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临床试验/NCT05341154
NCT05341154已完成不适用

Ketamine Versus Dexmedetomidine for Prevention of Postoperative Delirium in Elderly Patients Undergoing Emergency Surgery: A Comparative Study.

Huda Fahmy Mahmoud, PhD1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2021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
不适用
状态
已完成
发起方
入组人数
60
试验地点
1
主要终点
Postoperative delirium by Delirium Observation Screening Scale (DOS)

研究概览

简要总结

Delirium is a common postoperative complication in the elderly, often caused by multiple factors. It is defined as an acute neuropsychiatric disorder characterized by fluctuating disturbances in attention, awareness, and cognition. Postoperative delirium occurs in 17-61% of the major surgical procedures. It may be associated with cognitive decline, decreased functional independence, increased risk of dementia, caregiver burden, health care costs, morbidity, and mortality. Therefore, delirium is a possibly disastrous condition and is both a huge burden on a patient's health and on the health care system in general.

详细描述

Over the last few decades, numerous risk factors for delirium have been identified, emphasizing the importance of delirium prevention in patients undergoing surgery. It has already been identified as a state that may be associated with serious complications such as prolonged ICU and hospital stays, decreased quality of life, and increased mortality ). Previous studies on delirium pointed out old age and other factors as important predisposing factors. on the health care system in general. Extensive research on reducing the incidence of delirium has been conducted using both pharmacological and non-pharmacological preventive measures in the acute setting. As evidence recommending or opposing specific drugs for the prevention of postoperative delirium remains insufficient and the international guidelines can only recommend perioperative pharmacologic adjustments ("American Geriatrics Society Abstracted Clinical Practice Guideline for Postoperative Delirium in Older Adults," 2015) . Consequently, the challenge of developing reliable hospital algorithms for delirium prevention and treatment remains unresolved. Furthermore, there is a link between postoperative delirium and two biomarkers, cortisol and C- Reactive Protein (CRP), which have previously been linked to delirium but whose significance is unknown.

研究设计

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

入排标准

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

入选标准

  • 1- Patients aged ≥ 65 years. 2- Scheduled for visceral, orthopedic, vascular, obstetric, urology, or plastic surgery.

排除标准

  • 1- Delirium upon hospital admission or development of delirium prior to surgery stated by family members.
  • 2- Mini-Mental State Examination (MMSE) score < 24 points 3- Delirium Observation Scale (DOS) ≥4 points 4- preoperative neurological diseases affecting cognitive function (such as vascular dementia) 5- High risk for postoperative treatment in the intensive care unit (ICU) 6- Known to have dexmedetomidine and or ketamine intolerance. 7- Lack of cooperation or communication. 8- Parkinson's disease, parkinsonism, intake of dopaminergic drugs (levodopa, dopamine agonists) 9- Epilepsy. 10- Patients on steroid therapy 11- severe liver and renal insufficiency

研究组 & 干预措施

Ketamine group

Active Comparator

An anesthesiologist who is not involved in the study will prepare the intervention, ketamine1 mg/kg BW, in a standardized syringe with the same volume. Patients will be given the active comparator or placebo only once right before the induction of anesthesia.

All patients will be received standardized GA protocol as follows:

  1. Induction with propofol (1-2 mg/kg body weight).
  2. Esmeron (1 mg/kg body weight).
  3. Isoflurane is a volatile anesthetic agent in 50% O2 and air.
  4. Fentanyl (1 microgram/kg body weight) during induction of anesthesia and the total doses of fentanyl used during the operation will be recorded.
  5. All patients received a combination of intravenous paracetamol 1 g and ketorolac 30 mg at the conclusion of surgery. This regimen will be repeated regularly every 8 h.

干预措施: Ketamine Hcl 50Mg/Ml Inj (Drug)

Dexmedetomidine group

Active Comparator

An anesthesiologist who is not involved in the study will prepare the intervention, Dexmedetomidine 1 μg/kg BW, in a standardized syringe with the same volume. Patients will be given the active comparator or placebo only once right before the induction of anesthesia.

All patients will be received standardized GA protocol as follows:

  1. Induction with propofol (1-2 mg/kg body weight).
  2. Esmeron (1 mg/kg body weight).
  3. Isoflurane is a volatile anesthetic agent in 50% O2 and air.
  4. Fentanyl (1 microgram/kg body weight) during induction of anesthesia and the total doses of fentanyl used during the operation will be recorded.
  5. All patients received a combination of intravenous paracetamol 1 g and ketorolac 30 mg at the conclusion of surgery. This regimen will be repeated regularly every 8 h.

干预措施: Ketamine Hcl 50Mg/Ml Inj (Drug)

Placebo group

Placebo Comparator

An anesthesiologist who is not involved in the study will prepare the intervention, normal saline 0.9% in a standardized syringe with the same volume. Patients will be given the active comparator or placebo only once right before the induction of anesthesia.

All patients will be received standardized GA protocol as follows:

  1. Induction with propofol (1-2 mg/kg body weight).
  2. Esmeron (1 mg/kg body weight).
  3. Isoflurane is a volatile anesthetic agent in 50% O2 and air.
  4. Fentanyl (1 microgram/kg body weight) during induction of anesthesia and the total doses of fentanyl used during the operation will be recorded.
  5. All patients received a combination of intravenous paracetamol 1 g and ketorolac 30 mg at the conclusion of surgery. This regimen will be repeated regularly every 8 h.

干预措施: Ketamine Hcl 50Mg/Ml Inj (Drug)

结局指标

主要结局

Postoperative delirium by Delirium Observation Screening Scale (DOS)

时间窗: 72 hours

\>4 points

Postoperative cognitive impairment by Mini Mental State Examination (MMSE) score

时间窗: 72 hours

Mini Mental State Examination (MMSE) score \< 24 points

次要结局

未报告次要终点

研究者

发起方
Huda Fahmy Mahmoud, PhD
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Huda Fahmy Mahmoud, PhD

Assistant professor of Anesthesia and Intensive Care

Aswan University Hospital

研究点 (1)

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