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1.
J Family Med Prim Care ; 8(1): 220-224, 2019 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-30911510

RESUMO

BACKGROUND: The majority of oral diseases in children are preventable. The pediatricians owing to the unique position they occupy in child care are invaluable in achieving standard oral and dental healthcare in children. This study was aimed to assess pediatrician's knowledge, attitude, and awareness toward early childhood caries (ECC), oral health, and treatment needs of their patients. METHODS: A total of 65 pediatricians were randomly selected for the study and were requested to fill out an objective questionnaire pertaining to individual details, approach toward pediatric dentistry, and knowledge level of oral health, without providing any oral health information. RESULTS: About 58.5% of pediatricians acknowledged the importance of pediatric dentistry. About 72.7% of pediatricians perform oral examination regularly. Around 17% of pediatricians have knowledge of the ECC. Only 32.3% of pediatricians acknowledged the cariogenicity of medicated syrups. CONCLUSION: This study shows those pediatricians who were surveyed had poor knowledge regarding ECC, oral health, and dental treatment need in children. Pediatricians need to update themselves on recent recommendations.

2.
Contemp Clin Dent ; 9(4): 637-643, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-31772477

RESUMO

AIMS: The purpose of the study was to determine the best combination for chemomechanical preparation in primary teeth using two endo file systems (hand and rotary) along with two different irrigants. MATERIALS AND METHODS: Sixty primary molars indicated for pulpectomy, underwent chemomechanical preparation using endo files (H hand files and rotary Protaper files) and root canal irrigating solutions (Smearclear and QMiX). Samples from root canals were collected before and after the chemomechanical preparation of the canal and were cultured for microbial analysis of Enterococcus faecalis. RESULTS: Endodontic irrigating solutions showed significant differences of effectiveness on the growth inhibition of bacterial strain. The present study confirmed that the in vivo antimicrobial efficacy of QMiX solution was statistically significant when compared to the Smearclear solution. CONCLUSION: Based on the antimicrobial efficacy observed in the present study, it may be concluded that QMiX has a great potential than Smearclear as an intracanal irrigation solution in primary teeth and rotary preparation may be considered as more efficient and time-saving mechanical preparatory technique in primary molars.

3.
Invest Ophthalmol Vis Sci ; 59(2): 1045-1057, 2018 02 01.
Artigo em Inglês | MEDLINE | ID: mdl-29490341

RESUMO

Purpose: We tested the potential of bone morphogenic protein 7 (BMP7) and hepatocyte growth factor (HGF) combination gene therapy to treat preformed corneal fibrosis using established rabbit in vivo and human in vitro models. Methods: Eighteen New Zealand White rabbits were used. Corneal fibrosis was produced by alkali injury. Twenty-four hours after scar formation, cornea received topically either balanced salt solution (BSS; n = 6), polyethylenimine-conjugated gold nanoparticle (PEI2-GNP)-naked plasmid (n = 6) or PEI2-GNP plasmids expressing BMP7 and HGF genes (n = 6). Donor human corneas were used to obtain primary human corneal fibroblasts and myofibroblasts for mechanistic studies. Gene therapy effects on corneal fibrosis and ocular safety were evaluated by slit-lamp microscope, stereo microscopes, quantitative real-time PCR, immunofluorescence, TUNEL, modified MacDonald-Shadduck scoring system, and Draize tests. Results: PEI2-GNP-mediated BMP7+HGF gene therapy significantly decreased corneal fibrosis in live rabbits in vivo (Fantes scale was 0.6 in BMP7+HGF-treated eyes compared to 3.3 in -therapy group; P < 0.001). Corneas that received BMP7+HGF demonstrated significantly reduced mRNA levels of profibrotic genes: α-SMA (3.2-fold; P < 0.01), fibronectin (2.3-fold, P < 0.01), collagen I (2.1-fold, P < 0.01), collagen III (1.6-fold, P < 0.01), and collagen IV (1.9-fold, P < 0.01) compared to the -therapy corneas. Furthermore, BMP7+HGF-treated corneas showed significantly fewer myofibroblasts compared to the -therapy controls (83%; P < 0.001). The PEI2-GNP introduced >104 gene copies per microgram DNA of BMP7 and HGF genes. The recombinant HGF rendered apoptosis in corneal myofibroblasts but not in fibroblasts. Localized topical BMP7+HGF therapy showed no ocular toxicity. Conclusions: Localized topical BMP7+HGF gene therapy treats corneal fibrosis and restores transparency in vivo mitigating excessive healing and rendering selective apoptosis in myofibroblasts.


Assuntos
Apoptose/efeitos dos fármacos , Proteína Morfogenética Óssea 7/genética , Opacidade da Córnea/terapia , Terapia Genética/métodos , Fator de Crescimento de Hepatócito/genética , Miofibroblastos/patologia , Administração Oftálmica , Animais , Córnea/patologia , Opacidade da Córnea/patologia , Modelos Animais de Doenças , Combinação de Medicamentos , Feminino , Fibrose/terapia , Ouro/química , Marcação In Situ das Extremidades Cortadas , Pressão Intraocular , Nanopartículas Metálicas/química , Plasmídeos/genética , Polietilenoimina/química , Coelhos , Reação em Cadeia da Polimerase em Tempo Real , Tonometria Ocular
4.
Urology ; 60(5 Suppl 1): 78-80; discussion 80-1, 2002 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-12493362

RESUMO

In the United States alone, approximately 17 million men and women have symptoms of overactive bladder (OAB). For many years, oxybutynin was the drug of choice for treating OAB. Although it provided effective treatment, multiple daily doses were required, and adverse events, such as dry mouth and constipation, were decided drawbacks. Controlled drug delivery systems seen in commercially available OAB formulations alter the pharmacokinetics of antimuscarinic medications in ways that maintain efficacy and allow once-daily dosing and reduction of adverse events. In the future, OAB medications will not only incorporate new chemical entities, such as the S-enantiomer of oxybutynin, but will also use novel drug delivery technologies, including transdermal patches and bladder implants.


Assuntos
Antagonistas Colinérgicos/administração & dosagem , Antagonistas Colinérgicos/farmacocinética , Ácidos Mandélicos/administração & dosagem , Ácidos Mandélicos/farmacocinética , Transtornos Urinários/tratamento farmacológico , Administração Cutânea , Administração Oral , Compostos Benzidrílicos/administração & dosagem , Compostos Benzidrílicos/farmacocinética , Disponibilidade Biológica , Cresóis/administração & dosagem , Cresóis/farmacocinética , Preparações de Ação Retardada , Esquema de Medicação , Implantes de Medicamento , Feminino , Humanos , Masculino , Doenças da Bexiga Urinária/tratamento farmacológico , Doenças da Bexiga Urinária/metabolismo , Bexiga Urinaria Neurogênica/tratamento farmacológico , Bexiga Urinaria Neurogênica/metabolismo , Transtornos Urinários/metabolismo
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