Volume 18, Issue 2 pp. 176-183

Early awakening and extubation with remifentanil in ventilated premature neonates

YERKES PEREIRA E SILVA MD PhD

YERKES PEREIRA E SILVA MD PhD

Departments of Anesthesiology and Neonatology, Lifecenter Hospital

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RENATO SANTIAGO GOMEZ MD PhD

RENATO SANTIAGO GOMEZ MD PhD

Department of Surgery, Medical School, Federal University of Minas Gerais

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JULIANA DE OLIVEIRA MARCATTO RN

JULIANA DE OLIVEIRA MARCATTO RN

Departments of Anesthesiology and Neonatology, Lifecenter Hospital

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THADEU ALVES MAXIMO MD

THADEU ALVES MAXIMO MD

Department of Pediatrics, Medical School, Federal University of Minas Gerais, Avenida Alfredo Balena, Minas Gerais, Brazil

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ROSILU FERREIRA BARBOSA MD

ROSILU FERREIRA BARBOSA MD

Departments of Anesthesiology and Neonatology, Lifecenter Hospital

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ANA CRISTINA SIMÕES E SILVA MD PhD

ANA CRISTINA SIMÕES E SILVA MD PhD

Department of Pediatrics, Medical School, Federal University of Minas Gerais, Avenida Alfredo Balena, Minas Gerais, Brazil

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First published: 12 November 2007
Citations: 23
Yerkes Pereira e Silva, Rua Montevideu, 402 – Apt 402, Sion, Belo Horizonte, Minas Gerais 30315560, Brazil (email: [email protected], [email protected]).

Summary

Background: Morphine 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).

Methods: Twenty 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.

Results: After 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.

Conclusions: Our 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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