Effect of Low-Dose Dexmedetomidine on the Anesthetic and Recovery Profile of Sevoflurane-Based Anesthesia in Patients Presenting for Supratentorial Neurosurgeries: A Randomized Double-Blind Placebo-Controlled Trial.

Background  Dexmedetomidine could be a suitable adjuvant in neuroanesthesia due to its analgesic and anesthetic-sparing properties with the added advantage of facilitating intraoperative neuromonitoring. However, its recovery profile is still debated upon, as in neuroanesthesia, a prompt recovery is essential for postoperative neurologic assessment. We designed this study to evaluate the effect of dexmedetomidine on the anesthetic and recovery profile of patients presenting for supratentorial neurosurgeries. Materials and Methods  Forty adult patients undergoing supratentorial surgeries were recruited in this prospective, randomized, double-blinded study and were divided into two groups: group S and group SD. Both groups received sevoflurane and fentanyl for maintenance, whereas group SD alone received a low dose of dexmedetomidine infusion. Recovery parameters, opioid consumption, Richmond Agitation-Sedation Scale (RASS) and visual analogue scale (VAS) scores, incidence of nausea and vomiting, and intraoperative hemodynamics were analyzed. Results   There were no statistically significant differences between the groups S and SD in case of recovery parameters-time taken (in minutes, presented as median with interquartile range [IQR]) for (1) eye-opening to command: 9.5 (8-18) versus 22.5 (5-47.5) ( p = 0.414); 2) following verbal command: 10.5 (8.25-29.5) versus 25 (10-28.75) ( p = 0.512); (3) extubation: 11 (9.25-22) versus 25 (10-30) ( p = 0.277); and (4) getting oriented to place, time, and date: 23 (20-52.75) versus 27.5 (25-36.5) ( p = 0.121). Fentanyl consumption was significantly less in group SD (451 ± 39.3) versus group S (524.3 ± 144.1) ( p = 0.034). The median RASS score with IQR and the median VAS scores with IQR were comparable between the groups at all time points. Of the 20 patients in group S, 5 had complaints of nausea and vomiting compared with none in the group SD, although it was not statistically significant. The hemodynamic parameters did not show a significant difference between the groups except for a surge in mean arterial pressure at 30 minutes in group S. Conclusion  Low-dose dexmedetomidine as an adjuvant to sevoflurane- and fentanyl-based anesthesia could provide stable hemodynamics and lesser anesthetics and opioid consumption, without adversely affecting the recovery profile in patients undergoing supratentorial neurosurgical procedures.

RCT Entities:   Population Interventions Outcomes

Introduction

Anesthetic goal during the conduct of neurosurgery is to maintain a balance between optimal cerebral hemodynamics and oxygenation. An ideal anesthetic should provide a slack brain and excellent analgesia and facilitate a rapid recovery. Dexmedetomidine is a superselective α-2 agonist that can reduce the consumption of anesthetics and provide optimum analgesia through its opioid-sparing property. 1 It facilitates an ideal anesthetic background for neurosurgery as it does not interfere with intraoperative neuromonitoring and has an opioid-sparing effect, with the added advantage of preserving the respiratory drive in the immediate postoperative period. 2 Neurosurgeries differ from routine general surgeries in terms of the longer duration and differing anesthesia concerns. 2

The effect of dexmedetomidine in neurosurgeries has been evaluated in the past. However, these studies did not use the depth of anesthesia monitoring such as bispectral index scale (BIS) as an end point to titrate anesthetic drugs and therefore were inconclusive. 3 4 Moreover, these studies had varying outcomes ranging from a delayed recovery to the recovery time remaining unaffected. 1 2 3 4 The need for an early neurologic assessment in the postoperative period is of paramount importance in neuroanesthesia practice. Hence, a prompt recovery in the immediate postoperative period is one of the essential goals of neuroanesthesia practice. To address this lacuna in the scientific literature on dexmedetomidine, we decided to evaluate the effect of low-dose dexmedetomidine on the anesthetic and recovery profile of BIS-guided sevoflurane-based anesthesia in patients presenting for supratentorial neurosurgeries.

Materials and Methods

After obtaining approval from the Institutional Ethics Committee, the trial was registered in Clinical Trials Registry—India (CTRI/2019/01/017108). Forty consenting patients in the age group of 18 to 50 years, belonging to the ASA (American Society of Anesthesiologists) physical status I and II, undergoing elective supratentorial neurosurgeries were recruited in this prospective, randomized, double-blinded study. Patients allergic to dexmedetomidine, those with baseline heart rate (HR) < 50 bpm, those with a history of heart block, those on β-blockers, α-methyldopa, or clonidine, those with coronary artery disease or left ventricular dysfunction, and pregnant or nursing women were excluded from the study. Also, patients with signs and symptoms of raised intracranial pressure (ICP) were excluded. Tab alprazolam 0.5 mg was given on the previous night of the surgery as part of routine premedication.

Patients were randomized into two groups of 20 each. Group S patients received sevoflurane anesthesia for maintenance, and group SD patients received dexmedetomidine infusion along with sevoflurane anesthesia for maintenance. In group SD, we used dexmedetomidine diluted as 2 μg/mL at 0.2 μg/kg/h as an adjuvant. This corresponded to an infusion of 0.1 mL/kg/h of the diluted drug. In group S, we administered 0.1 mL/kg/h of normal saline.

Randomization

Patients were allocated randomly by envelope method using a random number table into two groups of 20 each by the principal investigator. Maintenance drugs, that is, dexmedetomidine/normal saline infusions, were prepared in identical syringes and were given to the attending anesthesiologist by the principal investigator. The assessment was performed by the attending anesthesiologist who was not an investigator of the study and was blinded to group allocation.

Study Protocol

In the operating room, the patient was connected to standard monitors, that is, electrocardiogram (ECG), pulse oximeter (SpO 2 ), and noninvasive blood pressure monitor. Additionally, the BIS Complete Monitoring System (Medtronic, Mansfield, Massachusetts, United States) also was used. BIS Quatro Sensor (Medtronic) was applied on the forehead as per the manufacturer’s instruction on the nonoperating side. Baselines values were recorded from all the monitors before induction. Under local anesthesia using 2% lignocaine, peripheral venous access was established. Postinduction, end-tidal carbon dioxide (EtCO 2 ), train of four (TOF), and invasive arterial blood pressure were also monitored. All patients received intravenous (IV) fentanyl 2 μg/kg and were induced with the total calculated dose of IV propofol 2 mg/kg titrated to the loss of verbal response and a target BIS of 40 followed by IV vecuronium 0.1 mg/kg after confirming the adequacy of ventilation. Postintubation, all patients were ventilated in a volume control mode with 8 to 10 mL/kg of tidal volume and respiratory rate set to achieve an end-tidal carbon dioxide pressure of 30 to 35 mm Hg. Anesthesia was maintained with O 2 , and air (50:50) mixture with sevoflurane titrated to a target BIS of 45 to 50. As the stimulus varied during surgery, volatile agent concentrations were adjusted by 0.2% increments whenever the BIS values were out of the target range to ensure a BIS of 45 to 50.

Postinduction, the study groups received the following drugs based on the group to which they were randomized:

Group S: 0.1 mL/kg/h IV normal saline + sevoflurane titrated to BIS of 45 to 50.

Group SD: 0.2 μg/kg/h dexmedetomidine + sevoflurane titrated to BIS of 45 to 50.

In both groups, additional vecuronium boluses were used to keep the TOF below 2 throughout the surgical procedure. All patients received an infusion of fentanyl at 0.5 μg/kg/h as a background analgesic agent till the end of the surgery. Apart from this constant maintenance dose, an additional bolus of fentanyl 1 μg/kg was administered before the application of skull clamps. Consistent elevation of 10% increase in HR and 10% increase in mean arterial pressure (MAP) without any confounding factors (such as neural reflex and iatrogenic changes in blood pressure for checking hemostasis) was considered as pain stimulus and was treated with a bolus of fentanyl 1 μg/kg.

Toward the end of surgery during dural closure, all patients received IV paracetamol 15 mg/kg and IV ondansetron 0.1 mg/kg. Maintenance drugs (dexmedetomidine/normal saline, fentanyl, and volatile agents) were stopped after the patient had been removed from surgical clamp. IV neostigmine 0.05 mg/kg and IV glycopyrrolate 4 μg/kg were given after the return of all the four twitches in TOF and a TOF ratio of >0.7. The patient was extubated once the patient started obeying commands and after ruling out any neurologic deficits. Rescue analgesia with 10 mg/kg of IV paracetamol was administered when the visual analogue scale (VAS) score was ≥3 or on-demand postoperatively. IV ondansetron 4 mg was administered immediately if the patient had nausea or vomiting.

Data

The following data were collected for each patient.

Anesthesia Parameters

The anesthesia parameters included the duration of anesthesia (intubation to extubation), the total dose of fentanyl administered, and end-tidal sevoflurane concentration (as %) values after intubation to discontinuation of volatile agents (assessed every 10 minutes from the trend of the gas monitor and averaged). The hemodynamic variables such as HR and MAP were recorded every 10 minutes.

Recovery Parameters

The recovery parameters included the following:

Time between discontinuation of maintenance drugs to:

Eye-opening to command

Following verbal command (handgrip)

Extubation

Orientation to place, time, and date

Sedation and pain assessment (extubation, 30, 60, 90, and 120 minutes):

Sedation assessment using the Richmond Agitation–Sedation Scale (RASS)

Pain assessment using VAS

Nausea and vomiting episodes

Statistical Analysis

Numerical data were expressed as mean ± standard deviation if the distribution was normal or as median with an interquartile range (IQR) if not, and categorical data were expressed as frequencies. Association between categorical variables was tested using the chi-square test and Fisher’s exact test. Continuous variables were compared using Student’s t -test or the Mann–Whitney U -test. Recovery parameters were compared between the two groups using time comparison analysis of variance with posthoc analysis. A p -value of less than 0.05 was considered statistically significant. The data analysis was performed using SPSS version 16 (IBM SPSS Inc., Chicago, Illinois, United States).

Results

Forty patients were recruited in this study. There were no statistically significant differences between the groups in terms of age, height, body weight, and body mass index, as shown in Table 1 . There was no significant difference in the mean duration of surgery and anesthesia, as described in Table 1 . The time needed to achieve the primary recovery end points—(1) eye-opening, (2) verbal response, (3) extubation, and (4) orientation in time and place—for groups S and SD is described in Table 2 . For eye-opening, the median time for group S was 9.5 minutes (IQR: 8–18 minutes), whereas for group SD, it was 22.5 minutes (IQR: 5–47.5 minutes). Though the time to eye- opening was longer in group SD, the difference was not statistically significant ( p = 0.414). In case of verbal response, for group S, the median time was 10.5 minutes (IQR: 8.25–29.5 minutes), whereas for group SD, it was 25 minutes (IQR: 10–28.75 minutes). This difference was not statistically significant ( p = 0.512). The median extubation time for group S was 11 minutes (IQR: 9.5–22 minutes), whereas for group SD, it was 25 minutes (IQR: 10–30 minutes), as seen in Table 2 . There was no statistically significant difference between the two groups with regard to the time taken for extubation ( p = 0.277). In terms of orientation postextubation, group S patients had taken a median time of 23 minutes (IQR: 20–52.75 minutes) to get oriented in time and place, while group SD patients had taken a median time of 27.5 (IQR: 25–36.5 minutes), which was not statistically significant ( p = 0.121) ( Table 2 ).

Table 1

Demographic parameters of patients in groups S and SD

Demographic parameters	Group S ( N = 20)		Group SD ( N = 20)		p -Value
	Mean	Standard deviation	Mean	Standard deviation
Abbreviations: BMI, body mass index; S, sevoflurane; SD, sevoflurane with dexmedetomidine.
Age (y)	43.60	10.88	46.40	3.36	0.589
Height (cm)	167.50	10.39	169.00	7.91	0.782
Weight (kg)	67.00	9.39	64.80	5.54	0.640
BMI (kg/m 2 )	23.82	1.92	22.70	1.61	0.284
Mean duration of surgery (min)	355.9	62.7	347	72.19	0.67
Mean duration of anesthesia (min)	372.9	56.8	380.2	62.4	0.62

Table 2

Recovery parameters of patients in groups S and SD

Recovery parameter	Group S ( N = 20), median time taken to reach recovery end point (minutes)	IQR	Group SD ( N = 20), median time taken to reach recovery end point (minutes)	IQR	p -Value
Abbreviations: IQR, interquartile range; S, sevoflurane; SD, sevoflurane with dexmedetomidine.
Eye-opening	9.5	8–18	22.5	5–47.5	0.414
Verbal response	10.5	8.2529.5	25	10–28.75	0.512
Extubation	11	9.25–22	25	10–30	0.277
Orientation in time and place	23	20–52.75	27.5	25–36.5	0.121

The total fentanyl consumption and end-tidal sevoflurane requirement to maintain a BIS of 45 to 50 in both the groups is shown in Table 3 . The consumption of fentanyl in group SD was found to be significantly lower than that in group S ( p = 0.034). Though the end-tidal sevoflurane was lower in group SD, it was not statistically significant as compared with the S group ( p = 0.065). The median RASS scores with IQR at various time points in both the groups were analyzed ( Fig. 1 ). There were no statistically significant differences between the median RASS scores with IQR between the groups at any time point. The median VAS scores with IQR at various time points were evaluated, and the results are depicted in Fig. 2 . The median VAS scores with IQR were comparable between the groups at all time points. Out of 20 patients, 5 had nausea and vomiting in group S compared with none in group SD, which was not statistically significant. Group S had a higher MAP compared with group SD, as shown in Fig. 3 , but it was not statistically significant except at 30 minutes postinduction ( p = 0.042). Though not statistically significant, the HR was lower in group SD at all time points as compared with group S.

Table 3

Comparison of fentanyl consumption and end-tidal sevoflurane in both the group of patients

Group	N	Fentanyl (mg)		p -Value	End-tidal sevoflurane (%) a		p -Value
		Mean	Standard deviation		Mean	Standard deviation
Abbreviations: S, sevoflurane; SD, sevoflurane with dexmedetomidine. a End-tidal sevoflurane (%) required to maintain bispectral index between 45 and 50.
S	20	524.3	144.1	0.034	1.89	0.4	0.065
SD	20	451.0	39.3		1.68	0.3

Fig. 1

Comparison of the median RASS score with interquartile range at various time points of both SEVO and SEVO + DEX groups. RASS, Richmond Agitation–Sedation Scale; SEVO, sevoflurane; SEVO + DEX, sevoflurane with dexmedetomidine.

Fig. 2

Comparison of the median VAS score with interquartile range at various time points of both SEVO and SEVO + DEX groups. SEVO, sevoflurane; SEVO + DEX, sevoflurane with dexmedetomidine; VAS, visual analogue scale.

Fig. 3

Comparison of the mean arterial pressure at various time points of both the sevoflurane group and the sevoflurane with dexmedetomidine group.

Discussion

Supratentorial neurosurgeries require an anesthetic regimen, which ensures optimal cerebral perfusion, stable hemodynamics, preserved autoregulation, excellent analgesia, and rapid recovery. 2 3 The ideal regimen should also facilitate intraoperative neuromonitoring, which has now become an integral part of neuroanesthesia practice. 5 Multiple drugs such as opioids, benzodiazepine, and dexmedetomidine can be used as adjuvants for facilitating these goals. Opioids in this scenario could affect the recovery, delay the neurologic assessment, and lead to a high incidence of postoperative nausea and vomiting (PONV), 2 whereas dexmedetomidine as an adjuvant achieves most of these targets without having any deleterious effects on the cerebral perfusion pressure, ICP, and cerebral oxygen demand (CMRO 2 ). 6 7 8 9 Dexmedetomidine as an adjuvant will facilitate intraoperative neuromonitoring as it does not affect the recording of motor evoked potential, somatosensory evoked potentials, and electrocorticography. 2 10 Additionally, it has analgesic and opioid-sparing properties along with antiemetic properties, making it the right choice for neuroanesthesia practice. 2 The main concern that limited the use of dexmedetomidine was the doubtful recovery profile when administered along with volatile agents. 1 11 Moreover, the recovery profile of neurosurgeries is different as the long duration can result in a cumulative drug effect, thereby delaying the recovery and thus hampering the prompt neurologic assessment in the immediate postoperative period. As there were limited data on the recovery characteristics of neurosurgical patients who received dexmedetomidine as an adjuvant, we designed this study to find the effect of dexmedetomidine on time taken for recovery and to assess the quality of recovery in patients undergoing supratentorial surgeries.

In our study, though there was a noticeable delay in the recovery parameters for the patients in the dexmedetomidine group, it was statistically not significant. We also found that the median RASS scores with IQR were comparable between both of the groups. Dexmedetomidine decreases the requirements of volatile agents in a dose-dependent manner. It also reduces the opioid requirement significantly in the perioperative period. 1 12 13 14 15 16 These factors must have helped in avoiding a significant delay in recovery of patients in the dexmedetomidine group. In our study, the requirement of fentanyl boluses was significantly lower in the dexmedetomidine group. Though not statistically significant, the end-tidal concentration of sevoflurane required to maintain a BIS of 45 to 50 was found to be lower in the dexmedetomidine group. This reduction in the requirement of anesthetics and opioids could have contributed to the favorable effect on the recovery. Apart from this, the avoidance of a loading dose and the use of BIS-guided titration of the depth of anesthesia might have further aided the optimal dosing of the anesthetics, leading to a normal recovery. 17 18

Chakrabarti et al evaluated the effects of dexmedetomidine as an adjuvant to propofol-based anesthesia in posterior fossa surgery. 19 They concluded that dexmedetomidine reduced propofol requirements in posterior fossa neurosurgeries, with comparable recovery profile to the group without dexmedetomidine. Therefore, this finding that the recovery is not getting affected, even in procedures involving the posterior fossa where the target area of action of dexmedetomidine, the locus ceruleus, is situated, reflects on the favorable safety profile of the drug in neurosurgical anesthesia practice. Ilhan et al studied the effects of dexmedetomidine as an adjuvant to isoflurane in one group and compared it with a group that received a combination of fentanyl and isoflurane in patients undergoing supratentorial surgeries. 16 They found that the dexmedetomidine group had shorter recovery time compared with the fentanyl group. They had administered additional boluses of fentanyl in the dexmedetomidine group for painful stimulus, which was not quantified, and the anesthesia was not titrated with the help of BIS or any other depth of anesthesia monitors. In neuroanesthesia practice, dexmedetomidine cannot totally replace fentanyl as an adjuvant as it has an inferior analgesic profile and neurosurgical population encounter higher pain stimulus. Dexmedetomidine plays a vital role as an adjuvant by reducing the perioperative opioid requirement. 14 15 20 To overcome the aforementioned issue, both the groups in our study received fentanyl-based anesthesia, and we evaluated the effects of dexmedetomidine as an adjuvant to one of the two groups while the anesthesia was titrated to a BIS of 45 to 50.

In our study, the dexmedetomidine group had a better hemodynamic profile. This concurred with the findings of the previous studies, which showed that intraoperative dexmedetomidine offers excellent hemodynamic stability at all phases of neurosurgeries. 3 20 We observed that the MAP was significantly lower in the dexmedetomidine group immediately after the application of the Mayfield clamp, indicating effective suppression of the sympathetic surge associated with the painful stimulus. Our study did not show any significant reduction of HR requiring intervention in the dexmedetomidine group. Tan and Ho had found that the incidence of bradycardia that requires intervention is higher with the administration of a loading dose and higher infusion rate. 21 In our study, we had omitted the loading dose of dexmedetomidine and used a low dose for maintenance, which could have resulted in stable hemodynamics while preserving dexmedetomidine’s desirable properties. Use of intraoperative BIS might have further optimized the anesthetic management, thus reducing the incidence of adverse hemodynamic events in the study group.

Optimal analgesia is of paramount importance in the neurosurgical population as poorly controlled pain results in raised ICP and unstable hemodynamics, both of which could affect the patient’s recovery and outcome. 22 Adequate analgesia also reduces the incidence of postoperative nausea, vomiting, and respiratory complications. The pharmacological armamentarium for perioperative analgesia includes nonsteroidal anti-inflammatory drugs (NSAIDs), opioids, and paracetamol. 23 NSAIDs are not recommended in neurosurgical procedures due to their potential to cause platelet dysfunction and due to an increased risk of causing bleeding inside a closed space. 24 Though opioids are routinely used agents in neurosurgeries, higher doses can depress the sensorium, resulting in delayed neurologic assessment along with respiratory depression and PONV. Respiratory depression could also lead to CO 2 retention, which, in turn, leads to a rise in ICP, thereby worsening the postoperative recovery. Dexmedetomidine as an adjuvant offers a good analgesic profile, reduces the requirement of opioids, and does not affect the respiratory drive. 1 20 25

The incidence of nausea and vomiting in neurosurgical patients has been reported as 55 to 70%. 26 27 28 It increases the ICP as well as the risk of hematoma formation. Also, the neurosurgical patients are at a high risk of aspiration due to their altered sensorium and weakened protective airway reflexes. 29 In our study also, the dexmedetomidine group had a lower incidence of nausea and vomiting, which was not statistically significant. The meta-analysis by Peng et al revealed that the administration of dexmedetomidine intraoperatively reduced the antiemetic requirements in the postoperative period, possibly by reducing hemodynamic fluctuations and due to the opioid-sparing action. 20 Gopalakrishna et al used the highest recommended maintenance dose of 0.7 μg/kg/h in patients undergoing pituitary surgeries and had got a more explicit benefit in reducing PONV (22.7% in the dexmedetomidine group vs 40.9% in the control group). 2 The lower maintenance dosage of dexmedetomidine in our study could have reduced its antiemetic potential in our study. 2

Limitation

Use of an analgesia nociception index monitor might have further quantified the analgesic potential of dexmedetomidine along with fentanyl.

Conclusion

Our study demonstrated that low-dose dexmedetomidine as an adjuvant to sevoflurane- and fentanyl-based anesthesia can provide stable hemodynamics and lesser anesthetic and opioid consumption, without adversely affecting the recovery profile in patients undergoing supratentorial neurosurgical procedures. Avoiding the loading dose and low-dose maintenance is the key to prevent the adverse effects of dexmedetomidine when used as an adjuvant to sevoflurane anesthesia.