AI Article Synopsis

  • The study aimed to evaluate the effectiveness, procedure time, and safety of two intravitreal injection techniques: an injection guide (IIG) and a dual blade speculum (DBS).
  • In a trial involving 200 adult eyes, both methods were successful, but the IIG had a significantly shorter mean procedure time (approximately 10 seconds) compared to the DBS (around 22 seconds).
  • The IIG also resulted in fewer instances of subconjunctival hemorrhage and was preferred by patients with prior IVI experience, highlighting its advantages over the DBS technique.

Article Abstract

Objective: To compare the effectiveness, procedure time and safety outcomes of two different intravitreal injections (IVI) techniques.

Methods: This was a prospective, single-center, randomized clinical trial of 200 adult eyes receiving intravitreal medications for various indications. Eyes were assigned (1:1) to undergo IVI using either an intravitreal injection guide (IIG) (n= 100) or conventional dual blade speculum plus surgical caliper (DBS) (n=100). All IVI were administered using a 30-gauge needle placed 4 mm posterior to the inferior limbus. The main outcome measures were rate of successful IVI administration, procedure time (seconds) as measured by a stopwatch from application to removal of IIG or DBS, patient preference for IVI technique and adverse events.

Results: The two groups were similar in terms of mean age (P=0.398), laterality (P=0.671), indication for treatment (P=0.175) and medication type (P=0.489). All IVI procedures were successfully completed in both groups. The mean procedure time was shorter using the IIG (9.94 ± 2.87 seconds) versus DBS (21.85 ± 7.25 seconds) technique (P ≤ 0.01). The incidence of post-injection subconjunctival hemorrhage was higher when the DBS was applied (OR = 2.35, 95% CI = 1.22-4.53). Patients with previous history of IVI preferred the IIG over the DBS. No other injection-related adverse events were observed in both groups.

Conclusion: DBS and IIG techniques are similarly effective and safe for the administration of intravitreal medications. The IIG appears to significantly reduce procedure time, be associated with a lower incidence of subconjunctival hemorrhage and engender better patient acceptance.

Clinical Trial Registration: ClinicalTrials.gov (NCT04455399).

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8197588PMC
http://dx.doi.org/10.2147/OPTH.S309501DOI Listing

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