Abstract | PURPOSE: METHODS: NTG patients with a baseline IOP of 16 mmHg or less were enrolled for a one-eye study in which tafluprost was applied once daily for 12 weeks. The presence of adverse drug reactions and the cumulative incidence of adverse events were also investigated. RESULTS: Among the 44 enrolled patients, 41/44 (93.2%) eyes completed the study. The baseline IOP was 13.2 ± 1.3 mmHg in the study eyes and 13.0 ± 1.3 mmHg in the fellow eyes, which was not statistically significant (P = 0.9173, Student's t test). The values obtained for IOP in the study eyes versus fellow eyes were 10.2 ± 1.6 versus 12.1 ± 1.5 mmHg at week 12. The IOP difference between the study eyes and the fellow eyes was statistically significant (P < 0.0001, Student's t test). The cumulative incidence of adverse events was 58.5% by week 12. Ocular itching was the most frequently observed adverse event (29.3%). All adverse events were clinically tolerable. CONCLUSIONS:
Tafluprost induced significant IOP reductions in NTG patients with a baseline IOP of 16 mmHg or less without raising any safety concerns.
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Authors | Tadashi Nakano, Keiji Yoshikawa, Tairo Kimura, Hirotaka Suzumura, Mami Nanno, Takahiko Noro |
Journal | Japanese journal of ophthalmology
(Jpn J Ophthalmol)
Vol. 55
Issue 6
Pg. 605-13
(Nov 2011)
ISSN: 1613-2246 [Electronic] Japan |
PMID | 21874307
(Publication Type: Journal Article, Multicenter Study)
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Chemical References |
- Antihypertensive Agents
- Ophthalmic Solutions
- Prostaglandins F
- tafluprost
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Topics |
- Antihypertensive Agents
(adverse effects, therapeutic use)
- Female
- Follow-Up Studies
- Humans
- Intraocular Pressure
(drug effects)
- Low Tension Glaucoma
(drug therapy, physiopathology)
- Male
- Middle Aged
- Ophthalmic Solutions
(adverse effects, therapeutic use)
- Prospective Studies
- Prostaglandins F
(adverse effects, therapeutic use)
- Tonometry, Ocular
- Treatment Outcome
- Visual Acuity
(physiology)
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