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Comparison of intubating conditions after induction with propofol and remifentanil or sufentanil

Randomized controlled REMIDENT trial for surgical tooth extraction

Vergleich der Intubationsbedingungen nach Induktion mit Propofol und Remifentanil oder Sufentanil

Randomisierte kontrollierte REMIDENT-Studie bei chirurgischer Zahnextraktion

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Abstract

Purpose

The aim of this study was to compare tracheal intubation conditions after induction of anesthesia with a bolus of propofol-sufentanil or propofol-remifentanil and a rapid induction technique.

Material and methods

A total of 70 patients (American Society of Anesthesiologists (ASA) classification I‑II) undergoing outpatient surgery under general anesthesia with intubation for tooth extraction were randomly assigned to two groups in this double-blind study. Patients received either a bolus of remifentanil (3 μg/kg) or sufentanil (0.3 μg/kg) together with 2.5 mg/kg propofol for intubation. The primary outcome was the percentage of excellent intubation conditions and the secondary outcomes were the percentage of patients with a decrease of over 20% in mean arterial pressure (MAP) or heart rate (HR), time to achieve spontaneous respiration, time between the end of surgery and extubation and time to achieve an Aldrete score of 10. VAS pain score was >3 or having laryngeal pain 15 min after arriving in the postanesthesia care unit (PACU) were also analyzed.

Results

Intubating conditions (perfect + good conditions) were significantly better with remifentanil than with sufentanil (88.5% vs. 68.6%; p = 0.01). When using remifentanil, the hemodynamic conditions were good. Using remifentanil did not significantly increase the pain score or the laryngeal pain in the recovery room. This was confirmed by no significant differences between the groups for morphine consumption. Remifentanil significantly decreased the time to achieve an Aldrete score of 10.

Conclusion

When intubation without muscle relaxants is required, intubating conditions are much better when a remifentanil bolus is used compared to a sufentanil bolus. The remifentanil/propofol rapid induction technique is a valuable technique to quickly intubate and achieve good conditions.

Zusammenfassung

Zweck

Ziel dieser Studie war es, die Bedingungen der Trachealintubation nach Narkoseeinleitung mit einem Bolus Propofol-Sufentanil oder Propofol-Remifentanil und einer schnellen Induktionstechnik zu vergleichen.

Material und Methoden

In dieser Doppelblindstudie wurden insgesamt 70 Patienten (American Society of Anesthesiologists(ASA)-Klassifikation I–II), bei denen ambulant unter Vollnarkose mit Intubation eine Operation zur Zahnextraktion durchgeführt wurde, in 2 Gruppen randomisiert. Die Patienten erhielten entweder einen Bolus Remifentanil (3 μg/kg) oder Sufentanil (0,3 μg/kg), zusammen mit 2,5 mg/kg Propofol zur Intubation. Das primäre Ergebnis war der Prozentsatz ausgezeichneter Intubationsbedingungen, und die sekundären Ergebnisse waren der prozentuale Anteil der Patienten mit einer Senkung des mittleren arteriellen Drucks (MAP) oder der Herzfrequenz (HR) um mehr als 20 %, die Zeit bis zum Erreichen der Spontanatmung, die Zeit zwischen dem Ende der Operation und der Extubation sowie die Zeit bis zum Erreichen eines Aldrete-Scores von 10. Der prozentuale Anteil der Patienten mit einem Schmerzscore >3 oder mit Kehlkopfschmerzen 15 min nach Ankunft auf der „postanesthesia care unit“ (PACU) wurde ebenfalls analysiert.

Ergebnisse

Die Intubationsbedingungen waren mit Remifentanil signifikant besser als mit Sufentanil (51,4 % vs. 20 %; p = 0,0064). Bei der Verwendung von Remifentanil waren die hämodynamischen Bedingungen gut. Die Verwendung von Remifentanil führte zu keiner signifikanten Erhöhung des Schmerzscores oder der Kehlkopfschmerzen im Aufwachraum. Dies wurde dadurch bestätigt, dass es keine signifikanten Unterschiede in den Gruppen für die Morphineinnahme gab. Remifentanil verkürzte die Zeit bis zum Erreichen eines Aldrete-Scores von 10 signifikant.

Schlussfolgerung

Wenn eine Intubation ohne Muskelrelaxanzien erforderlich ist, sind die Intubationsbedingungen bei Verwendung eines Remifentanil-Bolus wesentlich besser als bei Verwendung eines Sufentanil-Bolus. Die Methode der schnellen Induktion durch Remifentanil/Propofol ist eine wertvolle Technik, mit der eine schnelle Intubation möglich ist und gute Bedingungen erreicht werden können.

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Abbreviations

ASA:

American Society of Anesthesiologists

BMI:

Body mass index

HR:

Heart rate

IDS:

Intubation difficulty scale

IV:

Intravenous

MAP:

Mean arterial pressure

PACU:

Post anesthesia care unit

SpO2 :

Oxygen saturation

VAS:

Visual analog scale

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Acknowledgements

The authors thank Leonie Smith for the English editing of this article.

Funding

Support was provided solely from institutional and department sources. CHU Toulouse supported this work.

Author contributions

Conceived and designed the experiments: CR, VM. Performed the experiments: CR, LB, FF, AD. Wrote the paper: JMC, AD, LB, CR, VM.

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Correspondence to V. Minville.

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Conflict of interest

A. Dolsan, L. Bruneteau, C. Roche, F. Ferré, F. Labaste, A. Sommet, J.-M. Conil and V. Minville declare that they have no competing interests..

Ethical standards

All procedures performed in studies involving human participants or on human tissue were in accordance with the ethical standards of the institutional and/or national research committee and with the 1975 Helsinki declaration and its later amendments or comparable ethical standards. This study was approved by the research ethics board (protocol number 09.001.03, favorable opinion of the CPP Sud-Ouest et Outre-Mer 1) and written informed consent was obtained from each patient. This trial was registered at ClinicalTrials.gov (NCT01910285 dated July 29, 2013)

Additional information

The authors A. Dolsan and L. Bruneteau contributed equally to the manuscript.

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Dolsan, A., Bruneteau, L., Roche, C. et al. Comparison of intubating conditions after induction with propofol and remifentanil or sufentanil. Anaesthesist 69, 262–269 (2020). https://doi.org/10.1007/s00101-020-00739-0

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  • DOI: https://doi.org/10.1007/s00101-020-00739-0

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