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临床试验/NCT03318198
NCT03318198已完成不适用

The Effect of Intensive Inpatient Attending Supervision on Medical Errors, Patient Safety and Resident Education

Massachusetts General Hospital0 个研究点目标入组 134 人开始时间: 2015年9月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
134
主要终点
Measurement of the rate of medical errors defined as preventable adverse events and near misses. Patient Safety Outcome

研究概览

简要总结

Randomized cross over trial investigating the effect of intensive attending supervision of residents caring for inpatients on the medical service on both patient safety and educational outcomes. Hypothesis: increased attending supervision would improve patient safety and resident education.

详细描述

Background While the relationship between resident work hours and patient safety has been extensively studied, little research has evaluated the role of attending supervision on patient safety and education.

Investigators conducted a 9-month randomized, cross-over trial on an inpatient medicine teaching service where 22 faculty provided either: 1) direct supervision where attendings joined work rounds on established (previously admitted) patients or 2) standard supervision where attendings were available, but did not join work rounds. Each faculty member participated in both arms in random order. The primary safety outcome was rate of medical errors. Secondary safety outcomes included deaths and transfers to the intensive care unit. Resident education was evaluated via a time motion study to assess resident participation on rounds and surveys to measure resident and attending educational ratings.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Other
盲法
None

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

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Intervention Arm

Active Comparator

Attendings on the interventional arm attended daily work rounds with the resident teams in addition to established work rounds on the previously admitted patients on the care team.

干预措施: Enhanged Attending Supervision (Other)

Control Arm

Placebo Comparator

Attendings crossed over to the control arm in which they did not attend work rounds with the team and only say new admissions with the resident team. This was usual care.

干预措施: Standard of Care (Other)

结局指标

主要结局

Measurement of the rate of medical errors defined as preventable adverse events and near misses. Patient Safety Outcome

时间窗: 9 months

Using a previously validated protocol (PMID:24871238) to assess these outcomes, five research nurses reviewed the medical records, formal incident reports from the hospital incident-reporting system, daily pharmacy reports, pharmacy paging logs and solicited reports from nurses working on the study units and noted any adverse events or near misses. Four physician investigators, blinded to attending and intervention, classified each suspected incident as an adverse event, near miss or exclusion (an incident determined to be neither a medical error or adverse event). Physician reviewers further classified all adverse events as preventable or non-preventable. Medical Error rates are reports as number of events per 1,000 patient days

Resident Engagement on Rounds: Educational Outcome

时间窗: 9 months

Time motion study of the amount of time residents and faculty speak during rounds. Time was measured by a research assistant using a Microsoft access program embedded on an IPAD that recorded length of time. Time measurement outcomes are reported in minutes

次要结局

  • Resident and Faculty Perception of Education, Educational Outcome(9 months)
  • Deaths, Patient Safety Outcome(9 months)
  • Transfers to the Intensive Care Unit, Patient Safety Outcome(9 months)

研究者

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

Kathleen Finn

Inpatient Associate Program Director

Massachusetts General Hospital

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