Self-management of immunomodulatory drug treatment in multiple myeloma patients.

adherence immunomodulatory drugs multiple myeloma questionnaire self-management side effects

Journal

European journal of cancer care
ISSN: 1365-2354
Titre abrégé: Eur J Cancer Care (Engl)
Pays: England
ID NLM: 9301979

Informations de publication

Date de publication:
Jan 2021
Historique:
received: 07 10 2019
revised: 10 07 2020
accepted: 14 10 2020
pubmed: 8 11 2020
medline: 30 9 2021
entrez: 7 11 2020
Statut: ppublish

Résumé

Immunomodulatory drugs (IMIDs: thalidomide, lenalidomide and pomalidomide) are widely used in patients with multiple myeloma (MM). The aim of our study was to validate a questionnaire to evaluate the self-capacity of MM patients to manage IMID treatment including side effects. We used a method adapted from the recommendations of the European Organisation for Research and Treatment of Cancer (EORTC) to validate a French questionnaire for patients with MM treated with IMIDs. The face validity was evaluated in 15 patients and the construct validity in 56 patients. For discriminant validity, two groups were constituted by gender and depending on whether they had a previous IMID treatment. The median questionnaire score was 11.33/16 (IQR 9.75-12.08) with a minimum of 5.2 and a maximum of 14.75. For discriminant validity, a statistically significant difference was observed for patient capacity to contact healthcare professionals in specific situations and drug intake in case of swallowing disorder. Convergent validity showed an acceptable reliability for the scores of the different questions. The questionnaire has shown to be a valid tool for the assessment of the adherence and side-effect management skills for MM patients with IMID treatment.

Identifiants

pubmed: 33159353
doi: 10.1111/ecc.13356
doi:

Substances chimiques

Pharmaceutical Preparations 0
Lenalidomide F0P408N6V4

Types de publication

Journal Article

Langues

eng

Pagination

e13356

Informations de copyright

© 2020 John Wiley & Sons Ltd.

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Auteurs

Amélie Cransac (A)

Department of Pharmacy, Dijon University Hospital, Dijon, France.
LNC-UMR1231, University of Burgundy and Franche Comté, Dijon, France.

Serge Aho (S)

Hospital Epidemiology and Infection Control Department, Dijon University Hospital, Dijon, France.

Edouard Cosme (E)

Department of Pharmacy, Dijon University Hospital, Dijon, France.

Marie-Lorraine Chretien (ML)

Department of Clinical Hematology, Dijon University Hospital, Dijon, France.
SAPHIIR-UMR 1231, University of Burgundy and Franche Comté, Dijon, France.

Camille Favennec (C)

Department of Clinical Hematology, Dijon University Hospital, Dijon, France.

Laure Schreder (L)

Oncology Coordination Center, Dijon University Hospital, Dijon, France.

Mérédith Boutet (M)

Department of Pharmacy, Dijon University Hospital, Dijon, France.

Pauline Gueneau (P)

Department of Pharmacy, Dijon University Hospital, Dijon, France.

Maurice Giroud (M)

LNC-UMR1231, University of Burgundy and Franche Comté, Dijon, France.
Department of Neurology, Dijon University Hospital, Dijon, France.

Denis Caillot (D)

Department of Clinical Hematology, Dijon University Hospital, Dijon, France.

Mathieu Boulin (M)

Department of Pharmacy, Dijon University Hospital, Dijon, France.
EPICAD LNC-UMR1231, University of Burgundy and Franche Comté, Dijon, France.

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