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1.
J Acad Ophthalmol (2017) ; 15(2): e258-e260, 2023 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-38076402

RESUMO

Inpatient and emergency room ophthalmology consults are becoming an increasingly important issue as fewer providers are willing to provide hospital-based coverage. In this Editorial, I explore aspects of this challenge and highlight a potential solution via the role of an ophthalmic hospitalist.

2.
Pediatr Dermatol ; 40(6): 1107-1111, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-37202834

RESUMO

We present a case of cutaneous granulomatous disease associated with rubella virus in a 4-year-old girl without an identifiable immunodeficiency. In this case, a combination of anti-inflammatory, anti-viral, and anti-neutrophil therapies successfully treated vision-threatening eyelid, conjunctival, scleral, and orbital inflammation.


Assuntos
Síndromes de Imunodeficiência , Dermatopatias , Feminino , Humanos , Pré-Escolar , Vírus da Rubéola , Granuloma/tratamento farmacológico , Dermatopatias/complicações , Pálpebras , Inflamação/complicações
3.
Cornea ; 42(6): 751-754, 2023 Jun 01.
Artigo em Inglês | MEDLINE | ID: mdl-36728311

RESUMO

PURPOSE: The aim of this study was to describe a case of corneal involvement as an early manifestation of ocular disease in the 2022 human mpox (monkeypox) virus outbreak. METHODS: This is a single case report with longitudinal care. RESULTS: A 47-year-old immunocompetent man presented with viral conjunctivitis before development of skin lesions or systemic symptoms. Subsequently, he developed membranous keratoconjunctivitis and a corneal epithelial defect. Orthopoxvirus-positive polymerase chain reaction test from his ocular surface was positive. The epithelial defect did not heal with conservative treatment but was successfully treated with amniotic membrane transplantation over 8 days. Reduced corneal sensation was noted after epithelial healing, and polymerase chain reaction from the ocular surface remained positive at 17 days from symptom onset, with slowly recovering conjunctivitis at 21 days. Continued membrane formation required repeated removal but significantly improved with topical corticosteroid treatment after epithelial healing by 29 days of symptom onset. Corneal sensation normalized by 87 days from symptom onset at which time symblepharon were noted but PCR testing from the ocular surface was negative. CONCLUSIONS: Early corneal involvement of human monkeypox virus is possible. Transient corneal hypoesthesia may be due to acute inflammation. Chronic inflammatory changes can result in symblepharon. These findings have potential implications in patient care and corneal donation.


Assuntos
Doenças da Túnica Conjuntiva , Conjuntivite Viral , Doenças Palpebrais , Ceratoconjuntivite , Mpox , Masculino , Humanos , Pessoa de Meia-Idade , Hipestesia , Ceratoconjuntivite/diagnóstico , Ceratoconjuntivite/tratamento farmacológico , Cicatriz
4.
Orbit ; 41(2): 204-210, 2022 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-33386062

RESUMO

PURPOSE: To evaluate the predominant pathogens and clinical course in pediatric patients with orbital cellulitis (OC) complicated by subperiosteal abscess (SPA). METHODS: This is a single-center retrospective chart review evaluating pediatric patients with OC complicated by SPA treated at a tertiary care center in the Pacific Northwest. Data were analyzed for characteristics, rates of infection, and antibiotic resistance of the predominant pathogens in pediatric patients. RESULTS: Twenty-seven children were identified with OC complicated by SPA and bacterial cultures drawn. The average age (SD) of the patients was 9.2 years (4.8), median 9.6; 15 range 5 months to 17.2 years. Seventeen (63.0%) were male. Sinusitis was present in all patients. Streptococcus species were the most common pathogen accounting for 52% (17/33) of isolates. Streptococcus anginosus group (SAG) was the predominant species and were isolated in 10 out of 27 (37%) children in the study. Twenty-one (78%) patients required surgery for the treatment of SPA. Among surgically treated patients, females tended to be younger than males (p = .068). Pediatric patients with SAG infections required more surgery than children without this isolate, 100% and 65%, respectively (p = .030). Female patients tended to have SAG infections more often than males (p = .063). CONCLUSIONS: Orbital infections caused by SAG require surgical management more often than those caused by other pathogens. Our results suggest a difference in pathogenic organisms in male and female patients with SPA. SAG is one of the most common pathogens isolated in orbital cellulitis complicated by SPA in children.


Assuntos
Celulite Orbitária , Doenças Orbitárias , Abscesso/epidemiologia , Abscesso/etiologia , Abscesso/terapia , Antibacterianos/uso terapêutico , Celulite (Flegmão)/complicações , Celulite (Flegmão)/tratamento farmacológico , Criança , Feminino , Humanos , Masculino , Celulite Orbitária/tratamento farmacológico , Celulite Orbitária/terapia , Doenças Orbitárias/epidemiologia , Doenças Orbitárias/microbiologia , Doenças Orbitárias/terapia , Periósteo , Prevalência , Estudos Retrospectivos , Streptococcus anginosus
5.
Ophthalmology ; 129(1): 73-76, 2022 01.
Artigo em Inglês | MEDLINE | ID: mdl-34293405

RESUMO

The American Academy of Ophthalmology evaluated the practice of routine screening for intraocular infection from Candida septicemia. In the United States, ophthalmologists are consulted in the hospital to screen for intraocular infection routinely for patients with Candida bloodstream infections. This practice was established in the era before the use of systemic antifungal medication and the establishment of definitions of ocular disease with candidemia. A recent systematic review found a rate of less than 1% of routinely screened patients with endophthalmitis from Candida septicemia. Other studies found higher rates of endophthalmitis but had limitations in terms of inaccuracies in ocular disease classification, lack of vitreous biopsies, selection biases, and lack of longer-term visual outcomes. Some studies attributed ocular findings to Candida infections, rather than other comorbidities. Studies also have not demonstrated differences in medical management that are modified for eye disease treatment; therefore, therapy should be dictated by the underlying Candida infection, rather than be tailored on the basis of ocular findings. In summary, the Academy does not recommend a routine ophthalmologic consultation after laboratory findings of systemic Candida septicemia, which appears to be a low-value practice. An ophthalmologic consultation is a reasonable practice for a patient with signs or symptoms suggestive of ocular infection regardless of Candida septicemia.


Assuntos
Academias e Institutos/normas , Candidemia/diagnóstico , Endoftalmite/diagnóstico , Infecções Oculares Fúngicas/diagnóstico , Oftalmologia/organização & administração , Guias de Prática Clínica como Assunto , Candidemia/microbiologia , Endoftalmite/microbiologia , Infecções Oculares Fúngicas/microbiologia , Humanos , Incidência , Fatores de Risco , Estados Unidos
6.
Retin Cases Brief Rep ; 10(3): 249-51, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-26579594

RESUMO

PURPOSE: To report a case of frosted branch angiitis in a patient with granulomatosis with polyangiitis. METHODS: Clinical case report. Imaging was obtained with pseudo-color scanning laser ophthalmoscope photographs, fluorescein angiography, spectral domain optical coherence tomography, and B-scan ultrasound. RESULTS: A 24-year-old woman with a clinical history of granulomatosis with polyangiitis who presented with acute vision loss was found to have frosted branch angiitis with concurrent posterior scleritis and orbital inflammation. These findings improved rapidly after initiation of high-dose intravenous solumedrol. CONCLUSION: This is a unique case of frosted branch angiitis associated with granulomatosis with polyangiitis. The authors are not aware of a previous report of this association. Although rare, retinal vasculitis should be recognized as a potential complication of granulomatosis with polyangiitis and can respond rapidly to prompt initiation of therapy.


Assuntos
Granulomatose com Poliangiite/complicações , Vasculite Retiniana/etiologia , Doença Aguda , Cegueira/etiologia , Feminino , Humanos , Adulto Jovem
7.
J Glaucoma ; 19(8): 509-13, 2010.
Artigo em Inglês | MEDLINE | ID: mdl-20179621

RESUMO

PURPOSE: We previously described a group of patients of Chinese ancestry who presented with optic nerve appearance and visual field loss suggestive of glaucoma but did not show progression characteristic of this disease for up to 7 years. The purpose of this study was to assess whether axial length is a risk factor for visual field loss in patients presenting with this cluster of findings. PATIENTS AND METHODS: Twenty patients of Chinese ancestry with characteristics of this previously described condition including myopia, tilted discs, and glaucomatous visual field abnormalities who also had asymmetric visual field loss were enrolled in this study. Patients underwent axial length measurement of both eyes and a fellow eye analysis was performed to determine the relationship between axial length and visual field loss. RESULTS: Tilted discs were found in 30 out of 40 eyes, with cup/disc ratios ranging from 0.5 to 0.9. Myopia >6.00 diopters was also found in 30 out of 40 eyes. In these subjects with disease that was discordant between the 2 eyes, longer axial length was not found to be associated with greater visual field loss (P>0.99, Freeman-Halton extension of the Fisher exact test). No correlation was found between axial length and mean deviation on visual field testing (r=-0.06). CONCLUSIONS: We did not find axial length to be a risk factor for visual field loss in eyes with asymmetric disease in this patient population. These findings suggest that factors other than progressive lengthening of the eye play an important role in the etiology of glaucomatous appearing optic nerve damage and visual field loss in this specific subset of patients.


Assuntos
Comprimento Axial do Olho/patologia , Glaucoma de Ângulo Aberto/etiologia , Miopia/etiologia , Doenças do Nervo Óptico/etiologia , Transtornos da Visão/etiologia , Campos Visuais , Adulto , Idoso , Idoso de 80 Anos ou mais , Povo Asiático/genética , China , Feminino , Glaucoma de Ângulo Aberto/diagnóstico , Glaucoma de Ângulo Aberto/genética , Humanos , Masculino , Pessoa de Meia-Idade , Miopia/diagnóstico , Miopia/genética , Disco Óptico/anormalidades , Doenças do Nervo Óptico/diagnóstico , Doenças do Nervo Óptico/genética , Projetos Piloto , Estudos Retrospectivos , Fatores de Risco , Transtornos da Visão/diagnóstico , Transtornos da Visão/genética
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