跳至主要内容
临床试验/NCT04983329
NCT04983329已完成不适用

Systematic Quality Improvement With Realtime Event Support

Washington University School of Medicine2 个研究点 分布在 1 个国家目标入组 25,506 人开始时间: 2021年11月8日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
25,506
试验地点
2
主要终点
Improvement in administration of surgical antibiotic prophylaxis-after quality improvement intervention

研究概览

简要总结

The goal of this study is to improve perioperative quality metric performance in patients receiving anesthesia care provided by Washington University Department of Anesthesiology. In this protocol, we describe (1) the use of telemedicine-augmented quality improvement interventions to enhance on-time dosage of surgical prophylactic antibiotics, while (2) carrying out large scale monitoring of surgical site infection incidence in the target population. If this quality improvement framework is found to be feasible and successful, we plan subsequently to study its application to additional perioperative quality metrics, including many pertinent to surgical site infection incidence such as perioperative glucose monitoring and management, and intraoperative temperature management.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

入排标准

性别
All
接受健康志愿者

入选标准

  • Patients having procedures at Barnes-Jewish Hospital in suites not part of the TECTONICS trial will be included.

排除标准

  • Patients enrolled in the ongoing TECTONICS intraoperative Anesthesiology Control Tower telemedicine trial at Barnes-Jewish Hospital will be excluded from this study

结局指标

主要结局

Improvement in administration of surgical antibiotic prophylaxis-after quality improvement intervention

时间窗: 2 months

1b. Increase the rate of on-time surgical antibiotic prophylaxis administration prior to incision six weeks after the quality improvement intervention is completed.

Improvement in administration of surgical antibiotic prophylaxis- intervention period

时间窗: 3 months

1a. Increase the rate of on-time surgical antibiotic prophylaxis administration prior to incision during the intervention period.

Improvement in administration of surgical antibiotic prophylaxis

时间窗: 8 months

1c. Increase the rate of on-time re-dosing of antibiotic prophylaxis throughout the duration of the trial.

次要结局

  • Surgical site infection rate(8 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Paul Kerby

Assoc Prof of Anesthesiology

Washington University School of Medicine

研究点 (2)

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