TY - JOUR
T1 - Psychosocial Support Needs and Preferences Among Family Caregivers of ICU Patients with Severe Acute Brain Injury
T2 - A Qualitative Thematic Analysis
AU - the Coma Family Investigators
AU - Hwang, David Y.
AU - Reichman, Mira
AU - Bannon, Sarah M.
AU - Meurer, Kate
AU - Kubota, Rina
AU - Kim, Jisoo
AU - Baskaran, Nithyashri
AU - Zhang, Qiang
AU - Fishbein, Nathan S.
AU - Lichstein, Kaitlyn
AU - Presciutti, Alexander M.
AU - Woodworth, Emily C.
AU - Motta, Melissa
AU - Muehlschlegel, Susanne
AU - Reznik, Michael E.
AU - Jaffa, Matthew N.
AU - Creutzfeldt, Claire J.
AU - Fehnel, Corey R.
AU - Tomlinson, Amanda D.
AU - Williamson, Craig A.
AU - Vranceanu, Ana Maria
AU - Ensroth, Nick
AU - Dulak, Dominika
AU - Steinberg, Alexis
AU - Carter, Samuel
AU - Vilchinsky, Lauren
AU - Nuvvala, Nithya
AU - LaBuzetta, Jamie
AU - Smolen, Sigiriya E.
AU - Deb, Lena F.
AU - Latorre, Julius G.
AU - Threlkeld, Zachary D.
AU - Moody, Scott
AU - Rojas, Danielle A.
AU - Abukhadra, Sabine L.
AU - Agarwal, Sachin
AU - Marlette, Barbara J.
AU - Vijayan, Jaya
AU - Rose, Mariah Q.
AU - Freeman, William D.
AU - Popok, Paula
AU - Lester, Ethan G.
AU - Norton, Andrea C.
N1 - Publisher Copyright:
© Springer Science+Business Media, LLC, part of Springer Nature and Neurocritical Care Society 2025.
PY - 2025/8
Y1 - 2025/8
N2 - Background: Family caregivers of patients with severe acute brain injury (SABI) are at risk for clinically significant chronic emotional distress, including depression, anxiety, and posttraumatic stress. Existing psychosocial interventions for caregivers of intensive care unit (ICU) patients are not tailored to the unique needs of caregivers of patients with SABI, do not demonstrate long-term efficacy, and may increase caregiver burden. In this study, we explored the needs and preferences for psychosocial services among SABI caregivers to inform the development and adaptation of interventions to reduce their emotional distress during and after their relative’s ICU admission. Methods: In this multicenter longitudinal qualitative study, we conducted semistructed interviews with SABI caregivers at two time points: during their relative’s ICU admission (n = 30) and 2 months later (n = 20). We analyzed qualitative data using a hybrid of inductive and deductive analytic techniques. We recruited family caregivers of patients with SABI from 14 US neuroscience ICUs. We conducted interviews over live video. Our convenience sample of SABI caregivers (n = 30) was recruited through referral by medical teams and nursing staffs across participating neuroscience ICUs. Caregivers included spouses, children, parents, and siblings to patients with SABI. Results: We identified themes and subthemes related to participants’ preferences for (1) the content of psychosocial support services and (2) the delivery and implementation of psychosocial support services. Findings revealed an unmet need for psychosocial support around the time of ICU discharge and 2 months later, including information to understand their loved one’s condition and guide difficult decision-making, education regarding how best to communicate with the patient’s care team and other family members, and emotional and behavioral coping skills. Conclusions: Our findings provide specific recommendations to justify and inform the development and adaptation of psychosocial support services for SABI caregivers for delivery in the ICU and after discharge.
AB - Background: Family caregivers of patients with severe acute brain injury (SABI) are at risk for clinically significant chronic emotional distress, including depression, anxiety, and posttraumatic stress. Existing psychosocial interventions for caregivers of intensive care unit (ICU) patients are not tailored to the unique needs of caregivers of patients with SABI, do not demonstrate long-term efficacy, and may increase caregiver burden. In this study, we explored the needs and preferences for psychosocial services among SABI caregivers to inform the development and adaptation of interventions to reduce their emotional distress during and after their relative’s ICU admission. Methods: In this multicenter longitudinal qualitative study, we conducted semistructed interviews with SABI caregivers at two time points: during their relative’s ICU admission (n = 30) and 2 months later (n = 20). We analyzed qualitative data using a hybrid of inductive and deductive analytic techniques. We recruited family caregivers of patients with SABI from 14 US neuroscience ICUs. We conducted interviews over live video. Our convenience sample of SABI caregivers (n = 30) was recruited through referral by medical teams and nursing staffs across participating neuroscience ICUs. Caregivers included spouses, children, parents, and siblings to patients with SABI. Results: We identified themes and subthemes related to participants’ preferences for (1) the content of psychosocial support services and (2) the delivery and implementation of psychosocial support services. Findings revealed an unmet need for psychosocial support around the time of ICU discharge and 2 months later, including information to understand their loved one’s condition and guide difficult decision-making, education regarding how best to communicate with the patient’s care team and other family members, and emotional and behavioral coping skills. Conclusions: Our findings provide specific recommendations to justify and inform the development and adaptation of psychosocial support services for SABI caregivers for delivery in the ICU and after discharge.
KW - Caregiver burden
KW - Intensive care units
KW - Psychological adaptation
KW - Psychological distress
KW - Psychosocial intervention
KW - Psychosocial support systems
UR - https://www.scopus.com/pages/publications/85217562992
U2 - 10.1007/s12028-024-02202-z
DO - 10.1007/s12028-024-02202-z
M3 - Article
C2 - 39821565
AN - SCOPUS:85217562992
SN - 1541-6933
VL - 43
SP - 223
EP - 231
JO - Neurocritical Care
JF - Neurocritical Care
IS - 1
ER -