3.1. Study Design and Population
This is a prospective randomized controlled trial that was carried out on 60 patients undergoing elective cataract surgery by phacoemulsification with intraocular lens implantation. The patients assessed for eligibility were 100 patients. Forty patients were excluded (18 patients did not meet the inclusion criteria, 12 patients declined to participate, and 10 patients were excluded for other reasons). Sixty patients were randomly assigned into one of two groups; the first group received local anesthesia with lidocaine 2% (30 participants) (local anesthesia group), and the second group received topical anesthesia with Oxybuprocaine (30 participants) (topical anesthesia group). The patients, the neurologist, and the surgeons were blinded to the method of anesthesia. Randomization was done using a closed opaque envelope technique. In such a technique, the anesthetist selected a sealed envelope that contained a paper carrying the name of the group to which the patient was scheduled. No patients were lost to follow up or excluded from the analysis. The patients were recruited in the period from December 2016 to January 2018 from the Ophthalmology Outpatient Clinic of Beni-Suef University Hospital. Written informed consent was obtained from all participants on the day of surgery. The study was approved by the Local Ethics Committee in the Faculty of Medicine, Beni-Suef University (FWA00015574 in 8th of March 2018). The study was conducted in accordance with the Declaration of Helsinki. The study was registered in the Pan African Clinical Trial Registry (PACTR201903779653918).
3.2. Inclusion and Exclusion Criteria
Patients were included if they were between 40 years to 70 years old with immature cataracts.
The following patients were excluded from the study: patients with mature cataract, a history of previous ocular trauma or surgery, ocular co-morbidities such as exfoliation syndrome, posterior synechia, uveitis, phacodonesis, strabismus or poor fixation due to nystagmus, marked auditory dysfunction affecting their ability to complete testing, pre-existing cognitive disorder, allergy to either local or topical anesthetics, and inability to understand the instructions concerning the study or if the patient refused the local or topical anesthesia techniques.
The included patients were subjected to the following:
• Cognitive Assessment:
It was done for all patients preoperatively and one week postoperatively by a neurologist who was blinded to anesthesia technique. Verbal memory was assessed using paired-associate learning test (PALT). In such a test, the examiner would say ten pairs of words in front of the participant. These pairs contain four semantically unrelated pairs and six semantically related pairs. After two minutes, the first word of the pairs is mentioned to the participant and he/she is asked to recall the second one. The test is repeated three times. A score 1 was given for each correct incompatible pair while a score 0.5 was given for each correct compatible pair. The total score for the test ranges from 0 to 21 (
17). Attention and executive function were assessed using category verbal fluency test. In this test, the participant is asked to name as many animals as he can within 1 minute. Each animal he/she names, takes a score 1 (
18).
• Assessment of Patients’ Satisfaction:
Patients’ satisfaction was assessed by a neurologist who was blinded to the anesthesia technique using the Iowa satisfaction with anesthesia scale (ISAS). This questionnaire measures patient’s satisfaction with their monitored anesthesia care (MAC). Patients have to respond to 11 statements by placing a mark along a single response out of six options for responses. The responses are: -3 = disagree very much, -2 = disagree moderately, -1 = disagree slightly, 1 = agree slightly, 2 = agree moderately, and 3 = agree very much. A totally satisfied patient was given a score +3, and a totally dissatisfied patient was given a score −3. The mean score of their responses to all the statements ranged from -3 to +3. Patients were given the questionnaire immediately after the operation. The time required to fill in the questionnaire was not limited. None of the anesthesiologist or the operator was in contact with the patient during this time (
19).
• Anesthetic Technique:
Anesthesia for cataract surgery was done for all included patients by the same anesthesiologist. The included 60 patients in the study were randomly assigned to one of the two groups; the first group received local anesthesia with lidocaine 2% (total volume 6 mL) with hyaluronidase 30 IU (30 participants) (local anesthesia group), and the second group received topical anesthesia with Oxybuprocaine (benoxinate hydrochloride 0.4%) every 1 minute 3 times before the surgery (30 participants) (topical anesthesia group). All included patients were transferred to the preparation room. The anesthesia technique and the operation procedure were explained to the patients, no premedication was given, only psychological reassurance. Venous line was inserted under antiseptic technique. Standard monitoring was done for all included patients (oxygen saturation, electrocardiogram, and blood pressure measurement). In the local anesthesia group, peribulbar injection technique was done with a 25 G needle under complete antiseptic technique. The patients should look straight ahead, then injection of a volume 4 mL of the local anesthetic inferolaterally was done after negative aspiration followed by injection of 2 mL through the medial canthus. Digital pressure was applied after each injection for 5 seconds every 20 seconds over a period of 3 minutes. The patients were then transferred to the operation room, nasal mask with oxygen supply 3 - 4 L/min was applied and standard monitoring was done.
• Surgical Technique:
Cataract surgery was done for all participants by the same surgeon using the same surgical technique. In all patients, a 2.4 mm sized incision in the clear cornea was created at the most curved axis. A sutureless incision was made then phacoemulsification was performed with implantation of a foldable single piece lens into the capsular bag. In both groups, the surgical time was 15 - 20 minutes, the operation room stay was one hour, and the hospital stay 8 hours. The patients wear eye patches after surgery for 3 days.
3.3. Statistical Methods
Calculation of sample size was done using G*Power version 3.1.9.2 Software based on our pretrial pilot study. The power (1 - β) was 80% and the probability of type I error (α) was 5%. A total of 60 participants with 1:1 ratio of the two arms in our study were required for the two-sided significance of 95%. The data were coded and entered using: the statistical package for social science version 18 (SPSS V. 18) (Chicago, USA). For quantitative variable, student t-test was used for comparison between mean of responses of ISAS between local and topical anaesthesia groups, and Paired-sample t-test was used for comparison between means of preoperative and postoperative cognitive tests in local and topical anesthesia groups. For qualitative variables, number and percent were calculated and chi-square test was used for comparison between local and topical anesthesia groups. The significance value P < 0.05 is considered statistically significant.