Year : 2015 | Volume
| Issue : 4 | Page : 376-380
Comparative study between paracetamol and two different doses of pregabalin on postoperative pain in laparoscopic cholecystectomy
Ibrahim M Esmat, Hanan M Farag
Lecturer of Anesthesia and Intensive Care and Pain Management, Ain Shams University, Cairo, Egypt
Hanan M Farag
Africa St. project 41 building 14, district 8, Nasr city, Cairo, Zip code: 11817
Source of Support: None, Conflict of Interest: None
|Date of Web Publication||16-Sep-2015|
Background: Postoperative pain is the primary reason for prolonged hospital stay after laparoscopic cholecystectomy. This study compared the effect of a single oral preoperative administration of paracetamol (1 g) with 2 different doses of pregabalin (150 or 300 mg) for attenuating postoperative pain and analgesic consumption. Materials and Methods: Seventy-five patients, aged 18-60 years, American Society of Anesthesiologists' physical status I and II undergoing elective laparoscopic cholecystectomy were included in this randomized controlled study. Patients were divided into three groups, 25 each to receive either oral paracetamol 1 g (group I, control group) or pregabalin 150 (group II) or 300 mg (group III), 2 h before surgery. Postoperative pain was evaluated based on visual analog scale over a period of 6 h and 1 st time for rescue analgesia. Postoperative sedation, hemodynamic changes, serum cortisol level, and side effects were also evaluated. Results: There was a significant decrease in mean heart rate, mean systolic blood pressure, sedation score, pain score, and delayed the first request for analgesics postoperatively in group (II) and group (III) compared to group (I) 2 h postoperatively. There was no significant difference in group (III) compared to group (II) postoperatively. The incidence of postoperative side effects was more in group (III). Conclusion: The single oral preoperative dose administration of pregabalin had significant opioid-sparing effect in the first 6 h after surgery, whereas side effects were more common with administration of pregabalin 300 mg.
Keywords: Analgesia, cholecystectomy, pain, paracetamol, pregabalin
|How to cite this article:|
Esmat IM, Farag HM. Comparative study between paracetamol and two different doses of pregabalin on postoperative pain in laparoscopic cholecystectomy. Saudi J Anaesth 2015;9:376-80
|How to cite this URL:|
Esmat IM, Farag HM. Comparative study between paracetamol and two different doses of pregabalin on postoperative pain in laparoscopic cholecystectomy. Saudi J Anaesth [serial online] 2015 [cited 2022 Jan 26];9:376-80. Available from: https://www.saudija.org/text.asp?2015/9/4/376/159459
| Introduction|| |
"Freedom from pain should be a basic human right, limited only by our knowledge to achieve it."  Recent advances in the pathophysiology of pain have suggested that it is possible to prevent or to attenuate the central neural hyperexcitability that contributes to enhanced postoperative pain.  Early postoperative pain is the most common complaint after elective laparoscopic cholecystectomy. In 17-41% of the patients, pain is the main reason for overnight hospital stay after day case surgery.  Intense acute pain after laparoscopic cholecystectomy might predict the development of chronic pain (e.g., postlaparoscopic cholecystectomy syndrome). 
Pregabalin is a structural analog of γ-aminobutyric acid, which shows the analgesic, anticonvulsant, and anxiolytic effects. In many countries, it is approved for the treatment of neuropathic pain.  Like its predecessor, gabapentin, it binds to the α-2-d subunit of voltage-gated calcium channels, reducing the release of several excitatory neurotransmitters (including glutamate, norepinephrine, substance P, and calcitonin gene-related peptide) and blocking the development of hyperalgesia and central sensitization.  Pregabalin is more potent than the similar drug, gabapentin. It is rapidly absorbed orally with >90% bioavailability, achieves peak plasma levels within 30 min to 2 h. and shows linear pharmacokinetics.  The most common adverse events are dizziness and somnolence, and pregabalin has no effect on arterial blood pressure or heart rate. 
Paracetamol (acetaminophen; N-acetyl-p-aminophenol) is well-absorbed from the proximal small bowel and is not subject to significant first-pass metabolism in the liver, with oral bioavailability estimated at between 63% and 89% in adults.  The minimum plasma paracetamol level required for analgesia and antipyresis is thought to be 10 μg/ml, and the therapeutic range is usually stated to be 10-20 μg/ml.  150 μg/ml is considered to be the threshold for potential hepatotoxicity.  Peak plasma concentration (Cmax) is achieved approximately 45 min after 1 g orally.  Paracetamol inhibits both isoforms of cyclooxygenase (COX); the constitutive COX-1 and the inducible COX-2. Paracetamol displays weak anti-inflammatory activity, few or no gastrointestinal side effects and only a small dose-dependent alteration of platelet function. Current evidence points to multisite activity in the central nervous system, involving inhibition of prostaglandin synthesis and interaction with both serotonergic and cannabinoid pathways. 
The stress response to surgery is characterized by increased secretion of pituitary hormones and activation of the sympathetic nervous system. The changes in the pituitary secretions have secondary effects on hormone secretion from target organs (increased secretion of cortisol from the adrenal cortex). 
The present study was therefore designed to evaluate the role of a preoperative single oral dose of paracetamol (1 g) in comparison to preoperative single oral dose of two different doses of pregabalin (150 mg or 300 mg) for attenuating postoperative pain and analgesic consumption in patients undergoing laparoscopic cholecystectomy.
| Materials and Methods|| |
This randomized controlled study was conducted on 75 patients aged between 18 and 60 years old of both sex of American Society of Anesthesiologists (ASA) physical status I and II of 70-90 kg body weight and height 160-180 cm undergoing elective laparoscopic cholecystectomy under general anesthesia. The study protocol was approved from the Institutional Ethical Committee and written informed consent was obtained from all the patients.
Patients with impaired kidney or liver functions, history of cardiac or central nervous system disease, history of drug or alcohol abuse, history of chronic pain or daily intake of analgesics, uncontrolled medical disease (diabetes mellitus and hypertension), history of intake of nonsteroidal anti-inflammatory drugs within 24 h before surgery or allergy to the used medications, and duration of operation >90 min were excluded from the study.
Patients meeting the inclusion criteria during the preanesthetic evaluation were randomly assigned into three groups of 25 each to receive1 g paracetamol (group I, control group) or pregabalin 150 mg (group II) or pregabalin 300 mg (group III) orally 2 h before induction of anesthesia with sips of water. Assessment of postoperative pain, sedation, postoperative monitoring of heart rate, mean systolic and mean diastolic blood pressure, and side effects (e.g., vomiting, blurring of vision, and excessive sedation) were done every 30 min for 2 h and after 6 h.
Postoperative pain was evaluated based on visual analog scale (VAS), 1 st time to ask for rescue analgesia administered over a period of 6 h postoperatively. Before the surgery, patients were instructed in the use of VAS for pain assessment postoperatively where 0 cm defines no pain, and 10 cm defines the maximum intolerable pain. Patients with (VAS) >3 were given extra-analgesic doses in the form of 0.5 mg/kg pethidine intramuscularly. Assessment of sedation was according to sedation score where 0 = alert, 1 = sleepy and arousable by verbal command, 2 = sleepy and arousable by tactile stimulation and 3 = sleepy and arousable by painful stimulation.
Serum cortisol was measured by a fluorescence polarization immunoassay technology by the Abbott AxSYM system with the following reference ranges (morning serum cortisol 4.2-38.4 μg/dl) and evening serum cortisol 1.7-16.6 μg/dl). Serum cortisol level was measured 1 h postoperatively.
The general anesthesia technique was standardized for all the patients as well as monitors including 5 lead electrocardiography (ECG), noninvasive blood pressure (NIBP) monitor, pulse oximetry, and capnography after intubation using Datascope monitors. Neuromuscular function was also monitored using a peripheral nerve stimulator. After establishing an intravenous (IV) line, induction of general anesthesia with fentanyl (2 μg/dl) and sleeping dose of propofol followed by rocuronium (0.6 mg/kg) to facilitate orotracheal intubation was done. Anesthesia was maintained using sevoflurane in oxygen and air. Granisetron (1 mg IV) was given as a prophylactic antiemetic. At the end of the surgery, the residual neuromuscular paralysis was antagonized with neostigmine (0.05 mg/kg) and atropine (0.01 mg/kg). After satisfactory recovery, patients were extubated and transferred to the postanesthesia care unit where they were monitored with ECG, NIBP, and pulse oximetry.
| Results|| |
Analysis of data
Using PASS for sample size calculation, it was calculated that a sample size of 22 patients per group will achieve 80% power to detect differences in the mean-time to 1 st rescue analgesia of 90 min between the three groups with a standard deviation (SD) within a group assumed to be 41.77 using an F test with a 0.05000 significance level. Data were analyzed using SPSS 18.0 for Windows (SPSS, Chicago, IL, USA). Analysis of variance was used to compare the three groups for quantitative parametric data and if there was a significant difference among the groups, a post-hoc Tukey's test was performed. Kruskal-Wallis test was used for quantitative nonparametric data. Chi-square test was used for comparison of qualitative data. Continuous parametric data were presented as mean ± SD, nonparametric data as median (interquartile range) and categorical data were presented as number of patients. P < 0.05 were considered significant and < 0.001 highly significant.
A total of 85 patients were assessed for eligibility from March 2008 to April 2009 [Figure 1], out of which 78 patients received study medication after randomization and 75 patients completed the study (25 patients for each group) [Figure 1]. Seven patients were not included in this study on account of patient's refusal (4 patients) and history of chronic analgesic consumption (3 patients). Three patients were considered as drop-outs after initial randomization and were therefore not subjected to further statistical analysis (two patients underwent conversion to open cholecystectomy, and one patient needed re-exploration on account of the postoperative bleed).
Results of the current study did not show significant difference in the demographic data of the groups of patients as regard age, height, body weight, male to female ratio, ASA physical status and the length of surgery in minutes as shown in [Table 1].
There was a significant decrease in the mean heart rate in the group (II) and group (III) compared to group (I) 30 min, 1 h, 1.5 h, and 2 h postoperatively as shown in [Table 2]. There was not a significant difference in the mean heart rate in the group (III) compared to group (II) at any time postoperatively and there was not a significant difference in the mean heart rate between the three groups 6 h postoperatively.
There was a significant decrease in the mean systolic blood pressure in the group (II) and group (III) compared to group (I) 30 min, 1 h, 1.5 h, and 2 h postoperatively as shown in [Table 3]. There was not a significant difference in the mean systolic blood pressure in the group III compared to group (II) at any time postoperatively and there was no statistically significant difference between these groups of patients 6 h postoperatively.
There was no significant difference between the three groups 30 min, 1 h, 1.5 h, 2 h, and 6 h postoperatively as regard the mean diastolic blood pressure (P > 0.05).
Sedation score was significantly higher in group (II) and group (III) than in group (I) in the first 2 h postoperatively as shown in [Figure 2]. Sedation score was significantly higher in group (III) than in group (II) in the first 2 h postoperatively.
|Figure 2: Comparison between the three groups of patients as regard sedation score. The middle line in each box represents the median, the outer margins of the box represent the interquartile range, and whiskers represent minimum and maximum|
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There was a significant reduction in VAS in group (II) and group (III) in comparison to group (I) at the first 30 min to 2 h postoperatively as shown in [Figure 3]. Pain score was lower in group (III) compared to group (II) 2 h postoperatively and this was not significant.
|Figure 3: The visual analog scale. The middle line in each box represents the median, the outer margins of the box represent the interquartile range, and whiskers represent minimum and maximum|
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There was significant reduction as regards the time for first requirement for analgesia postoperatively between group (II) and group (III) in comparison to group (I) at the first 30 min to 2 h postoperatively [Table 4].
|Table 4: The time for the first requirement for analgesia (min) and serum cortisol changes (in μ g/dl) postoperatively|
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As regard serum cortisol level, there was a significant difference postoperatively between group (II) and group (III) in comparison to group (I) at 1 h postoperatively [Table 4].
There was no significant difference between group (II) and group (III) 1 h postoperatively as regards the time for the first requirement for analgesia and serum cortisol level [Table 4].
The occurrence of postoperative vomiting was significant (P < 0.01) in group (III) (9 patients) while it was absent in group (I) and group (II), in spite of premedication by granisetron (IV). There was significant excessive sedation and blurring of vision (P < 0.001) in group (III) (12 patients).
| Discussion|| |
Optimal pain relief postoperatively is important as it may reduce postoperative complications and encourage early discharge from hospital. The ideal method for postoperative pain relief should be simple to perform, inexpensive, and causes minimal morbidity. 
The results of the present study demonstrated that the single preoperative oral dose of pregabalin (150 mg or 300 mg) had delayed the first request for analgesics postoperatively compared to the group with single preoperative oral dose of paracetamol (1 g).
These results are in agreement with the findings of Girija et al. who reported that the administration of single preoperative dose of oral pregabalin 150 or 300 mg was effective in reducing postoperative pain and total fentanyl consumption in patients undergoing lumbar laminectomy and discectomy. 
Agarwal et al. also reported that oral pregabalin 150 mg administered before the operation was effective in reducing postoperative pain and the postoperative patient-controlled fentanyl requirement in patients undergoing laparoscopic cholecystectomy. 
Paech et al. found that no better pain relief than placebo and an increase in side effects, after a single preoperative dose of pregabalin 100 mg in patients have day-case uterine surgery. 
These results were partially consistent with Peng et al. who reported that multiple doses of pregabalin resulted in superior analgesia only in the first 90 min over placebo. Pregabalin 75 mg offered better analgesia compared with pregabalin 50 mg. However, pregabalin did not result in a reduction in opioid consumption, clinical meaningful side effects or an improvement in quality of recovery. 
In this study, sedation score was significantly higher in group (II) and group (III) than in group (I) in the first 2 h postoperatively.
This result was supported by the study of Girija et al. who reported that the sedation score was higher postoperatively in patients received single preoperative dose of oral pregabalin 300 mg than patients received single preoperative dose of oral pregabalin 150 mg undergoing lumbar laminectomy and discectomy. 
Hill et al., Chang et al. and Kim et al. had evaluated postoperatively the undesirable side effects of preoperative oral pregabalin 300 mg, e.g., excessive sedation, blurring of vision, dizziness, and postoperative nausea and vomiting. ,,
| Conclusion|| |
The single preoperative dose administration of pregabalin (150 or 300 mg) had a significant opioid-sparing effect in the first 2 h after surgery. The postoperative undesirable side effects of preoperative oral pregabalin 300 mg, e.g., excessive sedation, blurring of vision, and postoperative nausea and vomiting were significantly common. The use of preoperative oral pregabalin 150 mg was an effective and a safe adjuvant for acute pain after surgery.
| References|| |
Melzack R. Psychological aspects of pain: Implications for neural blockade. In: Cousins MJ, Bridenbaugh PO, editors. Neural Blockade in Clinical Anesthesia and Management of Pain. 2 nd
ed. Philadelphia: J.B. Lippincott; 1989. p. 845-60.
Wall PD. The prevention of postoperative pain. Pain 1988;33:289-90.
Lau H, Brooks DC. Predictive factors for unanticipated admissions after ambulatory laparoscopic cholecystectomy. Arch Surg 2001;136:1150-3.
Bisgaard T, Rosenberg J, Kehlet H. From acute to chronic pain after laparoscopic cholecystectomy: A prospective follow-up analysis. Scand J Gastroenterol 2005;40:1358-64.
Kavoussi R. Pregabalin: From molecule to medicine. Eur Neuropsychopharmacol 2006;16 Suppl 2:S128-33.
Shneker BF, McAuley JW. Pregabalin: A new neuromodulator with broad therapeutic indications. Ann Pharmacother 2005;39:2029-37.
Frampton JE, Scott LJ. Pregabalin: In the treatment of painful diabetic peripheral neuropathy. Drugs 2004;64:2813-20.
Reuben SS, Buvanendran A, Kroin JS, Raghunathan K. The analgesic efficacy of celecoxib, pregabalin, and their combination for spinal fusion surgery. Anesth Analg 2006;103:1271-7.
Ward B, Alexander-Williams JM. Paracetamol revisited: A review of the pharmacokinetics and pharmacodynamics. Acute Pain 1999;2:140-9.
Anderson BJ, Holford NH, Woollard GA, Kanagasundaram S, Mahadevan M. Perioperative pharmacodynamics of acetaminophen analgesia in children. Anesthesiology 1999;90:411-21.
Rumack B. Acetaminophen hepato-toxicity: The first 35 years. J Toxicol Clin Toxicol 2002;40:3-20.
Rygnestad T, Zahlsen K, Samdal FA. Absorption of effervescent paracetamol tablets relative to ordinary paracetamol tablets in healthy volunteers. Eur J Clin Pharmacol 2000;56:141-3.
Graham GG, Scott KF. Mechanism of action of paracetamol. Am J Ther 2005;12:46-55.
Desborough JP. The stress response to trauma and surgery. Br J Anaesth 2000;85:109-17.
Casey KL. Concepts of pain mechanisms: The contribution of functional imaging of the human brain. Prog Brain Res 2000;129:277-87.
Girija PR, Rahul Y, Arvind C, Hari HD.A63 Effects of pregabalin on postoperative pain and preoperative anxiety in patients undergoing lumbar discectomy. Eur J Anaesth 2012, Vol 29 Supplement 49 Neuroanaesth S19.
Agarwal A, Gautam S, Gupta D, Agarwal S, Singh PK, Singh U. Evaluation of a single preoperative dose of pregabalin for attenuation of postoperative pain after laparoscopic cholecystectomy. Br J Anaesth 2008;101:700-4.
Paech MJ, Goy R, Chua S, Scott K, Christmas T, Doherty DA. A randomized, placebo-controlled trial of preoperative oral pregabalin for postoperative pain relief after minor gynecological surgery. Anesth Analg 2007;105:1449-53.
Peng PW, Li C, Farcas E, Haley A, Wong W, Bender J, et al.
Use of low-dose pregabalin in patients undergoing laparoscopic cholecystectomy. Br J Anaesth 2010;105:155-61.
Hill CM, Balkenohl M, Thomas DW, Walker R, Mathé H, Murray G. Pregabalin in patients with postoperative dental pain. Eur J Pain 2001;5:119-24.
Chang SH, Lee HW, Kim HK, Kim SH, Kim DK. An evaluation of perioperative pregabalin for prevention and attenuation of postoperative shoulder pain after laparoscopic cholecystectomy. Anesth Analg 2009;109:1284-6.
Kim SY, Jeong JJ, Chung WY, Kim HJ, Nam KH, Shim YH. Perioperative administration of pregabalin for pain after robot-assisted endoscopic thyroidectomy: A randomized clinical trial. Surg Endosc 2010;24:2776-81.
[Figure 1], [Figure 2], [Figure 3]
[Table 1], [Table 2], [Table 3], [Table 4]
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