• J Clin Anesth · Mar 1996

    Randomized Controlled Trial Comparative Study Clinical Trial

    Patient-controlled analgesia with sufentanil: a comparison of two different methods of administration.

    • R S Sinatra, F B Sevarino, and D Paige.
    • Yale University School of Medicine, Department of Anesthesiology, New Haven, Connecticut 06510, USA.
    • J Clin Anesth. 1996 Mar 1;8(2):123-9.

    Study ObjectiveTo examine the safety and analgesic efficacy of sufentanil administered via either epidural or intravenous (i.v.) patient-controlled analgesia (PCA) in patients recovering from gynecologic surgery.DesignRandomized, double-blind comparison.SettingPatient care unit at a university medical center.Patients29 healthy women presenting for major intraabdominal gynecologic surgery with epidural anesthesia who requested postoperative PCA.InterventionsFollowing completion of surgery performed using epidural anesthesia with 2% lidocaine and i.v sedation, patients were assigned to one of three treatment groups: Group 1-epidural PCA (EPCA) with sufentanil: 0.3 microgram/kg bolus followed by 8 micrograms/hr infusion plus epidural PCA boluses of 4 micrograms every 6 min as needed; Group 2-i.v. PCA with sufentanil: 0.3 microgram/kg bolus followed by 8 micrograms/hr infusion plus IV PCA boluses of 4 micrograms every 6 min as needed; or Group 3-i.v. PCA with morphine: 0.1 mg/kg bolus followed by 0.5 mg/hr infusion plus i.v. PCA boluses of 1 mg every 6 min as needed.Measurements And Main ResultsPatients were observed at regular intervals during a 24-hour evaluation period. Visual analog scale (VAS) scores were used to assess analgesia and satisfaction with therapy. Pulmonary function was assessed by monitoring respiratory rate, oxygen (O2) saturation, and forced expiratory flow. Total opioid dose delivered and the presence/severity of side effects was also collected. Sufentanil plasma levels were measured in a subset of eight patients. Patients receiving either EPCA or i.v. PCA sufentanil experienced equivalent analgesia that was more rapid in onset than i.v. PCA morphine. Total dose administered and plasma concentration of drug were similar in both sufentanil groups; however, a greater number of patients in the i.v. delivery group experienced clinically significant O2 desaturation.ConclusionsThe main advantage of EPCA sufentanil in this postsurgical setting was its ability to provide a more rapid onset of analgesia than traditional i.v. PCA with morphine while offering greater safety than i.v. sufentanil.

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