請用此 Handle URI 來引用此文件:
http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/51848完整後設資料紀錄
| DC 欄位 | 值 | 語言 |
|---|---|---|
| dc.contributor.advisor | 鍾國彪 | |
| dc.contributor.author | Hsuan Peng | en |
| dc.contributor.author | 彭瑄 | zh_TW |
| dc.date.accessioned | 2021-06-15T13:53:09Z | - |
| dc.date.available | 2017-03-28 | |
| dc.date.copyright | 2016-03-28 | |
| dc.date.issued | 2015 | |
| dc.date.submitted | 2015-08-18 | |
| dc.identifier.citation | Abel, G. A., Saunders, C. L., & Lyratzopoulos, G. (2014). Cancer patient experience, hospital performance and case mix: evidence from England. Future Oncol, 10(9), 1589-1598. doi: 10.2217/fon.13.266
Armes, J., Crowe, M., Colbourne, L., Morgan, H., Murrells, T., Oakley, C., . . . Richardson, A. (2009). Patients' supportive care needs beyond the end of cancer treatment: a prospective, longitudinal survey. J Clin Oncol, 27(36), 6172-6179. doi: 10.1200/jco.2009.22.5151 Arora, N. K., Reeve, B. B., Hays, R. D., Clauser, S. B., & Oakley-Girvan, I. (2011). Assessment of quality of cancer-related follow-up care from the cancer survivor's perspective. J Clin Oncol, 29(10), 1280-1289. doi: 10.1200/jco.2010.32.1554 Ashing-Giwa, K. T., & Lim, J.-W. (2011). Examining emotional outcomes among a multiethnic cohort of breast cancer survivors. Oncol Nurs Forum, 38(3), 279-288. doi: 10.1188/11.onf.279-288 Avis, N. E., Smith, K. W., McGraw, S., Smith, R. G., Petronis, V. M., & Carver, C. S. (2005). Assessing quality of life in adult cancer survivors (QLACS). Qual Life Res, 14(4), 1007-1023. Ayanian, J. Z., Zaslavsky, A. M., Arora, N. K., Kahn, K. L., Malin, J. L., Ganz, P. A., . . . Harrington, D. P. (2010). Patients' experiences with care for lung cancer and colorectal cancer: findings from the Cancer Care Outcomes Research and Surveillance Consortium. J Clin Oncol, 28(27), 4154-4161. doi: 10.1200/jco.2009.27.3268 Baker, F., Denniston, M., Smith, T., & West, M. M. (2005). Adult cancer survivors: How are they faring? Cancer, 104(S11), 2565-2576. doi: 10.1002/cncr.21488 Baravelli, C., Krishnasamy, M., Pezaro, C., Schofield, P., Lotfi-Jam, K., Rogers, M., . . . Jefford, M. (2009). The views of bowel cancer survivors and health care professionals regarding survivorship care plans and post treatment follow up. J Cancer Surviv, 3(2), 99-108. doi: 10.1007/s11764-009-0086-1 Bardes, C. L. (2012). Defining “Patient-Centered Medicine”. New England Journal of Medicine, 366(9), 782-783. doi: doi:10.1056/NEJMp1200070 Beck, S., Towsley, G., Pett, M., Berry, P., Smith, E., Brant, J., & Guo, J.-W. (2010). Initial psychometric properties of the Pain Care Quality Survey (PainCQ). J Pain, 11, 1311 - 1319. Berg, P., Book, K., Dinkel, A., Henrich, G., Marten-Mittag, B., Mertens, D., . . . Herschbach, P. (2011). Fear of progression in chronic diseases. Psychother Psychosom Med Psychol, 61(1), 32-37. doi: 10.1055/s-0030-1267927 Bergman, J., Gore, J. L., Saigal, C. S., Kwan, L., & Litwin, M. S. (2009). Partnership and outcomes in men with prostate cancer. Cancer, 115(20), 4688-4694. doi: 10.1002/cncr.24544 Blanch-Hartigan, D., Blake, K. D., & Viswanath, K. (2014). Cancer Survivors' Use of Numerous Information Sources for Cancer-Related Information: Does More Matter? Journal of Cancer Education, 29(3), 488-496. doi: 10.1007/s13187-014-0642-x Brédart, A., Kop, J. L., Efficace, F., Beaudeau, A., Brito, T., Dolbeault, S., . . . for the, E. Q. o. L. G. (2014). Quality of care in the oncology outpatient setting from patients' perspective: a systematic review of questionnaires' content and psychometric performance. Psychooncology, n/a-n/a. doi: 10.1002/pon.3661 Brédart, A., Morvan, E., Savignoni, A., Giraud, P., & Stic-Rar, R. G. R. S. G. (2011). Patient's perception of care quality during radiotherapy sessions using respiratory gating techniques: validation of a specific questionnaire. Cancer Invest, 29(2), 145-152. doi: 10.3109/07357907.2010.543216 Chang, H.-R., Shih, S.-C., & Lin, F.-M. (2012). Impact of Comorbidities on the Outcomes of Older Patients Receiving Rectal Cancer Surgery. International Journal of Gerontology, 6(4), 285-289. doi: http://dx.doi.org/10.1016/j.ijge.2012.05.006 Clayton, M. F., Mishel, M. H., & Belyea, M. (2006). Testing a model of symptoms, communication, uncertainty, and well-being, in older breast cancer survivors. Res Nurs Health, 29(1), 18-39. doi: 10.1002/nur.20108 Cleary, P., & Edgman-Levitan, S. (1997). Health care quality. Incorporating consumer perspectives. JAMA, 278, 1608 - 1612. Costanzo, E. S., Lutgendorf, S. K., Mattes, M. L., Trehan, S., Robinson, C. B., Tewfik, F., & Roman, S. L. (2007). Adjusting to life after treatment: distress and quality of life following treatment for breast cancer. British Journal of Cancer, 97(12), 1625-1631. doi: 10.1038/sj.bjc.6604091 Couture, J., Chan, R., & Bouharaoui, F. (2005). Patient's preferences for adjuvant postoperative chemoradiation therapy in rectal cancer. Diseases of the Colon & Rectum, 48(11), 2055-2060. doi: 10.1007/s10350-005-0174-x Crist, J. V., & Grunfeld, E. A. (2013). Factors reported to influence fear of recurrence in cancer patients: a systematic review. Psychooncology, 22(5), 978-986. doi: 10.1002/pon.3114 Crow, R., Gage, H., Hampson, S., Hart, J., Kimber, A., Storey, L., & Thomas, H. (2002). The measurement of satisfaction with healthcare: implications for practice from a systematic review of the literature. Health Technol Assess, 6, 1 - 244. Currie, A., Askari, A., Nachiappan, S., Sevdalis, N., Faiz, O., & Kennedy, R. (2015). A systematic review of patient preference elicitation methods in the treatment of colorectal cancer. Colorectal Disease, 17(1), 17-25. doi: 10.1111/codi.12754 Damman, O. C., Hendriks, M., & Sixma, H. J. (2009). Towards more patient centred healthcare: A new Consumer Quality Index instrument to assess patients' experiences with breast care. Eur J Cancer, 45(9), 1569-1577. doi: 10.1016/j.ejca.2008.12.011 Dankert, A., Duran, G., Engst-Hastreiter, U., Keller, M., Waadt, S., Henrich, G., & Herschbach, P. (2003). Fear of progression in patients with cancer, diabetes mellitus and chronic arthritis. Rehabilitation, 42(3), 155-163. doi: 10.1055/s-2003-40094 Darzi, A. (2007). NHS Next Stage Review Interim Report Department of Health, London. de Kok, M., Sixma, H. J. M., van der Weijden, T., Kessels, A. G. H., Dirksen, C. D., Spijkers, K. F. J., . . . von Meyenfeldt, M. F. (2010). A patient-centred instrument for assessment of quality of breast cancer care: results of a pilot questionnaire. Qual Saf Health Care, 19(6), e40. doi: 10.1136/qshc.2007.025890 De Padova, S., Rosti, G., Scarpi, E., Salvioni, R., Amadori, D., De Giorgi, U., & Group, I. G. C. C. (2011). Expectations of survivors, caregivers and healthcare providers for testicular cancer survivorship and quality of life. Tumori, 97(3), 367-373. doi: 10.1700/912.10036 Defossez, G., Mathoulin-Pelissier, S., Ingrand, I., Gasquet, I., Sifer-Riviere, L., Ingrand, P., . . . network, t. R. r. (2007). Satisfaction with care among patients with non-metastatic breast cancer: development and first steps of validation of the REPERES-60 questionnaire. BMC Cancer, 7, 129. Deimling, G. T., Bowman, K. F., Sterns, S., Wagner, L. J., & Kahana, B. (2006). Cancer-related health worries and psychological distress among older adult, long-term cancer survivors. Psychooncology, 15(4), 306-320. doi: 10.1002/pon.955 Denlinger, C. S., & Barsevick, A. M. (2009). The challenges of colorectal cancer survivorship. J Natl Compr Canc Netw, 7(8), 883-893; quiz 894. DOH. (2010). National Cancer Patient Experience Survey Programme - 2010 National Survey Report. DOH. (2014). 2014 National Cancer Patient Experience Survey. Donabedian, A. (1988). The quality of care. How can it be assessed? JAMA, 260(12), 1743-1748. Elit, L. M., Charles, C., Gafni, A., Ranford, J., Tedford-Gold, S., & Gold, I. (2013). How oncologists communicate information to women with recurrent ovarian cancer in the context of treatment decision making in the medical encounter. Health Expect. doi: 10.1111/hex.12079 Elliott, M. N., Lehrman, W. G., Goldstein, E. H., Giordano, L. A., Beckett, M. K., Cohea, C. W., & Cleary, P. D. (2010). Hospital survey shows improvements in patient experience. Health Aff (Millwood), 29(11), 2061-2067. doi: 10.1377/hlthaff.2009.0876 Fink, R. (2000). Pain assessment: the cornerstone to optimal pain management. BUMC Proceedings, 13, 236 - 239. Ghazali, N., Cadwallader, E., Lowe, D., Humphris, G., Ozakinci, G., & Rogers, S. N. (2013). Fear of recurrence among head and neck cancer survivors: longitudinal trends. Psychooncology, 22(4), 807-813. doi: 10.1002/pon.3069 Glaser, A. W., Fraser, L. K., Corner, J., Feltbower, R., Morris, E. J., Hartwell, G., . . . Wagland, R. (2013). Patient-reported outcomes of cancer survivors in England 1-5 years after diagnosis: a cross-sectional survey. BMJ Open, 3(4). doi: 10.1136/bmjopen-2012-002317 Goldstein, E., Farquhar, M., Crofton, C., Darby, C., & Garfinkel, S. (2005). Measuring hospital care from the patients' perspective: an overview of the CAHPS Hospital Survey development process. Health Serv Res, 40(6 Pt 2), 1977-1995. doi: 10.1111/j.1475-6773.2005.00477.x Greenberg, D. B., Kornblith, A. B., Herndon, J. E., Zuckerman, E., Schiffer, C. A., Weiss, R. B., . . . Holland, J. C. (1997). Quality of life for adult leukemia survivors treated on clinical trials of cancer and leukemia group B during the period 1971-1988. Cancer, 80(10), 1936-1944. doi: 10.1002/(SICI)1097-0142(19971115)80:10<1936::AID-CNCR10>3.0.CO;2-Z Groß, S., Nitzsche, A., Gloede, T., Ansmann, L., Street, R., Pfaff, H., . . . Ernstmann, N. (2015). The initial clinical interview—can it reduce cancer patients’ fear? Supportive Care in Cancer, 23(4), 977-984. doi: 10.1007/s00520-014-2450-6 Hadi, M., Gibbons, E., & Fitzpatrick, R. (2010). A Structured Review of Patient Reported Outcome Measures (PROMS) for Colorectal Cancer. Patient-Reported Outcome Measurement Group, Oxford. Harley, C., Adams, J., Booth, L., Selby, P., Brown, J., & Velikova, G. (2009). Patient experiences of continuity of cancer care: development of a new medical care questionnaire (MCQ) for oncology outpatients. Value Health, 12(8), 1180-1186. doi: 10.1111/j.1524-4733.2009.00574.x Hart, S. L., Latini, D. M., Cowan, J. E., Carroll, P. R., & Investigators, C. (2008). Fear of recurrence, treatment satisfaction, and quality of life after radical prostatectomy for prostate cancer. Support Care Cancer, 16(2), 161-169. doi: 10.1007/s00520-007-0296-x Hayman, J. (2008). Measuring the quality of care in radiation oncology. Semin Radiat Oncol, 18, 201 - 206. Heins, M. J., Korevaar, J. C., Rijken, P. M., & Schellevis, F. G. (2013). For which health problems do cancer survivors visit their General Practitioner? European Journal of Cancer, 49(1), 211-218. doi: 10.1016/j.ejca.2012.07.011 Herschbach, P., Berg, P., Dankert, A., Duran, G., Engst-Hastreiter, U., Waadt, S., . . . Henrich, G. (2005). Fear of progression in chronic diseases: Psychometric properties of the Fear of Progression Questionnaire. Journal of Psychosomatic Research, 58(6), 505-511. doi: http://dx.doi.org/10.1016/j.jpsychores.2005.02.007 Herschbach, P., & Dinkel, A. (2014). Fear of progression. Recent Results Cancer Res, 197, 11-29. doi: 10.1007/978-3-642-40187-9_2 Hinz, A., Mehnert, A., Ernst, J., Herschbach, P., & Schulte, T. (2014). Fear of progression in patients 6 months after cancer rehabilitation—a validation study of the fear of progression questionnaire FoP-Q-12. Supportive Care in Cancer, 1-9. doi: 10.1007/s00520-014-2516-5 Hodgkinson, K., Butow, P., Fuchs, A., Hunt, G. E., Stenlake, A., Hobbs, K. M., . . . Wain, G. (2007). Long-term survival from gynecologic cancer: Psychosocial outcomes, supportive care needs and positive outcomes. Gynecol Oncol, 104(2), 381-389. doi: 10.1016/j.ygyno.2006.08.036 Humphris, G., & Ozakinci, G. (2008). The AFTER intervention: a structured psychological approach to reduce fears of recurrence in patients with head and neck cancer. Br J Health Psychol, 13(Pt 2), 223-230. doi: 10.1348/135910708x283751 IOM. (2001). Crossing the Quality Chasm: A New Health System for the 21st Century. Janz, N. K., Hawley, S. T., Mujahid, M. S., Griggs, J. J., Alderman, A., Hamilton, A. S., . . . Katz, S. J. (2011). Correlates of worry about recurrence in a multiethnic population-based sample of women with breast cancer. Cancer, 117(9), 1827-1836. doi: 10.1002/cncr.25740 Jenkinson, C., Coulter, A., Bruster, S., Richards, N., & Chandola, T. (2002). Patients' experiences and satisfaction with health care: results of a questionnaire study of specific aspects of care. Qual Saf Health Care, 11(4), 335-339. Kim, Y., Carver, C. S., Spillers, R. L., Love-Ghaffari, M., & Kaw, C.-K. (2012). Dyadic effects of fear of recurrence on the quality of life of cancer survivors and their caregivers. Qual Life Res, 21(3), 517-525. doi: 10.1007/s11136-011-9953-0 Koch, L., Bertram, H., Eberle, A., Holleczek, B., Schmid-Hopfner, S., Waldmann, A., . . . Arndt, V. (2014). Fear of recurrence in long-term breast cancer survivorsstill an issue. Results on prevalence, determinants, and the association with quality of life and depression from the Cancer Survivorship-a multi-regional populationbased study. Psychooncology, 23(5), 547-554. doi: 10.1002/pon.3452 Koch, L., Jansen, L., Brenner, H., & Arndt, V. (2013). Fear of recurrence and disease progression in long-term (≥5 years) cancer survivors—a systematic review of quantitative studies. Psychooncology, 22(1), 1-11. doi: 10.1002/pon.3022 Krouse, R. S., Herrinton, L. J., Grant, M., Wendel, C. S., Green, S. B., Mohler, M. J., . . . Hornbrook, M. C. (2009). Health-related quality of life among long-term rectal cancer survivors with an ostomy: manifestations by sex. J Clin Oncol, 27(28), 4664-4670. doi: 10.1200/jco.2008.20.9502 Kwakkenbos, L., van Lankveld, W. G. J. M., Vonk, M. C., Becker, E. S., van den Hoogen, F. H. J., & van den Ende, C. H. M. (2012). Disease-related and psychosocial factors associated with depressive symptoms in patients with systemic sclerosis, including fear of progression and appearance self-esteem. J Psychosom Res, 72(3), 199-204. doi: 10.1016/j.jpsychores.2011.12.005 Lebel, S., Tomei, C., Feldstain, A., Beattie, S., & McCallum, M. (2013). Does fear of cancer recurrence predict cancer survivors' health care use? Support Care Cancer, 21(3), 901-906. doi: 10.1007/s00520-012-1685-3 Lee-Jones, C., Humphris, G., Dixon, R., & Hatcher, M. B. (1997). Fear of cancer recurrence--a literature review and proposed cognitive formulation to explain exacerbation of recurrence fears. Psychooncology, 6(2), 95-105. doi: 10.1002/(sici)1099-1611(199706)6:2<95::aid-pon250>3.0.co;2-b Lipscomb, J., Gotay, C. C., & Snyder, C. F. (2007). Patient-reported outcomes in cancer: a review of recent research and policy initiatives. CA Cancer J Clin, 57(5), 278-300. doi: 10.3322/ca.57.5.278 Lis, C. G., Rodeghier, M., & Gupta, D. (2009). Distribution and determinants of patient satisfaction in oncology: A review of the literature. Patient Prefer Adherence, 3, 287-304. Liu, Y., Perez, M., Schootman, M., Aft, R. L., Gillanders, W. E., & Jeffe, D. B. (2011). Correlates of fear of cancer recurrence in women with ductal carcinoma in situ and early invasive breast cancer. Breast Cancer Research and Treatment, 130(1), 165-173. doi: 10.1007/s10549-011-1551-x Llewellyn, C. D., Weinman, J., McGurk, M., & Humphris, G. (2008). Can we predict which head and neck cancer survivors develop fears of recurrence? J Psychosom Res, 65(6), 525-532. doi: 10.1016/j.jpsychores.2008.03.014 Lohr, K. (2002). Assessing health status and quality-of-life instruments: Attributes and review criteria. Quality of Life Research, 11(3), 193-205. doi: 10.1023/A:1015291021312 Lyratzopoulos, G., Neal, R. D., Barbiere, J. M., Rubin, G. P., & Abel, G. A. (2012). Variation in number of general practitioner consultations before hospital referral for cancer: findings from the 2010 National Cancer Patient Experience Survey in England. Lancet Oncol, 13(4), 353-365. doi: 10.1016/s1470-2045(12)70041-4 McCarthy, M., Datta, P., Sherlaw-Johnson, C., Coleman, M., & Rachet, B. (2008). Is the performance of cancer services influenced more by hospital factors or by specialization? J Public Health (Oxf), 30(1), 69-74. doi: 10.1093/pubmed/fdm081 Mehnert, A., Berg, P., Henrich, G., & Herschbach, P. (2009). Fear of cancer progression and cancer-related intrusive cognitions in breast cancer survivors. Psychooncology, 18(12), 1273-1280. doi: 10.1002/pon.1481 Mehnert, A., Herschbach, P., Berg, P., Henrich, G., & Koch, U. (2006). Fear of progression in breast cancer patients-validation of the short form of the Fear of Progression Questionnaire (FoP-Q-SF). Z Psychosom Med Psychother, 52(3), 274-288. Mehnert, A., Koch, U., Sundermann, C., & Dinkel, A. (2013). Predictors of fear of recurrence in patients one year after cancer rehabilitation: A prospective study. Acta Oncologica, 52(6), 1102-1109. doi: doi:10.3109/0284186X.2013.765063 Mellon, S., Kershaw, T. S., Northouse, L. L., & Freeman-Gibb, L. (2007). A family-based model to predict fear of recurrence for cancer survivors and their caregivers. Psychooncology, 16(3), 214-223. doi: 10.1002/pon.1074 Mitchell, A. J., Chan, M., Bhatti, H., Halton, M., Grassi, L., Johansen, C., & Meader, N. (2011). Prevalence of depression, anxiety, and adjustment disorder in oncological, haematological, and palliative-care settings: a meta-analysis of 94 interview-based studies. Lancet Oncol, 12(2), 160-174. doi: 10.1016/s1470-2045(11)70002-x Muschalla, B., Glatz, J., & Linden, M. (2014). Heart-related anxieties in relation to general anxiety and severity of illness in cardiology patients. Psychol Health Med, 19(1), 83-92. doi: 10.1080/13548506.2013.774428 Ness, S., Kokal, J., Fee-Schroeder, K., Novotny, P., Satele, D., & Barton, D. (2013). Concerns across the survivorship trajectory: Results from a survey of cancer survivors. Oncology Nursing Forum, 40(1), 35-42. Ouwens, M., Hermens, R., Hulscher, M., Vonk-Okhuijsen, S., Tjan-Heijnen, V., Termeer, R., . . . Grol, R. (2010). Development of indicators for patient-centred cancer care. Supportive Care in Cancer, 18(1), 121-130. doi: 10.1007/s00520-009-0638-y Oxlad, M., Wade, T. D., Hallsworth, L., & Koczwara, B. (2008). 'I'm living with a chronic illness, not ... dying with cancer': a qualitative study of Australian women's self-identified concerns and needs following primary treatment for breast cancer. European Journal of Cancer Care, 17(2), 157-166. doi: 10.1111/j.1365-2354.2007.00828.x Park, C. L., Cho, D., Blank, T. O., & Wortmann, J. H. (2013). Cognitive and emotional aspects of fear of recurrence: predictors and relations with adjustment in young to middle-aged cancer survivors. Psychooncology, 22(7), 1630-1638. doi: 10.1002/pon.3195 Rabin, C., Leventhal, H., & Goodin, S. (2004). Conceptualization of disease timeline predicts posttreatment distress in breast cancer patients. Health Psychol, 23(4), 407-412. doi: 10.1037/0278-6133.23.4.407 Radwin, L., Alster, K., & Rubin, K. M. (2003). Development and testing of the Oncology Patients' Perceptions of the Quality of Nursing Care Scale. Oncol Nurs Forum, 30(2), 283-290. doi: 10.1188/03.onf.283-290 Reich, M., Leemans, C. R., Vermorken, J. B., Bernier, J., Licitra, L., Parmar, S., . . . Lefebvre, J. L. (2014). Best practices in the management of the psycho-oncologic aspects of head and neck cancer patients: recommendations from the European Head and Neck Cancer Society Make Sense Campaign. Annals of Oncology, 25(11), 2115-2124. doi: 10.1093/annonc/mdu105 Resnick, M. J., Guzzo, T. J., Cowan, J. E., Knight, S. J., Carroll, P. R., & Penson, D. F. (2013). Factors associated with satisfaction with prostate cancer care: Results from Cancer of the Prostate Strategic Urologic Research Endeavor (CaPSURE). BJU International, 111(2), 213-220. Rogers, S. N., Scott, B., Lowe, D., Ozakinci, G., & Humphris, G. M. (2010). Fear of recurrence following head and neck cancer in the outpatient clinic. Eur Arch Otorhinolaryngol, 267(12), 1943-1949. doi: 10.1007/s00405-010-1307-y Sarkar, S., Scherwath, A., Schirmer, L., Schulz-Kindermann, F., Neumann, K., Kruse, M., . . . Mehnert, A. (2014). Fear of recurrence and its impact on quality of life in patients with hematological cancers in the course of allogeneic hematopoietic SCT. Bone Marrow Transplant, 49(9), 1217-1222. doi: 10.1038/bmt.2014.139 Savard, J., & Ivers, H. (2013). The evolution of fear of cancer recurrence during the cancer care trajectory and its relationship with cancer characteristics. J Psychosom Res, 74(4), 354-360. doi: 10.1016/j.jpsychores.2012.12.013 Shim, E. J., Shin, Y. W., Oh, D. Y., & Hahm, B. J. (2010). Increased fear of progression in cancer patients with recurrence. General Hospital Psychiatry, 32(2), 169-175. doi: 10.1016/j.genhosppsych.2009.11.017 Simard, S., & Savard, J. (2009). Fear of Cancer Recurrence Inventory: development and initial validation of a multidimensional measure of fear of cancer recurrence. Supportive Care in Cancer, 17(3), 241-251. doi: 10.1007/s00520-008-0444-y Simard, S., Savard, J., & Ivers, H. (2010). Fear of cancer recurrence: specific profiles and nature of intrusive thoughts. J Cancer Surviv, 4(4), 361-371. doi: 10.1007/s11764-010-0136-8 Simard, S., Thewes, B., Humphris, G., Dixon, M., Hayden, C., Mireskandari, S., & Ozakinci, G. (2013). Fear of cancer recurrence in adult cancer survivors: A systematic review of quantitative studies. Journal of Cancer Survivorship, 7(3), 300-322. Singer, S., Das-Munshi, J., & Brähler, E. (2010). Prevalence of mental health conditions in cancer patients in acute care--a meta-analysis. Ann Oncol, 21(5), 925-930. doi: 10.1093/annonc/mdp515 Skaali, T., Fosså, S. D., Bremnes, R., Dahl, O., Haaland, C. F., Hauge, E. R., . . . Dahl, A. A. (2009). Fear of recurrence in long-term testicular cancer survivors. Psychooncology, 18(6), 580-588. doi: 10.1002/pon.1437 Smith, M. Y., Winkel, G., Egert, J., Diaz-Wionczek, M., & DuHamel, K. N. (2006). Patient-physician communication in the context of persistent pain: validation of a modified version of the patients' Perceived Involvement in Care Scale. J Pain Symptom Manage, 32(1), 71-81. doi: 10.1016/j.jpainsymman.2006.01.007 Stanton, A. L. (2006). Psychosocial Concerns and Interventions for Cancer Survivors. Journal of Clinical Oncology, 24(32), 5132-5137. doi: 10.1200/jco.2006.06.8775 Steele, N., Haigh, R., Knowles, G., & Mackean, M. (2007). Carcinoembryonic antigen (CEA) testing in colorectal cancer follow up: what do patients think? Postgraduate Medical Journal, 83(983), 612-614. doi: 10.1136/pgmj.2007.059634 Takayama, T., Yamazaki, Y., & Katsumata, N. (2001). Relationship between outpatients' perceptions of physicians' communication styles and patients' anxiety levels in a Japanese oncology setting. Soc Sci Med, 53(10), 1335-1350. Tarrant, C., Baker, R., Colman, A., Sinfield, P., Agarwal, S., Mellon, J., . . . Kockelbergh, R. (2009). The Prostate Care Questionnaire for Patients (PCQ-P): Reliability, validity and acceptability. BMC Health Services Research, 9(1), 199. Taylor, C., Richardson, A., & Cowley, S. (2011). Surviving cancer treatment: An investigation of the experience of fear about, and monitoring for, recurrence in patients following treatment for colorectal cancer. European Journal of Oncology Nursing, 15(3), 243-249. doi: http://dx.doi.org/10.1016/j.ejon.2011.03.010 Thewes, B., Butow, P., Zachariae, R., Christensen, S., Simard, S., & Gotay, C. (2012). Fear of cancer recurrence: a systematic literature review of self-report measures. Psychooncology, 21(6), 571-587. doi: 10.1002/pon.2070 Torbit, L. A., Albiani, J. J., Crangle, C. J., Latini, D. M., & Hart, T. L. (2014). Fear of recurrence: the importance of self-efficacy and satisfaction with care in gay men with prostate cancer. Psychooncology, n/a-n/a. doi: 10.1002/pon.3630 Tzelepis, F., Rose, S., Sanson-Fisher, R., Clinton-McHarg, T., Carey, M., & Paul, C. (2014). Are we missing the Institute of Medicine's mark? A systematic review of patient-reported outcome measures assessing quality of patient-centred cancer care. BMC Cancer, 14(1), 41. van Weert, J. C. M., Jansen, J., de Bruijn, G.-J., Noordman, J., van Dulmen, S., & Bensing, J. M. (2009). QUOTEchemo: a patient-centred instrument to measure quality of communication preceding chemotherapy treatment through the patient's eyes. Eur J Cancer, 45(17), 2967-2976. doi: 10.1016/j.ejca.2009.06.001 Vickberg, S. M. J. (2003). The Concerns About Recurrence Scale (CARS): a systematic measure of women's fears about the possibility of breast cancer recurrence. Ann Behav Med, 25(1), 16-24. Young, J., Walsh, J., Butow, P., Solomon, M., & Shaw, J. (2011). Measuring cancer care coordination: development and validation of a questionnaire for patients. BMC Cancer, 11(1), 298. 行政院衛生署. (2012). 醫療品質政策白皮書. 姚開屏、蕭宇佑、郭耿南、鄭守夏. (2010). 病人報告之醫院品質:問卷發展與信效度分析. [Patient Reported Hospital Quality (PRHQ): Scale Development, Reliability, and Validity]. 臺灣公共衛生雜誌, 29(5), 440-451. 國民健康署. (2014). 2011年癌症登記報告. 彭台光、高月慈、林鉦棽. (2005). 管理研究中的共同方法變異:問題本質、影響、測試和補救. 管理學報, 23(1), 77-98. 童伊迪. (2013). 醫療社會工作於腫瘤治療病患的處遇與發展. 社區發展季刊, 141, 477-488. 黃淑如. (2013). 頭頸部癌患者的害怕復發、因應型態與健康相關生活品質、創傷後成長間關係之追蹤研究. 中原大學心理學系碩士學位論文. 賴世華. (2010). 頭頸癌症患者復發擔憂對癌症關連疲勞之影響 - 以因應型態及負向情緒為中介變項. 中原大學心理學系碩士學位論文. | |
| dc.identifier.uri | http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/51848 | - |
| dc.description.abstract | 背景與目的:大腸直腸癌為國人癌症發生率中最高的,為了提升癌症照護與醫療品質,以癌症病人為中心的照護被提倡可以提供高品質的癌症醫療照護,同時,以癌症病人為中心的照護也被台灣癌症診療品質認證作為衡量癌症照護品質的項目,近年來,以病人報告為結果的測量方式(PROMs)逐漸被發展,病人主觀感受的醫療品質可以做為醫療照護服務接受者對於所接受到醫療品質優劣的評價,其中,以癌症病人就醫經驗調查最受到推崇,由於癌症病人的經驗評價可以避免過去在調查病人滿意度時,會受到病人喜好和期望的影響,可以較準確判斷癌症照護品質的優劣。復發擔憂是癌症存活者表示在其癌症治療結束後最大的未被滿足需求及困擾,因為復發擔憂會造成癌症病人生活品質的下降及過度使用醫療資源,變向增加全民健保的財務負擔及排擠其他醫療服務需求者的權益,若能了解癌症病人就醫的經驗對於其後續復發擔憂的影響,可以作為政府機關及醫療服務提供者做為癌症照護品質提升的發展策略參考,因此本研究欲探討癌症病人就醫經驗與其害怕復發之現況及其相關性。
研究方法:本研究為橫斷性研究,收案對象為接受過癌症相關治療的大腸直腸癌存活者,有效樣本為124份,收案期間為2015年3月10號至6月30號,問卷採用癌症病人就醫經驗問卷(CPES)及復發擔憂短版問卷(FoP-Q-SF)作為調查工具,在就醫經驗的部分將癌症病人在醫療過程中實際感受到的經驗轉換成構面的百分比來計算,在復發擔憂的部分採用Likert五點尺度的方式作為程度高低的分數加總,本研究將收集到的資料以描述性分析、獨立樣本T檢定、單因子變異數分析、皮爾森績差相關及複迴歸方法做資料分析。 研究結果:在病人特質與疾病特性的部分,大腸直腸癌病人的癌症是否復發、工作狀態、長期性症狀數目、共病症數目、癌症治療後的反應與其復發擔憂之間存在統計上的顯著關係。在大腸直腸癌病人就醫經驗的構面當中,控制其他變項後,病人在就醫過程中接受到以病人為中心的照護經驗、醫病間的溝通經驗、癌症資訊的提供及社會支持、病人參與治療決策與照護計畫與其復發擔憂存在統計上的顯著相關。經由逐步回歸(Stpewise)分析後的結果發現,在醫病間的溝通經驗與病人參與治療決策與照護計畫達統計上的顯著意義。 結論:在大腸直腸癌病人的就醫經驗中,以病人為中心的照護正向經驗、醫病間溝通的正向經驗、癌症資訊的提供及社會支持的正向經驗及病人參與治療決策與照護計畫的正向經驗與其復發擔憂的程度呈現負向的相關。在進一步的分析後,醫病間溝通的經驗及病人參與治療決策與照護計畫的經驗是最重要的兩個變項,建議在大腸直腸癌病人的癌症治療過程中,可以重視醫療人員與病人間的溝通狀況及是否需要溝通的橋梁,並在情況允許下,讓病人可以參與自己的治療決策和尊重病人的喜好,以減緩癌症病人對於自身癌症復發或病程進展的擔憂。 | zh_TW |
| dc.description.abstract | Background: In Taiwan, the annual incidence of newly-diagnosed colorectal cancer is in first place. In order to improve the quality of cancer care, cancer patient-centered care has been advocated to provide a high-quality cancer care, also became an evaluation included in Taiwan cancer care quality accreditation. In recent years, patient-reported outcome measures (PROMs) has been developed, patient subjective perception the quality of cancer care can be used as recipients for the receive medical care quality evaluation of the merits. However, the cancer patient experience survey is the most popular method, because it can avoid the previous cancer patient satisfaction survey would influenced by patient favor and expectation. Fear of recurrence is among the most commonly reported problems and one of the most prevalent areas of umet needs for cancer survivors, it will cause cancer patients to decrease quality of life and overuse medical resources, changing to increase the financial burden on national health insurance and other marginalized health care needs of those rights. This study attempt to explore the relationship among patient reported experience and fear of recurrence in patients with colorectal cancer.
Method: This is a cross-sectional study. The patients were recruited at 12 hospitals in Taiwan and 2 non-governmental organizations. All samples came from convenient sampling. There were 124 valid samples with collection period from March 10th to June 30th, year 2015. The questionnaire use Cancer Patient Experience Survey (CPES) and Fear of Progression Questionnaire - Short Form (FoP-Q-SF) as an investigative tool. In CPES, the cancer patient during a medical procedure practical experience, is converted into a percentage calculated under dimensions. In FoP, using the sum of Likert five-point scale as the scores of high and low degree. The data is analyzed by methods of descriptive analysis, independent-samples T test, one-way ANOVA, Pearson correlation underperformance and multiple linear regression. Results: In the part of the patient characteristics and disease characteristics, there is a statistically significant relationship between cancer recure, working conditions, the number of long-term symptoms, the number of comorbidities, the reaction of cancer after treatment with their fear of recurrence. In the part of medical treatment experience, controlling for other variables, the patient receives a patient-centered care experience in the process, communication experience with healthcare givers, hospital providing social support and cancer information, patient involvement in treatment-related decision-making and care planning are significant. Results via stepwise regression analysis found that communication experience with healthcare givers and involvement in treatment-related decision-making and care planning are significant. Conclusion: The colorectal cancer patients’ medical treatment experience during treatment, and there is a correlation between fears of recurrence. The positive treatment experience in patients with their fear of recurrence of exhibits negative correlation. After further analysis, communication experience with healthcare givers and involvement in treatment-related decision-making and care planning are the two most important dimensions. It is recommended during cancer treatment of colorectal cancer patients, we can pay attention to the patient-physician communication and physicians share the decision-making and care planning so that the patient can participate in their own treatment decisions and respect the patient's preferences, in order to decrease the cancer patients for cancer recurrence or progression of their own concerns. | en |
| dc.description.provenance | Made available in DSpace on 2021-06-15T13:53:09Z (GMT). No. of bitstreams: 1 ntu-104-R02848030-1.pdf: 3472418 bytes, checksum: 5e1a6c26d12099e941a9dbd41ba304a2 (MD5) Previous issue date: 2015 | en |
| dc.description.tableofcontents | 中文摘要 I
Abstract III 第一章 緒論 1 第一節 研究背景與動機 1 第二節 研究目的 4 第二章 文獻探討 5 第一節 大腸直腸癌病人流行病學、分期、診斷、治療方式 5 第二節 病人報告為結果的測量 (PROMs) 8 第三節 癌症病人就醫經驗 10 第四節 復發擔憂 20 第五節 癌症病人就醫經驗與復發擔憂相關之研究 31 第六節 綜合整理 32 第三章 研究方法 34 第一節 研究設計與研究架構 34 第二節 研究假說 37 第三節 研究工具與變項定義 38 第四節 資料處理及分析方法 46 第四章 資料分析結果 48 第一節 問卷信度與效度的檢定 48 第二節 描述性統計 49 第三節 雙變量分析 54 第四節 多變量分析 59 第五章 討論 73 第一節 研究資料品質 73 第二節 研究結果討論 75 第三節 研究限制 84 第六章 結論與建議 85 第一節 結論 85 第二節 未來研究建議 86 參考文獻 88 附件一 台灣大學附設醫院研究倫理試驗簡易審查公文 98 附件二 Cancer Paient Experience Survey Questionnaire 100 附件三 癌症病人就醫經驗問卷(中文版) 112 附件四 癌症病人就醫經驗問卷授權信 128 附件五 Fear of Progression Questionnaire - Short Form 130 附件六 復發擔憂問卷授權信 131 | |
| dc.language.iso | zh-TW | |
| dc.subject | 癌症病人就醫經驗 | zh_TW |
| dc.subject | 病人報告為結果的測量 | zh_TW |
| dc.subject | 大腸直腸癌 | zh_TW |
| dc.subject | 復發擔憂 | zh_TW |
| dc.subject | Cancer parient treatment experience | en |
| dc.subject | Patient reported outcome measure | en |
| dc.subject | Colorectal cancer | en |
| dc.subject | Fear of cancer recurrence | en |
| dc.title | 大腸直腸癌病人就醫經驗與復發擔憂之相關性探討 | zh_TW |
| dc.title | Exploring the relationship among patient reported experience and fear of recurrence in patients with colorectal cancer | en |
| dc.type | Thesis | |
| dc.date.schoolyear | 104-1 | |
| dc.description.degree | 碩士 | |
| dc.contributor.oralexamcommittee | 王拔群,王正旭 | |
| dc.subject.keyword | 大腸直腸癌,病人報告為結果的測量,癌症病人就醫經驗,復發擔憂, | zh_TW |
| dc.subject.keyword | Colorectal cancer,Patient reported outcome measure,Cancer parient treatment experience,Fear of cancer recurrence, | en |
| dc.relation.page | 132 | |
| dc.rights.note | 有償授權 | |
| dc.date.accepted | 2015-08-18 | |
| dc.contributor.author-college | 公共衛生學院 | zh_TW |
| dc.contributor.author-dept | 健康政策與管理研究所 | zh_TW |
| 顯示於系所單位: | 健康政策與管理研究所 | |
文件中的檔案:
| 檔案 | 大小 | 格式 | |
|---|---|---|---|
| ntu-104-1.pdf 未授權公開取用 | 3.39 MB | Adobe PDF |
系統中的文件,除了特別指名其著作權條款之外,均受到著作權保護,並且保留所有的權利。
