Table of Content - Volume 19 Issue 3 - September 2021
Comparative study of hemodynamic effects, quality of extubation and emergence - agitation response of the patients with dexmedetomidine versus lignocaine during and following the endotracheal extubation
Manasi Panat1*, Pranali Shukla2, Ramesh Talele3
1Associate Professor, 2Junior Resident, 3Professor, Department of Anaesthesia, JMF'S ACPM Medical College, Dhule, Maharashtra, INDIA. Email: mapanat7498@gmail.com
Abstract Background: Endotracheal extubation is the translaryngeal removal of a tube from the trachea via the nose or mouth. It is associated with hemodynamic changes because of reflex sympathetic discharge caused by epipharyngeal and laryngopharyngeal stimulation. Various drugs and techniques have been tried to attenuate the airway and stress responses during tracheal extubation. In present study, we have compared the effects of dexmedetomidine and intravenous lignocaine on the hemodynamic and recovery profiles during endotracheal extubation. Material and Methods: Present study was prospective randomised comparative study, conducted in patients from age group of 18-45 years, ASA grade I/II, scheduled for elective abdominal surgeries. The patients were categorised into two different groups using the sealed envelope method as Group D and group L. Results: In present study, patients were divided in following 2 groups with 50 patients in each group as group D (Dexmedetomidine) and group L (Lignocaine). Age, gender, mean BMI were comparable in both groups and difference was not significant statistically. The difference between mean heart rate, systolic BP, diastolic BP and mean arterial BP during extubation, after extubation at 1, 3, 5, 10, 15, 20, 25, 30 minutes in dexmedetomidine group and lignocaine group was statistically significant. In Dexmedetomidine group, 12% of the patients had no cough during extubation, 72% of the patients had smooth extubation with minimal cough while in Lignocaine group, 22% of the patients had smooth extubation with minimal cough, 74 % of the patients had moderate cough during extubation. Statistical analysis of the Emergence agitation score shows better results in group D. Conclusion: Administration of Dexmedetomidine before tracheal extubation was more effective in maintaining the hemodynamic stability, facilitated smooth tracheal extubation and had a better quality of recovery as compared to Lignocaine. Keywords: dexmedetomidine, tracheal extubation emergence - agitation response, lignocaine.
INTRODUCTION Endotracheal extubation is the translaryngeal removal of a tube from the trachea via the nose or mouth. It is associated with hemodynamic changes because of reflex sympathetic discharge caused by epipharyngeal and laryngopharyngeal stimulation. The rise in sympathoadrenal activity can cause tachycardia, hypertension and arrhythmias.1 Extubation causes airway irritation leading to increase in systolic blood pressure and diastolic blood pressure. Coughing during extubation increases intrathoracic pressure which impairs venous return to heart. 2 For smooth endotracheal extubation, the patient should not have any straining, coughing, bucking, movement, holding of breath, laryngospasm or bronchospasm. In patients with coronary artery disease or in patients who have risk factors for coronary artery disease ,the hemodynamic changes while extubation and emergence from anaesthesia will increase myocardial oxygen demand.3 Sudden increases in blood pressure during extubation maybe dangerous in patients undergoing neurosurgical procedure.4 Various drugs and techniques have been tried to attenuate the airway and stress responses during tracheal extubation. Studies have been done using fentanyl, sevoflurane, lignocaine, propofol, magnesium sulphate, nitroglycerine, clonidine, esmolol, labetalol, metoprolol, verapamil, nicardipine, diltiazem, etc., either as a sole agent or in comparison with each other.3,4,5,6 In present study, we have compared the effects of dexmedetomidine and intravenous lignocaine on the hemodynamic and recovery profiles during endotracheal extubation.
MATERIAL AND METHODS Present study was prospective randomised comparative study, conducted in Department of Anaesthesia, JMF'S ACPM Medical College, Dhule, India. Study period was from February 2019 to October 2020. Study was approved by institutional ethical committee. Inclusion criteria: Patients from age group of 18-45 years, ASA grade I/II, scheduled for elective abdominal surgeries Exclusion criteria: Patients with cardiovascular diseases, Respiratory, renal, liver diseases. Difficult airway: Cormack and Lehane grade 3 and 4. Obesity: BMI >30. History of sleep apnea. Emergency surgery. Patients having history of allergy or contraindications to the drugs being used in this study and those patients who do not give consent for the study. Pre-anaesthetic assessment of the patient was done with a complete history, physical examination and routine investigations. Written Informed consent was obtained from all the patients. All the patients were premedicated, preoxygenated and endotracheal intubation was done. Anaesthesia was maintained with nitrous oxide and oxygen. The patients were categorised into two different groups using the sealed envelope method. Sevoflurane was cut off in both the groups before drug administration. Group D received dexmedetomidine infusion of 0.75 microgram / kg in 100 ml of 0.9 % sodium chloride over a period of fifteen minutes before the anticipated time of extubation Group L received preservative free lignocaine 2 % at the dose of 1.5 mg / kg bolus intravenously, two minutes before the time of extubation. Reversal from the neuromuscular blockade was done with Inj. Glycopyrrolate 10 mcg / kg and Inj. Neostigmine 50 mcg / kg and the trachea was extubated when the spontaneous breathing efforts were adequate and the patient obeyed commands. Initial parameters like the heart rate, systolic arterial blood pressure, diastolic arterial blood pressure and mean arterial pressure were documented in both the groups during intubation and during extubation and at 1, 3, 5 minutes following endotracheal extubation and after that every five minutes for up to thirty minutes in both the groups D and L. Extubation response was analysed on a 5 point score (extubation quality score) based on the patient’s comfort and response. Emergence - agitation was analyzed on a six point score based on the patient’s response. Any adverse event like vomiting, respiratory depression, laryngospasm, bronchospasm, bradycardia (heart rate<60), hypotension (Mean Arterial Pressure<60 mm Hg) were recorded. The data was coded and entered into Microsoft Excel spreadsheet. Analysis was done using SPSS version 20, Windows software program. Descriptive statistics included computation of percentages, means and standard deviations. The unpaired t test (for quantitative data to compare two independent two groups) was used for quantitative data comparison of all clinical indicators. Chi-square test was used for qualitative data whenever two or more than two groups were used to compare. Level of significance was set atP≤0.05.
RESULTS In present study, patients were divided in following 2 groups with 50 patients in each group as group D (Dexmedetomidine) and group L (Lignocaine). Age, gender, mean BMI were comparable in both groups and difference was not significant statistically.
Table 1: General characteristics
The mean heart rate before extubation, during extubation and after extubation was calculated in both groups. The mean heart rate before extubation was comparable in Dexmedetomidine group and Lignocaine group, difference not significant statistically. The difference between mean heart rate during extubation, after extubation at 1, 3, 5, 10, 15, 20, 25, 30 minutes in dexmedetomidine group and lignocaine group was statistically significant. Table 2: Heart rate
The mean systolic blood pressure before extubation was comparable in Dexmedetomidine group and Lignocaine group, difference not significant statistically. The difference between mean systolic blood pressure during extubation, after extubation at 1, 3, 5, 10, 15, 20, 25, 30 minutes in dexmedetomidine group and lignocaine group was statistically significant. Table 3: Systolic Blood Pressure
The mean diastolic blood pressure before extubation was comparable in Dexmedetomidine group and Lignocaine group, difference not significant statistically. The difference between mean diastolic blood pressure during extubation, after extubation at 1, 3, 5, 10, 15, 20, 25, 30 minutes in dexmedetomidine group and lignocaine group was statistically significant. Table 4: Diastolic Blood Pressure
The mean arterial blood pressure before extubation was comparable in Dexmedetomidine group and Lignocaine group, difference not significant statistically. The difference between mean arterial blood pressure during extubation, after extubation at 1, 3, 5, 10, 15, 20, 25, 30 minutes in dexmedetomidine group and lignocaine group was statistically significant. Table 5: Mean arterial pressure
In Dexmedetomidine group, 12% of the patients had no cough during extubation, 72% of the patients had smooth extubation with minimal cough and 16% of the patients had moderate cough. In Lignocaine group, 22% of the patients had smooth extubation with minimal cough, 74 % of the patients had moderate cough during extubation and 4% of the patients had severe cough. Table 6: Extubation Quality Score
In Dexmedetomidine group, 36% of the patients were calm, oriented and co-operative during extubation. 64% of the patients were drowsy but responding to commands. In Lignocaine group, 12% of the patients were apprehensive, restless or agitated. 82% of the patients were calm, oriented and co-operative during extubation. 6% of the patients were drowsy but responded to commands. Statistical analysis of the Emergence agitation score shows a P value of 0.001 which is significant statistically. Table 7: Emergence Agitation Scale
In Dexmedetomidine group, 2% of the patients had vomiting during extubation and in Lignocaine group, 4% of the patients had vomiting. 11 patients in dexmedetomidine group had bradycardia (heart rate less than 60/minute) whereas 2 patients in the lignocaine group had bradycardia. Table 8: Adverse events
DISCUSSION During extubation of trachea, the cause of hemodynamic changes has multiple reasons such as pain at surgical site, anaesthesia emergence and irritation of trachea.6 Emergence from anaesthesia and extubation of trachea causes hemodynamic changes which is due to tracheal irritation and post-operative pain. Exaggerated responses to tracheal extubation can cause increased intracranial pressure, myocardial ischemia, arrhythmias, raised intraocular pressure. Coughing and bucking in intubated patients occurs in 40% of patients on emergence from general anaesthesia.7 Coughing maybe harmful because it causes increases in blood pressure, heart rate, intrathoracic pressure, intraabdominal pressure, intracranial pressure and intraocular pressure. Thus coughing exacerbates pain, edema, venous bleeding, hematoma and bronchospasm. Cough at extubation increases morbidity risk after surgical procedures. Smooth emergence from general anaestheisia with minimal coughing is desirable.8,9 These responses are well tolerated in healthy patients but maybe dangerous in patients with coronary artery disease, intracranial pathology and vascular anomalies. Many methods have been tried to attenuate the hemodynamic changes associated with extubation. Sharma et al.,10 found that heart rate increased during extubation in all three groups as compared to baseline values. The heart rate remained significantly high after 5 minutes of the drug administration in lignocaine group and placebo group, use of dexmedetomidine was associated with less increase in heart rate as compared to lignocaine group. In present study, heart rate variations between dexmedetomidine and lignocaine groups was statistically significant from the extubation time till the time the observations were recorded. Kotak et al.,11 observed that bolus dose of dexmedetomidine 0.5 microgram/kg given before extubation caused a better control of systolic blood pressure after extubation as compared to esmolol 1mg/kg. In present study, better control of systolic blood pressure was seen with the use of dexmedetomidine as compared to that of lignocaine. R. Amutharani et al.,12 observed that Dexmedetomidine group showed a lesser rise in diastolic blood pressure compared to fentanyl group from 5 minutes before extubation to 130 minutes after extubation which was statistically significant. In present study, the variations in diastolic blood pressure between Dexmedetomidine group and Lignocaine group were statistically significant from the time of extubation till the time the observations were done. Tung et al.,13 observed that all study medications- lignocaine (intravenous, intracuff, tracheal tube or topical applications), dexmedetomidine, remifentanil and fentanyl were better than placebo or no medication in reducing moderate to severe emergence cough, with dexmedetomidine ranked the most effective. Similar findings were noted in present study. Saidie, et al.,14 observed that dexmedetomidine reduced agitation in patients during extubation. Similar findings were noted in present study. Limitations of present study were small sample size,and from single hospital. Multicentric larger studies with are required to validate the results.
CONCLUSION From this prospective randomised comparative study, we can conclude that administration of Dexmedetomidine before tracheal extubation was more effective in maintaining the hemodynamic stability, facilitated smooth tracheal extubation and had a better quality of recovery as compared to Lignocaine.
REFERENCES
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