Hopelessness in Patients with Early-Stage Relapsing-Remitting Multiple Sclerosis.
depressive symptoms
hopelessness
relapsing-remitting multiple sclerosis
suicide
workplace difficulties
Journal
Patient preference and adherence
ISSN: 1177-889X
Titre abrégé: Patient Prefer Adherence
Pays: New Zealand
ID NLM: 101475748
Informations de publication
Date de publication:
2023
2023
Historique:
received:
04
03
2023
accepted:
25
05
2023
medline:
20
6
2023
pubmed:
20
6
2023
entrez:
20
6
2023
Statut:
epublish
Résumé
Hopelessness is a risk factor for depression and suicide. There is little information on this phenomenon among patients with relapsing-remitting multiple sclerosis (RRMS), one of the most common causes of disability and loss of autonomy in young adults. The aim of this study was to assess state hopelessness and its associated factors in early-stage RRMS. A multicenter, non-interventional study was conducted. Adult patients with a diagnosis of RRMS, a disease duration ≤ 3 years, and an Expanded Disability Status Scale (EDSS) score of 0-5.5 were included. The State-Trait Hopelessness Scale (STHS) was used to measure patients´ hopelessness. A battery of patient-reported and clinician-rated measurements was used to assess clinical status. A multivariate logistic regression analysis was conducted to determine the association between patients' characteristics and state hopelessness. A total of 189 patients were included. Mean age (standard deviation-SD) was 36.1 (9.4) years and 71.4% were female. Median disease duration (interquartile range-IQR) was 1.4 (0.7, 2.1) years. Symptom severity and disability were low with a median EDSS (IQR) score of 1.0 (0, 2.0). A proportion of 65.6% (n=124) of patients reported moderate-to-severe hopelessness. Hopelessness was associated with older age (p=0.035), depressive symptoms (p=<0.001), a threatening illness perception (p=0.001), and psychological and cognitive barriers to workplace performance (p=0.029) in the multivariate analysis after adjustment for confounders. Hopelessness was a common phenomenon in early-stage RRMS, even in a population with low physical disability. Identifying factors associated with hopelessness may be critical for implementing preventive strategies helping patients to adapt to the new situation and cope with the disease in the long term.
Sections du résumé
Background
UNASSIGNED
Hopelessness is a risk factor for depression and suicide. There is little information on this phenomenon among patients with relapsing-remitting multiple sclerosis (RRMS), one of the most common causes of disability and loss of autonomy in young adults. The aim of this study was to assess state hopelessness and its associated factors in early-stage RRMS.
Methods
UNASSIGNED
A multicenter, non-interventional study was conducted. Adult patients with a diagnosis of RRMS, a disease duration ≤ 3 years, and an Expanded Disability Status Scale (EDSS) score of 0-5.5 were included. The State-Trait Hopelessness Scale (STHS) was used to measure patients´ hopelessness. A battery of patient-reported and clinician-rated measurements was used to assess clinical status. A multivariate logistic regression analysis was conducted to determine the association between patients' characteristics and state hopelessness.
Results
UNASSIGNED
A total of 189 patients were included. Mean age (standard deviation-SD) was 36.1 (9.4) years and 71.4% were female. Median disease duration (interquartile range-IQR) was 1.4 (0.7, 2.1) years. Symptom severity and disability were low with a median EDSS (IQR) score of 1.0 (0, 2.0). A proportion of 65.6% (n=124) of patients reported moderate-to-severe hopelessness. Hopelessness was associated with older age (p=0.035), depressive symptoms (p=<0.001), a threatening illness perception (p=0.001), and psychological and cognitive barriers to workplace performance (p=0.029) in the multivariate analysis after adjustment for confounders.
Conclusion
UNASSIGNED
Hopelessness was a common phenomenon in early-stage RRMS, even in a population with low physical disability. Identifying factors associated with hopelessness may be critical for implementing preventive strategies helping patients to adapt to the new situation and cope with the disease in the long term.
Identifiants
pubmed: 37337517
doi: 10.2147/PPA.S411069
pii: 411069
pmc: PMC10277026
doi:
Types de publication
Journal Article
Langues
eng
Pagination
1431-1439Informations de copyright
© 2023 Sainz de la Maza et al.
Déclaration de conflit d'intérêts
Susana Sainz de la Maza received payment for lecturing or travel expenses from Merck, Biogen, Sanofi- Genzyme, Roche, and Novartis. Ana María Alonso Torres received compensation for consulting services from Biogen, BMS, Sanofi, Roche, Janssen and Novartis; and speaking honoraria from Biogen, BMS, Sanofi, Roche, Janssen, Merck, Almirall and Novartis. Ana B Caminero received courses and honoraria for her participation as speaker/meeting moderator/symposia organizer from Alter, Almirall, Bayer, Bial, Biogen, Bristol-Myers-Squibb, Lilly, Merck, Mylan, Novartis, Roche, Sanofi-Genzyme, Teva and UCB; and support to attend scientific meetings from Biogen, Bial, Merck-Serono, Novartis, Roche, Sanofi-Genzyme and Teva. Laura Borrega received compensation for consulting services, speaking honoraria and support to attend scientific meetings from Bayer, Celgene, Biogen, Genzyme, Merck, Novartis, Roche, Almirall and Teva. José L Sánchez-Menoyo received support to attend scientific meetings from Novartis, Merck, and Biogen; speaking honoraria from Biogen, Novartis, Sanofi, Merck, Almirall, Bayer and Teva; and participated in clinical trials from Biogen, Merck, and Roche. Francisco J Barrero-Hernández received compensation for consulting services and speaking honoraria from Almirall, Biogen, Genzyme, Merck, Novartis, Roche, Sanofi and Teva. Carmen Calles received compensation for consulting services, speaking honoraria and support to attend scientific meetings and courses from Merck, Teva, Sanofi-Genzyme, Novartis, Biogen, Roche, and Bristol-Myers-Squibb. Julio Dotor García-Soto received compensation for consulting services and speaking honoraria from Biogen, Novartis, Merck, UCB, Sanofi-Genzyme, Roche, Almirall and Teva. Laura Navarro-Cantó received compensations from Sanofi-Genzyme, Merk, Biogen and Roche. Eduardo Agüera-Morales received speaking honoraria from Roche, Novartis, Merck, Sanofi and Biogen. Moisés Garcés has received speaking honoraria from Biogen, Sanofi, Almirall and Novartis. Laura Gabaldón-Torres received speaking honoraria from Biogen, Novartis, Merck, Bayer, Sanofi-Genzyme, Almirall, Roche and Teva. Mariona Hervás participated in observational studies and received compensation for consulting services and speaking honoraria from Roche, Merck, Sanofi, Biogen, Novartis and Bayer. Jorge Maurino and Rocío Gómez-Ballesteros are employees of Roche Farma Spain. Tamara Castillo-Triviño reports personal fees from Almirall, Biogen, Bristol Myers Squibb, Janssen, Merck, Novartis, Roche, and Sanofi-Genzyme, outside the submitted work. The rest of the authors declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.
Références
Psychother Psychosom. 2018;87(3):190-192
pubmed: 29533948
Psychol Med. 2007 Jun;37(6):769-78
pubmed: 17202001
Health Psychol Rev. 2022 Sep;16(3):347-377
pubmed: 33461402
Mult Scler Relat Disord. 2020 Oct;45:102354
pubmed: 32629401
Curr Opin Psychol. 2018 Aug;22:38-43
pubmed: 30122276
Neurology. 1983 Nov;33(11):1444-52
pubmed: 6685237
Brain. 2001 May;124(Pt 5):962-73
pubmed: 11335698
Mult Scler. 2017 Apr;23(5):711-720
pubmed: 28206826
Int J Behav Med. 2022 Dec;29(6):691-704
pubmed: 35137362
J Int Neuropsychol Soc. 2015 Feb;21(2):156-68
pubmed: 25727930
JAMA. 2021 Feb 23;325(8):765-779
pubmed: 33620411
Mult Scler Relat Disord. 2022 May;61:103757
pubmed: 35367873
Mult Scler Relat Disord. 2019 Sep;34:83-90
pubmed: 31233959
Disabil Rehabil. 2014;36(8):635-41
pubmed: 23786346
Mult Scler Relat Disord. 2019 Jan;27:370-377
pubmed: 30476873
Mult Scler. 2022 Sep;28(10):1489-1490
pubmed: 35876470
West J Nurs Res. 2014 Apr;36(4):552-70
pubmed: 24122739
Int J Rehabil Res. 2010 Mar;33(1):26-33
pubmed: 19820406
Neurologia (Engl Ed). 2023 Jan-Feb;38(1):41-46
pubmed: 36167285
PLoS One. 2021 Oct 28;16(10):e0258740
pubmed: 34710124
J Cardiopulm Rehabil. 2006 May-Jun;26(3):152-9
pubmed: 16738453
Lancet Neurol. 2018 Feb;17(2):162-173
pubmed: 29275977
Mult Scler J Exp Transl Clin. 2019 Nov 09;5(4):2055217319887987
pubmed: 31741743
Mult Scler Relat Disord. 2022 Nov;67:104180
pubmed: 36130458
Mult Scler Relat Disord. 2022 Nov;67:104085
pubmed: 35977441
BMC Neurol. 2015 Mar 22;15:40
pubmed: 25886168
Mult Scler Relat Disord. 2020 Jun;41:102046
pubmed: 32179482
Arch Psychiatr Nurs. 2020 Apr;34(2):14-16
pubmed: 32248927
Acta Psychiatr Scand. 1983 Jun;67(6):361-70
pubmed: 6880820
Neurol Ther. 2020 Jun;9(1):173-179
pubmed: 31955391
J Pain Symptom Manage. 2019 Sep;58(3):437-444
pubmed: 31233844
Neurol Neuroimmunol Neuroinflamm. 2022 Aug 30;9(6):
pubmed: 36041861
Mult Scler. 2021 Sep;27(10):1477-1485
pubmed: 32613902
J Cardiovasc Nurs. 2020 Mar/Apr;35(2):126-130
pubmed: 32039949
Front Psychiatry. 2020 Jul 31;11:727
pubmed: 32848911
Ann Phys Rehabil Med. 2022 Jan;65(1):101491
pubmed: 33454397
Palliat Support Care. 2016 Jun;14(3):204-11
pubmed: 26155817
Occup Med (Lond). 2016 Jul;66(5):419-20
pubmed: 27317335
Medicine (Baltimore). 2019 Sep;98(38):e17184
pubmed: 31567960
Int J Psychiatry Med. 2002;32(2):155-65
pubmed: 12269596
Front Public Health. 2016 May 04;4:82
pubmed: 27200335
Int J MS Care. 2019 Sep-Oct;21(5):195-199
pubmed: 31680780
Neurology. 2013 Nov 19;81(21):1856-63
pubmed: 24174581