Rees C E, Bath P A
Behavioural Sciences Section, Division of Psychiatry, University of Nottingham, England.
J Adv Nurs. 2000 Apr;31(4):833-41. doi: 10.1046/j.1365-2648.2000.01341.x.
A comprehensive and critical literature review was conducted to examine the information needs and source preferences of women with breast cancer and their family members. Relevant papers published between 1988 and 1998 were reviewed and despite their having several methodological weaknesses, a number of conclusions can still be drawn. First, women with breast cancer have distinct needs for information throughout their breast cancer journeys, indicating that information needs change with time since diagnosis and with treatment-related events. Second, family members of women with breast cancer also have substantial needs for information. Third, women with breast cancer and their family members often prefer verbal forms of information from health care professionals (HCPs), particularly around the time of diagnosis. Women with breast cancer, however, are often dissatisfied with the information they receive from HCPs. Further, the family members of women with breast cancer often perceive their information needs to be ignored by HCPs. Finally, few studies have focused specifically on the information needs and source preferences of family members of women with breast cancer. These findings have a number of implications for nursing, both for clinical practice and nursing research, and these are discussed in the review.
开展了一项全面且批判性的文献综述,以研究乳腺癌女性患者及其家庭成员的信息需求和信息来源偏好。对1988年至1998年间发表的相关论文进行了回顾,尽管这些论文存在若干方法学上的缺陷,但仍能得出一些结论。首先,乳腺癌女性患者在整个乳腺癌病程中有着不同的信息需求,这表明信息需求会随着确诊后的时间以及与治疗相关的事件而变化。其次,乳腺癌女性患者的家庭成员也有大量的信息需求。第三,乳腺癌女性患者及其家庭成员通常更喜欢从医护人员那里获取口头形式的信息,尤其是在确诊前后。然而,乳腺癌女性患者往往对从医护人员那里获得的信息不满意。此外,乳腺癌女性患者的家庭成员常常觉得他们的信息需求被医护人员忽视了。最后,很少有研究专门关注乳腺癌女性患者家庭成员的信息需求和信息来源偏好。这些研究结果对护理工作在临床实践和护理研究方面都有诸多启示,本综述对此进行了讨论。