Literature DB >> 24379649

Efficacy and tolerability of preservative-free tafluprost 0.0015% in Korean patients with glaucoma.

Young Hoon Hwang1.   

Abstract

Entities:  

Year:  2013        PMID: 24379649      PMCID: PMC3872089          DOI: 10.2147/OPTH.S57089

Source DB:  PubMed          Journal:  Clin Ophthalmol        ISSN: 1177-5467


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Dear editor I read with interest the article entitled “Preservative-free tafluprost in the treatment of naive patients with glaucoma and ocular hypertension” by Lanzl et al.1 I have also experienced similar treatment outcomes in Korean patients. In Korea, preservative-free tafluprost (Taflotan-S; Santen Pharmaceutical Co, Ltd, Osaka, Japan) was introduced to the ophthalmic market in October 2012. Thus far, no data have been published on the efficacy and tolerability of preservative-free tafluprost in Korean patients. Thus, I investigated the intraocular pressure (IOP)-lowering efficacy and safety of preservative-free tafluprost in treatment-naïve Korean patients with glaucoma. This study included 58 Korean primary open-angle glaucoma patients who had not undergone previous glaucoma treatment. Preservative-free tafluprost was prescribed to the primary open-angle glaucoma patients and the patients were scheduled to visit the clinic after 1, 3, and 6 months of treatment. The mean (standard deviation) IOP of 58 eyes in 58 patients at the baseline visit was 20.0 (4.6) (range, 12–32) mmHg. After treatment with preservative-free tafluprost, the mean IOP decreased to 15.5 (2.5) mmHg (4.6 mmHg [23.0%] reduction from baseline) at 1 month after treatment, to 14.9 (2.8) mmHg (5.1 mmHg [25.5%] reduction from baseline) at 3 months after treatment, and to 15.1 (2.6) mmHg (4.9 mmHg [24.5%] reduction from baseline) at 6 months after treatment, respectively. No significant difference was found in IOP among 1, 3, and 6 months of treatment (P>0.05). Irritation/stinging/burning sensation, itching, tearing, and dryness were reported by 5 (8.6%), 2 (3.4%), 2 (3.4%), and 9 (15.5%) patients, respectively, during the treatment period. None, mild, moderate, and severe conjunctival hyperemia was observed in 43 (74.1%), 13 (22.4%), 2 (3.4%), and 0 (0%) eyes after treatment, respectively. No eye showed corneal staining during the treatment period. According to my clinical experience, preservative-free tafluprost was both well tolerated and effective for IOP reduction in treatment-naïve Korean glaucoma patients. Therefore, I think that preservative-free tafluprost may be a good treatment regimen for glaucoma in Korean patients.
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1.  Preservative-free tafluprost in the treatment of naive patients with glaucoma and ocular hypertension.

Authors:  Ines Lanzl; Thomas Hamacher; Klaus Rosbach; Mohammed Osman Ramez; Robert Rothe; Eva Růžičková; Marta Karhanová; Friedemann Kimmich
Journal:  Clin Ophthalmol       Date:  2013-05-16
  1 in total
  3 in total

1.  Twenty-four-hour efficacy of preservative-free tafluprost for open-angle glaucoma patients, assessed by home intraocular pressure (Icare-ONE) and blood-pressure monitoring.

Authors:  Soon Young Cho; Yong Yeon Kim; Chungkwon Yoo; Tae-Eun Lee
Journal:  Jpn J Ophthalmol       Date:  2015-09-28       Impact factor: 2.447

2.  Efficacy and tolerability of preservative-free 0.0015% tafluprost in glaucoma patients: a prospective crossover study.

Authors:  Wonseok Lee; Sunghoon Lee; HyoungWon Bae; Chan Yun Kim; Gong Je Seong
Journal:  BMC Ophthalmol       Date:  2017-04-28       Impact factor: 2.209

3.  Crossover randomized study comparing the efficacy and tolerability of preservative-free Tafluprost 0.0015% to Latanoprost 0.005% in patients with primary open-angle glaucoma.

Authors:  Sherein M Hagras; Omar K H Al-Duwailah; Mona A Nassief; Ameera G Abdelhameed
Journal:  Indian J Ophthalmol       Date:  2021-09       Impact factor: 1.848

  3 in total

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