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ocular hypertension/cefalea
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Severe ocular hypertension secondary to systemic corticosteroid treatment in a child with nephrotic syndrome.
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OBJECTIVE
To report a case of severe, acute ocular hypertension in a 6-year-old child, 7 days after initiating treatment with oral prednisolone, due to nephrotic syndrome.
METHODS
A 6-year-old female Caucasian child was diagnosed with nephrotic syndrome and treated with oral prednisolone (60
Safety and Efficacy of Adding Fixed-Combination Brinzolamide/Timolol Maleate to Prostaglandin Therapy for Treatment of Ocular Hypertension or Glaucoma.
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Purpose. To evaluate the safety and efficacy of adding brinzolamide 1%/timolol maleate 0.5% fixed combination (BTFC) to a prostaglandin analog (PGA). Methods. This was a 12-week, open-label, single-arm study of patients with open-angle glaucoma or ocular hypertension with intraocular pressure (IOP)
[Clinical evaluation of betaxolol in ophthalmic suspension with or without preservative agent in patients with glaucoma or ocular hypertension].
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A prospective, randomized, cross-over, double-blind trial was designed to compare the safety and intraocular pressure (IOP) lowering effect of betaxolol 0.25% ophthalmic suspension with and without preservative (benzalkonium chloride). Twenty-seven patients with primary open angle glaucoma or with
Preference for a fixed combination of brinzolamide/timolol versus dorzolamide/timolol among patients with open-angle glaucoma or ocular hypertension.
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OBJECTIVE
To assess ocular discomfort upon instillation and patient preference for brinzolamide/timolol relative to dorzolamide/timolol, in patients with open-angle glaucoma or ocular hypertension.
METHODS
This was a multicenter, prospective, patient-masked, randomized, crossover study. On day 0,
Headaches secondary to intraventricular silicone oil successfully managed with ventriculoperitoneal shunt.
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OBJECTIVE
To describe a case of intravitreal silicone oil (SO) migration into the cerebral ventricles with secondary chronic headaches.
METHODS
Retrospective case report. Chart review. Single patient.
RESULTS
A 51-year-old man with a history of proliferative diabetic retinopathy underwent surgery
Three-month comparison of bimatoprost and latanoprost in patients with glaucoma and ocular hypertension.
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A multicenter, randomized, investigator-masked, parallel-group trial compared bimatoprost and latanoprost for efficacy and safety in patients with glaucoma or ocular hypertension. Patients received bimatoprost 0.03% (n = 119) or latanoprost 0.005% (n = 113) once daily in the evening for 3 months.
A case of ocular hypertension complicated by SUNCT syndrome.
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We report a 53-year-old woman with laser iridotomy (LI)-resistant angle-closure and conjunctival injection, which was thought to be the cause of ciliochoroidal effusion associated with short-lasting unilateral neuralgiform headache with conjunctival injection and tearing (SUNCT) syndrome. LI had no
First day review after uncomplicated phacoemulsification: is it necessary?
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OBJECTIVE
To determine whether first day follow-up is necessary after routine uncomplicated phacoemulsification cataract surgery.
METHODS
Data collected prospectively at day 1 postoperative review.
RESULTS
In 510 consecutive cases, serious complications occurred in 8 (1.6%) (wound leak [4], corneal
Urrets-Zavalia syndrome with interface fluid syndrome following laser in situ keratomileusis.
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Efficacy and safety of fixed-combination travoprost 0.004%/timolol 0.5% in patients transitioning from bimatoprost 0.03%/timolol 0.5% combination therapy.
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OBJECTIVE
To determine the efficacy and safety of fixed-combination travoprost 0.004%/timolol 0.5% preserved with polyquaternium-1 in patients with insufficient response to bimatoprost 0.03%/timolol 0.5% preserved with benzalkonium chloride.
METHODS
In this open-label nonrandomized study conducted
Peyronie's disease and Dupuytren's contracture secondary to topical timolol.
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BACKGROUND
Topical beta-blockers are a proven and safe medication used in the treatment of glaucoma and ocular hypertension. Local and systemic side effects are, however, well documented. Systemic side effects can include severe cardio-respiratory impairment, endocrine dysfunction, as well as
[A case of cavernous dural arteriovenous fistula resulting in intracerebral extravasation during transvenous embolization].
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Cortical venous drainage has been described as one of the major risk factors for dural arteriovenous fistula, which may induce venous hypertension leading to venous ischemia or intracerebral hemorrhage. However, it is rather rare to observe cortical venous drainage manifesting in this way in the
Comparison of the intraocular pressure lowering effect of latanoprost and carteolol-pilocarpine combination in newly diagnosed glaucoma.
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OBJECTIVE
To evaluate the comparative efficacy of latanoprost monotherapy versus combined carteolol and pilocarpine therapy in patients with newly diagnosed glaucoma.
METHODS
Masked randomized prospective trial. This study included 51 patients (64 eyes) with newly diagnosed glaucoma or ocular
Comparison of the intraocular pressure lowering effect of latanoprost and a fixed combination of timolol-pilocarpine eye drops in patients insufficiently controlled with beta adrenergic antagonists. French Latanoprost Study Group, and the Swedish Latanoprost Study Group.
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OBJECTIVE
To compare the effect on intraocular pressure (IOP) of latanoprost monotherapy and timolol-pilocarpine in patients with glaucoma or ocular hypertension with inadequately controlled IOP on topical beta adrenergic antagonists.
METHODS
This was a multicentre, randomised, observer masked, 6
Comparison of the efficacy and safety of 2% dorzolamide and 0.5% betaxolol in the treatment of elevated intraocular pressure. Dorzolamide Comparison Study Group.
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A multicenter, parallel-design, randomized, double-masked study was conducted to compare the efficacy and safety of 2% dorzolamide with those of 0.5% betaxolol in the treatment of elevated intraocular pressure (i.o.p). A total of 311 adults with ocular hypertension or open-angle glaucoma were
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