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1.
Rev. chil. infectol ; Rev. chil. infectol;41(1): 184-186, feb. 2024. ilus
Artigo em Espanhol | LILACS | ID: biblio-1559669

RESUMO

Se presenta el caso clínico de persona viviendo con VIH, con mala adherencia a tratamiento, sin vacunación previa para mpox, que evolucionó con un cuadro clínico probable de síndrome de reconstitución inmune posterior a reinicio de TAR, debido a la progresión de las lesiones cutáneas. Recibió tratamiento con tecovirimat por siete días, con evolución clínica favorable. Corresponde al primer caso reportado que recibió terapia con tecovirimat en Chile.


We report a clinical case of a person living with HIV with poor adherence to treatment, no previous mpox vaccination, who had a probable mpox syndrome immune reconstitution after restarting ART, due to worsening of skin lesions. He received treatment with tecovirimat for 7 days, clinically improved and was discharged in good condition. We reported this first clinical case that received tecovirimat in Chile.


Assuntos
Humanos , Masculino , Adulto , Infecções por HIV/complicações , Mpox/complicações , Mpox/tratamento farmacológico , Síndrome Inflamatória da Reconstituição Imune/etiologia , Antivirais/uso terapêutico , Ftalimidas/uso terapêutico , Benzamidas/uso terapêutico
2.
J. appl. oral sci ; J. appl. oral sci;25(5): 575-584, Sept.-Oct. 2017. tab, graf
Artigo em Inglês | LILACS, BBO | ID: biblio-893651

RESUMO

Abstract Tooth whitening represents perhaps the most common aesthetic procedure in dentistry worldwide. The efficacy of bleaching depends on three aspects: bleaching agent, bleaching method, and tooth color. Objective: This in vivo study aimed to examine whitening effects on frontal teeth of the upper and lower jaws using an over-the-counter (OTC) non-hydrogen peroxide bleaching agent in comparison to a placebo after one single use. Material and methods: Forty subjects (25 female; 15 male) participated in this double-blind randomized placebo-controlled trial. The subjects were randomly allocated to two groups (n=20). The test group received the OTC product (iWhite Instant) and the placebo group received an identically composed product except for the active agents. Each subject was treated with a prefilled tray containing iWhite Instant or the placebo for 20 minutes. The tooth shade of the front teeth (upper and lower jaws) was assessed before (E_0), immediately after (E_1) and 24 h after treatment (E_2), using a shade guide (VITA classical). Statistical testing was accomplished using the Mann-Whitney U test (p<0.001). The dropout rate was 0%. Results: There were no significant differences at E_0 between placebo and test groups regarding the tooth color. Differences in tooth color changes immediately after (ΔE1_0) and 24 h after treatment (ΔE2_0) were calculated for both groups. The mean values (standard deviations) of tooth color changes for ΔE1_0 were 2.26 (0.92) in the test group and 0.01 (0.21) in the placebo group. The color changes for ΔE2_0 showed mean values of 2.15 (1.10) in the test group and 0.07 (0.35) in the placebo group. For ΔE1_0 and ΔE2_0 significant differences were found between the groups. Conclusion: In this short-term study, the results showed that a non-hydrogen peroxide bleaching agent has significant whitening effects immediately and 24 h after a single-use treatment.


Assuntos
Humanos , Masculino , Feminino , Adolescente , Adulto , Pessoa de Meia-Idade , Adulto Jovem , Ftalimidas/uso terapêutico , Clareamento Dental/métodos , Caproatos/uso terapêutico , Compostos de Cálcio/uso terapêutico , Clareadores Dentários/uso terapêutico , Gluconatos/uso terapêutico , Lactatos/uso terapêutico , Fatores de Tempo , Variações Dependentes do Observador , Efeito Placebo , Método Duplo-Cego , Reprodutibilidade dos Testes , Resultado do Tratamento , Colorimetria , Estatísticas não Paramétricas , Sensibilidade da Dentina/induzido quimicamente , Medicamentos sem Prescrição/uso terapêutico
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