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一扇了解未确诊疾病患者生活的窗口:来自未确诊疾病网络的患病经历叙述

A window into living with an undiagnosed disease: illness narratives from the Undiagnosed Diseases Network.

作者信息

Spillmann Rebecca C, McConkie-Rosell Allyn, Pena Loren, Jiang Yong-Hui, Schoch Kelly, Walley Nicole, Sanders Camilla, Sullivan Jennifer, Hooper Stephen R, Shashi Vandana

机构信息

Division of Medical Genetics, Department of Pediatrics, Duke University Medical Center, Durham, NC, USA.

Department of Allied Health Sciences, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.

出版信息

Orphanet J Rare Dis. 2017 Apr 17;12(1):71. doi: 10.1186/s13023-017-0623-3.

Abstract

BACKGROUND

Patients' stories of their illnesses help bridge the divide between patients and providers, facilitating more humane medical care. Illness narratives have been classified into three types: restitution (expectation of recovery), chaos (suffering and loss), and quest (unexpected positive effect from illness). Undiagnosed patients have unique illness experiences and obtaining their narratives would provide insights into the medical and emotional impact of living with an undiagnosed illness. Adults and children with undiagnosed diseases apply to be evaluated by the Undiagnosed Diseases Network (UDN). Written illness narratives from 40 UDN applicants, including 20 adult probands who applied for themselves and 20 parents who applied for their children, were analyzed for: 1) narrative content and 2) narrative type.

RESULTS

Narrative content: could be grouped into three themes: 1) Expectations of the UDN: the majority felt they had no further healthcare options and hoped the UDN would provide them with a diagnosis, with the adults expecting to return to their previously healthy life and the parents wanting information to manage their child's healthcare. 2) Personal medical information: the narratives reported worsening of symptoms and some offered opinions regarding the cause of their illness. The proband narratives had few objective findings, while parental narratives had detailed objective information. 3) Experiences related to living with their undiagnosed illness: frustration at being undiagnosed was expressed. The adults felt they had to provide validation of their symptoms to providers, given the lack of objective findings. The parents worried that something relevant to their child's management was being overlooked. Narrative type: All the narratives were of the chaos type, but for different reasons, with the probands describing loss and suffering and the parents expressing fear for their child's future. The parental narratives also had elements of restitution and quest, with acceptance of "a new normal", and an emphasis on the positive aspects of their child's illness which was absent from the probands.

CONCLUSIONS

These narratives illustrate the chaos that coexists with being undiagnosed. The differences between the proband and parental narratives suggest that these two groups have different needs that need to be considered during their evaluation and management.

摘要

背景

患者讲述自己的病情有助于弥合医患之间的分歧,促进更人性化的医疗护理。疾病叙事已被分为三种类型:恢复(对康复的期望)、混乱(痛苦和损失)和探索(疾病带来的意外积极影响)。未确诊的患者有独特的患病经历,获取他们的叙事将有助于深入了解患有未确诊疾病对医疗和情感方面的影响。患有未确诊疾病的成人和儿童申请接受未确诊疾病网络(UDN)的评估。对40名UDN申请者的书面疾病叙事进行了分析,其中包括20名成年先证者(为自己申请)和20名家长(为其子女申请),分析内容包括:1)叙事内容;2)叙事类型。

结果

叙事内容:可分为三个主题:1)对UDN的期望:大多数人觉得他们没有其他医疗选择,希望UDN能为他们提供诊断,成年人期望恢复到以前的健康生活,家长则希望获得信息以管理孩子的医疗护理。2)个人医疗信息:叙事中提到症状恶化,一些人还对自己疾病的病因发表了看法。先证者的叙事中客观发现较少,而家长的叙事中有详细的客观信息。3)与患有未确诊疾病相关的经历:表达了对未被确诊的沮丧。由于缺乏客观发现,成年人觉得他们必须向医疗服务提供者证实自己的症状。家长担心与孩子治疗相关的某些事情被忽视。叙事类型:所有叙事均为混乱型,但原因不同,先证者描述了损失和痛苦,家长则表达了对孩子未来的担忧。家长的叙事中也有恢复和探索的元素,接受“新常态”,并强调孩子疾病的积极方面,而先证者的叙事中没有这些。

结论

这些叙事说明了未被确诊所伴随的混乱。先证者和家长叙事之间的差异表明,这两组人有不同的需求,在对他们进行评估和管理时需要加以考虑。

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