Duration and Analgesic Quality of 1% Ropivacaine Ankle Blocks for Forefoot Surgeries - A Retrospective Analysis
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 56
- 试验地点
- 1
- 主要终点
- Duration sensory block
研究概览
简要总结
The goal of this observational study is to determine the analgesic duration and analgesic quality of a 1% ropivacaine ankle block in forefoot surgery. Bilateral cases of forefoot surgery, preoperative use of steroids, preexisting lower extremity neuropathy, or failed blocks were not included in this quality improvement program.
An ankle block with 1% ropivcaine and patient follow-up is part of the standard practice at Ziekenhuis Oost-Limburg.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Retrospective
入排标准
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients who underwent unilateral elective forefoot surgery under ankle block with 1% ropivacaine between December 2023 and April 2024 at Ziekenhuis Oost-Limburg, Genk, Belgium.
排除标准
- •Bilateral cases of forefoot surgery
- •Preoperative use of steroids,
- •Preexisting lower extremity neuropathy
- •Failed blocks
结局指标
主要结局
Duration sensory block
时间窗: A maximum of 72 hours until return of sensation is expected.
Every patient was contacted by phone to assess the duration of analgesia, maximum pain scores within the first 24 hours and patient satisfaction with analgesia on a 10-point visual analog scale (VAS), opioid consumption in the first 24 hours, sleep quality, side effects, and ease of mobilization. If the sensory block had not disappeared at the moment of the survey or if the patient could not be reached, the patient was called again the day after.
次要结局
未报告次要终点
研究者
Imré Van Herreweghe
Anesthesiologist, Principle Investigator
Ziekenhuis Oost-Limburg