Knee Injuries
Conditions
Keywords
knee arthroscopy, dexmedetomidine, neostigmine
Brief summary
Knee arthroscopy is a minimally invasive day case procedure which may be done for diagnosis, meniscectomy or debridement. Arthroscopic surgery is associated with a variable degree of postoperative pain, which is caused by an irritation of free nerve endings of the synovial tissue, anterior fat pad, and joint capsule due to surgical excision and resection
Detailed description
Many studies were done using different intra-articular agents as local anesthetics, opioids, ketamine and alfa2- adrenergic agonists for prevention and treatment of pain after knee surgeries. Dexmedetomidine is a potent and highly selective alfa2-adrenoreceptor agonist. It has sedative-hypnotic, anxiolytic, analgesic, anesthetic and sympatholytic effects. Intra-articular dexmedetomidine was used in several studies to enhance postoperative analgesia after knee arthroscopy with an increased time to first analgesic request and a decreased need for postoperative analgesia Neostigmine is an anticholinesterase and also has antinociceptive effects when administered intrathecally or peripherally.
Interventions
intraarticular injection of 1µg/kg dexametomidine +18ml 0.25%bubivacaine in a total volume of 20 ml.
intraarticular injection of 0.5mg/dose neostigmine +18ml 0.25%bubivacaine in a total volume of 20 ml.
Sponsors
Study design
Masking description
, Patients were randomly allocated (using random table assignment) into two groups to receive one of the following intra-articular solutions (prepared by an individual not involved in the study) which were injected into the knee joint through the cannular sheath after withdrawal of camera, by the orthopaedic surgeon (who was also unaware of the nature of the study drugs) before the arthroscope removed.
Intervention model description
Patients will be randomly allocated to one of two groups each including 50 patients; the group received either intraarticular dexametomidine or neostigmine .
Eligibility
Inclusion criteria
* patients aged above 18 years * scheduled for elective arthroscopic knee surgery under intrathecal anaesthesia
Exclusion criteria
* Absolute or relative contraindications for intrathecal anaesthesia, * Allergy for the studied drugs. * Patients having history of cardiovascular, cerebrovascular, and respiratory diseases, * Patients receiving chronic pain treatment or hypertension treated with alfa methyldopa, clonidine or beta adrenergic blockers were excluded from the study.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| postoperative pain | 36 hours after the end of the surgery. | visual analogue pain scale |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| nausea,vomiting | 36 hours after the end of the surgery. | nausea and vomiting scales |
| sedation | 36 hours after the end of the surgery. | Ramsay sedation score |
Countries
Egypt