Skip to content
CLADsolve

Paper

Chronic lung allograft dysfunction phenotypes and treatment

Evidence level: narrative review; abstract-only

A 2017 review of the BOS and RAS phenotypes of CLAD, their features and risk factors, and treatment strategies that have been tried.

As of . Primary source: Publisher record via DOI.

Summary

This review describes the two CLAD phenotypes, BOS and restrictive allograft syndrome or restrictive CLAD. According to the abstract, BOS is characterised by obstructive lung function, air trapping on CT and obliterative bronchiolitis on histopathology, while RAS or rCLAD shows restrictive lung function, persistent pleuroparenchymal infiltrates on CT and pleuroparenchymal fibroelastosis on biopsy. The abstract reports survival after diagnosis of 6 to 18 months for RAS or rCLAD, compared with 3 to 5 years for BOS. The review also covers risk factors and an overview of treatment strategies that have been tried with some success, and notes that adequate phenotyping remains difficult. The specific treatments were not read. This summary describes the literature and is not medical advice.

Details

doi
10.21037/jtd.2017.07.81
pmid
28932572
authors
Verleden SE, Vos R, Vanaudenaerde BM, Verleden GM
journal
Journal of Thoracic Disease
year
2017
volume
9
issue
8
pages
2650-2659

Sources and links

Related

Links from this record

Known gaps in this record

  • full text not read (abstract only)
  • funding statement and grant numbers
  • author affiliations

Information resource only. Not medical advice. Not a substitute for the care of the patient's transplant team.