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

被引:5
|
作者
Leso, Veruscka [1 ]
Romano, Rosaria [1 ]
Santocono, Carolina [1 ]
Caruso, Marilisa [1 ]
Iacotucci, Paola [2 ]
Carnovale, Vincenzo [2 ]
Iavicoli, Ivo [1 ]
机构
[1] Univ Naples Federico II, Dept Publ Hlth, Sect Occupat Med, Via S Pansini 5, I-80131 Naples, Italy
[2] Univ Naples Federico II, Adult Cyst Fibrosis Ctr, Dept Translat Med Sci, Via S Pansini 5, I-80131 Naples, Italy
关键词
Cystic fibrosis; Occupation; Employment; Work ability; Professional life; Risk assessment and management; ADULTS; EMPLOYMENT; PARTICIPATION; ATTAINMENT; DISABILITY; PREDICTORS; EXERCISE; QUALITY;
D O I
10.1016/j.jcf.2021.08.011
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
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 workrelated 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. (C) 2021 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:361 / 369
页数:9
相关论文
共 50 条
  • [21] The impact of pulmonary exacerbations on the quality of life of patients with cystic fibrosis
    Yi, MS
    Tsevat, J
    Wilmott, RW
    Kotagal, UR
    Britto, MT
    [J]. PEDIATRIC RESEARCH, 2004, 55 (04) : ER42 - ER42
  • [22] Telehealth in cystic fibrosis: a systematic review
    Cox, Narelle S.
    Alison, Jennifer A.
    Rasekaba, Tshepo
    Holland, Anne E.
    [J]. JOURNAL OF TELEMEDICINE AND TELECARE, 2012, 18 (02) : 72 - 78
  • [23] Impact of CFTR Modulator Therapies on Liver Function in Cystic Fibrosis Patients: A Systematic Review of Hepatic Biomarkers
    Moiceanu, Elena-Simona
    Leucua, Daniel-Corneliu
    Niescu, Viorela Gabriela
    Lescaie, Andreea
    Iacobescu, Maria
    Stan, Iustina Violeta
    Mosescu, Simona Elena
    Vivisenco, Iolanda Cristina
    Dumitrascu, Dan Lucian
    [J]. JOURNAL OF GASTROINTESTINAL AND LIVER DISEASES, 2024,
  • [24] Prevalence of constipation in cystic fibrosis patients: a systematic review of observational studies
    Stefano, Marina A.
    Poderoso, Rosana E.
    Mainz, Jochen G.
    Ribeiro, Jose D.
    Ribeiro, Antonio F.
    Lomazi, Elizete Aparecida
    [J]. JORNAL DE PEDIATRIA, 2020, 96 (06) : 686 - 692
  • [25] How do cystic fibrosis patients experience parenthood? A systematic review
    Jacob, Anne
    Journiac, Jonathan
    Fischer, Lotte
    Astrologo, Lisa
    Flahault, Cecile
    [J]. JOURNAL OF HEALTH PSYCHOLOGY, 2021, 26 (01) : 60 - 81
  • [26] Medication adherence to CFTR modulators in patients with cystic fibrosis: a systematic review
    Hansen, Carina M. E.
    Breukelman, Anna J.
    van den Bemt, Patricia M. L. A.
    Zwitserloot, Annelies M.
    van Dijk, Liset
    van Boven, Job F. M.
    [J]. EUROPEAN RESPIRATORY REVIEW, 2024, 33 (173):
  • [27] A systematic review of the clinical and genetic characteristics of Chinese patients with cystic fibrosis
    Shi, Ruihe
    Wang, Xiufang
    Lu, Xiaojing
    Zhu, Zhijie
    Xu, Qingrong
    Wang, Haoran
    Song, Li
    Zhu, Changlian
    [J]. PEDIATRIC PULMONOLOGY, 2020, 55 (11) : 3005 - 3011
  • [28] Is Gastroparesis Found More Frequently in Patients with Cystic Fibrosis? A Systematic Review
    Corral, Juan E.
    Dye, Corey W.
    Mascarenhas, Maria R.
    Barkin, Jamie S.
    Salathe, Matthias
    Moshiree, Baharak
    [J]. SCIENTIFICA, 2016, 2016
  • [29] Physical activity and its correlates in patients with Cystic Fibrosis: a systematic review
    Kinaupenne, M.
    De Craemer, M.
    Schaballie, H.
    Vandekerckhove, K.
    Van Biervliet, S.
    Demeyer, H.
    [J]. EUROPEAN RESPIRATORY JOURNAL, 2022, 60
  • [30] Hearing thresholds at high frequency in patients with cystic fibrosis: a systematic review
    Caumo, Debora T. M.
    Geyer, Lucia B.
    Teixeira, Adriana R.
    Barreto, Sergio S. M.
    [J]. BRAZILIAN JOURNAL OF OTORHINOLARYNGOLOGY, 2017, 83 (04) : 464 - 474