期刊论文详细信息
Health and Quality of Life Outcomes
Health-related quality of life in family members of patients with an advanced cancer diagnosis: A one-year prospective study
Gerd Ahlstrom3  Jan Mårtensson1  Johannes Järhult2  Bo Rolander2  Catarina Sjolander2 
[1] The School of Health Sciences, Jönköping University, P.O. Box 1026, SE-551 11, Jönköping, Sweden;The Ryhov County Hospital, SE-551 85, Jönköping, Sweden;The Swedish Institute for Health Sciences, Department of Health Sciences, Lund University, Box 187SE–221 00, Lund, Sweden
关键词: Physical health dimension;    Mental health dimension;    Health-related quality of life;    Advanced cancer;    Family member;   
Others  :  825324
DOI  :  10.1186/1477-7525-10-89
 received in 2012-01-21, accepted in 2012-07-16,  发布年份 2012
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【 摘 要 】

Background

Receiving a cancer diagnosis affects family members as well as the person diagnosed. Family members often provide support for the sick person in daily life out of duty and love, and may not always think of their own vulnerability to illness. To individualise support for them, family members who are most at risk for becoming ill must be identified.

The aim of this study was to investigate health-related quality of life (HRQOL) in family members of patients with advanced lung or gastrointestinal cancer 3 to 15 months after diagnosis.

Methods

Data on mental and physical dimensions of HRQOL were collected from family members of these patients in this prospective quantitative study. Five assessments using the Short Form 36 Health Survey (SF-36) and EuroQol (EQ-5D) were conducted during a 1-year period starting 3 months after diagnosis. Thirty-six family members completed the study, i.e. participated in all five data collections.

Results

No statistically significant changes in physical or mental HRQOL within the study group appeared over the 1-year follow-up. Compared with norm-based scores, family members had significantly poorer mental HRQOL scores throughout the year as measured by the SF-36. Family members also scored statistically significantly worse on the EQ-5D VAS in all five assessments compared to the norm-based score. Findings showed that older family members and partners were at higher risk for decreased physical HRQOL throughout the 1-year period, and younger family members were at higher risk for poorer mental HRQOL.

Conclusions

It is well known that ill health is associated with poor HRQOL. By identifying family members with poor HRQOL, those at risk of ill health can be identified and supported. Future large-scale research that verifies our findings is needed before making recommendations for individualised support and creating interventions best tailored to family members at risk for illness.

【 授权许可】

   
2012 Sjolander et al.; licensee BioMed Central Ltd.

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【 参考文献 】
  • [1]Couper JW, Bloch S, Love A, Duchesne G, Macvean M, Kissane DW: The psychosocial impact of prostate cancer on patients and their partners. Med J Aust 2006, 185:428-432.
  • [2]Cotrim H, Pereira G: Impact of colorectal cancer on patient and family: implications for care. Eur J Oncol Nurs 2008, 12:217-226.
  • [3]Steinberg T, Roseman M, Kasymjanova G, Dobson S, Lajeunesse L, Dajczman E, Kreisman H, MacDonald N, Agulnik J, Cohen V, et al.: Prevalence of emotional distress in newly diagnosed lung cancer patients. Support Care Canc 2009, 17:1493-1497.
  • [4]Clark KL, Loscalzo M, Trask PC, Zabora J, Philip EJ: Psychological distress in patients with pancreatic cancer–an understudied group. Psychooncology 2010, 19:1313-1320.
  • [5]Finfgeld-Connett D: Clarification of social support. J Nurs Scholarsh 2005, 37:4-9.
  • [6]Nausheen B, Gidron Y, Peveler R, Moss-Morris R: Social support and cancer progression: a systematic review. J Psychosom Res 2009, 67:403-415.
  • [7]Grunfeld E, Coyle D, Whelan T, Clinch J, Reyno L, Earle CC, Willan A, Viola R, Coristine M, Janz T, Glossop R: Family caregiver burden: results of a longitudinal study of breast cancer patients and their principal caregivers. CMAJ 2004, 170:1795-1801.
  • [8]Ostlund U, Wennman-Larsen A, Persson C, Gustavsson P, Wengstrom Y: Mental health in significant others of patients dying from lung cancer. Psychooncology 2010, 19:29-37.
  • [9]Braun M, Mikulincer M, Rydall A, Walsh A, Rodin G: Hidden morbidity in cancer: spouse caregivers. J Clin Oncol 2007, 25:4829-4834.
  • [10]Donnelly M, Anderson LA, Johnston BT, Watson RG, Murphy SJ, Comber H, McGuigan J, Reynolds JV, Murray LJ: Oesophageal cancer: caregiver mental health and strain. Psychooncology 2008, 17:1196-1201.
  • [11]Persson C, Ostlund U, Wennman-Larsen A, Wengstrom Y, Gustavsson P: Health-related quality of life in significant others of patients dying from lung cancer. Palliat Med 2008, 22:239-247.
  • [12]Song JI, Shin DW, Choi JY, Kang J, Baik YJ, Mo H, Park MH, Choi SE, Kwak JH, Kim EJ: Quality of life and mental health in family caregivers of patients with terminal cancer. Support Care Canc 2011, 19:1519-1526.
  • [13]Kim Y, Spillers RL: Quality of life of family caregivers at 2 years after a relative's cancer diagnosis. Psychooncology 2010, 19:431-440.
  • [14]Stenberg U, Ruland CM, Miaskowski C: Review of the literature on the effects of caring for a patient with cancer. Psychooncology 2010, 19:1013-1025.
  • [15]Fletcher BS, Paul SM, Dodd MJ, Schumacher K, West C, Cooper B, Lee K, Aouizerat B, Swift P, Wara W, Miaskowski CA: Prevalence, severity, and impact of symptoms on female family caregivers of patients at the initiation of radiation therapy for prostate cancer. J Clin Oncol 2008, 26:599-605.
  • [16]Swore Fletcher BA DM, Schumacher KL, Miaskowski C: Symptom experience of family caregivers of patients with cancer. Oncol Nurs Forum 2008, 35:E23-E44.
  • [17]Esbensen BA, Thome B: Being next of kin to an elderly person with cancer. Scand J Caring Sci 2010, 24:648-654.
  • [18]Lu L, Pan B, Sun W, Cheng L, Chi T, Wang L: Quality of life and related factors among cancer caregivers in China. Psychiatr Clin Neurosci 2010, 64:505-513.
  • [19]Tuinman MA, Hoekstra HJ, Sleijfer DT, Fleer J, Vidrine DJ, Gritz ER, Hoekstra-Weebers JE: Testicular cancer: a longitudinal pilot study on stress response symptoms and quality of life in couples before and after chemotherapy. Support Care Canc 2007, 15:279-286.
  • [20]Edvardsson T, Ahlstrom G: Being the next of kin of a person with a low-grade glioma. Psychooncology 2008, 17:584-591.
  • [21]Ringdal GI, Ringdal K, Jordhoy MS, Ahlner-Elmqvist M, Jannert M, Kaasa S: Health-related quality of life (HRQOL) in family members of cancer victims: results from a longitudinal intervention study in Norway and Sweden. Palliat Med 2004, 18:108-120.
  • [22]Ferlay J, Shin HR, Bray F, Forman D, Mathers C, Parkin DM: Estimates of worldwide burden of cancer in 2008: GLOBOCAN 2008. Int J Cancer 2010, 127:2893-2917.
  • [23]Sullivan M, Karlsson J, Taft C, Ware JE: SF-36 Health Survey: Swedish manual and interpretation guide (In Swedish). 2nd edition. Gothenburg: Sahlgrenska University Hospital, Unit of Health Research; 2002.
  • [24]Sullivan M, Karlsson J, Ware JE: SF-36 Health Survey: Swedish manual and interpretation guide (In Swedish). 2nd edition. Gothenburg: Sahlgrenska University Hospital, Unit of Health Research; 1994.
  • [25]The EuroQol Group: EuroQol - a new facility for the measurement of health-related quality of life. Health Pol 1990, 16:199-208.
  • [26]Kind PHG, Macran S: UK population norms for EQ-5D. In Working Papers 172chedp. York: Centre for Health Economics, University of York; 1999.
  • [27]Dolan P: Modeling valuations for EuroQol health states. Med Care 1997, 35:1095-1108.
  • [28]Wyrwich KW, Bullinger M, Aaronson N, Hays RD, Patrick DL, Symonds T: Estimating clinically significant differences in quality of life outcomes. Qual Life Res 2005, 14:285-295.
  • [29]Wyrwich KW, Fihn SD, Tierney WM, Kroenke K, Babu AN, Wolinsky FD: Clinically important changes in health-related quality of life for patients with chronic obstructive pulmonary disease: an expert consensus panel report. J Gen Intern Med 2003, 18:196-202.
  • [30]Lewis FM, Fletcher KA, Cochrane BB, Fann JR: Predictors of depressed mood in spouses of women with breast cancer. J Clin Oncol 2008, 26:1289-1295.
  • [31]Rhee YS, Yun YH, Park S, Shin DO, Lee KM, Yoo HJ, Kim JH, Kim SO, Lee R, Lee YO, Kim NS: Depression in family caregivers of cancer patients: the feeling of burden as a predictor of depression. J Clin Oncol 2008, 26:5890-5895.
  • [32]Sjolander C, Hedberg B, Ahlstrom G: Striving to be prepared for the painful: Management strategies following a family member's diagnosis of advanced cancer. BMC Nurs 2011, 10:18. BioMed Central Full Text
  • [33]Persson C, Sundin K: Being in the situation of a significant other to a person with inoperable lung cancer. Canc Nurs 2008, 31:380-388.
  • [34]van Andel J, Westerhuis W, Zijlmans M, Fischer K, Leijten FS: Coping style and health-related quality of life in caregivers of epilepsy patients. J Neurol 2011, 258:1788-1794.
  • [35]Sullivan M, Karlsson J, Ware JE: The Swedish SF-36 Health Survey--I. Evaluation of data quality, scaling assumptions, reliability and construct validity across general populations in Sweden. Soc Sci Med 1995, 41:1349-1358.
  • [36]Kim Y, Spillers RL, Hall DL: Quality of life of family caregivers 5 years after a relative's cancer diagnosis: follow-up of the national quality of life survey for caregivers. Psychooncology 2012, 3:273-281.
  • [37]Ko FC: The clinical care of frail, older adults. Clin Geriatr Med 2011, 27:89-100.
  • [38]Topinkova E: Aging, disability and frailty. Ann Nutr Metab 2008, 52(Suppl 1):6-11.
  • [39]Weiss CO: Frailty and chronic diseases in older adults. Clin Geriatr Med 2011, 27:39-52.
  • [40]Vinokur AD, Threatt BA, Vinokur-Kaplan D, Satariano WA: The process of recovery from breast cancer for younger and older patients. Changes during the first year. Cancer 1990, 65:1242-1254.
  • [41]Harden J: Developmental life stage and couples' experiences with prostate cancer: a review of the literature. Canc Nurs 2005, 28:85-98.
  • [42]Mor V, Allen S, Malin M: The psychosocial impact of cancer on older versus younger patients and their families. Cancer 1994, 74:2118-2127.
  • [43]Nijboer C, Triemstra M, Tempelaar R, Mulder M, Sanderman R, van den Bos GA: Patterns of caregiver experiences among partners of cancer patients. Gerontologist 2000, 40:738-746.
  • [44]Woods NF, Lewis FM: Women with chronic illness: their views of their families' adaptation. Health Care Women Int 1995, 16:135-148.
  • [45]Emslie C, Browne S, Macleod U, Rozmovits L, Mitchell E, Ziebland S: 'Getting through' not 'going under': a qualitative study of gender and spousal support after diagnosis with colorectal cancer. Soc Sci Med 2009, 68:1169-1175.
  • [46]Altschuler A, Ramirez M, Grant M, Wendel C, Hornbrook MC, Herrinton L, Krouse RS: The influence of husbands' or male partners' support on women's psychosocial adjustment to having an ostomy resulting from colorectal cancer. J Wound Ostomy Continence Nurs 2009, 36:299-305.
  • [47]Altman DG: Practical statistics for medical research. London: Chapman and Hall; 1991.
  • [48]Svensson E: Comparison of the quality of assessments using continuous and discrete ordinal rating scales. Biom J 2000, 42:417-434.
  • [49]Ferlay J, Parkin DM, Steliarova-Foucher E: Estimates of cancer incidence and mortality in Europe in 2008. Eur J Cancer 2010, 46:765-781.
  • [50]Polit DF, Hungler BP: Nursing research : principles and methods. 5th edition. Philadelphia: Lippincott; 1995.
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