Lian Beenhakker, Annemieke Witteveen, Kim A. E. Wijlens, Ester J. M. Siemerink, Marije L. van der Lee, Christina Bode, Sabine Siesling, Miriam M. R. Vollenbroek-Hutten
{"title":"电子健康干预癌症相关疲劳的患者偏好属性:范围综述","authors":"Lian Beenhakker, Annemieke Witteveen, Kim A. E. Wijlens, Ester J. M. Siemerink, Marije L. van der Lee, Christina Bode, Sabine Siesling, Miriam M. R. Vollenbroek-Hutten","doi":"10.1111/ecc.13754","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Introduction</h3>\n \n <p>Cancer-related fatigue (CRF) is one of the most reported long-term effects breast cancer patients experience after diagnosis. Many interventions for CRF are effective, however, not for every individual. Therefore, intervention advice should be adjusted to patients' preferences and characteristics. Our aim was to develop an overview of eHealth interventions and their (preference sensitive) attributes.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>eHealth interventions were identified using a scoping review approach. Eligible studies included breast cancer patients and assessed CRF as outcome. Interventions were categorised as physical activity, mind–body, psychological, ‘other’ or ‘combination’. Information was extracted on various (preference sensitive) attributes, like duration, intensity, peer support and costs.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>Thirty-five interventions were included and divided over the intervention categories. (Preference sensitive) attributes varied both within and between these categories. Duration varied from 4 weeks to 6 months, intensity from daily to own pace. Peer support was present in seven interventions and costs were known for six.</p>\n </section>\n \n <section>\n \n <h3> Conclusion</h3>\n \n <p>eHealth interventions exist in various categories, additionally, there is much variation in (preference sensitive) attributes. This provides opportunities to implement our overview for personalised treatment recommendations for breast cancer patients struggling with CRF. 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Patient preference attributes in eHealth interventions for cancer-related fatigue: A scoping review
Introduction
Cancer-related fatigue (CRF) is one of the most reported long-term effects breast cancer patients experience after diagnosis. Many interventions for CRF are effective, however, not for every individual. Therefore, intervention advice should be adjusted to patients' preferences and characteristics. Our aim was to develop an overview of eHealth interventions and their (preference sensitive) attributes.
Methods
eHealth interventions were identified using a scoping review approach. Eligible studies included breast cancer patients and assessed CRF as outcome. Interventions were categorised as physical activity, mind–body, psychological, ‘other’ or ‘combination’. Information was extracted on various (preference sensitive) attributes, like duration, intensity, peer support and costs.
Results
Thirty-five interventions were included and divided over the intervention categories. (Preference sensitive) attributes varied both within and between these categories. Duration varied from 4 weeks to 6 months, intensity from daily to own pace. Peer support was present in seven interventions and costs were known for six.
Conclusion
eHealth interventions exist in various categories, additionally, there is much variation in (preference sensitive) attributes. This provides opportunities to implement our overview for personalised treatment recommendations for breast cancer patients struggling with CRF. Taking into account patients' preferences and characteristics suits the complexity of CRF and heterogeneity of patients.
期刊介绍:
The European Journal of Cancer Care aims to encourage comprehensive, multiprofessional cancer care across Europe and internationally. It publishes original research reports, literature reviews, guest editorials, letters to the Editor and special features on current issues affecting the care of cancer patients. The Editor welcomes contributions which result from team working or collaboration between different health and social care providers, service users, patient groups and the voluntary sector in the areas of:
- Primary, secondary and tertiary care for cancer patients
- Multidisciplinary and service-user involvement in cancer care
- Rehabilitation, supportive, palliative and end of life care for cancer patients
- Policy, service development and healthcare evaluation in cancer care
- Psychosocial interventions for patients and family members
- International perspectives on cancer care