Liu Andy, Hammack-Aviran Catherine, Turnbull Jessica
Department of Pediatrics, Division of Critical Care, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
College of Law, Belmont University, Nashville, Tennessee, USA.
J Palliat Med. 2024 Sep;27(9):1163-1170. doi: 10.1089/jpm.2023.0699. Epub 2024 Jul 11.
The decision to place a tracheostomy in children is complex and involves factors beyond the medical procedure, including quality of life, values, and goals. Providers play an important role in counseling caregivers and guiding them through the decision-making process. There are no established guidelines for tracheostomy counseling, leading to variations in practice. Additionally, how caregivers receive information differs from how providers believe they deliver it. Although studies have explored caregivers' and providers' viewpoints, none have examined them concurrently. The primary aim of this exploratory study is to investigate differences between providers' and caregivers' perceptions of tracheostomy counseling and their perspectives regarding the decision-making process. Semi-structured interviews were conducted with both caregivers and providers for children being evaluated for a tracheostomy. Qualitative analysis was applied to the interview transcripts to identify emergent themes. Subsequently, a comparative analysis was performed to compare these themes between caregivers and healthcare providers. A total of 33 interviews were conducted, involving 16 caregivers and 17 providers. Notably, caregivers provided personal descriptions of their children in 81% of cases, whereas only 35% of providers did so. Concerns and fears for the children were expressed by 69% of caregivers and 59% of providers. In contrast, 75% of caregivers discussed their hopes and dreams for their children, compared with only 29% of providers. When it came to priorities, 69% of caregivers emphasized growth and development, and 38% mentioned discharge home, as opposed to 29% and 47% among providers, respectively. In conclusion, our study highlights a disconnect between caregivers and healthcare providers regarding tracheostomy counseling. These differing perspectives underscore the need for improved communication and understanding between the two groups. Recognizing these differences can help providers tailor their counseling approaches to better align with the values and priorities of families when making decisions about tracheostomy.
决定给儿童实施气管切开术是一个复杂的过程,涉及到医疗程序之外的诸多因素,包括生活质量、价值观和目标。医疗服务提供者在为护理人员提供咨询并指导他们完成决策过程中发挥着重要作用。目前尚无气管切开术咨询的既定指南,这导致了实践中的差异。此外,护理人员接收信息的方式与医疗服务提供者认为自己传递信息的方式有所不同。尽管已有研究探讨了护理人员和医疗服务提供者的观点,但尚无研究同时对二者进行考察。本探索性研究的主要目的是调查医疗服务提供者和护理人员对气管切开术咨询的认知差异,以及他们对决策过程的看法。对正在接受气管切开术评估的儿童的护理人员和医疗服务提供者都进行了半结构化访谈。对访谈记录进行了定性分析,以确定出现的主题。随后,进行了对比分析,以比较护理人员和医疗服务提供者之间的这些主题。总共进行了33次访谈,涉及16名护理人员和17名医疗服务提供者。值得注意的是,81%的护理人员在81%的案例中提供了关于其子女的个人描述,而只有35%的医疗服务提供者这样做了。69%的护理人员和59%的医疗服务提供者表达了对孩子的担忧和恐惧。相比之下,75%的护理人员讨论了他们对孩子的希望和梦想,而医疗服务提供者中只有29%这样做。在优先事项方面,69%的护理人员强调成长和发展,38%提到出院回家,而医疗服务提供者中这两个比例分别为29%和47%。总之,我们的研究突出了护理人员和医疗服务提供者在气管切开术咨询方面的脱节。这些不同的观点强调了两组之间改善沟通和理解的必要性。认识到这些差异有助于医疗服务提供者调整他们的咨询方法,以便在做出气管切开术决策时更好地与家庭的价值观和优先事项保持一致。