The perceptions and experiences of caregivers of patients with dysphagia: A qualitative meta‐synthesis

Abstract

AimsTo understand the perceptions and experiences of family caregivers of adult patients with dysphagia.BackgroundDysphagia is a common symptom and burdens caregivers greatly. There is a growing body of studies concentrating on caregivers and caregiving experiences. However, no qualitative meta‐synthesis has been conducted to explore the perceptions and experiences of family caregivers.DesignA qualitative meta‐ethnography.MethodsA search was conducted for relevant articles in six electronic databases (PubMed, Web of Science, CINAHL, Ovid, Cochrane Library, ProQuest) and two Chinese databases (CNKI, Wanfang Data) from inception to February 2023. The Joanna Briggs Institute Qualitative Assessment and Review Instrument (JBI‐QARI) was used to evaluate study quality. The meta‐ethnographic method was used to synthesize data from qualitative studies. The study was reported according to EQUATOR guidelines.ResultsEleven studies were included and three themes emerged: (1) emotion and perception, (2) change and challenge (3) adaption and coping.ConclusionThis review highlighted the challenges and positive coping experienced by caregivers. Findings directly inform the development and implementation of supportive interventions to reduce caregivers' stress and promote adaptive coping.Relevance to clinical practicePay attention to the needs of family caregivers of dysphagia. Family caregivers' perceived severity of dysphagia requires assessment. Caregivers need knowledge, support, and guidance to reduce their burden and fulfill their role.