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引用本文的文献

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本文引用的文献

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A catalyst for change: the European cancer Patient's Bill of Rights.变革的催化剂:《欧洲癌症患者权利法案》
Oncologist. 2014 Mar;19(3):217-24. doi: 10.1634/theoncologist.2013-0452. Epub 2014 Feb 3.
2
Nationwide continuous monitoring of end-of-life care via representative networks of general practitioners in Europe.通过欧洲全科医生代表性网络对临终关怀进行全国性持续监测。
BMC Fam Pract. 2013 Jun 3;14:73. doi: 10.1186/1471-2296-14-73.
3
Cancer incidence and mortality patterns in Europe: estimates for 40 countries in 2012.欧洲癌症发病率和死亡率模式:2012 年 40 个国家的估计数。
Eur J Cancer. 2013 Apr;49(6):1374-403. doi: 10.1016/j.ejca.2012.12.027. Epub 2013 Feb 26.
4
Ensuring quality cancer care: a follow-up review of the Institute of Medicine's 10 recommendations for improving the quality of cancer care in America.确保癌症治疗质量:对美国医学研究所改善癌症治疗质量的 10 项建议进行后续审查。
Cancer. 2012 May 15;118(10):2571-82. doi: 10.1002/cncr.26536. Epub 2011 Nov 1.
5
Expansion of cancer care and control in countries of low and middle income: a call to action.在中低收入国家扩大癌症的防治工作:行动呼吁。
Lancet. 2010 Oct 2;376(9747):1186-93. doi: 10.1016/S0140-6736(10)61152-X. Epub 2010 Aug 13.
6
Overview of the SEER-Medicare data: content, research applications, and generalizability to the United States elderly population.SEER-医疗保险数据概述:内容、研究应用及对美国老年人群的普遍性
Med Care. 2002 Aug;40(8 Suppl):IV-3-18. doi: 10.1097/01.MLR.0000020942.47004.03.

The European Cancer Patient's Bill of Rights: action steps for success.

作者信息

Friese Christopher R, Ayanian John Z

机构信息

Division of Systems Leadership and Effectiveness Science, School of Nursing, Institute for Healthcare Policy and Innovation, and Division of General Medicine, Medical School, and Department of Health Policy and Management, School of Public Health, and Gerald R. Ford School of Public Policy, University of Michigan, Ann Arbor, Michigan, USA.

出版信息

Oncologist. 2014 Mar;19(3):225-7. doi: 10.1634/theoncologist.2014-0050. Epub 2014 Feb 24.

DOI:10.1634/theoncologist.2014-0050
PMID:24567282
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3958471/
Abstract

The European Cancer Concord (ECC) has partnered with patients, caregivers, clinicians, and advocates to construct three articles that form a Patient’s Bill of Rights. We propose four key action steps that will advance the agenda of the ECC. These include (a) robust cancer registries, (b) monitoring of quality of care, (c) broader stakeholder engagement, and (d) dissemination of best practices.

摘要