Horbar J D
Department of Pediatrics, University of Vermont College of Medicine, Burlington, Vermont, and the Vermont Oxford Network, Burlington, Vermont 05401, USA.
Pediatrics. 1999 Jan;103(1 Suppl E):350-9.
The Vermont Oxford Network is a voluntary collaborative group of health professionals committed to improving the effectiveness and efficiency of medical care for newborn infants and their families through a coordinated program of research, education, and quality-improvement projects. In support of these activities, the Network maintains a clinical database of information about very low birth weight infants that now has more than 300 participating neonatal intensive care units (NICUs). We anticipate that these NICUs will submit data for 25 000 infants with birth weights of 401 to 1500 g born in 1998. The research program of the Network includes outcomes research and randomized clinical trials. The goal of Network outcomes research is to identify and explain the variations in clinical practice and patient outcomes that are apparent among NICUs. Network trials are designed to answer practical questions of importance to practitioners and families using pragmatic designs that can be integrated into the daily practice of neonatology. Quality improvement is a major focus of the Network. Members receive confidential quarterly and annual reports based on the Network database that document their performance and compare practices and outcomes at their unit with those at other units within the Network. These reports are intended to assist the members in identifying opportunities for improvement and to help them monitor the success of their improvement efforts. Although information is necessary for improvement to occur, it is not sufficient to foster lasting improvement by itself. Information must be translated into action. The Network is sponsoring an ongoing program of quality initiatives designed to provide members with the knowledge, skills, tools, and resources needed to foster action for improvement. The Network's first formal quality-improvement project, the NIC/Q Project, brought together 10 NICUs to apply the methods of collaborative improvement and benchmarking to neonatal intensive care. Building on the lessons learned in that initial project, the Network now is conducting the Vermont Oxford Network Evidence-Based Quality Improvement Collaborative for Neonatology, known as NIC/Q 2000. This 2-year collaborative will assist multidisciplinary teams from the 34 participating NICUs to develop four key habits for improvement: the habit for change, the habit for practice as a process, the habit for collaborative learning, and the habit for evidence-based practice. During the collaborative, participants will contribute to a knowledge bank of clinical, organizational, and operational change ideas for improving neonatal care. The coordinated program of research, education, and quality improvement described in this article is only possible because of the voluntary efforts of the members. The Network will continue to support these efforts by developing and providing improved tools and resources for the practice of evidence-based neonatology.neonatology, very low birth weight, database, network, quality improvement, evidence-based medicine, randomization, trials, outcomes, mortality, length of stay.
佛蒙特牛津网络是一个由健康专业人员组成的自愿合作组织,致力于通过协调的研究、教育和质量改进项目计划,提高对新生儿及其家庭的医疗护理效果和效率。为支持这些活动,该网络维护了一个关于极低出生体重婴儿的临床信息数据库,目前有300多个参与的新生儿重症监护病房(NICU)。我们预计这些NICU将提交1998年出生体重在401至1500克之间的25000名婴儿的数据。该网络的研究项目包括结果研究和随机临床试验。网络结果研究的目标是识别和解释NICU之间明显的临床实践和患者结果差异。网络试验旨在使用可融入新生儿学日常实践的实用设计,回答对从业者和家庭重要的实际问题。质量改进是该网络的主要重点。成员会收到基于网络数据库的保密季度和年度报告,这些报告记录了他们的表现,并将他们所在单位的实践和结果与网络内其他单位进行比较。这些报告旨在帮助成员识别改进机会,并帮助他们监测改进努力的成功情况。虽然信息是改进发生所必需的,但仅靠信息本身不足以促进持久的改进。信息必须转化为行动。该网络正在发起一个持续的质量倡议项目,旨在为成员提供促进改进行动所需的知识、技能、工具和资源。该网络的第一个正式质量改进项目,即NIC/Q项目,汇集了10个NICU,将协作改进和标杆管理方法应用于新生儿重症监护。基于在那个初始项目中吸取的经验教训,该网络现在正在开展佛蒙特牛津网络新生儿循证质量改进协作项目,即NIC/Q 2000。这个为期两年的协作项目将帮助来自34个参与NICU 的多学科团队养成四个关键的改进习惯:变革习惯、将实践视为一个过程的习惯、协作学习习惯和循证实践习惯。在协作过程中,参与者将为改善新生儿护理的临床、组织和运营变革想法知识库做出贡献。本文所述的研究、教育和质量改进协调计划只有通过成员的自愿努力才有可能实现。该网络将继续通过开发和提供改进的工具和资源来支持这些努力,以促进循证新生儿学的实践。新生儿学、极低出生体重、数据库、网络、质量改进、循证医学、随机化、试验、结果、死亡率、住院时间