Assessment of Quality of Life in Multiple Sclerosis through the MSQOL-54 and its relation to the health of the caregiver

Authors

DOI: https://doi.org/10.6018/eglobal.474161
Keywords: multiple sclerosis, quality of life, health-related quality of life, caregivers, mental health

Abstract

Objective: The aim of the present study was to evaluate the health-related quality of life (HRQoL) in patients with Multiple Sclerosis (MS) through the MSQOL-54 questionnaire and to analyse its relationship with the health of primary caregivers through the GHQ-12 questionnaire and a questionnaire on self-perceived physical health.
Materials and Methods: A total of 115 subjects diagnosed with MS and 79 primary caregivers were evaluated.
Results: The results obtained show the significance of effects on HRQoL of patients with MS and its relationship to the health of primary caregivers. Significant relationships were found between the physical and mental health of the person with MS and an increased number of illnesses, poorer mental health and lower self-perception of health in the caregiver.
Conclusions: The results obtained point to the significant impairment of the HRQoL of people with MS, and its direct relationship with the health of primary caregivers.

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References

Stenager, E.N., Stenager E., Koch-Henricksen, N., Bronnum-Hansen, H., Hyllested, K., Jensen K.,…Bille-Brahe, U. (1992). Suicide and multiple sclerosis: an epidemiological investigation. Journal of Neurology, Neurosurgery & Psychiatry, 55(7), 542-545. http://dx.doi.org/10.1136/jnnp.55.7.542

Mitchell, A.J., Benito-León, J., González, J.M., & Rivera-Navarro, J. (2005). Quality of life and its assessment in multiple sclerosis: integrating physical and psychological components of wellbeing. The Lancet Neurology, 4(9), 556-566. http://dx.doi.org/10.1016/s1474-4422(05)70166-6

Schwartzman, L. (2003). Calidad de vida relacionada con la salud: Aspectos conceptuales. Ciencia y Enfermería, 9(2), 9-21.http://dx.doi.org/10.4067/s0717-95532003000200002

Testa, M., & Simonson, D.C. (1996). Assessment of Quality-of-Life Outcomes. New England Journal of Medicine, 334(13), 835-840. http://dx.doi.org/10.1056/nejm199603283341306

Hernández, M.A. (2000). Tratamiento de la esclerosis múltiple y calidad de vida. Revista de Neurología, 30(12), 1242-1245. https://www.neurologia.com/articulo/99517

Rivera-Navarro, J., Morales-González, J.M., Benito-León, J., & Mitchell, A.J. (2008). Dimensión social y familiar: experiencias de cuidadores y personas con esclerosis múltiple. El estudio GEDMA. Revista de Neurología, 47(6), 281-285. https://www.neurologia.com/articulo/2008071

Olascoaga, J. (2010). Calidad de vida y esclerosis múltiple. Revista de Neurología, 51(5), 279-288. https://www.neurologia.com/articulo/2010277

Aymerich, M., Guillamón, I., & Jovell, A. J. (2009). Health-related quality of life assessment in people with multiple sclerosis and their family caregivers. A multicenter study in Catalonia (Southern Europe). Patient Prefer Adherence, 3, 311–321.http://dx.doi.org/10.2147/ppa.s6217

McKeown, L.P., Porter-Armstrong, A.P., & Baxter, G.D. (2003). The needs and experiences of caregivers of individuals with multiple sclerosis: a systematic review. Clinical Rehabilitation, 17(3), 234-248. http://dx.doi.org/10.1191/0269215503cr618oa

Carreón-Guarnizo, E., Andreu-Reinon, E., Cerdán-Sánchez, M., Carrasco-Torres R., Hernández-Clares, R., Prieto-Valiente L.,…Meca-Lallana, J.E. (2016). Prevalencia de la Esclerosis Múltiple en la Región de Murcia [Prevalence of multiple sclerosis in the Region of Murcia]. Revista de Neurología, 62(9), 396–402.

Vickrey, B.G., Hays, R.D., Harooni, R., Myers, L.W., & Ellison, G.W. (1995). A health-related quality of life measure for multiple sclerosis. Quality of Life Research, 4, 187-206. http://dx.doi.org/10.1007/bf02260859

Aymerich, M., Guillamón, I., Perkal, H., Nos, C., Porcel, J., Berra, S.,…Montalbán, X. (2006). Adaptación al español del cuestionario específico MSQOL-54 para pacientes con esclerosis múltiple. Neurología, 21(4), 181-187.

Goldberg, D., & Williams, P. (1988). A user’s guide to the General Health Questionnaire. Windsor, UK: NFER-Nelson.

Sánchez-López, M.P., & Dresch, V. (2008). The 12-item General Health Questionnaires (GHQ-12): reliability, external validity and factor structure in the Spanish population. Psicothema, 20(4), 839-843.

Instituto Nacional de Estadística, INE. (2013). Encuesta Nacional de Salud 2011-2012. Ministerio de Sanidad, Servicios Sociales e Igualdad. Gobierno de España.

Sánchez-López, M.P., & Limiñana-Gras, R.M. (2017). Health from a Gender Perspective. In M.P. Sánchez-López & R.M. Limiñana-Gras (Eds.), The Psychology of Gender and Health: Conceptual and Applied Global Concerns (pp.1-52). Elseiver/Academic Press. http://dx.doi.org/10.1016/b978-0-12-803864-2.00001-8

Delgado-Mendilívar, J.M., Cadenas-Díaz, J.C., Fernández-Torrico, J.M., Navarro-Mascarell, G., & Izquierdo, G. (2005). Estudio de la calidad de vida en la Esclerosis Múltiple. Revista de Neurología, 41(5), 257-262.

Grasso, M.G., Clemenzi, A., Tonini, A., Pace, L., Casillo, P., Cuccaro, A.,…Troisi, E. (2008). Pain in multiple sclerosis: a clinical and instrumental approach. Multiple Sclerosis, 14(4), 506-513. http://dx.doi.org/10.1177/1352458507085553

Amato, M.P., Ponziani, G., Siracusa, G., & Sorbi, S. (2001). Cognitive dysfunction in early-onset multiple sclerosis: a reappraisal after 10 years. Archives of Neurology, 58(10), 1602-1606. http://dx.doi.org/10.1001/archneur.58.10.1602

Alarcón, G. S., McGwin, G., Uribe, A., Friedman, A. W., Roseman, J. M.,… Fessler, B. J. (2004). Systemic lupus erythematosus in a multiethnic lupus cohort (LUMINA). XVII. Predictors of self-reported health-related quality of life early in the disease course. Arthritis Care & Research, 51(3), 465–474. http://dx.doi.org/10.1002/art.20409

Hopman, W. M., Coo, H., Edgar, C. M., McBride, E. V., Day, A. G., & Brunet, D. G. (2007). Factors Associated with Health-Related Quality of Life in Multiple Sclerosis. The Canadian Journal of Neurological Sciences, 34(02), 160–166. http://dx.doi.org/10.1017/s0317167100005989

Cuéllar-Flores, I., & Sánchez-López, M. P. (2012). Adaptación psicológica en personas cuidadoras de familiares dependientes. Clínica y Salud, 23(2), 141-152. http://dx.doi.org/10.5093/cl2012a9

De Andrés-Jiménez, Elena y Limiñana-Gras, Rosa María (2014). El afrontamiento del cuidado en familiares cuidadores de personas con demencia: dimensiones cognitivas y el manejo de la ira. Revista Iberoamericana de Diagnóstico y Evaluación - e Avaliação Psicológica [Internet]. 2014;1(37),169-185.

Manso-Martínez, M. E., Sánchez-López, M. P., & Cuéllar-Flores, I. (2013). Salud y sobrecarga percibida en personas cuidadoras familiares de una zona rural. Clínica y Salud, 24(1), 37-45. http://dx.doi.org/10.5093/cl2013a5

Figved, N., Myhr, K.M., Larsen, J.P., & Aarsland, D. (2007) Caregiver burden in multiple sclerosis: the impact of neuropsychiatric symptoms. Journal of Neurology, Neurosurgery and Psychiatry, 78(10), 1097–1102. http://dx.doi.org/10.1136/jnnp.2006.104216

Patti, F., Pozzilli, C., Montanari, E., Pappalardo, A., Piazza, L., Levi, A.,…Pesci, I. (2007). Effects of education level and employment status on HRQoL in early relapsing-remitting multiple sclerosis. Multiple Sclerosis, 13(6), 783-791. http://dx.doi.org/10.1177/1352458506073511

Cuéllar-Flores, I., Sánchez-López, M. P., Limiñana-Gras, R. M., & Colodro-Conde, L. (2014). The GHQ-12 for the Assessment of Psychological Distress of Family Caregivers. Behavioral Medicine, 40(2), 65–70. http://dx.doi.org/10.1080/08964289.2013.847815

Pinquart, M., & Sörensen, S. (2006). Gender differences in caregiver stressors, social resources, and heath: an update meta-analysis. Journal of Gerontology, Series B: Psychological Sciences, 61(1), 33-45. http://dx.doi.org/10.1093/geronb/61.1.p33

Yee, J., & Schulz, R. (2000). Gender differences in psychiatric morbidity among family caregivers: a review and analysis. The Gerontologist, 40(2), 147-164. http://dx.doi.org/10.1093/geront/40.2.147

Acaster, S., Perard, R., Chauhan, D., & Lloyd, A.J. (2013). A forgotten aspect of the NICE reference case: an observational study of the health related quality of life impact on caregivers of people with multiple sclerosis. BMC Health Services Research, 13(1), 346. http://dx.doi.org/10.1186/1472-6963-13-346

Forbes, A., While, A., & Mathes, L. (2007). Informal carer activities, carer burden and health status in multiple sclerosis. Clinical Rehabilitation, 21(6), 563–575. http://dx.doi.org/10.1177/0269215507075035

Published
08-10-2021
How to Cite
[1]
Martínez-Espejo, M.D. et al. 2021. Assessment of Quality of Life in Multiple Sclerosis through the MSQOL-54 and its relation to the health of the caregiver . Global Nursing. 20, 4 (Oct. 2021), 217–249. DOI:https://doi.org/10.6018/eglobal.474161.
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Section
ORIGINAL RESEARCH