Korsvold Live, Mellblom Anneli Viktoria, Finset Arnstein, Ruud Ellen, Lie Hanne Cathrine
Department of Behavioural Sciences in Medicine, Institute of Basic Medical Sciences, Faculty of Medicine, University of Oslo, Norway; Department of Paediatric Medicine, Children's and Adolescents Division, Oslo University Hospital, Norway.
Department of Behavioural Sciences in Medicine, Institute of Basic Medical Sciences, Faculty of Medicine, University of Oslo, Norway.
Eur J Oncol Nurs. 2017 Feb;26:1-8. doi: 10.1016/j.ejon.2016.10.005. Epub 2016 Nov 16.
Little is known about the emotional concerns expressed by adolescent and young adult (AYA) patients in consultations when a diagnosis of cancer is delivered. Here, we investigated the content of such concerns and how health care providers respond to them.
We audio-recorded nine consultations with AYA cancer patients (ages: 12-25 years) at the time of diagnosis. We have previously identified and coded 135 emotional concerns and the responses to these in the nine consultations using the Verona Coding Definitions of Emotional Sequences (VR-CoDES) framework. Here, we used qualitative content analysis to study these emotional concerns and categorize them according to overarching themes. We then quantitatively explored associations between the themes of the concerns and whether the responses to them varied according to their themes.
We identified four themes for the content of concerns: "Side-effects/late-effects" (39%), "What happens in the near future/practical aspects" (16%), "Fear" (27%) and "Sadness" (17%) (e. g. crying, sighing or other sounds that expressed sadness). Health care providers' responses did not appear to vary according to the different themes of concerns, but typically consisted of providing medical information.
The content analysis revealed that patients and family members expressed a wide range of emotional concerns. Health care providers tended to respond to the content-aspect of the concerns, but did rarely explicitly acknowledge the affective-aspect of the concerns. The effect of responses to patients' emotional concerns in the important first consultations about the cancer diagnosis and planned treatment should be investigated in future studies.
对于青少年及青年(AYA)癌症患者在确诊时咨询过程中表达的情感担忧,我们了解甚少。在此,我们调查了此类担忧的内容以及医疗服务提供者如何回应这些担忧。
我们对9名AYA癌症患者(年龄:12 - 25岁)确诊时的咨询过程进行了录音。我们之前使用维罗纳情感序列编码定义(VR - CoDES)框架,在这9次咨询中识别并编码了135种情感担忧及其相应回应。在此,我们采用定性内容分析法研究这些情感担忧,并根据总体主题对其进行分类。然后,我们定量探索了担忧主题之间的关联,以及对这些担忧的回应是否因主题而异。
我们确定了担忧内容的四个主题:“副作用/后期效应”(39%)、“近期会发生什么/实际方面”(16%)、“恐惧”(27%)和“悲伤”(17%)(例如哭泣、叹息或其他表达悲伤的声音)。医疗服务提供者的回应似乎并未因担忧的不同主题而有所不同,但通常包括提供医疗信息。
内容分析表明,患者及其家属表达了广泛的情感担忧。医疗服务提供者倾向于回应担忧的内容方面,但很少明确承认担忧的情感方面。在未来的研究中,应调查在关于癌症诊断和计划治疗的重要首次咨询中,对患者情感担忧的回应所产生的影响。