TY - JOUR
T1 - The signs of ocular-surface disorders after switching from latanoprost to tafluprost/timolol fixed combination
T2 - A prospective study
AU - Okumichi, Hideaki
AU - Kiuchi, Yoshiaki
AU - Baba, Tetsuya
AU - Kanamoto, Takashi
AU - Naito, Tomoko
AU - Nakakura, Shunsuke
AU - Tabuchi, Hitoshi
AU - Nii, Hiroki
AU - Sueoka, Chie
AU - Sugimoto, Yosuke
N1 - Funding Information:
Joji Takenaka, Masahide Yanagi, Ken Kobayashi (Hiroshima University) and Takaaki Sasaki (Hiroshima Prefectural Hos-pital) provided and cared for study patients, and reviewed the manuscript. Masayo Hashimoto, Naomi Otsuka, Hiroaki Kurashima, Takeshi Hizume, and Etsuyo Miyamoto (Depart-ment of Medical Affairs, Santen Pharmaceutical Co., Ltd., Osaka, Japan) provided assistance with study design and review of the manuscript. This study was sponsored and funded by Santen Pharmaceutical Co., Ltd., Osaka, Japan. The funding organization participated in the design of the study, interpretation of the data, review and approval of the manuscript and had no role in the conduct, data collection, or analysis of data derived from this study.
Publisher Copyright:
© 2017 Okumichi et al.
PY - 2017/6/21
Y1 - 2017/6/21
N2 - Purpose: To evaluate the ocular-surface safety of a 0.001% benzalkonium chloride-containing tafluprost/timolol fixed combination (TTFC) in patients with primary open-angle glaucoma (POAG) or ocular hypertension who have inadequate intraocular pressure (IOP) control with latanoprost monotherapy. Methods: This study is a multicenter, prospective, single-arm, open-label clinical study. Patients with POAG or ocular hypertension who have inadequate IOP control with latanoprost monotherapy were considered eligible. After providing informed consent, patients continued latanoprost monotherapy for 12 weeks, followed by a switch to TTFC. We evaluated the extent of ocular-surface damage using superficial punctate keratopathy (SPK) score, tear breakup time (TBUT), hyperemia score, IOP, systolic blood pressure (SBP), diastolic blood pressure (DBP), and heart rate at 0, 4, and 12 weeks after switching. Results: A total of 68 patients were enrolled, of whom, 64 patients were included in the final analysis. No significant changes in SPK score, TBUT, or hyperemia score were observed at 4 and 12 weeks compared with week 0. IOP decreased significantly at 4 (13.9±2.5 mmHg) and 12 (14.1±2.5 mmHg) weeks, relative to week 0 (15.3±2.7 mmHg). No significant changes in either SBP or DBP were observed during the study, although patients’ mean heart rate decreased significantly after switching to TTFC. Adverse drug reactions to TTFC occurred in seven patients including two incidences of asthma and one of arrhythmia, and no events were serious. Conclusion: The ocular-surface safety of TTFC is not significantly different to that of latanoprost. Furthermore, switching from latanoprost to TTFC in patients with insufficient IOP control has additive IOP-lowering effects. TTFC is an effective approach for patients receiving latanoprost monotherapy who require more intensive IOP reduction.
AB - Purpose: To evaluate the ocular-surface safety of a 0.001% benzalkonium chloride-containing tafluprost/timolol fixed combination (TTFC) in patients with primary open-angle glaucoma (POAG) or ocular hypertension who have inadequate intraocular pressure (IOP) control with latanoprost monotherapy. Methods: This study is a multicenter, prospective, single-arm, open-label clinical study. Patients with POAG or ocular hypertension who have inadequate IOP control with latanoprost monotherapy were considered eligible. After providing informed consent, patients continued latanoprost monotherapy for 12 weeks, followed by a switch to TTFC. We evaluated the extent of ocular-surface damage using superficial punctate keratopathy (SPK) score, tear breakup time (TBUT), hyperemia score, IOP, systolic blood pressure (SBP), diastolic blood pressure (DBP), and heart rate at 0, 4, and 12 weeks after switching. Results: A total of 68 patients were enrolled, of whom, 64 patients were included in the final analysis. No significant changes in SPK score, TBUT, or hyperemia score were observed at 4 and 12 weeks compared with week 0. IOP decreased significantly at 4 (13.9±2.5 mmHg) and 12 (14.1±2.5 mmHg) weeks, relative to week 0 (15.3±2.7 mmHg). No significant changes in either SBP or DBP were observed during the study, although patients’ mean heart rate decreased significantly after switching to TTFC. Adverse drug reactions to TTFC occurred in seven patients including two incidences of asthma and one of arrhythmia, and no events were serious. Conclusion: The ocular-surface safety of TTFC is not significantly different to that of latanoprost. Furthermore, switching from latanoprost to TTFC in patients with insufficient IOP control has additive IOP-lowering effects. TTFC is an effective approach for patients receiving latanoprost monotherapy who require more intensive IOP reduction.
KW - Glaucoma
KW - Intraocular pressure
KW - Latanoprost
KW - Ocular-surface safety
KW - Tafluprost/timolol fixed combination
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UR - http://www.scopus.com/inward/citedby.url?scp=85021423464&partnerID=8YFLogxK
U2 - 10.2147/OPTH.S136418
DO - 10.2147/OPTH.S136418
M3 - Article
AN - SCOPUS:85021423464
SN - 1177-5467
VL - 11
SP - 1175
EP - 1181
JO - Clinical Ophthalmology
JF - Clinical Ophthalmology
ER -