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GAP Index for Idiopathic Pulmonary Fibrosis

Gender, Age, Physiology (GAP) index predicts 1, 2, and 3-year mortality in idiopathic pulmonary fibrosis (IPF) using clinical and physiological variables.

Score interpretation

GAP Stage I 0–3

GAP Stage I — 1-year mortality ~6%, 3-year mortality ~16%

→ Initiate antifibrotic therapy (nintedanib or pirfenidone); monitor FVC every 3–6 months; O₂ assessment; pulmonary rehab

GAP Stage II 4–5

GAP Stage II — 1-year mortality ~16%, 3-year mortality ~43%

→ Antifibrotic therapy; lung transplant evaluation; palliative care discussion; early enrolment in trials

GAP Stage III 6–8

GAP Stage III — 1-year mortality ~39%, 3-year mortality ~77%

→ Urgent transplant evaluation; palliative care; symptom management (cough, dyspnoea, anxiety); advance care planning

Interpretation bands for the GAP Index. Apply clinical judgement and local guidance.

References

Related

Curated clinical cross-links plus same-class fallbacks.

Decision support only — verify against a current formulary, NICE, or your local guideline before clinical use.