Abstract | BACKGROUND: METHODS: Prospective, placebo-controlled consecutive case-series trial. Sixty three patients were divided into two groups: group 1 consisting of 32 patients previously diagnosed with and treated for primary or recurrent chalazia with 2-5 international units (IU) in 0.2-0.5 ml of preserved saline solution of botulinum toxin injection, and group 2 consisting of 31 patients receiving placebo. The main outcome measures were localization and duration of the disease, size of chalazion before and after treatment, clinical resolution of chalazion, time to resolution, and complications of treatment. RESULTS: There was a clinically and statistically significant between-group difference in the rate of therapeutic success and post-therapeutic chalazion regression, but not in the rate of complications. CONCLUSIONS:
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Authors | Tamara Knezevic, Renata Ivekovic, Jasna Pavicic Astalos, Katia Novak Laus, Zdravko Mandic, Aljosa Matejcic |
Journal | Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie
(Graefes Arch Clin Exp Ophthalmol)
Vol. 247
Issue 6
Pg. 789-94
(Jun 2009)
ISSN: 1435-702X [Electronic] Germany |
PMID | 19002481
(Publication Type: Controlled Clinical Trial, Journal Article)
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Chemical References |
- Neuromuscular Agents
- Botulinum Toxins, Type A
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Topics |
- Adolescent
- Adult
- Aged
- Botulinum Toxins, Type A
(administration & dosage, adverse effects)
- Chalazion
(drug therapy)
- Female
- Humans
- Injections, Intralesional
- Male
- Middle Aged
- Neuromuscular Agents
(administration & dosage, adverse effects)
- Prospective Studies
- Recurrence
- Treatment Outcome
- Young Adult
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