Skip to main content
main-content
Top

Tip

Swipe om te navigeren naar een ander artikel

Gepubliceerd in: Quality of Life Research 3/2018

05-10-2017

Establishing clinical severity for PROMIS® measures in adult patients with rheumatic diseases

Auteurs: Vivek Nagaraja, Constance Mara, Puja P. Khanna, Rajaie Namas, Amber Young, David A. Fox, Timothy Laing, William J. McCune, Carol Dodge, Debra Rizzo, Maha Almackenzie, Dinesh Khanna

Gepubliceerd in: Quality of Life Research | Uitgave 3/2018

Log in om toegang te krijgen
share
DELEN

Deel dit onderdeel of sectie (kopieer de link)

  • Optie A:
    Klik op de rechtermuisknop op de link en selecteer de optie “linkadres kopiëren”
  • Optie B:
    Deel de link per e-mail

Abstract

Purpose

Different patient-reported outcome (PRO) measures are used for rheumatic diseases (RD). The aims of this study are—(1) Identify PROMIS® domains most relevant to care of patients with RD, (2) Collect T-Score metrics in patients with RD, and (3) Identify clinically meaningful cut-points for these domains.

Methods

A convenience sample of RD patients was recruited consecutively during clinic visits, and asked to complete computer-adaptive tests on thirteen Patient-Reported Outcomes Measurement Information System (PROMIS®) instruments. Based on discussion with clinical providers, four measures were chosen to be relevant and actionable (from rheumatologists’ perspective) in RD patients. Data from RD patients were used to develop clinical vignettes across a range of symptom severity. Vignettes were created based on most likely item responses at different levels on the T-score metric (mean = 50; SD = 10) and anchored at 5-point intervals (0.5 SDs). Patients with RD (N = 9) and clinical providers (N = 10) participated as expert panelists in separate one-day meetings using a modified educational standard setting method.

Results

Four domains (physical function, pain interferences, sleep disturbance, depression) that are actionable at the point-of-care were selected. For all domains, patients endorsed cut-points at lower levels of impairment than providers by 0.5 to 1 SD (e.g., severe impairment in physical function was defined as a T-score of 35 by patients and 25 by providers).

Conclusions

We used a modified educational method to estimate clinically relevant cut-points to classify severity for PROMIS measures This allows for meaningful interpretation of PROMIS® measures in a clinical setting of RD population.
Bijlagen
Alleen toegankelijk voor geautoriseerde gebruikers
Literatuur
1.
go back to reference Khanna, D., Krishnan, E., Dewitt, E. M., Khanna, P. P., Spiegel, B., & Hays, R. D. (2011). The future of measuring patient-reported outcomes in rheumatology: Patient-Reported Outcomes Measurement Information System (PROMIS). Arthritis Care and Research, 63(Suppl 11), S486-490. Khanna, D., Krishnan, E., Dewitt, E. M., Khanna, P. P., Spiegel, B., & Hays, R. D. (2011). The future of measuring patient-reported outcomes in rheumatology: Patient-Reported Outcomes Measurement Information System (PROMIS). Arthritis Care and Research, 63(Suppl 11), S486-490.
2.
go back to reference Centers for Disease Control and Prevention, and Centers for Disease Control and Prevention. (2000). Measuring healthy days: Population assessment of health-related quality of life (pp. 4–6). Atlanta: CDC. Centers for Disease Control and Prevention, and Centers for Disease Control and Prevention. (2000). Measuring healthy days: Population assessment of health-related quality of life (pp. 4–6). Atlanta: CDC.
3.
go back to reference Devilliers, H., Amoura, Z., Besancenot, J. F., Bonnotte, B., Pasquali, J. L., Wahl, D., Maurier, F., Kaminsky, P., Pennaforte, J. L., Magy-Bertrand, N., Arnaud, L., Binquet, C., Guillemin, F., & Bonithon-Kopp, C. (2015). Responsiveness of the 36-item Short Form Health Survey and the Lupus Quality of Life questionnaire in SLE. Rheumatology, 54(5), 940–949. CrossRefPubMed Devilliers, H., Amoura, Z., Besancenot, J. F., Bonnotte, B., Pasquali, J. L., Wahl, D., Maurier, F., Kaminsky, P., Pennaforte, J. L., Magy-Bertrand, N., Arnaud, L., Binquet, C., Guillemin, F., & Bonithon-Kopp, C. (2015). Responsiveness of the 36-item Short Form Health Survey and the Lupus Quality of Life questionnaire in SLE. Rheumatology, 54(5), 940–949. CrossRefPubMed
4.
go back to reference Husted, J. A., Gladman, D. D., Farewell, V. T., & Cook, R. J. (2001). Health-related quality of life of patients with psoriatic arthritis: A comparison with patients with rheumatoid arthritis. Arthritis and Rheumatism, 45(2), 151–158. CrossRefPubMed Husted, J. A., Gladman, D. D., Farewell, V. T., & Cook, R. J. (2001). Health-related quality of life of patients with psoriatic arthritis: A comparison with patients with rheumatoid arthritis. Arthritis and Rheumatism, 45(2), 151–158. CrossRefPubMed
5.
go back to reference Uhlig, T., Loge, J. H., Kristiansen, I. S., & Kvien, T. K. (2007). Quantification of reduced health-related quality of life in patients with rheumatoid arthritis compared to the general population. The Journal of Rheumatology, 34(6), 1241–1247. PubMed Uhlig, T., Loge, J. H., Kristiansen, I. S., & Kvien, T. K. (2007). Quantification of reduced health-related quality of life in patients with rheumatoid arthritis compared to the general population. The Journal of Rheumatology, 34(6), 1241–1247. PubMed
6.
go back to reference Health, U. S. D. o., Human Services, F. D. A. C. f. D. E., Research, Health, U. S. D. o., Human Services, F. D. A. C. f. B. E., Research, Health, U. S. D. o., Human Services, F. D. A. C. f. D., & Radiological, H. (2006). Guidance for industry: patient-reported outcome measures: Use in medical product development to support labeling claims: Draft guidance. Health Quality Life Outcomes, 4, 79. CrossRef Health, U. S. D. o., Human Services, F. D. A. C. f. D. E., Research, Health, U. S. D. o., Human Services, F. D. A. C. f. B. E., Research, Health, U. S. D. o., Human Services, F. D. A. C. f. D., & Radiological, H. (2006). Guidance for industry: patient-reported outcome measures: Use in medical product development to support labeling claims: Draft guidance. Health Quality Life Outcomes, 4, 79. CrossRef
7.
go back to reference Singh, J. A., Saag, K. G., Bridges, S. L. Jr., Akl, E. A., Bannuru, R. R., Sullivan, M. C., Vaysbrot, E., McNaughton, C., Osani, M., Shmerling, R. H., Curtis, J. R., Furst, D. E., Parks, D., Kavanaugh, A., O’Dell, J., King, C., Leong, A., Matteson, E. L., Schousboe, J. T., Drevlow, B., Ginsberg, S., Grober, J., Clair, E. W., Tindall, E., Miller, A. S., & McAlindon, T. (2016). 2015 American College of Rheumatology guideline for the treatment of rheumatoid arthritis. Arthritis Rheumatology, 68(1), 1–26. CrossRefPubMed Singh, J. A., Saag, K. G., Bridges, S. L. Jr., Akl, E. A., Bannuru, R. R., Sullivan, M. C., Vaysbrot, E., McNaughton, C., Osani, M., Shmerling, R. H., Curtis, J. R., Furst, D. E., Parks, D., Kavanaugh, A., O’Dell, J., King, C., Leong, A., Matteson, E. L., Schousboe, J. T., Drevlow, B., Ginsberg, S., Grober, J., Clair, E. W., Tindall, E., Miller, A. S., & McAlindon, T. (2016). 2015 American College of Rheumatology guideline for the treatment of rheumatoid arthritis. Arthritis Rheumatology, 68(1), 1–26. CrossRefPubMed
8.
go back to reference Witter, J. P. (2016). The Promise Of Patient-Reported Outcomes Measurement Information System-turning theory into reality: A uniform approach to patient-reported outcomes across rheumatic diseases. Rheumatic Diseases Clinics of North America, 42(2), 377–394. CrossRefPubMed Witter, J. P. (2016). The Promise Of Patient-Reported Outcomes Measurement Information System-turning theory into reality: A uniform approach to patient-reported outcomes across rheumatic diseases. Rheumatic Diseases Clinics of North America, 42(2), 377–394. CrossRefPubMed
9.
go back to reference Cella, D., Yount, S., Rothrock, N., Gershon, R., Cook, K., Reeve, B., Ader, D., Fries, J. F., Bruce, B., Rose, M., & Group, P. C. (2007). The Patient-Reported Outcomes Measurement Information System (PROMIS): progress of an NIH Roadmap cooperative group during its first two years. Medical Care, 45(5 Suppl 1), S3–S11. CrossRefPubMedPubMedCentral Cella, D., Yount, S., Rothrock, N., Gershon, R., Cook, K., Reeve, B., Ader, D., Fries, J. F., Bruce, B., Rose, M., & Group, P. C. (2007). The Patient-Reported Outcomes Measurement Information System (PROMIS): progress of an NIH Roadmap cooperative group during its first two years. Medical Care, 45(5 Suppl 1), S3–S11. CrossRefPubMedPubMedCentral
10.
go back to reference Reeve, B. B., Hays, R. D., Bjorner, J. B., Cook, K. F., Crane, P. K., Teresi, J. A., Thissen, D., Revicki, D. A., Weiss, D. J., Hambleton, R. K., Liu, H., Gershon, R., Reise, S. P., Lai, J. S., Cella, D., & Group, P. C. (2007). Psychometric evaluation and calibration of health-related quality of life item banks: plans for the Patient-Reported Outcomes Measurement Information System (PROMIS). Medical Care, 45(5 Suppl 1), S22-31. PubMed Reeve, B. B., Hays, R. D., Bjorner, J. B., Cook, K. F., Crane, P. K., Teresi, J. A., Thissen, D., Revicki, D. A., Weiss, D. J., Hambleton, R. K., Liu, H., Gershon, R., Reise, S. P., Lai, J. S., Cella, D., & Group, P. C. (2007). Psychometric evaluation and calibration of health-related quality of life item banks: plans for the Patient-Reported Outcomes Measurement Information System (PROMIS). Medical Care, 45(5 Suppl 1), S22-31. PubMed
11.
go back to reference Hays, R. D., Liu, H., Spritzer, K., & Cella, D. (2007). Item response theory analyses of physical functioning items in the medical outcomes study. Medical Care, 45(5 Suppl 1), S32–S38. CrossRefPubMed Hays, R. D., Liu, H., Spritzer, K., & Cella, D. (2007). Item response theory analyses of physical functioning items in the medical outcomes study. Medical Care, 45(5 Suppl 1), S32–S38. CrossRefPubMed
12.
go back to reference Khullar, O. V., Rajaei, M. H., Force, S. D., Binongo, J. N., Lasanajak, Y., Robertson, S., Pickens, A., Sancheti, M. S., Lipscomb, J., Gillespie, T. W., & Fernandez, F. G. (2017). Pilot study to integrate patient reported outcomes after lung cancer operations into the Society of Thoracic Surgeons Database. The Annals of Thoracic Surgery, 104(1), 245–253. CrossRefPubMed Khullar, O. V., Rajaei, M. H., Force, S. D., Binongo, J. N., Lasanajak, Y., Robertson, S., Pickens, A., Sancheti, M. S., Lipscomb, J., Gillespie, T. W., & Fernandez, F. G. (2017). Pilot study to integrate patient reported outcomes after lung cancer operations into the Society of Thoracic Surgeons Database. The Annals of Thoracic Surgery, 104(1), 245–253. CrossRefPubMed
13.
go back to reference Karantonis, A., & Sireci, S. G. (2006). The bookmark standard-setting method: A literature review. Educational Measurement: Issues and Practice, 25(1), 4–12. CrossRef Karantonis, A., & Sireci, S. G. (2006). The bookmark standard-setting method: A literature review. Educational Measurement: Issues and Practice, 25(1), 4–12. CrossRef
14.
go back to reference Cook, K. F., Victorson, D. E., Cella, D., Schalet, B. D., & Miller, D. (2015). Creating meaningful cut-scores for Neuro-QOL measures of fatigue, physical functioning, and sleep disturbance using standard setting with patients and providers. Quality of life research, 24(3), 575–589. CrossRefPubMed Cook, K. F., Victorson, D. E., Cella, D., Schalet, B. D., & Miller, D. (2015). Creating meaningful cut-scores for Neuro-QOL measures of fatigue, physical functioning, and sleep disturbance using standard setting with patients and providers. Quality of life research, 24(3), 575–589. CrossRefPubMed
15.
go back to reference Cella, D., Choi, S., Garcia, S., Cook, K. F., Rosenbloom, S., Lai, J. S., Tatum, D. S., & Gershon, R. (2014). Setting standards for severity of common symptoms in oncology using the PROMIS item banks and expert judgment. Quality of Life Research, 23(10), 2651–2661. CrossRefPubMedPubMedCentral Cella, D., Choi, S., Garcia, S., Cook, K. F., Rosenbloom, S., Lai, J. S., Tatum, D. S., & Gershon, R. (2014). Setting standards for severity of common symptoms in oncology using the PROMIS item banks and expert judgment. Quality of Life Research, 23(10), 2651–2661. CrossRefPubMedPubMedCentral
16.
go back to reference Morgan, E. M., Mara, C. A., Huang, B., Barnett, K., Carle, A. C., Farrell, J. E., & Cook, K. F. (2017). Establishing clinical meaning and defining important differences for Patient-Reported Outcomes Measurement Information System (PROMIS(R)) measures in juvenile idiopathic arthritis using standard setting with patients, parents, and providers. Quality of Life Research, 26(3), 565–586. CrossRefPubMed Morgan, E. M., Mara, C. A., Huang, B., Barnett, K., Carle, A. C., Farrell, J. E., & Cook, K. F. (2017). Establishing clinical meaning and defining important differences for Patient-Reported Outcomes Measurement Information System (PROMIS(R)) measures in juvenile idiopathic arthritis using standard setting with patients, parents, and providers. Quality of Life Research, 26(3), 565–586. CrossRefPubMed
18.
go back to reference Cella, D., Riley, W., Stone, A., Rothrock, N., Reeve, B., Yount, S., Amtmann, D., Bode, R., Buysse, D., Choi, S., Cook, K., Devellis, R., DeWalt, D., Fries, J. F., Gershon, R., Hahn, E. A., Lai, J. S., Pilkonis, P., Revicki, D., Rose, M., Weinfurt, K., Hays, R., & Group, P. C. (2010). The Patient-Reported Outcomes Measurement Information System (PROMIS) developed and tested its first wave of adult self-reported health outcome item banks: 2005–2008. Journal of Clinical Epidemiology, 63(11), 1179–1194. CrossRefPubMedPubMedCentral Cella, D., Riley, W., Stone, A., Rothrock, N., Reeve, B., Yount, S., Amtmann, D., Bode, R., Buysse, D., Choi, S., Cook, K., Devellis, R., DeWalt, D., Fries, J. F., Gershon, R., Hahn, E. A., Lai, J. S., Pilkonis, P., Revicki, D., Rose, M., Weinfurt, K., Hays, R., & Group, P. C. (2010). The Patient-Reported Outcomes Measurement Information System (PROMIS) developed and tested its first wave of adult self-reported health outcome item banks: 2005–2008. Journal of Clinical Epidemiology, 63(11), 1179–1194. CrossRefPubMedPubMedCentral
19.
go back to reference Idzerda, L., Rader, T., Tugwell, P., & Boers, M. (2014). Can we decide which outcomes should be measured in every clinical trial? A scoping review of the existing conceptual frameworks and processes to develop core outcome sets. The Journal of rheumatology, 41(5), 986–993. CrossRefPubMed Idzerda, L., Rader, T., Tugwell, P., & Boers, M. (2014). Can we decide which outcomes should be measured in every clinical trial? A scoping review of the existing conceptual frameworks and processes to develop core outcome sets. The Journal of rheumatology, 41(5), 986–993. CrossRefPubMed
20.
go back to reference Bartlett, S. J., Orbai, A. M., Duncan, T., DeLeon, E., Ruffing, V., Clegg-Smith, K., & Bingham, C. O. 3rd. (2015). Reliability and validity of selected PROMIS measures in people with rheumatoid arthritis. PLoS ONE, 10(9), e0138543. CrossRefPubMedPubMedCentral Bartlett, S. J., Orbai, A. M., Duncan, T., DeLeon, E., Ruffing, V., Clegg-Smith, K., & Bingham, C. O. 3rd. (2015). Reliability and validity of selected PROMIS measures in people with rheumatoid arthritis. PLoS ONE, 10(9), e0138543. CrossRefPubMedPubMedCentral
21.
go back to reference Bartlett, S. J., Hewlett, S., Bingham, C. O. 3rd, Woodworth, T. G., Alten, R., Pohl, C., Choy, E. H., Sanderson, T., Boonen, A., Bykerk, V., Leong, A. L., Strand, V., Furst, D. E., Christensen, R., & Group, O. R. F. W. (2012). Identifying core domains to assess flare in rheumatoid arthritis: an OMERACT international patient and provider combined Delphi consensus. Annals of the Rheumatic Diseases, 71(11), 1855–1860. CrossRefPubMed Bartlett, S. J., Hewlett, S., Bingham, C. O. 3rd, Woodworth, T. G., Alten, R., Pohl, C., Choy, E. H., Sanderson, T., Boonen, A., Bykerk, V., Leong, A. L., Strand, V., Furst, D. E., Christensen, R., & Group, O. R. F. W. (2012). Identifying core domains to assess flare in rheumatoid arthritis: an OMERACT international patient and provider combined Delphi consensus. Annals of the Rheumatic Diseases, 71(11), 1855–1860. CrossRefPubMed
22.
go back to reference Mahieu, M. A., Ahn, G. E., Chmiel, J. S., Dunlop, D. D., Helenowski, I. B., Semanik, P., Song, J., Yount, S., Chang, R. W., & Ramsey-Goldman, R. (2016). Fatigue, patient reported outcomes, and objective measurement of physical activity in systemic lupus erythematosus. Lupus, 25, 1190–1199. CrossRefPubMedPubMedCentral Mahieu, M. A., Ahn, G. E., Chmiel, J. S., Dunlop, D. D., Helenowski, I. B., Semanik, P., Song, J., Yount, S., Chang, R. W., & Ramsey-Goldman, R. (2016). Fatigue, patient reported outcomes, and objective measurement of physical activity in systemic lupus erythematosus. Lupus, 25, 1190–1199. CrossRefPubMedPubMedCentral
23.
go back to reference Jensen, R. E., Rothrock, N. E., DeWitt, E. M., Spiegel, B., Tucker, C. A., Crane, H. M., Forrest, C. B., Patrick, D. L., Fredericksen, R., Shulman, L. M., Cella, D., & Crane, P. K. (2015). The role of technical advances in the adoption and integration of patient-reported outcomes in clinical care. Medical Care, 53(2), 153–159. CrossRefPubMedPubMedCentral Jensen, R. E., Rothrock, N. E., DeWitt, E. M., Spiegel, B., Tucker, C. A., Crane, H. M., Forrest, C. B., Patrick, D. L., Fredericksen, R., Shulman, L. M., Cella, D., & Crane, P. K. (2015). The role of technical advances in the adoption and integration of patient-reported outcomes in clinical care. Medical Care, 53(2), 153–159. CrossRefPubMedPubMedCentral
24.
go back to reference Basu, N., Jones, G. T., Fluck, N., MacDonald, A. G., Pang, D., Dospinescu, P., Reid, D. M., & Macfarlane, G. J. (2010). Fatigue: A principal contributor to impaired quality of life in ANCA-associated vasculitis. Rheumatology, 49(7), 1383–1390. CrossRefPubMedPubMedCentral Basu, N., Jones, G. T., Fluck, N., MacDonald, A. G., Pang, D., Dospinescu, P., Reid, D. M., & Macfarlane, G. J. (2010). Fatigue: A principal contributor to impaired quality of life in ANCA-associated vasculitis. Rheumatology, 49(7), 1383–1390. CrossRefPubMedPubMedCentral
25.
go back to reference Druce, K. L., Jones, G. T., Macfarlane, G. J., & Basu, N. (2015). Patients receiving anti-TNF therapies experience clinically important improvements in RA-related fatigue: Results from the British Society for Rheumatology Biologics Register for Rheumatoid Arthritis. Rheumatology, 54(6), 964–971. CrossRefPubMed Druce, K. L., Jones, G. T., Macfarlane, G. J., & Basu, N. (2015). Patients receiving anti-TNF therapies experience clinically important improvements in RA-related fatigue: Results from the British Society for Rheumatology Biologics Register for Rheumatoid Arthritis. Rheumatology, 54(6), 964–971. CrossRefPubMed
26.
go back to reference Lai, J. S., Beaumont, J. L., Jensen, S. E., Kaiser, K., Van Brunt, D. L., Kao, A. H., & Chen, S. Y. (2017). An evaluation of health-related quality of life in patients with systemic lupus erythematosus using PROMIS and Neuro-QoL. Clinical Rheumatology, 36(3), 555–562. CrossRefPubMed Lai, J. S., Beaumont, J. L., Jensen, S. E., Kaiser, K., Van Brunt, D. L., Kao, A. H., & Chen, S. Y. (2017). An evaluation of health-related quality of life in patients with systemic lupus erythematosus using PROMIS and Neuro-QoL. Clinical Rheumatology, 36(3), 555–562. CrossRefPubMed
27.
go back to reference Druce, K. L., Jones, G. T., Macfarlane, G. J., & Basu, N. (2015). Determining pathways to improvements in fatigue in rheumatoid arthritis: Results from the British Society for Rheumatology Biologics Register for Rheumatoid Arthritis. Arthritis Rheumatology, 67(9), 2303–2310. CrossRefPubMed Druce, K. L., Jones, G. T., Macfarlane, G. J., & Basu, N. (2015). Determining pathways to improvements in fatigue in rheumatoid arthritis: Results from the British Society for Rheumatology Biologics Register for Rheumatoid Arthritis. Arthritis Rheumatology, 67(9), 2303–2310. CrossRefPubMed
28.
go back to reference Hifinger, M., Putrik, P., Ramiro, S., Keszei, A. P., Hmamouchi, I., Dougados, M., Gossec, L., & Boonen, A. (2016). In rheumatoid arthritis, country of residence has an important influence on fatigue: Results from the multinational COMORA study. Rheumatology, 55(4), 735–744. CrossRefPubMed Hifinger, M., Putrik, P., Ramiro, S., Keszei, A. P., Hmamouchi, I., Dougados, M., Gossec, L., & Boonen, A. (2016). In rheumatoid arthritis, country of residence has an important influence on fatigue: Results from the multinational COMORA study. Rheumatology, 55(4), 735–744. CrossRefPubMed
29.
go back to reference Wagner, L. I., Spiegel, D., & Pearman, T. (2013). Using the science of psychosocial care to implement the new american college of surgeons commission on cancer distress screening standard. Journal of the National Comprehensive Cancer Network, 11(2), 214–221. CrossRefPubMed Wagner, L. I., Spiegel, D., & Pearman, T. (2013). Using the science of psychosocial care to implement the new american college of surgeons commission on cancer distress screening standard. Journal of the National Comprehensive Cancer Network, 11(2), 214–221. CrossRefPubMed
30.
go back to reference Snyder, C. F., Smith, K. C., Bantug, E. T., Tolbert, E. E., Blackford, A. L., Brundage, M. D., & the PRO Data Presentation Stakeholder Advisory Board. (2017). What do these scores mean? Presenting patient-reported outcomes data to patients and clinicians to improve interpretability. Cancer, 123(10), 1848–1859. CrossRefPubMedPubMedCentral Snyder, C. F., Smith, K. C., Bantug, E. T., Tolbert, E. E., Blackford, A. L., Brundage, M. D., & the PRO Data Presentation Stakeholder Advisory Board. (2017). What do these scores mean? Presenting patient-reported outcomes data to patients and clinicians to improve interpretability. Cancer, 123(10), 1848–1859. CrossRefPubMedPubMedCentral
31.
go back to reference Basch, E., Iasonos, A., McDonough, T., Barz, A., Culkin, A., Kris, M. G., Scher, H. I., & Schrag, D. (2006). Patient versus clinician symptom reporting using the National Cancer Institute Common Terminology Criteria for Adverse Events: Results of a questionnaire-based study. The Lancet Oncology, 7(11), 903–909. CrossRefPubMed Basch, E., Iasonos, A., McDonough, T., Barz, A., Culkin, A., Kris, M. G., Scher, H. I., & Schrag, D. (2006). Patient versus clinician symptom reporting using the National Cancer Institute Common Terminology Criteria for Adverse Events: Results of a questionnaire-based study. The Lancet Oncology, 7(11), 903–909. CrossRefPubMed
Metagegevens
Titel
Establishing clinical severity for PROMIS® measures in adult patients with rheumatic diseases
Auteurs
Vivek Nagaraja
Constance Mara
Puja P. Khanna
Rajaie Namas
Amber Young
David A. Fox
Timothy Laing
William J. McCune
Carol Dodge
Debra Rizzo
Maha Almackenzie
Dinesh Khanna
Publicatiedatum
05-10-2017
Uitgeverij
Springer International Publishing
Gepubliceerd in
Quality of Life Research / Uitgave 3/2018
Print ISSN: 0962-9343
Elektronisch ISSN: 1573-2649
DOI
https://doi.org/10.1007/s11136-017-1709-z