2004, Number 1
Estudio comparativo de la eficacia clínica y seguridad de la rimexolona al 1% vs el clorhidrato de olopatadina al 0.1% en pacientes pediátricos con conjuntivitis alérgica moderada a severa
Lombardo-Velásquez II, Juárez EJC, Ordaz FJC
Language: Spanish
References: 7
Page: 22-25
PDF size: 215.43 Kb.
ABSTRACT
Purpose: To compare the efficacy and safety of Rimexolone 1% vs. Olopatadine hydrochloride 0.1% in the management of allergic conjunctivitis.Materials and methods: In a randomized, double masked, parallel controlled study, 11 patients with allergic conjunctivitis were studied. Those who met inclusion criteria, received masked study medication with instructions to instil drops twice daily (Olopatadine hydrochloride), and three times daily (Rimexolone 1%) in each eye. The patients underwent a complete ophthalmologic examination, and were asked to describe their symptoms, at the beginning, first, second, forth and sixth week.
Results: 9 patients had been treated, 5 girls and 6 boys. Four of them were treated with more than one drug at the same time.
Clinical improvement of the signs and symptoms occurred in six patients with Rimexolone 1%, two with Olopatadine hydrochloride and one with both.
There was an increase of 5 mmHg in the intraocular pressure in one patient. The level returned to the original value after two weeks.
Two patients did not complete the follow up and were excluded from the study.
Conclusion: Both Rimexolone 1% and Olopatadine hydrochloride 0.1% were effective. Rimexolone 1% acted more rapidly and safety with minimal effect on the intraocular pressure.
REFERENCES