• Paediatric anaesthesia · Feb 2008

    Randomized Controlled Trial

    Early awakening and extubation with remifentanil in ventilated premature neonates.

    • Yerkes Pereira e Silva, Renato Santiago Gomez, Juliana de Oliveira Marcatto, Thadeu Alves Maximo, Rosilu Ferreira Barbosa, and Ana Cristina Simões e Silva.
    • Department of Anesthesiology and Neonatology, Lifecenter Hospital, Belo Horizonte, Minas Gerais, Brazil. yerkesps@uol.com.br
    • Paediatr Anaesth. 2008 Feb 1;18(2):176-83.

    BackgroundMorphine is one of the most commonly used drugs for sedation and analgesia during mechanical ventilation, but its pharmacological profile has limitations, such as prolonged duration of action, especially in premature neonates. Because of its very short context-sensitive half-time, remifentanil has rapid onset and quickly decreases in plasma concentration after interrupting administration. The aim of the present study was to compare a continuous infusion of remifentanil and morphine during mechanical ventilation of premature neonates with respiratory distress syndrome (RDS).MethodsTwenty premature neonates (28-34 weeks) with RDS were randomized in a prospective double-blinded study to receive either a continuous infusion of morphine (n = 10) or remifentanil (n = 10) for mechanical ventilation. The length of time to awaken and extubate the neonate after interrupting opioid administration was recorded. We also recorded stress (COMFORT scale), pain response [Neonatal Infant Pain Scale (NIPS)], hemodynamic and ventilatory variables as well as adverse effects secondary to infusion of the specific opioid.ResultsAfter terminating infusion, the length of time required to awaken and extubate the neonates was 18.9- and 12.1-fold longer, respectively, in the morphine group than in the remifentanil group. Both groups produced good quality sedation and analgesia as evaluated by the NIPS and COMFORT scores. No major side effects were observed.ConclusionsOur results show an interesting potential for the use of remifentanil in premature neonates. Remifentanil allowed an adequate level of sedation and analgesia as well as rapid recovery after discontinuation. However, further properly designed clinical trials are needed before it can be generally recommended.

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