Switching from concomitant therapy to tafluprost/timolol fixed combination
Autor: | Minako Shiokawa, Seiki Katakura, Kenji Inoue, Kyoko Shidara, Hiromi Kohmoto, Ryoko Okayama, Taku Kawashima, Takayuki Fujimoto, Ryo Moriyama |
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Jazyk: | angličtina |
Rok vydání: | 2018 |
Předmět: |
medicine.medical_specialty
Intraocular pressure genetic structures Timolol Glaucoma 03 medical and health sciences 0302 clinical medicine Blurred vision Ophthalmology Concomitant Therapy medicine adverse reactions Original Research business.industry switching tafluprost Tafluprost timolol fixed combination Clinical Ophthalmology medicine.disease eye diseases Blood pressure Concomitant 030221 ophthalmology & optometry sense organs medicine.symptom business 030217 neurology & neurosurgery medicine.drug intraocular pressure |
Zdroj: | Clinical Ophthalmology (Auckland, N.Z.) |
ISSN: | 1177-5483 1177-5467 |
Popis: | Kenji Inoue, Taku Kawashima, Seiki Katakura, Kyoko Shidara, Takayuki Fujimoto, Hiromi Kohmoto, Minako Shiokawa, Ryo Moriyama, Ryoko Okayama Inouye Eye Hospital, Tokyo, Japan Purpose: To evaluate the efficacy and safety of tafluprost/timolol fixed combination (TTFC). Study design: A prospective clinical study. Methods: Twenty-eight patients (28 eyes) with primary open-angle glaucoma, who had used tafluprost and timolol gel for at least 3 months with good adherence, were enrolled. Concomitant administration of tafluprost and timolol was switched to TTFC without a washout period. The intraocular pressure (IOP), blood pressure, pulse rate, and ocular signs were compared between before switching (baseline), and 4 and 8 weeks after switching. A questionnaire survey was also performed 4 weeks after switching to investigate ocular comfort and patient preferences. Results: The IOP showed no significant change after switching to TTFC (14.8 ± 2.8, 14.6 ± 3.4, and 14.8 ± 3.7 mmHg at baseline, Week 4, and Week 8, respectively). The pulse rate and systolic blood pressure showed no changes, but diastolic blood pressure was significantly lower at Week 8. At baseline, fluorescein staining revealed corneal abnormalities in 3 patients, which resolved by Week 8 in 1 patient. Hyperemia was noted in 2 patients at baseline, and this also resolved by Week 8 in 1 patient. Three patients discontinued study treatment for the following reasons (1 patient each): blurred vision; ocular irritation, eyelid erythema, and asthenopia; and loss to follow-up from Week 8. The questionnaire survey revealed no significant differences between the 2 treatments, although more patients preferred TTFC. Conclusion: Among 28 patients enrolled, only 2 patients discontinued the study treatment due to adverse reactions. In patients whose adherence was considered relatively good to concomitant therapy, switching to TTFC achieved similar IOP control with good safety and a high level of patient acceptance. Keywords: tafluprost/timolol fixed combination, switching, intraocular pressure, adverse reactions |
Databáze: | OpenAIRE |
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