Proxy Evaluation of Health-Related Quality of Life: A Conceptual Framework for Understanding Multiple Proxy Perspectives
暂无分享,去创建一个
[1] P. Dorman,et al. Doctors and patients don't agree: cross sectional study of patients' and doctors' perceptions and assessments of disability in multiple sclerosis , 1997, BMJ.
[2] D. Cook,et al. Dying in the ICU: perspectives of family members. , 2003, Chest.
[3] D. Schwappach,et al. Resource allocation, social values and the QALY: a review of the debate and empirical evidence , 2002, Health expectations : an international journal of public participation in health care and health policy.
[4] George Loewenstein,et al. Whose quality of life? A commentary exploring discrepancies between health state evaluations of patients and the general public , 2003, Quality of Life Research.
[5] D. Streiner,et al. Health‐related Quality of Life in Children with Epilepsy: Development and Validation of Self‐report and Parent Proxy Measures , 2003, Epilepsia.
[6] D. Feeny,et al. Use of the Health Utilities Index with stroke patients and their caregivers. , 1997, Stroke.
[7] F. Guillemin,et al. Use of the EQ-5D among patients suffering from dementia. , 2003, Journal of clinical epidemiology.
[8] R. Deber,et al. Family and Physicians' Views of Surrogate Decision-Making: The Roles and How to Choose , 1996, International Psychogeriatrics.
[9] S Larry Goldenberg,et al. Assessing Information and Decision Preferences of Men With Prostate Cancer and Their Partners , 2002, Cancer nursing.
[10] Deborah J. Cook,et al. Decision-making in the ICU: perspectives of the substitute decision-maker , 2002, Intensive Care Medicine.
[11] N. Dendukuri,et al. Proxy Reporting of Quality of Life Using the EQ-5D , 2002, Medical care.
[12] J. Whyte,et al. Concordance of patient and family report of neurobehavioral symptoms at 1 year after traumatic brain injury. , 2003, Archives of physical medicine and rehabilitation.
[13] R. Doughty,et al. Measuring health-related quality of life. , 1999, The New Zealand medical journal.
[14] W. F. Shaffer,et al. Use of an empathy algorithm with a role-played client. , 1984, Journal of clinical psychology.
[15] Clara E. Hill,et al. The current state of empathy research , 1996 .
[16] R. Hogan,et al. The theory and measurement of empathy. , 1973 .
[17] M. Weinstein,et al. Health utilities in Alzheimer's disease: a cross-sectional study of patients and caregivers. , 1999, Medical care.
[18] J. Cramer,et al. Agreement between self reports and proxy reports of quality of life in epilepsy patients , 1995, Quality of Life Research.
[19] M. Brundage,et al. Practical issues in assisting shared decision‐making , 2000, Health expectations : an international journal of public participation in health care and health policy.
[20] C. Moinpour,et al. Substituting proxy ratings for patient ratings in cancer clinical trials: An analysis based on a Southwest Oncology Group trial in patients with brain metastases , 2000, Quality of Life Research.
[21] T. M. Kashner,et al. Patient-proxy response comparability on measures of patient health and functional status. , 1988, Journal of clinical epidemiology.
[22] D. Feeny,et al. Multiattribute approach to the assessment of health-related quality of life: Health Utilities Index. , 1998, Medical and pediatric oncology.
[23] J. Hanley,et al. Proxy use of the Canadian SF-36 in rating health status of the disabled elderly. , 1998, Journal of clinical epidemiology.
[24] Mohamed Abdolell,et al. Perception of quality of life by patients, partners and treating physicians , 2004, Quality of Life Research.
[25] E. Caine,et al. Older Age and the Underreporting of Depressive Symptoms , 1995, Journal of the American Geriatrics Society.
[26] G. Natvig,et al. Health-related quality of life and pain beliefs among people suffering from chronic pain. , 2004, Pain management nursing : official journal of the American Society of Pain Management Nurses.
[27] C. Rogers. The necessary and sufficient conditions of therapeutic personality change. , 1992, Psychotherapy.
[28] K. Calman,et al. QultIflf ncne ains-a Quality of life in cancer patients -an hypothesis , 2006 .
[29] S. Bassett,et al. Reliability of proxy response on mental health indices for aged, community-dwelling women. , 1990, Psychology and aging.
[30] F. D. de Charro,et al. Sensitivity and perspective in the valuation of health status: whose values count? , 2000, Health economics.
[31] N. Aaronson,et al. Value of caregiver ratings in evaluating the quality of life of patients with cancer. , 1997, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[32] J. Wit,et al. The proxy problem: child report versus parent report in health-related quality of life research , 2004, Quality of Life Research.
[33] P. Dolan,et al. To what extent can we explain time trade-off values from other information about respondents? , 2002, Social science & medicine.
[34] S. Dunn,et al. Patient barriers to optimal cancer pain control , 2003, Psycho-oncology.
[35] Ruth McCorkle,et al. From “Death Sentence” to “Good Cancer”: Couples’ Transformation of a Prostate Cancer Diagnosis , 2002, Nursing research.
[36] D. Osoba,et al. The use of significant others as proxy raters of the quality of life of patients with brain cancer. , 1997, Medical care.
[37] Judith A. Hall,et al. Using Proxies to Evaluate Quality of Life: Can They Provide Valid Information About Patients' Health Status and Satisfaction with Medical Care? , 1989, Medical care.
[38] P. Dolan,et al. An inquiry into the different perspectives that can be used when eliciting preferences in health. , 2003, Health economics.
[39] N. Aaronson,et al. Comparison of patient and proxy EORTC QLQ-C30 ratings in assessing the quality of life of cancer patients. , 1998, Journal of clinical epidemiology.
[40] A. Glaser,et al. Influence of proxy respondents and mode of administration on health status assessment following central nervous system tumours in childhood , 2004, Quality of Life Research.
[41] L. Sharp,et al. Spouse ratings of quality of life in patients with metastatic prostate cancer of lower socioeconomic status: an assessment of feasibility, reliability, and validity. , 2001, Urology.
[42] N. Aaronson,et al. Comparison of patient and spouse assessments of health related quality of life in men with metastatic prostate cancer. , 2001, The Journal of urology.
[43] E. Bruera,et al. A survey of mouth pain and dryness in patients with advanced cancer , 2000, Supportive Care in Cancer.
[44] S. Gadow. Clinical subjectivity. Advocacy with silent patients. , 1989, The Nursing clinics of North America.
[45] A. Barsky,et al. Forgetting, fabricating, and telescoping: the instability of the medical history. , 2002, Archives of internal medicine.
[46] B. Penninx,et al. Self-reports and general practitioner information on the presence of chronic diseases in community dwelling elderly. A study on the accuracy of patients' self-reports and on determinants of inaccuracy. , 1996, Journal of clinical epidemiology.
[47] J. Varni,et al. The Pediatric Cancer Quality of Life Inventory (PCQL). I. Instrument Development, Descriptive Statistics, and Cross-Informant Variance , 1998, Journal of Behavioral Medicine.
[48] R. Willke,et al. Measuring agreement between patient and proxy responses to multidimensional health-related quality-of-life measures in clinical trials. An application of psychometric profile analysis. , 2002, Journal of clinical epidemiology.
[49] M. Maltoni,et al. Quality of Life of homebound patients with advanced cancer : Assessments by patients, family members, and oncologists , 1996 .
[50] J. Landgraf. Measuring health‐related quality of life in pediatric oncology patients: A brief commentary on the state of the art of measurement and application (discussion) , 1999, International journal of cancer. Supplement = Journal international du cancer. Supplement.
[51] D. Lollar,et al. Proxy reliability: Health-related quality of life (HRQoL) measures for people with disability , 2004, Quality of Life Research.
[52] L. Degner,et al. Patients With Cancer and Next-of-Kin Response Comparability on Physical and Psychological Symptom Well-being: Trends and Measurement Issues , 2002, Cancer nursing.
[53] D. Fryback. Whose quality of life? or Whose decision? , 2003, Quality of Life Research.
[54] N. Aaronson,et al. The role of health care providers and significant others in evaluating the quality of life of patients with chronic disease. , 2002, Journal of clinical epidemiology.
[55] A Simon Pickard,et al. Agreement Between Patient and Proxy Assessments of Health-Related Quality of Life After Stroke Using the EQ-5D and Health Utilities Index , 2004, Stroke.
[56] J. Ankri,et al. Agreement between patients' and proxies' reports of quality of lifein Alzheimer's disease , 2004, Quality of Life Research.
[57] P Sandercock,et al. Are proxy assessments of health status after stroke with the EuroQol questionnaire feasible, accurate, and unbiased? , 1997, Stroke.
[58] R. Adelman,et al. The Effects of the Presence of a Third Person on the Physician‐Older Patient Medical Interview , 1994, Journal of the American Geriatrics Society.
[59] D. Hickam,et al. The Validity of Proxy-Generated Scores as Measures of Patient Health Status , 1991, Medical care.
[60] J. Rabkin,et al. Disparities in perceptions of distress and burden in ALS patients and family caregivers , 2004, Neurology.
[61] M. Limburg,et al. Assessing quality of life after stroke. The value and limitations of proxy ratings. , 1997, Stroke.
[62] Stirling Bryan,et al. EQ-5D in Patients With Dementia An Investigation of Inter-Rater Agreement , 2001, Medical care.
[63] G. Guyatt,et al. Children and adult perceptions of childhood asthma. , 1997, Pediatrics.