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Título : Dexmedetomidine, Application in Pediatrics: Paper Review
Creador: Perez Guillé, Maria Gabriela
Nivel de acceso: Open access
Palabras clave : Dexmedetomidina - Farmacología
Dexmedetomidina - farmacocinética
Dexmedetomidina -líquido cefalorraquídeo
Dexmedetomidina -efectos adversos
Hipnóticos y Sedantes - farmacocinética
Hipnóticos y Sedantes - efectos adversos
Analgésicos - farmacocinética
Analgésicos - efectos adversos
Unidades de Cuidados Intensivos
Respiración Artificial - utilización
Dexmedetomidine - pharmacology
Dexmedetomidine - pharmacokinetics
Dexmedetomidine - cerebrospinal fluid
Dexmedetomidine - adverse effects
Hypnotics and Sedatives - pharmacokinetics
Analgesics - pharmacokinetics
Analgesics - adverse effects
Intensive Care Units
Respiration, Artificial - utilization
"Dexmedetomidina farmacocinética/farmacodinámica, pacientes pediátricos, reacción adversa,
Dexmedetomidine, Pharmacokinetic/pharmacodynamic, Paediatric patients, Adverse reaction, Applications.
Descripción : Introduction: Dexmedetomidine is a drug with sedative, hypnotic, and analgesic properties. Its use in adult sedation was approved in 1999. In children, although the use has not been approved, its application by paediatricians is common. The drug offers many advantages in sedative procedures of paediatric patients. First, the half-life is relatively short. Second, it has little or no effect on respiratory management, and lastly, it is well tolerated by intensive care unit patients found with mechanical ventilation. Pharmacokinetics: 93% of the drug bonds with plasma proteins on absorption. Then, it undergoes a rapid phase of distribution with a half-life of 7 min. It has a depuration rate of 15 ml/kg/min, and half-life elimination rate of 2 h. Pharmacodynamics: The drug has antinociceptive action on α-2A adrenergic receptor of the spinal cord. It has hypnotic-sedative action, and inhibitory effect on central noradrenergic transmission. Applications: It is used as a premedication agent with the objective of getting better cooperation of the patient on starting anaesthetic procedures. Adverse reactions: Bradycardia and hypotension. Conclusion: Its use appears to have a promising future in paediatric population; however, it is pertinent that more controlled clinical studies be carried out in order to demonstrate its safety and efficacy. © 2016, Association of Pharmaceutical Teachers of India. All rights reserved.
Colaborador(es) u otros Autores: Murata Chiharu
Reyes-Reyes Rosa Eugenia
Perez Guillé Beatriz
Bobadilla-Chavez José
Alemon Medina Radames
Corral G Ismene
Osnaya-Romero Neydi
Fecha de publicación : 2016
Tipo de publicación: Revisión
Formato: pdf
Identificador del Recurso : 10.5530/ijper.50.2.31
Fuente: Indian Journal of Pharmaceutical Education and Research 50(2):S153 - S158
URI : http://repositorio.pediatria.gob.mx:8180/handle/20.500.12103/2279
Idioma: eng
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