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Use of low-dose β1-blocker for sinus tachycardia in patients with catecholamine support following cardiovascular surgery: a retrospective study
Journal of Cardiothoracic Surgeryvolume 14, Article number: 145 (2019)
Sinus tachycardia coupled with high-dose catecholamine is common after cardiopulmonary bypass (CPB). The present study assessed the hemodynamic efficacy and safety of combination therapy using low-dose β1-selective adrenergic blocker (landiolol) and inotropes.
This was a retrospective, single center, self-comparison study at post-anesthesia care unit within a tertiary care center. The study included adults who underwent cardiac surgery with CPB and received landiolol between April 2007 and November 2011. We assessed hemodynamic data prior to and 1 h after initiation of landiolol therapy.
We evaluated 11 patients who were administered 2.6 ± 1.3 μg/kg/min (mean ± SD) landiolol with sinus tachycardia and received catecholamine therapy after on-pump cardiovascular surgery. Landiolol administration led to a significant reduction in heart rate (HR; 112.4 ± 5.8 vs 126.0 ± 7.6 beats/min, p < 0.001), and a significant increase in stroke volume index (SVI) assessed by pulmonary artery catheterization (22.4 ± 5.4 vs. 18.9 ± 4.2 mL/m2, p = 0.04). Only one patient showed no HR reduction, whereas seven patients showed decreased HR and increased SVI (64, 95% confidence interval: 30–98%). Moreover, all five patients who received high-dose catecholamine support showed improved hemodynamics. In terms of safety, no patients required cessation of landiolol therapy.
Low-dose landiolol therapy may safely decrease HR and improve hemodynamics among patients with sinus tachycardia receiving catecholamine treatment after cardiovascular surgery.
This study is retrospective. Registration number: 11. Duration of registration: April 2007~November 2011.
Sinus tachycardia coupled with high-dose catecholamine is a common problem after cardiopulmonary bypass (CPB). Since tachycardia is associated with mortality and cardiac morbidity in the general population [1, 2] as well as in patients following surgery [3, 4], heart failure , and/or coronary artery disease , anesthesiologists should carefully manage heart rate (HR) throughout the perioperative period.
Catecholamine therapy after CPB aids cardiac performance by stabilizing hemodynamic conditions. However, high-dose catecholamine therapy frequently induces sinus tachycardia, and its treatment remains highly controversial. Continuation of tachycardia may compromise the myocardial oxygen balance, ultimately followed by global cardiac performance deterioration. However, reducing inotropic stimulation can induce a decrease in cardiac output, followed by deterioration of hemodynamic conditions. Therefore, an effective approach that avoids this vicious circle is necessary.
Landiolol is an injectable, ultra-short-acting, highly selective β1-adrenoreceptor blocker with a potency ratio (β1/β2) of 255 and an elimination half-life value of 4 min in healthy individuals, compared with esmolol, which has a potency ratio of 33 and elimination half-life of 9 min [7, 8]. Since landiolol is more likely to have high β1-selectivity and a short half-life compared with esmolol or other β1-blockers, a bolus shot of landiolol may be used to safely attenuate tachycardia in response to endotracheal intubation under general anesthesia [9, 10]. Recent studies have demonstrated the efficacy and safety of continuous intravenous landiolol infusion in different clinical settings to treat atrial fibrillation and/or atrial flutter after cardiac surgery [11,12,13] as well as acute heart failure . However, these reports excluded unstable hemodynamic cases requiring high-dose catecholamine support. There have been some reports of clinical observations of combination therapy with β-blocker and low-dose inotrope in decompensated heart failure . However, to date, the hemodynamic efficacy and safety of ultra-short-acting β1-blockers remains largely unclear in cases with concomitant administration of high-dose inotropes. We hypothesized that ultra-short-acting β1-blocker therapy could represent a valuable therapeutic option in cases of sinus tachycardia under high-dose catecholamine support. As a preliminary investigation, we conducted a retrospective, single center, self-comparison study.
The Research Ethics Review Board of National Cerebral and Cardiovascular Center approved the present study. Due to the use of de-identified data, informed consent was waived. Cardiac surgical intensive care unit charts for all adult patients who underwent on-pump cardiovascular surgery between April 2007 and November 2011 at the National Cerebral and Cardiovascular Center Hospital, Suita, Osaka were reviewed. The inclusion criteria were as follows: (1) patients who had persistent sinus tachycardia (HR > 100 beats/min) induced by catecholamine support after CPB; (2) patients who received continuous intravenous landiolol for sinus tachycardia based on the decision of the attending physician; (3) landiolol administration overlapped with constant dose of inotropic drugs (catecholamine, vasodilator, and/or phosphodiesterase 3 inhibitor) for at least for 1 h; (4) patients who had a pulmonary artery catheter; and (5) patients who were sedated and supported via mechanical ventilation. The exclusion criteria were as follows: (1) patients who had a temporary or permanent pacemaker; (2) patents who had any atrial arrhythmia except for sinus tachycardia; or (3) patients who had any mechanical circulatory support, including continuous renal replacement therapy.
Assessment of clinical features
In addition to general clinical features, we collected data on preoperative EuroSCORE, preoperative left ventricular ejection fraction, and fractional shortening via transthoracic echocardiography.
To comprehensively assess the various regimens of catecholamine, we used a modified Wernovsky inotrope score , calculated using the following formula: cardiac agent index (CAI) = dopamine dose (μg/kg/min) + dobutamine dose (μg/kg/min) + 100 × epinephrine dose (μg/kg/min) + 100 × norepinephrine dose (μg/kg/min) + 10 × phosphodiesterase 3 inhibitor dose (μg/kg/min). High-dose catecholamine use was defined as CAI > 10. Definitions of hemodynamic instability and the approaches used to maintain hemodynamic conditions were based on the assessment by individual anesthesiologists.
To evaluate adverse events, plasma creatine kinase-MB isozyme levels were measured every 6 h, as part of the routine daily clinical practice at our intensive care unit.
We evaluated hemodynamic variables just before and 1 h after landiolol infusion. Using a 7.5 Fr. Continuous Cardiac Output Thermodilution Catheter (Edwards Lifescience, CA, USA) and TruWave Disposable Pressure Transducer (Edwards Lifescience, CA, USA), the following variables were measured: HR (beats/min), cardiac output (L/min), cardiac index (CI, L/min/m2), stroke volume (SV, mL), stroke volume index (SVI, mL/m2), mixed venous oxygen saturation (SvO2, %), systolic arterial blood pressure (mmHg), diastolic arterial pressure (mmHg), mean arterial blood pressure (mmHg), systolic pulmonary artery pressure (mmHg), diastolic pulmonary artery pressure (mmHg), mean pulmonary artery pressure (mmHg), and central venous pressure (mmHg). Blood temperature (BT, °C) was also measured.
All data are presented as mean ± SD unless otherwise stated. Paired t test was used to compare hemodynamic variables. Pearson’s correlation coefficient (r) was used to study the relationship between changes in rate of HR reduction and SVI elevation. All p-values < 0.05 (two-tailed) were considered significant. Statistical analyses were performed using SPSS software version 11.0.1 J (IBM SPSS Inc., IL, USA).
Table 1 summarizes the clinical characteristics of the patients.
We identified 11 out of 1762 adult patients who underwent on-pump cardiovascular surgery (0.6%). The average continuous infusion dose of β1-blocker landiolol was 2.6 ± 1.3 μg/kg/min (range, 1.1–5.0 μg/kg/min), indicating that our dose was lower than the manufacturer’s recommended dose for tachycardia prevention (20–40 μg/kg/min). All landiolol infusions were started without an initial loading dose. No bolus shots or up- or down-titrations were used, even beyond the observation phase. The average CAI value was 14.6 ± 13.4. Five of the 11 patients (45%) received high-dose catecholamine therapy (> 10), but none of these used epinephrine.
Landiolol administration led to a reduction in HR by approximately 11%, and was significantly different (Table 2) within our study population (p < 0.001). Notably, administration of low-dose landiolol with concomitant used of inotropes led to an 18.5% increase in SVI (p = 0.04), with no deterioration in hemodynamic parameters.
A correlation between HR and SVI was observed (Fig. 1), and there was no evidence that SVI deterioration was caused by HR reduction. HR increased in response to landiolol in only one case (patient no. 1), followed by a decrease in SVI, suggesting that excess tachycardia harmed output. Three cases showed no changes in SVI despite reductions in HR (patient nos. 2, 5, and 8).
Plasma creatine kinase-MB isozyme levels did not differ significantly between pre- and post-landiolol administration (142.3 ± 271.5 vs. 199.9 ± 424.6 ng/mL, respectively; p = 0.31).
Five patients received high-dose catecholamine support (CAI > 10), and are shown as a subgroup in Table 3. HR reduction led to an increase in SVI as well as improved CI, suggesting that low-dose landiolol may not only confer control rate ability, but may also exert a positive impact on cardiac function in conjunction with high doses of catecholamine.
The findings of the present study highlight the usefulness of a low-dose infusion of the β1-blocker, landiolol, during the acute postoperative phase in patients with sinus tachycardia receiving high-dose catecholamine support. The successful use of landiolol for HR control was shown previously in clinical settings, including atrial fibrillation  and sepsis . However, there is some uncertainty regarding administration of β-blockers in patients who require a potent inotropic agent to guard against serious hemodynamic instability . Some reports have shown beneficial effects of intravenous β-blocker in a clinical setting of low-dose catecholamine support [20, 21]. However, to the best our knowledge, no previous trials have examined this issue from the standpoint of high-dose inotropes. In the cases we studied, relatively low-dose landiolol reduced HR and increased SVI without adversely affecting patients treated with high-dose catecholamines.
Catecholamines are the first-line drug treatment to support cardiac performance after CPB. Since excess sinus tachycardia induced by high-dose catecholamine can reduce the duration of coronary perfusion  and coronary vasoconstriction , efforts must be made to prevent sinus tachycardia following cardiac surgery. Epinephrine is a choice catecholamine used to avoid tachycardia , but is not a first-line drug for low cardiac output syndrome treatment due to its detrimental effects on splanchnic blood flow and its ability to induce lactic acidosis . The present study indicates the possibility of using the ultra-short-acting β1-blocker, landiolol, to optimize HR without inhibiting the favorable hemodynamic response brought about by the conventional use of inotropes.
Administration of landiolol should be initiated at a loading dose of 40 μg/kg/min, and then titrated to a maintenance dose. However, this method has been shown to cause hypotension . Additionally, several reports have shown that landiolol administration without an initial loading dose was effective in preventing atrial fibrillation/atrial flutter/paroxysmal atrial tachycardia (maintenance dose range, 1–5 μg/kg/min) in surgical patients with left ventricular dysfunction [27, 28]. Therefore, we did not administer a loading dose to patients receiving high-dose catecholamine support.
Surprisingly, our results suggest that landiolol has multiple beneficial effects, both in terms of controlling HR and positively affecting SVI under high-dose catecholamine support. This is similar to the manner by which a low-dose β-blocker infusion may decrease the undesirable response associated with catecholamine without significantly reversing the desired inotropic effects. Additionally, a slower HR facilitates a lengthier diastolic filling time and subsequently increases the static arterial elastance. Improved ventricular–arterial coupling is thought to increase the SVI . Therefore, accurate evaluation of diastolic function may have a positive impact on HR reduction.
Human ventricular myocardium contains a mixed population of β1 and β2 adrenergic receptors, and patients with heart failure have lower a β1/β2 ratio compared with healthy hearts . Moreover, both β1 and β2 receptors in the ventricle were coupled to a positive inotropic response. Therefore, one can speculate that the β2 receptor acts as an inotropic mediator to maintain systolic function in cases where there is concomitant use of landiolol and inotropes. The reaction stemming from combination of landiolol and inotropes may be altered depending upon the population of β-adrenergic receptors in the ventricle. However, landiolol cannot be administered based solely on the molecular evidence regarding the β1/β2 ratio in the human ventricle. Therefore, careful titration and monitoring of the patient is required to assess the efficacy and safety of landiolol.
Sinus tachycardia induced by high-dose catecholamine immediately after surgery requires a prompt strategy to control HR to avoid impaired impair cardiac systolic function. The present study provides important evidence supporting use of a safe and effective therapeutic regimen combining landiolol and inotropes.
The present study has several limitations. First, our sample size was small and only included 11 patients because concomitant use of catecholamine with β1-blocker agent is still not specified as a clinical treatment regimen. Second, our analysis was retrospective in nature. Prospective multicenter trials are required. However, a prospective design is not easy since a therapeutic approach should be dependent upon the judgment of the attending physician. Third, our comparison was between pre-administration and post-administration and involved only a single time point. We limited the study duration to only 1 h to minimize the effects of other clinical factors, such as fluid resuscitation, temperature recovery, and reduced bleeding. Fourth, this study did not have a control group; therefore, our findings are not definitive. Future studies are required to overcome these limitations.
In the present study, low-dose β1-blocker landiolol therapy reduced HR and also increased SVI in patients who received sinus tachycardia-induced inotropic agents following on-pump cardiovascular surgery. While this study has some limitations in terms of low patient numbers and the study design, our findings suggest that landiolol is a promising therapy for the management of sinus tachycardia after CPB.
Reproducing these results using a large, appropriately powered and designed study could provide cardiovascular anesthesiologists and intensivists with a great addition to their pharmacological armamentarium.
Availability of data and materials
All data were retrieved from the institutional database and are available from the corresponding author upon reasonable request.
Cardiac agent index
Stroke volume index
Kannel WB, Kannel C, Paffenbarger RS Jr, Cupples LA. Heart rate and cardiovascular mortality: the Framingham study. Am Heart J. 1987;113:1489–94.
Jouven X, Empana JP, Schwartz PJ, Desnos M, Courbon D, Ducimetiere P. Heart-rate profile during exercise as a predictor of sudden death. N Engl J Med. 2005;352:1951–8.
Raby KE, Brull SJ, Timimi F, Akhtar S, Rosenbaum S, Naimi C, Whittemore AD. The effect of heart rate control on myocardial ischemia among high-risk patients after vascular surgery. Anesth Analg. 1999;88:477–82.
Fillinger MP, Surgenor SD, Hartman GS, Clark C, Dodds TM, Rassias AJ, et al. The association between heart rate and in-hospital mortality after coronary artery bypass graft surgery. Anesth Analg. 2002;95:1483–8.
Bohm M, Swedberg K, Komajda M, Borer JS, Ford I, Dubost-Brama A, et al. Heart rate as a risk factor in chronic heart failure (SHIFT): the association between heart rate and outcomes in a randomised placebo-controlled trial. Lancet. 2010;376:886–94.
Fox K, Ford I, Steg PG, Tendera M, Robertson M, Ferrari R, et al. Heart rate as a prognostic risk factor in patients with coronary artery disease and left-ventricular systolic dysfunction (BEAUTIFUL): a subgroup analysis of a randomised controlled trial. Lancet. 2008;372:817–21.
Iguchi S, Iwamura H, Nishizaki M, Hayashi A, Senokuchi K, Kobayashi K, et al. Development of a highly cardioselective ultra short-acting beta-blocker, ONO-1101. Chem Pharm Bull. 1992;40:1462–9.
Sugiyama A, Takahara A, Hashimoto K. Electrophysiologic, cardiohemodynamic and beta-blocking actions of a new ultra-short-acting beta-blocker, ONO-1101, assessed by the in vivo canine model in comparison with esmolol. J Cardiovasc Pharmacol. 1999;34:70–7.
Sugiura S, Seki S, Hidaka K, Masuoka M, Tsuchida H. The hemodynamic effects of landiolol, an ultra-short-acting beta1-selective blocker, on endotracheal intubation in patients with and without hypertension. Anesth Analg. 2007;104:124–9.
Yamazaki A, Kinoshita H, Shimogai M, Fujii K, Nakahata K, Hironaka Y, et al. Landiolol attenuates tachycardia in response to endotracheal intubation without affecting blood pressure. Can J Anaesth. 2005;52:254–7.
Sezai A, Minami K, Nakai T, Hata M, Yoshitake I, Wakui S, et al. Landiolol hydrochloride for prevention of atrial fibrillation after coronary artery bypass grafting: new evidence from the PASCAL trial. J Thorac Cardiovasc Surg. 2011;141:1478–87.
Sakamoto A, Kitakaze M, Takamoto S, Namiki A, Kasanuki H, Hosoda S, et al. Landiolol, an ultra-short-acting beta(1)-blocker, more effectively terminates atrial fibrillation than diltiazem after open heart surgery: prospective, multicenter, randomized, open-label study (JL-KNIGHT study). Circ J. 2012;76:1097–101.
Sezai A, Nakai T, Hata M, Yoshitake I, Shiono M, Kunimoto S, et al. Feasibility of landiolol and bisoprolol for prevention of atrial fibrillation after coronary artery bypass grafting: a pilot study. J Thorac Cardiovasc Surg. 2012;144:1241–8.
Adachi T, Sato A, Baba M, Hiraya D, Hasegawa T, Kuroki K, et al. Novel use of the ultra-short-acting intravenous beta1-selective blocker landiolol for supraventricular tachyarrhythmias in patients with congestive heart failure. Heart Vessel. 2014;29:464–9.
Jaiswal A, Nguyen VQ, Carry B, Le Jemetel TH. Combination therapy with beta blocker and inotrope in decompensated heart failure: a clinical observation. Heart Res Open J. 2017;4:18–22.
Wernovsky G, Wypij D, Jonas RA, Mayer JE Jr, Hanley FL, Hickey PR, et al. Postoperative course and hemodynamic profile after the arterial switch operation in neonates and infants. A comparison of low-flow cardiopulmonary bypass and circulatory arrest. Circulation. 1995;92:2226–35.
Yoshida Y, Terajima K, Sato C, Akada S, Miyagi Y, Hongo T, et al. Clinical role and efficacy of landiolol in the intensive care unit. J Anesth. 2008;22:64–9.
Okajima M, Takamura M, Taniguchi T. Landiolol, an ultra-short-acting β1-blocker, is useful for managing supraventricular tachyarrhythmias in sepsis. World J Crit Care Med. 2015;4:251–7.
Bohm M, Link A, Cai D, Nieminen MS, Filippatos GS, Salem R, et al. Beneficial association of beta-blocker therapy on recovery from severe acute heart failure treatment: data from the survival of patients with acute heart failure in need of intravenous inotropic support trial. Crit Care Med. 2011;39:940–4.
Kobayashi S, Murakami W, Myoren T, Tateishi H, Okuda S, Doi M, et al. A low-dose beta1-blocker effectively and safely slows the heart rate in patients with acute decompensated heart failure and rapid atrial fibrillation. Cardiology. 2014;127:105–13.
Yasumura Y. Combination of b-blocker and milrinone for acute heart failure. Circ J. 2012;76:1589–97.
Mulder P, Barbier S, Chagraoui A, Richard V, Henry JP, Lallemand F, et al. Long-term heart rate reduction induced by the selective I(f) current inhibitor ivabradine improves left ventricular function and intrinsic myocardial structure in congestive heart failure. Circulation. 2004;109:1674–9.
Sambuceti G, Marzilli M, Marraccini P, Schneider-Eicke J, Gliozheni E, Parodi O, et al. Coronary vasoconstriction during myocardial ischemia induced by rises in metabolic demand in patients with coronary artery disease. Circulation. 1997;95:2652–9.
Butterworth JF, Prielipp RC, Royster RL, Spray BJ, Kon ND, Wallenhaupt SL, et al. Dobutamine increases heart rate more than epinephrine in patients recovering from aortocoronary bypass surgery. J Cardiothorac Vasc Anesth. 1992;6:535–41.
Lomivorotov VV, Efremov SM, Kirov MY, Fominskiy EV, Karaskov AM. Low-cardiac-output syndrome after cardiac surgery. J Cardiothorac Vasc Anesth. 2017;31:291–308.
Hasegawa T, Oshima Y, Maruo A, Matsuhisa H, Kadowaki T, Noda R. Landiolol for junctional ectopic tachycardia refractory to amiodarone after pediatric cardiac surgery. Gen Thorac Cardiovasc Surg. 2013;61:350–2.
Ito N, Tashiro T, Morishige N, Nishimi M, Hayashida Y, Minematsu N, et al. Safety and efficacy of an ultrashort-acting beta1-blocker on left ventricular dysfunction. Heart Surg Forum. 2012;15:E189–94.
Morisaki A, Hosono M, Sasaki Y, Hirai H, Sakaguchi M, Nakahira A, et al. Very-low-dose continuous drip infusion of landiolol hydrochloride for postoperative atrial tachyarrhythmia in patients with poor left ventricular function. Gen Thorac Cardiovasc Surg. 2012;60:386–90.
Morelli A, Singer M, Ranieri VM, D'Egidio A, Mascia L, Orecchioni A, et al. Heart rate reduction with esmolol is associated with improved arterial elastance in patients with septic shock: a prospective observational study. Intensive Care Med. 2016;42:1528–34.
Bristow MR, Ginsburg R, Umans V, Fowler M, Minobe W, Rasmussen R, et al. Beta 1- and beta 2-adrenergic-receptor subpopulations in nonfailing and failing human ventricular myocardium: coupling of both receptor subtypes to muscle contraction and selective beta 1-receptor down-regulation in heart failure. Circ Res. 1986;59:297–309.
This work was not supported by any resource.
Ethics approval and consent to participate
The Institutional Review Board reviewed and approved the study. Consent to participate for this study was waived as no individual patients were identified.
Consent for publication
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