CB03.1

ICD-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

  • 01 – Certain infectious or parasitic diseases
  • 05 – Endocrine, nutritional or metabolic diseases
  • 18 – Complications of pregnancy, childbirth and the puerperium
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  • 19 – Certain conditions originating in the perinatal period
  • 20 – Congenital malformations, deformations and chromosomal abnormalities
  • 22 – Injury, poisoning or certain other consequences of external causes

Sibling codes

  • CB03.0 – Acute interstitial pneumonitis
  • CB03.2 – Cryptogenic organizing pneumonitis
  • CB03.3 – Desquamative interstitial pneumonitis
  • CB03.4 – Idiopathic pulmonary fibrosis
  • CB03.5 – Lymphoid interstitial pneumonia
  • CB03.6 – Respiratory bronchiolitis - interstitial lung disease
  • CB03.Y – Other specified idiopathic interstitial pneumonitis
  • CB03.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