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Ultrasound Guided Peribulbar Anaesthesia - A Novel Dual Quadrant Injection Technique

Not Applicable
Completed
Conditions
Eye Diseases
Interventions
Procedure: Ultrasound guided Dual Quadrant Peribulbar Anaesthesia
Registration Number
NCT02459782
Lead Sponsor
Sunnybrook Health Sciences Centre
Brief Summary

Peribulbar anaesthesia for ocular surgery depends on the spread of local anaesthetic throught the orbit to be successful and has a relatively high failure rate. This study will examine a novel ultrasound guided approach to peribulbar anaesthesia which should extend the depostion of local anaesthetic by using a dual quadrant injection technique. The study will assess the feasibility of this technique, how successful it is and whether any obvious safety issues arise with its use.

Detailed Description

Peribulbar anesthesia is widely used for anterior and posterior chamber ophthalmic procedures. It is a blind technique which is traditionally carried out by inserting a needle in the infero-lateral aspect of the orbit below the globe and injecting a volume of 8 - 12 mL of local anesthetic in the periorbital space. The goal of this inejction is to achieve akinesia and anesthesia of the eye sufficient for surgery. The technique has a relatively high failure rate of up to 30%. A failure or insufficient block requires a second or rarely a third peribulbar injection to achieve success. Ultrasound can be used to guide needles in the human body and has been successfully used in many anatomic locations for anaesthesia. This study will assess whether ultrasound can guide the block needle in ophthalmic anesthesia to deliver local anesthetic via a single entry into two discrete locations within the periorbital space - the first in the infero-lateral quadrant and the second in the infero-medial quadrant. If this can be done the investigators may achieve a higher success rate for this block with a lower volume potentially improving the quality of the block and its safety.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
22
Inclusion Criteria
  • ASA score less than III and ability to provide a written informed consent
  • 22 patients presenting for opthalmic surgery
Exclusion Criteria
  • Coagulation disorder or anticoagulated with INR > 1.5
  • Platelet count < 75 X 10*9/L
  • Significant Myopia (axial length > 28mm)
  • Patients unable to lie supine for 2 hours
  • Patients with recent gas or silicone injections in/around the eye

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
US Guided Dual Quadrant Peribulbar blockUltrasound guided Dual Quadrant Peribulbar AnaesthesiaUltrasound guided Dual Quadrant Peribulbar Anaesthesia
Primary Outcome Measures
NameTimeMethod
Block Success10 minutes post intervention

Block will be deemed a failure if a supplementary block is required for the operative procedure

Secondary Outcome Measures
NameTimeMethod
Block Quality (standardized Ocular Scoring System for akinesia and anaesthesia)5 and 10 minutes

Block will be assessed according to a standardized Ocular Scoring System for akinesia and anaesthesia at 5 minutes and 10 minutes post block. This is a composite measure

Duration of Procedure1 to 10 minutes

The duration of the entire procedure will be recorded

Complications6 Weeks

Any complications during the procedure or in follow up clinical visits will be recorded

Image Visualization1 minute

Operator's ability to see the needle in both the infero-lateral and infero-medial injection will be recorded. Ability to see perineural, retrobulbar and medial rectus spread of local anaesthetic will be recorded. This is a composite qualitative measure.

Block Volume1 minute

Total volume of local anaesthetic will be recorded. Volume for each part of the dual injection technique will also be recorded. This is a composite measure.

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