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1.
Orbit ; 41(2): 150-161, 2022 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-34396904

RESUMO

PURPOSE: Epiphora remains an often difficult to manage ocular complaint for ophthalmologists in all subspecialties. This review seeks to examine the safety and efficacy of botulinum toxin injection for management of chronic epiphora. METHODS: The authors conducted a Pubmed search for studies on the use of lacrimal and transplanted salivary gland botulinum toxin injections for the management of epiphora within the past 20 years. Studies included had a minimum of four glandular injections. RESULTS: The authors identified 14 studies and divided them by indication for injection; either functional epiphora, non-functional epiphora, or mixed studies. Seven studies examined injections for cases of functional epiphora, four for non-functional epiphora, and four for mixed cases. The number of glandular injections reported ranged from 4 to 65. Side effects reported were limited to diplopia, eyelid or lacrimal gland hematoma, papillary conjunctivitis, dry eye, ptosis, and bleeding. CONCLUSIONS: Glandular botulinum toxin injection should be considered as a viable treatment strategy for both functional and nonfunctional epiphora. From the studies reviewed, botulinum toxin injection was shown to be effective in both children and adults. Injection can be performed in the outpatient setting, is minimally invasive, technically easy to administer, has a favorable side effect profile, and good efficacy. Furthermore, repeat injections can be performed with similar efficacy.


Assuntos
Blefaroptose , Toxinas Botulínicas Tipo A , Aparelho Lacrimal , Obstrução dos Ductos Lacrimais , Adulto , Blefaroptose/tratamento farmacológico , Toxinas Botulínicas Tipo A/uso terapêutico , Criança , Humanos , Injeções , Resultado do Tratamento
2.
Ophthalmic Plast Reconstr Surg ; 35(1): e3-e6, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-30407994

RESUMO

The authors report the use of a 0.35-mm-thickness nylon implant for medial orbital wall reconstruction to facilitate functional endoscopic sinus surgery (FESS) for severe erosive polypoidal sinus disease while minimizing iatrogenic injuries to the orbital contents. A retrospective chart review identified 4 patients with extensive polypoidal sinus disease who underwent medial orbital wall reconstruction in the setting of FESS. All patients underwent successful reconstruction of bilateral eroded medial orbital walls using a 0.35-mm Supramid Foil Nylon Implant immediately followed by FESS. There were no permanent complications or iatrogenic injuries to the orbital contents due to FESS. All patients experienced improvement in sinus symptoms. Medial orbital wall reconstruction in the setting of erosive polypoidal sinus disease is a useful tool to help facilitate FESS. It allows the sinus surgeon to clear sinus disease aggressively with the orbits being protected from iatrogenic injury.


Assuntos
Endoscopia/métodos , Procedimentos Cirúrgicos Oftalmológicos/métodos , Órbita/cirurgia , Implantes Orbitários , Doenças dos Seios Paranasais/cirurgia , Procedimentos de Cirurgia Plástica/métodos , Pólipos/cirurgia , Idoso , Humanos , Masculino , Pessoa de Meia-Idade , Órbita/diagnóstico por imagem , Doenças dos Seios Paranasais/diagnóstico , Seios Paranasais/diagnóstico por imagem , Seios Paranasais/cirurgia , Pólipos/diagnóstico , Tomografia Computadorizada por Raios X
5.
Am J Ophthalmol Case Rep ; 19: 100836, 2020 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-32760852

RESUMO

PURPOSE: To report a case of chronic neuropathic ocular pain in a patient without visual complaints. OBSERVATIONS: A 37-year-old male with a history of bilateral laser-assisted in situ keratomileusis (LASIK) presented with pain symptoms of 8 months duration in the left eye. The prior LASIK surgery was complicated by corneal ectasia in the left eye requiring penetrating keratoplasty and subsequent placement of a glaucoma drainage implant for uncontrolled, elevated intraocular pressure. The patient was evaluated with a complete clinical examination, including Goldmann applanation tonometry, dilated fundus examination, fluorescein angiography, optical coherence tomography, and magnetic resonance imaging. After 3 weeks of treatment with gabapentin 300 mg BID, the patient reported complete resolution of the ocular pain. CONCLUSIONS AND IMPORTANCE: The pathophysiology of neuropathic ocular pain remains poorly understood. Clinical evaluation often reveals minimal ophthalmic exam findings, leading to an underdiagnosis of the condition by ophthalmologists. Gabapentin may be an underutilized medication in the treatment of chronic ocular pain.

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