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1.
Cleft Palate Craniofac J ; 47(3): 322-3, 2010 May.
Artigo em Inglês | MEDLINE | ID: mdl-20426680

RESUMO

Securing an endotracheal tube in completely edentulous patients undergoing maxillofacial surgery can pose difficulties. In this report, a readily available and easy method of securing the endotracheal tube to gums of the teeth using the suture in such a circumstance is described. This technique has been used successfully in more than 100 patients at our institutions. Our experience suggests that it can provide reliable tube fixation and does not hinder surgical access.


Assuntos
Intubação Intratraqueal/instrumentação , Arcada Edêntula , Procedimentos Cirúrgicos Bucais , Técnicas de Sutura , Humanos
2.
Anesth Analg ; 108(2): 536-43, 2009 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-19151284

RESUMO

BACKGROUND: We designed this randomized, double-blind clinical study to compare the safety and efficacy of 2% and 4% lidocaine during airway topical anesthesia with a spray-as-you-go technique via the fiberoptic bronchoscope. METHODS: Fifty-two adult patients with a difficult airway were randomly assigned to 1 of 2 study groups to receive 2% (Group 1) or 4% lidocaine (Group 2) by a spray-as-you-go technique with the fiberoptic bronchoscope, in a double-blind manner. After airway topical anesthesia, awake fiberoptic orotracheal intubation (FOI) was performed. Level of sedation, time for each lidocaine spray in different targeted areas, total times for airway sprays, total dosages of lidocaine used for airway sprays, intubation times, and number of intubation attempts were noted. An independent investigator scored patients' comfort during airway topical anesthesia, patients' reaction, coughing severity, and intubating condition during awake FOI, and observed changes of arterial blood pressure and heart rate during each stage in the airway manipulation process. Serial blood samples were obtained for analysis of plasma lidocaine concentrations. RESULTS: Except for the total dosages and plasma concentrations of lidocaine, there were no significant differences in any of the observed variables between groups. All patients exhibited excellent or acceptable intubating conditions. The total dosages of lidocaine were significantly smaller in Group 1 (3.4 +/- 0.6 mg/kg) than in Group 2 (7.1 +/- 2.1 mg/kg). The plasma lidocaine concentrations in all observed points after the supraglottic sprays were larger in Group 2 than in Group 1. CONCLUSIONS: Both 2% and 4% lidocaine administered topically by a spray-as-you-go technique can provide clinically acceptable intubating conditions for awake FOI in sedated patients with a difficult airway. As compared with 4% lidocaine, however, 2% lidocaine requires a smaller dosage and results in lower plasma concentrations.


Assuntos
Anestésicos Locais/administração & dosagem , Intubação Intratraqueal/métodos , Lidocaína/administração & dosagem , Adulto , Aerossóis , Anestesia por Inalação , Anestésicos Locais/efeitos adversos , Anestésicos Locais/farmacocinética , Pressão Sanguínea/efeitos dos fármacos , Tosse/induzido quimicamente , Tosse/epidemiologia , Método Duplo-Cego , Feminino , Tecnologia de Fibra Óptica , Frequência Cardíaca/efeitos dos fármacos , Humanos , Hipnóticos e Sedativos , Complicações Intraoperatórias/induzido quimicamente , Complicações Intraoperatórias/epidemiologia , Lidocaína/efeitos adversos , Lidocaína/farmacocinética , Masculino , Midazolam
3.
Dis Model Mech ; 11(9)2018 09 27.
Artigo em Inglês | MEDLINE | ID: mdl-30061297

RESUMO

Transgenic animals are invaluable for modeling cancer genomics, but often require complex crosses of multiple germline alleles to obtain the desired combinations. Zebrafish models have advantages in that transgenes can be rapidly tested by mosaic expression, but typically lack spatial and temporal control of tumor onset, which limits their utility for the study of tumor progression and metastasis. To overcome these limitations, we have developed a method referred to as Transgene Electroporation in Adult Zebrafish (TEAZ). TEAZ can deliver DNA constructs with promoter elements of interest to drive fluorophores, oncogenes or CRISPR-Cas9-based mutagenic cassettes in specific cell types. Using TEAZ, we created a highly aggressive melanoma model via Cas9-mediated inactivation of Rb1 in the context of BRAFV600E in spatially constrained melanocytes. Unlike prior models that take ∼4 months to develop, we found that TEAZ leads to tumor onset in ∼7 weeks, and these tumors develop in fully immunocompetent animals. As the resulting tumors initiated at highly defined locations, we could track their progression via fluorescence, and documented deep invasion into tissues and metastatic deposits. TEAZ can be deployed to other tissues and cell types, such as the heart, with the use of suitable transgenic promoters. The versatility of TEAZ makes it widely accessible for rapid modeling of somatic gene alterations and cancer progression at a scale not achievable in other in vivo systems.


Assuntos
Envelhecimento/genética , Eletroporação , Transgenes , Peixe-Zebra/genética , Animais , Animais Geneticamente Modificados , Sistemas CRISPR-Cas/genética , Carcinogênese/genética , Carcinogênese/patologia , Modelos Animais de Doenças , Progressão da Doença , Embrião não Mamífero/metabolismo , Técnicas de Transferência de Genes , Melanoma/patologia , Plasmídeos/genética , Regiões Promotoras Genéticas , Peixe-Zebra/embriologia
4.
Dev Cell ; 45(5): 580-594.e7, 2018 06 04.
Artigo em Inglês | MEDLINE | ID: mdl-29804876

RESUMO

Patterning of vertebrate melanophores is essential for mate selection and protection from UV-induced damage. Patterning can be influenced by circulating long-range factors, such as hormones, but it is unclear how their activity is controlled in recipient cells to prevent excesses in cell number and migration. The zebrafish wanderlust mutant harbors a mutation in the sheddase bace2 and exhibits hyperdendritic and hyperproliferative melanophores that localize to aberrant sites. We performed a chemical screen to identify suppressors of the wanderlust phenotype and found that inhibition of insulin/PI3Kγ/mTOR signaling rescues the defect. In normal physiology, Bace2 cleaves the insulin receptor, whereas its loss results in hyperactive insulin/PI3K/mTOR signaling. Insulin B, an isoform enriched in the head, drives the melanophore defect. These results suggest that insulin signaling is negatively regulated by melanophore-specific expression of a sheddase, highlighting how long-distance factors can be regulated in a cell-type-specific manner.


Assuntos
Secretases da Proteína Precursora do Amiloide/metabolismo , Padronização Corporal , Insulina/metabolismo , Melanóforos/fisiologia , Pigmentação , Proteínas de Peixe-Zebra/metabolismo , Peixe-Zebra/fisiologia , Secretases da Proteína Precursora do Amiloide/genética , Animais , Movimento Celular/fisiologia , Embrião não Mamífero/citologia , Embrião não Mamífero/fisiologia , Regulação da Expressão Gênica no Desenvolvimento , Insulina/genética , Melanóforos/citologia , Mutação , Fenótipo , Fosfatidilinositol 3-Quinases , Transdução de Sinais , Serina-Treonina Quinases TOR/genética , Serina-Treonina Quinases TOR/metabolismo , Peixe-Zebra/embriologia , Proteínas de Peixe-Zebra/genética
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