• Anaesthesia · Aug 2007

    Clinical Trial

    Remifentanil for tracheal tube tolerance: a case control study.

    • A M Machata, U M Illievich, B Gustorff, C Gonano, K Fässler, and C K Spiss.
    • Department of Anaesthesiology and General Intensive Care, Medical University of Vienna, General Hospital, Waehringer Geurtel 18-20, 1090 Vienna, Austria. anette-marie.machata@meduniwien.ac.at
    • Anaesthesia. 2007 Aug 1;62(8):796-801.

    AbstractWe assessed the minimal remifentanil dosage required for tracheal tube tolerance in awake and spontaneously breathing patients after major abdominal surgery. Forty postoperative patients received remifentanil 0.1 microg.kg(-1).min(-1), which was reduced in steps of 0.025 microg.kg(-1).min(-1) every 30 min. Respiratory response subscore of comfort scale (CSRR), Ramsay sedation scale (RSS), visual analogue scale (VAS), respiratory rate, and minute ventilation were recorded. Spontaneous respiration with no or little response to ventilation (CSRR 2) in co-operative, oriented and tranquil patients (RSS 2) was defined as the main outcome and study endpoint. Thirty-one patients (77.5%) reached a CSRR 2 and RSS 2 with remifentanil 0.025 microg.kg(-1).min(-1) and nine patients (22.5%) required remifentanil 0.05 microg.kg(-1).min(-1). Analgesia was sufficient in all patients (VAS = 30). Remifentanil 0.025-0.05 microg.kg(-1).min(-1) achieves satisfactory tracheal tube tolerance in awake and spontaneously breathing patients.

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