Intra-operative Ketamine Infusions in Opioid-dependent Patients With Chronic Lower Back Pain
Information source: Dartmouth-Hitchcock Medical Center
ClinicalTrials.gov processed this data on August 23, 2015 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Chronic Low Back Pain
Intervention: Ketamine (Drug); Normal saline (Other)
Phase: N/A
Status: Completed
Sponsored by: Dartmouth-Hitchcock Medical Center Official(s) and/or principal investigator(s): Jeffrey A Clark, MD, Principal Investigator, Affiliation: DHMC
Summary
Noxious stimuli occurring intraoperatively and postoperatively generate central
sensitization, decreasing pain thresholds and ultimately increasing analgesic requirements.
The pathophysiology of central sensitization is thought to involve excitatory amino acid
receptors such as N-methyl-d-aspartate (NMDA) (1, 2). Ketamine is a N-methyl-d-aspartate
(NMDA) receptor antagonist that has been shown to be useful in the reduction of acute
postoperative pain and analgesic consumption in a variety of surgical interventions (3).
Spine surgery provides a unique opportunity to evaluate the preemptive and preventative
impact of ketamine on the primary end points of postoperative 24 and 48 hour opioid
consumption in patients with chronic pain. The goal of this IRB approved double blinded,
prospective, randomized placebo controlled trial is to quantify the preemptive and
preventative analgesic effects of ketamine infusions in this patient population. Such
insight may lead to better pain control, improved satisfaction, and ultimately a reduction
in side-effects related to postoperative opioid use.
Clinical Details
Official title: Intra-operative Ketamine Infusions in Patients With Chronic Lower Back Discomfort Undergoing Laminectomies.
Study design: Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
Primary outcome: Morphine Consumption in the First 48 Hours After Surgery
Secondary outcome: Hospital DurationMortality Hemodynamic Changes Complications Related to Ketamine
Detailed description:
Noxious stimuli occurring intra-operatively and post-operatively generate central
sensitization, decreasing pain thresholds and ultimately increasing analgesic requirements.
The pathophysiology of central sensitization is thought to involve excitatory amino acid
receptors that have been implicated in the prolongation of painful states in animal models.
The N-methyl-d-aspartate (NMDA) receptor is one such excitatory amino acid receptor (1, 2).
The underlying mechanism of central sensitization is thought to involve c-fiber associated
injury occurring with incision. Crile and Wall brought about the concept that attenuation of
central sensitization could be accomplished via the provision of analgesic interventions
(opioids, local anesthesia) prior to the noxious insult. They termed the central
sensitization attenuation preemptive analgesia. The concept of preemptive analgesia was
later expanded to implicate both pre and post-incisional noxious stimuli as part of this
process, resulting in studies designed to provide interventions throughout the surgical
intervention (peri-procedural) (3). Reduction in analgesic requirements or pain scores for
more than five half-lives (1st order kinetics) following the provision of the intervening
analgesic agent peri-procedurally is now known as preventative analgesia. The term
preemptive analgesia is now reserved for interventions that occur only before the noxious
stimuli.
Multiple studies have investigated the concepts of preemptive analgesia and preventative
analgesia by providing a variety of analgesic interventions at various times throughout the
surgical insult in addition to more conventional means of anesthesia provision, including
opioids, Non-Steroidal Anti-Inflammatory Drugs (NSAID)s, Cyclooxygenase-II (COX-2)
inhibitors, alpha-2 agonists, and ketamine (4, 5, 6). Preemptive and preventative analgesia
using a variety of pharmacological agents with at least partially known mechanisms of
actions has provided some insight into potential mechanisms of central sensitization.
Ketamine is a N-methyl-d-aspartate (NMDA) receptor antagonist that has been shown to be
useful in the reduction of acute postoperative pain and analgesic consumption in a variety
of surgical interventions with variable routes of administration. It has also been shown to
be effective in the presence and absence of opioids, suggesting that it has more than one
mechanism of action in preemptive and preventative analgesia, including but not limited to
decreasing central excitability, decreasing acute post-operative opioid tolerance, and a
possible modulation of opioid receptors (7). Ketamine is a common anesthetic agent and has
been in use since the Vietnam War. Clinically, ketamine provides pain relief with minimal
respiratory depression, and at higher doses (1-2mg/kg) can induce general anesthesia while
maintaining blood pressure and cardiac output.
Recently, a qualitative systematic review of the role of NMDA receptor antagonists was
completed. Twenty-four studies investigating the role of ketamine met the inclusion
criteria of the study, 58% of which demonstrated a preemptive or preventative analgesic
effect. Patients underwent a variety of surgical procedures, both ambulatory and inpatient,
and there was no obvious effect of either surgical type or dose of ketamine (range 0. 15 to
1mg/kg) on the success of preventative intervention. However, the authors were unable to
quantify the degree of reduction in primary end-points (opioid consumption, pain scores,
both) due to variability in recording of such data. In addition, most inpatient studies were
limited to abdominal procedures while the outpatient studies investigated mainly knee
arthroscopies, providing no insight into the degree of impact of NMDA receptor antagonism in
the setting of high pre-operative opioid tolerance combined with surgical procedures known
to be associated with an invariably high degree of post-operative pain. Of note, only 1/24
studies documented a significant difference in side effects related to ketamine provision
in patients who had received 20mg of epidural ketamine (7).
Laminectomy procedures provide a unique opportunity to evaluate the preemptive and
preventative impact of ketamine on the primary end points of acute post-operative pain
scores and opioid consumption in a patient population with opioid dependence and a high
degree of post-operative and intra-operative noxious stimuli. The goal of this double
blinded, randomized placebo controlled trial will be to test for the presence of, and
quantify, the preemptive and preventative analgesic effects of ketamine infusions in this
patient population. Such insight may lead to better pain control, improved satisfaction,
and ultimately a reduction in side-effects related to post-operative opioid use including
but not limited to respiratory depression, constipation, and delirium.
Eligibility
Minimum age: 18 Years.
Maximum age: 90 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- Laminectomy procedures.
- History of chronic back pain.
- Daily opioid use.
- Capable of providing informed consent.
Exclusion Criteria:
- Intolerance/allergy to ketamine.
- Intolerance/true allergy to morphine.
- Elevated intra-ocular pressure.
- Uncontrolled hypertension.
- Elevated intra-cranial pressure.
- Any history of a psychosis.
- Pregnancy.
Locations and Contacts
Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire 03756, United States
Additional Information
Related publications: 1. Wall PD. The prevention of postoperative pain. Pain 1988; 33: 289-90. 2. Katz J. George Washington Crile, anoci-association, and preemptive analgesia. Pain 1993;53: 243-5. 3. McQual HJ. Pre-emptive analgesia. Br J Anaesth 1992;69: 1-3. 4. Moiniche S, Kehlet H, Dahl JB. A qualitative and quantitative systematic review of preemptive analgesia for postoperative pain relief: the role of timing of analgesia. Anesthesiology 2002;96: 725-41. 5. Katz J. Pre-emptive analgesia: evidence, current status and future directions. Eur J Anaesthesiol Suppl 995;10:8-13. 6. Katz J, McCartney CJ. Update on pre-emptive analgesia. Curr Opin Anesthesiol 2002; 15: 435-41. 7. McCartney et al. A qualitative systematic review of the role of N-Methyl-D-Aspartate receptor antagonists in preventative analgesia. Anesth Analg 2004; 98: 1385-1400. 8. Wu CT, Yeh CC, Yu JC, et al. Pre-incisional epidural ketamine, morphine and bupivacaine combined with epidural and general anesthesia provides pre-emptive analgesia for upper abdominal surgery. Acta Anaesthesiol Scand 2000;44: 63-8.
Starting date: February 2007
Last updated: May 3, 2013
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