2009
DOI: 10.1016/j.ijoa.2008.06.006
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A double-blind randomized controlled trial of patient-controlled epidural analgesia with or without a background infusion following initial spinal analgesia for labor pain

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Cited by 21 publications
(15 citation statements)
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“…5 In contrast to the COMET study, a number of other studies have shown no difference in AVD. [11][12][13][14] These studies differed in the local anesthetic utilized, the concentrations of local anesthetic solution, or the varying combinations of bolus and/or continuous background infusion rates. Although the COMET study showed that the concentration of local anesthetic had an effect on AVD in nulliparous women, it was performed in only two tertiary delivery centres within the U.K., which may limit the broad generalizability of their findings to other obstetric populations and practices within and outside the U.K. A recent review by Loubert et al highlighted the need for further studies to elucidate the impact of epidural solutions and regimens on outcomes such as the rate of AVD and the duration of labour.…”
Section: Résumémentioning
confidence: 99%
“…5 In contrast to the COMET study, a number of other studies have shown no difference in AVD. [11][12][13][14] These studies differed in the local anesthetic utilized, the concentrations of local anesthetic solution, or the varying combinations of bolus and/or continuous background infusion rates. Although the COMET study showed that the concentration of local anesthetic had an effect on AVD in nulliparous women, it was performed in only two tertiary delivery centres within the U.K., which may limit the broad generalizability of their findings to other obstetric populations and practices within and outside the U.K. A recent review by Loubert et al highlighted the need for further studies to elucidate the impact of epidural solutions and regimens on outcomes such as the rate of AVD and the duration of labour.…”
Section: Résumémentioning
confidence: 99%
“…Although lower consumption of local anesthetic was reported in women who received PCEA without the basal infusion, none of the other outcomes were significantly better in patients who received PCEA without the basal infusion. A double-blind randomized controlled trial was carried out by Okutomi et al [7] on 67 nulliparous women, who received a standard PCEA protocol (5-ml demand bolus, 10-min lockout interval) with or without a continuous basal infusion (CBI) of 6 ml/h after initial spinal analgesia (part of CSE technique). The median number of analgesic boluses per hour (as assessed with the demanded : delivered ratio) was significantly higher in the demand-only group.…”
Section: Patient-controlled Epidural Analgesia Plus Basal Infusionmentioning
confidence: 99%
“…[1][2][3][4] Additionally, PCEA leads to decreased anesthetic administration, smaller rescue doses, and a lower incidence of motor blockade. 2,[5][6][7][8] PCEA has been used during labor with or without continuous background infusion, 1,4,[7][8][9][10] with boluses of different volumes, and with variable lockout intervals.…”
Section: Introductionmentioning
confidence: 99%