1 |
Stajduhar KI (2013). Burdens of family caregiving at the end of life. Clin and Investigative Med, 36, 121-6.
DOI
|
2 |
Shih WMJ, Hsiao PJ, Chen ML, Lin MH (2013). Experiences of family of patient with newly diagnosed advanced terminal stage hepatocellular cancer. Asian Pac J Cancer Prev, 14, 4655-60.
과학기술학회마을
DOI
ScienceOn
|
3 |
Silveira MJ, Given CW, Given B, Rosland AM, Piette JD (2010) Patient-caregiver concordance in symptom assessment and improvement in outcomes for patients undergoing cancer chemotherapy. Chronic Illness, 6, 46-56.
DOI
ScienceOn
|
4 |
Speziale HJ, Carpenter DR (2003). Qualitative Research in Nursing: Advancing the Humanistic Imperative. 4th ed, Lippincott Williams &Wilkins, Philadelphia, 36-39.
|
5 |
Tamayo GJ, Broxson A, Munsell M, Cohen MZ (2010). Caring for the caregiver. Oncol Nurs Forum, 37, 50-7.
DOI
ScienceOn
|
6 |
Terakye G (2011). Interaction with cancer patients' relatives. Electronic Journal of Dokuz Eylul University School of Nursing, 4, 78-82.
|
7 |
Turkoglu N, Kilic D (2012). Effects of care burdens of caregivers of cancer patients on their quality of life. Asian Pac J Cancer Prev, 13, 4141-5.
과학기술학회마을
DOI
ScienceOn
|
8 |
Tsigaroppoulos T, Mazaris E, Chatzidarellis E, et al (2009). Problems faced by relatives caring for cancer patients at home. Int J Nurs Practices, 15, 1-6.
DOI
ScienceOn
|
9 |
Ugur O, Elcigil A, Arslan D, Sonmez A (2014). Responsibilities and difficulties of caregivers of cancer patients in home care. Asian Pac J Cancer Prev, 15, 725-9 .
과학기술학회마을
DOI
ScienceOn
|
10 |
Yildirim A, Simsek H (2005). Qualitative research methods in social sciences 5th ed, Seckin press, Ankara, Turkey, 151-163, 227-241, 255-273.
|
11 |
Liu JE, Mok E, Wong T (2005). Perceptions of supportive communication in Chinese patients with cancer: experiences and expectations. J Adv Nur, 52, 262-70.
DOI
ScienceOn
|
12 |
National Profile of Family Caregivers in Canada (2002). National Profile of Family Caregivers in Canada, Final Report, pg: 1-38. (Access date: december 2013) http://www.hc-sc.gc.ca/hcs-sss/alt_formats/hpb-dgps/pdf/pubs/2002-caregivinterven/2002-caregiv-interven-eng.pdf
|
13 |
Kurtz ME, Kurtz JC, Given CW, Given B (2005). A randomized, controlled trial of a patient/caregiver symptom control intervention: effects on depressive symptomatology of caregivers of cancer patients. J Pain Symptom Manage, 30, 112-22.
DOI
ScienceOn
|
14 |
Lee J, Bell K (2011). The impact of cancer on family relationships among chinese patients. J Transcultural Nur, 22, 225-34 .
DOI
ScienceOn
|
15 |
Lethborg CE, Kissane D, Burns WI (2003). 'It's not the easy part': the experience of significant others of women with early stage breast cancer, at treatment completion. Soc Work Health Care, 37, 63-85.
DOI
ScienceOn
|
16 |
Ogce F, Ozkan S, Okcin F, Yaren A, Demiray G (2013). Evaluation of quality of life of breast cancer patient nextof-kin in Turkey. Asian Pac J Cancer Prev, 14, 2771-6.
과학기술학회마을
DOI
ScienceOn
|
17 |
Schmid-Buchi S, Halfens RJG, Dassen T, Borne B (2008). A review of psychosocial needs of breast-cancer patients and their relatives. J Clin Nur, 17, 2895-909.
DOI
ScienceOn
|
18 |
Schmid-Buchi S, Halfens R JG, Dassen T, Borne B (2011). Psychosocial problems and needs of posttreatment patients with breast cancer and their relatives. J Oncol Nur, 15, 260-6.
DOI
ScienceOn
|
19 |
Graneheim UH, Lundman B (2004). Qualitative content analysis in nursing research: concepts, procedures and measures to achieve trustworthiness. Nurse Education Today, 24, 105-12.
DOI
ScienceOn
|
20 |
Deeken JF, Taylor KL, Mangan P, Yabroff KR, Ingham JM (2003). Care for the caregivers: a review self-report intruments developed to measure the burden, needs, and quality of life of informal caregivers. J Pain and Symptom Management, 26, 922-53.
DOI
ScienceOn
|
21 |
Dew MA, Myaskovsky L, Dimartini AF, et al (2004). Onset, timing and risk for depression and anxiety in family caregivers to heart transplant recipients. Psychological Medicine, 34, 1065-82.
DOI
ScienceOn
|
22 |
Eriksson E, Lauri S (2000). Informational and emotional support for cancer patients' relatives. Eur J Cancer Care, 9, 8-15.
DOI
ScienceOn
|
23 |
Gopalan N, Brannon LA (2006). Increasing family members' appreciation of family caregiving stress. J Psychology, 140, 85-94.
DOI
|
24 |
Haley W (2003). The costs of family caregiving: implications for geriatric oncology. Crit Rev Oncol Hematol, 48, 151-8.
DOI
ScienceOn
|
25 |
Harandy TF, Ghofranipour F, Montazeri A, et al (2010). Muslim breast cancer survivor spirituality: coping strategy or health seeking behavior hindrance? Health Care Women Int, 31, 88-98.
|
26 |
Hilton BA, Crawford JA, Tarko MA (2000). Men's perspectives on individual and family coping with their wives' breast cancer and chemotherapy. West J Nurs Res, 22, 438-59.
DOI
|
27 |
Huang X, Meiser B, Butow P, Goldstein D (1999). Attitudes and information needs of Chinese migrant cancer patients and their relatives. Aus and NZ J Med, 29, 207-2013.
DOI
ScienceOn
|
28 |
Hudson P, Aranda S, McMurray N (2002). Intervention development for enhanced lay palliative caregiver support-the use of focus groups. Eur J Cancer Care, 11, 262-70.
DOI
ScienceOn
|
29 |
Chang YJ, Kwon YC, Lee WJ, et al (2013). Burdens, needs and satisfaction of terminal cancer patients and their caregivers. Asian Pac J Cancer Prev, 14, 209-16.
과학기술학회마을
DOI
ScienceOn
|
30 |
Bee PE, Barnes P, Luker KA (2008). A systematic review of informal caregivers' needs in providing home-based endof-life care to people with cancer. J Clin Nur, 18, 1379-93.
|
31 |
Chindaprasirt J, Limpawattana P, Pakkaratho P, et al (2014). Burdens among caregivers of older adults with advanced cancer and risk factors. Asian Pac J Cancer Prev, 15, 1643-8.
과학기술학회마을
DOI
ScienceOn
|
32 |
Pinkert C, Holtgrawe M, Remmers H (2013). Needs of relatives of breast cancer patients-the perspectives of families and nurses. Eur J Oncol Nur, 17, 81-7.
DOI
ScienceOn
|
33 |
Ugur O, Fadiloglu Zc (2012). The effect of planned education applied to caregivers of cancer patients on caregiver burdens. Cumhuriyet Nurs J, 1, 53-8.
|