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Various drugs and methods have been studied to prevent hemodynamic alterations due to stress
of surgery and anaesthesia. Dexmedetomidine, a highly selective α2 – agonist has been used by
many workers like Jalonen J et al, Bhattacharjee DP et al, Aantaa R et al, Kang WS et al,
Scheinin B et al, Jaakola ML et al, Levanen J et al, Guler G et al, Yildiz M et al, Tanskanen
PE et al, Bajwa SS Et al, Gupta K et al etc. for attenuation of hemodynamic responses in various
doses and along with various anaesthetic regimens for various types of surgeries Aho Met al
conducted a study in which dexmedetomidine was given, for the first time, to patients
undergoing a laparoscopic procedure, i.e. gynaecologic diagnostic laparoscopy, and the
hemodynamic and endocrine effects of three different doses of dexmedetomidine were
compared. All the workers have been quite successful in their efforts and have found
dexmedetomidine effective in attenuating the responses but their findings need to be further
substantiated and effectiveness of dexmedetomidine needs to be evaluated in laparoscopic
cholecystectomy.
Duration of Surgery:
The mean duration of surgery in Group A (dexmedetomidine group) was 46.67 ± 4.35 minutes
and that in group B (Control) was 47.43±396 minutes (p-value 0.478).
Extubation:
In our study, in Group A (dexmedetomidine group) during extubation, the mean
HR (81.47 ± 4.01/min), SBP(125.13 ± 2.18mmHg), DBP(82.13 ± 4.02mmHg) and
MAP(96.47 ± 5.40 mmHg) were noted and compared with group B (control group) which
were: the mean HR (86.83 ± 8.40/min), SBP (126.07 ± 8.56 mmHg), DRP(83.43 ± 6.73 mmHg)
and MAP(97.64 ± 6.86 mmHg). When compared to the baseline parameters in group B
(control group) HR, SBP, DBP and MAP were significantly higher at the time of extubation
(p value <0.05) as compared to baseline, whereas in Group A (study), SBP, DBP and MAP
were comparable to the baseline parameters Above data suggests that hemodynamics were
much more stable in dexmedetomidine group than control group during extubation
Turan Get al in 2008 examined the effects of dexmedetomidine given at the end of the
procedure to prevent hyper dynamic responses during extubation and to allow a comfortable
and high-quality recovery. They concluded that dexmedetomidine 05 mcg kg administered 5
min. before the end of surgery stabilizes hemodynamics, allows easy extubation, provides a
more comfortable recovery and early neurological examination following intracranial
operations.
Emergence from Anaesthesia:
We also observed the hemodynamics during emergence from anaesthesia i.e. time for
extubation and time to respond to oral commands and found that it was similar in both the
groups. The mean duration of surgery in group A(Study) was 46.67 ± 4.35 minutes and in
Group B (Control) was 47.43 ± 3.96 minutes (p-value 0.478). The mean duration of extubation
time in group A (dexmedetomidine group) was 6.77 ± 0.73/minutes and in control group it was
7.00 ± 0.58minutes (p-value 0.184). The mean duration of response to oral commands in Group
A(dexmedetomidinegroup) was 8.59 ± 0.70 /minutes and in group B (control group) it was
8.78 ± 0.72/minutes (p value=0.304). There was no statistically significant difference found in
the duration of surgery, extubation time and response to oral commands when compared in
both the groups (p>0.05) dexmedetomidine does not seems to have significant respiratory
depression property.
Bhattacharjee DP compared infusion of dexmedetomidine 0.2g/kg/hr and normal saline
0.2g/kg/hr in patients undergoing laparoscopic cholecystectomy and found that there was no
difference in extubation time and response to oral commands in both the groups and the
hemodynamics were much more stable as compared to placebo group during extubation in
dexmedetomidine group. These findings are similar to our study results.
Guler G et al all studied the effect of Single-dose dexmedetomidine attenuates airway and
circulatory reflexes during extubation. Five minutes before the end of surgery, patients were
given dexmedetomidine 0.5µg/kg (Group D) or saline placebo (Group P) intravenous over 60
sec. The blinded anaesthetist awoke all the patients, and the number of coughs per patient was
continuously monitored for 15 min after extubation, coughing was evaluated on a 4-point scale.
Heart rate (HR) and systolic and diastolic blood pressure (SAP, DAP) were measured before,
during and after tracheal extubation. The time from tracheal extubation and emergence from
anaesthesia were recorded, there were no differences between the groups in the incidence of
breath holding or desaturation. HR, SAP and DAP increased at extubation in both groups
(P<0.05), but the increase was less significant with dexmedetomidine. The time from tracheal
extubation and emergence from anaesthesia were similar in both groups.
Adverse complications:
We observed in our study that none of the patients had any episode of bradycardia and
hypotension in Group A (dexmedetomidine) and Group B (control). Studies using
dexmedetomidine have commonly reported cardiovascular side effects such as bradycardia,
sinus arrest and hypotension mainly because of sympatholytic effect. But none of the patient
in our study had an episode of bradycardia or hypotension which could be because we used
lower loading dose of 0.6µg/kg followed by 0.3 µg/kg/hr maintenance dose. In several study
reports, dexmedetomidine infusion rates ranging from 0.1 to 10 µg/kg/hr have been used. The
studies with higher infusion rates had more incidences of adverse effects like hypotension and
bradycardia. Also no significant respiratory depression, apnea, muscle rigidity or decrease in
SpO2 was seen in any of our patients.
In our study, none of the patients in dexmedetomidine group had nausea or vomiting in the
post-operative period, whereas 4 patients (135) in group B(control) had nausea and vomiting
(p-value 0.038).
Massad IM et al, reported that combining dexmedetomidine to other anaesthetic agents,
resulted in more balanced anaesthesia and a significant drop in the incidence of postoperative
nausea and vomiting after laparoscopic gynaecological surgeries.
Tulungullari B et al also found that those patients receiving dexmedetomidine had lesser
incidence of postoperative nausea and vomiting.
Turgut N et al used dexmedetomidine infusion in lumbar laminectomy patients Group D
received Dexmedetomidine 0.6µg/kg as bolus before induction and 0.2µg/kg/hr by infusion.
They found that before and after extubation, MAP values in Group F (fentanyl) were
significantly higher than those in Group D (dexmedetomidine). There was no statistical
difference in heart rate between the groups. Extubation time and post anaesthesia care unit
discharge time were similar in both groups. The fentanyl group patients required supplemental
analgesia earlier than the dexmedetomidine group. Postoperative nausea and vomiting were
significantly higher in Group F.
The findings of our study are in agreement with the findings of various above mentioned
investigators in that dexmedetomidine infusion intraoperatively is an effective agent to reduce
the hemodynamic fluctuations associated with laparoscopic surgery. It also reduces the
incidence of postoperative nausea vomiting.
1. There were certain limitations as our study was done in surgeries of short duration
(around one hour) and on small number of patients (30 in each group). More studies are
required to establish the effect of dexmedetomidine on surgeries of longer duration and
on large number of patients.
2. Moreover the study was done on ASA I and II patients, but the usefulness will of
immense help in high risk cardiac patients.
3. Further studies are required to modify dosage of dexmedetomidine in order to have
wider margin of safety in terms of hemodynamic perturbations without affecting its
analgesic or sedative potentials.
RECOMMENDATIONS
Aim of the study was to evaluate the efficacy of dexmedetomidine in the dose of 0.6µg/kg as
a single bolus followed by 03µg/kg infusion dose in maintaining hemodynamic response to
laryngoscopy, tracheal intubation and carboperitoneum creation in adult patients undergoing
laparoscopic surgeries and opioid requirement. After approval by the Hospital Ethics
Committee, the present study was conducted on sixty adult ASA Grade I or II patients of either
sex in the age group 18 to 60 years admitted to Batra Hospital & Medical Research Centre,
New Delhi, who underwent elective laparoscopic surgeries under general anaesthesia.
There was no statistically significant difference in the demographic data between both groups.
Both groups were comparable in terms of age, weight, sex, ASA grade distribution, duration
of surgery and volume of intra-venous fluids administered intra operatively.
The mean baseline variables (HR. SBP. DBP, MAP, SpO2) were comparable in both
groups.
When the mean Heart Rate's at different time points were compared in both groups,
significant differences were found at all time-points.
When the mean Systolic Blood Pressure’s at different time points were compared in
both groups, significant differences were found at all time-points till just after reversal.
When the mean Diastolic Blood Pressures at different points were compared in both
groups, Diastolic BP values in Group A (Study) were lower than in Group B at all time-
points, differences being significant at all time-points from skin incision till extubation.
When the averages of Mean Arterial Pressure at different time points were compared
in both groups, significant differences were found at all time points just after intubation
till just after reversal.
The mean duration of surgery in Group A and Group B were comparable and the
difference was not statistically significant (46.67 ± 4.35 minutes vs 47.43 ± 3.96
minutes)
The mean extubation time (time from end of all infusions to intubation) in Group A
(dexmedetomidine) and group B(control) were comparable and the difference was not
statistically significant (6.77 ± 0.73 minutes vs 7.00 ± 0.58). Similarly, response to oral
commands in both the groups was comparable (8.59 ± 0.7 minutes vs 8,78 ± 0.72).
In Group A(dexmedetomidine) requirement of fentanyl citrate (opioid agent used) was
significantly less as compared to that of Group B(control) (6.7% patients required single
top up fentanyl in group A and 83.3% patients required single top up, 16.7% patients
required 2 top-ups in group B (control) the difference being statistically significant.
Four patients (13%) in the control group had nausea and vomiting in the post-operative
period, difference being statistically significant and none of the patients had episode of
bradycardia, hypotension or hypertension.
CONCLUSIONS
We conclude from our study the dexmedetomidine intravenous infusion in the dose
range of loading 0.6µg/kg followed by maintenance of 0.3µg/kg/hr reduces the rise in
heart rate, systolic blood pressure, diastolic blood pressure and mean arterial pressure
associated with the creation and maintenance of pneumoperitoneum during the
laparoscopy surgical procedures.
Thus, it provides perioperative hemodynamic stability in ASA I and II grade patients
during laparoscopic surgeries because of their sedative, hypnotic anxiolytic and
sympatholytic properties.
Hence, dexmedetomidine infusion of 0.6 µg/kg followed by 0.3 µg/kg/hr as an
anaesthetic adjuvant can be used in laparoscopic surgeries to provide perioperative
hemodynamic stability and to facilitate smooth emergence from anaesthesia. It also
affords added advantage of opioid sparing properties and in preventing post op nausea
and vomiting. However further study is required to evaluate its effect on hemodynamic
parameters in high risk group patients with compromised cardio-respiratory function
undergoing laparoscopic surgical procedures.