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Effects of esmolol on QTc interval changes during tracheal intubation: a systematic review
  1. Venkatesan Thiruvenkatarajan1,
  2. Jenn Yuan Lee2,
  3. Manesha Sembu3,
  4. Richard Watts1,
  5. Roelof Markus Van Wijk1
  1. 1 Anaesthesia, The Queen Elizabeth Hospital, Adelaide, South Australia, Australia
  2. 2 The University of Adelaide, Adelaide, South Australia, Australia
  3. 3 University of New South Wales, Sydney, New South Wales, Australia
  1. Correspondence to Dr Venkatesan Thiruvenkatarajan; Venkatesan.Thiruvenkatarajan{at}sa.gov.au

Abstract

Introduction and aims Esmolol is an ultra-short-acting β1 antagonist that has been shown to attenuate the corrected QT (QTc) interval prolongation associated with laryngoscopy and endotracheal intubation (LTI). Prolongation of the QTc interval can precipitate arrhythmias, the most serious of which is torsades de pointes . The aim of this systematic review was to compare esmolol and placebo on QTc changes occurring during LTI.

Materials and methods PubMed, EMBASE, Cochrane Registry of Clinical Trials and CINAHL databases (up to August 2018) were screened for randomised controlled trials comparing esmolol and placebo on QTc changes during LTI in cardiac and non-cardiac surgeries. The primary outcome was QTc changes during LTI and secondary outcome was related to adverse effects from esmolol such as bradycardia and hypotension.

Results Seven trials were identified involving 320 patients, 160 patients receiving esmolol or placebo apiece. A shortening of the QTc post-LTI was evident in the esmolol group compared with the placebo in four studies. Compared with the baseline, the QTc was reduced post-LTI in the esmolol group. In the placebo group, the QTc was prolonged compared with the baseline post LTI. Nonetheless, esmolol did not prevent QTc prolongation in the remaining three studies, and much of this was attributed to employing QTc prolonging agents for premedication and anaesthetic induction. No significant adverse events were noted.

Conclusion Compared with placebo, esmolol reduced the LTI-induced QTc prolongation when current non-QTc prolonging agents were chosen for tracheal intubation. Future studies should explore whether transmural dispersion (a marker of torsadogenicity) is also affected during LTI by analysing parameters such as the Tp-e interval (interval between the peak to the end of the T-wave) and Tp-e/QTc (rate corrected Tp-e interval).

Trial registration number CRD42018090282.

  • general anaesthesia
  • laryngoscopy
  • tracheal intubation
  • esmolol
  • QTc interval
  • arrhythmia

This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.

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Strengths and limitations of this study

  • This is the first systematic review to explore the effect of an adjuvant medication in mitigating the corrected QT response secondary to laryngoscopy and tracheal intubation.

  • The Preferred Reporting Items for Systematic Reviews and Meta-analyses guidelines were strictly adhered to in conducting this review.

  • Studies were included irrespective of the language and trials were spread across a diverse subset; for example, American Society of Anaesthesiologists I-II to cardiac surgeries.

  • Medication regimen chosen by the older studies are no longer applicable in contemporary practice, thus contributed to heterogeneity.

Introduction

Prolongation of the corrected QT (QTc) interval of the electrocardiogram (QT interval corrected for heart rate) can occur throughout anaesthetic induction and tracheal intubation, maintenance and emergence during a general anaesthetic.1 Airway manoeuvres such as laryngoscopy and tracheal intubation (LTI) are associated with an intense sympathetical surge and have been identified as critical periods of QTc interval disturbances precipitating arrhythmias.1 2 Torsades de pointes (TdP) has been described during LTI.3 The use of a supraglottic airway device has been shown to produce less QTc perturbations compared with LTI.4 While this may not be a significant concern in otherwise healthy patients, it can lead to significant morbidity in specific high-risk patient population. This group includes those with coronary artery disease,5–7 hypertension,8 9 and patients undergoing coronary artery bypass grafting (CABG) procedures.10 Hypertension could exacerbate the sympathetical response during LTI predisposing to QTc changes apart from haemodynamic response.8 QTc interval prolongation has been identified as a risk factor for cardiovascular events in hypertensive as well as diabetic patients.11 12 Perioperative QTc prolongation predisposes to complications such as polymorphic ventricular tachycardia, myocardial ischaemia and sudden cardiac death.1 2 Nonetheless, this phenomenon is probably less appreciated in clinical practice.

Various agents have been used during induction of general anaesthesia to attenuate LTI-induced QTc prolongation such as beta blockers,7–9 intravenous lignocaine13 and opioids (fentanyl and remifentanil).14–16 Esmolol, a selective β1 antagonist, is among one of the most studied drugs, due to its ability to dampen the sympathetic tone, which is one of the underlying mechanisms of QTc prolongation.

The primary objective of this systematic review was to evaluate the effect of esmolol compared with control, in mitigating the LTI-induced QTc interval prolongation in adult patients aged 18 years and above who were undergoing elective surgery.

The secondary objective was to define any adverse effects associated with esmolol administration during anaesthetic induction and LTI.

Methods

The review was conducted in compliance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines and the protocol was registered on PROSPERO.

Search strategy

The relevant studies were identified through PubMed, EMBASE and Cochrane Central Registry of Clinical Trials and CINAHL databases, and were subsequently recruited by applying our inclusion criteria. The initial literature search strategy on PubMed included appropriate use of medical subject headings (MeSH) terms, adequate descriptors and Boolean operators and was performed as follows: ([esmolol] and [anaesthesia or general anaesthesia or induction of anaesthesia] and [QT interval or QTc interval]). Details of the search strategy is given in online supplementary appendix 1. Complementary search strategies were used for other databases according to their particulars. A manual search was performed on the articles that were cross-referenced in the selected studies. No language restriction was applied.

Supplemental material

Study selection

Two authors (VT and JYL) independently assessed abstracts and titles of all the studies that were a potential inclusion based on the search strategy. The non-English abstracts were translated with google translate, and if found eligible or ambiguous, full translation of the manuscript was undertaken. The full texts of all eligible studies were independently screened by two investigators (VT and JYL), any discrepancies were resolved by discussion and consensus. The PRISMA flow chart for selection of studies is shown in figure 1.

Figure 1

The Preferred Reporting Items for Systematic Reviews and Meta Analyses flowchart reflecting the literature search process.

Eligibility criteria

Studies were included based on the following criteria: (1) randomised trials in adult patients comparing fixed or various doses of esmolol with an active placebo control during induction of anaesthesia and (2) reporting various parameters of the QT interval such as QTc, QTd ([QT dispersion], difference between maximum and minimum QT), QTcd (QTd corrected for heart rate), Tp-e interval (interval between the peak to the end of the T-wave) and Tp-e/QTc (rate corrected Tp-e interval). It was considered essential that the studies reported baseline values of the QTc parameters prior to esmolol administration as well as at least two values reported within 5 min of endotracheal intubation. Non-controlled studies and studies where airway management was carried out without a single lumen endotracheal tube (eg, supraglottic airway) were excluded.

Data extraction and definition of outcome parameters

A data extraction sheet (template attached as online supplementary appendix 2) was created that contained information on the following: author, year and journal, American Society of Anaesthesiologists (ASA) physical status, type of surgery, cohort type in terms of co-morbidities, nature of premedication, induction agents, dose and timing of esmolol, QT parameters assessed, formula used for QTc correction, timing of assessment of QT interval post intubation, type of control (placebo or no treatment), any adverse events recorded such as severe bradycardia or other arrhythmias or allergic reactions. Also, conflicts of interest and source of funding were also extracted. Two authors (VT and DL) independently extracted the data from the included trials and discrepancies were resolved by discussion and consensus. Data were originally extracted from text or tables and from figures or graphs if not available in tables.

Supplemental material

Our primary outcome included all the QT parameters captured at any time frame during the first 5 min after LTI. The difference in outcome between the esmolol and the control group within the 5 min post-LTI were assessed. Secondary outcomes were significant adverse events such as bradycardia, hypotension and arrhythmias.

Risk of bias assessment

The risk of bias was assessed using the Cochrane Collaboration’s risk of bias tool and the risk of bias was summarised. Three authors independently assessed the risk of bias for each study, and disagreements resolved by consensus.

Patient and public involvement

There were involvement of any patients or the public in the study.

Results

The search and recruitment of papers were performed up to August 2018. The search strategy generated a total of 297 citations. The full texts of 25 articles were screened for further relevance after excluding 272 articles based on consideration of the title and abstract and duplicates. We included seven randomised controlled trials (RCTs) with a total of 409 participants. Of the included trials, six were in English and one in Chinese. Figure 1 depicts the flow diagram of the studies, screened, identified and retained as per the PRISMA guidelines.

The details of the included studies are shown in table 1. Of the seven studies included, four compared esmolol versus placebo,7–10 17 whereas in three studies esmolol was compared with placebo as well as with an alternative therapeutic agent.18–20 We analysed data from 409 patients of whom 160 each had either received esmolol or placebo (320 in total). The remaining 89 had received alternative therapeutic agents mostly opiates or lignocaine. The average trial size was 58 patients (range 40 to 80).

Table 1

Summary of findings for the outcome measures and the quality of evidence

Only one study reported the data on variance of the QT parameter. Further, the studies varied in terms of the population that was assessed, adjuvant drugs used during the intubation process, mode of administration (some studies used just a bolus while others used bolus followed by an infusion), timings of assessing the QT parameters and the formulas used in analysing. As a result of these clinical and methodological heterogeneity, a qualitative narrative synthesis of the findings are presented.

Study population

Four studies had patients with an ASA status I-II undergoing various elective surgeries,17–20 two had patients with documented coronary artery disease7 and hypertension9 respectively and one study was conducted in patients undergoing CABG.10

Premedication regime/induction agents/anaesthetic agents

Premedication administration was described in five studies. While midazolam was used in two studies (one intramuscular and other unspecified route),10 18 intramuscular oxycodone and atropine was used in three studies.17 19 20 Thiopentone sodium and suxamethonium were used as induction agents in three studies,17 19 20 propofol and vecuronium in three studies,7 9 18 etomidate and vecuronium in one study.10 Opiates were used during induction in three studies,7 9 10 whereas four studies did not use opioids at induction.17–20

Administration of study drug

Several esmolol regimens were tested including intravenous bolus, infusion or combination of both. Five studies7 9 10 17 18 used a bolus (ranging from 300 mcg/kg to 1000 mcg/kg) followed by infusion (ranging from 100 mcg/kg/min to 250 mcg/kg/min). Of the two remaining studies, one study used a bolus alone at 2 mg/kg,20 and the remaining study used two different combination of boluses, 2 mg/kg and 3 mg/kg.19 Esmolol was commenced from 1 min up to 5 min prior to administration of induction agents. Most of the infusions were ceased 4 min post LTI.

QT interval assessment

The QTc analysis was carried out at multiple time frames post intubation from 30 s until 10 min. All the studies assessed corrected QTc, and one study assessed QTcd as well.9 Bazzett’s formula was used for rate correction in five studies, whereas the remaining studies used Hodges’10 and Fredericia’s7 formulas, respectively. A QTc of 440 ms was considered normal regardless of the gender of the patients.

Outcomes

The mean baseline QTc was 424 ms in the esmolol group and 420 ms in the control group. Four studies7 9 10 18 (recruiting patients with known coronary artery disease, known hypertensives, undergoing CABG and ASA status I-II) have shown consistent results in terms of esmolol’s effect on the QTc interval. Prolongation of QTc was observed in the control group post LTI. The groups treated with esmolol had a reduced QTc interval compared with the controls. Further, compared with the baseline values, elevation of the QTc interval was not observed at any time post LTI in the esmolol group. Nonetheless, compared with the baseline values, QTc was prolonged post LTI in the control group. A similar pattern post LTI was noted for QTcd as well in patients treated with esmolol compared with controls.9 The mean QTcd was 19 ms in the esmolol group and 24 ms in the control group, and the maximun QTcd noted in the control group after intubation was 35 ms.

Esmolol did not prevent the LTI QTc prolongation in three studies that used thiopentone and suxamethonium (without opioids) for intubation following intramuscular atropine premedication.17 19 20 The maximum QTc observed was 450 ms in the trials that avoided thiopentone and suxamethonium, whereas it was 490 ms in trials that employed those agents. The summary of findings is presented in table 2.

Table 2

Summary of findings for the outcome measures and the quality of evidence (GRADE, Grading of Recommendations, Assessment, Development and Evaluation)

Risk of bias

The potential sources of bias have been outlined in figure 2 and an overall estimate of the risk of bias has been created for each study. Five of the seven studies were of sufficiently good quality with a low risk of bias.

Figure 2

Risk of bias assessment of included studies.

Adverse effects

Adverse events were reported in two trials, one involving hypertensive patients and the other analysing patients undergoing CABG.9 10 Of the combined 120 patients in these studies (60 esmolol and 60 control), eleven patients in the control group developed less severe ventricular arrhythmias as compared with two in the esmolol group. The difference was reported as significant in one study. No other haemodynamic adverse events were reported in any of the trials.

Source of funding for the included studies

Five studies did not report any conflict of interest or source of funding. Two studies by the same sources (done in 1995) reported support from Paivikki and Sakari Sohlberg foundation.19 20 This foundation supports the well-being of children and seniors in Finland.

Discussion

The main findings from this review are that compared with placebo, esmolol administration during anaesthetic induction attenuated the QTc prolongation post LTI. This was evident only in studies that used anaesthetic inducing agents that had no effect on the QTc interval.7 9 10 18 Meta-analyses was precluded by the lack of data on variability and the clinical and methodological heterogeneity of the included studies.

Our review had three trials done in the 1990’s by a single group17 19 20 and four studies done in the last decade since 2009.7 9 10 18 Interestingly, the three older studies had used agents that could prolong the QTc interval, such as atropine and suxamethonium (without opioids) prior to intubation. Unsurprisingly, esmolol did not reduce the LTI-induced QTc prolongation in those trials. However, the later studies that used non-QTc disturbing induction medications showed a consistent protective effect on LTI-induced QTc response. Esmolol was noted to blunt the QTc prolongation compared with the control group and no prolongation was noticed compared with the baseline in the esmolol group unlike the control group.

There are multiple theories as to how esmolol is able to achieve its effects on the QTc interval. Esmolol, being a β1-adrenergic antagonist is able to directly mitigate the heightened sympathetic tone caused by LTI. Coupled with an anti-ischaemic effect, the antisympathetical effect helps in reducing the QTc prolongation.10 Similar effects have been shown for other beta blockers such as landiolol.21

The favourable pharmacokinetic profile (direct alpha antagonism, ultra-short acting, rapid onset and offset) makes it an ideal agent in this regard. Also, it can be employed as an infusion post intubation in vulnerable patients or those who present with a baseline acquired QTc prolongation if their perioperative pathway is likely to be vulnerable to QTc triggering insults. Indeed, beta blockers are the first line therapeutical options for congenital long QT syndrome (LQTS).2 Although some sources have used opioids alone and shown a favourable QTc response post LTI,14–16 it is conceivable that esmolol may have more profound sympatholytical effect compared with opioids. Because it is a standard practice to use opioids at induction, a synergistical effect on the QTc interval could be anticipated with co-administration of esmolol. The aforementioned properties of esmolol makes it a unique agent during anaesthetic induction and LTI offering protection against both QTc and haemodynamic response. Yet, esmolol should be cautiously used during anaesthesia induction and tracheal intubation in view of its potent haemodynamic effects.

Perioperative QTc interval burden has been a subject of interest recently. Acquired LQTS is grossly underrecognised in the perioperative period, and it warrants caution when encountered.2 The perioperative management of LQTS is based on low level of evidence, and no consensus guidelines exist.2 Minor QTc interval prolongation (an average of 23 ms) up to 48 hours postoperatively was noted in 80% of patients in a cohort of 469 patients undergoing non-cardiac procedures. A QTc over 440 ms was noted in 51% of them, 4% had marked QTc prolongation (over 500 ms), and one patient developed TdP.22 A combined data on 1600 patients across three studies has shown that preexisting QTc prolongation is an independent risk factor for major postoperative cardiovascular events.23–25 For every 10 ms prolongation of the QTc interval above 436 ms, a 13% increase in adverse events were observed.23

In the non-operative environment, the risk of TdP increases either when the QTC interval exceeds 500 ms or with a 20 ms increase from baseline.26 27 In the perioperative setting, an increase of over 100 ms from baseline was noted as a risk factor for TdP in a recent systematic review analysing the reported cases of perioperative TdP.3 The same review found that during the TdP event, the mean QTc was 575 ms. It has been proven that prolongation of the QTc interval alone is not a marker for TdP development. Unless the transmural dispersion of the myocardium is also distorted, the risk of TdP is less.27 It is reflected by intervals other than QTc such as the Tp-e interval, Tp-e/QTc ratio. Although it is known that the transmural dispersion of repolarisation is affected by anaesthetic and other perioperative agents, it is unclear whether airway manipulations elicit similar effects. Nevertheless, vigilance is required in the susceptible whenever the perioperative milieu is likely to be exposed to QTc modifying factors.

Our review could not find major adverse events or serious haemodynamic compromise with esmolol administration during anaesthetic induction and tracheal intubation. The number of subjects in our review was probably low for this outcome. A large review assessing the safety of prolonged esmolol infusion following a bolus failed to show significant bradycardia as an adverse event.28 Likewise, another meta-analysis on the safety of esmolol demonstrated no significant hypotension or bradycardia in non-cardiac surgery.29 The authors concluded that the ultra-short acting nature of esmolol only causes reversible episode of hypotension and bradycardia, and the concerns of a negative inotropic effect are minimal. It is plausible that employing esmolol for shorter duration during LTI may not produce significant haemodynamic changes since it is likely to counter balance the sympathetical surge induced hypertension and tachycardia. Preparation of an esmolol infusion may insert a layer of complexity during anaesthetic induction, yet, the best clinical management should not be influenced by comfort, as echoed by a meta-analysis evaluating the effects of esmolol in attenuating the haemodynamic response during LTI.30 The meta-analysis on 38 trials including 2009 patients found that esmolol was very effective in attenuating the haemodynamic response to LTI.30 Ultra-short acting beta blockers have a wide range of application in the perioperative and critical care setting including cardiac surgery, acute myocardial infarction, critically ill septic patients, improving oxygenation in extracorporeal membrane oxygenation and perioperative cardioprotection for non-cardiac surgery.31

This review had few shortcomings. The inconsistency noted in the choice of inducing agents attributed to earlier trials is a limitation. Varying dose range was described, and a dose- seeking pilot study was attempted in only three of the trials. Adverse effects were poorly reported.

An extensive literature search without language restriction is a major strength of our review. Our review offers scope to design future trials. Hodges’ formula may be appropriate to evaluate the QTc parameters during LTI as it is less likely to be influenced by heart rate changes.7

Conclusion

The review on seven RCTs presents the evidence that esmolol can prevent LTI0induced QTc prolongation compared with placebo, in healthy patients as well as in those at risk. This effect was appreciated when non-QT prolonging anaesthetic medications were chosen to facilitate induction and LTI. No major adverse events were reported. A loading dose of 500 mcg/kg followed by an infusion of 100 to 200 mcg/kg/min continuing for at least 5 to 7 min post LTI seems logical. Esmolol is uniquely poised to attenuate both the QTc response as well as the haemodynamical response secondary to LTI. These findings may have clinical implications in patients at risk of developing QTc interval prolongation perioperatively. Future studies should explore whether transmural dispersion is also affected during LTI by analysing parameters such as Tp-e and Tp-e/QTc apart from identifying the safest dose regime.

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Footnotes

  • Contributors VT conceived the review, designed the protocol and wrote the manuscript. VT and JYL were involved in the literature search, data extraction and study quality assessment. MS assisted in data analysis, study quality and PRISMA checklist. RW conceived the idea, assisted in the discussion. RVW assisted with clinical suggestions, data analysis and discussion. All the authors reviewed and approved the final version.

  • Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.

  • Competing interests None declared.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Data sharing statement No additional data are available.

  • Patient consent for publication Not required.

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