Como publicado no v.48, n.2, de 2014, nas páginas 278 a 284, nas referências do artigo “Cancer patients caregivers comfort”, exclua-se a lista publicada e leia-se a lista a seguir:
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2. Chavez ARM, Vasconcelos AM. O cuidador no provimento do cuidado ao paciente com câncer avançado no Instituto Nacional do Câncer [resumo de tese]. RevBrasCancerol. 2006;52(1):111.
3. Lahan CF. Percepção de perdas e ganhos subjetivos entre cuidadores de pacientes atendidos em um programa de assistência domiciliar [dissertação]. São Paulo: Faculdade de Medicina, Universidade de São Paulo; 2003.
4. Vieira MCU. Sentimentos, saberes e fazeres do cuidador principal do idoso com câncer [dissertação]. Maringá: UniversidadeEstadual de Maringá; 2006.
5. Kolcaba KY. A taxonomic structure for the concept comfort. Image J Nurs Sch. 1991;23(4):237-40.
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7. Mussi FC, Friedlander MR, Arruda EN. Os significados da palavra conforto segundo a perspectiva do paciente com infarto agudo do miocárdio. Rev Latino AmEnferm. 1996;3(4):19-39.
8. Rezende VL, Derchain SFM, Botega NJ, Vial DL. Revisão crítica dos instrumentos utilizados para avaliar aspectos emocionais, físicos e sociais do cuidador de pacientes com câncer na fase terminal da doença. Rev Bras Cancer. 2005;51(1):79-87.
9. Karnofsky DA, Burchenal JH. The clinical evaluation of chemotherapeutic agents. In: MacLeod CM, editor. Evaluation of chemotherapeutic agents. New York: Columbia University Press; 1949.
10. Grunfeld E, Coyle D, Whelan T, Clinch J, Reyno L, Earle CC, et al. Family caregiver burden: results of a longitudinal study of breast cancer patients and their principal caregivers. Can Med Assoc J. 2004;170(12):1795-801.
11. Hinton J. Can home care maintain na acceptable quality of life for patients with terminal cancer and their relatives?Palliat Med. 1994;8(3):183-96.
12. Alptekin S, Gönülü G, Yücel I, Yaris F. Characteristics and quality of life analysis of caregivers of cancer patients. Med Oncol. 2010;27(3):607-17.
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14. Seon YK, Yoon-Jung C, Young RD, Sam YK, Sang YP, Hyun SJ, et al. Employment status and work-related difficulties among family members of terminally ill patients compared with the general population. Asian Pac J Cancer Prev. 2013;14(1):373-9.
15. Delgado-Guay MO, Parsons HA, Hui D, De la Cruz MG, Thorney S, Bruera E. Spirituality, religiosity, and spiritual pain among caregivers of patients with advanced cancer. Am J HospPalliat Care. 2013;30(5):455-61.
16. Steele RG, Fitch MI. Coping strategies of family caregivers of home hospice patients with cancer. OncolNurs Forum. 1996;23(6):955-60.
17. Osse BH, Vernooij-Dassen MJ, Schadé E, Grol RP. Problems experienced by the informal caregivers of cancer patients and their needs for support. Cancer Nurs. 2006;29(5):378-88; quiz 389-90.
18. Shirayama H, Iuchi M, Asada H, Yokoi H, Fujita T. The influence of family willingness to home palliative care. GanTo Kagaku Ryoho. 2006;33Suppl 2:341-4.
19. Khalili Y. Ongoing transitions: the impact of a malignant brain tumor on patient and family. Axone. 2007;28(3):5-13.
20. Aranda SK, Hayman-White K. Home caregivers of the person with advanced cancer: an Australian perspective. Cancer Nurs. 2001;24(4):300-7.
Datas de Publicação
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Publicação nesta coleção
Ago 2014
