The Australian experiment: the use of evidence based medicine for the reimbursement of surgical and diagnostic procedures (1998-2004).

Sue P O'Malley
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引用次数: 1

Abstract

Background: In 1998 a formal process using the criteria of safety, effectiveness and cost-effectiveness (evidence based medicine) on the introduction and use of new medical procedures was implemented in Australia. As part of this process an expert panel, the Medical Services Advisory Committee (MSAC) was set up. This paper examines the effectiveness of this process based on the original criteria, that is, evidence based medicine.

Method: The data for this analysis was sourced primarily from that made available in the public domain. The MSAC web site provided Minutes from MSAC meetings; Annual Reports; Assessment and Review reports; Progress status; and Archived material.

Results: The total number of applications submitted to the MSAC has been relatively low averaging approximately only fourteen per year. Additionally, the source of applications has quickly shifted to the medical devices, equipment and diagnostic industry as being the major source of applications. An overall average time for the processing of an application is eighteen months. Negative recommendations were in most cases based on insufficient clinical evidence rather than clinical evidence that clearly demonstrated a lack of clinical effectiveness. It was rare for a recommendation, either positive or negative, to be based on cost-effectiveness.

Conclusion: New medical procedures are often the result of a process of experimentation rather than formally conducted research. Affordability and the question of who should pay for the generation, collection and analysis of the clinical evidence is perhaps the most difficult to answer. This is especially the case where the new procedure is the result of a process of experimentation with an old procedure. A cost-effective way needs to be found to collect acceptable levels of evidence proving the clinical effectiveness of these new procedures, otherwise the formal processes of evaluation such as that used by the Australian MSAC since 1998 will continue to run the risk of committing Type II errors, that is, denying access to medical procedures that are beneficial and efficient.

澳大利亚实验:在外科和诊断程序的报销中使用循证医学(1998-2004)。
背景:1998年,澳大利亚根据安全性、有效性和成本效益(循证医学)标准,对引进和使用新的医疗程序实施了正式程序。作为这一进程的一部分,设立了一个专家小组,即医疗服务咨询委员会。本文根据原始标准,即循证医学,检验了这一过程的有效性。方法:本分析的数据主要来源于公共领域提供的数据。MSAC网站提供MSAC会议纪要;年度报告;评估及检讨报告;进步状态;和存档材料。结果:提交给MSAC的申请总数相对较低,平均每年大约只有14份。此外,应用程序的来源已迅速转移到医疗设备、设备和诊断行业,成为应用程序的主要来源。处理申请的总体平均时间为18个月。在大多数情况下,否定建议是基于临床证据不足,而不是基于明确证明缺乏临床有效性的临床证据。以成本效益为基础的建议,无论是积极的还是消极的,都是罕见的。结论:新的医疗程序往往是实验过程的结果,而不是正式进行的研究。负担能力和谁应该为临床证据的产生、收集和分析买单的问题可能是最难回答的。当新程序是对旧程序进行实验的结果时,尤其如此。需要找到一种具有成本效益的方法来收集证明这些新程序的临床有效性的可接受水平的证据,否则,澳大利亚MSAC自1998年以来使用的正式评估程序将继续有犯第二类错误的风险,即拒绝接受有益和有效的医疗程序。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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