Understanding the Caregiver Perspective: The Impact of Caring for Patients with Advanced Cancer
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Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1245/s10434-024-14990-x.pdf
Reference6 articles.
1. Stenberg U, Ruland CM, Miaskowski C. Review of the literature on the effects of caring for a patient with cancer. Psycho-Oncology. 2010;19(10):1013–25. https://doi.org/10.1002/pon.1670.
2. Goren A, Gilloteau I, Lees M, daCosta DiBonaventura M. Quantifying the burden of informal caregiving for patients with cancer in Europe. Support Care Cancer. 2014;22(6):1637–46. https://doi.org/10.1007/s00520-014-2122-6.
3. Weitzner MA, Jacobsen PB, Wagner H, Friedland J, Cox C. The Caregiver quality of life index-cancer (CQOLC) scale: development and validation of an instrument to measure quality of life of the family caregiver of patients with cancer. Qual Life Res. 1999;8(1):55–63. https://doi.org/10.1023/A:1026407010614.
4. Avery J, Geist A, D’Agostino NM, et al. “It’s more difficult…”: clinicians’ experience providing palliative care to adolescents and young adults diagnosed with advanced cancer. J Oncol Pract. 2020;16(1):e100–8. https://doi.org/10.1200/JOP.19.00313.
5. Mack JW, Fisher L, Kushi L, et al. Patient, family, and clinician perspectives on end-of-life care quality domains and candidate indicators for adolescents and young adults with cancer. JAMA Netw Open. 2021;4(8):e2121888. https://doi.org/10.1001/jamanetworkopen.2021.21888.
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