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Effect of Different Concentrations of Esmolol on Perioperative Hemodynamics and Analgesia in Patients Undergoing Colectomy: A Prospective, Randomized Controlled Study

Authors Song F , Jin Y, Li P, Zheng C , Zhao X 

Received 1 September 2021

Accepted for publication 29 November 2021

Published 14 December 2021 Volume 2021:15 Pages 5025—5033

DOI https://doi.org/10.2147/DDDT.S337201

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 2

Editor who approved publication: Dr Tin Wui Wong



Fuxi Song,1 Yanwu Jin,1 Peng Li,1 Chao Zheng,2 Xin Zhao1

1Department of Anesthesiology, The Second Hospital, Cheeloo College of Medicine, Shandong University, Jinan, Shandong, People’s Republic of China; 2Department of Breast Surgery, The Second Hospital, School of Medicine, Cheeloo College of Medicine, Shandong University, Jinan, Shandong, People’s Republic of China

Correspondence: Xin Zhao
Department of Anesthesiology, The Second Hospital, Cheeloo College of Medicine, Shandong University, No. 247 Beiyuan Street, Jinan, Shandong, 250033, People’s Republic of China
Fax +86-531-88962544
Email [email protected]

Purpose: The aim of this study was to investigate the efficacy of esmolol on intraoperative hemodynamic and perioperative analgesic management.
Methods: Totally, 125 patients undergoing colectomy were randomly divided into three groups. Group S (saline group) was administered 0.75 mL/kg/h of normal saline for 5 min before anesthesia induction and maintenance of 0.25 mL/kg/h; Group E1 and Group E2 were administered 0.5 mg/kg and 1.0 mg/kg esmolol for 5 min before anesthesia induction, and maintained of 0.5 mg/kg/h and 2.0 mg/kg/h, respectively. Several parameters including indexes of hemodynamics variation (primary outcome), intra- and postoperative analgesic usage, and pain score were measured.
Results: Group E1 and Group E2 had significantly lower intubation response than Group S (P = 0.007, P = 0.001), and extubation response of Group E2 was significantly lower than Group S (P = 0.007). The opioid consumption in Group E1 and Group E2 was significantly lower than in Group S intraoperatively (P = 0.020 and 0.007). The incidence of postoperative adverse reactions among the three groups was not statistically significant (P = 0.368 and 0.772).
Conclusion: Esmolol 0.5 mg/kg and 1.0 mg/kg infusion before intubation both can effectively inhibit the intubation response, while only maintenance with 2.0 mg/kg/h of esmolol can reduce the incidence of extubation response. At the same time, esmolol can decrease intraoperative opioid requirement without increasing the risk of adverse reactions.
Trial Registration: ChiCTR1900024538 and the date of registration was July 15, 2019 at http://www.chictr.org.cn.

Keywords: esmolol, hemodynamics, analgesia, intubation response, extubation response

Introduction

Surgical stress is a kind of non-specific defense reaction, which is mainly characterized by sympathetic excitation and enhancement of the hypothalamic–pituitary–adrenal axis (HPA or HTPA axis).1 For patients undergoing colectomy, a variety of reasons, especially tracheal intubation and extubation, can cause strong stress response, which leads to obvious hemodynamic instability and cardiovascular or cerebrovascular accidents, and brings great challenges for perioperative anesthesia and analgesia.2

Opioids are the mainstay of treatment for perioperative pain, but their administration increases the incidence of respiratory complications, slows down normal gastrointestinal motility, and prolongs hospital stay.3,4 With the development of enhanced recovery after surgery (ERAS), reducing the use of opioids in perioperative period has become the common goal of anesthesiologists. The dosage of opioids should be strictly controlled whenever possible, which should not only meet the needs of analgesia perioperatively, but also minimize the incidence of adverse reactions.5 Due to various factors that cause the stress reaction in colectomy, such as intestinal traction, stimulation of nerves and baroreceptors caused by surgical or anaesthetic operation, it is unscientific to use opioids only inhibiting it. To seek corresponding auxiliary therapy inhibiting the stress response is crucial.

Esmolol is an ultra-short acting, cardio-selective β1-adrenergic receptor blocker with the characteristics of quick onset, short half-value period, strong controllability, and rarely side effects,6 which is effective in blunting adrenergic responses to perioperative stimuli including the tracheal intubation, intraoperative events, and tracheal extubation. Previous clinical studies have demonstrated that perioperative infusion of esmolol reduced opioid consumption and stress response.7–9 However, in previous studies, the dosage of esmolol was used in a wide range.10 The meta-analysis results of Figueredo et al,11 which reported that the most effective method to inhibit adrenergic response to intubation was to use esmolol with loading dose of 500 ug/kg/min, followed by continuous infusion of 200–300 ug/kg/min. In the study of Ratnani et al, administration of 1.5 mg/kg esmolol 2 minutes before extubation could effectively inhibit hypertension and tachycardia.12 However, we have not found relevant reference supporting the influence of continuous intraoperative infusion of esmolol on extubation. Considering that our patients are relatively older, and many patients’ basal heart rate is maintained between 60 and 70 bpm, the application safety range of esmolol is narrower than that of normal people. Esmolol is an ultra-short-acting β -blocker with a short duration of action for a single dose. Continuous administration can prolong the drug action of esmolol, at the same time, decrease the risk of bradycardia caused by a rapid single injection, which is often very dangerous for the elderly. Therefore, after fully consideration of the tolerance of patients and clinical experience of our anesthesiologists, we selected two relatively low doses to compare the effect of intraoperative esmolol administration on hemodynamics and perioperative analgesia for patients undergoing colectomy.

Methods

Trial Design

This study is a single center, prospective, randomized, controlled clinical trial conducted at The Second Hospital, Cheeloo College of Medicine, Shandong University, Jinan, Shandong, China, approved by the Ethics Committee of the Second Hospital of Shandong University with the approval number KYLL-2019(LW)009 on June 10, 2019. The study was prospectively registered at http://www.chictr.org.cn on July 15, 2019, identifier ChiCTR1900024538.

Participants

One hundred and fifty-two consecutive patients with the age of 20–70 years old, American Society of Anesthesiologists (ASA) physical status I–III, undergoing selective colectomy for colon cancer were identified from July 20, 2019 to August 31, 2020. One hundred and thirty-eight were enrolled and randomly allocated into three groups using computer-generated randomization numbers contained in sealed opaque envelopes and 14 were excluded because of exclusion criteria; What is more, 4 patients were excluded due to occurring severe hemodynamic fluctuation; 9 patients were lost to follow-up; 125 patients were included in the final statistical analysis. Exclusion criteria were: patient refusal, pregnant, history of bradycardia or atrioventricular block; history of hypotension; history of bronchial asthma or severe chronic obstructive pulmonary disease (COPD); history of relevant allergy to related perioperative medications, patients with severe organ damage such as heart, hepatic and renal failure; body mass index (BMI) less than 18 or more than 30 Kg/m2; patients who cannot cooperate with the trial. All the enrolled patients provided a written informed consent.

Anesthesia and Analgesia

Grouping

All patients enrolled were divided into three groups according to the random number generated by computer. Before induction, Group S (saline group) were administered 0.75 mL/kg/h of normal saline for 5 min and maintenance of 0.25 mL/kg/h; Group E1 and Group E2 were administered 0.5 mg/kg and 1.0 mg/kg for 5 min, and maintenance of 0.5 mg/kg/h and 2.0 mg/kg/h, respectively. Esmolol (2 mL: 0.2 g*2, Qilu Pharmaceutical Company, China) used in this trial was diluted with normal saline to 50 mL (8 mg/mL). Saline and esmolol infusion stopped immediately upon extubation.

Anesthesia Method

After ASA standard monitors were applied, induction of general anesthesia was standardized in the three groups using propofol (1.5 ~ 2.0 mg/kg) and sufentanil (0.3 ~ 0.5 µg/kg). Endotracheal intubation was facilitated with cis-atracurium (0.2 mg/kg). After induction, the radial arterial line and the catheterization of right internal jugular vein were given and ultrasound-guided quadratus lumborum block (US-QLB) was performed using 60mL of 0.3% ropivacaine (30 mL into each side). Sufentanil 0.1 ug/kg (could be reused 1 time if there was no adequate improvement in 10 minutes) would be given when the patient’s MAP or HR exceeds 20% or more of their baseline value during surgical procedures such as skin dissection and intestinal traction. During the operation, vasoactive drugs (phenylephrine, ephedrine, nitroglycerin, urapidil, atropine, or isoprenaline) were administered to maintain blood pressure and heart rate within 20% fluctuation after enough opioids. If the MAP was higher than 120 mmHg or lower than 60 mmHg, the HR was higher than 100 bpm or lower than 50 bpm, the vasoactive drugs were also necessary for correcting the fluctuation. Intractable hypotension or bradycardia was recorded when hypotension or bradycardia recurred within 5 minutes of returning to normal range with vasoactive agents and continuous vasoactive agents were required to maintain normal MAP or HR. When intractable hypotension or bradycardia occurred, the test drug was stopped and vasoactive drugs or other necessary measures such as blood transfusion and rapid fluid infusion were used for improving the situation.

Maintenance of anesthesia was achieved with sevoflurane (2~4% in 100% oxygen), and its concentration was adjusted based on BIS which was kept between 40 and 60. Cis-atracurium (0.1 mg/kg/h) was administered during maintenance at the discretion of the anesthesiologist. Decrease the anesthesia depth and use remifentanil 3–5 ug/kg/h (regulated according to MAP and HR) when a drainage tube was placed. All the patients were admitted to postanesthesia care unit (PACU) for at least half an hour after extubation until vitals are stable before being discharged to regular floor.

Postoperative Analgesia

All patients were provided with a patient-controlled analgesia (PCA) pump that delivered a mixture of sufentanil 1µg/kg, dexmedetomidine 1 µg/kg, and palonosetron 0.25 mg to 150 mL at the basal rate 3 mL/hour, a 2 mL per demand dose with a lock-out time of 20 minutes. The PCA pump was started immediately after the operation upon arrival in the PACU. When the patient’s numerical rating scale (NRS) ≥4, a demand dose of the PCA pump was given to relieve the pain. And intravenous flurbiprofen axetil 50 mg iv. and intramuscular pethidine 50 mg im. were the first- and second-line treatments for breakthrough pain, respectively, for numerical rating scale (NRS) ≥4 or at the patient’s request. Breakthrough nausea and vomiting were managed with intravenous palonosetron at 0.25 mg as needed.

Measurement Index

The mean arterial pressure (MAP) and heart rate (HR) were recorded at entering the room (T1), after loading dosage (T2), after anesthesia induction (T3), 1 min after intubation (T4), 5 min after skin cutting (T5), 1h after skin cutting (T6), 2h after skin cutting (T7) and 5min after extubation (T8), respectively. Intubation response was considered to have occurred when MAP or HR at 5 minutes after intubation exceeds 15% or more than that at 5 minutes after induction of anesthesia (before intubation). At the same time, when the MAP or HR at 5 minutes after extubation was 15% or higher than that at 5 minutes before spontaneous breathing occurred before extubation, it was considered as extubation response. The incidences of intubation and extubation response were recorded separately. The NRS (0 for painless and 10 for maximum pain) was recorded 5 minutes, 30 minutes, 1h, 4h, 24h, and 48h after operation.

The primary outcomes were the incidences of intubation and extubation response. The second outcomes were perioperative opioid consumption and pain scores, intraoperative hemodynamic, number of postoperative rescue analgesic usage, frequency of adverse events such as nausea, vomiting, refractory hypotension and bradycardia.

Sample Size Calculation and Randomization

The sample size was calculated based on a 30% expected difference in intubation and extubation responses based on previous study12 and our pre-trial. For a study power of 80% (α = 0.05, β = 0.2), the total sample size was 114 with 38 patients in each group (PASS 15.0; NCSS Statistical Software, Kaysville, Utah). Assuming a presumably dropout rate of 20% (including loss to follow-up and cessation of the test due to severe hemodynamic instability), the final sample size was determined as total 138 (with 46 patients in each group). We applied the Visual Binning function of Statistical Program for Social Sciences (SPSS) to randomly divide 138 patients into three groups (33.33% for each group). The grouped results were wrapped in opaque envelopes. The anesthesiologists responsible for data collection did not know the grouped results until the day of surgery.

Statistical Analysis

Statistical Program for Social Sciences (SPSS) was used for statistical analysis of the collected data. For scale (quantitative data), such as age, BMI, opioid dosage, MAP, HR, we statistically described them in the form of mean ± standard deviation, and used Kolmogorov–Smirnov to test their normal distribution and applied analysis of variance (ANOVA) to test them. If the significance (P value) <0.05, then the data were analyzed by the least significant difference (LSD) test. For nominal (qualitative data), such as gender, intubation response, extubation response, we used frequency (percentage) to describe them statistically and applied the Chi-square test to verify its significance. If P value <0.05, then proceeded Chi-square test between each two groups. For ordinal (grade data), such as NRS, we used median (range) for statistical description. Kruskal–Wallis test was used to compare the overall differences, and the Wilcoxon test was applied to further analysis if P value <0.05. All test results determined that P value <0.05 was statistically significant.

Results

There were totally 125 patients completed the test (Figure 1).

Figure 1 Flow chart of inclusion, exclusion, and randomization of all patients.

Basic Information and Intraoperative General Conditions

In the statistical analysis of the patients’ basic information and general conditions during operation, it was found that there were no statistical differences (P > 0.05; Table 1).

Table 1 Basic Information and Intraoperative General Conditions

Perioperative Hemodynamics

In the statistical analysis of the MAP and HR, there was a significant difference in MAPT4, HRT2, HRT5, HRT6, and HRT8 among the three groups (P < 0.05, Figure 2), while there was no statistical difference between Group E1 and Group E2 (P > 0.05, Figure 2). The MAPT8 of Group E2 were significantly lower than the other two groups (P < 0.05, Figure 2). The number of intubation responses in Group S was higher than that in the other two groups (P < 0.05, Table 2). While the incidence of extubation response in Group E2 was significantly less than Group S and Group E1 (P < 0.05, Table 2). In the use of vasoactive drugs, only nitroglycerin in Group S was significantly more than that in Group E1 and Group E2 (P < 0.05, Table 2).

Table 2 Hemodynamic Fluctuation and Vasoactive Drugs

Figure 2 Changes in MAP (A) and HR (B) among the three groups; scale variables presented as mean±standard deviation; *P < 0.05 between Group S and Group E1; #P < 0.05 between Group S and Group E2.

Abbreviations: MAP, mean arterial pressure; HR, heart rate.

Analgesia and Adverse Reactions

In the use of analgesic drugs, the amount of intraoperative opioids in Group E1 and Group E2 was significantly less than that in Group S (P < 0.05, Table 3), while there was no significant difference between the two groups (P > 0.05, Table 3). Also, no statistical difference was showed in the amount of opioids and NRS within 48 hours after surgery among the three groups (P > 0.05, Table 3, Figure 3). The comparison of the incidence of adverse reactions among the three groups found no statistical difference (P > 0.05, Table 3).

Table 3 Opioids Dosage and Side Effects

Figure 3 NRS changes among three groups; ordinal variables described as median (range). No statistical significance is found (P > 0.05).

Abbreviation: NRS, numerical rating scale.

Discussion

From the results of this randomized controlled trial, it can be seen that the continuous administration of esmolol in the perioperative period has a positive impact on the stability of hemodynamics. Before anesthesia induction, esmolol 0.5 mg/kg (Group E1) and 1.0 mg/kg (Group E2) infusion can significantly reduce the incidence of intubation response without increasing the risk of hypotension. The dose of esmolol used in this study is lower than that of previous studies.13,14 Through the comparison of several studies, we believe that a low dose of esmolol could already significantly improve the increase in blood pressure caused by intubation. The main reason is that enough analgesics are given in anesthesia induction, and propofol itself has an antihypertensive effect, so combining with a small amount of esmolol can inhibit intubation response. In previous studies, most of them are about the influence of single-dose of esmolol on extubation response,15,16 while articles of the effect of continuous esmolol administration during the operation on extubation are little. Our trial indicates that continuous infusion of esmolol 2.0mg/kg/h can inhibit the extubation response, while esmolol administration of 0.5 mg/kg/h can only stabilize the HR after extubation without affecting MAP, so it cannot reduce the occurrence of extubation response. What is more, infusion of esmolol 2.0 mg/kg/h cannot completely inhibit extubation response. It is probably a consequence of the weakening or disappearance of anesthetic effect, together with the pain of surgical wound and the stimulation of extubation on trachea. Therefore, it is difficult to inhibit the extubation response completely caused by various reasons by using esmolol simply.

In our study, we find that continuous administration of esmolol during the operation can inhibit the remarkable increase of blood pressure during intubation, skin incision, extubation (only with continuous infusion of esmolol 2.0 mg/kg/h) and can promote the heart rate to maintain a lower level in the relatively stable stage of operation. On the one hand, it can cut down the increase of cardiac afterload and work caused by increased blood pressure. On the other hand, lower heart rate can reduce myocardial oxygen consumption, thus reducing the occurrence of cardiovascular accidents. A meta-analysis showed that esmolol seems to be beneficial for the prevention of perioperative myocardial ischaemia.17 Another study proved that esmolol 0.5 mg/kg combined with nicardipine 20 ug/kg during rapid-sequence induction can effectively reduce cardiovascular response.18 Esmolol can also be used for controlled hypotension in various operations such as functional endoscopic sinus surgery (FESS), tympanoplasty and laparoscopic surgeries.19–21 These studies have shown that esmolol has a positive effect on the maintenance of intraoperative hemodynamic stability.

In addition, we find that esmolol can reduce intraoperative opioids dosage, which is consistent with the previous results of Hamed et al.22 What is more, it has also been proved that intraoperative infusion of esmolol can reduce postoperative opioid dosage in Gelineau study.23 Esmolol itself has no analgesic effect, but some studies consider that its auxiliary analgesic effect is achieved through extending the effect of opioids.24 In this study, different doses of esmolol do not affect the dosage of postoperative analgesic drugs. It may be that all patients in this trial took QLB before surgery, which is a new trunk block method based on the transverse abdominis plane block (TAPB). Blanco et al showed that QLB was closer to the axon and sympathetic trunk, which had more obvious advantages in the duration of trunk analgesia and the weakening of visceral pain than TAPB.25 The doses of postoperative opioids in the three group are all obviously reduced. As a result, it is difficult to find their statistical significance. What is more, we do not use esmolol continuously after extubation so that we cannot find the persistent influence of esmolol on postoperative analgesia.

In the analysis of postoperative adverse reactions, it is found that esmolol does not increase the incidence of postoperative nausea and vomiting (PONV), persistent hypotension and bradycardia, which benefited from the ultra-short effect of esmolol.26 Some other studies have shown that esmolol can reduce PONV,27 which is mostly achieved by reducing the amount of postoperative opioids.

This trial has the following limitations in the design process. Firstly, the quadratus lumborum block was performed after anesthesia induction. Although the anesthesiologist used the same approach, we did not judge the range and effect of QLB which might influence the study results. Secondly, this study did not collect the time of first flatus and defecation, so that there was no theoretical basis for the effect of esmolol on the recovery of postoperative gastrointestinal function. Thirdly, we only selected one time point after intubation and extubation for MAP and HR statistics, which may obscure reliable estimates of the true incidence of intubation and extubation reactions. Finally, this study only compared the MAP and HR at the same time point, but did not compare the hemodynamic fluctuation of patients in a short time, and MAP and HR monitoring every 5 minutes may be a better approach.

Conclusions

Esmolol 0.5 mg/kg or 1.0 mg/kg short-term infusion can effectively inhibit the intubation response, while only continuous infusion of esmolol 2.0 mg/kg/h intraoperatively was safe and effectively to reduce the occurrence of extubation response. Both 0.5 mg/kg/h and 2.0 mg/kg/h continuous infusion of esmolol can reduce the dosage of intraoperative opioids without increasing the risk of adverse reactions.

Abbreviations

ANOVA, analysis of variance; ASA, American Society of Anesthesiologists; BMI, body mass index; COPD, chronic obstructive pulmonary disease; ERAS, enhanced recovery after surgery; FESS, functional endoscopic sinus surgery; HPA(HTPA), hypothalamic–pituitary–adrenal; HR, heart rate; LSD, least significant difference; MAP, mean arterial pressure; NCSS, number crunching statistical system; NRS, numerical rating scale; PACU, postanesthesia care unit; PASS, power analysis and sample size; PCA, patient-controlled analgesia; PONV, post-operative nausea and vomiting; QLB, quadratus lumborum block; SPSS, statistical program for social sciences; TAPB, abdominis plane block; US-QLB, ultrasound-guided quadratus lumborum block.

Data Sharing Statement

All data generated or analyzed during this study were included in this published article. Further inquiries can be directed to Professor Xin Zhao on reasonable request.

Ethics Approval and Consent to Participate

This study was approved by the Ethics Committee of the Second Hospital of Shandong University with the approval number KYLL-2019(LW)009 on June 10, 2019, and in accordance with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. The study was prospectively registered at http://www.chictr.org.cn on July 15, 2019, identifier ChiCTR1900024538. Informed consent was obtained from all of the participants.

Consent for Publication

All authors have read the manuscript, attest to the validity and legitimacy of the data and its interpretation, and agree to its publication.

Acknowledgments

The authors gratefully thank Santosh Kumar Paidi from Johns Hopkins University, USA, for useful comments, suggestions and language editing for improving the manuscript. Chao Zheng acknowledges support from the Taishan Scholars Program of Shandong Province (tsqn201812135). We would like to thank all participants involved in the study for their cooperation.

Disclosure

The authors declare that they have no competing interests.

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