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首页> 外文期刊>International Journal of Circumpolar Health >Caring for Alaska Native prostate cancer survivors in primary care: a survey of Alaska Tribal Health System providers
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Caring for Alaska Native prostate cancer survivors in primary care: a survey of Alaska Tribal Health System providers

机译:照顾阿拉斯加初级保健中的天然前列腺癌幸存者:对阿拉斯加部落卫生系统提供者的调查

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Background. Little is known about the constraints of optimizing health care for prostate cancer survivors in Alaska primary care.Objective. To describe the experiences and attitudes of primary care providers within the Alaska Tribal Health System (ATHS) regarding the care of prostate cancer survivors.Design. In late October 2011, we emailed a 22-item electronic survey to 268 ATHS primary care providers regarding the frequency of Prostate Specific Antigen (PSA) monitoring for a hypothetical prostate cancer survivor; who should be responsible for the patient’s life-long prostate cancer surveillance; who should support the patient’s emotional and medical needs as a survivor; and providers’ level of comfort addressing recurrence monitoring, erectile dysfunction, urinary incontinence, androgen deprivation therapy, and emotional needs. We used simple logistic regression to examine the association between provider characteristics and their responses to the survivorship survey items.Results. Of 221 individuals who were successfully contacted, a total of 114 responded (52% response rate). Most ATHS providers indicated they would order a PSA test every 12 months (69%) and believed that, ideally, the hypothetical patient’s primary care provider should be responsible for his life-long prostate cancer surveillance (60%). Most providers reported feeling either “moderately” or “very” comfortable addressing topics such as prostate cancer recurrence (59%), erectile dysfunction (64%), urinary incontinence (63%), and emotional needs (61%) with prostate cancer survivors. These results varied somewhat by provider characteristics including female sex, years in practice, and the number of prostate cancer survivors seen in their practice.Conclusions. These data suggest that most primary care providers in Alaska are poised to assume the care of prostate cancer survivors locally. However, we also found that large minorities of providers do not feel confident in their ability to manage common issues in prostate cancer survivorship, implying that continued access to specialists with more expert knowledge would be beneficial.
机译:背景。关于阿拉斯加初级保健中优化前列腺癌幸存者医疗保健的限制知之甚少。描述阿拉斯加部落卫生系统(ATHS)中初级保健提供者对前列腺癌幸存者的护理经历和态度。设计。在2011年10月下旬,我们通过电子邮件向22个ATHS基层医疗服务提供者发送了22个项目的电子调查,内容涉及对假设的前列腺癌幸存者进行前列腺特异性抗原(PSA)监测的频率;谁应该负责患者的终生前列腺癌监测;谁应该支持患者作为幸存者的情感和医疗需求;以及提供者的舒适度,以应对复发监测,勃起功能障碍,尿失禁,雄激素剥夺疗法和情绪需求。我们使用简单的逻辑回归分析了提供者特征与其对生存调查项目的响应之间的关联。在成功联系的221个人中,有114人做出了回应(回复率为52%)。大多数ATHS提供者表示,他们将每12个月订购一次PSA测试(69%),并认为,理想情况下,假设患者的初级保健提供者应对他的终生前列腺癌监测负责(60%)。大多数医疗服务提供者表示,对前列腺癌复发(59 %),勃起功能障碍(64 %),尿失禁(63 %)和情绪需要(61 %)这样的话题感到“中等”或“非常”舒服与前列腺癌幸存者。这些结果因提供者的特征而有所不同,包括女性,实践年限以及实践中见到的前列腺癌幸存者的数量。这些数据表明,阿拉斯加的大多数初级保健提供者都准备在当地接受前列腺癌幸存者的照顾。但是,我们还发现,少数医疗服务提供者对他们处理前列腺癌生存中常见问题的能力没有信心,这意味着继续与具有更多专业知识的专家接触将是有益的。

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