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临床试验/NCT04679025
NCT04679025已完成不适用

Quality Gaps in Screening and Monitoring for Postoperative Hyperglycemia in a Canadian Hospital: A Cross-sectional, Exploratory Study

University of Calgary1 个研究点 分布在 1 个国家目标入组 7,633 人开始时间: 2019年4月1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
7,633
试验地点
1
主要终点
Number of point of care blood glucose measurements in 24-hours after surgery

研究概览

简要总结

Patients with and without diabetes who have postoperative hyperglycemia have worse outcomes than patients with in-target blood sugars. Previous quality improvement work suggests numerous barriers and clinical inertia may contribute to quality gaps in glycemic management for surgical patients. Using a framework for perioperative glycemic management, we sought to measure quality gaps in perioperative glycemic care.

This cross-sectional study used administrative data to measure the proportion of surgical patients with and without known diabetes who underwent preoperative hemoglobin A1c measurement, postoperative point-of-care testing for glucose (POCT), had hyperglycemia, and received basal bolus insulin regimens for treatment. We performed an exploratory analysis comparing length of stay (LOS) in patients with and without diabetes who had and did not have postoperative hyperglycemia.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Cross Sectional

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Underwent inpatient surgical procedure at the Foothills Medical Centre between Apr 1 2019 and March 31 2020
  • Stayed in hospital for more than 24-hours after surgery

排除标准

  • Younger than 18 years of age

结局指标

主要结局

Number of point of care blood glucose measurements in 24-hours after surgery

时间窗: 24-hours post surgery

Proportion of patients who have hyperglycemia

时间窗: 24-hours after surgery

blood or capillary glucose \> 10 mmol/L

次要结局

  • Proportion of patients who have moderate hyperglycemia(24-hours after surgery)
  • Proportion of patients who have severe hyperglycemia(24-hours after surgery)
  • Hospital Length of stay(Until study completion (up to one year from surgical procedure))

研究者

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

Shannon Ruzycki

Clinical Assistant Professor

University of Calgary

研究点 (1)

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