Abstract | PURPOSE: METHODS: We retrospectively analyzed the data of RP patients at Kyushu University Hospital. We included patients who showed a treatment response to 1.0% topical dorzolamide. The day of treatment initiation was set as the baseline. Topical dorzolamide treatment was continued during the follow-up. The recurrence of CME (defined as a >20% increase in central subfield thickness compared to previous visit, or a central subfield thickness value that exceed baseline value) was evaluated at each follow-up visit. Risk factors for RP-CME recurrence were analyzed by Cox proportional hazards modeling. A Kaplan-Meier survival analysis was used to evaluate the time to recurrent RP-CME. RESULTS: Forty RP-CME patients showed a treatment response to topical dorzolamide. During the mean 3.9-year follow-up, 14 patients exhibited recurrence; its rate was 15.6%, 34.7%, and 48.7% at 1, 3, and 5 years, respectively. A high baseline central subfield thickness was significantly associated with recurrent (hazard ratio 1.11, 95% CI: 1.05-1.18, P = 0.0004). CONCLUSION: The recurrence rate of RP-CME increased with time. A high baseline central subfield thickness value was a risk factor for recurrence.
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Authors | Shotaro Shimokawa, Yusuke Murakami, Kohta Fujiwara, Jun Funatsu, Shunji Nakatake, Yoshito Koyanagi, Masato Akiyama, Noriko Yoshida, Atsunobu Takeda, Yasuhiro Ikeda, Koh-Hei Sonoda |
Journal | Retina (Philadelphia, Pa.)
(Retina)
Vol. 42
Issue 1
Pg. 168-173
(01 01 2022)
ISSN: 1539-2864 [Electronic] United States |
PMID | 34393209
(Publication Type: Journal Article, Observational Study)
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Chemical References |
- Carbonic Anhydrase Inhibitors
- Sulfonamides
- Thiophenes
- dorzolamide
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Topics |
- Administration, Topical
- Carbonic Anhydrase Inhibitors
(administration & dosage)
- Female
- Follow-Up Studies
- Humans
- Incidence
- Japan
(epidemiology)
- Macula Lutea
(growth & development)
- Macular Edema
(drug therapy, epidemiology, etiology)
- Male
- Middle Aged
- Prospective Studies
- Recurrence
- Retinitis Pigmentosa
(complications, diagnosis)
- Risk Assessment
(methods)
- Risk Factors
- Sulfonamides
(administration & dosage)
- Thiophenes
(administration & dosage)
- Time Factors
- Tomography, Optical Coherence
(methods)
- Visual Acuity
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