• Minerva stomatologica · Mar 2006

    Randomized Controlled Trial Comparative Study

    Neurosedation in dentistry of the disabled patient: the use of midazolam, propofol, and remifentanil.

    • S Collini, G Pinto, L Lejeune, S Di Carlo, S Meloncelli, G Barraco, and R Gatto.
    • Department of Anesthesia and Resuscitation, 2nd Faculty of Medicine and Surgery, La Sapienza University, Rome, Italy.
    • Minerva Stomatol. 2006 Mar 1;55(3):99-113.

    AimThis prospective randomized study, deals with neurosedation in dental treatment of 200 disabled patients and unable to cooperate, subdivided in 4 groups of 50 male only patients, with age ranging from 28 to 59 (39+/-11), ASA I-III.MethodsThe pharmaceuticals used were Midazolam (group MID) Propofol (group Prop) and Remifentanil. Midazolam and Propofol were used following a bolus-infusion sequence, both separately and in combination among themselves (MID\PROP group), or with an opioid, Remifentanil (MID\PROP\REMI group). ECG, heart rate , non invasive blood pressure (NIBP), SaO(2), EtCO(2) during the procedure were monitored. Induction time, duration of the sedation, recovery time and discharge were reported.ResultsThe statistical analysis demonstrated the superiority of the PROP group for induction time in minute (3.1+/-0.5) in comparison with the MID group (10.6+/-2.1), the MID\PROP group (4.3+/-1.3) and MID\PROP\REMI (3.7+/-1.2). The recovery and discharge times have confirmed the superiority of the MID\PROP\REMI group in comparison with the other 3 groups.ConclusionThis combination proved best at leveraging the synergistic characteristics of each single pharmaceutical and minimizing the collateral effects of each individually.

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