Details

Autor(en) / Beteiligte

• Thompson, Jake R.
• Fu, Hong
• Saw, Robyn P. M.
• Sherman, Kerry A.
• Beedle, Victoria
• Atkinson, Victoria
• Boyle, Frances
• O’Sullivan, Niamh A.
• Martin, Linda K.
• Bartula, Iris

Titel

Supportive care needs in Australian melanoma patients and caregivers: results from a quantitative cross-sectional survey

Ist Teil von

• Quality of life research, 2023-12, Vol.32 (12), p.3531-3545

Ort / Verlag

Cham: Springer International Publishing

Erscheinungsjahr

2023

Quelle

Alma/SFX Local Collection

Beschreibungen/Notizen

• Purpose This study aimed to investigate the supportive care needs of Australian melanoma patients and their caregivers to form the basis for improving services. Methods General and melanoma-related supportive care needs in melanoma patients were measured using the SCNS-SF34 and SCNS-M12 respectively, whereas caregivers completed the SCNS-P&C. Patients also completed the MCQ-28 and FCRI-9, with all participants completing the QLQ-C30, DASS-21, and questions measuring utilisation and preference for supportive health services. Multivariable stepwise logistic regression was used to identify variables associated with unmet needs in melanoma patients. Results A total of 56 early-stage patients, 100 advanced-stage patients, and 37 caregivers participated. At least three-quarters ( ≥ 75%) of each participant group reported at least one unmet need. Of the ten most reported unmet needs in each participant group, at least six ( ≥ 60%) were related to psychological and emotional well-being, with access to a psychologist the most desired service (> 25%). Fear of cancer recurrence was equally prevalent in both patient groups at a level indicative of need for intervention. Advanced-stage patients reported significantly (p < 0.05) more unmet psychological, physical and daily living, and sexuality needs, and significantly (p < 0.05) worse functioning than early-stage patients. Conclusion Australian melanoma patients and caregivers report substantial unmet supportive care needs, particularly regarding their psychological and emotional well-being. Psychological and emotional well-being services, such as access to a clinical psychologist or implementation of patient-reported outcome measures, should be incorporated into routine melanoma care to address unmet patient and caregiver needs and improve well-being.