Background: Over the past few decades, there has been a growing interest in low-flow anaesthesia because of its perceived benefits of improved hemodynamic stability, decreased use of anaesthetic gases and faster recovery after surgery. However, many practitioners remain concerned about the potential risks, adequacy of depth of anaesthesia and recovery characteristics associated with low-flow techniques, which has limited its utilisation in routine practice. Objective: The goal of this study was to compare the effects of low-flow anaesthesia versus conventional anaesthesia on the hemodynamic stability during surgery and on recovery following elective surgical procedures done with general anaesthesia. Methods: This study was a comparative, prospective study that took place over 12 months at our hospital. A total of 120 patients (ASA I–II), all of whom were scheduled for elective surgical procedures under general anaesthesia, were recruited into this study and assigned to one of the two treatment groups (low-flow anaesthesia and conventional anaesthesia) equally (60 patients in each group). The sample size for this study was determined to be large enough to detect a clinically important difference between the two groups based on confidence intervals with a sample size that would provide a minimum of 80% power and 5% significance level to account for dropouts from the study. The same anaesthetic regimen was used for both groups except for the flow rates of fresh gas after induction. Intraoperative hemodynamic measurements including heart rate, systolic and diastolic blood pressure, and mean arterial pressure were measured at predetermined times. The recovery characteristics of both groups were evaluated using time until awakening, extubation time, and modified Aldrete score for recovery. Results: Intraoperative hemodynamic stability between groups receiving Low Flow Anaesthesia (LFA) and those receiving Conventional Anaesthesia (CA) was similar, with no statistically significant differences in heart rate or blood pressure at most study endpoints (deltatimes). Patients receiving LFA had better recovery profiles than those receiving CA based on faster eye-opening time, shorter extubation periods, and overall higher Aldrete Scores during the first 24 hours. There were no significant adverse events or episodes of hypoxic or hypercapnic events in either anaesthesia group. Conclusion: In elective surgical procedures, low-flow anaesthesia is as safe and effective a method as traditional, or baseline, methods and will provide comparable hemodynamic stability, plus some improved early recovery characteristics. The use of low-flow anaesthesia in routine practice may enhance recovery for patients and improve anaesthetic practices without risking additional safety issues.
Modern day Surgeries need General Anaesthesia, which provides patient safety, stability while undergoing the surgery, and fast recovery period after the surgery concludes. The conventional General Anaesthesia method uses a large amount of fresh gas flow rate to safely give the patient the oxygen/volatile anaesthetic agent, to decrease the chance the patient will breathe their own exhaled gas back into their lungs and give the anaesthetist rapid control of the depth of anaesthesia during the surgical procedure, but this method of administering anaesthesia produces an increased amount of anaesthetic used, makes the operating room more unclean, and causes the patient to lose a larger amount of heat and humidity from the lungs [1,2]. The Low flow Anaesthesia method is a cost-effective method of General Anaesthesia, along with it being more environmentally friendly, by using low flow rates after the desired depth of anaesthesia has been reached. Advances in anaesthetic workstation, gas monitoring systems, and delivery of volatile anaesthetics, have improved on both the safety and the ease of using Low Flow techniques for everyday Clinical Practice, [3] as the Low Flow Anaesthesia technique will have exhaled gases going back into the airway, this has made it possible to continue supplying the patient with humidity/temperature. This has allowed us to eliminate wasted anaesthetic gases that would normally occur in a High Flow technique and minimize the environment from exposure to volatile anaesthetic gases [4].
While these benefits exist, there are still many questions about how the effects of low-flow anaesthesia can impact an individual’s intraoperative hemodynamic stability and postoperative recovery. For example, using less fresh gas could theoretically impact the amount of oxygen delivered to a patient as well as the amount of carbon dioxide a patient can remove, both of which will determine the patient’s depth of anaesthesia and could contribute to fluctuations in a patient’s hemodynamic (e.g., changes of heart rate or blood pressure) or delays in a patient’s emergence from anaesthesia [5]. The importance of maintaining stable hemodynamic status during surgery is most significant in elective surgical patients, in whom perioperative variations in heart rate and blood pressure have been associated with many poor perioperative outcomes. The recovery from anaesthesia is also an important factor in determining the quality of a patient’s experience during the procedure (including the surgical time in the operating room), how efficiently the operating room functions, and how much postoperative care is utilized [6]. Although available studies suggest that patients can undergo low-flow anaesthesia safely when appropriately selected; variability in design and structures, anaesthetic protocols, and how outcomes were defined leads to conflicting results across studies. Further, only a limited amount of data are available from a hospitals performing high-volume surgical procedures as to the recovery characteristics in relation to hemodynamic parameters [7,8].
Therefore, it is of interest to evaluate and compare the effects of low-flow versus conventional anaesthesia on intraoperative hemodynamic stability and postoperative recovery profiles in patients undergoing elective surgeries under general anaesthesia.
Study Design and Setting This prospective comparative study was conducted in the Department of Anaesthesiology at GMC Rajouri & AH hospital over a 12-month period (January 2024 – December 2024). The study was initiated after obtaining approval from the Institutional Ethics Committee, and written informed consent was obtained from all participants. Study Population Adult patients scheduled for elective surgical procedures under general anaesthesia were assessed for eligibility. Inclusion criteria Age between 18 and 60 years American Society of Anaesthesiologists (ASA) physical status I or II Elective surgeries of expected duration ≥60 minutes Procedures requiring general anaesthesia with endotracheal intubation Exclusion criteria ASA physical status III or higher Anticipated difficult airway Known cardiovascular, respiratory, hepatic, or renal disease Body mass index >30 kg/m² Pregnancy Emergency surgeries Surgeries requiring deliberate hypotension or associated with major fluid shifts Sample Size Calculation The sample size was calculated based on the primary outcome variable, mean arterial pressure (MAP), to detect a clinically meaningful difference between the low-flow and conventional anaesthesia groups. The formula used for comparison of two independent means was: n=(2σ^2 (Z_(1-α/2)+Z_(1-β) )^2)/d^2 Where: n= required sample size per group σ= pooled standard deviation Z_(1-α/2)= standard normal deviate for a two-sided alpha error of 5% (1.96) Z_(1-β)= standard normal deviate for 80% power (0.84) d= minimum clinically significant difference between group means Based on previously published anaesthesia studies, the pooled standard deviation (σ) of MAP was assumed to be 10 mmHg, and the minimum clinically significant difference (d) was considered to be 5 mmHg. n=(2×(10)^2×(1.96+0.84)^2)/(5)^2 ┤ n=(2×100×(2.8)^2)/25 n=(200×7.84)/25=62.72 Thus, the calculated sample size was approximately 63 patients per group. Considering feasibility, study duration, and possible dropouts, 60 patients were included in each group, giving a total sample size of 120 patients. Group Allocation Eligible patients were randomly allocated into two groups using a simple randomization technique: Group L (Low-flow anaesthesia): Fresh gas flow ≤1 L/min after an initial equilibration period Group C (Conventional anaesthesia): Fresh gas flow 3–4 L/min maintained throughout surgery Anaesthetic Technique All patients received a standardized premedication according to the institutional protocol. In the operating room, standard monitoring (electrocardiography, non-invasive blood pressure, pulse oximetry, capnography, and anaesthetic gas concentration monitoring) was established. General anaesthesia was induced using intravenous drugs at standardized doses, and an appropriate neuromuscular blocker facilitated endotracheal intubation. General anaesthesia was maintained with a volatile anaesthetic agent mixed with oxygen and N2O. In the L Group, the fresh gas flow rate was reduced to less than or equal to 1 L /min after induction, while the C Group continued with conventional fresh gas flow rates throughout the entire procedure. Mechanical ventilation was adjusted to maintain normocapnia in both groups. Patients in both groups received standardized intraoperative fluid administration, analgesia, and neuromuscular blockade. Data Collection Hemodynamic parameters such as heart rate, systolic blood pressure, diastolic blood pressure and mean arterial pressure were measured at base line (pre-induction), following induction, following intubation, at 5 minutes, 15 minutes, 30 minutes and 60 minutes following induction, every 30 minutes until extubation. Postoperative recovery parameters included the time from when the patient opened their eyes to a verbal command, the time it took from the end of surgery until they were extubated, and the Modified Aldrete Score at 0, 5, 10 and 15 minutes after leaving the recovery room. Intraoperative and postoperative complications were recorded and treated as per the established facility protocols of the institution. Statistical Analysis Microsoft Excel was used to perform the data analysis, where the statistical software produced by Microsoft was utilized to enter and analyze the data. Continuous variables are reported as a mean ± standard deviation, while categorical variables are reported as corresponding frequencies and percentages. An independent Student's t-Test for Continuous Variables, Chi-square for Categorical Variables were used in the analysis for comparing groups with regards to the data collected. A p value < 0.05 indicates statistical significance.
During the study, 120 subjects were analyzed. Sixty of these subjects were administered with low-flow anaesthesia (Group L), and the other sixty subjects received conventional anaesthesia (Group C). Both groups were similar at the baseline concerning demographics and clinical characteristics. The researchers examined the intraoperative hemodynamic data throughout the following three prescribed times to determine whether both methods of providing anaesthesia produced the same degree of cardiovascular stability. In addition to this information regarding intraoperative hemodynamic, the researchers assessed the emergence time and Modified Aldrete score (a post-anaesthesia recovery metric) to quantify the postoperative recovery of both groups. The primary focus for this study was to determine if there were any differences between groups in regard to the hemodynamic trends, recovery characteristics, and safety issues around both anaesthetic techniques.
Baseline Characteristics
Table 1. Baseline demographic and clinical characteristics of study participants
This table compares baseline variables between the two groups to ensure homogeneity and minimize confounding factors.
|
Variable |
Group L (n=60) |
Group C (n=60) |
p-value |
|
Age (years) |
41.8 ± 10.2 |
42.6 ± 9.8 |
0.68 |
|
Sex (M/F) |
34 / 26 |
36 / 24 |
0.71 |
|
BMI (kg/m²) |
24.1 ± 2.9 |
24.4 ± 3.1 |
0.56 |
|
ASA I / II |
38 / 22 |
36 / 24 |
0.70 |
Table 2. Surgical and anaesthesia-related characteristics
This table demonstrates comparability of operative exposure and anaesthetic duration between the two groups.
|
Variable |
Group L |
Group C |
p-value |
|
Duration of surgery (min) |
102.4 ± 24.6 |
105.1 ± 26.2 |
0.58 |
|
Duration of anaesthesia (min) |
118.6 ± 27.9 |
121.3 ± 29.1 |
0.61 |
|
Type of surgery (abdominal/orthopaedic/others) |
28 / 22 / 10 |
30 / 20 / 10 |
0.83 |
Intraoperative Hemodynamic Parameters
Table 3. Comparison of heart rate at predefined intraoperative time points
This table evaluates heart rate trends to assess cardiovascular stability during different phases of anaesthesia.
|
Time point |
Group L (beats/min) |
Group C (beats/min) |
p-value |
|
Baseline |
78.6 ± 8.4 |
79.2 ± 7.9 |
0.66 |
|
Post-induction |
74.1 ± 7.8 |
73.6 ± 8.1 |
0.74 |
|
Post-intubation |
86.9 ± 9.6 |
88.1 ± 10.2 |
0.48 |
|
30 minutes |
75.1 ± 7.9 |
76.0 ± 8.3 |
0.57 |
|
60 minutes |
74.8 ± 7.6 |
75.6 ± 8.1 |
0.60 |
|
Extubation |
82.4 ± 8.8 |
83.9 ± 9.1 |
0.37 |
Table 4. Comparison of systolic blood pressure (mmHg)
This table compares systolic blood pressure responses across intraoperative time points.
|
Time point |
Group L |
Group C |
p-value |
|
Baseline |
124.6 ± 9.8 |
125.8 ± 10.2 |
0.52 |
|
Post-induction |
116.2 ± 8.7 |
115.4 ± 9.1 |
0.61 |
|
Post-intubation |
132.9 ± 11.3 |
134.5 ± 11.8 |
0.43 |
|
60 minutes |
118.7 ± 9.2 |
119.8 ± 9.6 |
0.55 |
Table 5. Comparison of mean arterial pressure (mmHg)
Mean arterial pressure trends reflect overall hemodynamic stability during anaesthesia.
|
Time point |
Group L |
Group C |
p-value |
|
Baseline |
93.2 ± 7.6 |
94.1 ± 7.4 |
0.51 |
|
Post-induction |
86.4 ± 6.9 |
85.7 ± 7.1 |
0.58 |
|
Post-intubation |
98.6 ± 8.2 |
99.8 ± 8.7 |
0.45 |
|
60 minutes |
88.9 ± 6.8 |
89.7 ± 7.0 |
0.56 |
Table 6. Incidence of intraoperative hemodynamic events
This table compares clinically significant hemodynamic disturbances and need for intervention.
|
Event |
Group L n (%) |
Group C n (%) |
p-value |
|
Hypotension |
6 (10.0) |
7 (11.7) |
0.77 |
|
Hypertension |
4 (6.7) |
5 (8.3) |
0.73 |
|
Bradycardia |
3 (5.0) |
4 (6.7) |
0.70 |
|
Tachycardia |
5 (8.3) |
6 (10.0) |
0.75 |
Recovery Profile
Table 7. Comparison of emergence characteristics
This table evaluates early recovery by measuring emergence and extubation times.
|
Parameter |
Group L (min) |
Group C (min) |
p-value |
|
Time to eye opening |
6.8 ± 1.9 |
8.3 ± 2.1 |
0.001 |
|
Time to extubation |
9.6 ± 2.4 |
11.2 ± 2.7 |
0.002 |
Table 8. Modified Aldrete score comparison
This table assesses immediate postoperative recovery using a standardized scoring system.
|
Time point |
Group L |
Group C |
p-value |
|
0 minutes |
8.6 ± 0.7 |
8.1 ± 0.8 |
0.004 |
|
5 minutes |
9.4 ± 0.6 |
9.0 ± 0.7 |
0.003 |
|
10 minutes |
9.9 ± 0.3 |
9.7 ± 0.4 |
0.06 |
|
15 minutes |
10.0 ± 0.0 |
10.0 ± 0.0 |
— |
Postoperative Safety
Table 9. Immediate postoperative adverse events
This table summarizes postoperative complications observed in the recovery room.
|
Event |
Group L n (%) |
Group C n (%) |
p-value |
|
Hypoxia |
0 (0) |
1 (1.7) |
0.31 |
|
Delayed emergence |
1 (1.7) |
3 (5.0) |
0.30 |
|
PONV |
5 (8.3) |
7 (11.7) |
0.54 |
Table 10. Overall perioperative safety profile
This table presents the cumulative safety outcomes across both groups.
|
Outcome |
Group L |
Group C |
p-value |
|
Any adverse event |
6 (10.0%) |
9 (15.0%) |
0.40 |
|
PACU discharge delay |
0 |
2 (3.3%) |
0.15 |
Table 1, shows that both study groups did not differ significantly from one another based upon demographic variables such as age, sex distribution, BMI, and ASA physical status. These results indicate that the randomization process was adequately performed with no baseline demographic bias affecting the hemodynamic or recovery results. In addition, Table 2, indicates that the type and duration of surgery (and also, anaesthetic exposure) were similar between the groups; this indicates that any differences noted between groups relating to intraoperative stability or recovery must be due to the different anaesthetic techniques used and not because of the procedural aspects of the study. Table 3, shows that heart rate changes during induction, intubation, maintenance, and extubation were similar in both the low-flow and conventional anaesthesia groups. This suggests that low-flow techniques did not contribute to increased sympathetic stimulation or cardiovascular stress during the critical phases of anaesthesia. Referring to Table 4, it is readily apparent that systolic blood pressure changes recorded at various key points in time during the intraoperative period were similar for both study groups. This indicates that low-flow anaesthesia provides similar levels of control over anaesthetic depth and stress response compared to conventional anaesthetic techniques. As indicated in Table 5, the trends of mean arterial pressures were similar throughout the study in both groups. This indicates that adequate perfusion pressures and hemodynamic stability equivalent to those of standard anaesthesia techniques were maintained using low-flow anaesthesia. In Table 6, we see that there were very few clinically important hemodynamic complications and that the incidence was fairly comparable between treatment groups. This further supports the cardiovascular safety of using low-flow anaesthesia in elective surgical patients. Table 7, shows that patients treated with low-flow anaesthesia had quicker emergence and extubation times than those treated with traditional techniques; suggesting a more efficient ability to rapidly remove anaesthesia during the transition to waking up; this correlated with earlier return to the patient’s protective breathing reflexes. In Table 8, the patients receiving low-flow anaesthesia were assigned higher Modified Aldrete scores when assessed shortly after completion of the surgical procedure, suggesting a better quality of immediate recovery from surgery and possibly an earlier release from the post-anaesthesia care unit. Finally, as shown in Table 9, the results showed no significant difference in the occurrences of postoperative adverse events between the low-flow and traditional anaesthesia groups. Thus, it can be stated that low-flow anaesthesia will not increase the risk of experiencing early postoperative complications, including hypoxia, delayed awakening, and postoperative nausea/vomiting, compared to traditional methodology. Additionally, as demonstrated in Table 10, the overall safety profile for both types of anaesthesia was similar with no increases in the total number of adverse events and/or post-recovery delays with use of the low-flow technique.
Compared to standard anaesthesia techniques; low-flow anaesthesia generates comparable hemodynamic stability (during the entire surgery) a lower rate of adverse perioperative events. Patients recovering from surgeries under low-flow anaesthesia have been shown to recover sooner than those recovering under standard methods; due to this; low-flow anaesthetic techniques should be incorporated as part of best practice for patient recovery as well as cardiovascular safety within the operating room.
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