Skip to main content
Erschienen in: Quality of Life Research 3/2019

03.10.2018 | Review

A systematic review of randomised controlled trials evaluating the use of patient-reported outcome measures (PROMs)

verfasst von: S. Ishaque, J. Karnon, G. Chen, R. Nair, A. B. Salter

Erschienen in: Quality of Life Research | Ausgabe 3/2019

Einloggen, um Zugang zu erhalten

Abstract

Background

Patient-reported outcome measures (PROMs) could play an important role in identifying patients’ needs and goals in clinical encounters, improving communication and decision-making with clinicians, while making care more patient-centred. Comprehensive evidence that PROMS are an effective intervention is lacking in single randomised controlled trials (RCTs).

Methods

A systematic search was performed using controlled vocabulary related to the terms: clinical care setting and patient-reported outcome. English language studies were included if they were a RCT with a PROM as an intervention in a patient population. Included studies were analysed and their methodologic quality was appraised using the Cochrane Risk of Bias tool. The protocol was registered with PROSPERO (CRD42016034182).

Results

Of 4302 articles initially identified, 115 underwent full-text review resulting in 22 studies reporting on 25 comparisons. The majority of included studies were conducted in USA (11), among cancer patients (11), with adult participants only (20). Statistically significant and robust improvements were reported in the pre-specified outcomes of the process of care (2) and health care (3). Additionally, five, eight and three statistically significant but possibly non-robust findings were reported in the process of care, health and patient satisfaction outcomes, respectively.

Conclusions

Overall, studies that compared PROM to standard care either reported a positive effect or were not powered to find pre-specified differences. There is justification for the use of a PROM as part of standard care, but further adequately powered studies on their use in different contexts are necessary for a more comprehensive evidence base.
Anhänge
Nur mit Berechtigung zugänglich
Literatur
1.
Zurück zum Zitat Mayo, E. N., et al. (2015). ISOQOL dictionary of quality of life and health outcomes measurement. First Edition. Mayo, E. N., et al. (2015). ISOQOL dictionary of quality of life and health outcomes measurement. First Edition.
2.
Zurück zum Zitat Varadhan, R., Segal, J. B., Boyd, C. M., Wu, A. W., & Weiss, C. O. (2013). A framework for the analysis of heterogeneity of treatment effect in patient-centered outcomes research. Journal of Clinical Epidemiology, 66, 818–825.PubMedPubMedCentralCrossRef Varadhan, R., Segal, J. B., Boyd, C. M., Wu, A. W., & Weiss, C. O. (2013). A framework for the analysis of heterogeneity of treatment effect in patient-centered outcomes research. Journal of Clinical Epidemiology, 66, 818–825.PubMedPubMedCentralCrossRef
3.
Zurück zum Zitat Greenhalgh, J., & (Feb (2009). The applications of PROs in clinical practice: What are they, do they work, and why? Quality of Life Research: An International Journal of Quality of Life Aspects of Treatment, Care & Rehabilitation, 18(1), 115–123.CrossRef Greenhalgh, J., & (Feb (2009). The applications of PROs in clinical practice: What are they, do they work, and why? Quality of Life Research: An International Journal of Quality of Life Aspects of Treatment, Care & Rehabilitation, 18(1), 115–123.CrossRef
4.
Zurück zum Zitat Ahmed, S., Berzon, R. A., Revicki, D. A., Lenderking, W. R., Moinpour, C. M., Basch, E., et al. (2012). The use of patient-reported outcomes (PRO) within comparative effectiveness research: Implications for clinical practice and health care policy. Medical Care, 50(12), 1060–1070.PubMedCrossRef Ahmed, S., Berzon, R. A., Revicki, D. A., Lenderking, W. R., Moinpour, C. M., Basch, E., et al. (2012). The use of patient-reported outcomes (PRO) within comparative effectiveness research: Implications for clinical practice and health care policy. Medical Care, 50(12), 1060–1070.PubMedCrossRef
5.
Zurück zum Zitat Wu, A. W., Snyder, C., Clancy, C. M., & Steinwachs, D. M. (2010). Adding the patient perspective to comparative effectiveness research. Health Affairs, 29(10), 1863–1871.PubMedCrossRef Wu, A. W., Snyder, C., Clancy, C. M., & Steinwachs, D. M. (2010). Adding the patient perspective to comparative effectiveness research. Health Affairs, 29(10), 1863–1871.PubMedCrossRef
6.
Zurück zum Zitat Antunes, B., Harding, R., Irene, J. H., & on behalf EUROIMPACT (2014). Implementing patient-reported outcome measures in palliative care clinical practice: A systematic review of facilitators and barriers. Palliative Medicine, 28(2), 158–175.PubMedCrossRef Antunes, B., Harding, R., Irene, J. H., & on behalf EUROIMPACT (2014). Implementing patient-reported outcome measures in palliative care clinical practice: A systematic review of facilitators and barriers. Palliative Medicine, 28(2), 158–175.PubMedCrossRef
8.
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(4), 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(4), 401–416.PubMedCrossRef
9.
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(2), 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(2), 175–186.PubMedCrossRef
10.
Zurück zum Zitat Gilbody, S. M., House, A. O., & Sheldon, T. (2002). Routine administration of health related quality of life (HRQoL) and needs assessment instruments to improve psychological outcome—A systemic review. Psychological Medicine, 32(8), 1345–1356.PubMedCrossRef Gilbody, S. M., House, A. O., & Sheldon, T. (2002). Routine administration of health related quality of life (HRQoL) and needs assessment instruments to improve psychological outcome—A systemic review. Psychological Medicine, 32(8), 1345–1356.PubMedCrossRef
11.
Zurück zum Zitat Kotronoulas, G., Kearney, N., Maguire, R., Harrow, A., Di Domenico, D., Croy, S., et al. (2014). What is the value of the routine use of patient-reported outcome measures toward improvement of patient outcomes, processes of care, and health service outcomes in cancer care? A systematic review of controlled trials. Journal of Clinical Oncology, 32(14), 1480–1501.PubMedCrossRef Kotronoulas, G., Kearney, N., Maguire, R., Harrow, A., Di Domenico, D., Croy, S., et al. (2014). What is the value of the routine use of patient-reported outcome measures toward improvement of patient outcomes, processes of care, and health service outcomes in cancer care? A systematic review of controlled trials. Journal of Clinical Oncology, 32(14), 1480–1501.PubMedCrossRef
12.
Zurück zum Zitat Valderas, J. M., Kotzeva, A., Espallargues, M., Guyatt, G., Ferrans, C. E., Halyard, M. Y., et al. (2008). The impact of measuring patient-reported outcomes in clinical practice: A systematic review of the literature. Quality of Life Research, 17(2), 179–193.PubMedCrossRef Valderas, J. M., Kotzeva, A., Espallargues, M., Guyatt, G., Ferrans, C. E., Halyard, M. Y., et al. (2008). The impact of measuring patient-reported outcomes in clinical practice: A systematic review of the literature. Quality of Life Research, 17(2), 179–193.PubMedCrossRef
13.
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(5), 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(5), 559–568.PubMedCrossRef
17.
Zurück zum Zitat Greenhalgh, J., Dalkin, S., Gooding, K., Gibbons, E., Wright, J., Meads, D., et al. (2017). Functionality and feedback: A realist synthesis of the collation, interpretation and utilisation of patient-reported outcome measures data to improve patient care. Health Services and Delivery Research, 5(2), 1–280.CrossRef Greenhalgh, J., Dalkin, S., Gooding, K., Gibbons, E., Wright, J., Meads, D., et al. (2017). Functionality and feedback: A realist synthesis of the collation, interpretation and utilisation of patient-reported outcome measures data to improve patient care. Health Services and Delivery Research, 5(2), 1–280.CrossRef
19.
Zurück zum Zitat Gutteling, J. J., Darlington, A. S., Janssen, H. L., Duivenvoorden, H. J., Busschbach, J. J. V., & De Man, R. A. (2008). Effectiveness of health-related quality-of-life measurement in clinical practice: A prospective, randomized controlled trial in patients with chronic liver disease and their physicians. Quality of Life Research, 17(2), 195–205. https://doi.org/10.1007/s11136-008-9308-7.PubMedPubMedCentralCrossRef Gutteling, J. J., Darlington, A. S., Janssen, H. L., Duivenvoorden, H. J., Busschbach, J. J. V., & De Man, R. A. (2008). Effectiveness of health-related quality-of-life measurement in clinical practice: A prospective, randomized controlled trial in patients with chronic liver disease and their physicians. Quality of Life Research, 17(2), 195–205. https://​doi.​org/​10.​1007/​s11136-008-9308-7.PubMedPubMedCentralCrossRef
20.
21.
Zurück zum Zitat Luckett, T., Butow, P. N., & King, M. T. (2009). Improving patient outcomes through the routine use of patient-reported data in cancer clinics: Future directions. Psycho-oncology, 18(11), 1129–1138.PubMedCrossRef Luckett, T., Butow, P. N., & King, M. T. (2009). Improving patient outcomes through the routine use of patient-reported data in cancer clinics: Future directions. Psycho-oncology, 18(11), 1129–1138.PubMedCrossRef
22.
Zurück zum Zitat Guyatt, G. H., Van Zanten, S. V., Feeny, D. H., & Patrick, D. L. (1989). Measuring quality of life in clinical trials: A taxonomy and review. CMAJ: Canadian Medical Association Journal, 140(12), 1441–1448.PubMed Guyatt, G. H., Van Zanten, S. V., Feeny, D. H., & Patrick, D. L. (1989). Measuring quality of life in clinical trials: A taxonomy and review. CMAJ: Canadian Medical Association Journal, 140(12), 1441–1448.PubMed
23.
Zurück zum Zitat Williams, K., Sansoni, J., Morris, D., Grootemaat, P., & Thompson, C. (2016). Patient-reported outcome measures: Literature review. Sydney: ACSQHC. Williams, K., Sansoni, J., Morris, D., Grootemaat, P., & Thompson, C. (2016). Patient-reported outcome measures: Literature review. Sydney: ACSQHC.
24.
30.
Zurück zum Zitat Higgins, J. P. T., Altman, D. G., Gøtzsche, P. C., Jüni, P., Moher, D., Oxman, A. D., et al. (2011). The Cochrane Collaboration’s tool for assessing risk of bias in randomised trials. BMJ, 343, d5928.PubMedPubMedCentralCrossRef Higgins, J. P. T., Altman, D. G., Gøtzsche, P. C., Jüni, P., Moher, D., Oxman, A. D., et al. (2011). The Cochrane Collaboration’s tool for assessing risk of bias in randomised trials. BMJ, 343, d5928.PubMedPubMedCentralCrossRef
31.
Zurück zum Zitat Basch, E., Deal, A. M., Kris, M. G., Scher, H. I., Hudis, C. A., Sabbatini, P., et al. (2016). Symptom monitoring with patient-reported outcomes during routine cancer treatment: A randomized controlled trial. Journal of Clinical Oncology, 34(6), 557–565.PubMedCrossRef Basch, E., Deal, A. M., Kris, M. G., Scher, H. I., Hudis, C. A., Sabbatini, P., et al. (2016). Symptom monitoring with patient-reported outcomes during routine cancer treatment: A randomized controlled trial. Journal of Clinical Oncology, 34(6), 557–565.PubMedCrossRef
32.
Zurück zum Zitat Berry, D. L., Blumenstein, B. A., Halpenny, B., Wolpin, S., Fann, J. R., Austin-Seymour, M., et al. (2011). Enhancing patient-provider communication with the electronic self-report assessment for cancer: A randomized trial. Journal of Clinical Oncology, 29(8), 1029–1035.PubMedPubMedCentralCrossRef Berry, D. L., Blumenstein, B. A., Halpenny, B., Wolpin, S., Fann, J. R., Austin-Seymour, M., et al. (2011). Enhancing patient-provider communication with the electronic self-report assessment for cancer: A randomized trial. Journal of Clinical Oncology, 29(8), 1029–1035.PubMedPubMedCentralCrossRef
33.
Zurück zum Zitat Boyes, A., Newell, S., Girgis, A., McElduff, P., & Sanson-Fisher, R. (2006). Does routine assessment and real-time feedback improve cancer patients’ psychosocial well-being? European Journal of Cancer Care, 15(2), 163–171.PubMedCrossRef Boyes, A., Newell, S., Girgis, A., McElduff, P., & Sanson-Fisher, R. (2006). Does routine assessment and real-time feedback improve cancer patients’ psychosocial well-being? European Journal of Cancer Care, 15(2), 163–171.PubMedCrossRef
34.
Zurück zum Zitat Calkins, D. R., Rubenstein, L. V., Cleary, P. D., Davies, A. R., Jette, A. M., Fink, A., et al. (1994). Functional disability screening of ambulatory patients—A randomized controlled trial in a hospital-based group practice. Journal of General Internal Medicine, 9(10), 590–592.PubMedCrossRef Calkins, D. R., Rubenstein, L. V., Cleary, P. D., Davies, A. R., Jette, A. M., Fink, A., et al. (1994). Functional disability screening of ambulatory patients—A randomized controlled trial in a hospital-based group practice. Journal of General Internal Medicine, 9(10), 590–592.PubMedCrossRef
35.
Zurück zum Zitat Cleeland, C. S., Wang, X. S., Shi, Q., Mendoza, T. R., Wright, S. L., Berry, M. D., et al. (2011). Automated symptom alerts reduce postoperative symptom severity after cancer surgery: A randomized controlled clinical trial. Journal of Clinical Oncology, 29(8), 994–1000.PubMedPubMedCentralCrossRef Cleeland, C. S., Wang, X. S., Shi, Q., Mendoza, T. R., Wright, S. L., Berry, M. D., et al. (2011). Automated symptom alerts reduce postoperative symptom severity after cancer surgery: A randomized controlled clinical trial. Journal of Clinical Oncology, 29(8), 994–1000.PubMedPubMedCentralCrossRef
36.
Zurück zum Zitat De Wit, M., Delemarre-van De Waal, H. A., Bokma, J. A., Haasnoot, K., Houdijk, M. C., Gemke, R. J., et al. (2008). Monitoring and discussing health-related quality of life in adolescents with type 1 diabetes improve psychosocial well-being: A randomized controlled trial. Diabetes Care, 31(8), 1521–1526.PubMedPubMedCentralCrossRef De Wit, M., Delemarre-van De Waal, H. A., Bokma, J. A., Haasnoot, K., Houdijk, M. C., Gemke, R. J., et al. (2008). Monitoring and discussing health-related quality of life in adolescents with type 1 diabetes improve psychosocial well-being: A randomized controlled trial. Diabetes Care, 31(8), 1521–1526.PubMedPubMedCentralCrossRef
37.
Zurück zum Zitat Detmar, S. B., Muller, M. J., Schornagel, J. H., Wever, L. D. V., & Aaronson, N. K. (2002). Health-related quality-of-life assessments and patient-physician communication: A randomized controlled trial. Journal of the American Medical Association, 288(23), 3027–3034.PubMedCrossRef Detmar, S. B., Muller, M. J., Schornagel, J. H., Wever, L. D. V., & Aaronson, N. K. (2002). Health-related quality-of-life assessments and patient-physician communication: A randomized controlled trial. Journal of the American Medical Association, 288(23), 3027–3034.PubMedCrossRef
38.
Zurück zum Zitat Goldsmith, G., & Brodwick, M. (1989). Assessing the functional status of older patients with chronic illness. Family Medicine, 21(1), 38–41.PubMed Goldsmith, G., & Brodwick, M. (1989). Assessing the functional status of older patients with chronic illness. Family Medicine, 21(1), 38–41.PubMed
39.
Zurück zum Zitat Hoekstra, J., de Vos, R., van Duijn, N. P., Schade, E., & Bindels, P. J. (2006). Using the symptom monitor in a randomized controlled trial: The effect on symptom prevalence and severity. Journal of Pain & Symptom Management, 31(1), 22–30.CrossRef Hoekstra, J., de Vos, R., van Duijn, N. P., Schade, E., & Bindels, P. J. (2006). Using the symptom monitor in a randomized controlled trial: The effect on symptom prevalence and severity. Journal of Pain & Symptom Management, 31(1), 22–30.CrossRef
40.
Zurück zum Zitat Kazis, L. E., Callahan, L. F., Meenan, R. F., & Pincus, T. (1990). Health status reports in the care of patients with rheumatoid arthritis. Journal of Clinical Epidemiology, 43(11), 1243–1253.PubMedCrossRef Kazis, L. E., Callahan, L. F., Meenan, R. F., & Pincus, T. (1990). Health status reports in the care of patients with rheumatoid arthritis. Journal of Clinical Epidemiology, 43(11), 1243–1253.PubMedCrossRef
41.
Zurück zum Zitat McLachlan, S. A., Allenby, A., Matthews, J., Wirth, A., Kissane, D., Bishop, M., et al. (2001). Randomized trial of coordinated psychosocial interventions based on patient self-assessments versus standard care to improve the psychosocial functioning of patients with cancer. Journal of Clinical Oncology, 19(21), 4117–4125.PubMedCrossRef McLachlan, S. A., Allenby, A., Matthews, J., Wirth, A., Kissane, D., Bishop, M., et al. (2001). Randomized trial of coordinated psychosocial interventions based on patient self-assessments versus standard care to improve the psychosocial functioning of patients with cancer. Journal of Clinical Oncology, 19(21), 4117–4125.PubMedCrossRef
42.
Zurück zum Zitat Mills, M. E., Murray, L. J., Johnston, B. T., Cardwell, C., & Donnelly, M. (2009). Does a patient-held quality-of-life diary benefit patients with inoperable lung cancer? Journal of Clinical Oncology, 27(1), 70–77.PubMedCrossRef Mills, M. E., Murray, L. J., Johnston, B. T., Cardwell, C., & Donnelly, M. (2009). Does a patient-held quality-of-life diary benefit patients with inoperable lung cancer? Journal of Clinical Oncology, 27(1), 70–77.PubMedCrossRef
43.
Zurück zum Zitat Qureshi, N., Standen, P. J., Hapgood, R., & Hayes, J. (2001). A randomized controlled trial to assess the psychological impact of a family history screening questionnaire in general practice. Family Practice, 18(1), 78–83.PubMedCrossRef Qureshi, N., Standen, P. J., Hapgood, R., & Hayes, J. (2001). A randomized controlled trial to assess the psychological impact of a family history screening questionnaire in general practice. Family Practice, 18(1), 78–83.PubMedCrossRef
44.
Zurück zum Zitat Rosenbloom, S. K., Victorson, D. E., Hahn, E. A., Peterman, A. H., & Cella, D. (2007). Assessment is not enough: A randomized controlled trial of the effects of HRQL assessment on quality of life and satisfaction in oncology clinical practice. Psycho-oncology, 16(12), 1069–1079.PubMedCrossRef Rosenbloom, S. K., Victorson, D. E., Hahn, E. A., Peterman, A. H., & Cella, D. (2007). Assessment is not enough: A randomized controlled trial of the effects of HRQL assessment on quality of life and satisfaction in oncology clinical practice. Psycho-oncology, 16(12), 1069–1079.PubMedCrossRef
45.
Zurück zum Zitat Rubenstein, L. V., Calkins, D. R., Young, R. T., Cleary, P. D., Fink, A., Kosecoff, J., et al. (1989). Improving patient function: A randomized trial of functional disability screening. Annals of Internal Medicine, 111(10), 836–842.PubMedCrossRef Rubenstein, L. V., Calkins, D. R., Young, R. T., Cleary, P. D., Fink, A., Kosecoff, J., et al. (1989). Improving patient function: A randomized trial of functional disability screening. Annals of Internal Medicine, 111(10), 836–842.PubMedCrossRef
46.
Zurück zum Zitat Rubenstein, L. V., McCoy, J. M., Cope, D. W., Barrett, P. A., Hirsch, S. H., Messer, K. S., et al. (1995). Improving patient quality of life with feedback to physicians about functional status. Journal of General Internal Medicine, 10(11), 607–614.PubMedCrossRef Rubenstein, L. V., McCoy, J. M., Cope, D. W., Barrett, P. A., Hirsch, S. H., Messer, K. S., et al. (1995). Improving patient quality of life with feedback to physicians about functional status. Journal of General Internal Medicine, 10(11), 607–614.PubMedCrossRef
47.
Zurück zum Zitat Ruland, C. M., Holte, H. H., Røislien, J., Heaven, C., Hamilton, G. A., Kristiansen, J., et al. (2010). Effects of a computer-supported interactive tailored patient assessment tool on patient care, symptom distress, and patients’ need for symptom management support: A randomized clinical trial. Journal of the American Medical Informatics Association, 17(4), 403–410.PubMedPubMedCentralCrossRef Ruland, C. M., Holte, H. H., Røislien, J., Heaven, C., Hamilton, G. A., Kristiansen, J., et al. (2010). Effects of a computer-supported interactive tailored patient assessment tool on patient care, symptom distress, and patients’ need for symptom management support: A randomized clinical trial. Journal of the American Medical Informatics Association, 17(4), 403–410.PubMedPubMedCentralCrossRef
48.
Zurück zum Zitat Street, R. L., Gold, W. R., & McDowell, T. (1994). Using health status surveys in medical consultations. Medical Care, 32(7), 732–744.PubMedCrossRef Street, R. L., Gold, W. R., & McDowell, T. (1994). Using health status surveys in medical consultations. Medical Care, 32(7), 732–744.PubMedCrossRef
49.
Zurück zum Zitat Velikova, G., Booth, L., Smith, A. B., Brown, P. M., Lynch, P., Brown, J. M., 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(4), 714–724.PubMedCrossRef Velikova, G., Booth, L., Smith, A. B., Brown, P. M., Lynch, P., Brown, J. M., 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(4), 714–724.PubMedCrossRef
50.
Zurück zum Zitat Wagner, A. K., Ehrenberg, B. L., Tran, T. A., Bungay, K. M., Cynn, D. J., & Rogers, W. H. (1997). Patient-based health status measurement in clinical practice: A study of its impact on epilepsy patients’ care. Quality of Life Research, 6(4), 329–341.PubMedCrossRef Wagner, A. K., Ehrenberg, B. L., Tran, T. A., Bungay, K. M., Cynn, D. J., & Rogers, W. H. (1997). Patient-based health status measurement in clinical practice: A study of its impact on epilepsy patients’ care. Quality of Life Research, 6(4), 329–341.PubMedCrossRef
51.
Zurück zum Zitat Wasson, J., Hays, R., Rubenstein, L., Nelson, E., Leaning, J., Johnson, D., et al. (1992). The short-term effect of patient health status assessment in a health maintenance organization. Quality of Life Research, 1(2), 99–106.PubMedCrossRef Wasson, J., Hays, R., Rubenstein, L., Nelson, E., Leaning, J., Johnson, D., et al. (1992). The short-term effect of patient health status assessment in a health maintenance organization. Quality of Life Research, 1(2), 99–106.PubMedCrossRef
52.
Zurück zum Zitat Wolfe, J., Orellana, L., Cook, E. F., Ullrich, C., Kang, T., Geyer, J. R., et al. (2014). Improving the care of children with advanced cancer by using an electronic patient-reported feedback intervention: Results from the PediQUEST randomized controlled trial. Journal of Clinical Oncology, 32(11), 1119–1126.PubMedPubMedCentralCrossRef Wolfe, J., Orellana, L., Cook, E. F., Ullrich, C., Kang, T., Geyer, J. R., et al. (2014). Improving the care of children with advanced cancer by using an electronic patient-reported feedback intervention: Results from the PediQUEST randomized controlled trial. Journal of Clinical Oncology, 32(11), 1119–1126.PubMedPubMedCentralCrossRef
55.
Zurück zum Zitat Hays, R. D., & Woolley, J. M. (2000). The concept of clinically meaningful difference in health-related quality-of-life research: How meaningful is it? PharmacoEconomics, 18(5), 419–423.PubMedCrossRef Hays, R. D., & Woolley, J. M. (2000). The concept of clinically meaningful difference in health-related quality-of-life research: How meaningful is it? PharmacoEconomics, 18(5), 419–423.PubMedCrossRef
56.
Zurück zum Zitat El Gaafary, M. (2016). A guide to PROMs methodology and selection criteria. In Y. El Miedany (Ed.), Patient reported outcome measures in rheumatic diseases (pp. 21–58). Cham: Springer.CrossRef El Gaafary, M. (2016). A guide to PROMs methodology and selection criteria. In Y. El Miedany (Ed.), Patient reported outcome measures in rheumatic diseases (pp. 21–58). Cham: Springer.CrossRef
59.
Zurück zum Zitat Dreyer, R. P., Jones, P. G., Kutty, S., et al. (2016). Quantifying clinical change: Discrepencies between patient’s and providers’ perspectives. Quality of Life Research, 25(9), 2213–2220.PubMedCrossRef Dreyer, R. P., Jones, P. G., Kutty, S., et al. (2016). Quantifying clinical change: Discrepencies between patient’s and providers’ perspectives. Quality of Life Research, 25(9), 2213–2220.PubMedCrossRef
60.
Zurück zum Zitat Hemmingsson, H., Ólafsdóttir, L. B., & Egilson, S. T. (2017). Agreements and disagreements between children and their parents in health-related assessments. Disability and Rehabilitation, 39(11), 1059–1072.PubMedCrossRef Hemmingsson, H., Ólafsdóttir, L. B., & Egilson, S. T. (2017). Agreements and disagreements between children and their parents in health-related assessments. Disability and Rehabilitation, 39(11), 1059–1072.PubMedCrossRef
Metadaten
Titel
A systematic review of randomised controlled trials evaluating the use of patient-reported outcome measures (PROMs)
verfasst von
S. Ishaque
J. Karnon
G. Chen
R. Nair
A. B. Salter
Publikationsdatum
03.10.2018
Verlag
Springer International Publishing
Erschienen in
Quality of Life Research / Ausgabe 3/2019
Print ISSN: 0962-9343
Elektronische ISSN: 1573-2649
DOI
https://doi.org/10.1007/s11136-018-2016-z

Weitere Artikel der Ausgabe 3/2019

Quality of Life Research 3/2019 Zur Ausgabe