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1.
Pediatr Emerg Care ; 40(7): 562-565, 2024 Jul 01.
Artigo em Inglês | MEDLINE | ID: mdl-38718800

RESUMO

OBJECTIVE: The aim of this study was to describe how specific mental health-trained social workers can assist in the evaluations and follow-up of patients presenting with mental health concerns in the pediatric emergency department (ED). METHODS: Work was performed at a quaternary children's hospital ED with 95,000 annual ED visits across 2 locations. Patients requiring mental health services identified based on presenting complaint or from universal suicide screen were included. Emergency department team first evaluates the patients for medical screening and then consults a team of social workers specialized in acute mental health screening (AMHS). The team evaluates and provides recommendation for disposition and assists in plan completion. For patients not admitted, AMHS team makes 24- and 48-hour calls to ensure safety. We collected and analyzed the data on all eligible patients from September 2015 through June 2019 for (1) demographic information, (2) trends in number of consults to AMHS, (3) disposition plans and trends by year, and (4) frequency of follow-up phone calls. RESULTS: A total of 5950 patient visits were reviewed, for 4454 distinct patients. Most patients were 12 to 17 years of age, female, and White, with Medicaid being the predominant insurance. The most common chief complaint was suicidal ideation/plan/attempt. Self-referrals were the majority of assessments, and 59% of patients were already receiving mental health services. Median team response time was 19 minutes. There was an upward trend in consults. Psychiatric hospitalization was the most common disposition; more than 95% of the other visits had timely follow-up phone calls. CONCLUSION: Despite an increasing number of patients presenting to the ED with mental health crisis, safe and efficient management is possible with ED staff-social worker partnership. This approach can ensure that eligible patients receive consistent and evidence-based evaluations and can allow ED clinicians to respond to medical emergencies that require their attention.


Assuntos
Serviço Hospitalar de Emergência , Programas de Rastreamento , Transtornos Mentais , Humanos , Serviço Hospitalar de Emergência/estatística & dados numéricos , Feminino , Masculino , Criança , Adolescente , Programas de Rastreamento/métodos , Transtornos Mentais/epidemiologia , Transtornos Mentais/diagnóstico , Assistentes Sociais , Hospitais Pediátricos , Ideação Suicida , Serviços de Saúde Mental , Saúde Mental
2.
Environ Sci Pollut Res Int ; 30(32): 77981-78003, 2023 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-37300726

RESUMO

Waste cooking oil (WCO) as a rejuvenator is gaining attention in the pavement industry to incorporate higher reclaimed asphalt (RA) in asphalt mixture. This review article provides a comprehensive review on the current state and the feasibility of turning WCO and RA into cleaner and sustainable asphalt pavement material. Considering the advancements in research related to the utilization of WCO in RA mixture, it was necessary to critically review the past and recent studies to provide a methodological scope for future research. The review discusses a plethora of characteristics focusing on chemical, rheological, simulation, environmental, and economical findings related to the utilization of WCO in RA mixtures. Based on the review, WCO can be adjudged as a potential material to rejuvenate asphalt mixtures with higher recycled asphalt content. Furthermore, although WCO enhances low-to-intermediate temperature performance, studies indicated that moisture damage and higher temperature properties are compromised. Future research scope exists in understanding the rejuvenation capabilities of different WCOs and blends of different types of WCO, optimizing the transesterification process of WCO to improve its quality, molecular dynamic simulations focusing on transesterified WCO, quantification of environmental and economic benefits of recycled asphalt mixtures with WCO, and field performance studies.


Assuntos
Temperatura Baixa , Rejuvenescimento , Culinária , Simulação de Dinâmica Molecular
3.
Mol Syst Biol ; 16(12): e9310, 2020 12.
Artigo em Inglês | MEDLINE | ID: mdl-33438817

RESUMO

Many proteins involved in signal transduction contain peptide recognition modules (PRMs) that recognize short linear motifs (SLiMs) within their interaction partners. Here, we used large-scale peptide-phage display methods to derive optimal ligands for 163 unique PRMs representing 79 distinct structural families. We combined the new data with previous data that we collected for the large SH3, PDZ, and WW domain families to assemble a database containing 7,984 unique peptide ligands for 500 PRMs representing 82 structural families. For 74 PRMs, we acquired enough new data to map the specificity profiles in detail and derived position weight matrices and binding specificity logos based on multiple peptide ligands. These analyses showed that optimal peptide ligands resembled peptides observed in existing structures of PRM-ligand complexes, indicating that a large majority of the phage-derived peptides are likely to target natural peptide-binding sites and could thus act as inhibitors of natural protein-protein interactions. The complete dataset has been assembled in an online database (http://www.prm-db.org) that will enable many structural, functional, and biological studies of PRMs and SLiMs.


Assuntos
Bases de Dados de Proteínas , Peptídeos/metabolismo , Inquéritos e Questionários , Sequência de Aminoácidos , Bacteriófagos/metabolismo , Humanos , Ligantes , Peptídeos/química
4.
Pediatrics ; 144(4)2019 10.
Artigo em Inglês | MEDLINE | ID: mdl-31511313

RESUMO

BACKGROUND: Although pharyngitis is common, group A Streptococcus is an uncommon etiology, and sequelae are rare in patients <3 years old. Inappropriate testing leads to increased cost of health care and unnecessary exposure to antibiotics. Rapid streptococcal tests (RSTs) for group A Streptococcus pharyngitis are not routinely indicated in this age group. At our urban, tertiary pediatric emergency department (ED), on average, 20 RSTs were performed each month for patients <3 years of age. Our objective was to reduce RSTs in the ED in patients aged <3 years by 50% in 18 months. METHODS: We initiated this project in October 2016 at an urban, tertiary pediatric ED. We surveyed pertinent multidisciplinary stakeholders to identify factors leading to RSTs in children <3 years of age. We conducted multiple interventions and collected weekly data on the number of RSTs in children aged <3 years (outcome measure) and the number of family complaints and return visits for complications of pharyngitis (balancing measure). We used statistical process control for analysis. RESULTS: The mean number of RSTs ordered per month in patients aged <3 years declined by 52% in 10 months. The majority of tests during the study phase were ordered by nurse practitioners (62%) for patients aged 25 to 36 months (66%). There has been 1 family grievance and no patient complications attributable to the project. CONCLUSIONS: Our interventions led to a successful and sustained reduction of RSTs in patients aged <3 years. A local clinical practice guideline was developed, and the project was expanded to other acute care settings.


Assuntos
Serviço Hospitalar de Emergência , Testes de Sensibilidade Microbiana/estatística & dados numéricos , Faringite/microbiologia , Infecções Estreptocócicas/diagnóstico , Procedimentos Desnecessários , Pré-Escolar , Sistemas de Apoio a Decisões Clínicas , Registros Eletrônicos de Saúde , Feminino , Humanos , Capacitação em Serviço , Masculino , Missouri , Streptococcus pyogenes/isolamento & purificação
5.
J Educ Health Promot ; 7: 75, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-29963568

RESUMO

BACKGROUND: Substance abuse and mental disorder often coexist and may cause several consequences in sociooccupational functioning and health care and management. Indian data are sparse in this area. OBJECTIVES: The aim of the study was to examine the sociodemographic profile, pattern, and prevalence of alcohol and substance use among person suffering with mental illness and to compare with those without mental illness. METHODS: A total of 80 treatment-seeking patients with mental illness and 80 nontreatment seeking healthy accompanying persons were assessed for current substance use. Mental illness was screened using Structured Clinical Interview for DSM-IV Axis I Disorders and the diagnosis was made as per DSM IV, semi-structured sociodemographic pro forma was also applied. The data collected were analyzed using the Chi-square and Student's t-test. RESULTS: Substance use was found 2.5 times higher among cases (56.2%) than controls (22.5%). Substance-using participants comprised mainly males belonging to rural residence. The substance using cases were more unmarried, less educated, poorer economically, and more nuclear family structures that substance-using controls. When compared with non-substance using cases, cases with substance use had more males than females and lower education. Although both groups were almost similar in term of marital status, family structure, residence, and socioeconomic status. Among both groups, most common substance use was tobacco, followed by alcohol and cannabis. Although all the substances were more prevalent among cases than controls. The prevalence of any substance use was highest among cases with psychotic disorder (77.3%), followed by unipolar depression (62.5%), bipolar affective disorder (41.7%), and anxiety disorders (21.4%). Tobacco and cannabis use was most prevalent among cases suffering with psychotic disorders, whereas alcohol use was most prevalent among cases suffering with unipolar depression. CONCLUSIONS: Mentally ill individuals are vulnerable to develop substance use, thus they are doubly jeopardized. The susceptibility of these individuals stem from lesser insight, need for stimulation, to decrease the anhedonia induced by psychoactive medicines and poor awareness hence this group of individuals has several health and social consequences; therefore, they require due attention. A better care, support, and education are needed for substance using patients with mental illness to improve their prognosis and also help in their appropriate rehabilitation.

6.
Structure ; 25(10): 1598-1610.e3, 2017 10 03.
Artigo em Inglês | MEDLINE | ID: mdl-28890361

RESUMO

SH3 domains are protein modules that mediate protein-protein interactions in many eukaryotic signal transduction pathways. The majority of SH3 domains studied thus far act by binding to proline-rich sequences in partner proteins, but a growing number of studies have revealed alternative recognition mechanisms. We have comprehensively surveyed the specificity landscape of human SH3 domains in an unbiased manner using peptide-phage display and deep sequencing. Based on ∼70,000 unique binding peptides, we obtained 154 specificity profiles for 115 SH3 domains, which reveal that roughly half of the SH3 domains exhibit non-canonical specificities and collectively recognize a wide variety of peptide motifs, most of which were previously unknown. Crystal structures of SH3 domains with two distinct non-canonical specificities revealed novel peptide-binding modes through an extended surface outside of the canonical proline-binding site. Our results constitute a significant contribution toward a complete understanding of the mechanisms underlying SH3-mediated cellular responses.


Assuntos
Sequenciamento de Nucleotídeos em Larga Escala/métodos , Proteínas/química , Proteínas/metabolismo , Análise de Sequência de Proteína/métodos , Animais , Humanos , Modelos Moleculares , Biblioteca de Peptídeos , Peptídeos/metabolismo , Ligação Proteica , Conformação Proteica , Proteínas/genética , Domínios de Homologia de src
7.
Bioinformatics ; 32(12): 1865-72, 2016 06 15.
Artigo em Inglês | MEDLINE | ID: mdl-26861823

RESUMO

MOTIVATION: Many intracellular signaling processes are mediated by interactions involving peptide recognition modules such as SH3 domains. These domains bind to small, linear protein sequence motifs which can be identified using high-throughput experimental screens such as phage display. Binding motif patterns can then be used to computationally predict protein interactions mediated by these domains. While many protein-protein interaction prediction methods exist, most do not work with peptide recognition module mediated interactions or do not consider many of the known constraints governing physiologically relevant interactions between two proteins. RESULTS: A novel method for predicting physiologically relevant SH3 domain-peptide mediated protein-protein interactions in S. cerevisae using phage display data is presented. Like some previous similar methods, this method uses position weight matrix models of protein linear motif preference for individual SH3 domains to scan the proteome for potential hits and then filters these hits using a range of evidence sources related to sequence-based and cellular constraints on protein interactions. The novelty of this approach is the large number of evidence sources used and the method of combination of sequence based and protein pair based evidence sources. By combining different peptide and protein features using multiple Bayesian models we are able to predict high confidence interactions with an overall accuracy of 0.97. AVAILABILITY AND IMPLEMENTATION: Domain-Motif Mediated Interaction Prediction (DoMo-Pred) command line tool and all relevant datasets are available under GNU LGPL license for download from http://www.baderlab.org/Software/DoMo-Pred The DoMo-Pred command line tool is implemented using Python 2.7 and C ++. CONTACT: gary.bader@utoronto.ca SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.


Assuntos
Domínios de Homologia de src , Sequência de Aminoácidos , Teorema de Bayes , Sítios de Ligação , Peptídeos , Ligação Proteica , Saccharomyces cerevisiae
8.
Nature ; 509(7502): 575-81, 2014 May 29.
Artigo em Inglês | MEDLINE | ID: mdl-24870542

RESUMO

The availability of human genome sequence has transformed biomedical research over the past decade. However, an equivalent map for the human proteome with direct measurements of proteins and peptides does not exist yet. Here we present a draft map of the human proteome using high-resolution Fourier-transform mass spectrometry. In-depth proteomic profiling of 30 histologically normal human samples, including 17 adult tissues, 7 fetal tissues and 6 purified primary haematopoietic cells, resulted in identification of proteins encoded by 17,294 genes accounting for approximately 84% of the total annotated protein-coding genes in humans. A unique and comprehensive strategy for proteogenomic analysis enabled us to discover a number of novel protein-coding regions, which includes translated pseudogenes, non-coding RNAs and upstream open reading frames. This large human proteome catalogue (available as an interactive web-based resource at http://www.humanproteomemap.org) will complement available human genome and transcriptome data to accelerate biomedical research in health and disease.


Assuntos
Proteoma/metabolismo , Proteômica , Adulto , Células Cultivadas , Bases de Dados de Proteínas , Feto/metabolismo , Análise de Fourier , Perfilação da Expressão Gênica , Genoma Humano/genética , Células-Tronco Hematopoéticas/citologia , Células-Tronco Hematopoéticas/metabolismo , Humanos , Internet , Espectrometria de Massas , Anotação de Sequência Molecular , Fases de Leitura Aberta/genética , Especificidade de Órgãos , Biossíntese de Proteínas , Isoformas de Proteínas/análise , Isoformas de Proteínas/genética , Isoformas de Proteínas/metabolismo , Sinais Direcionadores de Proteínas , Transporte Proteico , Proteoma/análise , Proteoma/química , Proteoma/genética , Pseudogenes/genética , RNA não Traduzido/genética , Reprodutibilidade dos Testes , Regiões não Traduzidas/genética
9.
FEBS Lett ; 586(17): 2751-63, 2012 Aug 14.
Artigo em Inglês | MEDLINE | ID: mdl-22561014

RESUMO

Protein-protein interactions (PPIs), involved in many biological processes such as cellular signaling, are ultimately encoded in the genome. Solving the problem of predicting protein interactions from the genome sequence will lead to increased understanding of complex networks, evolution and human disease. We can learn the relationship between genomes and networks by focusing on an easily approachable subset of high-resolution protein interactions that are mediated by peptide recognition modules (PRMs) such as PDZ, WW and SH3 domains. This review focuses on computational prediction and analysis of PRM-mediated networks and discusses sequence- and structure-based interaction predictors, techniques and datasets for identifying physiologically relevant PPIs, and interpreting high-resolution interaction networks in the context of evolution and human disease.


Assuntos
Genoma , Mutação , Mapeamento de Interação de Proteínas/métodos , Sequência de Aminoácidos , Animais , Inteligência Artificial , Biologia Computacional/métodos , DNA/química , Humanos , Conformação Molecular , Dados de Sequência Molecular , Peptídeos/química , Ligação Proteica , Domínios e Motivos de Interação entre Proteínas , Estrutura Terciária de Proteína , Proteínas/química , Domínios de Homologia de src
10.
Int J Pediatr Endocrinol ; 2011: 11, 2011 Oct 13.
Artigo em Inglês | MEDLINE | ID: mdl-21995344

RESUMO

CHARGE is a phenotypically heterogeneous autosomal dominant disorder recognized as a cohesive syndrome since the identification of CHD7 as a genetic etiology. Classic features include: Coloboma, Heart defects, Atresia choanae, Retarded growth and development, Genitourinary abnormalities, and Ear anomalies and/or deafness. With greater accessibility to genetic analysis, a wider spectrum of features are emerging, and overlap with disorders such as DiGeorge syndrome, Kallmann syndrome, and Hypoparathyroidism Sensorineural Deafness and Renal Disease syndrome, is increasingly evident. We present a patient with a unique manifestation of CHARGE syndrome, including primary hypoparathyroidism and a limb anomaly; to our knowledge, he is also the first CHARGE subject reported with bilateral multicystic dysplastic kidneys. Furthermore, with structural modeling and murine expression studies, we characterize a putative CHD7 G744S missense mutation. Our report continues to expand the CHARGE phenotype and highlights that stringent fulfillment of conventional criteria should not strictly guide genetic analysis.

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