Efficacy and safety of intraoperative use of tropicamide 0.02%/phenylephrine0.31%/lidocaine1% intracameral combination during pediatric cataract surgery

Author:

Nucci Paolo1,Lembo Andrea2,Caputo Roberto3,Dellavalle Andrea1,Serafino Massimiliano4,Schiavetti Irene5,Pichi Francesco6

Affiliation:

1. University of Milan

2. San Giuseppe Hospital

3. Anna Meyer Children's University Hospital

4. IRCCS Istituto Giannina Gaslini

5. University of Genoa

6. Cleveland Clinic Abu Dhabi

Abstract

Abstract Background: to demonstrate the safety and efficacy of the intracameral use of tropicamide 0.02%/phenylephrine 0.31%/lidocaine 1% in pediatric cataract surgery, a combination widely used in adult patients but still off-label in childrenMethods: Design: two-center, prospective, observational studySetting: San Giuseppe Hospital, Milan and Meyer Children's Hospital, FlorenceStudy population: children from 0 to 4 years of age undergoing cataract surgery with or without intraocular IOL implantation, in the absence of clinically significant systemic conditions, history of ocular surgery, concurrent ocular medication, hypersensitivity to any of the substances and post-traumatic cataracts. During the surgery, patients received the combination drug after the primary access to the anterior chamber. Efficacy was evaluated by achieving an adequate mydriasis in order to perform capsulorhexis, while safety was assessed by recording vital signs (heart rate, blood pressure, respiratory rate, temperature) pre and post administration of the substance.Results: this study included 53 surgical procedures of 36 patients: 41 eyes were left aphakic while 12 eyes received primary IOL implantation. The pupil size was adequate to safely perform capsulorhexis in 52 procedures of 53. The difference in pupil enlargement was significant (6.0 ± 1.14mm, P = < 0.001). There were no notable changes in vital parameters. Conclusions: the administration of intracameral tropicamide 0.02%/phenylephrine 0.31%/lidocaine 1% in pediatric cataract surgery is effective for obtaining an adequate mydriasis without any vital parameters changes throughout the procedure.

Publisher

Research Square Platform LLC

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