Micropulse transscleral cyclophotocoagulation: initial results using a reduced energy protocol in refractory glaucoma.
Aged
Aged, 80 and over
Ciliary Body
/ surgery
Female
Glaucoma, Open-Angle
/ physiopathology
Humans
Intraocular Pressure
/ physiology
Laser Coagulation
/ methods
Lasers, Semiconductor
/ therapeutic use
Male
Middle Aged
Ocular Hypertension
/ physiopathology
Prognosis
Retrospective Studies
Sclera
/ surgery
Tonometry, Ocular
Visual Acuity
/ physiology
Cyclophotocoagulation
Glaucoma
Intraocular pressure
Micropulse laser
Journal
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie
ISSN: 1435-702X
Titre abrégé: Graefes Arch Clin Exp Ophthalmol
Pays: Germany
ID NLM: 8205248
Informations de publication
Date de publication:
May 2020
May 2020
Historique:
received:
31
07
2019
accepted:
27
01
2020
revised:
22
01
2020
pubmed:
10
2
2020
medline:
6
3
2021
entrez:
10
2
2020
Statut:
ppublish
Résumé
This study evaluates the 6-month safety and efficacy of micropulse transscleral cyclophotocoagulation (MP-TSCPC) in cases of uncontrolled glaucoma/ocular hypertension using a reduced energy protocol. Retrospective analysis of patients undergoing MP-TSCPC from January-April 2018 was carried out. Patients received up to 90 s of laser with settings of 2000 mW/Cm2 and a duty cycle of 31.3%. A total of 29 patients were included, with a mean age of 64.7 ± 15.1 years. The most common diagnosis was primary open angle glaucoma (41.4%) with a mean Logmar visual acuity of 1.5 ± 1.2. All subjects had either undergone intraocular surgery (58.6% filtration surgery) or continuous wave diode laser prior to micropulse treatment. Mean pre-laser IOP was 26.2 ± 11.1 mmHg. There was a significant reduction (p < 0.05) in IOP at 1 month to 15.8 ± 5.4 mmHg (39.7% reduction), at 3 months to 15.04 ± 5.25 mmHg (42.6% reduction) and at 6 months to 18.19 ± 7.47 mmHg (30.6% reduction). There was also a corresponding reduction (p < 0.05) in the number of topical agents required to control pressure from a baseline of 3.31 ± 0.97, to 2.72 ± 0.88 at 1 month, 2.76 ± 0.91 at 3 months and 2.90 ± 1.08 at 6 months. Requirements for oral acetazolamide reduced from 41.3% (1/29) at baseline to 3.4% (1/29) at 6 months. Success rates were 75.9% at 1 month, 79.3% at 3 months and 58.6% at 6 months. There was no drop in the visual acuity, no change in central retinal thickness and no cases of intraocular inflammation. MP-TSCPC at a decreased duration is effective at reducing intraocular pressure in ethnically diverse glaucoma patients refractory to previous glaucoma laser or surgeries at 6 months follow-up, with no significant complications. Further work is needed to confirm efficacy in the long term and to determine optimal settings.
Identifiants
pubmed: 32036425
doi: 10.1007/s00417-020-04611-0
pii: 10.1007/s00417-020-04611-0
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
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