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Subconjunctival liposomal sirolimus vs. cyclosporine or tacrolimus as treatment of keratoconjunctivitis sicca in dogs: A double-blind, randomized study.
García-Santisteban, Rodrigo; Linares-Alba, Mónica Anayatzin; Botello-Bárcenas, Andrés; Margay, Paola; Soto, Carlos; Fonzar-Furtado, Joice; Brooks, Dennis; García, Diego; Sánchez, Gustavo Adolfo García.
Afiliação
  • García-Santisteban R; Hospital Veterinario Oftalvet, Mexico City, Mexico.
  • Linares-Alba MA; Laboratorio Santgar, Mexico City, Mexico.
  • Botello-Bárcenas A; Hospital Veterinario Oftalvet, Mexico City, Mexico.
  • Margay P; Hospital Veterinario Oftalvet, Mexico City, Mexico.
  • Soto C; Hospital Veterinario Oftalvet, Mexico City, Mexico.
  • Fonzar-Furtado J; Hospital Veterinario Oftalvet, Mexico City, Mexico.
  • Brooks D; University of Florida, Gainesville, Florida, USA.
  • García D; Brookseyes LLC, Alachua, Florida, USA.
  • Sánchez GAG; Laboratorio Santgar, Mexico City, Mexico.
Vet Ophthalmol ; 2024 Feb 08.
Article em En | MEDLINE | ID: mdl-38329299
ABSTRACT

PURPOSE:

To compare the safety and efficacy of a 100 microgram subconjunctival injection of liposome-encapsulated sirolimus (SCJS) to cyclosporine (CsA) or tacrolimus (CsA/T) for the treatment of keratoconjunctivitis sicca (KCS) in dogs.

METHODS:

Dogs with signs and symptoms of KCS were block-randomized to one of two treatment groups Biweekly SCJS or conventional treatment (CsA/T). Schirmer tear test 1 (STT-1) scores, conjunctival hyperemia (CH) scores, corneal opacity (CO) scores, and clinical evaluation of potential side effects were recorded every 2 weeks for 14 weeks for both groups. Differences between groups were analyzed using the mixed results ANOVA and U-Mann Whitney tests (p < .05 was considered significant).

RESULTS:

A total of 30 eyes were included in the study, of which 20 eyes completed follow-up. There was no statistically significant interaction between the treatment group and time on STT-1 score (p = .165), and median CH and CO scores showed no statistically significant differences between groups (p = .353 and p = .393, respectively). There were no clinically significant side effects present in any subject at any time.

CONCLUSION:

In this trial, a 1 mg/mL (100 micrograms) SCJS every 2 weeks showed similar safety and efficacy profiles as daily CsA/T in dogs with KS after 14 weeks of treatment. Larger studies should be performed to further assess SCJS as an alternative treatment for KCS.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article