"Are you listening?" : experiences shared online by family caregivers of patients in the palliative phase during the covid-19-pandemic

Article

HOFFSTADT, Hinke E. | VERHOEF, Mary-Joanne | AKKERMANS, Aranka | VAN DER STEEN, Jenny T. | STOPPELENBURG, Arianne | DE VRIES, Sita | DE GRAAF, Everlien | TEUNISSEN, Saskia C. C. M. | HARTOG, Iris D. | VAN DER LINDEN, Yvette M.

OBJECTIVES: In palliative care, it is important for family caregivers to spend time with and care for the patient, and to receive (in)formal support. These elements were compromised during the Covid-19-pandemic. This study investigates what family caregivers of non-Covid-19-patients in the palliative phase shared online during the first wave of the pandemic, and what their communicative intentions were with posting online. METHODS: To investigate what family caregivers shared online, a reflexive thematic analysis was performed on online newspaper articles and posts on Twitter, Facebook and online forums. To investigate family caregivers' communicative intentions with social media posts, content analysis was conducted guided by Speech Act Theory. RESULTS: In total, 412 posts and articles were included, the majority being Tweets (86.7%). Four themes were constructed: 1) 'Being out of touch', 2) 'Fear, worries and uncertainties, 3) 'Disbelief, anger and resistance', and 4) 'Understanding, acceptance and gratitude'. Family caregivers felt overwhelmed with anger, sadness and anxiety, yet some expressing milder or positive attitudes towards the new circumstances. Family caregivers mostly posted online to share their personal experiences and emotions, and to express their opinions about the restrictions. CONCLUSIONS: The pandemic had distinct implications for family caregivers of non-Covid-19-patients in the palliative phase. In future similar circumstances, restrictions should be tailored to individual conditions and interventions should be in place to facilitate contact between patients, family caregivers and healthcare professionals and to support family caregivers.

http://dx.doi.org/10.1371/journal.pone.0310624

Voir la revue «Plos one, 19»

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