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通过卒中中心及系统提高医疗质量的建议:卒中中心识别选项的审查:美国卒中协会卒中中心识别选项咨询工作组的多学科共识建议

Recommendations for improving the quality of care through stroke centers and systems: an examination of stroke center identification options: multidisciplinary consensus recommendations from the Advisory Working Group on Stroke Center Identification Options of the American Stroke Association.

作者信息

Adams Robert, Acker Joe, Alberts Mark, Andrews Liz, Atkinson Richard, Fenelon Kathy, Furlan Anthony, Girgus Meighan, Horton Katie, Hughes Richard, Koroshetz Walter, Latchaw Richard, Magnis Ellen, Mayberg Marc, Pancioli Arthur, Robertson Rose Marie, Shephard Tim, Smith Rene, Smith Sidney C, Smith Suzanne, Stranne Steven K, Kenton Edgar J, Bashe Gil, Chavez Altagracia, Goldstein Larry, Hodosh Richard, Keitel Cindy, Kelly-Hayes Margaret, Leonard Anne, Morgenstern Lewis, Wood Jack Owen

出版信息

Stroke. 2002 Jan;33(1):e1-7.

Abstract

BACKGROUND AND PURPOSE

The American Stroke Association (ASA) assembled a multidisciplinary group of experts to develop recommendations regarding the potential effectiveness of establishing an identification program for stroke centers and systems. "Identification" refers to the full spectrum of models for assessing and recognizing standards of quality care (self-assessment, verification, certification, and accreditation). A primary consideration is whether stroke center identification might improve patient outcomes.

METHODS

In February 2001, ASA, with the support of the Stroke Council's Executive Committee, decided to embark on an evaluation of the potential impact of stroke center identification. HealthPolicy R&D was selected to prepare a comprehensive report. The investigators reported on models outside the area of stroke, ongoing initiatives within the stroke community (such as Operation Stroke), and state and federal activities designed to improve care for stroke patients. The investigators also conducted interviews with thought leaders in the stroke community, representing a diverse sampling of specialties and affiliations. In October 2001, the Advisory Working Group on Stroke Center Identification developed its consensus recommendations. This group included recognized experts in neurology, emergency medicine, emergency medical services, neurological surgery, neurointensive care, vascular disease, and stroke program planning.

RESULTS

There are a variety of existing identification programs, generally falling within 1 of 4 categories (self-assessment, verification, certification, and accreditation) along a continuum with respect to intensity and scope of review and consumption of resources. Ten programs were evaluated, including Peer Review Organizations, trauma centers, and new efforts by the National Committee on Quality Assurance and the Joint Commission on the Accreditation of Healthcare Organizations to identify providers and disease management programs. The largest body of literature on clinical outcomes associated with identification programs involves trauma centers. Most studies support that trauma centers and systems lead to improved mortality rates and patient outcomes. The Advisory Working Group felt that comparison to the trauma model was most relevant given the need for urgent evaluation and treatment of stroke. The literature in other areas generally supports the positive impact of identification programs, although patient outcomes data have less often been published. In the leadership interviews, participants generally expressed strong support for pursuing some form of voluntary identification program, although concerns were raised that this effort could meet with some resistance.

CONCLUSIONS

Identification of stroke centers and stroke systems competencies is in the best interest of stroke patients in the United States, and ASA should support the development and implementation of such processes. The purpose of a stroke center/systems identification program is to increase the capacity for all hospitals to treat stroke patients according to standards of care, recognizing that levels of involvement will vary according to the resources of hospitals and systems.

摘要

背景与目的

美国心脏协会(ASA)组建了一个多学科专家小组,以制定关于建立卒中中心及系统识别计划潜在效果的建议。“识别”指的是评估和认可优质护理标准的全系列模式(自我评估、核实、认证和认可)。一个主要考量因素是卒中中心识别是否可能改善患者预后。

方法

2001年2月,在卒中委员会执行委员会的支持下,ASA决定着手评估卒中中心识别的潜在影响。选择了卫生政策研发部门来编写一份综合报告。研究人员报告了卒中领域之外的模式、卒中社区内正在开展的举措(如卒中行动)以及旨在改善卒中患者护理的州和联邦活动。研究人员还对卒中社区的思想领袖进行了访谈,这些思想领袖代表了不同专业和背景的抽样群体。2001年10月,卒中中心识别咨询工作组制定了其共识性建议。该小组包括神经病学、急诊医学、紧急医疗服务、神经外科、神经重症监护、血管疾病和卒中项目规划等领域的知名专家。

结果

存在多种现有的识别计划,一般可分为四类(自我评估、核实、认证和认可)中的一类,在审查强度和范围以及资源消耗方面呈连续统一体。评估了10个计划,包括同行评审组织、创伤中心以及国家质量保证委员会和医疗保健组织认证联合委员会为识别医疗服务提供者和疾病管理计划所做的新努力。关于与识别计划相关的临床结果的最大文献量涉及创伤中心。大多数研究支持创伤中心及系统可降低死亡率并改善患者预后。鉴于卒中需要紧急评估和治疗,咨询工作组认为与创伤模式进行比较最为相关。其他领域的文献总体上支持识别计划的积极影响,尽管关于患者预后的数据较少发表。在领导层访谈中,参与者普遍表示强烈支持推行某种形式的自愿识别计划,尽管有人担心这一努力可能会遇到一些阻力。

结论

识别卒中中心和卒中系统的能力符合美国卒中患者的最佳利益,ASA应支持此类流程的制定和实施。卒中中心/系统识别计划的目的是提高所有医院按照护理标准治疗卒中患者的能力,同时认识到参与程度将因医院和系统的资源而异。

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