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临床实践中的乳腺癌治疗与最佳证据及实践指南的对比。

Breast cancer treatment in clinical practice compared to best evidence and practice guidelines.

作者信息

Bloom B S, de Pouvourville N, Chhatre S, Jayadevappa R, Weinberg D

机构信息

Division of Geriatrics, Department of Medicine, University of Pennsylvania, PA, USA.

出版信息

Br J Cancer. 2004 Jan 12;90(1):26-30. doi: 10.1038/sj.bjc.6601439.

Abstract

There is sparse evidence on community practice patterns in treating women with breast cancer. This study compared care of women with breast cancer with evidence from meta-analyses and US National Comprehensive Cancer Network (NCCN) clinical guidelines. Records of 4395 women with breast cancer were abstracted from practices of 19 surgeon oncologists in six specialty practices in the Philadelphia region during 1995-1999. Patients were followed through December 2001. Low-frequency data were obtained on all patients. All other data were from a random sample of 464 women, minimum of 50 patients per practice. Actual care provided was compared to NCCN guidelines and results of meta-analyses. Fewer than half the women received treatments reflecting meta-analysis results or NCCN guidelines, by disease stage/TNM status. Adherence to either standard varied from 0% for LCIS to 87% for stages IIA or IIB node positive. There are multiple interactive reasons for low adherence to guidelines or meta-analyses results, including insufficient health system supports to clinicians, inadequate organisation and delivery systems and ineffective continuing medical education. The paucity of written information from patient records on physician/patient interactions limits the understanding of treatment decisions.

摘要

关于社区治疗乳腺癌女性的实践模式,证据稀少。本研究将乳腺癌女性的治疗情况与荟萃分析及美国国立综合癌症网络(NCCN)临床指南的证据进行了比较。1995年至1999年期间,从费城地区六个专科诊所的19位外科肿瘤学家的实践记录中提取了4395名乳腺癌女性的记录。对患者随访至2001年12月。获取了所有患者的低频数据。所有其他数据来自464名女性的随机样本,每个诊所至少50名患者。将实际提供的治疗与NCCN指南及荟萃分析结果进行了比较。按疾病分期/ TNM状态来看,接受反映荟萃分析结果或NCCN指南治疗的女性不到一半。对任一标准的依从性从LCIS的0%到IIA期或IIB期淋巴结阳性的87%不等。对指南或荟萃分析结果依从性低有多种相互作用的原因,包括卫生系统对临床医生的支持不足、组织和提供系统不完善以及继续医学教育效果不佳。患者记录中关于医患互动的书面信息匮乏,限制了对治疗决策的理解。

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