Perioperative Outcomes in Patients Received Spinal Chloroprocaine for Hip or Knee Arthroplasty
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 65
- 试验地点
- 1
- 主要终点
- Spinal anesthesia failure
研究概览
简要总结
This study evaluates the perioperative course in adult patients undergoing total or partial knee arthroplasty, or total hip arthroplasty under chloroprocaine spinal anesthesia.
详细描述
This study evaluates the failure rate of spinal anesthesia, the duration of surgical anesthesia, the needs for complementary intraoperative analgesia, the time for recovery, the incidence of urinary retention, postoperative nausea and vomiting, and length of stay in the recovery room in patients operated for knee or hip arthroplasty under spinal anesthesia with chloroprocaine 50 mg.
研究设计
- 研究类型
- Observational
- 观察模型
- Case Only
- 时间视角
- Retrospective
入排标准
- 接受健康志愿者
- 否
入选标准
- •adult patients
- •with spinal anesthesia using 50 mg of chloroprocaine
- •operated for total knee, unicompartment knee or anterior access hip arthroplasty
- •in the period of years 2020 - 2021
排除标准
- •expressed disagreement to to participate after receiving information notice
研究组 & 干预措施
chloroprocaine anesthesia for arthroplasty
patients having predicted uncomplicated surgery for total or unicompartment knee arthroplasty of anterior access total hip arthroplasty, operated under spinal anesthesia with 50 mg of chloroprocaine
干预措施: Chloroprocaine Injection (Drug)
结局指标
主要结局
Spinal anesthesia failure
时间窗: Day 0
proportion of patients with the necessity to convert initially planned spinal anesthesia into general anesthesia
次要结局
- Urinary retention(24 hours)
- Postoperative nausea and vomiting(24 hours)
- Need for sedation(Day 0)
- Surgical block duration(Day 0)
- PACU analgesia requirement(Day 0)
- Hemodynamic instability(Day 0)
- Length of stay in recovery room(Day 0)
研究者
Mikhail Dziadzko, MD, PhD
Senior physician
Hôpital de la Croix-Rousse