Eye Diseases Surgery Eye Block Anaesthesia
Conditions
Interventions
Eye Block Fentanyl Group
Eye Block Control Group
Eye Block Midazolam Group
Sponsors
Authors
Kasr Al Ainy Hospitals-Cairo University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: All patients were clinically evaluated for fitness for anesthesia and categorized according to ASA l grade and patients who had co-morbidities underwent preoperative contro and continued on their treatment during postoperative (PO) course.
Exclusion criteria
Exclusion criteria: 1-Patients with impaired orbital/periorbital sensation, 2-Patients had history of bleeding tendency 3-Patients on current anticoagulants or antiplatelets 4-Patients had allergy to local anesthetics, 5-Patients had posterior staphyloma or with axial length >30 mm were excluded from the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1.Motor block was evaluated using a three point scoring (14). The onset of eyelid and globe akinesia was assessed at 1, 3, 5, 10 and 15 minute and then every 15 minutes after surgery until complete recovery of the block. Duration of block was calculated starting from 15-min after LAM injection till complete recovery. | — |
Secondary
| Measure | Time frame |
|---|---|
| 2. Hemodynamic variables were assessed every 15 minutes during the entire procedure and every 30 minutes during the first two postoperative (PO) hours. Hypotension and bradycardia were defined as a 20% decrease in MAP and HR in relation to baseline measures.;3. PO analgesia was assessed by using 11-points Visual Analogue Score (VAS) every hour for 6-hrs PO and was scored as 0 if no pain up to 10 which indicates intolerable pain sensation. PO analgesia was provided as if VAS was >5 in the form of intramuscular injection of diclofenac 75 mg. | — |
Countries
Egypt
Contacts
Public ContactAhmed Shaker
Lecturer of Anesthesia
Outcome results
None listed