Tusharbhai D. M, Baliga M, Kamath S, Mishra A. Comparison of Propofol-Fentanyl Versus Propofol-Ketamine Combination as Total Intravenous Anesthesia in Maxillofacial Surgical Procedures – A Prospective Randomized Controlled Study. Biomed Pharmacol J 2022;15(2)
Manuscript received on :23-04-2021
Manuscript accepted on :03-06-2022
Published online on: 30-06-2022
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Dani Mihir Tusharbhai 1*, Mohan Baliga1, Shaila Kamathand Aananya Mishra1

1Department of Oral and Maxillofacial Surgery, Manipal College of Dental Sciences, Mangalore, Manipal Academy of Higher Education, India.

2Department of Anesthesiology, Kasturba Medical College, Mangalore, Manipal Academy of Higher Education, India.

Corresponding Author E-mail: mihirdani26@gmail.com

DOI : https://dx.doi.org/10.13005/bpj/2428

Abstract

Background: Total intravenous anesthesia (TIVA) is a technique where drugs are administered intravenously for the induction and maintenance of anesthesia instead of volatile drugs, avoiding some of the drawbacks of inhalation anesthesia providing rapid and complete recovery making it suitable for daycare surgeries. Aim: To compare the intraoperative and postoperative hemodynamic patterns, postoperative recovery time, and unwanted consequences such as post-operative nausea and vomiting (PONV) in various maxillofacial procedures using a combination of two drug regimens, namely propofol-ketamine and propofol-fentanyl. Patient & methods: 40 patients between the age group of 18-40 years of either gender were randomly divided into two groups with propofol-ketamine (group 1, n=20) and propofol-fentanyl (group 2, n=20) who underwent various surgical procedures like cyst enucleation, open reduction and internal fixation (ORIF) of facial fractures, orthognathic procedures such as maxillary or mandibular segmental osteotomy and genioplasty with the procedure lasting 60 to 75 minutes. This study compared the total amount of propofol, time of the infusion, and hemodynamic parameters like mean pulse rate (PR), oxygen saturation level (SpO2), systolic blood pressure (SBP) & diastolic blood pressure (DBP), emergence time & recovery time, undesirable sequels like postoperative nausea and vomiting (PONV) and any other side effects between both the groups.  Results were analyzed statistically using an independent t-test and chi-square test. Results: A comparison of two groups revealed a significant rise in systolic blood pressure in group 1 as compared to group 2 and group 2 showed better emergence time & recovery time with fewer incidences of postoperative nausea and vomiting and other side effects. Conclusion: Since the propofol-fentanyl provided significantly good results it can be considered as an alternative to gaseous anesthetic agents in various maxillofacial surgical procedures mentioned in the materials with the surgical procedure lasting 60-75 minutes.

Keywords

Fentanyl; Intravenous anesthesia; Ketamine; Maxillofacial Surgical Procedures; Propofol

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Tusharbhai D. M, Baliga M, Kamath S, Mishra A. Comparison of Propofol-Fentanyl Versus Propofol-Ketamine Combination as Total Intravenous Anesthesia in Maxillofacial Surgical Procedures – A Prospective Randomized Controlled Study. Biomed Pharmacol J 2022;15(2)

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Tusharbhai D. M, Baliga M, Kamath S, Mishra A. Comparison of Propofol-Fentanyl Versus Propofol-Ketamine Combination as Total Intravenous Anesthesia in Maxillofacial Surgical Procedures – A Prospective Randomized Controlled Study. Biomed Pharmacol J 2022;15(2). Available from: https://bit.ly/3Ow3bwh

Introduction

Various Maxillofacial surgeries are executed globally under general anesthesia amid which volatile agents have remained the conventional choice for the maintenance of anesthesia, often imperiled to added stress to the patients, increased side effects, the higher cost feature and uneasiness for the patient. Economic constraints including prolonged hospital stays have encouraged both the surgeons and anesthesiologists for the alteration and improvements in the existing anesthetic procedures. 1

Ever since GA’s establishment in surgery, its recent variation total intravenous anesthesia has undergone lots of evolution. Total intravenous anesthesia (TIVA) is a technique where drugs are administered intravenously instead of volatile drugs. The benefits of TIVA includes it evades several shortcomings of inhalation anesthesia while delivering rapid and painstaking recovery in addition to fewer incidence of post-operative nausea and vomiting (PONV), which makes it convenient for daycare surgeries. It is relatively less noxious and it diminishes the risk of malignant hyperthermia and environmental hazards such as ozone depletion in stratosphere and greenhouse warming in the troposphere. 2,3 As compared to inhalational anesthesia, TIVA has numerous benefits such as no operational room pollution, marginal cardiac depression, minor neuro-humoral response, and reduced oxygen consumption. 4

In the current era, TIVA has added more popularity with the development of newer induction agents, amnestic agents and opioids and along with advances of automated infusion pumps including target-controlled infusion system (TCI) and syringe pumps. 5

Several drugs have been tried in the search for an ideal intravenous drug but none of the single-agent can deliver all properties, hence various combinations of different drugs are advocated to offer balanced in TIVA. 6, 7

This randomized study was aimed to compare and evaluate the combination of two drugs regimen i.e. propofol-ketamine and propofol-fentanyl for total intravenous anesthesia in terms of intraoperative and postoperative hemodynamic profile, postoperative recovery and undesirable sequels like PONV and other side effects in various maxillofacial procedures.

Materials and Methods

After obtaining the ethical committee approval (Ref. No. 17096) a prospective randomized study was carried out from November 2017 to June 2019 in our hospital.

The sample size was calculated using the formula:

Vol15No2_Com_Dan_eq1

With 95% confidence level and 90% power, 40 participants with the age group between 18-40 years were divided into two groups.

Group 1 contained propofol-ketamine (N =20)

Group 2 contained propofol-fentanyl (N =20)

For randomization of the study population, a toss of coin method to decide whether to use group 1 or group 2.

Inclusion criteria consist of patients with American Society of Anesthesiologists (ASA) status I & II, who underwent various maxillofacial procedures such as cystic enucleation (5 patients in each group), open and internal reduction (ORIF) of facial fractures (12 patients in each group) and segmental maxillary or mandibular osteotomy and genioplasty (3 patients in each group) with procedure lasting for 60-75 minutes. Exclusion criteria were patients with a history of allergy to the given drug, patients having immune-compromised state and suffering from cardiovascular disease and renal disease and with obstructive sleep apnea (OSA).

All the patients received tablet pantoprazole 40 mg along with tablet alprazolam 0.25 mg night before and 2 h before as a premedication. After the initial surgical evaluation, all the patients were evaluated by an anesthetist, assessing the patient’s medical condition and nil per oral status. Various monitors were used including a non-invasive blood pressure cuff (NIBP), electrocardiogram leads (ECG), pulse oximeter along with salter nasal cannula, after which initial vital signs were recorded. 18 gauge IV cannula was placed in the hand to obtain intravenous access for infusing drugs and fluid administration. After securing IV line injection midazolam 0.04mg/kg was injected before induction in each group. Induction of anesthesia in group 1 patients was performed with propofol in a dose of 1.0 mg/kg body weight & ketamine in the dose of 1.0 mg/kg body weight as intravenous boluses. While in group 2, it was performed with propofol in the dose of 1.0 mg/kg body weight & fentanyl 2 μg/kg body weights as intravenous boluses.

Injection succinylcholine in the dose of 1.5 mg/kg body weight was injected as a muscle relaxant in both the groups prior to intubation, after which patients were intubated with endotracheal intubation technique. Thereafter hemodynamic parameters were recorded at every 1 minute for the initial 5 minutes. Maintenance of anesthesia in group I was done with propofol in the dose of 2.0 mg/kg/hour & ketamine in the dose of 1.5 mg/kg/hour, while in group II, propofol in the dose of 2.0 mg/kg/hour & fentanyl 1.5 μg/kg/hour were administered for maintenance. Hemodynamic parameters were recorded every 10 minutes until the procedure is completed, with all the patients being ventilated with 100% oxygen. The infused drugs were terminated 5 minutes prior to the end of the surgical procedure. For the reversal of neuromuscular blockade injection neostigmine in the dose of 0.05 mg/kg body weight and injection glycopyrrolate in the dose of 10 μg/kg body weight were injected over duration of 2 to 4 minutes. Extubation was carried out when the patients were able to retain rhythmic respiration & ample tidal volume.

Following Extubation, the patients were asked to open eyes by anesthetist every minute until the patient was able to obey. The time elapsed for the patient to open the eyes after cessation of the infusion was noted as the emergence time. After Extubation, the patients were shifted to post-anesthetic care room where recovery time was recorded along with the physiological parameters were also recorded every 5 minutes up to 20 minutes. Any untoward sequel or any adverse events such as post-operative nausea, vomiting, awareness of procedure or any excitatory movements that occurred in the recovery was recorded and addressed accordingly by the surgeon and the anesthetists. After that patients were given appropriate postsurgical instructions and analgesics were administered as required for pain control.

Results

This study compared the total amount of propofol, time of the infusion, hemodynamic parameters like mean pulse rate (PR), oxygen saturation level (SpO2), systolic blood pressure (SBP) & diastolic blood pressure (DBP), emergence time & recovery time, undesirable sequels like postoperative nausea and vomiting (PONV) and any other side effects between both the groups. 22 males & 18 females belonging to ASA grade I & II in the age group of 18 to 40 years were part of the study & the results obtained were statistically analyzed using SPSS version 17. Statistical analysis was done by independent t-test & Pearson’s chi-squared test.

Comparison of age distribution, time of infusion and total propofol infused in both the group showed statistically no significant difference (Table 1).

Table 1: Comparison of age, average time infusion and total propofol infusion between two groups.

Parameters Group Mean SD   P Value
Age

(Year)

1 35.15 8.24 0.895
2 35.55 10.69

 

Average Infusion

(min)

 

1 53.00 8.01 0.846
2 53.50 8.12
Total

Propofol (mg)

1 120.00 26.75 0.735
           2 117.50 18.88

Abbreviations: SD, Standard Deviation; min, minutes; µg, microgram.

Comparison of oxygen saturation level showed higher values in group 2 both preoperatively and intraoperatively, while postoperatively it is higher in group 1. However, there was statistically no significant difference in oxygen saturation level between the 2 groups. (Table 2).

Table 2:  Comparison of oxygen saturation of both the groups.

Variable Group Mean SD P Value
Oxygen Saturation Preoperative 1 98.750 1.164 0.178
2 99.200 0.894

 

Oxygen Saturation Intraoperative 1 99.900 0.308 0.163
2 100.000 0.000

 

Oxygen Saturation

Postoperative

1 99.850 0.366 1
2 99.850 0.489

Abbreviations: SD, Standard Deviation

Comparison of SBP between both the groups at pre-induction it was higher in group 1and was statistically non- significant with a P-value of 0.054. From 1 minute (1M) of induction to 20 minutes (20M) intraoperatively shows a statistically highly significant difference with P value ˂ 0.05 with group 2 providing better values. While at 30 and 40 minutes intraoperatively shows no statistically significant difference among the two groups and at 50 minutes the comparison showed a statistically significant difference with P-value 0.013. Also comparing the systolic blood pressure postoperatively showed statistically no significant difference (Graph 1) and (Table 3).

Table 3: Comparison of systolic blood pressure of both the groups at different stages of anesthesia.

Parameter GROUP N Mean Std. Deviation P VALUE
Systolic Blood Pressure Pre-induction GROUP 1 20 133.750 7.461 0.054
GROUP 2 20 129.300 6.658
Systolic Blood Pressure 1M GROUP 1 20 135.700 8.603 0.007
GROUP 2 20 128.400 7.500
Systolic Blood Pressure 2M GROUP 1 20 135.250 10.721 0.009
GROUP 2 20 126.950 8.204
Systolic Blood Pressure 3M GROUP 1 20 135.700 10.367 0.009
GROUP 2 20 128.200 5.926
Systolic Blood Pressure 4M GROUP 1 20 136.000 10.084 0.006
GROUP 2 20 128.250 5.821
Systolic Blood Pressure 5M GROUP 1 20 135.350 11.944 0.018
GROUP 2 20 127.900 5.581
Systolic Blood Pressure 10M GROUP 1 20 135.250 10.939 0.006
GROUP 2 20 126.600 7.493
Systolic Blood Pressure 20M GROUP 1 20 135.100 8.717 0.037
GROUP 2 20 130.100 5.619
Systolic Blood Pressure 30M GROUP 1 20 134.600 11.330 0.114
GROUP 2 20 130.050 5.155
Systolic Blood Pressure 40M GROUP 1 20 132.550 10.039 0.358
GROUP 2 20 130.100 6.103
Systolic Blood Pressure 50M GROUP 1 16 137.560 9.838 0.013
GROUP 2 17 129.820 6.858
Systolic Blood Pressure 60M GROUP 1 10 133.500 9.925 0.448
GROUP 2 12 130.670 7.253
Systolic Blood Pressure PO 1M GROUP 1 20 135.100 8.669 0.098
GROUP 2 19 130.790 7.076
Systolic Blood Pressure PO 5M GROUP 1 20 133.200 7.445 0.132
GROUP 2 20 129.300 8.535
Systolic Blood Pressure PO 10M GROUP 1 20 132.700 7.767 0.094
GROUP 2 20 128.300 8.411
Systolic Blood Pressure P0 20M GROUP 1 20 129.100 8.084 0.406
GROUP 2 20 127.850 7.719

 

Vol15No2_Com_Dan_gra1 Graph 1: Comparison of systolic blood pressure of both the groups at different stages of anesthesia.

Click here to view graph

Comparison of DBP between two groups from Pre-induction to 30 minutes (30M) intraoperatively showed statistically no significant difference. While at 40 minutes (40M) comparison shows a statistically significant difference with a P-value of 0.042. Also at 20 minutes postoperatively comparison between two groups shows a statistical difference with a P value of 0.044 (Graph 2) and (Table 4).

Table 4: Comparison of diastolic blood pressure in both the groups.

 Parameter GROUP   N    Mean    Std.   Deviation         P VALUE
Diastolic Blood Pressure Pre-induction GROUP 1 20 85.850 8.580 0.295
GROUP 2 20 88.100 3.905
Diastolic Blood Pressure 1M GROUP 1 20 83.750 11.116 0.256
GROUP 2 20 86.950 5.316
Diastolic Blood Pressure 2M GROUP 1 20 86.900 9.176 0.652
GROUP 2 20 88.000 5.767
Diastolic Blood Pressure 3M GROUP 1 20 85.750 8.168 0.399
GROUP 2 20 87.650 5.696
Diastolic Blood Pressure 4M GROUP 1 20 85.300 6.959 0.681
GROUP 2 20 86.100 5.119
Diastolic Blood Pressure 5M GROUP 1 20 86.300 9.559 0.544
GROUP 2 20 87.800 5.337
Diastolic Blood Pressure 10M GROUP 1 20 86.750 7.745 0.246
GROUP 2 20 89.000 3.598
Diastolic Blood Pressure 20M GROUP 1 20 85.350 8.119 0.172
GROUP 2 20 88.250 4.447
Diastolic Blood Pressure 30M GROUP 1 20 84.550 9.058 0.133
GROUP 2 20 88.150 5.153
Diastolic Blood Pressure 40M GROUP 1 20 83.800 6.354 0.042
GROUP 2 20 87.450 4.419
Diastolic Blood Pressure 50M GROUP 1 15 85.470 5.181 0.196
GROUP 2 17 88.060 5.815
Diastolic Blood Pressure 60M GROUP 1 12 86.830 6.073 0.846
GROUP 2 12 86.420 4.122
Diastolic Blood Pressure PO 1M GROUP 1 19 86.740 5.486 0.4
GROUP 2 20 88.300 5.957
Diastolic Blood Pressure PO 5M GROUP 1 20 86.700 4.953 0.246
GROUP 2 20 88.400 4.135
Diastolic Blood Pressure PO 10M GROUP 1 20 85.100 4.855 0.913
GROUP 2 20 85.250 3.740
Diastolic Blood Pressure PO 15M GROUP 1 20 83.400 3.912 0.314
GROUP 2 20 84.800 4.731
Diastolic Blood Pressure PO 20M GROUP 1 20 80.550 3.720 0.044
GROUP 2 20 83.200 4.312

 

Vol15No2_Com_Dan_gra2 Graph 2: Comparison of diastolic blood pressure in both the groups.

Click here to view graph

Comparison of the mean pulse rate between the two groups from pre-induction to postoperatively 20 minutes shows a statistically non-significant difference with P value ˂ 0.05 (Graph 3) and (Table 5).

Table 5: Comparison of mean pulse rate between the groups.

 Parameter GROUP   N     Mean       Std. Deviation           P VALUE
Pulse Rate Pre-induction GROUP 1 20 81.600 8.840 0.215
GROUP 2 20 78.300 7.651
Pulse Rate 1M GROUP 1 20 80.400 6.533 0.896
GROUP 2 20 80.700 7.855
Pulse Rate 2M GROUP 1 20 78.700 9.493 0.329
GROUP 2 20 81.500 8.382
Pulse Rate 3M GROUP 1 20 78.950 10.050 0.264
GROUP 2 20 82.000 6.561
Pulse Rate 4M GROUP 1 20 77.700 9.734 0.401
GROUP 2 20 80.000 7.226
Pulse Rate 5M GROUP 1 20 78.700 9.565 0.603
GROUP 2 20 80.150 7.822
Pulse Rate 10M GROUP 1 20 79.200 9.671 0.693
GROUP 2 20 78.150 6.784
Pulse Rate 20M GROUP 1 20 77.850 8.580 0.857
GROUP 2 20 78.300 7.079
Pulse Rate 30M GROUP 1 20 75.700 8.323 0.731
GROUP 2 20 76.600 8.127
Pulse Rate 40M GROUP 1 20 74.450 7.437 0.458
GROUP 2 20 76.300 8.144
Pulse Rate 50M GROUP 1 16 74.000 8.319 0.205
GROUP 2 16 77.440 6.572
Pulse Rate 60M GROUP 1 10 74.400 7.749 0.752
GROUP 2 11 75.640 9.698
Pulse Rate PO 1M GROUP 1 20 73.800 7.571 0.313
GROUP 2 20 76.200 7.274
Pulse Rate PO 5M GROUP 1 20 71.300 7.841 0.178
GROUP 2 20 74.500 6.871
Pulse Rate PO 10M GROUP 1 20 70.600 6.524 0.208
GROUP 2 20 73.250 6.552
Pulse Rate PO 15M GROUP 1 20 71.100 7.532              0.749
GROUP 2 20 71.800 6.135
Pulse Rate PO 20M GROUP 1 20 70.150 7.206              0.716
GROUP 2 20 71.000 7.469

 

Vol15No2_Com_Dan_gra3 Graph 3: Comparison of mean pulse rate between the groups.

Click here to view graph

Comparison of emergence time & recovery time between both the groups was done using independent t-test, which showed emergence time and recovery time (in minutes) was higher in group 1 and was statistically non-significant with a P-value of 0.211 and 0.003 (Graph 4).

Vol15No2_Com_Dan_gra4 Graph 4: Comparison of emergence and recovery time (in minutes) of both the groups.

Click here to view figure

Comparison of postoperative incidence of nausea among two groups showed that one patient in group 1 and two patients in group 2 had an incidence of postoperative nausea which is statistically non-significant with a P-value of 0.548. While Comparing the incidence of postoperative vomiting revealed only one patient in group 1 had an incidence of postoperative vomiting which is statistically non-significant while in group 2 none of the  patient had an incidence of postoperative vomiting (Table 6).

Table 6: Comparison of post-operative side effects in both the groups.

Parameters   Group Absent count Present count P value
Nausea 1

2

18

19

2

1

0.548
Vomiting 1

2

19

20

1

0

0.311
Excitatory Movements 1

2

18

19

2

1

0.548
Awareness of procedure 1

2

20

20

0

0

Comparison of postoperative excitatory movements was done using the chi-square test showed 2 patients had an incidence of excitatory movements in group 1 and only 1 patient in group 2 had an incidence of postoperative excitatory movements. The data is statistically non-significant with a P-value of 0.54.Comparison of postoperative awareness between the two groups showed no incidence of postoperative awareness of procedure (Table 6).

Comparison of surgeon satisfaction at the end of the procedure between two groups showed group 1 had a mean value of 7.45 with SD± 0.75 and group 2 had a mean value of 7.95 with SD± 0.82. It is higher in group 2 and was statistically non-significant having P-value of 0.053 (Table 7)

Table 7: Comparison of surgeon’s satisfaction of both the groups.

Parameter Group Mean SD  P Value
Surgeon’s  Satisfaction     1 7.450 0.759 0.053
    2 7.950 0.826

Abbreviations: SD, Standard Deviation

Discussion

Total intravenous anesthesia is evolved in recent years that induces anesthesia, along with amnesia and loss of consciousness for several surgical procedures.8 The accessibility of rapid & short-acting sedative-hypnotic, analgesics & muscle relaxants has refocused the consideration of balanced anesthesia by intravenous route.9Lately TIVA has become more prevalent, beneficial and favorable for two main reasons- the first one is its  pharmacokinetics & pharmacodynamics effects of drugs like propofol and recent short-acting various opioids that make it apt for intravenous administration. And the second reason being the newer infusion techniques &latest drug delivery methods like TCI & automated infusion pumps. 10, 11

In the present study two-drug regimen, propofol-ketamine (group 1) and propofol-fentanyl (group 2) for TIVA were compared for a number of maxillofacial surgical procedures. Group 1 showed statistically no significant variation in HR & DBP throughout induction & maintenance of anesthetic procedure in comparison to group 2. But while comparing systolic blood pressure between both the groups statistically significant difference was observed with P values higher in group 1 than group 2.

Comparison of demographic data was quite similar to other studies and doesn’t show any significant difference. The mean duration time for cystic enucleation of jaws was 40-52 minutes, while mean duration time for ORIF was 51-63 minutes and for segmental maxillary and mandibular osteotomy was 58-69 minutes respectively. Our study compared the oxygen saturation between both the groups preoperatively, intraoperatively and postoperatively which showed statistically non-significant, which is clinically relevant as none of our patients had apnea intraoperatively and postoperatively.

A similar study was done where the combination of two drugs viz. propofol-ketamine & propofol-fentanyl as an I.V. anesthesia were compared on 18 patients who undertook non-cardiac surgical procedure, where they observed a decrease in both the SBP & DBP after induction, in patients who received propofol & fentanyl which were very similar to our study. And their results stated as propofol-ketamine as hemodynamically stable drug combination as compared to propofol-fentanyl without the need for additional analgesics. 12

Another study was done where they compared the two-drug combinations using propofol–ketamine & propofol–fentanyl for TIVA on 100 patients with the age group of 20-50 years in patients who underwent elective surgery, where Propofol–fentanyl drug combination resulted in a significantly higher drop in HR (9.28% VS 0.23%) and SBP (7.94% VS 0.12%) and DBP (8.10% VS 0.35%) as compared to propofol–ketamine drug combination. They stated that Propofol–ketamine drug combination resulted in the stable hemodynamic profile during maintenance phase whereas propofol–fentanyl was related with a mild rise in HR and SBP & DBP 13 which in contrast to our study results where propofol-fentanyl combinations showed better hemodynamic stability both during induction and maintenance phase with very fewer side effects.

Comparing the surgeon satisfaction between two groups, showed that group 2 had higher satisfaction scores and ease of performing surgery and there were minimal side effects noted by the operating surgeon with good patient compliance. Whereas comparing the postoperative awareness and excitatory movements between both the groups shows no incidence of postoperative awareness. Moreover out of 40 patients only 2 patients in propofol- ketamine and 1 patient in propofol-fentanyl group had an incidence of excitatory movements.

TIVA can be used in ASA grade I and II without any intra and postoperative complications, however, continuous monitoring of the patient during the entire procedure can be considered as a limitation.

Conclusion

In conclusion we found that propofol-fentanyl combination has the advantage of offering better in terms of hemodynamic stability and postoperative recovery profile along with minimal complications like PONV, awareness of the procedure and excitatory movements with surgeon’s satisfaction in various maxillofacial procedures. Maintaining hemodynamic stability, reducing pain on injection with propofol and preventing PONV, in TIVA technique is a contentious subject and there is no perfect method to reduce it. Propofol-Fentanyl drug combination showed good results. Hence it can be considered as a novel alternative to gaseous anesthetic agents in various maxillofacial surgical procedures lasting 60-75 minutes.

Acknowledgments: None

Conflict of Interest

We have no conflicts of interest.

Funding Sources

There is no funding source.

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