Evidence map›Paper›PMID 42340007›Full record

ArticleRevista paulista de pediatria : orgao oficial da Sociedade de Pediatria de Sao Paulo2026

Caregiver burden in children with medical complexity: an approach based on the identification of associated factors.

Fernando Sarin da Mota E Albuquerque, Danton Matheus de Souza, Lidice Valeriana Oliveira Diop, Ana Paula Scoleze Ferrer

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Article in Revista paulista de pediatria : orgao oficial da Sociedade de Pediatria de Sao Paulo, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Fernando Sarin da Mota E AlbuquerqueUniversidade de São Paulo, Faculdade de Medicina, São Paulo, SP, Brazil.ORCID http://orcid.org/0009-0005-3684-2677
Danton Matheus de SouzaUniversidade Federal de São Paulo, Escola Paulista de Enfermagem, São Paulo, SP, Brazil.ORCID http://orcid.org/0000-0001-6320-4826
Lidice Valeriana Oliveira DiopUniversidade de São Paulo, Faculdade de Medicina, São Paulo, SP, Brazil.ORCID http://orcid.org/0009-0009-6173-4503
Ana Paula Scoleze FerrerUniversidade de São Paulo, Faculdade de Medicina, São Paulo, SP, Brazil.ORCID http://orcid.org/0000-0003-2364-8443

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe aim of this study was to identify factors associated with increased caregiver burden of children with medical complexity and to guide management strategies.

methodsThis cross-sectional study was conducted in a specialized service for patients with complex chronic conditions. Caregiver burden was assessed using the Zarit Burden Interview, which measures subjective burden, encompassing emotional, social, and personal impacts associated with caregiving, and is categorized as mild, moderate, or severe according to the total score. Bivariate analyses used chi-square tests, followed by multivariable Poisson regression with robust variance estimation, with results expressed as prevalence ratios (PRs) and 95% confidence intervals; p<0.05 was considered significant.

resultsA total of 173 caregivers were interviewed, predominantly mothers (88.4%), with a mean age of 38.8 years, from low-income households. Among the patients, 28.7% had cerebral palsy, 59.4% used assistive devices, and 57.2% required help with daily life activities. A severe burden score was reported by 31.2%. Polypharmacy was associated with a higher prevalence of moderateto-severe caregiver burden (PR=1.48; p=0.015), whereas daily care support (PR=0.79; p=0.039) and adequate sleep (PR=0.78; p=0.027) were associated with a lower prevalence of the outcome.

conclusionsCare-related needs, particularly polypharmacy, daily care support, and sleep quality, were associated with caregiver burden level. These findings highlight potentially modifiable factors and support the integration of a family-centered approach in the clinical follow-up of children and adolescents with medical complexity.

Indexed as

Caregiver BurdenCaregiversCost of IllnessAdolescentAdultChildChild, PreschoolChronic DiseaseCross-Sectional StudiesFemaleHumansMale

Identifiers

PMID42340007
PMCPMC13286575

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