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Anaesth Intensive Care ; 33(4): 452-6, 2005 Aug.
Article in English | MEDLINE | ID: mdl-16119485

ABSTRACT

Patient-controlled epidural analgesia (PCEA) is used to maintain epidural analgesia following initial intrathecal analgesia. This trial investigated whether a continuous background infusion with PCEA provides superior analgesia to PCEA alone among patients who received combined spinal-epidural (CSE) analgesia during labour Eighty parturients were randomized to either PCEA alone (PCEA) or PCEA with a background infusion of ropivacaine 0.15% with sufentanil 0.75 microg/ml at 2 ml/h (PCEA + CEI). PCEA settings were a bolus of 4 ml of the same analgesic solution with a lockout interval of 15 minutes. Significantly more patients in the PCEA group required at least one anaesthetist intervention for breakthrough pain (27 [71%] vs 10 [25%] in the PCEA + CEI group, P<0.05). Consumption of local anaesthetic (excluding manually administered boluses) was similar between the groups. If anaesthetist-administered boluses were included, more local anaesthetic was consumed by the PCEA group (47.1 +/- 19.4 mg vs 35.6 +/- 12.0 mg in the PCEA + CEI group, P<0.05). We conclude that PCEA with a background infusion provides effective analgesia with less anaesthetist workload and reduced local anaesthetic consumption as compared with PCEA without a background infusion.


Subject(s)
Analgesia, Epidural/methods , Analgesia, Obstetrical/methods , Analgesia, Patient-Controlled/methods , Anesthetics, Combined/therapeutic use , Adult , Amides/administration & dosage , Analgesia, Epidural/adverse effects , Analgesia, Obstetrical/adverse effects , Analgesia, Patient-Controlled/adverse effects , Analgesics, Opioid/administration & dosage , Anesthetics, Combined/administration & dosage , Anesthetics, Local/administration & dosage , Double-Blind Method , Female , Humans , Infusions, Intravenous/methods , Injections, Spinal/methods , Pain/prevention & control , Pain Measurement/statistics & numerical data , Ropivacaine , Sufentanil/administration & dosage , Sufentanil/adverse effects , Time Factors , Treatment Outcome
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