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1.
Medicine (Baltimore) ; 98(1): e14035, 2019 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-30608457

RESUMO

This retrospective study investigated the application of the sedation-agitation scale (SAS) in pediatric bronchoscopy by observing its effects on sedative dosages and adverse reactions.Children who underwent sedation before bronchoscopy, during the period from January 2014 to June 2017, were divided into control and SAS groups. Patients in the control group were administered a single dose of 0.1 to 0.3 mg/kg midazolam, based on physicians' clinical experience. The initial dose of midazolam in the SAS group was 0.1 mg/kg, and was adjusted based on the SAS score, as evaluated by physicians. Between-group comparisons were made of midazolam dose; adverse reactions of midazolam, such as agitation, delirium, excessive sedation, and respiratory depression; operating time of bronchoscopy; and number of participants.No statistically significant differences in gender, age distribution, weight, or disease composition were observed between the groups. The midazolam dose, operating time, and number of participants at different ages were all lower in the SAS group than in the control group. Fewer adverse drug reactions, such as intraoperative agitation and delirium, were noted in the SAS group. Moreover, the overall number of participants was reduced, and the overall operating time was less than that in the control group.Application of SAS for assessment of sedation during pediatric bronchoscopy can guide individualized administration of midazolam, reduce midazolam dose while achieving an ideal sedative effect, reduce adverse reactions, and improve operator experience. Hence, its use should be promoted for pediatric patients undergoing bronchoscopy under local anesthesia and conscious sedation.


Assuntos
Ansiedade/tratamento farmacológico , Broncoscopia/normas , Sedação Consciente/efeitos adversos , Midazolam/efeitos adversos , Acatisia Induzida por Medicamentos , Anestesia Local/métodos , Ansiolíticos/administração & dosagem , Ansiolíticos/efeitos adversos , Ansiolíticos/uso terapêutico , Criança , Pré-Escolar , Sedação Consciente/métodos , Delírio/induzido quimicamente , Relação Dose-Resposta a Droga , Feminino , Humanos , Hipnóticos e Sedativos/normas , Lactente , Masculino , Midazolam/administração & dosagem , Midazolam/uso terapêutico , Duração da Cirurgia , Estudos Retrospectivos
2.
Med Pregl ; 66(3-4): 170-6, 2013.
Artigo em Sérvio | MEDLINE | ID: mdl-23653996

RESUMO

INTRODUCTION: Rational phytotherapy is a modern concept of using plant-originated drugs which has emerged from the need to improve phytotherapy in order to make the use of herbal remedies more efficient and safer. The aim of this study was to give the health-care workers more information on the manufacturing process of high quality phytopreparation following principles of Good Manufacturing Practice and Good Laboratory Practice on the example of herbal sedative, Odoval S capsules. MATERIAL AND METHODS: This study was designed to reflect the production process of a high-quality and safe herbal remedy, starting from defining the formulation and the production procedure to the quality control of raw materials, characterization of the final product, and testing stability of active ingredients in the capsules. RESULTS: Formulation of the phytopreparation, validation of the production process, quality control and stability testing, all together have resulted in the production of capsules with defined valeric acid content (1 mg valeric acid per capsule). DISCUSSION: The preparation is recommended to relieve the symptoms caused by chronic stress (anxiety, irritability, fatigue, lack of concentration, heart palpitations) and for mild insomnia. CONCLUSION: This paper presents the complete cycle of the production of a phytopreparation on the example of a new herbal sedative--Odoval S capsules.


Assuntos
Hipnóticos e Sedativos/normas , Fitoterapia , Preparações de Plantas/normas , Valeriana , Humanos , Controle de Qualidade
3.
Fortschr Med ; 97(29): 1289-92, 1979 Aug 02.
Artigo em Alemão | MEDLINE | ID: mdl-457024

RESUMO

Vita-Dor is a drug inducing sleep and acting as an intermediate type of a hypnotic. Regarding the dosis the age of the patient has to be considered. As an average dose for adults 2 sugar coated tablets are recommended to be administered in the evening. Elderly patients should start with 1 tablet in the evening.


Assuntos
Hipnóticos e Sedativos/normas , Adulto , Idoso , Avaliação de Medicamentos , Humanos , Pessoa de Meia-Idade , Extratos Vegetais , Plantas Medicinais , Tiamina
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