Literature DB >> 24717908

A comparative study of two remifentanil doses for procedural pain in ventilated preterm infants: a randomized, controlled study*.

Seung Han Shin1, Han-Suk Kim, Juyoung Lee, Ka Young Choi, Jang Hoon Lee, Ee-Kyung Kim, Moon Sung Park, Jung-Hwan Choi.   

Abstract

OBJECTIVES: Remifentanil is an ultrashort-acting synthetic opioid, and the metabolism of which is not influenced by hepatic or renal function. This study aims to compare the efficacy of two remifentanil doses during procedures in ventilated preterm infants.
DESIGN: Prospective, randomized, double-blind, noninferiority trial.
SETTING: Neonatal ICU. PATIENTS: Preterm infants who were supported by a mechanical ventilator with tracheal tube and requiring central venous access.
INTERVENTIONS: Two remifentanil dosages were administered in mechanically ventilated preterm infants during peripherally inserted central catheter insertion. Fourteen preterm infants were randomly assigned to low-dose (0.1 μg/kg/min) or high-dose (0.25 μg/kg/min) remifentanil infusion. The Premature Infant Pain Profile was used to score pain during the procedure, and changes in the Premature Infant Pain Profile score between needle puncture and baseline were analyzed to investigate the noninferiority of low-dose to high-dose remifentanil. Occurrence of cardiorespiratory complications was also recorded.
MEASUREMENTS AND MAIN RESULTS: The median gestational age (minimum, maximum) was 26 weeks (24, 31), and the median birth weight was 825 g (610, 1,280). Changes in Premature Infant Pain Profile in the high-dose and low-dose groups were 1.43 ± 3.10 and -0.60 ± 5.32, respectively. The difference in changes in the Premature Infant Pain Profile score between the high-dose and low-dose groups was -2.03 ± 4.13. The corresponding lower limit of one-tailed 97.5% CI was -7.24, below the noninferiority margin. Apneic events and bradycardia did not occur in the low-dose group; however, there were three episodes of apnea (42.9%) and one of bradycardia (14.3%) in the high-dose group (p = 0.683 and 0.366, respectively).
CONCLUSION: For mechanically ventilated preterm infants, the use of remifentanil at 0.25 μg/kg/min as an analgesic for short procedures represents a therapeutic option. Our pilot study suggests the need for larger randomized trials.

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Year:  2014        PMID: 24717908     DOI: 10.1097/PCC.0000000000000123

Source DB:  PubMed          Journal:  Pediatr Crit Care Med        ISSN: 1529-7535            Impact factor:   3.624


  5 in total

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Authors:  Mineto Kamata; Joseph D Tobias
Journal:  J Anesth       Date:  2016-01-13       Impact factor: 2.078

2.  Randomized Controlled Trial Comparing Different Single Doses of Intravenous Paracetamol for Placement of Peripherally Inserted Central Catheters in Preterm Infants.

Authors:  Daniella W E Roofthooft; Sinno H P Simons; Richard A van Lingen; Dick Tibboel; John N van den Anker; Irwin K H Reiss; Monique van Dijk
Journal:  Neonatology       Date:  2017-05-31       Impact factor: 4.035

3.  Eligibility Criteria and Representativeness of Randomized Clinical Trials That Include Infants Born Extremely Premature: A Systematic Review.

Authors:  Leeann R Pavlek; Brian K Rivera; Charles V Smith; Joanie Randle; Cory Hanlon; Kristi Small; Edward F Bell; Matthew A Rysavy; Sara Conroy; Carl H Backes
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Review 4.  Randomized controlled trials in central vascular access devices: A scoping review.

Authors:  Mari Takashima; Gillian Ray-Barruel; Amanda Ullman; Samantha Keogh; Claire M Rickard
Journal:  PLoS One       Date:  2017-03-21       Impact factor: 3.240

5.  Efficacy and Safety Aspects of Remifentanil Sedation for Intubation in Neonates: A Retrospective Study.

Authors:  Clément Chollat; Arielle Maroni; Marie-Stéphanie Aubelle; Cyril Guillier; Juliana Patkai; Elodie Zana-Taïeb; Aurélie Keslick; Héloïse Torchin; Pierre-Henri Jarreau
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  5 in total

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