Maccallum Fiona, Breen Lauren J, Ivynian Serra, DiGiacomo Michelle, Luckett Tim, Lobb Elizabeth A
School of Psychology, University of Queensland, Brisbane, QLD, Australia.
School of Population Health and Enable Institute, Curtin University, Perth, Australia.
J Affect Disord. 2025 Apr 1;374:467-476. doi: 10.1016/j.jad.2025.01.056. Epub 2025 Jan 13.
The COVID-19 pandemic disrupted many care systems limiting bereaved peoples' ability to access social, community, and professional support. This study investigated help-seeking of people living with probable prolonged grief disorder (PGD) to identify challenges and facilitators of care, with the aim of informing bereavement practice and policy recommendations.
Participants (N = 786; 96.3 % female, Mage = 54.51. SD = 11.64) who were 12 or more months post-bereavement completed an online survey indexing pandemic bereavement experiences, mental health and functional outcomes, and help-seeking experiences. Probable PGD was defined as a score ≥30 on the Prolonged Grief Scale 13-Revised (PG-13-R). Results were analyzed using univariate statistics for closed questions and content analysis for free-text responses.
Participants living with probable PGD (39.4 %) were more likely than others to: have sought help from professional or other structured grief supports (χ(1) = 41.18, p < .001); have unmet bereavement needs (χ(1) = 91.87, p < .001); and be living with significant functional impairment (t = -26.55, p < .001) and suicidal ideation (χ(3) = 117.38, p < .001). Lack of provider availability and lack of relevant skills in working with grief and trauma were identified as challenges to care.
The study used a convenience sample recruited online and so care is required before generalizing to less represented populations.
We identified both pandemic-specific and more general gaps within bereavement support systems. Our findings highlight a need to recognize care needs and elevate bereavement care within pandemic planning and health care systems more generally.
新冠疫情扰乱了许多医疗系统,限制了丧亲者获得社会、社区和专业支持的能力。本研究调查了可能患有持续性悲伤障碍(PGD)的人群的求助情况,以确定护理的挑战和促进因素,旨在为丧亲护理实践和政策建议提供信息。
丧亲12个月或更长时间的参与者(N = 786;96.3%为女性,年龄中位数Mage = 54.51,标准差SD = 11.64)完成了一项在线调查,该调查涉及疫情期间的丧亲经历、心理健康和功能结果以及求助经历。可能的PGD被定义为在修订版13项持续性悲伤量表(PG - 13 - R)上得分≥30。对封闭式问题的结果使用单变量统计进行分析,对自由文本回复使用内容分析进行分析。
可能患有PGD的参与者(39.4%)比其他人更有可能:寻求专业或其他结构化悲伤支持的帮助(χ(1) = 41.18,p <.001);有未满足的丧亲需求(χ(1) = 91.87,p <.001);以及存在严重的功能障碍(t = -26.55,p <.001)和自杀意念(χ(3) = 117.38,p <.001)。护理的挑战包括提供者可及性不足以及在处理悲伤和创伤方面缺乏相关技能。
本研究使用了通过在线招募的便利样本,因此在推广到代表性较低的人群之前需要谨慎。
我们确定了丧亲支持系统中特定于疫情的以及更普遍的差距。我们的研究结果强调需要认识到护理需求,并在疫情规划和更广泛的医疗保健系统中提升丧亲护理水平。