Factors of psychosocial resource and their importance in functioning of families where a patient with endogenous mental disorder lives
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Keywords

family anxiety
type of attitude towards mental illness
psycho-emotional sphere
family caregivers
endogenous mental disorders

How to Cite

Kaminska, A., & Agisheva, N. (2020). Factors of psychosocial resource and their importance in functioning of families where a patient with endogenous mental disorder lives. Medicine Today and Tomorrow, 83(2), 43–52. https://doi.org/10.35339/msz.2019.83.02.05

Abstract

As in many countries, in Ukraine, family caregivers of mentally ill patients face a liability to which they are not usually prepared, that requires maximum involvement of personal adaptation resources of all family members and the activation of psychosocial resource of the family as a whole as an environment where a patient with endogenous mental illness lives, in order to ensure his re-socialization and rehabilitation. Family burden and family anxiety are factors that determine psychosocial resource of family and its potential in terms of providing optimal conditions for promoting psychosocial rehabilitation of patients with endogenous mental disorders. We examined 168 reference relatives of patients with paranoid schizophrenia and 75 reference relatives of patients with affective disorders (bipolar affective and recurrent depressive disorders), in which the levels of family stress and family anxiety were determined in the context of the psychosocial functioning of the subjects. The control group consisted of 55 mentally healthy individuals. The degree of family burden was assessed using a family burden rating scale according to G. Szmukler et al. (1994), the level of family anxiety was assessed according to the questionnaire «Analysis of family anxiety» E.G. Eidemiller and V. Justickis. It was revealed that high levels of family anxiety in reference relatives persist with a disease duration of up to 4 years and from 5 to 8 years, after which the indicators decrease to values that slightly differ from the control group. This probably indicates a gradual distance from the current family situation with a switch to other areas of life. With an increase in the duration of the disease, the level of family burden increases according to the subscales of negative assessments, while the decrease in the subscales of positive assessments, which reflects the focus of family members on the negative aspects of the disease. These patterns must be taken into account when developing an appropriate integrated system of medical and psychological support for families where patients with endogenous mental disorders live.

https://doi.org/10.35339/msz.2019.83.02.05
PDF (Українська)

References

Buhorskii A.V. (2017). Psikhiatricheskoie prosveshcheniie rodstvennikov patsiientov, stradaiushchikh shyzofreniiei i rasstroistvami shyzofrenicheskoho spektra [Psychiatric education for relatives of patients with schizophrenia and schizophrenic spectrum disorders]. Psikhoterapiia i psikhosotsialnaia rabota v psikhiatrii – Psychotherapy and psychosocial work in psychiatry. O.V. Limankin, S.M. Babin (Ed.). SPb.: Taro, issue IV, pp. 49–56 [in Russian].

Hurovich I.Ya., Shmukler A.B., Salnikova L.I. (2002). Praktikum po psikhosotsialnomu lecheniiu i psikhosotsialnoi reabilitatsii psikhicheski bolnykh [Guide for psychosocial treatment and psychosocial rehabilitation of the mentally ill patients]. Мoscow: Media-praktika, 180 p. [in Russian].

Perlick D.A., Rosenheck R.A., Miklowitz D.J., Kaczynski R., Link B., Ketter T. et al. (2008). Caregiver burden and health in bipolar disorder: a cluster analytic approach. The Journal of Nervous and Mental Disease, vol. 196 (6), pp. 484–491.

Souza A.L.R., Guimarães R.A., de Araújo Vilela D., de Assis R.M., Oliveira L.M.A.C., Souza M.R., Nogueira M.R., Barbosa M.A. (2017). Factors associated with the burden of family caregivers of patients with mental disorders: a cross-sectional study. BMC Psychiatry, № 17 (1), рр. 353, DOI 10.1186/s12888-017-1501-1.

Zendjidjian X.Y., Boyer L. (2014). Challenges in measuring outcomes for caregivers of people with mental health problems. Dialogues Clin. Neurosci., № 16 (2), рр. 159–169.

Gupta S., Isherwood G., Jones K., Van Impe K. (2015). Assessing health status in informal schizophrenia caregivers compared with health status in non-caregivers and caregivers of other conditions. BMC Psychiatry, № 15, DOI 10.1186/s12888-015-0547-1.

Ochoa S., Vilaplana M., Haro J.M., Villalta-Gil V., Martínez F., Negredo M.C. et al. (2008). Do needs, symptoms or disability of outpatients with schizophrenia influence family burden? Soc. Psychiatry and Psychiatric Epidemiol., vol. 43 (8), pp. 612–618.

Alzahrani S.H., Fallata E.O., Alabdulwahab M.A., Alsafi W.A., Bashawri J. (2017). Assessment of the burden on caregivers of patients with mental disorders in Jeddah, Saudi Arabia. BMC Psychiatry, № 17 (1), рр. 202, DOI 10.1186/s12888-017-1368-1.

Awad A.G., Voruganti L.N. (2008). The burden of schizophrenia on caregivers: a review. Pharmacoeconomics, № 26 (2), pp. 149–162.

Eidemiller E.H., Yustitskis V. (1999). Psikholohiia i psikhoterapiia semi [Family psychology and psychotherapy]. St. Peterburg, pp. 38, 555–556 [in Russian].

Berk L., Berk M., Dodd S., Kelly C., Cvetkovski S., Jorm A.F. (2013). Evaluation of the acceptability and usefulness of an information website for caregivers of people with bipolar disorder. BMC Medicine, № 11 (1), pp. 162.

Bustillo J., Lauriello J., Horan W., Keith S. (2001). The psychosocial treatment of schizophrenia: an update. The American Journal of Psychiatry, № 158 (2), pp. 163–175.

Geriani D., Savithry K.S., Shivakumar S., Kanchan T. (2015). Burden of care on caregivers of schizophrenia patients: a correlation to personality and coping. Journal of Clinical and Diagnostic Research, № 9 (3), VC01–VC04, DOI 10.7860/JCDR/2015/11342.5654.