ArticleRevista Cuidarte
Needs of family caregivers of older adults with post-stroke sequelae.
Article in Revista Cuidarte. 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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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Introduction: Stroke is the leading cause of disability, resulting in mobility deficits, cognitive and functional impairments that lead to dependence. As a result, caregivers experience stress, anxiety, and uncertainty during the transition from hospital to home due to inadequate preparation for taking on the role. Objective: To describe the needs of family caregivers of older adults with post-stroke sequelae. Materials and Methods: A qualitative, phenomenological study was conducted using in-depth, open-ended interviews, audio-recorded and transcribed, accompanied by field notes. A convenience sample of six participants was selected. An interpretative phenomenological analysis was conducted in light of Edmund Husserl's theoretical and referential framework. Results: Six participants, daughters of older adults with post-stroke sequelae, took part in the study. Most were married, had a secondary education, were homemakers, and reported low economic income. Three core themes of meaning emerged from their caregiving experiences: Awareness of reality, perceived needs, and caregiving coping strategies. They expressed their feelings and interpretations in detail, sharing from their lived experiences the challenges and care required in response to their family member's health deterioration. Discussion: Caregivers face emotional and knowledge-related challenges when caring for older adults after a stroke. According to various studies, professional training and spiritual and family support are key strategies for reducing caregiver burden and improving the quality of care. Conclusion: The identified needs include caregiving support, highlighting preparation for home care, and access to psychological assistance.
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