Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 4 de 4
Filtrar
1.
S D Med ; 72(7): 299-302, 2019 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-31461584

RESUMO

INTRODUCTION: Many organizations recommend childhood vision screenings. Furthermore, 42 out of 50 states in the U.S. have laws requiring these examinations looking for multiple ocular abnormalities that can lead to amblyopia, which has the potential to result in lifelong visual impairment. Currently, South Dakota is not a state with similar aforementioned law. The purpose of this research was to examine vision screening laws and programs across America to potentially provide a framework from which South Dakota could adopt its own law. METHODS: This is a healthcare policy review of childhood vision screenings across the U.S. government websites and departments of education and/or health were contacted for information regarding laws and their processes of vision screenings. The University of South Dakota Sanford School of Medicine (USD SSOM) Pediatric Residency Program was queried on their current practice. The 14 largest school districts in South Dakota were questioned on their policies. Other current regular childhood health screenings in South Dakota were also investigated. RESULTS: Most states utilize the public school systems and school personnel in performing screenings. The USD SSOM Pediatric Residency Program routinely screens children at kindergarten physical exams. The majority of the largest school districts in South Dakota routinely screen their students using a variety of methods. There are a few other routine health screenings covered by insurance and Medicaid in South Dakota. CONCLUSION: South Dakota does not have a law requiring childhood vision screenings. Despite this, many screenings are still performed in schools or in medical offices.


Assuntos
Política de Saúde , Seleção Visual , Criança , Atenção à Saúde , Humanos , South Dakota , Estudantes , Estados Unidos
2.
S D Med ; 71(4): 158-163, 2018 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-29996032

RESUMO

INTRODUCTION: Trabecular microbypass stents are effective at lowering intraocular pressure in patients with mild to moderate glaucoma. Corneal hysteresis has been shown to correlate with reduction in intraocular pressure in patients using topical prostaglandin analogues and selective laser trabeculoplasty to treat glaucoma. The purpose of this study was to investigate whether baseline corneal hysteresis measurements were predictive of effectiveness of trabecular microbypass stents in treating glaucoma. METHODS: This was a retrospective chart review of 163 eyes from 109 patients with primary open angle glaucoma that underwent simultaneous trabecular microbypass stenting and cataract surgery. This was a single center study with one surgeon performing all procedures. RESULTS: The eyes were grouped into quartiles according to baseline corneal hysteresis measurements. Baseline intraocular pressures among the four quartiles of baseline corneal hysteresis groups were similar (p=0.082, ANOVA). The average intraocular pressure reduction at 3 months post-operative visits were 3.67, 1.51, 2.83, and 2.09 mmHg for the first through fourth quartiles respectively, and these differences are insignificant overall (p=0.34, ANOVA). Likewise, no significant difference was detected in terms of reduction in glaucoma medications among the quartiles three months after surgery (p=0.78, ANOVA). CONCLUSION: Baseline corneal hysteresis does not appear to show any value in predicting intraocular pressure reduction in response to placement of a trabecular microbypass stent for treating glaucoma.


Assuntos
Extração de Catarata , Córnea/fisiopatologia , Implantes para Drenagem de Glaucoma , Glaucoma de Ângulo Aberto/cirurgia , Stents , Malha Trabecular/cirurgia , Análise de Variância , Terapia Combinada/métodos , Glaucoma de Ângulo Aberto/fisiopatologia , Humanos , Pressão Intraocular/fisiologia , Estudos Retrospectivos
3.
J Cataract Refract Surg ; 44(1): 56-62, 2018 01.
Artigo em Inglês | MEDLINE | ID: mdl-29502618

RESUMO

PURPOSE: To evaluate the safety and efficacy of intravitreal administration of a steroid and antibiotics during cataract surgery compared with the typical postoperative topical regimen in preventing postoperative inflammation, pain, cystoid macular edema (CME), and endophthalmitis. SETTING: Private practice, Sioux Falls, South Dakota, USA. DESIGN: Retrospective case series. METHODS: The study group included eyes that had an intravitreal injection of triamcinolone-moxifloxacin-vancomycin at the time of cataract surgery with concomitant trabecular microbypass stent insertion. The control eyes had the same procedure but were prescribed topical antibiotics, steroids, and nonsteroidal antiinflammatory drugs postoperatively. Data were recorded preoperatively and 1 day, 1 week, 1 month, and 3 months postoperatively. Primary outcomes included the number of glaucoma medications, intraocular pressure (IOP), and IOP spikes of at least 15 mm Hg from baseline. RESULTS: There were 234 eyes in the study group and 249 eyes in the control group. The mean reduction in glaucoma medications was 0.24 drops in the study group and 0.80 drops in the control group 3 months postoperatively, whereas the mean IOP reduction was 2.59 mm Hg in the study group and 3.63 mm Hg in the control group. Pressure spikes were detected at 54 (5.7%) of 936 postoperative visits in the study group and at 37 (3.7%) of 996 visits in the control group. There were no cases of severe inflammation, CME, infection, or retinal detachments. CONCLUSIONS: Both groups had similar postoperative pressure reductions and incidence of IOP spikes. The results indicate that intravitreal injections of a steroid and antibiotics might be a safe option for glaucomatous eyes having cataract surgery with trabecular microbypass stent insertion.


Assuntos
Antibacterianos/administração & dosagem , Extração de Catarata/métodos , Cirurgia Filtrante/métodos , Glucocorticoides/administração & dosagem , Complicações Pós-Operatórias/prevenção & controle , Stents , Malha Trabecular/cirurgia , Idoso , Catarata/complicações , Feminino , Humanos , Pressão Intraocular , Masculino , Microcirurgia/métodos , Estudos Retrospectivos , Resultado do Tratamento , Acuidade Visual
4.
Front Neurosci ; 11: 608, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-29163012

RESUMO

Targeting neuropeptide systems is important for future advancements in treatment of neurological and psychiatric illnesses. However, many of the peptides and their analogs do not cross the blood-brain barrier (BBB) efficiently. Nanoparticles such as iron oxide can cross the BBB, and here we describe a novel method for the conjugation of a peptide antisauvagine-30 (ASV-30) to iron oxide nanoparticles. Previous research has shown that direct infusion of ASV-30 into the brain reduces anxiety-like behavior in animal models via actions on corticotropin releasing factor type 2 (CRF2) receptors. Therefore, we tested whether iron oxide+ASV-30 complexes cross the BBB of rats and then determined whether iron oxide+ASV-30 nanoparticles are localized with CRF2-expressing neurons. Finally we tested the hypothesis that systemic infusion of iron oxide+ASV-30 can reduce anxiety-like behavior. First we describe the synthesis and demonstrate the stability of iron oxide-peptide nanoparticle complexes. Next, nanoparticles (87.7 µg/kg Fe2O3) with or without ASV-30 (200 µg/kg, ip) were injected into male rats 30 min prior to transcardial perfusion and brain fixation for immunohistochemical analysis, or before testing on the elevated plus maze (EPM) in an amphetamine withdrawal model of anxiety. Systemically administered iron oxide+ASV-30 particles were present in the brain and associated with neurons, including those that express CRF2 receptors, but did not localize with the iron storage protein ferritin. Furthermore, systemic administration of ironoxide+ASV-30 reduced amphetamine withdrawal-induced anxiety without affecting locomotion, suggesting that the anxiolytic effects of ASV-30 were preserved and the bioavailability of ASV-30 was sufficient. The findings demonstrate a novel approach to peptide delivery across the BBB and provide insight as to the neural distribution and efficacy of this nanotechnology.

SELEÇÃO DE REFERÊNCIAS
Detalhe da pesquisa