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妇科癌症幸存者的信息需求。

Informational needs of gynecologic cancer survivors.

机构信息

Patient Education and Survivorship, Princess Margaret Hospital, Toronto, Canada.

出版信息

Gynecol Oncol. 2012 Mar;124(3):452-7. doi: 10.1016/j.ygyno.2011.10.030. Epub 2011 Oct 30.

DOI:10.1016/j.ygyno.2011.10.030
PMID:22047740
Abstract

OBJECTIVES

In preparation for the launch of a gynecologic oncology survivorship program, this study looked at the informational needs of women with gynecologic cancers. Although studies have touched on some of these needs, no published literature has investigated the comprehensive informational needs of gynecologic oncology patients within all sites of gynecologic cancers.

METHODS

A needs assessment, consisting of a self-administered questionnaire, was conducted at an ambulatory gynecologic oncology clinic from August 2010 to March 2011. This study investigated the informational needs of patients, including the importance of information, the amount desired, and the preferred mode of delivery. Informational needs were grouped into six domains: medical, practical, physical, emotional, social, and spiritual.

RESULTS

185 surveys were analyzed and the majority of the respondents were Caucasian (77%) and over the age of 50 (66%). Forty-nine percent of respondents were diagnosed with ovarian cancer, and there was an even distribution between newly diagnosed patients (38%), those in long-term follow-up (27%), and those with recurrent disease (37%). Overall, respondents placed more importance on receiving medical information (P<0.01). The three preferred education modalities were; pamphlets, one-on-one discussions with health care professionals and websites. Age, education, and disease site were associated with differing informational needs.

CONCLUSIONS

This study has highlighted the most important informational needs of patients with gynecologic malignancies in our patient population. This information may guide the development of clinical survivorship programs and educational resources for patients in the future.

摘要

目的

在筹备妇科肿瘤生存项目之际,本研究着眼于妇科癌症女性的信息需求。尽管已有研究触及到其中部分需求,但目前尚无文献调查妇科癌症所有部位的妇科肿瘤患者的全面信息需求。

方法

2010 年 8 月至 2011 年 3 月,在一家门诊妇科肿瘤诊所进行了一项需求评估,采用自我管理问卷形式。本研究调查了患者的信息需求,包括信息的重要性、所需数量以及首选传递模式。信息需求分为六个领域:医疗、实际、身体、情感、社会和精神。

结果

共分析了 185 份调查,大多数受访者为白人(77%)且年龄超过 50 岁(66%)。49%的受访者被诊断为卵巢癌,新诊断患者(38%)、长期随访患者(27%)和复发性疾病患者(37%)之间分布均匀。总体而言,受访者更重视获得医疗信息(P<0.01)。三种首选的教育方式是:宣传册、与医疗保健专业人员的一对一讨论和网站。年龄、教育程度和疾病部位与不同的信息需求相关。

结论

本研究突出了我们患者群体中妇科恶性肿瘤患者最重要的信息需求。这些信息可能指导未来为患者制定临床生存项目和教育资源。

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