Relief of Periorbital Pain After Acute Angle Closure Glaucoma Attack by Botulinum Toxin Type A
Male
Iridectomy
Palliative Care
Gonioscopy
Middle Aged
Pain, Intractable
3. Good health
Tonometry, Ocular
03 medical and health sciences
0302 clinical medicine
Neuromuscular Agents
Acute Disease
Orbital Diseases
Eye Pain
Humans
Female
Prospective Studies
Botulinum Toxins, Type A
Glaucoma, Angle-Closure
Antihypertensive Agents
Intraocular Pressure
Aged
Pain Measurement
DOI:
10.1097/ijg.0b013e3181ca76a9
Publication Date:
2010-03-24T08:13:12Z
AUTHORS (5)
ABSTRACT
To assess the efficacy and safety of botulinum toxin type A (BoNT-A) injection in patients suffering from intractable periorbital pain after acute angle closure glaucoma (AACG).In this prospective randomized intervention study, 19 patients suffering from periorbital pain after an AACG attack were injected with BoNT-A or placebo for pain relief. Patients were assessed on days 1, 2, 7, 14, 30, 60, and 90. The main outcomes were mean change of visual analog rating scale (VARS) and index scores measured through a quality-of-life questionnaire (EQ-5D), and changes in the visual analog scale (VAS), all of which were assessed at each visit. A secondary outcome was the frequency and nature of adverse events and the number of patients who withdrew from the study as a result.In the treatment group (n=10), the mean index score of EQ-5D and VAS changed significantly from the placebo group (by 0.299 and 2.61, respectively) from day 2 (P<0.01). The VARS of EQ-5D also disclosed significant changes from day 2 (17, P<0.01). In addition, efficacy was maintained mainly between days 2 and 60 but declined slightly by day 90. The most frequently reported treatment-related adverse events in the treatment and placebo groups were local tenderness (21%), subcutaneous hemorrhage (10.5%), and conjunctivitis (10.5%). No severe adverse events were reported during the study or follow-up period.BoNT-A is effective and well tolerated for the treatment of periorbital pain after an AACG attack. Its effects may be maintained for 3 months.
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CITATIONS (5)
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