Evaluación de la calidad de vida en Esclerosis Múltiple a través del MSQOL-54 y su relación con la salud de la persona

  1. Martínez-Espejo, María Dolores 1
  2. Limiñana-Gras, Rosa María 1
  3. Patró-Hernández, Rosa María 1
  4. Meca Lallana, José Eustasio 2
  5. Aznar Robles, Encarnación 2
  6. Márquez Rebollo, María del Carmen 2
  1. 1 Universidad de Murcia
    info

    Universidad de Murcia

    Murcia, España

    ROR https://ror.org/03p3aeb86

  2. 2 Unidad de Esclerosis Múltiple, Hospital Clínico Universitario Virgen de la Arrixaca, Murcia.
Journal:
Enfermería global: revista electrónica trimestral de enfermería

ISSN: 1695-6141

Year of publication: 2021

Issue Title: #64 Octubre

Volume: 20

Issue: 4

Pages: 217-249

Type: Article

DOI: 10.6018/EGLOBAL.474161 DIALNET GOOGLE SCHOLAR lock_openDIGITUM editor

More publications in: Enfermería global: revista electrónica trimestral de enfermería

Sustainable development goals

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.

Bibliographic 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
Data source: Dialnet