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The impact of cystic fibrosis on the working life of patients: A systematic review

  • V. Leso
  • , R. Romano
  • , C. Santocono
  • , M. Caruso
  • , P. Iacotucci
  • , V. Carnovale
  • , Ivo Iavicoli*
  • *Corresponding author
  • University of Naples Federico II

Research output: Contribution to journalArticlepeer-review

Abstract

Advances in the treatment and management of cystic fibrosis (CF) have led to a substantial increase in patient life expectancy, thus facilitating healthier lives and labour force participation. This review aimed to address the impact of CF on the occupational functioning of patients. A significant proportion of patients were reported to retain a job on a full- or part-time schedule. Less physically demanding occupations were most frequently performed, perhaps due to CF-related inability to sustain a heavy workload. Disease severity parameters (e.g., lung function measurements, or personal, psycho-social, or economic conditions) have been reported as determinant or co-determinant factors for the development of work-related disability. Although further research is necessary, our results may be useful to inform interdisciplinary CF healthcare management, including the assessment of work function, and to define career counselling plans and workplace risk assessment and management strategies to support the personal, social and professional lives of patients.
Original languageEnglish
Pages (from-to)361-369
Number of pages9
JournalJournal of Cystic Fibrosis
Volume21
Issue number2
DOIs
Publication statusPublished - 2022

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

All Science Journal Classification (ASJC) codes

  • Pediatrics, Perinatology, and Child Health
  • Pulmonary and Respiratory Medicine

Keywords

  • Cystic fibrosis
  • Employment
  • Occupation
  • Professional life
  • Risk assessment and management
  • Work ability

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