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. 2019 Mar 8:13:6.
doi: 10.1186/s13030-019-0147-2. eCollection 2019.

Psychosocial factors related with caregiver burden among families of children with chronic conditions

Filiberto Toledano-Toledano  1 , Miriam Teresa Domínguez-Guedea  2
Affiliations

Psychosocial factors related with caregiver burden among families of children with chronic conditions

Filiberto Toledano-Toledano et al. Biopsychosoc Med. .

Abstract

Background: The impact of looking after children who live with complex chronic conditions is a growing public health issue. However, it is unclear whether sociodemographic and psychosocial variables can be used to predict the burden on the caregiver and how the profiles of families of children with chronic diseases are defined and structured. The objective of this study was to identify multivariate sociodemographic and psychosocial variables as well as sociocultural and familial factors to analyze the caregiver burden of family caregivers of children with chronic diseases.

Methods: A cross-sectional study was conducted involving 416 family caregivers of children with chronic diseases at the National Institute of Health in Mexico City. The participants responded to a questionnaire on sociodemographic variables and a battery of 7 instruments that examined caregiver burden, family support, parental stress, anxiety, support networks, family functioning, historic-psycho-socio-cultural premises and the World Health Organization Well-Being Index.

Results: A multivariate analysis using hierarchical multiple regression models showed that the variables included in the psychosocial and sociodemographic profile as a whole explained 40% of the variance in caregiver burden, taking sociocultural historical premises, stressors and anxiety into account as positive individual predictors. Negative individual predictors for caregiver burden included upper secondary education, social support networks, family support, family functioning and well-being. The sociodemographic profiles of family caregivers were as follows: female (81.7%); mean age, 31.7 years (standard deviation [SD], 8 years); married (79.3%); nuclear family (60%); basic education (62.7%); unpaid work (66.3%); and a daily household income of approximately 4 USD (61.1%).

Conclusions: The caregiver burden of family caregivers of children with chronic diseases is defined and structured based on personal, family, and sociocultural factors. These features provide evidence to conduct research and implement intervention strategies with regard to families facing adversity, risk and vulnerability during a child's disease.

Keywords: Caregiver burden; Family caregivers; Family functioning; Family support; Pediatric chronic diseases; Psychosocial factors; Social support networks; Sociodemographic variables; Well-being.

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Conflict of interest statement

This research project, HIM/2013/019/SSA.1141, was approved by the Research, Ethics and Biosafety Commission [Comisiones de Investigación, Ética y Bioseguridad] of the Hospital Infantil de México Federico Gómez National Institute of Health. All participants signed an informed consent form.Consent to publish this study has been provided, and all participants have signed an informed consent form.The authors declare that they have no competing interests. The authors declare that we have no conflicts of interest. All of the authors have given their approval for the article to be published.Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

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