Antihyperalgesic effects of dexmedetomidine on high-dose remifentanil-induced hyperalgesia.

BACKGROUND: Dexmedetomidine is a highly selective α2 adrenergic agonist that has been shown to decrease the intensity of opioid-induced hyperalgesia (OIH). We aimed to investigate the antihyperalgesic effects of dexmedetomidine on high-dose remifentanil-induced hyperalgesia.
METHODS: Ninety American Society of Anesthesiologists physical status I-II patients undergoing laparoscopically assisted vaginal hysterectomy (LAVH) were randomly assigned to one of the following three groups, each of which received either dexmedetomidine (an initial dose of 1.0 µg/kg for 10 min, followed by a continuous infusion of 0.7 µg/kg/hr) or placebo saline 15 min before the induction of anesthesia and intraoperative remifentanil infusion: group C received a placebo and 0.05 µg/kg/min remifentanil; group RH received a placebo and 0.3 µg/kg/min remifentanil; and group DRH received dexmedetomidine and 0.3 µg/kg/min remifentanil.
RESULTS: The mechanical hyperalgesia threshold 24 hr after surgery was significantly lower in group RH than in the other two groups. Postoperative pain intensity using visual analog scale (VAS) and cumulative volume of a patient-controlled analgesia (PCA) containing morphine over 24 hr were significantly greater in group RH than in group DRH. The time to the first postoperative analgesic requirement was significantly shorter in group RH than in the other two groups. The desflurane requirement was significantly greater in group C than in the other groups. The frequency of hypotension and bradycardia was significantly higher, but shivering and postoperative nausea and vomiting were significantly lower in group DRH than in the other two groups.
CONCLUSIONS: High-doses of remifentanil induced hyperalgesia, which presented a decreased mechanical hyperalgesia threshold, enhanced pain intensity, a shorter time to first postoperative analgesic requirement, and greater morphine consumption, but dexmedetomidine efficiently alleviated those symptoms. Dexmedetomidine may be a novel and effective treatment option for preventing or attenuating OIH.

RCT Entities:   Population Interventions Outcomes

Introduction

Dexmedetomidine is a highly selective and potent α2 adrenergic receptor agonist with an α1/α2 ratio of 1 : 1,620, comparing with clonidine, which is only a partial agonist with an α1/α2 ratio of 1 : 220 [1]. Belgrade and Hall [2] showed that dexmedetomidine could reboot opioid sensitivity in patients with opioid-induced hyperalgesia (OIH) to attenuate pain intensity and lower opioid doses. In addition, dexmedetomidine might contribute to the recovery of normal nociceptive and antinociceptive responses.

Some studies have reported the role of α2 adrenergic receptor agonists in modulating pain sensitivity known as OIH. These studies showed that α2 adrenergic receptor agonists attenuate opioid-induced post-infusion antianalgesia and prevents opioid-induced post-infusion secondary hyperalgesia. These data suggest that α2 adrenergic receptor agonists may play a role in OIH modulation [3-5].

Remifentanil is an ultra-short-acting µ-opioid receptor agonist associated with a predictable and rapid recovery that is independent of the dose and duration of infusion. Its unique pharmacokinetic characteristics make it an effective anesthetic adjuvant, commonly used in general anesthesia [6]. However, considerable evidence suggests that exposure to high-dose remifentanil paradoxically enhances pain sensitivity and increases analgesic requirements [7-9].

In this study, we evaluated the antihyperalgesia effects of a two-step intravenous infusion of dexmedetomidine on high-dose remifentanil-induced hyperalgesia, which presented a decreased mechanical hyperalgesia threshold, enhanced pain intensity, a shorter time to first postoperative analgesic requirement, and greater morphine consumption.

Materials and Methods

We obtained approval from our Institution Review Board and written informed consent from all participants. Ninety (n = 30 per group) American Society of Anesthesiologists physical status I-II patients aged 20-65 years who were scheduled for laparoscopically assisted vaginal hysterectomy (LAVH) were enrolled in this study. Exclusion criteria included allergy to dexmedetomidine, clinically significant medical or psychiatric conditions, pregnancy, a history of alcohol or drug abuse, or opioid-containing pain or sedative medications.

On the day before surgery, patients were taught how to use the visual analog scale (VAS) and the patient-controlled analgesia (PCA) device. They were instructed to self-deliver analgesia whenever they began to feel pain.

All patients were premedicated with intramuscular midazolam (2-3 mg) before arrival in the operating room. The patients were placed on pulse oximeter, automated blood pressure (BP) cuff, electrocardiogram (EKG), and end-tidal CO2 (ETCO2) devices. In addition, arterial and urinary catheters were attached as part of the patient's management. Tympanic temperature was measured immediately before induction of anesthesia, and again just before extubation.

The patients were randomly assigned using a computer-generated random number table into one of three treatment groups, each of which received either dexmedetomidine (two-step infusion; an initial dose of 1.0 µg/kg for 10 min, followed by a continuous infusion of 0.7 µg/kg/h) or placebo saline 15 min before the induction of anesthesia and intraoperative remifentanil infusion: group C received a placebo and 0.05 µg/kg/min remifentanil; group RH received a placebo and 0.3 µg/kg/min remifentanil; and group DRH received dexmedetomidine and 0.3 µg/kg/min remifentanil.

Induction of anesthesia was commenced with a slow (30-60 s) intravenous (i.v.) bolus dose of remifentanil (1 µg/kg), followed by propofol (1-2 mg/kg); tracheal intubation was facilitated with rocuronium (0.9 mg/kg) in all groups. As mentioned above, infusion of dexmedetomidine or remifentanil in all groups was fixed, and anesthesia was maintained with desflurane and an oxygen/air mixture (fraction of oxygen, 50%). When desflurane was required, its administration was started at the end-tidal concentration of 1 minimum alveolar concentration (MAC), and the concentration was adjusted by a 1% stepwise titration according to acceptable hemodynamic limits (mean arterial blood pressure between -30% and +15% and heart rate between -40% and +15%) and to a target bispectral index (BIS) between 40 and 60. Ephedrine (20 mg) or atropine (0.5 mg) was administered if a patient's preoperative baseline values went below the acceptable limits.

Upon completion of surgery, a neuromuscular blockade was reversed with pyridostigmine (0.2 mg/kg) and glycopyrrolate (0.008 mg/kg) when the train-of-four (TOF) ratio had returned to 25%. When BIS values reached 80 and spontaneous breathing was achieved, extubation was performed. Dexmedetomidine or remifentanil infusion was discontinued when the final surgical stitch had been placed. Each patient was administered analgesics using a PCA pump containing morphine (60 mg), ketorolac (150 mg), and ramosetron (0.6 mg) in a total volume of 100 ml of saline. This device was set to deliver a basal infusion of 2 ml/hr and bolus doses of 0.5 ml with a 15 min lockout period. Postoperative pain intensity was documented using a 100 mm linear VAS. The VAS consisted of a straight line with the left end of the line representing no pain and the right end of the line representing the worst pain. Patients were asked to mark the position on the line corresponding to their perception of pain. An i.v. dose of ketorolac (30 mg) was administered if patients reported a VAS score ≥ 40, and 15 mg ketorolac was added as needed during their postanesthesia care unit (PACU) stay.

The mechanical hyperalgesia threshold was measured preoperatively and 24 hr after surgery using Von Frey filaments (Bioseb™, Chaville, France) on peri-incisional areas, 2 cm above from the perpendicular line of the optical port site. This device consists of 20 monofilaments of constant length with a stepwise progression of diameters. The numerical grade of the filaments (1.65-6.65) corresponds to a logarithmic function of the equivalent forces of 0.008-300 g. When the tip of a fiber of given length and diameter is pressed against a test area at a right angle, the applied force increases as the researcher continues to advance the probe, until the fiber bends. After the fiber bends, further advancement of the probe may induce more bending, but does not apply more force to the test area. This makes it possible to apply reproducible forces within a wide tolerance range to the tested surface. The force is continuously applied for 1 s and then removed. Subjects are instructed to respond "yes" to indicate that contact was felt during the stimulation or "no" to indicate that contact was not felt during the stimulation. If the subject reports a negative answer, a filament with a larger diameter is used and applied with increasing intensity until the subject reacts. The mechanical hyperalgesia threshold was defined as the lowest force (g/mm2) necessary to bend a Von Frey filament, which was perceived to be painful.

The primary endpoint was a mechanical hyperalgesia threshold at 24 hr after surgery. Secondary endpoints were the time to the first postoperative analgesic requirement, postoperative pain intensity using VAS, and cumulative volume of a PCA containing morphine over 24 hr. Side effects related to the study drugs included hypotension, bradycardia, dysrhythmia, shivering, and postoperative nausea and vomiting (PONV). Shivering was treated using a forced-air warming blanket. Nausea or vomiting was treated with i.v. ondansetron (4 mg).

A preliminary investigation showed that the means of the three treatment groups (group C, group RH, and group DRH) for mechanical hyperalgesia threshold after surgery were 132, 84, and 116 g/mm2, respectively, with effect size of 0.37 and a standard deviation among subjects of 39.55 g/mm2. Thus, a sample size of 26 patients per group was needed to demonstrate a significant difference with a power of 80% and an α-coefficient of 0.05. Assuming a 10% dropout rate, the final sample size was determined to be 30 patients per group. The results are presented as mean ± SD or number (percentage) of patients. Comparisons of age, body weight, % volume of desflurane, duration of anesthesia, mechanical hyperalgesia threshold, time to first postoperative analgesic requirement, pain intensity, and cumulative PCA volume over 24 hr after surgery among the groups were conducted using one-way ANOVA. Post-hoc comparisons were performed with Bonferroni correction of the significance level. Chi-square tests were used to analyze categorical data, such as hypotension, bradycardia, shivering, dysrhythmia, and PONV. P < 0.05 was considered statistically significant.

Results

A total of 90 patients were assessed for eligibility and received study medication after randomization. Five of the 90 patients initially enrolled were withdrawn because of conversion to open surgery or re-exploration for postoperative bleeding (Fig. 1).

Fig. 1

The COSORT flowchart.

There were no significant differences between the three groups with respect to age, weight, duration of anesthesia, or perioperative tympanic temperature. Extubation time after surgery was significantly longer in group C than in the other two groups. The % volume of desflurane was significantly higher in group C than in the other two groups, and that in group DRH was significantly lower than in group RH (Table 1).

Table 1

Demographic and Anesthetic Data

Values are expressed as mean ± SD. Group C: placebo and 0.05 µg/kg/min remifentanil, group RH: placebo and 0.3 µg/kg/min remifentanil, and group DRH: dexmedetomidine and 0.3 µg/kg/min remifentanil. *P < 0.05 versus the other 2 groups. †P < 0.05 versus group DRH.

The time to first postoperative analgesic requirement was significantly shorter in group RH than in the other two groups. Analgesic consumption (ketorolac) during PACU stay was significantly higher in group C than in the other two groups. Pain intensity using VAS was significantly greater in group RH than in group DRH and group C at 24 hr and 12 hr after surgery, respectively. The preoperative mechanical hyperalgesia threshold was not significantly different between the three groups. The mechanical hyperalgesia threshold around the surgical incision 24 hr after surgery was significantly lower in group RH than in the other two groups. The volume of PCA containing morphine was significantly greater in group RH than in the other two groups (Table 2).

Table 2

Clinically Relevant Pain and Mechanical Hyperalgesia Threshold

Values are expressed as mean ± SD. PACU: postanesthesia care unit. Group C: placebo and 0.05 µg/kg/min remifentanil, group RH: placebo and 0.3 µg/kg/min remifentanil, and group DRH: dexmedetomidine and 0.3 µg/kg/min remifentanil. *P < 0.05 versus the other 2 groups. †P < 0.05 versus group DRH.

The frequency of hypotension and bradycardia was significantly higher in group DRH than in the other two groups. Postanesthetic shivering was significantly lower in group DRH than in the other two groups, and that in group RH was significantly higher than in group C. PONV was significantly lower in group DRH than in the other two groups, and that in group C was significantly higher than in group RH (Table 3).

Table 3

Postoperative Side Effects

Values are expressed as numbers (%). PONV: postoperative nausea and vomiting. Group C: placebo and 0.05 µg/kg/min remifentanil, group RH: placebo and 0.3 µg/kg/min remifentanil, and group DRH: dexmedetomidine and 0.3 µg/kg/min remifentanil. *P < 0.05 versus group the other 2 groups. †P < 0.05 versus group C.

Discussion

The major finding of this study was that dexmedetomidine (two-step infusion; an initial dose of 1.0 µg/kg for 10 min, followed by a continuous infusion of 0.7 µg/kg/h) attenuated high-dose remifentanil-induced hyperalgesia in patients undergoing LAVH.

OIH is characterized by a paradoxical increase in pain intensity, distribution, or sensitivity in patients receiving high-doses or long durations of opioids for the treatment of pain [7]. As a result, patients become more sensitive to certain painful stimuli. However, epidemiologic reports regarding the incidence or prevalence of OIH are limited. Although the precise molecular mechanism of OIH is not yet understood, acute receptor desensitization via uncoupling of the receptor from G-proteins, up-regulation of the cAMP pathway, activation of the N-methyl-D-aspartate (NMDA)-receptor system, and descending facilitation have been proposed to be involved. Of these, the central NMDA system is considered the most likely player. NMDA receptors are comprised of two types of subunits: the principal subunit NR1 and the modulatory subunit NR2A-D. Particularly crucial is the NMDA receptor 2B (NR2B) subunit, which plays an important role in spinal dorsal horn sensory pathways [10,11].

In the present study, we found that intraoperative high-dose remifentanil induced a decreased mechanical hyperalgesia threshold, enhanced pain intensity, shorter time to first postoperative analgesic requirement, and greater morphine consumption, all indicative of OIH. Enhanced tyrosine phosphorylation of NR2B in the spinal cord is associated with remifentanil-induced postoperative hyperalgesia. In fact, it plays a key role in the NMDA receptor activation, and contributes to nociceptor activity-induced spinal plasticity and the development of central sensitization that leads to OIH [12]. Strategies for preventing, reversing, or managing OIH have been attempted. These include the NMDA receptor antagonists ketamine [1,12] or magnesium [9], the GABA receptor antagonist propofol [8], the α2 agonists clonidine [1] or dexmedetomidine [2,3,5], the β-blocker propranolol [13], and the COX-2 inhibitor parecoxib [14].

Dexmedetomidine, a highly selective and potent α2 adrenergic receptor agonist attenuates high-dose remifentanil-induced hyperalgesia by decreasing spinal tyrosine phosphorylation of the NR2B subunit [3]. As mentioned above, in the present study, the dexmedetomidine (group DRH) alleviated clinically relevant pain by relieving symptoms such as enhanced pain intensity, inducing a shorter time to first postoperative analgesic requirement and high morphine consumption; mechanically evoked pain up to 24 hr after surgery was also alleviated. It has been shown that the effect of dexmedetomidine on the cumulative consumption of morphine persisted for 24 hr, and its effect on postoperative pain intensity for 48 hr, as compared to controls [15].

α2 adrenergic receptor agonists with sedation properties have been shown to decrease anesthetic requirements in animal models [16,17] and human clinical trials [18,19]. The locus ceruleus of the brainstem is the major site of the hypnotic action of α2 adrenergic receptor agonists, which cause a reduction in noradrenergic activity. In addition to synaptic noradrenergic depletion, the mechanism of the hypnotic action of α2 adrenergic receptor agonists can be explained by the fact that α2 adrenergic receptor agonists and general anesthetics increase K+ efflux through the neuronal cell membrane and reduce intracellular cyclic adenosine monophosphate (cAMP), which in turn induces changes in transmembrane hyperpolarization of excitable neuronal cells [20,21]. In the present study, the dexmedetomidine (group DRH) significantly reduced the desflurane requirement for anesthetic maintenance by 49%, and 16% compared with the groups receiving placebo concomitant with low- or high-dose remifentanil (groups C and RH, respectively). Our data correspond with some studies showing that dexmedetomidine diminished anesthetic requirements by 30-90% [22,23].

Tufanogullari et al. [24] reported that although dexmedetomidine showed better early recovery (e.g., PACU stay), later recovery events (e.g., hospital discharge, resumption of oral intake and bowel function) were similar as compared to controls. In the present study, time to extubation in group DRH (dexmedetomidine and high-dose remifentanil) was significantly shorter than in group C (placebo and low-dose remifentanil) but not significantly different from time to extubation in group RH (placebo and high-dose remifentanil). As mentioned above, the significant difference in desflurane requirements between group DRH and group C might have affected time to extubation. However, more data are necessary to confirm the effect of dexmedetomidine on time to extubation.

The hemodynamic effects of α2 adrenergic receptor agonists may be explained through a reduction of sympathetic tone. A decreased sympathetic activity results in lower blood pressure and reduced heart rate [25]. Because high catecholamine concentrations may trigger PONV, the antiemetic effect of α2 adrenergic receptor agonists may result from a decreased sympathetic activity [26]. In the present study, we found that the frequency of hypotension and bradycardia in group DRH was significantly higher, and PONV was significantly lower, as compared to the other two groups. However, dexmedetomidine combined with high-doses of remifentanil should be used cautiously, as this present study showed that patient's preoperative hemodynamic baseline values in group DRH significantly went below the acceptable limits compared to the two groups.

Postanesthetic shivering or OIH is associated with high-dose remifentanil and may be prevented by NMDA receptor antagonists [27]. The antishivering action of dexmedetomidine results from lowering vasoconstriction and shivering thresholds [28]. In the present study, we found that OIH and shivering induced by high-dose remifentanil were alleviated by dexmedetomidine. The findings of the present study provide an indirect support to the fact that antihyperalgesic and antishivering effects of α2 adrenergic receptor agonists are associated with NMDA receptors.

In conclusion, high-doses of remifentanil induced hyperalgesia, which presented a decreased mechanical hyperalgesia threshold, enhanced pain intensity, shorter time to first postoperative analgesic requirement, and greater morphine consumption. A two-step dexmedetomidine infusion efficiently alleviated OIH symptoms. Therefore, dexmedetomidine may be a novel and effective treatment option for preventing or attenuating OIH. Further studies are required to investigate the use of dexmedetomidine as part of a multimodal approach for OIH.