Microsoft powerpoint - reuben_iarsposter

Analgesic Efficacy of Administering Celecoxib, Pregabalin, or the Combination for Spinal Fusion Surgery
Scott S. Reuben, MD, Asokumar Buvanendran, MD, Jeff S. Kroin, PhD, Karthik Raghunathan, MD, MPH
Department of Anesthesiology, Baystate Medical Center, Springfield, MA ~ The Western Campus of Tufts University School of Medicine
Department of Anesthesiology, Rush University Medical Center, Chicago, IL
BACKGROUND
MATERIALS AND METHODS
A multimodal analgesic approach is currently
Following hospital IRB approval, 80 patients scheduled to undergo
• There were no differences in demographics, surgical recommended for the management of acute pain (1).
elective decompressive lumbar laminectomy with posterior spinal fusion
duration, or number of spinal levels fused. • Recent evidence suggests that alpha-2-delta subunit
were randomized to receive oral medications:
• The pregabalin/celecoxib group consumed the least calcium channel ligands (gabapentin and pregabalin),
1) placebo 1 h before and 12 h after surgery
amount of patient-controlled morphine (Figure 1).
may provide effective post-surgical analgesia (2).
2) celecoxib 400 mg 1 h before and celecoxib 200 mg 12 h after surgery
• Celecoxib alone or pregabalin alone also reduced • Further, these drugs can interact synergistically
pregabalin 150 mg 1 h before and 12 h after surgery
opioid use compared to placebo, but not as much as with NSAIDs to produce antihyperalgesia (3).
4) pregabalin/celecoxib combination of 150 mg/400 mg 1 h before and 150
The combination of gabapentin and rofecoxib, a
mg/200 mg 12 h after surgery.
• The pregabalin/celecoxib combination was the most COX-2 NSAID, was shown to be superior to either
Morphine consumption with patient-controlled anesthesia (PCA), and
effective treatment for reducing pain both at rest and single agent for postoperative pain (4).
pain scores (0-10 verbal rating scale) at rest and with movement, were
with movement over the 24-h postoperative time period.
Celecoxib (5) and gabapentin (6) have demonstrated
evaluated for 24 h after the patient arrived in the post-anesthesia care
• Hemodynamics and respiratory rate did not differ analgesic efficacy following spinal fusion surgery.
unit (PACU).
Sedation scores, heart rate, oxygen saturation, mean blood pressure,
• Fewer patients experienced nausea or excessive respiratory rate, and opioid-related side-effects were also recorded.
sedation in the pregabalin/celecoxib group compared to Morphine consumption, pain, heart rate, mean arterial blood pressure,
and respiratory rate were compared among the 4 groups over the
postoperative time points with repeated measures linear fixed model.

CONCLUSIONS
PURPOSE AND HYPOTHESIS
• This study revealed that the perioperative Figure 1. PCA Morphine Use over 24 h
administration of the combination of celecoxib and • Although structurally similar to gabapentin,
pregabalin resulted in improved analgesia, with less pregabalin has demonstrated greater analgesic
opioid consumption and fewer side effects, compared to efficacy in rodent models of neuropathic pain (7), and
either analgesic agent alone following spinal fusion exhibits linear pharmacokinetics across its
therapeutic dose range with low inter-subject
variability (8).

BIBLIOGRAPHY
The goal of this study was to assess the combination
of celecoxib and pregabalin for pain following spinal

fusion surgery.
Acta Anaesthesiol Scand 2004;48:1130-6.
J Bone Joint Surg Am 2005;87(3):536-42.

Source: http://www.oaprs.org/news/2006/media/Reuben_IARSposter.pdf

Wallsandfloors20130107~2.xlsx

Whilst every effort has been made to ensure that this price list is accurate Tile Supply Ltd can not accept responsibility for any errors or omissions. Tile Supply Ltd Unit 10B Broadmeadow Industrial Estate Teignmouth TQ14 9AE Tel:01626 776606 Email: [email protected] www.TileSupply.co.ukTrade Prices exclude delivery charge, please call the sales team for your delivery rate. Tile Supply

Cem_templates

gaming operations Itsoundslikeafunnyquestion,butwhenyoustarttothinkabout it, it can lead to a little bit of panic. Jeez, how do I know what Idon’t know? Where do you go to find the answer when you don’teven know the question to ask? When I do training on technologyrisk assessments, I start by asking this question. People don’t knowhow to answer and sit there with a puzzled look on th

Copyright © 2008-2018 All About Drugs