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2.
Maedica (Bucur) ; 14(4): 343-349, 2019 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-32153664

RESUMO

Introduction:An effective pain control significantly contributes to an optimal dental treatment in pediatric dentistry. This study was conducted to compare children's pain perception and behavioral feedback during local anesthetic injection accompanied with counter-irritation, refrigerant, ice precooling or topical benzocaine. Methods:This study was conducted on 99 children who needed dental treatment in bilateral maxillary primary molars by local anesthesia. Subjects were randomly assigned to three groups, in which the injection site was prepared using counter-irritation in group I, ice precooling in group II, and refrigerant spray precooling in group III. In all three groups, 20% benzocaine gel was used in the injection site of opposite quadrant as a control. The perceived pain and behavioral feedback of children during injection were evaluated using the visual analogue scale (VAS) and sound, eye, and motor (SEM) indexes. Sign and Kruskal-Wallis tests were used to analyze data at a significance level of P < 0.05. Results:The perceived pain was significantly lower when using benzocaine compared to the other three methods (P < 0.05). Behavioral feedback of children when using benzocaine was not significantly different from the counter-irritation method (P=1.00). However, behavioral feedback with counter-irritation was significantly better than precooling (P < 0.05). Counter-irritation was significantly more effective than precooling methods in reduction of pain perception and improvement of behavioral feedback (P < 0.05). Conclusions:The perceived pain was significantly lower when the benzocaine method was used. Behavioral feedback was significantly better with benzocaine and counter-irritation methods compared to precooling procedures.

3.
Acta Cardiol ; 64(4): 571-3, 2009 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-19725457

RESUMO

Cardiac myxomas are the most common type of primary cardiac tumours. Nevertheless, it is still a rare tumour and its relation with immunosuppressive therapy, which is essential after organ transplantation, remains uncertain. We report the case of a 30-year-old woman, who underwent kidney and pancreatic transplantation for severe nephropathy due to type I diabetes mellitus and since then, under heavy immunosuppressive treatment. Four years after surgery, a left atrial myxoma was discovered. Three other cases of cardiac myxomas following transplantation and immunodepressive status have been reported in the literature, which raises the question of an association between immunosuppression and the development of cardiac myxomas.


Assuntos
Neoplasias Cardíacas/etiologia , Terapia de Imunossupressão/efeitos adversos , Mixoma/etiologia , Adulto , Feminino , Humanos , Transplante de Rim , Neoplasias Pancreáticas
4.
Eur J Echocardiogr ; 10(4): 579-81, 2009 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-19383642

RESUMO

Left ventricular (LV) to right atrial (RA) communication, also known as Gerbode defect, is very rare, usually congenital but sometimes also acquired. Cases of Gerbode defect have been reported after left valve surgery, usually valve replacement. We describe the first case of LV-RA communication following a tricuspid annuloplasty not combined to a left valve surgery. The case we report concerns a 73-year-old woman who underwent a double-valve surgery (pulmonary valve replacement and tricuspid annuloplasty) for symptomatic severe right heart failure due to post-endocarditis pulmonary valve regurgitation. A LV-RA shunt was discovered 1 year after surgery. This case report confirms the responsibility of a tricuspid annuloplasty in an acquired LV-RA shunt.


Assuntos
Defeitos dos Septos Cardíacos/diagnóstico por imagem , Complicações Pós-Operatórias/diagnóstico por imagem , Insuficiência da Valva Tricúspide/cirurgia , Valva Tricúspide/cirurgia , Idoso , Velocidade do Fluxo Sanguíneo , Ecocardiografia Doppler em Cores , Ecocardiografia Transesofagiana , Feminino , Defeitos dos Septos Cardíacos/etiologia , Humanos , Sopros Sistólicos , Valva Tricúspide/diagnóstico por imagem
5.
J Exp Med ; 199(7): 1011-6, 2004 Apr 05.
Artigo em Inglês | MEDLINE | ID: mdl-15051764

RESUMO

To gain insight into the inability of newborns to mount efficient Th1 responses, we analyzed the molecular basis of defective IL-12(p35) expression in human neonatal monocyte-derived dendritic cells (DCs). Determination of IL-12(p35) pre-mRNA levels by real-time RT-PCR revealed that transcriptional activation of the gene in lipopolysaccharide-stimulated neonatal DCs was strongly impaired compared with adult DCs. We next showed that p50/p65 and p65/p65 dimers interact with kB#1 site, a critical cis-acting element of the IL-12(p35) promoter. We found that LPS-induced p65 activation was similar in adult and newborn DCs. Likewise, in vitro binding activity to the Sp1#1 site, previously shown to be critical for IL-12(p35) gene activation, did not differ in adults and newborns. Since the accessibility to this Sp1#1 site was found to depend on nucleosome remodeling, we used a chromatin accessibility assay to compare remodeling of the relevant nucleosome (nuc-2) in adult and neonatal DCs. We observed that nuc-2 remodeling in neonatal DCs was profoundly impaired in response to lipopolysaccharide. Both nuc-2 remodeling and IL-12(p35) gene transcription were restored upon addition of recombinant interferon-gamma. We conclude that IL-12(p35) transcriptional repression in neonatal DCs takes place at the chromatin level.


Assuntos
Células Dendríticas/imunologia , Células Dendríticas/metabolismo , Interleucina-12/genética , Nucleossomos/metabolismo , Subunidades Proteicas/genética , Adulto , Sequência de Bases , Montagem e Desmontagem da Cromatina/efeitos dos fármacos , Células Dendríticas/efeitos dos fármacos , Humanos , Técnicas In Vitro , Recém-Nascido , Interferon gama/farmacologia , Subunidade p35 da Interleucina-12 , Lipopolissacarídeos/farmacologia , NF-kappa B/metabolismo , Nucleossomos/efeitos dos fármacos , Precursores de RNA/genética , Precursores de RNA/metabolismo , Proteínas Recombinantes , Fator de Transcrição Sp1/metabolismo , Transcrição Gênica/efeitos dos fármacos
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