Not marked
Service records
0 of 1 collectedMilitary medical records showing in-service treatment, complaints, or injuries related to this condition.
Not marked
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