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Table of Content - Volume 11 Issue 1 -July 2019


Attenuation of haemodynamic response to laryngoscopy and endotracheal intubation:

A comparative study between fentanyl and esmolol

 

Rajiv Aggarwal1, Manjula Sudhakar Rao2*, Alok Basu Roy3, Ravindra Kumar Arora4

 

1Consultant, Department of Anesthesiology, Regency Hospital, Kanpur, INDIA.

2Senior Resident, Department of Anesthesiology, Father Mullers Medical College Hospital, Kankanady, Mangalore, Karnataka, INDIA.

3,4Senior Consultant, Department of Anesthesiology, Max Superspeciality Hospital, Vaishali, Ghaziabad, Uttar Pradesh, INDIA.

Email: manjularao1010@gmail.com

 

Abstract               Background: Laryngoscopy and endotracheal intubation have become the integral part of general anaesthesia and critical care of patients. It has been practiced since its description by Rowbothom and Magill in 1921. These are noxious stimuli which provoke a transient but marked sympathetic response manifesting as hypertension and tachycardia, more severe in hypertensive patients. Materials and methods: This prospective study was conducted in the Department of Anaesthesiology, Max Hospital Vaishali Gaziabad during the period of 12 months from December 2014 to December 2015. A total of 100 normotensive patients between 18 and 60 years of age with ASA grade 1 and 2 risk, undergoing elective surgical procedures under general anaesthesia were included. Patients undergoing emergency surgical procedures, anaesthesia with non-invasive airway devices haemodynamically unstable patients, patients on beta blockers and calcium channel blockers and patients with difficult airway were excluded. Results: In the fentanyl group, the average heart rate increased by 1.85 bpm during laryngoscopy and intubation. In the esmolol group, the rise in heart rate was 3.1bpm which is higher than that of fentanyl group. The increase in heart rate in the esmolol group as a response to intubation was statistically significant. Hence our study showed that Fentanyl is a better drug to control the tachycardia as a response to laryngoscopy and intubation. Both fentanyl and esmolol effectively prevented rise of SBP as a response to intubation. Conclusion: 1Fentanyl is better than esmolol in controlling tachycardia in response to laryngoscopy and endotracheal intubation. 2Both fentanyl and esmolol are effective in controlling the rise in SBP as a response to laryngoscopy and endotracheal intubation. 3Esmolol is more effective than fentanyl in controlling SBP and RPP. In conclusion, both fentanyl and esmolol are effective in attenuation of hemodynamic response to laryngoscopy and intubation. Fentanyl is more effective in preventing tachycardia while esmolol is more effective in controlling rise in systolic blood pressure and rate pressure product.

Key Word: haemodynamic.

 

INTRODUCTION

Laryngoscopy and endotracheal intubation have become the integral part of general anaesthesia and critical care of patients. It has been practiced since its description by Rowbothom and Magill in 1921.1 Laryngoscopy and tracheal intubation are noxious stimuli which provoke a transient but marked sympathetic response manifesting as hypertension and tachycardia.2 Hypertensive patients are more prone to have significant increase in blood pressure (BP), whether they have been treated beforehand or not.3 In susceptible patients, particularly those with systemic hypertension, coronary artery disease, cerebrovascular disease and intracranial aneurysm, even these transient changes can result in potentially deleterious effects like left ventricular failure, arrhythmias, myocardial ischaemia, cerebral haemorrhage and rupture of cerebral aneurysm.3,4 Many pharmacological methods have been devised to reduce the extent of these haemodynamic events. These include opioids, local anaesthestics, beta adrenergic blockers and vasodilator drugs. Beta adrenergic blockers have been used to successfully attenuate this undesirable response to intubation. They act by blocking the effect of the hyperactive sympathetic system on the cardiovascular system. A short acting and cardio selective blocker may be more useful with minimal adverse effects.5 Esmolol is an ultra-short acting, β1 cardio selective, β blocking agent with a short half-life (9min). This agent has been used to reduce the increase in heart rate and blood pressure in response to tracheal intubation, thereby reducing the myocardial oxygen demand.6 Fentanyl is a synthetic opioid agonist used as an adjuvant to provide analgesia during general anaesthesia. Studies have shown its efficacy in reducing the hemodynamic response to laryngoscopy and endotracheal intubation. It acts by blunting the tracheal sensitivity to the stimulus of laryngoscopy and intubation.7 In this study we have compared the efficacy of Esmolol and Fentanyl in attenuating the pressor response to laryngoscopy and intubation during general anaesthesia.

 

AIMS AND OBJECTIVES

  1. To study the effect of esmolol and fentanyl on haemodynamic response to laryngoscopy and endotracheal intubation.
  2. To compare the effects of esmolol and fentanyl on attenuation of the haemodynamic response to laryngoscopy and endotracheal intubation.
  3. To evaluate any adverse effects of these drugs during anaesthesia and recovery.

 

MATERIALS AND METHODS

This prospective randomised single blind comparative study was conducted in the department of anaesthesiology, Pushpanjali Crosslay Hospital Ghaziabad during the period of 12 months from December 2014 to December 2015. A total of 100 patients who underwent elective surgical procedures under general anaesthesia were randomly enrolled for this study using table of random numbers.

Inclusion criteria

  1. All normotensive patients undergoing surgical procedures under general anaesthesia.
  2. Patients aged between 18 to 60 years with ASA grade 1 and 2 risk.

Exclusion criteria

  1. Patients not willing to be part of the study.
  2. Emergency surgical procedures.
  3. General anaesthesia with non-invasive airway devices.
  4. Haemodynamically unstable patients.
  5. Patients on beta blockers and calcium channel blockers.
  6. Difficult airway.

 

METHODOLOGY

Sample size- Sample size was calculated using the following formula

Zα = 1.96 at 95% confidence level

Zβ = 1.28 at 90% power.

σ and d are combined SD and mean difference from reference no 35

Hence the sample size was calculated as 98.

100 patients who met the defined inclusion and exclusion criteria were enrolled for this study. A written informed consent was taken from the patients who were enrolled. Block randomisation method was used to assign patients into two groups- Group A (Fentanyl group) and Group B (Esmolol group). A number was assigned to each patient of the day using random number chart. Patient with even number was taken into esmolol group and the one with odd number was taken into fentanyl group, thus avoiding selection bias. Patients were evaluated by taking detailed history, physical examination, airway assessment and relevant investigations preoperatively. They were asked to fast overnight. Group A patients received Inj. Fentanyl 1.5 microgram per kg intravenously 5 minutes prior to laryngoscopy. Group B patients received Inj. Esmolol 2 milligram per kg intravenously 3 minutes prior to laryngoscopy. All patients received standard premedications like H2 blockers, prokinetics, antisialogogues and anxiolytics prior to induction. They were pre-oxygenated and induced with Inj.Propofol 2mg per kg intravenously and intubated after paralysing with intermediate acting non depolarising muscle relaxant. General anaesthesia was maintained with volatile agents and oxygen nitrous oxide mixture during the surgery. Patient’s heart rate (HR), systolic blood pressure(SBP), diastolic blood pressure (DBP) were recorded prior to induction, at the time of intubation and at intervals of 1, 3 and 5 minutes after intubation. Mean arterial pressure (MAP) and rate pressure product (RPP) were calculated. At the conclusion of the surgery, patients were reversed using Inj. Neostigmine 0.05mg per kg and Inj.Glycopyrolate 0.01mg per kg and extubated. Any adverse effects of the medications were noted. The data was recorded and tabulated in a standard format. After completion of 100 cases, the data was analysed to compare the efficacy of Fentanyl and Esmolol to attenuate the haemodynamic response to laryngoscopy and intubation. Statistical analysis was done to assess the significance of differences between the two groups. Mean and standard deviations were calculated for all the readings. Two tailed paired student t tes was used to determine whether the observed differences were significant. P value of 0.05 or less was taken as significant at 95% confidence.


 

OBSERVATIONS AND RESULTS

A total of 100 patients were enrolled for this study. All patients underwent elective surgical procedures under general anaesthesia.

Table 1: Distribution of cases by gender

 

Drug used

Total

gender

Male

Count

23

26

49

%

46.0%

52.0%

49.0%

Female

Count

27

24

51

%

54.0%

48.0%

51.0%

Total

 

Count

50

50

 

%

100.0%

100.0%

x2=0.36 p=0.548 ns

Chi square test showed a p value of 0.543 for difference between the two groups with reference to gender composition. This p value was statistically not significant. Hence the two groups were comparable.

 

Table 2: Age and weight comparison

 

Drug used

N

Mean

Std. Deviation

t

Age

Esmolol

50

45.600

8.997

1.654

Fentanyl

50

42.640

8.903

p=0.101 ns

Weight

Esmolol

50

65.480

10.839

.418

Fentanyl

50

66.400

11.178

p=0.677 ns

Heart Rate

Table 3: Comparison of HR between fentanyl and esmolol groups

 

drugused

N

Mean

Std. Deviation

t

Hr pre

Esmolol

50

83.040

11.146

1.149

Fentanyl

50

86.340

16.971

p=0.253 ns

Hr intub

Esmolol

50

86.100

6.119

1.006

Fentanyl

50

87.960

11.549

p=0.317 ns

Hr 1min

Esmolol

50

84.180

6.880

1.069

Fentanyl

50

85.940

9.406

p=0.288 ns

Hr 3min

Esmolol

50

87.420

8.199

1.384

Fentanyl

50

84.940

9.662

p=0.17 ns

Hr 5min

Esmolol

50

87.560

7.675

3.525

Fentanyl

50

80.700

11.420

p=0.001 vhs

 

Systolic Blood Pressure

Table 4: Comparison of systolic BP between fentanyl and esmolol groups

 

Drug used

N

Mean

Std. Deviation

t

Sbp preinduction

Esmolol

50

124.560

11.634

3.938

Fentanyl

50

135.040

14.792

p=0.001 vhs

Sbp intubation

Esmolol

50

115.540

14.204

.789

Fentanyl

50

113.100

16.642

p=0.432 ns

sbp1min

Esmolol

50

114.460

12.786

1.312

Fentanyl

50

118.300

16.271

p=0.193 ns

Sbp 3min

Esmolol

50

105.780

14.406

2.070

Fentanyl

50

110.620

8.109

p=0.041 sig

Sbp 5min

Esmolol

50

108.800

10.108

.056

Fentanyl

50

108.680

11.293

p=0.955 ns

 

Diastolic Blood Pressure

Table 15: Comparison of diastolic BP between the fentanyl and esmolol groups.

 

Drug used

N

Mean

Std. Deviation

t

Dbp pre-intubation

Esmolol

50

81.000

10.535

.161

Fentanyl

50

80.600

14.010

p=0.872 ns

Dbp intubation

Esmolol

50

77.240

14.244

1.907

Fentanyl

50

70.840

18.987

p=0.06 ns

dbp1min

Esmolol

50

71.420

8.069

.887

Fentanyl

50

73.500

14.479

p=0.377 ns

Dbp 3min

Esmolol

50

65.900

11.014

.044

Fentanyl

50

65.980

6.723

p=0.965 ns

Dbp 5min

Esmolol

50

66.820

9.077

.773

Fentanyl

50

68.200

8.781

p=0.442 ns


Mean arterial pressure

Table 6: comparison of MAP between fentanyl and esmolol groups

 

drugused

N

Mean

Std. Deviation

t

mappreinduction

Esmolol

50

92.200

10.392

2.077

Fentanyl

50

97.140

13.220

p=0.04 sig

mapintubation

Esmolol

50

87.360

13.127

.999

Fentanyl

50

84.260

17.574

p=0.32 ns

map1min

Esmolol

50

83.160

8.747

1.756

Fentanyl

50

87.540

15.321

p=0.082 ns

map3min

Esmolol

50

77.280

11.375

1.168

Fentanyl

50

79.420

6.201

p=0.246 ns

map5min

Esmolol

50

78.760

8.463

.856

Fentanyl

50

80.160

7.888

p=0.394 ns

 

Rate pressure product:

Table 7: Comparison of RPP in fentanyl and esmolol group

 

drugused

N

Mean

Std. Deviation

t

Rate pressure product

Esmolol

50

10313.820

1905.039

2.961

Fentanyl

50

11624.660

2484.333

p=0.004 hs

Rpp intubation

Esmolol

50

9946.920

1535.634

.155

Fentanyl

50

10007.840

2317.119

p=0.877 ns

rpp1min

Esmolol

50

9648.480

1441.017

1.608

Fentanyl

50

10129.300

1547.799

p=0.111 ns

rpp3min

Esmolol

50

9229.920

1429.468

.603

Fentanyl

50

9391.180

1238.238

p=0.548 ns

rpp5min

Esmolol

50

9570.620

1269.701

2.793

Fentanyl

50

8779.940

1547.592

p=0.006 hs


Table 8: Difference From Preinduction To 5 Min

 

drugused

N

Mean

Std. Deviation

t

HR

Esmolol

50

-4.5200

13.09345

3.93800

Fentanyl

50

5.6400

12.70346

P<0.001 VHS

SBP

Esmolol

50

15.7600

11.83485

3.46700

Fentanyl

50

26.3600

18.08908

P<0.001 VHS

DBP

Esmolol

50

14.1800

7.98389

.83400

Fentanyl

50

12.4000

12.81421

P=0.407 NS

MAP

Esmolol

50

13.4400

8.51208

1.56500

Fentanyl

50

16.9800

13.53829

P=0.121 NS

RPP

Esmolol

50

743.2000

2327.43367

4.30400

Fentanyl

50

2844.7200

2550.03203

P<0.001 VHS

DISCUSSION

A hemodynamic response of increased HR and BP to manipulation in the area of the larynx, by means of laryngoscopy and intubation, has been well recognized for 60 years. Stimulation of mechanoreceptors in the pharyngeal wall, epiglottis, and vocal cords is thought to be the cause for the haemodynamic response. The receptors are abundant over arytenoid cartilage, vocal cords, epiglottis and hypopharynx. Transitory hypertension and tachycardia are probably of no consequence in healthy individuals, but either one or both may be hazardous to those with hypertension, myocardial insufficiency or cerebrovascular diseases. The transient changes can result in potentially deleterious effect like left ventricular failure, pulmonary edema, myocardial ischemia and cerebral haemorrhage.4 Numerous studies have been published with different drugs to attenuate this response to laryngoscopy and intubation. In this study we have compared the efficacy of fentanyl and esmolol in attenuation the pressor response to laryngoscopy and intubation. We found that in the fentanyl group, the average heart rate increased by1.85% during laryngoscopy and intubation. In the esmolol group, the rise in heart rate was 3.1% which is higher than that of fentanyl group. The increase in heart rate in the esmolol group as a response to intubation was not statistically significant. However, at 5 min after intubation, the HR in fentanyl group was 8 bpm lower compared to esmolol group. P value for this difference was 0.001 making this very highly significant. Hence our study showed that Fentanyl is a better drug to control the tachycardia as a response to laryngoscopy and intubation. Gupta A et al37 found Esmolol beneficial in controlling tachycardia as response to laryngoscopy and intubation. Lars et al also found that esmolol controlled tachycardia.5 However Ranganathan et al38 found Fentanyl effectively supressed the tachycardia during intubation. Ebert et al (39)in their study found Fentanyl more effective than esmolol in controlling heart rate as response to laryngoscopy and intubation. Their finding was similar to the present study. On the contrary, Bostan et al found esmolol controlled HR better than Fentanyl.35 We found both fentanyl and esmolol effectively prevented rise of SBP as a response to intubation. In fact there was a fall of SBP noted in both the groups as compared to pre induction levels. When compared to fentanyl group, the average SBP was significantly lower in esmolol group during pre-induction and 3 min post intubation periods. Hence esmolol is more effective in controlling SBP as compared to fentanyl. DBP fell significantly in the fentanyl group as compared to esmolol group. Esmolol was also effective in supressing the rise of DBP, however there was no significant fall in DBP in esmolol group. However when the two groups were compared, there was no statistically significant differences in DBP. Both fentanyl and esmolol were effective in blocking the rise MAP as response to laryngoscopy and intubation. There was a statistically significant reduction in MAP in both the groups. MAP was significantly lower in the esmolol group in the pre induction period only. Both fentanyl and esmolol were able to prevent the rise of RPP as a response to laryngoscopy and intubation. In the fentanyl group, it reduced by a statistically significant amount. The RPP was significantly lower in the esmolol group during the pre induction period and 5 min after intubation. Ebert et al39 found that Fentanyl decreased the SBP, MAP and DBP significantly below the baseline, while these were either maintained at or elevated slightly in the esmolol group. Helfman et al.40 did not find any attenuation of the pressor response with 200 mcg fentanyl, however they intubated 2 minutes after study drug injection. Lars et al5 did not find any statistically significant difference in MAP between esmolol and placebo groups while our study showed esmolol effectively prevented rise of MAP during laryngoscopy and intubation. Gupta et al37 found esmolol effectively attenuated the rise of SBP and DBP as response to laryngoscopy and intubation. Yushi et al7 found fentanyl was more effective in controlling the stress response to intubation when compared to the stress response to laryngoscopy. Dahlgren and Masseter also found fentanyl effectively controlled the stress response to laryngoscopy and intubation. 29

 

CONCLUSION

Based on findings of this study, we conclude that,

  1. Fentanyl is better than esmolol in controlling tachycardia in response to laryngoscopy and endotracheal intubation.
  2. Both fentanyl and esmolol are effective in controlling the rise in systolic blood pressue as a response to laryngoscopy and endotracheal intubation.
  3. Esmolol is more effective than fentanyl in controlling rise in systolic blood pressure and rate pressure product.

In conclusion, both fentanyl and esmolol are effective in attenuation of hemodynamic response to laryngoscopy and intubation. Fentanyl is more effective in preventing tachycardia while esmolol is more effective in controlling rise in systolic BP and rate pressure product.

 

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