CB03.1ICD-11 MMS 2026-01
Combined pulmonary fibrosis and emphysema syndrome
Description
Combined pulmonary fibrosis and emphysema (CPFE) is a syndrome of combined emphysema of the upper lobes and fibrosis of the lower lobes defined on chest computed tomography, and characterised by subnormal spirometry, severe impairment of gas exchange, high prevalence of pulmonary hypertension, and poor survival. Characteristic functional profile of CPEF is strongly impaired carbon monoxide diffusing capacity of the lung, and hypoxaemia at exercise, with preserved lung volumes. Despite subnormal spirometry, which may be responsible for its under recognition, CPFE is a severe entity. The presence of pulmonary arterial hypertension at diagnosis is a critical determinant of prognosis.
Index terms
- Combined pulmonary fibrosis and emphysema syndrome
- CPFE - [Combined pulmonary fibrosis and emphysema syndrome]
Exclusions from above levels
Sibling codes
CB03.0– Acute interstitial pneumonitisCB03.2– Cryptogenic organizing pneumonitisCB03.3– Desquamative interstitial pneumonitisCB03.4– Idiopathic pulmonary fibrosisCB03.5– Lymphoid interstitial pneumoniaCB03.6– Respiratory bronchiolitis - interstitial lung diseaseCB03.Y– Other specified idiopathic interstitial pneumonitisCB03.Z– Idiopathic interstitial pneumonitis, unspecified
Foundation entity
Combined pulmonary fibrosis and emphysema syndrome – http://id.who.int/icd/entity/1361267223
Allowed postcoordination axes
Part of: CB03: Idiopathic interstitial pneumonitis › 12: Diseases of the respiratory system