Cargando…
Raising the standards of patient‐centered outcomes research in myelodysplastic syndromes: Clinical utility and validation of the subscales of the QUALMS from the MDS‐RIGHT project
BACKGROUND: Clinical decision‐making for patients with myelodysplastic syndromes (MDS) is challenging, and both disease and treatment effects heavily impact health‐related quality of life (HRQoL) of these patients. Therefore, disease‐specific HRQoL measures can be critical to harness the patient voi...
Autores principales: | , , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10067097/ https://www.ncbi.nlm.nih.gov/pubmed/36533415 http://dx.doi.org/10.1002/cam4.5487 |
_version_ | 1785018395719106560 |
---|---|
author | Efficace, Fabio Koinig, Karin Cottone, Francesco Bowen, David Mittelman, Moshe Sommer, Kathrin Langemeijer, Saskia Culligan, Dominic Filanovsky, Kalman Storck, Michael Smith, Alexandra van Marrewijk, Corine Dugas, Martin Stojkov, Igor Siebert, Uwe de Witte, Theo Stauder, Reinhard |
author_facet | Efficace, Fabio Koinig, Karin Cottone, Francesco Bowen, David Mittelman, Moshe Sommer, Kathrin Langemeijer, Saskia Culligan, Dominic Filanovsky, Kalman Storck, Michael Smith, Alexandra van Marrewijk, Corine Dugas, Martin Stojkov, Igor Siebert, Uwe de Witte, Theo Stauder, Reinhard |
author_sort | Efficace, Fabio |
collection | PubMed |
description | BACKGROUND: Clinical decision‐making for patients with myelodysplastic syndromes (MDS) is challenging, and both disease and treatment effects heavily impact health‐related quality of life (HRQoL) of these patients. Therefore, disease‐specific HRQoL measures can be critical to harness the patient voice in MDS research. METHODS: We report a prospective international validation study of the Quality of Life in Myelodysplasia Scale (QUALMS) with a main focus on providing information on the psychometric characteristics of its three subscales: physical burden (QUALMS‐P), emotional burden (QUALMS‐E), and benefit finding (QUALMS‐BF). The analysis is based on patients enrolled from three European countries and Israel, participating to the MDS‐RIGHT Project. The scale structure and psychometric properties of the QUALMS were assessed. RESULTS: Overall, 270 patients with a median age of 74 years were analyzed and the majority of them (60.3%) had a low MDS‐Comorbidity Index score. Results of the confirmatory factor analysis supported the underlying scale structure of the QUALMS, which, in addition to a total score, includes three subscales: QUALMS‐P, QUALMS‐E, and the QUALMS‐BF. The QUALMS‐P exhibited the highest Cronbach's alpha coefficients. Discriminant validity analysis indicated good results with the QUALMS‐P and QUALMS‐E distinguishing between patients with different performance status, comorbidity, anemia, and transfusion dependency status. No floor and ceiling effects were observed. Responsiveness to change analysis supported the validity of the measure. Patients with a hemoglobin (Hb) level of <11 g/dL at study entry, who subsequently showed an improvement in their Hb levels, also reported a mean score change of 9 and 8 points (scales ranging between 0 and 100) in the expected direction of the QUALMS‐E and QUALMS‐P, respectively. CONCLUSIONS: Our study provides additional validation data on the QUALMS from the international MDS‐RIGHT Project. The use of this disease‐specific HRQoL measure may contribute to raise quality standards of patient‐centered outcomes research in MDS. |
format | Online Article Text |
id | pubmed-10067097 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100670972023-04-03 Raising the standards of patient‐centered outcomes research in myelodysplastic syndromes: Clinical utility and validation of the subscales of the QUALMS from the MDS‐RIGHT project Efficace, Fabio Koinig, Karin Cottone, Francesco Bowen, David Mittelman, Moshe Sommer, Kathrin Langemeijer, Saskia Culligan, Dominic Filanovsky, Kalman Storck, Michael Smith, Alexandra van Marrewijk, Corine Dugas, Martin Stojkov, Igor Siebert, Uwe de Witte, Theo Stauder, Reinhard Cancer Med RESEARCH ARTICLES BACKGROUND: Clinical decision‐making for patients with myelodysplastic syndromes (MDS) is challenging, and both disease and treatment effects heavily impact health‐related quality of life (HRQoL) of these patients. Therefore, disease‐specific HRQoL measures can be critical to harness the patient voice in MDS research. METHODS: We report a prospective international validation study of the Quality of Life in Myelodysplasia Scale (QUALMS) with a main focus on providing information on the psychometric characteristics of its three subscales: physical burden (QUALMS‐P), emotional burden (QUALMS‐E), and benefit finding (QUALMS‐BF). The analysis is based on patients enrolled from three European countries and Israel, participating to the MDS‐RIGHT Project. The scale structure and psychometric properties of the QUALMS were assessed. RESULTS: Overall, 270 patients with a median age of 74 years were analyzed and the majority of them (60.3%) had a low MDS‐Comorbidity Index score. Results of the confirmatory factor analysis supported the underlying scale structure of the QUALMS, which, in addition to a total score, includes three subscales: QUALMS‐P, QUALMS‐E, and the QUALMS‐BF. The QUALMS‐P exhibited the highest Cronbach's alpha coefficients. Discriminant validity analysis indicated good results with the QUALMS‐P and QUALMS‐E distinguishing between patients with different performance status, comorbidity, anemia, and transfusion dependency status. No floor and ceiling effects were observed. Responsiveness to change analysis supported the validity of the measure. Patients with a hemoglobin (Hb) level of <11 g/dL at study entry, who subsequently showed an improvement in their Hb levels, also reported a mean score change of 9 and 8 points (scales ranging between 0 and 100) in the expected direction of the QUALMS‐E and QUALMS‐P, respectively. CONCLUSIONS: Our study provides additional validation data on the QUALMS from the international MDS‐RIGHT Project. The use of this disease‐specific HRQoL measure may contribute to raise quality standards of patient‐centered outcomes research in MDS. John Wiley and Sons Inc. 2022-12-19 /pmc/articles/PMC10067097/ /pubmed/36533415 http://dx.doi.org/10.1002/cam4.5487 Text en © 2022 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | RESEARCH ARTICLES Efficace, Fabio Koinig, Karin Cottone, Francesco Bowen, David Mittelman, Moshe Sommer, Kathrin Langemeijer, Saskia Culligan, Dominic Filanovsky, Kalman Storck, Michael Smith, Alexandra van Marrewijk, Corine Dugas, Martin Stojkov, Igor Siebert, Uwe de Witte, Theo Stauder, Reinhard Raising the standards of patient‐centered outcomes research in myelodysplastic syndromes: Clinical utility and validation of the subscales of the QUALMS from the MDS‐RIGHT project |
title | Raising the standards of patient‐centered outcomes research in myelodysplastic syndromes: Clinical utility and validation of the subscales of the QUALMS from the MDS‐RIGHT project |
title_full | Raising the standards of patient‐centered outcomes research in myelodysplastic syndromes: Clinical utility and validation of the subscales of the QUALMS from the MDS‐RIGHT project |
title_fullStr | Raising the standards of patient‐centered outcomes research in myelodysplastic syndromes: Clinical utility and validation of the subscales of the QUALMS from the MDS‐RIGHT project |
title_full_unstemmed | Raising the standards of patient‐centered outcomes research in myelodysplastic syndromes: Clinical utility and validation of the subscales of the QUALMS from the MDS‐RIGHT project |
title_short | Raising the standards of patient‐centered outcomes research in myelodysplastic syndromes: Clinical utility and validation of the subscales of the QUALMS from the MDS‐RIGHT project |
title_sort | raising the standards of patient‐centered outcomes research in myelodysplastic syndromes: clinical utility and validation of the subscales of the qualms from the mds‐right project |
topic | RESEARCH ARTICLES |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10067097/ https://www.ncbi.nlm.nih.gov/pubmed/36533415 http://dx.doi.org/10.1002/cam4.5487 |
work_keys_str_mv | AT efficacefabio raisingthestandardsofpatientcenteredoutcomesresearchinmyelodysplasticsyndromesclinicalutilityandvalidationofthesubscalesofthequalmsfromthemdsrightproject AT koinigkarin raisingthestandardsofpatientcenteredoutcomesresearchinmyelodysplasticsyndromesclinicalutilityandvalidationofthesubscalesofthequalmsfromthemdsrightproject AT cottonefrancesco raisingthestandardsofpatientcenteredoutcomesresearchinmyelodysplasticsyndromesclinicalutilityandvalidationofthesubscalesofthequalmsfromthemdsrightproject AT bowendavid raisingthestandardsofpatientcenteredoutcomesresearchinmyelodysplasticsyndromesclinicalutilityandvalidationofthesubscalesofthequalmsfromthemdsrightproject AT mittelmanmoshe raisingthestandardsofpatientcenteredoutcomesresearchinmyelodysplasticsyndromesclinicalutilityandvalidationofthesubscalesofthequalmsfromthemdsrightproject AT sommerkathrin raisingthestandardsofpatientcenteredoutcomesresearchinmyelodysplasticsyndromesclinicalutilityandvalidationofthesubscalesofthequalmsfromthemdsrightproject AT langemeijersaskia raisingthestandardsofpatientcenteredoutcomesresearchinmyelodysplasticsyndromesclinicalutilityandvalidationofthesubscalesofthequalmsfromthemdsrightproject AT culligandominic raisingthestandardsofpatientcenteredoutcomesresearchinmyelodysplasticsyndromesclinicalutilityandvalidationofthesubscalesofthequalmsfromthemdsrightproject AT filanovskykalman raisingthestandardsofpatientcenteredoutcomesresearchinmyelodysplasticsyndromesclinicalutilityandvalidationofthesubscalesofthequalmsfromthemdsrightproject AT storckmichael raisingthestandardsofpatientcenteredoutcomesresearchinmyelodysplasticsyndromesclinicalutilityandvalidationofthesubscalesofthequalmsfromthemdsrightproject AT smithalexandra raisingthestandardsofpatientcenteredoutcomesresearchinmyelodysplasticsyndromesclinicalutilityandvalidationofthesubscalesofthequalmsfromthemdsrightproject AT vanmarrewijkcorine raisingthestandardsofpatientcenteredoutcomesresearchinmyelodysplasticsyndromesclinicalutilityandvalidationofthesubscalesofthequalmsfromthemdsrightproject AT dugasmartin raisingthestandardsofpatientcenteredoutcomesresearchinmyelodysplasticsyndromesclinicalutilityandvalidationofthesubscalesofthequalmsfromthemdsrightproject AT stojkovigor raisingthestandardsofpatientcenteredoutcomesresearchinmyelodysplasticsyndromesclinicalutilityandvalidationofthesubscalesofthequalmsfromthemdsrightproject AT siebertuwe raisingthestandardsofpatientcenteredoutcomesresearchinmyelodysplasticsyndromesclinicalutilityandvalidationofthesubscalesofthequalmsfromthemdsrightproject AT dewittetheo raisingthestandardsofpatientcenteredoutcomesresearchinmyelodysplasticsyndromesclinicalutilityandvalidationofthesubscalesofthequalmsfromthemdsrightproject AT stauderreinhard raisingthestandardsofpatientcenteredoutcomesresearchinmyelodysplasticsyndromesclinicalutilityandvalidationofthesubscalesofthequalmsfromthemdsrightproject |