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加利福尼亚大学雅典娜乳腺健康网络(雅典娜)中乳腺癌幸存者的治疗后护理质量

Quality of Posttreatment Care Among Breast Cancer Survivors in the University of California Athena Breast Health Network (Athena).

作者信息

Ganz Patricia A, Hahn Erin E, Petersen Laura, Melisko Michelle E, Pierce John P, Von Friederichs-Fitzwater Marlene, Lane Karen T, Hiatt Robert A

机构信息

Jonsson Comprehensive Cancer Center, University of California, Los Angeles, CA.

Jonsson Comprehensive Cancer Center, University of California, Los Angeles, CA.

出版信息

Clin Breast Cancer. 2016 Oct;16(5):356-363. doi: 10.1016/j.clbc.2016.05.003. Epub 2016 May 14.

Abstract

INTRODUCTION

Multiple oncology providers are involved in the initial breast cancer treatment. To better understand the patterns and quality of posttreatment breast cancer care, we surveyed patients who had been treated at each of the 5 University of California (UC) cancer centers.

PATIENTS AND METHODS

We identified breast cancer patients diagnosed in 2008-2009 from hospital tumor registries; invitations for the mailed survey on posttreatment care were sent between September 2011 and November 2012. The survey requested information on the number and type of provider visits, discussion of key topics, use of treatment summaries, and survivorship care plans (SCP).

RESULTS

A total of 329 patients completed the survey. The mean age of respondents was 60.5 years, and they were 3.2 years since diagnosis (range, 1.6-4.8 years). A total of 82% had continued posttreatment care at a UC facility, and they reported high numbers of clinical follow-up visits, with an average of > 2 providers (range, 1-5). Surgery-only patients reported an average of 4 to 5 office visits a year; patients who received surgery, radiation, and chemotherapy reported 5 to 6 office visits a year. Overall, 45% of women reported receiving a treatment summary; receipt of a SCP was reported by 59%, occurring significantly more often among those in follow-up at a UC (P = .004).

CONCLUSION

Patients reported visits to multiple providers during their follow-up care, in excess of what is recommended by current guidelines. This was in spite of many women reporting that they had received a SCP.

摘要

引言

多个肿瘤学医疗服务提供者参与乳腺癌的初始治疗。为了更好地了解乳腺癌治疗后护理的模式和质量,我们对在加利福尼亚大学(UC)的5个癌症中心接受治疗的患者进行了调查。

患者与方法

我们从医院肿瘤登记处识别出2008 - 2009年诊断出的乳腺癌患者;在2011年9月至2012年11月期间发送了关于治疗后护理的邮寄调查问卷。该调查询问了医疗服务提供者就诊的次数和类型、关键话题的讨论、治疗总结的使用以及生存护理计划(SCP)。

结果

共有329名患者完成了调查。受访者的平均年龄为60.5岁,自诊断以来已有3.2年(范围为1.6 - 4.8年)。共有82%的患者在UC机构继续接受治疗后护理,他们报告临床随访就诊次数较多,平均有超过2名医疗服务提供者(范围为1 - 5名)。仅接受手术的患者报告每年平均有4至5次门诊就诊;接受手术、放疗和化疗的患者报告每年有5至6次门诊就诊。总体而言,45%的女性报告收到了治疗总结;59%的女性报告收到了SCP,在UC接受随访的患者中发生的频率明显更高(P = .004)。

结论

患者报告在随访护理期间拜访了多个医疗服务提供者,超过了当前指南的建议。尽管许多女性报告她们已经收到了SCP。

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