J Korean Ophthalmol Soc.  2013 Feb;54(2):303-309. 10.3341/jkos.2013.54.2.303.

Analysis of Clinical Effectiveness of Tafluprost by Ocular Pulse Amplitude

Affiliations
  • 1Department of Ophthalmology, Soonchunhyang University College of Medicine, Seoul, Korea. sjha@schmc.ac.kr

Abstract

PURPOSE
To analyze the clinical effectiveness of tafluprost used in the treatment of glaucoma, using ocular pulse amplitude (OPA) measurements with dynamic contour tonometry (DCT).
METHODS
Sixty patients (119 eyes) with normal tension glaucoma (NTG) or primary open angle glaucoma (POAG) treated with tafluprost or other eyedrops were investigated in the present study. Intraocular pressure (IOP) was measured with Goldmann applanation tonometry (GAT), and OPA was measured with DCT, before and after treatment, retrospectively.
RESULTS
In 20 patients treated with tafluprost, IOP decreased from 17.1 mm Hg before treatment to 13.0 mm Hg 3 months after treatment (24.0% descent rate), and OPA decreased from 2.35 to 1.57 (33.2% descent rate). For 20 patients who switched from another monotherapy to tafluprost, IOP decreased from 15.7 mm Hg to 13.2 mm Hg from 15.7 mm Hg (15.3%) and OPA from 2.38 to 1.69 (27.7%).
CONCLUSIONS
Tafluprost used to treat glaucoma has a large OPA and IOP lowering effect and, therefore can be applied to patients who have a large OPA with glaucoma progression in spite of well controlled IOP.

Keyword

Normal tension glaucoma; Ocular pulse amplitude; Primary open angle glaucoma; Tafloprost

MeSH Terms

Glaucoma
Glaucoma, Open-Angle
Humans
Intraocular Pressure
Low Tension Glaucoma
Manometry
Ophthalmic Solutions
Prostaglandins F
Ophthalmic Solutions
Prostaglandins F

Figure

  • Figure 1. Time course of IOP change after treatment. Data represent: mean ± SD. **p < 0.01, compared with start or switch value (ANOVA test: Scheffe, Dunnet T3 test). Not significant, comparison between three groups, only significant at base line point between Group 1 and Group 3. IOP reduction from base line to 12 weeks after treatment. Group 1: 24.0%, Group 2: 15.3%, Group 3: 10.1%. Group 1 = Initiation of glaucoma treatment with tafluprost. Group 2 = Switching of anti-glaucoma eye drop (monotherapy) to tafluprost. Group 3 = Switching of anti-glaucoma eye drop to another eye drop except tafluprost.

  • Figure 2. Time course of OPA change after treatment. Data represent: mean ± SD. **p < 0.01, compared with start or switch value (ANOVA test : Scheffe, Dunnet T3 test Not significant, comparison between Group 1 and Group 2, but significant Group 1, 2 vs Group 3, at all time points. OPA reduction from base line to 12 weeks after treatment. Group 1: 33.2%, Group 2: 27.7%, Group 3: 11.7%. Group 1 = Initiation of glaucoma treatment with tafluprost. Group 2 = Switching of anti-glaucoma eye drop (monotherapy) to tafluprost. Group 3 = Switching of anti-glaucoma eye drop to another eye drop except tafluprost.

  • Figure 3. Linear graph of reduction % of cOPA after treatment. Data represent efficacy of cOPA reduction. cOPA: corrected the OPA values by the IOP difference by the time course (ΔIOP). cOPA = OPA − (ΔIOP × 0.12). cOPA means the value of OPA, excluding influence of intraocular pressure. Not significant difference in cOPA, comparison between 3 Groups (ANOVA test), but differ in reduction % of cOPA between 3 Groups, because of difference ΔIOP in each groups. High reduction % of cOPA is meaningful in Group 2, in which IOP has already reduced by another eyedrop. cOPA reduction. Group 1: 16.3%, Group 2: 12.3%, Group 3: 6.7%. Group 1 = Initiation of glaucoma treatment with tafluprost. Group 2 = Switching of anti-glaucoma eye drop (monotherapy) to tafluprost. Group 3 = Switching of anti-glaucoma eye drop to another eye drop except tafluprost.


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Comparison of Dorzolamide-Timolol Fixed Combination and Latanoprost, Effects on Intraocular Pressure and Ocular Pulse Amplitude
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