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Performance of the PROMIS After Operative Interventions for Shoulder Instability

BACKGROUND: The Patient-Reported Outcomes Measurement Information System (PROMIS) was developed to capture patient-reported outcomes (PROs) in an efficient manner. Few studies have assessed this instrument postoperatively. PURPOSE: To compare the PROMIS Physical Function computer adaptive test (PROM...

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Autores principales: Hajewski, Christina J., Glass, Natalie A., Westermann, Robert W., Bollier, Matthew, Wolf, Brian R., Hettrich, Carolyn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6537071/
https://www.ncbi.nlm.nih.gov/pubmed/31205969
http://dx.doi.org/10.1177/2325967119846920
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author Hajewski, Christina J.
Glass, Natalie A.
Westermann, Robert W.
Bollier, Matthew
Wolf, Brian R.
Hettrich, Carolyn
author_facet Hajewski, Christina J.
Glass, Natalie A.
Westermann, Robert W.
Bollier, Matthew
Wolf, Brian R.
Hettrich, Carolyn
author_sort Hajewski, Christina J.
collection PubMed
description BACKGROUND: The Patient-Reported Outcomes Measurement Information System (PROMIS) was developed to capture patient-reported outcomes (PROs) in an efficient manner. Few studies have assessed this instrument postoperatively. PURPOSE: To compare the PROMIS Physical Function computer adaptive test (PROMIS PF CAT) and Upper Extremity (PROMIS UE) item bank to other previously validated PRO instruments and to evaluate ceiling and floor effects and construct validity responsiveness in patients who underwent operative interventions for shoulder instability. STUDY DESIGN: Cohort study (diagnosis); Level of evidence, 2. METHODS: A total of 72 patients who underwent operative interventions for shoulder instability completed the American Shoulder and Elbow Surgeons (ASES) assessment form, Marx shoulder activity scale (Marx), 36-Item Short Form Health Survey physical function (SF-36 PF) and general health (SF-36 GH), Western Ontario Shoulder Instability Index (WOSI), PROMIS PF CAT, and PROMIS UE before surgery and then at 6 weeks and 6 months postoperatively. Correlation coefficients were calculated among these tools. The effect size of change was also calculated for each tool at each time point. A total of 91 patients who had also undergone surgery for shoulder instability completed these PRO instruments 2 years postoperatively. The percentage of patients hitting the ceiling and floor effects of each of the PRO instruments was calculated at all time points. RESULTS: The PROMIS PF CAT demonstrated excellent-good correlation with the SF-36 PF at all postoperative time points (0.61 at 6 weeks, 0.68 at 6 months, and 0.64 at 2 years; P < .01 for all). The PROMIS UE showed excellent correlation with the ASES at 6 weeks postoperatively (0.73, P < .01). Both the PROMIS PF CAT and PROMIS UE demonstrated the ability to detect change after surgical interventions with a medium to large effect size. The PROMIS UE demonstrated a ceiling effect at 6 months (68.1%) and 2 years (67.0%) postoperatively. The PROMIS PF CAT demonstrated no ceiling effect at any time point. CONCLUSION: The PROMIS PF CAT demonstrated good to excellent correlation with other previously validated PRO instruments that assess physical function in patients with shoulder instability postoperatively. The PROMIS UE demonstrated good correlation with other PRO tools but had a significant ceiling effect and is not recommended for this patient population. Both tools demonstrated an ability to detect change after surgical interventions with a good effect size.
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spelling pubmed-65370712019-06-14 Performance of the PROMIS After Operative Interventions for Shoulder Instability Hajewski, Christina J. Glass, Natalie A. Westermann, Robert W. Bollier, Matthew Wolf, Brian R. Hettrich, Carolyn Orthop J Sports Med Article BACKGROUND: The Patient-Reported Outcomes Measurement Information System (PROMIS) was developed to capture patient-reported outcomes (PROs) in an efficient manner. Few studies have assessed this instrument postoperatively. PURPOSE: To compare the PROMIS Physical Function computer adaptive test (PROMIS PF CAT) and Upper Extremity (PROMIS UE) item bank to other previously validated PRO instruments and to evaluate ceiling and floor effects and construct validity responsiveness in patients who underwent operative interventions for shoulder instability. STUDY DESIGN: Cohort study (diagnosis); Level of evidence, 2. METHODS: A total of 72 patients who underwent operative interventions for shoulder instability completed the American Shoulder and Elbow Surgeons (ASES) assessment form, Marx shoulder activity scale (Marx), 36-Item Short Form Health Survey physical function (SF-36 PF) and general health (SF-36 GH), Western Ontario Shoulder Instability Index (WOSI), PROMIS PF CAT, and PROMIS UE before surgery and then at 6 weeks and 6 months postoperatively. Correlation coefficients were calculated among these tools. The effect size of change was also calculated for each tool at each time point. A total of 91 patients who had also undergone surgery for shoulder instability completed these PRO instruments 2 years postoperatively. The percentage of patients hitting the ceiling and floor effects of each of the PRO instruments was calculated at all time points. RESULTS: The PROMIS PF CAT demonstrated excellent-good correlation with the SF-36 PF at all postoperative time points (0.61 at 6 weeks, 0.68 at 6 months, and 0.64 at 2 years; P < .01 for all). The PROMIS UE showed excellent correlation with the ASES at 6 weeks postoperatively (0.73, P < .01). Both the PROMIS PF CAT and PROMIS UE demonstrated the ability to detect change after surgical interventions with a medium to large effect size. The PROMIS UE demonstrated a ceiling effect at 6 months (68.1%) and 2 years (67.0%) postoperatively. The PROMIS PF CAT demonstrated no ceiling effect at any time point. CONCLUSION: The PROMIS PF CAT demonstrated good to excellent correlation with other previously validated PRO instruments that assess physical function in patients with shoulder instability postoperatively. The PROMIS UE demonstrated good correlation with other PRO tools but had a significant ceiling effect and is not recommended for this patient population. Both tools demonstrated an ability to detect change after surgical interventions with a good effect size. SAGE Publications 2019-05-24 /pmc/articles/PMC6537071/ /pubmed/31205969 http://dx.doi.org/10.1177/2325967119846920 Text en © The Author(s) 2019 http://creativecommons.org/licenses/by-nc-nd/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 License (http://www.creativecommons.org/licenses/by-nc-nd/4.0/) which permits non-commercial use, reproduction and distribution of the work as published without adaptation or alteration, without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Article
Hajewski, Christina J.
Glass, Natalie A.
Westermann, Robert W.
Bollier, Matthew
Wolf, Brian R.
Hettrich, Carolyn
Performance of the PROMIS After Operative Interventions for Shoulder Instability
title Performance of the PROMIS After Operative Interventions for Shoulder Instability
title_full Performance of the PROMIS After Operative Interventions for Shoulder Instability
title_fullStr Performance of the PROMIS After Operative Interventions for Shoulder Instability
title_full_unstemmed Performance of the PROMIS After Operative Interventions for Shoulder Instability
title_short Performance of the PROMIS After Operative Interventions for Shoulder Instability
title_sort performance of the promis after operative interventions for shoulder instability
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6537071/
https://www.ncbi.nlm.nih.gov/pubmed/31205969
http://dx.doi.org/10.1177/2325967119846920
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