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临床试验/NCT04648540
NCT04648540已完成早期 1 期

Multimodal Opioid-free Anesthesia Versus Opioid-based Anesthesia for Patients Undergoing Cardiac Valve Surgeries: A Randomized Controlled Trial

Cairo University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2020年12月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
早期 1 期
状态
已完成
入组人数
60
试验地点
1
主要终点
Extubation time (min)

研究概览

简要总结

Several studies demonstrated the effectiveness of OFA in patients undergoing non-cardiac surgery. Preoperative use of Cox inhibitors, GABA analogues and acetaminophen have been shown to decrease use of opioids postoperatively . Intraoperative use of agents that lead to opioid sparing effects via sodium channel blockade, blockade of G protein-coupled receptors, NMDA blockade, central alpha-2 agonists and anti-inflammatory effects can make opioid-free anesthesia (OFA) possible. On the other hand, there have been no studies demonstrating the effectiveness of an OFA technique in patients undergoing cardiac surgery except for two case reports who successfully implemented the OFA regimen in two patients undergoing valve replacement surgeries. The investigators therefore propose this prospective randomized controlled trial to investigate whether a multimodal opioid-free anesthesia regimen will be suitable as an alternative to conventional opioid-based regimen in patients undergoing valve surgery

详细描述

High-dose opioid anesthesia during cardiac surgery has been the mainstay of cardiac anesthesia for decades due to its ability to preserve hemodynamic stability and attenuate hormonal and metabolic response to surgical stress (1) . However, large doses of long-acting opioids required patients to be ventilated post-operatively for 12-24 h. Modifications in these practices have been dictated by the increasing cost, complications of prolonged mechanical ventilation, and the changes in demographics of patients presenting for cardiac surgery (2) . Moreover, the intraoperative use of large bolus doses or continuous infusions of potent opioids may be associated with postoperative hyperalgesia and tolerance (3). When it comes to ambulatory surgery, opioid related side effects, such as postoperative nausea and vomiting (PONV), prolonged sedation, ileus and urinary retention may delay recovery and discharge or cause unanticipated hospital readmission (4) . Such complications might, at least in part, also apply to cardiac anesthesia.

Recent evidence suggests that increased total dose of opioids during cardiac surgery may lead to increased in-hospital, as well as long-term post-operative pain medication requirements for up to one year (5). Moreover, according to Hirji et al study , ongoing opioid use three months after CABG was present in 21.7% of opioid-exposed patients versus 3.2% of opioid-naive patients (6). In addition, Opioids have many known side effects such as somnolence, brainstem and respiratory depression , and chronic opioid dependence (7-9), and there is a national trend to decrease opioid use during non-cardiac surgery to promote faster recovery and decrease narcotic use post-operatively (1) .

Several studies demonstrated the effectiveness of Opioid-free Anesthesia (OFA) in patients undergoing non-cardiac surgery(4,10,11). Preoperative use of COX inhibitors, GABA analogues and acetaminophen have been shown to decrease use of opioids postoperatively(10). Intraoperative use of agents that lead to opioid sparing effects via sodium channel blockade, blockade of G protein-coupled receptors, NMDA blockade, central alpha-2 agonists and anti-inflammatory effects can make opioid-free anesthesia (OFA) possible (12,13). On the other hand, there have been no studies demonstrating the effectiveness of an OFA technique in patients undergoing cardiac surgery except for two case reports who successfully implemented the OFA regimen in two patients undergoing valve replacement surgeries (14,15). The investigators therefore propose this prospective randomized controlled trial to investigate whether a multimodal opioid-free anesthesia regimen will be suitable as an alternative to conventional opioid-based regimen in patients undergoing valve surgery.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients undergoing cardiac valve surgeries ( replacement or repair ) .
  • Age (18-80) years

排除标准

  • Patient refusal
  • Known allergy to any of the medications used in the study
  • Combined valve and CABG surgeries
  • Redo surgery
  • Infective endocarditis
  • Patients in heart failure or heart block or with significant systolic dysfunction (EF < 40%) or diastolic dysfunction more than grade II
  • Pregnant females
  • Patients being treated for chronic pain or with recent use (< two weeks) of opioids, gabapentin, or pregabalin.
  • Substance abuse
  • Patients with renal impairment (creatinine > 2 mg/dL) or hepatic impairment (ALT > 2 folds, INR > 1.5 and/or serum albumin < 2.5 g/dl)

研究组 & 干预措施

Opioid-Free Anesthesia (OFA)

Experimental

The following drugs will be administered 10 minutes before induction of anesthesia in group I (OFA):

  • Pregabalin 150 mg orally with a small sip of water
  • Acetaminophen 1 gm and Ketorolac 30 mg in 100 mL i.v. over 10 minutes
  • Dexmedetomidine loading dose of 0.5 mic/kg i.v. over 10 minutes
  • Lidocaine loading dose of 1.5 mg/kg i.v. over 10 minutes

For simplicity, the weight-based doses of dexmedetomidine and lidocaine will be prepared in a 20 mL syringe

the following drugs will be administered as a continuous infusion:

  • Dexmedetomidine 0.5 mic/kg/h
  • Lidocaine 0.5 mg/kg/h

Patients in both groups will be extubated when they meet our institutional criteria for extubation. Postoperative analgesia will be started as follows:

Group I (OFA):

  • Acetaminophen 1 gm/6h
  • ketorolac 30 mg/8h
  • Pregabalin 150 mg once at night
  • Celecoxib 200 mg/24 hours

干预措施: Dexmedetomidine 0.5 mic/kg/h (Drug)

Opioid Anesthesia (OA)

Active Comparator

Before induction In Group II (OA) patients will receive placebo pills and normal saline in equivalent volumes .

Maintenance

In Group II (OA) patients will receive a continuous infusion of Fentanyl (1 mic/kg/h)

Patients in both groups will be extubated when they meet our institutional criteria for extubation. Postoperative analgesia will be started as follows:

• Morphine 0.1 mg /kg PRN every 8 hours

干预措施: Fentanyl 1 mic/kg/hr (Drug)

结局指标

主要结局

Extubation time (min)

时间窗: 24 hours

Extubation time, defined as the time from discontinuation of inhalation agents to extubation

次要结局

  • Heart rate (beats/min)(24 hours)
  • Blood pressure (mm Hg)(24 hours)
  • Postoperative rescue analgesia (number)(24)
  • Postoperative morphine consumption (mg)(24 hours)

研究者

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

Hossam El-Ashmawi

Professor of anesthiology and pain management

Cairo University

研究点 (1)

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