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1.
Ophthalmic Physiol Opt ; 36(3): 266-78, 2016 05.
Artigo em Inglês | MEDLINE | ID: mdl-27112224

RESUMO

PURPOSE: To introduce a newly developed instrument for measuring the topography of the anterior eye, provide principles of its operation and to assess its accuracy and precision. METHODS: The Eye Surface Profiler is a new technology based on Fourier transform profilometry for measuring the anterior eye surface encompassing the corneo-scleral area. Details of technical principles of operation are provided for the particular case of sequential double fringe projection. Technical limits of accuracy have been assessed for several key parameters such as the carrier frequency, image quantisation level, sensor size, carrier frequency inaccuracy, and level and type of noise. Further, results from both artificial test surfaces as well as real eyes are used to assess precision and accuracy of the device (here benchmarked against one of popular Placido disk videokeratoscopes). RESULTS: Technically, the Eye Surface Profiler accuracy can reach levels below 1 µm for a range of considered key parameters. For the unit tested and using calibrated artificial surfaces, the accuracy of measurement (in terms of RMS error) was below 10 µm for a central measurement area of 8 mm diameter and below 40 µm for an extended measurement area of 16 mm. In some cases, the error reached levels of up to 200 µm at the very periphery of the measured surface (up to 20 mm). The SimK estimates of the test surfaces from the Eye Surface Profiler were in close agreement with those from a Placido disk videokeratoscope with differences no greater than ±0.1 D. For real eyes, the benchmarked accuracy was within ±0.5D for both the spherical and cylindrical SimK components. CONCLUSIONS: The Eye Surface Profiler can successfully measure the topography of the entire anterior eye including the cornea, limbus and sclera. It has a great potential to become an optometry clinical tool that could substitute the currently used videokeratoscopes and provide a high quality corneo-scleral topography.


Assuntos
Córnea/anatomia & histologia , Topografia da Córnea/normas , Modelos Anatômicos , Esclera/anatomia & histologia , Topografia da Córnea/métodos , Humanos , Processamento de Imagem Assistida por Computador , Reprodutibilidade dos Testes
2.
J Womens Health (Larchmt) ; 24(4): 257-60, 2015 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-25860106

RESUMO

Maternal and child health (MCH) surveillance data are important for understanding gaps in services and disparities in burden of disease, access to care, risk behaviors, and health outcomes. However, national and state surveillance systems are not always designed to gather sufficient data for calculating reliable estimates of the health conditions among high-risk or underrepresented population subgroups living in smaller geographic areas. The Centers for Disease Control and Prevention's Pregnancy Risk Assessment Monitoring System (PRAMS) has conducted surveillance for over 25 years in collaboration with state and city health departments. In 2012, PRAMS embarked on a multiyear collaboration with the W.K. Kellogg Foundation (WKKF) to include oversampling of minority and low-income women in selected geographic areas in four states (Louisiana, Michigan, Mississippi, and New Mexico) where the WKKF funded extensive place-based initiatives are located. The PRAMS-WKKF collaboration has broad implications for promoting meaningful collaboration between public, private, local, state, and federal organizations to address MCH data gaps on disparities, and for improving the availability of information needed for MCH programs, policy makers, and women.


Assuntos
Comportamento Cooperativo , Comportamentos Relacionados com a Saúde/etnologia , Comportamento Materno/etnologia , Cuidado Pós-Natal/estatística & dados numéricos , Cuidado Pré-Natal/estatística & dados numéricos , Medição de Risco/métodos , Adolescente , Proteção da Criança , Pré-Escolar , Feminino , Humanos , Lactente , Cuidado do Lactente , Recém-Nascido , Assistência Perinatal/estatística & dados numéricos , Vigilância da População , Gravidez , Assunção de Riscos , Fatores Socioeconômicos , Estados Unidos
4.
CNS Spectr ; 19(5): 403-10, 2014 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-24284256

RESUMO

OBJECTIVE: Clozapine is used in the management of treatment-resistant schizophrenia and is effective in reducing aggression; however a subgroup of patients is poorly responsive. For violent patients in this group, there is limited literature on the use of strategies to augment clozapine with other agents. Here we present a case series of 6 schizophrenia patients, within a high-security hospital, who have a history of serious violence and who were treated with clozapine augmented with amisulpride. METHODS: We reviewed case notes and health records for evidence of violence/aggression and positive factors such as engagement in activities, and Clinical Global Impression (CGI) scores were formulated. We also examined metabolic parameters before and after augmentation. RESULTS: All 6 of the patients showed clinical improvement in symptoms and a reduction in their risk of violence to others. Five patients had a reduction in number of violent/aggressive incidents, and all patients showed improvement in engagement in occupational, vocational, and/or psychological work. Metabolic parameters were largely unchanged except for 1 patient whose Body Mass Index (BMI) increased. Five patients reported side effects as unchanged or improved. CONCLUSION: These schizophrenia patients with a history of violence showed clinical improvement and reduced aggression and violence with amisulpride augmentation of clozapine. To our knowledge, this is the first report of an antiaggressive benefit of this combination in forensic psychiatric patients. Further studies are warranted to establish the efficacy and anti-aggressive effects of amisulpride augmentation of clozapine.


Assuntos
Antipsicóticos/uso terapêutico , Clozapina/uso terapêutico , Hospitais Psiquiátricos , Esquizofrenia/tratamento farmacológico , Psicologia do Esquizofrênico , Sulpirida/análogos & derivados , Violência/prevenção & controle , Adulto , Agressão/psicologia , Amissulprida , Glicemia/metabolismo , Índice de Massa Corporal , Colesterol/metabolismo , HDL-Colesterol/metabolismo , Estudos de Coortes , Quimioterapia Combinada , Humanos , Masculino , Estudos Retrospectivos , Medidas de Segurança , Sulpirida/uso terapêutico , Resultado do Tratamento , Reino Unido , Violência/psicologia , Adulto Jovem
5.
J Biol Chem ; 279(19): 19401-6, 2004 May 07.
Artigo em Inglês | MEDLINE | ID: mdl-14966136

RESUMO

As a member of the tetraspanin superfamily of proteins, CD81 has been linked to a number of biologic functions including cellular proliferation, differentiation, activation, and degranulation. As a co-receptor for hepatitis C virus, and a requirement for hepatocytes for infectivity of human Plasmodium falciparum and rodent P. yoelii sporozoite infectivity, CD81 may also play a vital role in pathology. Despite the importance of CD81 in multiple cellular functions, the molecular mechanism of action of CD81 in these processes has remained elusive. Here we report an association between CD81 and the epsilon isoform of 14-3-3, a serine/threonine-binding intracellular signaling protein. Furthermore, we provide evidence that in human, this association is influenced by the palmitoylation state of the CD81 cytoplasmic tails. We have generated a series of CD81 cysteine mutants to identify palmitoylated intracellular motifs of CD81, and reveal palmitoylation on the N- and C-terminal tails as well as the intracellular loop between transmembrane domains 2 and 3. One of these mutants lacks all five of its intracellular cysteines and therefore cannot be palmitoylated. This unpalmitoylated version of CD81 shows constitutive association with 14-3-3. Interestingly, we find that under oxidative conditions, CD81 palmitoylation is inhibited and that condition correlates with the association of CD81 and 14-3-3. These finding suggest that CD81 signaling events could be mediated by 14-3-3 adapter proteins, and these signals may be dependent on cellular redox.


Assuntos
Antígenos CD/metabolismo , Oxirredução , Ácido Palmítico/metabolismo , Tirosina 3-Mono-Oxigenase/metabolismo , Proteínas 14-3-3 , Motivos de Aminoácidos , Sequência de Aminoácidos , Animais , Western Blotting , Células COS , Divisão Celular , Clonagem Molecular , Cisteína/química , Citoplasma/metabolismo , Eletroforese em Gel de Poliacrilamida , Hepatócitos/metabolismo , Humanos , Peróxido de Hidrogênio/farmacologia , Células Jurkat , Camundongos , Dados de Sequência Molecular , Células NIH 3T3 , Estresse Oxidativo , Oxigênio/metabolismo , Plasmídeos/metabolismo , Testes de Precipitina , Ligação Proteica , Isoformas de Proteínas , Estrutura Terciária de Proteína , Homologia de Sequência de Aminoácidos , Transdução de Sinais , Tetraspanina 28 , Transfecção
6.
Clin Lab Sci ; 15(1): 9-12, 2002.
Artigo em Inglês | MEDLINE | ID: mdl-12778949

RESUMO

This study examined the utility of performing urine cultures on biochemically negative urine specimens and details the implementation of a policy to cancel these cultures. Four reactions of the Multistix SG (Bayer, Elkhart IN) urine dipstick (protein, occult blood, leukocyte esterase, and nitrite) were used as biochemical indicators. A three-month retrospective study examining the results of 843 urinalysis/ urine culture pairs indicated that one-third of these cultures were probably unnecessary (negative dipstick/negative culture). Based on these results, a policy was implemented to screen those urine samples having both a urinalysis and urine culture ordered. Over a six-month period, 6,192 urine specimens were evaluated. Of these, 36% (2,260 cultures) were cancelled. Of the 3,932 samples cultured 22.4% (883) were true positives (positive dipstick/positive culture) while 31.6% (1245) had a positive dipstick but grew organisms considered contaminants. The false positive rate was 40% (positive dipstick/negative culture), and the false negative rate was 6%. Implementation of this policy reduced the number of urines cultured by 36%.


Assuntos
Técnicas de Cultura de Células/métodos , Citodiagnóstico/métodos , Urinálise/métodos , Algoritmos , Humanos , Sensibilidade e Especificidade
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