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1.
Public Health Rep ; 138(3): 493-499, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-36734190

RESUMO

OBJECTIVES: Limited data are available on how the closure of pediatric dental clinics because of the COVID-19 pandemic affected hospital pediatric emergency department (ED) visits in the United States. We evaluated changes in dental-related visits at a pediatric ED and associated urgent care centers (UCCs) after the shutdown of a large pediatric dental clinic because of the COVID-19 pandemic. METHODS: We conducted a single-center retrospective medical record review of 811 patients aged 0 to 17 years who presented to a pediatric ED or associated UCC at Rady Children's Hospital-San Diego for dental-related concerns from March 19, 2019, through January 17, 2021. Patients were classified into 3 periods: before shutdown, during shutdown, and after shutdown. We collected data on demographic characteristics; International Classification of Diseases, Tenth Revision codes; dental diagnosis; treatment; and COVID-19 test results. We compared the frequency and proportion of patients seen for dental-related concerns, dental diagnosis, and treatment during the 3 periods. RESULTS: The proportion of dental-related concerns in the ED doubled during the shutdown (0.7%) and was 1.5 times higher after the shutdown (0.6%) compared with before the shutdown (0.4%; P < .001). Significantly more patients were seen in EDs than in UCCs during and after the shutdown than before the shutdown (P = .005). During and after the shutdown, admission to the hospital for antibiotic treatment increased significantly to 6.5% and 7.9%, respectively, compared with before the shutdown (2.8%; P = .022), and nonaerosolized procedures and ED/UCC discharge increased to 13.4% and 9.3%, respectively, compared with before the shutdown (6.2%; P = .015). CONCLUSIONS: Mitigating future closures of dental offices is important given the shifted burden of dental care to the ED.


Assuntos
COVID-19 , Clínicas Odontológicas , Humanos , Criança , Estados Unidos/epidemiologia , COVID-19/epidemiologia , Estudos Retrospectivos , Pandemias , Serviço Hospitalar de Emergência , Instituições de Assistência Ambulatorial
2.
J Dent Child (Chic) ; 88(3): 210-222, 2021 Sep 15.
Artigo em Inglês | MEDLINE | ID: mdl-34937633

RESUMO

The purpose of this article was to present the case of a 12-year-old patient with Pallister-Killian syndrome and 45, X/46, XY mosaicism. Dental clinical and radiographic findings and treatment are discussed. The patient presented multiple unerupted supernumerary teeth, ankylosed primary teeth, abnormal root formation of permanent teeth, possible odontomas, and talon cusps on permanent teeth. These unique findings can assist providers in treating patients with these medical conditions.


Assuntos
Anormalidades Múltiplas , Transtornos Cromossômicos , Criança , Cromossomos Humanos Par 12 , Humanos , Mosaicismo
3.
Am J Physiol Lung Cell Mol Physiol ; 293(1): L114-23, 2007 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-17384087

RESUMO

Pulmonary host defense employs a combination of biochemical and biophysical activities to recognize, inactivate, and mediate clearance of environmental agents as well as modulate the overall response to such challenge. Dysregulation of the inflammatory arm of this response is associated with chronic lung diseases (CLD) including cystic fibrosis and chronic obstructive lung disease. Although mechanisms mediating immunoregulation are incompletely characterized, decrements in levels of the nonciliated secretory cell product Clara cell secretory protein (CCSP) in numerous CLD and identification of proinflammatory state in mice homozygous for a null allele of the CCSP gene (CCSP-/-) suggest a central role for the nonciliated secretory cell in this process. In an effort to determine the molecular basis for immunoregulatory defects associated with CCSP deficiency, we utilized difference gel electrophoresis in combination with matrix-assisted laser desorption ionization time-of-flight to compare the proteomes of wild-type and CCSP-/- mice. We demonstrate a shift in the isoelectric point of the immunomodulatory protein annexin A1 (ANXA1) to more acidic isoforms in CCSP-/- mice. Similar ANXA1 mRNA and protein abundance in wild-type and CCSP-/- tissue and identical localization of ANXA1 protein to alveolar macrophages and the ciliary bed of ciliated cells demonstrated that CCSP deficiency was associated exclusively with altered posttranslational modification of ANXA1. These results suggest that both long- and short-range paracrine signaling between nonciliated secretory cells and cells of the immune system and epithelium impact modification of cell type-specific proteins and implicate nonciliated secretory cells in a regulatory axis that might integrate critical aspects of host defense.


Assuntos
Pulmão/citologia , Pulmão/metabolismo , Macrófagos/citologia , Macrófagos/metabolismo , Uteroglobina/metabolismo , Sequência de Aminoácidos , Animais , Anexina A1/química , Anexina A1/genética , Anexina A1/metabolismo , Polaridade Celular , Eletroforese em Gel Bidimensional , Epitélio/metabolismo , Regulação da Expressão Gênica , Camundongos , Camundongos Endogâmicos C57BL , Dados de Sequência Molecular , Isoformas de Proteínas/química , Isoformas de Proteínas/genética , Isoformas de Proteínas/metabolismo , Processamento de Proteína Pós-Traducional , Transporte Proteico , RNA Mensageiro/genética , RNA Mensageiro/metabolismo , Espectrometria de Massas por Ionização e Dessorção a Laser Assistida por Matriz , Uteroglobina/deficiência
4.
Arch Biochem Biophys ; 435(1): 32-41, 2005 Mar 01.
Artigo em Inglês | MEDLINE | ID: mdl-15680904

RESUMO

Hsp70 and Hsp90 molecular chaperones play essential roles in protein expression and maturation, and while catalyzing protein folding they can "decide" to target mis-folded substrates for degradation. In this report, we show for the first time distinct but partially overlapping requirements for Hsp90, Hsp70, and an Hsp70 nucleotide exchange factor (NEF) at different steps during the biogenesis of a model substrate, firefly luciferase (FFLux), in yeast. By examining the inducible expression of FFLux in wild type cells and in specific yeast mutants, we find that the Fes1p NEF is required for efficient FFLux folding, whereas the Hsp70, Ssa1p, is required for both protein folding and stability, and to maintain maximal FFLux mRNA levels. In contrast, Hsp90 function was primarily necessary to express the FFLux-encoding gene from an inducible promoter. Together, these data indicate previously unknown roles for these proteins and point to the complexity with which chaperones and cochaperones function in the cell.


Assuntos
Proteínas de Transporte/metabolismo , Proteínas de Choque Térmico HSP70/metabolismo , Proteínas de Choque Térmico HSP90/metabolismo , Luciferases de Vaga-Lume/biossíntese , Biossíntese de Proteínas/fisiologia , Leveduras/metabolismo , Proteínas Adaptadoras de Transdução de Sinal , Regulação Fúngica da Expressão Gênica/fisiologia , Leveduras/genética
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