Overview
Efficacy and Safety of Adding Atracurium to Percaruncular Block for High Myopes Undergoing Cataract Surgery
Status:
Completed
Completed
Trial end date:
2016-05-01
2016-05-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
There are several local anesthetic techniques available for cataract surgery and the choice depends on patient, surgical and operator factors. The eyes of patients with axial myopia (the eye globe is abnormally elongated) have thin wall (sclera), limited space for needle insertion for local anesthetic injection between the globe and the orbit and out-pouching of the back of the eye (staphyloma). These factors increased the risk of perforation following conventional needle techniques of eye block The current study technique is per-caruncular injection (the needle insertion site is between the nasal side of the globe and bony orbit) which may provide a safer alternative to the conventional needle techniques for myopic patients. The space of injection is devoid of blood vessels moreover, myopic staphylomata are infrequently located on the nasal side of the globe. Local injection of muscle relaxant added to local anesthetic solution may provide earlier onset of eye muscle paralysis thus earlier onset of favorable surgical condition than local anesthetic solution alone. The current study will demonstrate the effect of adding low dose atracurium (a muscle relaxant) to local anesthetic mixture in providing early onset of eye muscle paralysis and favorable surgical condition in per-caruncular technique of eye block in high myopes undergoing cataract surgery.Phase:
Phase 4Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Kasr El Aini HospitalTreatments:
Atracurium
Bupivacaine
Lidocaine
Criteria
Inclusion Criteria:- American Society of Anesthesiologists (ASA) physical status I-III
- high myopia (axial length 26mm or more)
Exclusion Criteria:
- Pregnant patients.
- ASA physical status >III.
- Axial length less than 26 mm.
- Contraindication of regional anesthesia:
Absolute contraindications: Patient refusal to participate in the study, Local anesthetic
allergy and Infection/marked orbital inflammation or, Relative contraindications: unable to
lie flat for a sufficient length of time, Confusion or psychiatric illness, communication
difficulties, bleeding diathesis or taking anticoagulants, Previous scleral buckling or
space-occupying lesions within the orbit