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Implementation of a Dexmedetomidine Stewardship Program at a Tertiary Academic Medical Center

机译:在大专院校医学中心实施右美托咪定管理计划

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Background: Brigham and Women's Hospital implemented a dexmedetomidine stewardship program in October 2010 beginning with an institution-specific prescribing guideline. To ensure continued adherence to the prescribing guideline, a pharmacist-driven quality assurance program was implemented in November 2011. Objective: The primary objective of this study is to describe the role and impact of a dexmedetomidine stewardship program on dexmedetomidine use at a tertiary academic medical center. Methods: This is a prospective descriptive analysis of a dexmedetomidine stewardship program. Dexmedetomidine stewardship data were collected prospectively from January 2012 through June 2012, in all intensive care units (ICUs) at a single academic medical center. Adult patients (>18 years old) receiving dexmedetomidine therapy continuously for sedation and in the ICU were included in the analysis. Results: A total of 99 patients were identified during the study time frame, during which 71 (71.7%) were identified as compliant with the institutional guideline. The total number of patients receiving dexmedetomidine for greater than 24 hours was 13 (13.1%), of whom 10 (76.9%) received targeted interventions; 15 (15.2%) targeted interventions were made on all patients receiving dexmedetomidine during the study time frame. The total use of dexmedetomidine during the study period was 1310 vials, compared with 5404 vials during the equivalent time frame in 2010-a 76% reduction. Conclusions: A dexmedetomidine stewardship program, including an institution-specific prescribing guideline and a pharmacist-driven quality assurance program may ensure guideline compliance and decreased use of dexmedetomidine at an academic medical center.
机译:背景:百翰妇女医院于2010年10月实施了右美托咪定管理计划,该计划始于特定于机构的处方指南。为了确保继续遵守处方指南,2011年11月实施了以药剂师为主导的质量保证计划。目的:本研究的主要目的是描述在第三级学术医学上右美托咪定管理计划对右美托咪定使用的作用和影响。中央。方法:这是右美托咪定管理计划的前瞻性描述性分析。从2012年1月至2012年6月,在一个学术医学中心的所有重症监护病房(ICU)中收集了右美托咪定的管理数据。分析中包括连续接受右美托咪定治疗并在ICU中接受镇静的成年患者(> 18岁)。结果:在研究时间范围内共鉴定出99名患者,其中71名(71.7%)被鉴定为符合机构指南。接受右美托咪定治疗24小时以上的患者总数为13(13.1%),其中10(76.9%)名接受了靶向干预。在研究时间范围内,对所有接受右美托咪定的患者进行了15例(15.2%)靶向治疗。在研究期间,右美托咪定的总使用量为1310个小瓶,而2010年同期的总使用量为5404个小瓶-减少了76%。结论:右美托咪定管理计划,包括特定于机构的处方指南和药剂师驱动的质量保证计划,可确保在学术医疗中心遵守该准则并减少右美托咪定的使用。

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