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Erschienen in: Quality of Life Research 8/2012

01.10.2012 | Review

Implementing patient-reported outcomes assessment in clinical practice: a review of the options and considerations

verfasst von: Claire F. Snyder, Neil K. Aaronson, Ali K. Choucair, Thomas E. Elliott, Joanne Greenhalgh, Michele Y. Halyard, Rachel Hess, Deborah M. Miller, Bryce B. Reeve, Maria Santana

Erschienen in: Quality of Life Research | Ausgabe 8/2012

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Abstract

Purpose

While clinical care is frequently directed at making patients “feel better,” patients’ reports on their functioning and well-being (patient-reported outcomes [PROs]) are rarely collected in routine clinical practice. The International Society for Quality of Life Research (ISOQOL) has developed a User’s Guide for Implementing Patient-Reported Outcomes Assessment in Clinical Practice. This paper summarizes the key issues from the User’s Guide.

Methods

Using the literature, an ISOQOL team outlined considerations for using PROs in clinical practice; options for designing the intervention; and strengths, weaknesses, and resource requirements associated with each option.

Results

Implementing routine PRO assessment involves a number of methodological and practical decisions, including (1) identifying the goals for collecting PROs in clinical practice, (2) selecting the patients, setting, and timing of assessments, (3) determining which questionnaire(s) to use, (4) choosing a mode for administering and scoring the questionnaire, (5) designing processes for reporting results, (6) identifying aids to facilitate score interpretation, (7) developing strategies for responding to issues identified by the questionnaires, and (8) evaluating the impact of the PRO intervention on the practice.

Conclusions

Integrating PROs in clinical practice has the potential to enhance patient-centered care. The online version of the User’s Guide will be updated periodically.
Literatur
1.
Zurück zum Zitat Department of Health. (2010). Equity and excellence: Liberating the NHS. London. Department of Health. (2010). Equity and excellence: Liberating the NHS. London.
2.
Zurück zum Zitat Greenhalgh, J., & Meadows, K. (1999). The effectiveness of the use of patient-based measures of health in routine practice in improving the process and outcomes of patient care: A literature review. Journal of Evaluation in Clinical Practice, 5, 401–416.PubMedCrossRef Greenhalgh, J., & Meadows, K. (1999). The effectiveness of the use of patient-based measures of health in routine practice in improving the process and outcomes of patient care: A literature review. Journal of Evaluation in Clinical Practice, 5, 401–416.PubMedCrossRef
3.
Zurück zum Zitat Marshall, S., Haywood, K., & Fitzpatrick, R. (2006). Impact of patient-reported outcome measures on routine practice: A structured review. Journal of Evaluation in Clinical Practice, 12, 559–568.PubMedCrossRef Marshall, S., Haywood, K., & Fitzpatrick, R. (2006). Impact of patient-reported outcome measures on routine practice: A structured review. Journal of Evaluation in Clinical Practice, 12, 559–568.PubMedCrossRef
4.
Zurück zum Zitat Valderas, J. M., Kotzeva, A., Espallargues, M., et al. (2008). The impact of measuring patient-reported outcomes in clinical practice: A systematic review of the literature. Quality of Life Research, 17, 179–193.PubMedCrossRef Valderas, J. M., Kotzeva, A., Espallargues, M., et al. (2008). The impact of measuring patient-reported outcomes in clinical practice: A systematic review of the literature. Quality of Life Research, 17, 179–193.PubMedCrossRef
5.
Zurück zum Zitat Greenhalgh, J. (2009). The applications of PROs in clinical practice: What are they, do they work and why? Quality of Life Research, 18, 115–123.PubMedCrossRef Greenhalgh, J. (2009). The applications of PROs in clinical practice: What are they, do they work and why? Quality of Life Research, 18, 115–123.PubMedCrossRef
6.
Zurück zum Zitat Devlin, N. J., & Appleby, J. (2010). Getting the most out of PROMS: Putting health outcomes at the heart of NHS decision-making. London, United Kingdom: The King’s Fund. Devlin, N. J., & Appleby, J. (2010). Getting the most out of PROMS: Putting health outcomes at the heart of NHS decision-making. London, United Kingdom: The King’s Fund.
7.
Zurück zum Zitat Ackerley, S. J., Gordon, H. J., Elston, A. F., Crawford, L. M., & McPherson, K. M. (2009). Assessment of quality of life, participation within an outpatient rehabilitation setting. [Erratum appears in Disability, Rehabilitation;31:1107]. Disability and Rehabilitation, 31, 906–913.PubMedCrossRef Ackerley, S. J., Gordon, H. J., Elston, A. F., Crawford, L. M., & McPherson, K. M. (2009). Assessment of quality of life, participation within an outpatient rehabilitation setting. [Erratum appears in Disability, Rehabilitation;31:1107]. Disability and Rehabilitation, 31, 906–913.PubMedCrossRef
8.
Zurück zum Zitat Masskulpan, P., Riewthong, K., Dajpratham, P., & Kuptniratsaikul, V. (2008). Anxiety and depressive symptoms after stroke in 9 rehabilitation centers. Journal of the Medical Association of Thailand, 91, 1595–1602.PubMed Masskulpan, P., Riewthong, K., Dajpratham, P., & Kuptniratsaikul, V. (2008). Anxiety and depressive symptoms after stroke in 9 rehabilitation centers. Journal of the Medical Association of Thailand, 91, 1595–1602.PubMed
9.
Zurück zum Zitat Veenstra, M., Moum, T., & Garratt, A. M. (2006). Patient experiences with information in a hospital setting: associations with coping and self-rated health in chronic illness. Quality of Life Research, 15, 967–978.PubMedCrossRef Veenstra, M., Moum, T., & Garratt, A. M. (2006). Patient experiences with information in a hospital setting: associations with coping and self-rated health in chronic illness. Quality of Life Research, 15, 967–978.PubMedCrossRef
10.
Zurück zum Zitat Rose, M., & Bezjak, A. (2009). Logistics of collecting patient-reported outcomes (PRO) in clinical practice: an overview and practical examples. Quality of Life Research, 18, 125–136.PubMedCrossRef Rose, M., & Bezjak, A. (2009). Logistics of collecting patient-reported outcomes (PRO) in clinical practice: an overview and practical examples. Quality of Life Research, 18, 125–136.PubMedCrossRef
11.
Zurück zum Zitat Lohr, K. N., & Zebrack, B. J. (2009). Using patient-reported outcomes in clinical practice: Challenges and opportunities. Quality of Life Research, 18, 99–107.PubMedCrossRef Lohr, K. N., & Zebrack, B. J. (2009). Using patient-reported outcomes in clinical practice: Challenges and opportunities. Quality of Life Research, 18, 99–107.PubMedCrossRef
12.
Zurück zum Zitat Santana, M. J., Feeny, D., Johnson, J. A., et al. (2010). Assessing the use of health related quality of life measures in the routine clinical care of lung transplant patients. Quality of Life Research, 19, 371–379.PubMedCrossRef Santana, M. J., Feeny, D., Johnson, J. A., et al. (2010). Assessing the use of health related quality of life measures in the routine clinical care of lung transplant patients. Quality of Life Research, 19, 371–379.PubMedCrossRef
13.
Zurück zum Zitat Santana, M. J., & Feeny, D. (2009). Using the health utilities index in routine clinical care: Process, feasibility and acceptability. Patient, 2, 1–9.CrossRef Santana, M. J., & Feeny, D. (2009). Using the health utilities index in routine clinical care: Process, feasibility and acceptability. Patient, 2, 1–9.CrossRef
14.
Zurück zum Zitat Frost, M. H., Bonomi, A. E., Cappelleri, J. C., et al. (2007). Applying quality-of-life data formally and systematically into clinical practice. Mayo Clinic Proceedings, 82, 1214–1228.PubMedCrossRef Frost, M. H., Bonomi, A. E., Cappelleri, J. C., et al. (2007). Applying quality-of-life data formally and systematically into clinical practice. Mayo Clinic Proceedings, 82, 1214–1228.PubMedCrossRef
15.
Zurück zum Zitat Donaldson, M. S. (2008). Taking PROs and patient-centered care seriously: Incremental and disruptive ideas for incorporating PROs in oncology practice. Quality of Life Research, 17, 1323–1330.PubMedCrossRef Donaldson, M. S. (2008). Taking PROs and patient-centered care seriously: Incremental and disruptive ideas for incorporating PROs in oncology practice. Quality of Life Research, 17, 1323–1330.PubMedCrossRef
16.
Zurück zum Zitat Fung, C., & Hays, R. D. (2008). Prospects and challenges in using patient-reported outcomes in clinical practice. Quality of Life Research, 17, 1297–1302.PubMedCrossRef Fung, C., & Hays, R. D. (2008). Prospects and challenges in using patient-reported outcomes in clinical practice. Quality of Life Research, 17, 1297–1302.PubMedCrossRef
17.
Zurück zum Zitat Greenhalgh, J., Long, A. F., & Flynn, R. (2005). The use of patient reported outcome measures in routine clinical care: Lack of impact or lack of theory? Social Science and Medicine, 60, 833–843.PubMedCrossRef Greenhalgh, J., Long, A. F., & Flynn, R. (2005). The use of patient reported outcome measures in routine clinical care: Lack of impact or lack of theory? Social Science and Medicine, 60, 833–843.PubMedCrossRef
18.
Zurück zum Zitat Bush, N., Donaldson, G., Moinpour, C., et al. (2005). Development, feasibility and compliance of a web-based system for very frequent QOL and symptom home self-assessment after hematopoietic stem cell transplantation. Quality of Life Research, 14, 77–93.PubMedCrossRef Bush, N., Donaldson, G., Moinpour, C., et al. (2005). Development, feasibility and compliance of a web-based system for very frequent QOL and symptom home self-assessment after hematopoietic stem cell transplantation. Quality of Life Research, 14, 77–93.PubMedCrossRef
19.
Zurück zum Zitat Donaldson, M. S. (2007). Use of patient-reported outcomes in clinical oncology practice. A nonvisit approach to patient care based on the IOM report. Journal of Ambulatory Care Management, 30, 302–307.PubMed Donaldson, M. S. (2007). Use of patient-reported outcomes in clinical oncology practice. A nonvisit approach to patient care based on the IOM report. Journal of Ambulatory Care Management, 30, 302–307.PubMed
20.
Zurück zum Zitat Snyder, C. F., Jensen, R., Courtin, O., & Wu, A. W. (2009). PatientViewpoint: A website for patient-reported outcomes assessment. Quality of Life Research, 18, 793–800.PubMedCrossRef Snyder, C. F., Jensen, R., Courtin, O., & Wu, A. W. (2009). PatientViewpoint: A website for patient-reported outcomes assessment. Quality of Life Research, 18, 793–800.PubMedCrossRef
21.
Zurück zum Zitat McColl, E., & Fayers, P. (2005). Context effects and proxy assessments. In P. Fayers & R. D. Hays (Eds.), Assessing quality of life in clinical trials (pp. 131–148). New York: Oxford. McColl, E., & Fayers, P. (2005). Context effects and proxy assessments. In P. Fayers & R. D. Hays (Eds.), Assessing quality of life in clinical trials (pp. 131–148). New York: Oxford.
22.
Zurück zum Zitat Seid, M., Limbers, C. A., Driscoll, K. A., Opipari-Arrigan, L. A., Gelhard, L. R., & Varni, J. W. (2010). Reliability, validity, and responsiveness of the pediatric quality of life inventory (PedsQL) generic core scales and asthma symptoms scale in vulnerable children with asthma. Journal of Asthma, 47, 170–177.PubMedCrossRef Seid, M., Limbers, C. A., Driscoll, K. A., Opipari-Arrigan, L. A., Gelhard, L. R., & Varni, J. W. (2010). Reliability, validity, and responsiveness of the pediatric quality of life inventory (PedsQL) generic core scales and asthma symptoms scale in vulnerable children with asthma. Journal of Asthma, 47, 170–177.PubMedCrossRef
23.
Zurück zum Zitat Naglie, G., Tomlinson, G., Tansey, C., et al. (2006). Utility-based quality of life measures in Alzheimer’s disease. Quality of Life Research, 15, 631–643.PubMedCrossRef Naglie, G., Tomlinson, G., Tansey, C., et al. (2006). Utility-based quality of life measures in Alzheimer’s disease. Quality of Life Research, 15, 631–643.PubMedCrossRef
24.
Zurück zum Zitat Novella, J. L., Jochum, C., Jolly, D., et al. (2001). Agreement between patients’ and proxies’ reports of quality of life in Alzheimer’s disease. Quality of Life Research, 10, 443–452.PubMedCrossRef Novella, J. L., Jochum, C., Jolly, D., et al. (2001). Agreement between patients’ and proxies’ reports of quality of life in Alzheimer’s disease. Quality of Life Research, 10, 443–452.PubMedCrossRef
25.
Zurück zum Zitat Ready, R. E., Ott, B. R., & Grace, J. (2004). Patient versus informant perspectives of quality of life in mild cognitive impairment and Alzheimer’s disease. International Journal of Geriatric Psychiatry, 19, 256–265.PubMedCrossRef Ready, R. E., Ott, B. R., & Grace, J. (2004). Patient versus informant perspectives of quality of life in mild cognitive impairment and Alzheimer’s disease. International Journal of Geriatric Psychiatry, 19, 256–265.PubMedCrossRef
26.
Zurück zum Zitat Pickard, A. S., & Knight, S. J. (2005). Proxy evaluation of health-related quality of life: a conceptual framework for understanding multiple proxy perspectives. Medical Care, 43, 493–499.PubMedCrossRef Pickard, A. S., & Knight, S. J. (2005). Proxy evaluation of health-related quality of life: a conceptual framework for understanding multiple proxy perspectives. Medical Care, 43, 493–499.PubMedCrossRef
27.
Zurück zum Zitat Chen, T. H., Li, L., & Kochen, M. M. (2005). A systematic review: How to choose appropriate health-related quality of life (HRQOL) measures in routine general practice? Journal of Zhejiang University Science B, 6, 936–940.PubMedCrossRef Chen, T. H., Li, L., & Kochen, M. M. (2005). A systematic review: How to choose appropriate health-related quality of life (HRQOL) measures in routine general practice? Journal of Zhejiang University Science B, 6, 936–940.PubMedCrossRef
28.
Zurück zum Zitat Osoba, D. (2007). Translating the science of patient-reported outcomes assessment into clinical practice. Journal of the National Cancer Institute Monographs, 37, 5–11.PubMedCrossRef Osoba, D. (2007). Translating the science of patient-reported outcomes assessment into clinical practice. Journal of the National Cancer Institute Monographs, 37, 5–11.PubMedCrossRef
29.
Zurück zum Zitat Snyder, C. F., Dy, S. M., Hendricks, D. E., et al. (2007). Asking the right questions: investigating needs assessments and health-related quality-of-life questionnaires for use in oncology clinical practice. Supportive Care in Cancer, 15, 1075–1085.PubMedCrossRef Snyder, C. F., Dy, S. M., Hendricks, D. E., et al. (2007). Asking the right questions: investigating needs assessments and health-related quality-of-life questionnaires for use in oncology clinical practice. Supportive Care in Cancer, 15, 1075–1085.PubMedCrossRef
30.
Zurück zum Zitat Miller, D. M., Kattan, M. W., & Fu, A. Z. (2007). Health related quality of life assessment in multiple sclerosis. In J. A. Cohen & R. A. Rudick (Eds.), Multiple sclerosis therapeutics (3rd ed., pp. 101–112). Abingdon: Informa. Miller, D. M., Kattan, M. W., & Fu, A. Z. (2007). Health related quality of life assessment in multiple sclerosis. In J. A. Cohen & R. A. Rudick (Eds.), Multiple sclerosis therapeutics (3rd ed., pp. 101–112). Abingdon: Informa.
31.
Zurück zum Zitat Nowels, D., McGloin, J., Westfall, J. M., & Holcomb, S. (2005). Validation of the EQ-5D quality of life instrument in patients after myocardial infarction. Quality of Life Research, 14, 95–105.PubMedCrossRef Nowels, D., McGloin, J., Westfall, J. M., & Holcomb, S. (2005). Validation of the EQ-5D quality of life instrument in patients after myocardial infarction. Quality of Life Research, 14, 95–105.PubMedCrossRef
32.
Zurück zum Zitat Zimmerman, M., Ruggero, C. J., Chelminski, I., et al. (2006). Developing brief scales for use in clinical practice: the reliability and validity of single-item self-report measures of depression symptom severity, psychosocial impairment due to depression, and quality of life. Journal of Clinical Psychiatry, 67, 1536–1541.PubMedCrossRef Zimmerman, M., Ruggero, C. J., Chelminski, I., et al. (2006). Developing brief scales for use in clinical practice: the reliability and validity of single-item self-report measures of depression symptom severity, psychosocial impairment due to depression, and quality of life. Journal of Clinical Psychiatry, 67, 1536–1541.PubMedCrossRef
33.
Zurück zum Zitat Cella, D., Gershon, R., Lai, J. S., & Choi, S. (2007). The future of outcomes measurement: Item banking, tailored short-forms, and computerized adaptive assessment. Quality of Life Research, 161(Suppl 1), 133–141.CrossRef Cella, D., Gershon, R., Lai, J. S., & Choi, S. (2007). The future of outcomes measurement: Item banking, tailored short-forms, and computerized adaptive assessment. Quality of Life Research, 161(Suppl 1), 133–141.CrossRef
34.
Zurück zum Zitat Cella, D., Riley, W., Stone, A., et al. (2010). Initial adult health item banks and first wave testing of the patient-reported outcomes measurement information system (PROMIS) network: 2005–2008. Journal of Clinical Epidemiology, 63, 1179–1194.PubMedCrossRef Cella, D., Riley, W., Stone, A., et al. (2010). Initial adult health item banks and first wave testing of the patient-reported outcomes measurement information system (PROMIS) network: 2005–2008. Journal of Clinical Epidemiology, 63, 1179–1194.PubMedCrossRef
35.
Zurück zum Zitat Walter, O. B., Becker, J., Bjorner, J. B., Fliege, H., Klapp, B. F., & Rose, M. (2007). Development and evaluation of a computer adaptive test for ‘Anxiety’ (Anxiety-CAT). Quality of Life Research, 16(Suppl 1), 143–155.PubMedCrossRef Walter, O. B., Becker, J., Bjorner, J. B., Fliege, H., Klapp, B. F., & Rose, M. (2007). Development and evaluation of a computer adaptive test for ‘Anxiety’ (Anxiety-CAT). Quality of Life Research, 16(Suppl 1), 143–155.PubMedCrossRef
37.
Zurück zum Zitat Dillman, D. A., Smyth, J. D., & Christian, L. M. (2009). Internet, mail, and mixed-mode surveys: The tailored design method (3rd ed.). New Jersey: Wiley. Dillman, D. A., Smyth, J. D., & Christian, L. M. (2009). Internet, mail, and mixed-mode surveys: The tailored design method (3rd ed.). New Jersey: Wiley.
38.
Zurück zum Zitat Bickman, L., & Rog, D. J. (2009). The Sage handbook of applied social research methods. London: Sage Publications Ltd. Bickman, L., & Rog, D. J. (2009). The Sage handbook of applied social research methods. London: Sage Publications Ltd.
39.
Zurück zum Zitat Fowley, F. J., Jr. (2009). Survey research methods (4th ed.). London: Sage Publications Ltd. Fowley, F. J., Jr. (2009). Survey research methods (4th ed.). London: Sage Publications Ltd.
40.
Zurück zum Zitat Wasson, J. H., Stukel, T. A., Weiss, J. E., Hays, R. D., Jette, A. M., & Nelson, E. C. (1999). A randomized trial of the use of patient self-assessment data to improve community practices. Effective Clinical Practice, 2, 1–10.PubMed Wasson, J. H., Stukel, T. A., Weiss, J. E., Hays, R. D., Jette, A. M., & Nelson, E. C. (1999). A randomized trial of the use of patient self-assessment data to improve community practices. Effective Clinical Practice, 2, 1–10.PubMed
41.
Zurück zum Zitat Hess, R., Santucci, A., McTigue, K., Fischer, G., & Kapoor, W. (2008). Patient difficulty using tablet computers to screen in primary care. Journal of General Internal Medicine, 23, 476–480.PubMedCrossRef Hess, R., Santucci, A., McTigue, K., Fischer, G., & Kapoor, W. (2008). Patient difficulty using tablet computers to screen in primary care. Journal of General Internal Medicine, 23, 476–480.PubMedCrossRef
42.
Zurück zum Zitat Detmar, S. B., Muller, M. J., Schornagel, J. H., Wever, L. D., & Aaronson, N. K. (2002). Health-related quality-of-life assessments and patient-physician communication: A randomized controlled trial. JAMA, 288, 3027–3034.PubMedCrossRef Detmar, S. B., Muller, M. J., Schornagel, J. H., Wever, L. D., & Aaronson, N. K. (2002). Health-related quality-of-life assessments and patient-physician communication: A randomized controlled trial. JAMA, 288, 3027–3034.PubMedCrossRef
43.
Zurück zum Zitat Velikova, G., Booth, L., Smith, A. B., et al. (2004). Measuring quality of life in routine oncology practice improves communication and patient well-being: A randomized controlled trial. Journal of Clinical Oncology, 22, 714–724.PubMedCrossRef Velikova, G., Booth, L., Smith, A. B., et al. (2004). Measuring quality of life in routine oncology practice improves communication and patient well-being: A randomized controlled trial. Journal of Clinical Oncology, 22, 714–724.PubMedCrossRef
44.
Zurück zum Zitat Wright, E. P., Selby, P. J., Crawford, M., et al. (2003). Feasibility and compliance of automated measurement of quality of life in oncology practice. Journal of Clinical Oncology, 21, 374–382.PubMedCrossRef Wright, E. P., Selby, P. J., Crawford, M., et al. (2003). Feasibility and compliance of automated measurement of quality of life in oncology practice. Journal of Clinical Oncology, 21, 374–382.PubMedCrossRef
45.
Zurück zum Zitat Espallargues, M., Valderas, J. M., & Alonso, J. (2000). Provision of feedback on perceived health status to health care professionals: A systematic review of its impact. Medical Care, 38, 175–186.PubMedCrossRef Espallargues, M., Valderas, J. M., & Alonso, J. (2000). Provision of feedback on perceived health status to health care professionals: A systematic review of its impact. Medical Care, 38, 175–186.PubMedCrossRef
46.
Zurück zum Zitat Guyatt, G. H., Ferrans, C. E., Halyard, M. Y., et al. (2007). Exploration of the value of health-related quality-of-life information from clinical research and into clinical practice. Mayo Clinic Proceedings, 82, 1229–1239.PubMedCrossRef Guyatt, G. H., Ferrans, C. E., Halyard, M. Y., et al. (2007). Exploration of the value of health-related quality-of-life information from clinical research and into clinical practice. Mayo Clinic Proceedings, 82, 1229–1239.PubMedCrossRef
47.
Zurück zum Zitat MacArthur, C., Winter, H. R., Bick, D. E., et al. (2002). Effects of redesigned community postnatal care on womens’ health 4 months after birth: A cluster randomised controlled trial. Lancet, 359, 378–385.PubMedCrossRef MacArthur, C., Winter, H. R., Bick, D. E., et al. (2002). Effects of redesigned community postnatal care on womens’ health 4 months after birth: A cluster randomised controlled trial. Lancet, 359, 378–385.PubMedCrossRef
48.
Zurück zum Zitat Wagner, E. H. (1998). Chronic disease management: What will it take to improve care for chronic illness? Effective Clinical Practice, 1, 2–4.PubMed Wagner, E. H. (1998). Chronic disease management: What will it take to improve care for chronic illness? Effective Clinical Practice, 1, 2–4.PubMed
49.
Zurück zum Zitat Brundage, M., Leis, A., Bezjak, A., et al. (2003). Cancer patients’ preferences for communicating clinical trial quality of life information: A qualitative study. Quality of Life Research, 12, 395–404.PubMedCrossRef Brundage, M., Leis, A., Bezjak, A., et al. (2003). Cancer patients’ preferences for communicating clinical trial quality of life information: A qualitative study. Quality of Life Research, 12, 395–404.PubMedCrossRef
50.
Zurück zum Zitat Brundage, M., Feldman-Stewart, D., Leis, A., et al. (2005). Communicating quality of life information to cancer patients: A study of six presentation formats. Journal of Clinical Oncology, 23, 6949–6956.PubMedCrossRef Brundage, M., Feldman-Stewart, D., Leis, A., et al. (2005). Communicating quality of life information to cancer patients: A study of six presentation formats. Journal of Clinical Oncology, 23, 6949–6956.PubMedCrossRef
51.
Zurück zum Zitat Hilarius, D. L., Kloeg, P. H., Gundy, C. M., & Aaronson, N. (2008). Use of health related quality of life assessments in daily clinical oncology nursing practice: A community hospital based intervention study. Cancer, 113, 628–637.PubMedCrossRef Hilarius, D. L., Kloeg, P. H., Gundy, C. M., & Aaronson, N. (2008). Use of health related quality of life assessments in daily clinical oncology nursing practice: A community hospital based intervention study. Cancer, 113, 628–637.PubMedCrossRef
52.
Zurück zum Zitat Mathias, S. D., Fifer, S. K., Mazonson, P. D., Lubeck, D. P., Buesching, D. P., & Patrick, D. L. (1994). Necessary but not sufficient: The effect of screening and feedback on outcomes of primary care patients with untreated anxiety. Journal of General Internal Medicine, 9, 606–615.PubMedCrossRef Mathias, S. D., Fifer, S. K., Mazonson, P. D., Lubeck, D. P., Buesching, D. P., & Patrick, D. L. (1994). Necessary but not sufficient: The effect of screening and feedback on outcomes of primary care patients with untreated anxiety. Journal of General Internal Medicine, 9, 606–615.PubMedCrossRef
53.
Zurück zum Zitat Magruder-Habib, K., Zung, W. W. K., & Feussner, J. R. (1990). Improving physicians’ recognition and treatment of depression in general medical care. Results from a randomized clinical trial. Medical Care, 28, 239–250.PubMedCrossRef Magruder-Habib, K., Zung, W. W. K., & Feussner, J. R. (1990). Improving physicians’ recognition and treatment of depression in general medical care. Results from a randomized clinical trial. Medical Care, 28, 239–250.PubMedCrossRef
54.
Zurück zum Zitat Reifler, D. R., Kessler, H. S., Bernhard, E. J., Leon, A. C., & Martin, G. J. (1996). Impact of screening for mental health concerns on health service utilization and functional status in primary care patients. Archives of Internal Medicine, 156, 2593–2599.PubMedCrossRef Reifler, D. R., Kessler, H. S., Bernhard, E. J., Leon, A. C., & Martin, G. J. (1996). Impact of screening for mental health concerns on health service utilization and functional status in primary care patients. Archives of Internal Medicine, 156, 2593–2599.PubMedCrossRef
55.
Zurück zum Zitat Gilbody, S., Sheldon, T., & Wessely, S. (2006). Should we screen for depression? BMJ, 332, 1027–1030.PubMedCrossRef Gilbody, S., Sheldon, T., & Wessely, S. (2006). Should we screen for depression? BMJ, 332, 1027–1030.PubMedCrossRef
56.
Zurück zum Zitat Rosenbloom, S. K., Victorson, D. E., Hahn, E. A., Peterman, A., & Cella, D. (2007). Assessment is not enough: A randomized controlled trial of the effects of HRQoL assessment on quality of life and satisfaction in oncology clinical practice. Psychooncology, 16, 1069–1079.PubMedCrossRef Rosenbloom, S. K., Victorson, D. E., Hahn, E. A., Peterman, A., & Cella, D. (2007). Assessment is not enough: A randomized controlled trial of the effects of HRQoL assessment on quality of life and satisfaction in oncology clinical practice. Psychooncology, 16, 1069–1079.PubMedCrossRef
57.
Zurück zum Zitat Gutteling, J. J., Darlington, A. S., Janssen, H. L., Duivenvoorden, H. J., Busschbach, J. J., & de Man, R. A. (2008). Effectiveness of health related quality of life measurement in clinical practice: a prospective, randomised controlled trial in patients with chronic liver disease and their physicians. Quality of Life Research, 17, 195–205.PubMedCrossRef Gutteling, J. J., Darlington, A. S., Janssen, H. L., Duivenvoorden, H. J., Busschbach, J. J., & de Man, R. A. (2008). Effectiveness of health related quality of life measurement in clinical practice: a prospective, randomised controlled trial in patients with chronic liver disease and their physicians. Quality of Life Research, 17, 195–205.PubMedCrossRef
58.
Zurück zum Zitat Donaldson, G. (2008). Patient reported outcomes and the mandate for measurement. Quality of Life Research, 17, 1303–1313.PubMedCrossRef Donaldson, G. (2008). Patient reported outcomes and the mandate for measurement. Quality of Life Research, 17, 1303–1313.PubMedCrossRef
59.
Zurück zum Zitat Hays, R., Brodsky, M., Johnston, M. F., Spritzer, K. L., & Hui, K.-K. (2005). Evaluating the statistical significance of health related quality of life change in individual patients. Evaluation & the Health Professions, 28, 160–171.CrossRef Hays, R., Brodsky, M., Johnston, M. F., Spritzer, K. L., & Hui, K.-K. (2005). Evaluating the statistical significance of health related quality of life change in individual patients. Evaluation & the Health Professions, 28, 160–171.CrossRef
60.
Zurück zum Zitat Kemmler, G., Zabernigg, A., Gattringer, K., et al. (2010). A new approach to combining clinical relevance and statistical significance for evaluation of quality of life changes in the individual patient. Journal of Clinical Epidemiology, 63, 171–179.PubMedCrossRef Kemmler, G., Zabernigg, A., Gattringer, K., et al. (2010). A new approach to combining clinical relevance and statistical significance for evaluation of quality of life changes in the individual patient. Journal of Clinical Epidemiology, 63, 171–179.PubMedCrossRef
61.
Zurück zum Zitat De Vet, H. C., & Terwee, C. B. (2010). The minimal detectable change should not replace the minimal important change. Journal of Clinical Epidemiology, 63, 804–805.PubMedCrossRef De Vet, H. C., & Terwee, C. B. (2010). The minimal detectable change should not replace the minimal important change. Journal of Clinical Epidemiology, 63, 804–805.PubMedCrossRef
62.
Zurück zum Zitat Norman, G. R., Sloan, J. A., & Wyrwich, K. W. (2003). Interpretation of changes in health-related quality of life: The remarkable universality of half a standard deviation.[comment]. Medical Care, 41, 582–592.PubMed Norman, G. R., Sloan, J. A., & Wyrwich, K. W. (2003). Interpretation of changes in health-related quality of life: The remarkable universality of half a standard deviation.[comment]. Medical Care, 41, 582–592.PubMed
63.
Zurück zum Zitat Kosinski, M., Zhao, S. Z., Dedhiya, S., Osterhaus, J. T., & Ware, J. E. (2000). Determining minimally important changes in generic and disease specific health related quality of life questionnaires in clinical trials of rheumatoid arthritis. Arthritis and Rheumatism, 43, 1478–1487.PubMedCrossRef Kosinski, M., Zhao, S. Z., Dedhiya, S., Osterhaus, J. T., & Ware, J. E. (2000). Determining minimally important changes in generic and disease specific health related quality of life questionnaires in clinical trials of rheumatoid arthritis. Arthritis and Rheumatism, 43, 1478–1487.PubMedCrossRef
64.
Zurück zum Zitat Cella, D., Eton, D. T., Lai, J. S., Peterman, A. H., & Merkel, D. E. (2002). Combining anchor and distribution-based methods to derive minimal clinically important differences on the functional assessment of cancer therapy (FACT) anemia and fatigue scales. Journal of Pain and Symptom Management, 24, 547–561.PubMedCrossRef Cella, D., Eton, D. T., Lai, J. S., Peterman, A. H., & Merkel, D. E. (2002). Combining anchor and distribution-based methods to derive minimal clinically important differences on the functional assessment of cancer therapy (FACT) anemia and fatigue scales. Journal of Pain and Symptom Management, 24, 547–561.PubMedCrossRef
65.
Zurück zum Zitat Wyrwich, K. W., Bullinger, M., Aaronson, N., et al. (2005). Estimating clinically significant differences in quality of life outcomes. Quality of Life Research, 14, 285–295.PubMedCrossRef Wyrwich, K. W., Bullinger, M., Aaronson, N., et al. (2005). Estimating clinically significant differences in quality of life outcomes. Quality of Life Research, 14, 285–295.PubMedCrossRef
66.
Zurück zum Zitat Wyrwich, K. W., Nienaber, N. A., Tierney, W. M., & Wolinsky, F. D. (1999). Linking clinical relevance and statistical significance in evaluating intra-individual changes in health-related quality of life. Medical Care, 37, 469–478.PubMedCrossRef Wyrwich, K. W., Nienaber, N. A., Tierney, W. M., & Wolinsky, F. D. (1999). Linking clinical relevance and statistical significance in evaluating intra-individual changes in health-related quality of life. Medical Care, 37, 469–478.PubMedCrossRef
67.
Zurück zum Zitat Wyrwich, K. W., & Wolinsky, F. D. (2000). Identifying meaningful intra-individual change standards for health-related quality of life measures. Journal of Evaluation in Clinical Practice, 6, 39–49.PubMedCrossRef Wyrwich, K. W., & Wolinsky, F. D. (2000). Identifying meaningful intra-individual change standards for health-related quality of life measures. Journal of Evaluation in Clinical Practice, 6, 39–49.PubMedCrossRef
68.
Zurück zum Zitat Donaldson, M. S. (2004). Taking stock of health-related quality-of-life measurement in oncology practice in the United States. Journal of the National Cancer Institute Monographs, 33, 155–167.PubMedCrossRef Donaldson, M. S. (2004). Taking stock of health-related quality-of-life measurement in oncology practice in the United States. Journal of the National Cancer Institute Monographs, 33, 155–167.PubMedCrossRef
69.
Zurück zum Zitat Callahan, M. B. (2001). Using quality of life measurement to enhance interdisciplinary collaboration. Advances in Renal Replacement Therapy, 8, 148–151.PubMedCrossRef Callahan, M. B. (2001). Using quality of life measurement to enhance interdisciplinary collaboration. Advances in Renal Replacement Therapy, 8, 148–151.PubMedCrossRef
70.
Zurück zum Zitat Greenhalgh, J., Flynn, R., Long, A. F., & Tyson, S. (2008). Tacit and encoded knowledge in the use of standardised outcome measures in multidisciplinary team decision making: a case study of in-patient neurorehabilitation. Social Science and Medicine, 67, 183–194.PubMedCrossRef Greenhalgh, J., Flynn, R., Long, A. F., & Tyson, S. (2008). Tacit and encoded knowledge in the use of standardised outcome measures in multidisciplinary team decision making: a case study of in-patient neurorehabilitation. Social Science and Medicine, 67, 183–194.PubMedCrossRef
71.
Zurück zum Zitat Meyer, K. B., Espindle, D. M., DeGiacomo, J. M., Jenuleson, C. S., Kurtin, P. S., & Davies, A. R. (1994). Monitoring dialysis patients’ health status. American Journal of Kidney Diseases, 24, 267–279.PubMed Meyer, K. B., Espindle, D. M., DeGiacomo, J. M., Jenuleson, C. S., Kurtin, P. S., & Davies, A. R. (1994). Monitoring dialysis patients’ health status. American Journal of Kidney Diseases, 24, 267–279.PubMed
72.
Zurück zum Zitat Gilbody, S. M., House, A. O., & Sheldon, T. A. (2002). Psychiatrists in the UK do not use outcomes measures. National survey. British Journal of Psychiatry, 180, 101–103.PubMedCrossRef Gilbody, S. M., House, A. O., & Sheldon, T. A. (2002). Psychiatrists in the UK do not use outcomes measures. National survey. British Journal of Psychiatry, 180, 101–103.PubMedCrossRef
73.
Zurück zum Zitat Campbell, D. T., & Stanley, J. C. (1963). Experimental and Quasi-experimental designs for research. Chicago: Rand McNally College Publishing Company. Campbell, D. T., & Stanley, J. C. (1963). Experimental and Quasi-experimental designs for research. Chicago: Rand McNally College Publishing Company.
75.
Zurück zum Zitat Nelson, E. C., Splaine, M. E., Plume, S. K., & Batalden, P. (2004). Good measurement for good improvement work. Quality Management in Health Care, 13, 1–16.PubMed Nelson, E. C., Splaine, M. E., Plume, S. K., & Batalden, P. (2004). Good measurement for good improvement work. Quality Management in Health Care, 13, 1–16.PubMed
76.
Zurück zum Zitat Pawson, R., & Tilley, N. (1997). Realistic evaluation. London: Sage Publications, Ltd. Pawson, R., & Tilley, N. (1997). Realistic evaluation. London: Sage Publications, Ltd.
77.
Zurück zum Zitat Baker, G. R. (2006). Strengthening the contributions of quality improvement research to evidence based healthcare. Quality and Safety in Health Care, 15, 150–151.PubMedCrossRef Baker, G. R. (2006). Strengthening the contributions of quality improvement research to evidence based healthcare. Quality and Safety in Health Care, 15, 150–151.PubMedCrossRef
78.
Zurück zum Zitat Campbell, M., Fitzpatrick, R., Haines, A., et al. (2000). Framework for design and evaluation of complex interventions to improve health. BMJ, 321, 694–696.PubMedCrossRef Campbell, M., Fitzpatrick, R., Haines, A., et al. (2000). Framework for design and evaluation of complex interventions to improve health. BMJ, 321, 694–696.PubMedCrossRef
79.
Zurück zum Zitat Berwick, D. M. (1998). Developing and testing changes in delivery of care. Annals of Internal Medicine, 128, 651–656.PubMed Berwick, D. M. (1998). Developing and testing changes in delivery of care. Annals of Internal Medicine, 128, 651–656.PubMed
80.
Zurück zum Zitat Batalden, P. B., & Davidoff, F. (2007). What is “quality improvement” and how can it transform healthcare? Quality and Safety in Health Care, 16, 2–3.PubMedCrossRef Batalden, P. B., & Davidoff, F. (2007). What is “quality improvement” and how can it transform healthcare? Quality and Safety in Health Care, 16, 2–3.PubMedCrossRef
81.
Zurück zum Zitat Cook, T. D., & Campbell, D. T. (1979). Quasi-experimentation: Design and analysis issues for field settings. Chicago: Rand McNally College Publishing Company. Cook, T. D., & Campbell, D. T. (1979). Quasi-experimentation: Design and analysis issues for field settings. Chicago: Rand McNally College Publishing Company.
82.
Zurück zum Zitat Donner, A., & Klar, N. (2000). Design and analysis of cluster-randomized trials in health research. London: Arnold. Donner, A., & Klar, N. (2000). Design and analysis of cluster-randomized trials in health research. London: Arnold.
83.
Zurück zum Zitat Fayers, P. M. (2008). Evaluating the effectiveness of using PROs in clinical practice: A role for cluster-randomized trials. Quality of Life Research, 17, 1315–1321.PubMedCrossRef Fayers, P. M. (2008). Evaluating the effectiveness of using PROs in clinical practice: A role for cluster-randomized trials. Quality of Life Research, 17, 1315–1321.PubMedCrossRef
84.
Zurück zum Zitat Murray, D. M. (1998). Design and analysis of group-randomized trials. New York: Oxford University Press, Inc. Murray, D. M. (1998). Design and analysis of group-randomized trials. New York: Oxford University Press, Inc.
Metadaten
Titel
Implementing patient-reported outcomes assessment in clinical practice: a review of the options and considerations
verfasst von
Claire F. Snyder
Neil K. Aaronson
Ali K. Choucair
Thomas E. Elliott
Joanne Greenhalgh
Michele Y. Halyard
Rachel Hess
Deborah M. Miller
Bryce B. Reeve
Maria Santana
Publikationsdatum
01.10.2012
Verlag
Springer Netherlands
Erschienen in
Quality of Life Research / Ausgabe 8/2012
Print ISSN: 0962-9343
Elektronische ISSN: 1573-2649
DOI
https://doi.org/10.1007/s11136-011-0054-x

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