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患者对家族性腺瘤性息肉病手术和监测的看法。

Patients' views of surgery and surveillance for familial adenomatous polyposis.

机构信息

The Swedish Polyposis Registry, Department of Gastroenterology and Hepatology, Karolinska University Hospital, Stockholm, Sweden.

出版信息

Cancer Nurs. 2010 Mar-Apr;33(2):E17-23. doi: 10.1097/NCC.0b013e3181bb0cf1.

Abstract

BACKGROUND

Familial adenomatous polyposis (FAP) is an inherited condition that requires prophylactic surgery (colectomy) followed by a lifetime program of endoscopic surveillance to prevent colorectal cancer. Patients are normally free of symptoms before surgery but a majority report problems related to bowel function postoperatively.

OBJECTIVE

The aim of the study was to gain a deeper understanding of how FAP affects life by exploring patients' view of what it is like living with the illness and being committed to a lifelong screening program.

METHODS

Three focus group interviews were conducted, and data were analyzed using descriptive qualitative content analysis.

RESULTS

The analysis resulted in two categories related to the participants' view of living with FAP. The first category was associated with concerns related to the hereditary and lifelong nature of the disease as well as to the prophylactic surgery and the second category was related to patients' ways of managing life.

CONCLUSION

Most participants expressed unmet needs, such as lack of healthcare providers with good knowledge about FAP, practical and psychosocial support, FAP educational programs, and organized meetings with other persons with the condition.

IMPLICATIONS FOR PRACTICE

One important aspect of living with FAP shared by the participants concerned ways of managing life concerns, something that healthcare providers caring for patients with FAP should identify and support. Furthermore, continuity of care by health care providers with good knowledge about FAP can be an important way of reducing patient concerns.

摘要

背景

家族性腺瘤性息肉病(FAP)是一种遗传性疾病,需要进行预防性手术(结肠切除术),并终身进行内镜监测,以预防结直肠癌。患者在手术前通常没有症状,但大多数患者报告手术后存在与肠道功能相关的问题。

目的

本研究旨在通过探讨患者对患病和终生筛查计划的看法,深入了解 FAP 如何影响生活。

方法

进行了三次焦点小组访谈,并使用描述性定性内容分析对数据进行分析。

结果

分析结果得出两个与参与者对 FAP 生活看法相关的类别。第一类与疾病的遗传性和终生性质、预防性手术以及第二类与患者管理生活的方式相关的担忧有关。

结论

大多数参与者表示存在未满足的需求,例如缺乏对 FAP 有良好了解的医疗保健提供者、实用和心理社会支持、FAP 教育计划以及与其他患有该病的人组织的会议。

实践意义

参与者共同分享的 FAP 生活的一个重要方面涉及管理生活的方式,这是照顾 FAP 患者的医疗保健提供者应该识别和支持的方面。此外,具有良好 FAP 知识的医疗保健提供者的连续性护理可以成为减轻患者担忧的重要方式。

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