Opioids are a prerequisite for perioperative analgesia in the anesthetic setting, but can be a double-edged sword due to the side effect of opioid-induced hyperalgesia (OIH). OIH is related to high opioid dosage, long duration of opioid use, and abrupt discontinuation of opioids after surgery. Therefore, many mechanism- based combinations of other adjuvant drugs have been used to attenuate sensitization of the central pronociceptive process and reduce the unpleasant hyperalgesic response [1].

Ketamine, an N-methyl-D-aspartate (NMDA) antagonist, efficiently decreases the hyperalgesic response induced by opioids. Ketamine modulates the pronociceptive sensitization process and attenuates postoperative hyperalgesic responses. Multiple modes of administration have been used to evaluate the effects of ketamine on postoperative hyperalgesic response, including a single bolus, a bolus plus an intraoperative intravenous infusion, and an intraoperative infusion plus a consecutive postoperative infusion [2]. Reduction of postoperative hyperalgesia can be evaluated by decrease in pain scores, a delay of time to the first request for analgesic drugs, a decrease in total opioid consumption, and a decrease in additional analgesics. Rarely, a postoperative hyperalgesic response was the primary endpoint [345] for evaluation of the hyperalgesic effect of ketamine. In this study we tried to make a point of confirming the antihyperalgesic ability of ketamine in a view point of not only reduction of opioid consumption but also increase of tactile sensitivity by Touch- Test sensory evaluator.

We attempted to demonstrate the antihyperalgesic effect of ketamine on high-dose remifentanil-based anesthesia. Ketamine was administrated as an intravenous bolus and as a subsequent intraoperative infusion. In addition, the Touch-Test sensory threshold was used to evaluate the periumbilical area to detect changes in tactile sensitization and hyperalgesic response, instead of the Von Frey monofilament.

We enrolled seventy five patients (n = 25 per group) scheduled for elective laparoscopic gynecological surgery. All patients were 23 to 60 years old, American Society of Anesthesiologists physical status I or II. Patients were excluded from the study when they had previous history of sedative and opioid medications, alcohol abuse, or significant medical or psychiatric conditions. When patients visited the preoperative anesthetic clinic, they were taught how to handle the numerical rating scale (NRS) score, the patient-controlled analgesia (PCA) device, and the Touch-Test sensory evaluation [6]. After obtaining Institutional Review Board approval [No: 2014-10-044-002] and written informed consent, patients were randomly divided into three groups on the day of surgery. Postoperative fentanyl consumption was used to calculate the statistical power. A sample size estimate indicated that 24 patients per group would give a power of 80% at a α level of 0.05 for detecting a difference in fentanyl consumption of at least 30%. All patients were noninvasively monitored to collect data on blood pressure (BP), oxygen saturation (SpO₂) with pulse oximetry, electrocardiogram, end-tidal concentration of desflurane and CO₂, bispectral index (BIS) and esophageal temperature. Total fluid infusion and urine output were also monitored and recorded during anesthesia. Induction of anesthesia was conducted with an intravenous bolus dose of remifentanil (0.5 µg/kg), followed by propofol (1.5 mg/kg), glycopyrrolate (0.2 mg), and midazolam (0.05 mg/kg). Endotracheal intubation was conducted after rocuronium (0.6 mg/kg) in all groups. All patients were assigned into three groups: group RL received 0.05 µg/kg/min remifentanil; group RH received 0.3 µg/kg/min remifentanil; and group KRH received 5 µg/kg/min ketamine and 0.3 µg/kg/min remifentanil during maintenance. Group KRH only received an intravenous bolus dose of ketamine (0.5 mg/kg) during induction. The infusion rates of ketamine and remifentanil did not change during anesthetic maintenance. The end-tidal concentration of desflurane (volume %) of desflurane mixed with oxygen (O₂ 50%) was recorded and changed according to the target BIS (40 to 60) and acceptable blood pressure and heart rate (± 20% of baseline). Ephedrine (5 mg) or glycopyrrolate (0.2 mg) was administered when a patient's hemodynamic parameters left the acceptable range. Infusion of ketamine and remifentanil was discontinued at the final surgical suture. When BIS reached 90 and hand grip (5 s) was possible, extubation was performed. The time to extubation (min) was measured from discontinuation of the study drug infusion to extubation. An intravenous bolus of ramosetron (0.3 mg) was administered after the final stitch and another bolus of ramosetron (0.3 mg) was mixed with the PCA pump, which contained 800 µg fentanyl in a total volume of 60 ml of saline and was connected to each patient. This PCA device was set at a basal infusion of 0.5 ml/hr, with a bolus dose of 0.5 ml with 15 min lockout interval. Postoperative pain intensity was measured by verbal NRS score at 0 h (immediately after surgery) and then after 1, 6, and 24 h after surgery by an investigator who was blinded to the patients' group (NRS0, NRS1, NRS6, NRS24, respectively). Time (min) to first analgesic, which was ketorolac, and total additional analgesic dose (mg) were also recorded. If the pain scores by NRS of the patient were over 4, 30 mg ketorolac was administered and if the pain scores by NRS were still over 4 again, another consecutive 15 mg of ketorolac was added repeatedly during the patient's stay in the postanesthetic care unit (PACU).

The Touch-Test sensory threshold was measured preoperatively and 24 h after surgery using a Semmes-Weinstein monofilament (SWMF, North Coast Medical, Inc., San Jose, CA, USA) 20 piece full kit (NC12775), with an evaluator size of 1.65-6.65 and a target force of 0.008-300 g. The Touch-Test sensory evaluator was applied on peri-incisional areas 2 cm above the perpendicular line of the optimal port site. The filament was pressed at a 90° angle against the skin until it bowed and was held in place for 1.5 s and then removed. For monofilaments from 1.65 to 4.08, the stimulus was applied in the same location up to 3 times to elicit a response. A single response indicated a positive response. For filaments 4.17 to 6.65, the stimulus was applied one time only. The patient was instructed to respond by saying "yes" or "touch" when the stimulus was felt. The patient's vision was occluded by using a shield or by having the patient look away. If the patient did not respond to the stimulus, the process was repeated with the next largest monofilament. A diminished threshold of sensory evaluation compared with the preoperative baseline suggested desensitization of peripheral sensory perception. Side effects including hypotension, bradycardia, delirium, shivering, and postoperative nausea and vomiting (PONV) were recorded. Shivering and PONV were treated in the PACU with a warm air-blanket and additional intravenous ramosetron (0.3 mg), respectively.

Comparisons of the following parameters among the three groups were performed by one-way ANOVA with Bonferroni post-hoc analysis using GraphPad Prism (Prism version 6.0, GraphPad Software, Inc., San Diego, CA, USA): age, body weight, baseline hemodynamics (blood pressure, heart rate), duration of anesthesia, input, output, the end-tidal concentration of desflurane (volume %), time to extubation after surgery, time to first analgesic requirement, additional analgesic consumption during PACU stay, pain scores by NRS (0, 1, 6, and 24 h after surgery), Touch-Test sensory evaluation (preoperative, postoperative 24 h, and differences), and cumulative fentanyl dose for 48 h after surgery. P < 0.05 was considered statistically significant

No patient was dropped during the study. There were no significant differences among the three groups related to demographic and anesthetic parameters, such as age, body weight, baseline blood pressure (systolic, diastolic, mean), baseline heart rate, duration of anesthesia, input, output, or time to extubation after surgery. The mean end-tidal concentration of desflurane group RL was higher than other 2 groups (P < 0.05, Table 1).

Additional analgesic (ketorolac) consumption during the PACU stay was significantly higher in group RH than in group RL. Pain scores by NRS at 6 and 24 h after surgery were significantly higher in group RH than in the other two groups. The preoperative value of the Touch-Test sensory evaluation did not differ significantly between the three groups. The postoperative value of the Touch-Test sensory evaluation was significantly lower in group RH than in the other two groups. The value difference [postoperative - preoperative] was also significantly higher in group RH than in the other two groups, along with the cumulative fentanyl dose (µg) for 48 h after surgery (Table 2).

No additional intravenous ramosetron was needed for PONV. Two cases of shivering were detected in group RH, but subsided after application of a warm air-blanket.

Remifentanil, a commonly used perioperative ultrashortacting opioid analgesic, commonly induces postoperative hyperalgesia associated with high dosage, long duration of use, and acute withdrawal [78910], though the specifics vary based on clinical experimental designs and settings [111213]. Hyperalgesia is defined as "increased pain from a stimulus that normally provokes pain" [14]. Sensitization induced by opioids is initially characterized by "an increased nociceptive response to a drug that follows its repeated intermittent administration," known as "reverse opioid tolerance" [15]. Although sensitization and tolerance are opposite phenomena, they are expressed concomitantly at the same level of biological processes [16]. It is believed that pain modulation occurs during this biologic process, and a new set equilibrium can be established between nociception and antinociception. In this case, more hyperalgesia can be expected, but more sensitization and tolerance can also be developed. Group RH had significantly higher 6 and 24 h NRS scores and a higher 48 h fentanyl dose than group RL. Analgesic consumption in the PACU was also significantly higher in group RH than in group RL, indicating the development of remifentanilinduced hyperalgesia.

Proposed mechanisms of acute opioid tolerance include activation of NMDA antagonists [17], inactivation of mu (µ) opioid receptor peptide [18], and increased secretion of dynorphin and calcitonin-gene related peptide in the dorsal horn of the spinal cord [20]. Sensitization and concomitant development of acute tolerance can produce postoperative hyperalgesia. Therefore, hyperalgesia could be attenuated by administration of ketamine [202122], which is an NMDA antagonist. Group RH showed a significantly higher pain score by NRS (24 h after surgery) and higher fentanyl consumption (48 h) than patients who received high dose remifentanil with a ketamine infusion (group KRH). The total fentanyl consumption (48 h) in group KRH was significantly reduced up to 32% compared to group RH. A low-dose infusion of ketamine reduced opioid consumption up to 40% [2]. Reduction of pain scores and postoperative opioid consumption demonstrated that an intraoperative infusion of ketamine was clinically effective enough to attenuate the hyperalgesic response induced by high-dose remifentanil. Reduction of pain score by NRS among three groups was investigated at the independent time point (0, 1, 6, 24 h respectively) by ANOVA not at the dependent serial time point by repeated measures of ANOVA. Therefore, the intergroup differences of pain score by NRS at the specific time point should be considered.

The Touch-Test sensory evaluator is indicated for diagnoses including nerve compression syndromes, peripheral neuropathy, thermal injuries, and postoperative nerve repair. Each Touch-Test sensory evaluator is individually calibrated to deliver its targeted force within a 5% standard deviation and provides a noninvasive evaluation of the cutaneous sensation threshold throughout the body with objective and repeatable results [623242526]. The Touch-Test sensory evaluation using SWMF can demonstrate changes in tactile sensitivity. If the postoperative value minus the preoperative value shows a higher negative number, that means that tactile sensitivity increased and that a hyperalgesic response may occur. The Touch-Test sensory evaluation is seldom used for acute postoperative conditions; it is more commonly used to evaluate neuroplasticity, central and peripheral desensitization of neuronal damage, and neuronal inflammation [23242526]. Group RH showed significantly higher negative SMWF numbers on the Touch-Test sensory evaluation than group KRH and group RL. This demonstrates that infusion of ketamine was clinically effective enough to attenuate tactile sensitivity and the hyperalgesic response induced by high dose remifentanil.

Lee et al. [5] showed antihyperalgesic effects of dexmedetomidine on high-dose remifentanil-induced hyperalgesia. This group used Von Frey filaments to evaluate mechanical hyperalgesia as the primary endpoint. We opted to use the Touch-Test sensory evaluation as it is less invasive and easier to conduct than the Von Frey filament test. Ketamine has fewer side effects than dexmedetomidine, especially hypotension, and has its intrinsic sympathomimetic activities in combination with high-dose remifentanil based anesthesia. Moreover, dexmedetomidine and ketamine have similar antihyperalgesic effects on high-dose remifentanil-induced hyperalgesia. Although dexmedetomidine creates less respiratory depression, the time to extubation ranged from 3.6 to 4.3 min in our subjects, which was shorter than the previously reported 13 to 16 min [5]. Ketamine also has an economic advantage over dexmedetomidine.

Taken together, high-dose remifentanil-induced hyperalgesia can be efficiently attenuated by an intraoperative infusion of ketamine. Ketamine also can decrease peripheral tactile sensitivity induced by high-dose remifentanil, based on Touch-Test sensory evaluation. To increase the quality of perioperative life in high-dose remifentanil based anesthesia, intraoperative ketamine could be used safely to modulate hyperalgesic responses to opioids and increase patient satisfaction.