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Intensive care unit (ICU) visitation restrictions during the coronavirus disease (COVID-19) pandemic have drastically reduced family-engaged care. Understanding the impact of physical distancing on family members of ICU patients is needed to inform future policies. To understand the experiences of family members of critically ill patients with COVID-19 when physically distanced from their loved ones and to explore ways clinicians may support them. This qualitative study of an observational cohort study reports data from 74 family members of ICU patients with COVID-19 at 10 United States hospitals in four states, chosen based on geographic and demographic diversity. Adult family members of patients admitted to the ICU with COVID-19 during the early phase of the pandemic (February-June 2020) were invited to participate in a phone interview. Interviews followed a semistructured guide to assess four constructs: illness narrative, stress experiences, communication experiences, and satisfaction with care. Interviews were transcribed verbatim and analyzed using an inductive approach to thematic analysis. Among 74 interviewees, the mean age was 53.0 years, 55% were white, and 76% were female. Physical distancing contributed to substantial stress and harms (nine themes). Participants described profound suffering and psychological illness, unfavorable perceptions of care, and weakened therapeutic relationship between family members and clinicians. Three communication principles emerged as those most valued by family members: contact, consistency, and compassion (the 3Cs). Family members offered suggestions to guide clinicians faced with communicating with physically distanced families. Visitation restrictions impose substantial psychological harms upon family members of critically ill patients. Derived from the voics of family members, our findings warrant strong consideration when implementing visitation restrictions in the ICU and advocate for investment in infrastructure (including staffing and videoconferencing) to support communication. This study offers family-derived recommendations to operationalize the 3Cs to guide and improve communication in times of physical distancing during the COVID-19 pandemic and beyond.
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http://dx.doi.org/10.1513/AnnalsATS.202105-629OC | DOI Listing |
JMIR Res Protoc
September 2025
Division of Physical Therapy and Rehabilitation Science, Department of Family Medicine and Community Health, Medical School, University of Minnesota-Twin Cities, Minneapolis, MN, United States.
Background: Approximately 69% of Americans with spinal cord injury (SCI) have neuropathic pain. Research suggests that impairments in mental body representations (MBRs; ie, representations of the body in the brain) likely contribute to neuropathic pain. Clinical trials in adults with SCI, focused on restoring MBR, led to improvements in sensation and movement as well as neuropathic pain relief.
View Article and Find Full Text PDFJMIR Pediatr Parent
September 2025
Division of Prevention Science, Department of Medicine, University of California, San Francisco, San Francisco, CA, United States.
Background: Alone time with health care providers is critical for adolescents, and several professional organizations recommend it. Alone time with providers promotes better utilization of health services, empowers adolescents to manage their health, and facilitates discussions on sensitive issues. However, only 40% of adolescents have private conversations with clinicians during visits.
View Article and Find Full Text PDFJ Appl Gerontol
September 2025
Department of Medical Psychology and Sociology, Faculty of Medicine, Institute of Theoretical Medicine, University of Augsburg, Germany.
Research on the relatives' well-being during the critical time point when their family member is hospitalized in an acute psychiatric hospital is still lacking. Therefore, we investigated psychological well-being, care-related burden, and communication challenges of 67 relatives of older patients with dementia (RPwD) versus 60 relatives of older patients with a psychiatric disorder (RPP) at the time of hospitalization. RPwD reported significantly higher levels of depression and care-related burden compared to RPP (there was a similar non-significant trend for anxiety).
View Article and Find Full Text PDFJ Vis Exp
September 2025
Human Development and Family Studies, Iowa State University.
This corrects the article 10.3791/55393.
View Article and Find Full Text PDFPLoS One
September 2025
School of Law, Society and Criminology, UNSW, Sydney, New South Wales, Australia.
In this paper we analyse gender-based biases in the language within complex legal judgments. Our aims are: (i) to determine the extent to which purported biases discussed in the literature by feminist legal scholars are identifiable from the language of legal judgments themselves, and (ii) to uncover new forms of bias represented in the data that may promote further analysis and interpretation of the functioning of the legal system. We consider a large set of 2530 judgments in family law in Australia over a 20 year period, examining the way that male and female parties to a case are spoken to and about, by male and female judges, in relation to their capacity to provide care for children subject to the decision.
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