乳腺放射治疗幸存者和癌症支持小组:通过 "解决乳腺癌皮肤副作用 (ABCDEs) 计划 "开展社区参与和教育的机会。

IF 1.4 4区 医学 Q3 EDUCATION, SCIENTIFIC DISCIPLINES
Shriya Veluri, Jiwon Park, Clark Anderson, Joshua Asper, Margaret Walsh, Mark Bonnen, Caesar Ramirez, Shraddha Dalwadi
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引用次数: 0

摘要

在美国,乳腺癌是最常见的癌症,也是导致女性癌症死亡的第二大原因。为了服务得克萨斯州南部保险不足的乳腺癌患者,我们设计了一项患者教育计划,以提高患者对放疗后继发性皮肤病变化的健康知识的了解。我们分发了一份需求评估调查表,以更好地了解患者的治疗阶段、对放射治疗引起的皮肤副作用的经历以及使用的非处方皮肤产品和家庭疗法。在参与该计划的 33 名患者中,几乎所有患者(93.94%,n = 31)都正在接受治疗或已完成治疗。在这 31 人中,74.19% 的患者(n = 23)至少在 9-12 个月前完成了治疗,22.58% 的患者(n = 7)目前正在接受化疗,3.23% 的患者(n = 1)目前正在接受放疗。在皮肤科副作用中,患者肤色改变、发红和灼伤/烧灼感最为严重。调查参与者使用最多的产品是处方强度的局部皮质类固醇激素(65.63%),其次是口服镇痛药(28.13%)和压力袖(25.00%)。芦荟(15.63%)是使用最多的补充和替代治疗方法。通过调查资源匮乏和少数民族社区的辐射引起的皮肤病副作用,我们可以更好地定制患者教育计划,以反映患者的经历。总之,这项计划可以增强临床医生对资源不足的患者经历的洞察力,提高健康素养,消除对乳腺癌治疗、管理和生存期的常见误解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Breast Radiation Therapy Survivorship and Cancer Support Groups: an Opportunity for Community Engagement and Education Through the Addressing Breast Cancer Dermatologic Side Effects (ABCDEs) Program.

Breast cancer is the most commonly diagnosed cancer and the second leading cause of cancer deaths in women in the USA. To serve under-insured breast cancer patients in South Texas, we designed a patient education program to improve health literacy of secondary dermatologic changes after completing radiation therapy. A needs assessment survey was distributed to better understand the patients' stage of treatment, experiences with radiation-induced dermatologic side effects, and over-the-counter skin products and home remedies used. Of the 33 patients that participated in this program, nearly all patients (93.94%, n = 31) are either currently undergoing treatment or have completed treatment. Of the 31 individuals, 74.19% of patients (n = 23) have completed treatment at least 9-12 months ago, 22.58% (n = 7) are currently receiving chemotherapy, and 3.23% (n = 1) are currently undergoing radiation therapy. Among the dermatologic side effects, patients experienced changes to skin color, redness, and burns/burning sensation at the greatest severity. The top products used by survey participants were prescription-strength topical corticosteroids (65.63%) followed by oral analgesics (28.13%) and compression sleeves (25.00%). Aloe vera (15.63%) was the most used complementary and alternative therapeutic treatment. By surveying experiences of radiation-induced dermatologic side effects in predominantly under-resourced and minority communities, we can better tailor patient education programs to reflect patients' experiences. Overall, this program can enhance clinicians' insight on under-resourced patient experiences to improve health literacy and dispel common misconceptions surrounding breast cancer treatment, management, and survivorship.

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来源期刊
Journal of Cancer Education
Journal of Cancer Education 医学-医学:信息
CiteScore
3.40
自引率
6.20%
发文量
122
审稿时长
4-8 weeks
期刊介绍: The Journal of Cancer Education, the official journal of the American Association for Cancer Education (AACE) and the European Association for Cancer Education (EACE), is an international, quarterly journal dedicated to the publication of original contributions dealing with the varied aspects of cancer education for physicians, dentists, nurses, students, social workers and other allied health professionals, patients, the general public, and anyone interested in effective education about cancer related issues. Articles featured include reports of original results of educational research, as well as discussions of current problems and techniques in cancer education. Manuscripts are welcome on such subjects as educational methods, instruments, and program evaluation. Suitable topics include teaching of basic science aspects of cancer; the assessment of attitudes toward cancer patient management; the teaching of diagnostic skills relevant to cancer; the evaluation of undergraduate, postgraduate, or continuing education programs; and articles about all aspects of cancer education from prevention to palliative care. We encourage contributions to a special column called Reflections; these articles should relate to the human aspects of dealing with cancer, cancer patients, and their families and finding meaning and support in these efforts. Letters to the Editor (600 words or less) dealing with published articles or matters of current interest are also invited. Also featured are commentary; book and media reviews; and announcements of educational programs, fellowships, and grants. Articles should be limited to no more than ten double-spaced typed pages, and there should be no more than three tables or figures and 25 references. We also encourage brief reports of five typewritten pages or less, with no more than one figure or table and 15 references.
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