학술논문

Nefopam as an adjunct to intravenous patient-controlled analgesia after renal transplantation: a randomised trial.
Document Type
Article
Source
Acta Anaesthesiologica Scandinavica. Sep2015, Vol. 59 Issue 8, p1068-1075. 8p. 1 Diagram, 3 Charts, 2 Graphs.
Subject
*KIDNEY transplantation
*RANDOMIZED controlled trials
*GLOMERULAR filtration rate
*ANALGESIA
*ANALGESICS
*CONTROL groups
Language
ISSN
0001-5172
Abstract
Background Nefopam has been used as an adjuvant to opioid analgesia after operation. We investigated the efficacy of nefopam as an adjunct to fentanyl-based intravenous patient-controlled analgesia ( IV PCA) on post-operative pain relief in patients undergoing renal transplantation. Methods Ninety-eight patients undergoing elective renal transplantation were randomised into two groups: nefopam or control groups. The former received nefopam (160 mg in 200 ml at a rate of 4 ml/h) whereas the latter received normal saline during the first 48 h after reperfusion of grafted kidney. Pain intensity scores, cumulative dose of fentanyl, and the incidence of adverse events were assessed at 1, 6, 12, 24, and 48 h post-operatively. Serum creatinine and estimated glomerular filtration rate were evaluated on post-operative days 1, 2, 4, and 7. Results The cumulative fentanyl consumption during the first 48 h after operation was 19% less in the nefopam group than that in the control group (1005 ± 344 μg vs. 1246 ± 486 μg, mean ± SD; P = 0.006). Pain intensity scores at rest and on coughing were significantly lower in the nefopam group throughout the first 12 and 48 h after operation, respectively. Adverse events and early graft function were comparable between the groups, except a significantly lower incidence of drowsiness observed in the nefopam group (4% vs. 21%, P = 0.027). Conclusion In combination with fentanyl PCA, nefopam reduced post-operative fentanyl consumption with superior analgesia after renal transplantation. [ABSTRACT FROM AUTHOR]