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Using the internet for information about breast cancer: A questionnaire-based study

机译：使用互联网获取有关乳腺癌的信息：基于问卷的研究

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Objectives: To identify the proportion of breast cancer patients that used the Internet for breast cancer information; to classify patterns of use based on patient demographics; and to evaluate whether using the Internet for this purpose was beneficial or problematic. Also to recognize whether a specific demographic group was more likely to experience problems when using the Internet for breast cancer information. Methods: A 10-item questionnaire was given to patients who attended the breast unit at the University Hospital of South Manchester between May and June 2011 following breast cancer treatment within the last 5 years. Results: 200 questionnaires were completed. 50.5% of patients had used the Internet for breast cancer information, with younger (p < 0.001) patients with a higher household income (p < 0.001) being most likely to do so. The majority (73%) found it beneficial; however 31% had experienced problems. Ethnicity affected the likelihood of experiencing problems with white patients encountering fewer problems (25%) than non-white patients (64%) (p= 0.008). Conclusion: A significant proportion of breast cancer patients will encounter difficulties when using the Internet for breast cancer information, particularly those from ethnic minorities. Practice implications: Health professionals need to include a discussion about Internet use in consultations with breast cancer patients.
机译：目的：确定使用互联网获取乳腺癌信息的乳腺癌患者的比例;根据患者的人口统计学分类使用方式;并评估为此目的使用互联网是有益还是有问题。还可以识别特定人群在使用Internet获取乳腺癌信息时是否更有可能遇到问题。方法：对最近5年内接受乳腺癌治疗后于2011年5月至6月在南曼彻斯特大学医院就诊的乳腺癌患者进行了10项问卷调查。结果：完成问卷200份。 50.5％的患者使用互联网获取乳腺癌信息，而家庭收入较高（p <0.001）的年轻患者（p <0.001）最有可能这样做。绝大多数（73％）认为它有益。但是31％的人遇到了问题。种族影响白人患者遇到问题的可能性（25％）比非白人患者（64％）少（p = 0.008）。结论：相当一部分乳腺癌患者在使用互联网获取乳腺癌信息时会遇到困难，尤其是少数民族患者。实践意义：卫生专业人员需要在与乳腺癌患者的咨询中纳入有关互联网使用的讨论。

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