Effect of adding 8 milligrams ondansetron to lidocaine for Bier's block on post-operative pain
Azim Honarmand, Mohammadreza Safavi, Leili Adineh-Mehr
Anesthesiology and Critical Care Research Center, Isfahan University of Medical Sciences, Isfahan, Iran
|Date of Submission||09-Jul-2012|
|Date of Acceptance||25-Aug-2012|
|Date of Web Publication||29-Jun-2013|
Anesthesiology and Critical Care Research Center, Isfahan University of Medical Sciences, Isfahan
Source of Support: Anesthesiology and Critical Care Research Center,
Isfahan University of Medical Sciences, Isfahan, Iran., Conflict of Interest: None
Background: Ondansetron has analgesic properties. The aim of the present study was to assess the analgesic effect of 8 mg ondansetron when added to lidocaine for intravenous regional anesthesia (IVRA).
Materials and Methods: Ninety patients undergoing hand surgery were randomly allocated to the three groups to receive 3 mg/kg 2% lidocaine diluted with saline to a total dose of 40 mL (Group L, n = 30) or 8 mg ondansetron plus 3 mg/kg 2% lidocaine diluted with saline to a total dose of 40 mL (group LO, n = 30) or 3 mg/kg 2% lidocaine diluted with saline to a total dose of 40 mL plus 8 mg ondansetron intravenously (Group IO, n = 30). Tourniquet pain and analgesic use were recorded before and after the tourniquet application.
Results: The sensory and motor block onset times were significantly shorter in Group LO compared with Group L and Group IO (4.2 ± 1.7 vs. 5.2 ± 0.8 and 5.1 ± 1.2 respectively, P < 0.05; 4.5 ± 1.4 vs. 5.8 ± 1.5 and 5.7 ± 1.4 respectively, P < 0.05). The sensory and motor block recovery times were significantly longer in Group LO compared with Group L and Group IO (6.1 ± 1.1 vs. 4.1 ± 1.3 and 4.5 ± 0.9 respectively, P < 0.05; 6.7 ± 1.4 vs. 4.4 ± 0.9 and 4.7 ± 0.7 respectively, P < 0.05). Post-operative VAS scores were significantly less in Group LO compared with Group L and Group IO till 24 h after tourniquet deflation ( P < 0.05).
Conclusion: The addition of 8 mg ondansetron to lidocaine for IVRA reduced intraoperative and post-operative analgesic use till 24 h.
Keywords: Anesthetic techniques, intravenous regional, lidocaine, ondansetron, pain, post-operative
|How to cite this article:|
Honarmand A, Safavi M, Adineh-Mehr L. Effect of adding 8 milligrams ondansetron to lidocaine for Bier's block on post-operative pain. Adv Biomed Res 2013;2:52
|How to cite this URL:|
Honarmand A, Safavi M, Adineh-Mehr L. Effect of adding 8 milligrams ondansetron to lidocaine for Bier's block on post-operative pain. Adv Biomed Res [serial online] 2013 [cited 2019 Jul 21];2:52. Available from: http://www.advbiores.net/text.asp?2013/2/1/52/114197
| Introduction|| |
Intravenous regional anesthesia (IVRA) is a simple, reliable and cost-effective technique of regional anesthesia that used for short operative procedures of extremities. , There are some disadvantages related to the IVRG that include: Toxicity of local anesthetic (LA), slow onset of sensory and motor block, poor muscle relaxation, tourniquet pain, and short duration of post-operative analgesia. ,
For improving block quality, prolonging post-operative analgesia, and decreasing tourniquet pain different additives combined with LA. These additives include opioids, tramadol, muscle relaxants, dexmedetomidine and non-steroidal anti-inflammatory drugs. ,,,,
Ondansetron is a specific 5-Hydroxy tryptamine-3 (5-HT3) antagonist, which is used as an antiemetic drug while has no significant side effect.  It was shown by Glaum and colleagues  that 5-HT3 antagonists interfere with peripheral effects of serotonin on nociception. Also, as Ye et al.,  showed, ondansetron has local anesthetic effects. Ondansetron can bind to the opioid mμ receptors in human and acts as an agonist. 
In a study that was performed by Farouk et al.,  it was shown that adding ondansetron 4 mg to the lidocaine for IVRA can decrease intraoperative and post-operative analgesic uses while improved sensory and motor block. The analgesic effect of this combination was limited to the first 4 h after tourniquet deflation. It was not clear that if higher dose of ondansetron (for example 8 mg) was used for this purpose, it could be prolonged the analgesic effect of lidocaine use for IVRG. The analgesic effect of ondansetron which showed in Farouk et al., study might be due to its peripheral local anesthetic effect on the nerve ending or its effect on the pain control center in the brain. This important point was not investigated in Farouk and colleagues study.
So, we designed the present study to evaluate the effect of adding ondansetron 8 mg to the lidocaine for IVRG on sensory and motor block onset and recovery time, intraoperative and post-operative pain, tourniquet pain, the quality of anesthesia, intraoperative and post-operative hemodynamic variables, and the side effects. We compared the effect of 8 mg ondansetron added to IVRG with another group which received 8 mg ondansetron intravenously to show that the analgesic effect of ondansetron was peripheral or central effect.
| Materials and Methods|| |
After obtaining institutional approval from Ethic committee of our university and written informed consent from the patients, ninety American Society of Anesthesiologist (ASA) physical status I-II patients, aged 18-65 years old, scheduled for elective hand or forearm surgery gave written informed consent to participate in this randomized prospective double-blind study. Other inclusion criteria were patients without Reynaud disease, without sickle cell anemia or who had no history of allergy to any drug used. All surgeries were tendon repair following soft tissue injury to the forearm and hand.
Two 18 gauge intravenous cannula were inserted; one in a dorsal vein of the operative hand and the other in the opposite hand for infusion of crystalloid before beginning the anesthetic block. After exsanguinations of operating arm with an Esmarch bandage, it was elevated for 3 min. After that, a 10 cm pneumatic padded double-tourniquet was placed around the upper arm and proximal cuff was inflated to 250 mmHg.
After generation of a randomization list, an anesthesiologist who was blinded to the study prepared identical syringes. Another anesthesiologist blinded to the group allocation administered concealed syringes and recorded all data. IVRA was administered in three groups. In the first group, IVRA begins in hand injury with 3 mg/kg 2% lidocaine diluted with saline (Group L, n0 = 30) to a total dose of 40 mL and in the other hand with 3 mL normal saline intravenously. In second group, IVRA begins in hand injury with 8 mg ondansetron plus 3 mg/kg 2% lidocaine diluted with saline to a total dose of 40 mL (Group LO respectively; n = 30) and in the other hand with 3 mL normal saline intravenously. In third group, IVRA begins in hand injury with 3 mg/kg 2% lidocaine diluted with saline (Group IO, n0 = 30) to a total dose of 40 mL and in the other hand with 8 mg ondansetron in volume of 3 mL intravenously.
An anesthesiologist that did not involve in data collection prepared study drug solution in similar syringe in equal volume and coded them. The administration of coded study drugs was done by resident of anesthesiologist. Data collection was performed by resident of anesthesiologist who was not aware from the study group. The sensory block was evaluated continuously at 30 seconds intervals by a pinprick performed with a 22 gauge short beveled needle. The response of patient was evaluated in the dermatomal sensory distribution of the medial and lateral antebrachial cutaneous, ulnar, median, and radial nerves. Motor function was evaluated by asking the patient to flex and extend his/her wrist and fingers, and complete motor block was considered when voluntary movement was impossible.
Onset of sensory block (defined as the time elapsed from injection of study drug to sensory block achieved in all dermatomes), and onset of motor block (defined as the time elapsed from injection of study drug to complete motor block) were also recorded. After completion of sensory and motor block, the distal cuff was inflated to 250 mmHg, and the proximal tourniquet was released. After that the surgery was begun.
MAP, HR, Spo2, visual analog scale (VAS) scores (0 = no pain and 10 = worst pain imaginable) and degree of sedation (scale 1-5, 1 = completely awake, 2 = awake but drowsy, 3 = asleep but responsive to verbal commands, 4 = asleep but responsive to tactile stimulus, 5 = asleep and not responsive to any stimulus)  were recorded before and just after tourniquet inflation, at 1, 5, 10, 15, 30 min after the injection of study drugs and at 1, 5, 10, 15, 30 min after tourniquet release.
If patients developed tourniquet pain with VAS more than 3 during operation, boluses of fentanyl 1 μg/kg were administered for tourniquet pain and total fentanyl usage was recorded. The time elapsed after tourniquet inflation to the first patient request for fentanyl was also recorded. Tourniquet duration was defined as time from initial proximal tourniquet inflation until deflation of the distal tourniquet at the end of operation. The VAS and hemodynamic parameters were recorded at 2, 4, 8, 12, and 24 h after operation.
During post-operative periods, if VAS was more than 3, 75 mg of suppository diclofenac were administered and total dose diclofenac usage was recorded. The time elapsed after tourniquet release to the first patient request for diclofenac was also recorded. All evaluations were done by an anesthesia resident blinded to the study group assignment.
Qualification of surgical condition such as disturbing movement of the arm and too much bleeding was assessed by the surgeon who did not know group allocation according to the following numeric scale: 0 = unsuccessful, 1 = poor, 2 = acceptable and 3 = perfect. In addition, the patients was asked to qualify the operative conditions according to following numeric scale: 4 (excellent) = no complaint from patient, 3 (good) = minor complaint with no need for supplemental analgesics, 2 (moderate) = complaint that required supplemental analgesics, and 1 (unsuccessful) = patient given general anesthesia at post-operative period. 
Sensory recovery time (defined as the time elapsed after tourniquet deflation up to recovery of pain in all dermatomes determined by pinprick test) was recorded. Motor block recovery time (defined as the time elapsed after tourniquet deflation up to movement of fingers) was also recorded.
The statistical analysis was performed by the SPSS 16 statistical software package. A sample size of 30, in each group had 80% power to detect a difference in means amount of intraoperative fentanyl requirement of 17.9 μg assuming that standard deviation (SD) in Group L and Group LO was 13.3 and 25.6 respectively using a 0.050 two-sided significance level.
Statistical comparisons for quantitative variables were done by using two-way ANOVA, followed by unpaired t-tests with Bonferroni's correction nominal or categorical data were analyzed and compared using the Chi-square test and Fisher's exact test, when it was appropriate. Sedation score and the quality of the anesthesia between the four groups were compared using the Kruskal-Wallis test. P < 0.05 was considered statistically significant.
| Results|| |
Ninety patients were included in the present study. No patient was excluded from the study due to any problem. Flow diagram of randomized patients was shown in [Figure 1]. No significant difference was noted among three groups with respect to demographic data, duration of surgery and tourniquet time [Table 1].
|Table 1: Patients' demographic data, duration of surgery and tourniquet inflation in three groups |
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Hear rate, mean arterial pressure and SpO 2 recorded at different time intervals was not significantly different between three groups ( P > 0.05). The sensory and motor block onset times were significantly shorter in Group LO compared with Group L and Group IO ( P < 0.05) [Table 2]. The sensory and motor block recovery times were significantly longer in Group LO compared with Group L and Group IO ( P < 0.05) [Table 2]. No significant difference was noted between Group L with Group IO regarding the above variables.
|Table 2: Onset and recovery times of sensory and motor block, initial time of tourniquet and post-operative pain, and the amount of intraoperative and post-operative analgesic needs in three groups |
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Median sedation level was no significantly difference at any intraoperative and post-operative period between three groups. The VAS scores for tourniquet pain during the intraoperative period were significantly less in Group LO compared with Group L and Group IO at 5, 10, 20, and 30 min after tourniquet inflation ( P < 0.05) [Figure 2]. There was no significant difference between Group L with Group IO in this regards.
|Figure 2: Intraoperative (tourniquet pain) visual analogue scale scores. Data are presented as mean±SD. Group L=Lidocaine group; Group LO=Lidocaine-ondansetron group; Group IO=Intravenous ondansetron group. ATI=After tourniquet inflation. *P< 0.05 vs. Group L and Group IO|
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The first time for initiation of tourniquet pain was significantly longer in Group LO compared with Group L and Group IO ( P < 0.05) [Table 2]. The total dosage of fentanyl used for relieving tourniquet pain was significantly less in Group LO compared with Group L and Group IO ( P < 0.05) [Table 2]. No significant difference was noted between Group L with Group IO regarding these variables.
The post-operative VAS scores were significantly less in Group LO compared with Group L and Group IO at 1, 3, 5, 10, 15, and 30 min after tourniquet deflation in ( P < 0.05) [Figure 3]. There was no significant difference between Group L with Group IO in this regards. Also, post-operative VAS scores were significantly less in Group LO compared with Group L and Group IO at 2, 4, 8, 12, and 24 h after tourniquet deflation ( P < 0.05) [Figure 4]. No significant difference was noted between Group L with Group IO in this regards.
|Figure 3: Post-operative visual analogue scale scores at 1, 3, 5, 10, 15, and 30 min after tourniquet release. Data are presented as mean ± SD. Group L=Lidocaine group; Group LO=Lidocaine-ondansetron group; Group IO=Intravenous ondansetron group. ATR=After tourniquet release. *P<0.05 vs. Group L and Group IO|
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|Figure 4: Post-operative visual analogue scale scores at 2, 4, 8, 12, and 24 h after tourniquet release. Data are presented as mean ± SD. Group L=Lidocaine group; Group LO=Lidocaine-ondansetron group; Group IO=Intravenous ondansetron group. ATR=After tourniquet release. *P<0.05 versus Group L and Group IO|
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The first time for rescue analgesic was significantly longer in Group LO compared with Group L and Group IO ( P < 0.05) [Table 2]. The total dosage of analgesic used for relieving post-operative pain was significantly less in Group LO compared with Group L and Group IO (P < 0.05) [Table 2]. No significant difference was noted between Group L with Group IO regarding these variables.
Quality of anesthesia which assessed by the patients and the surgeon was significantly more in Group LO compared with Group L and Group IO (P < 0.05) [Table 3]. No significant difference was noted between Group L with Group IO in this regards. No adverse effect was noted in any patient throughout the study period.
| Discussion|| |
The results of our study showed that addition of ondansetron 8 mg to lidocaine for IVRG significantly improved the onset time and duration of sensory and motor block, decreased tourniquet pain, decreased intra-operative and post-operative analgesic use till 24 h compared with Group L and Group IO without causing important side effects. The quality of anesthesia was also significantly better in Group LO compared with Group L and Group IO.
In one previous study, which was performed by Farouk,  it showed that the addition of ondansetron 4 mg to lidocaine for IVRG significantly improved the quality of anesthesia, shortened onset time and duration of sensory and motor block, lessened tourniquet pain, decreased intraoperative and post-operative analgesic use for the first 4 h after surgery. It was not clear that addition higher dose of ondansetron prolonged duration of analgesia beyond 4 h after surgery or not. Our study showed that addition of higher dose of ondansetron (8 mg) prolonged duration of postoperative analgesia till 24 h without causing significant side effects.
Ondansetron is an antagonist of 5-hydroxytryptamine-3, which used commonly for prevention or treatment of postoperative nausea and vomiting.  Also, it was shown by Ye et al.,  that ondansetron could block sodium channels similar to local anesthetics and had anti-nociceptive effect. It was demonstrated that peripheral 5-hydroxytryptamine-3 receptors were participated in the pathway of nociception. These peripheral receptors could bind to the opioid receptor and show agonist activity.  Gregory et al.,  showed that ondansetron may be effective in preventing pain following injection of propofol by binding to the opioid receptors. Ambesh et al.,  found that pain during injection of propofol can successfully prevent by administration of 4 mg ondansetron. Also, in another study performed by Reddy and colleagues,  it was shown that ondansetron 4 mg could reduce significantly pain during injection of rocuronium and propofol.
Ye and et al. colleagues  showed that ondansetron, as a local anesthetic, seems to be approximately fifteen times more potent than lidocaine because 0.1 percent ondansetron produced local anesthetic effect similar to that 1.5% lidocaine. They concluded that ondansetron's local anesthetic properties may contribute to its antiemetic effects. It was shown that there is receptors similar to enteric neuron 5-HT3 on the nociceptive primary afferent fibers (PAF) not only on the peripheral free terminal but also centrally on their spinal terminal. , These receptors are present on the neurons of the superficial lamina of the dorsal horn also. ,
Fassoulaki et al.,  showed that ondansetron could antagonize the sensory block produced by intrathecal injection of lidocaine. Cui and colleagues  concluded that stimulation of periaqueductal gray matter could increase release of 5-HT in dorsal horns of spinal cord that consequently might inhibit the nociception of dorsal horn neurons. Arcionic et al.,  showed that ondansetron was administered by continuous infusion for prevention of post-operative nausea and vomiting could reduce the analgesic effect of tramadol, which probably was due to blocking of spinal 5-HT3 receptors. The 5-HT3 receptors, which are present on PAF (from the nociceptors up to the dorsal horn) mediate pronociceptive action while those receptors located postsynaptically in relation to PAF mediate the antinociceptive effect of endogenous (5-HT) or administered agonist. ,
It was showed by the Zeitz et al.,  that peripheral 5-HT3 receptors acts as a novel complement for the primary afferent nociceptors. As tourniquet inflation prevent whole body distribution of ondansetron. Our study may be useful model for investigating mechanism of peripheral action of ondansetron. Stratz and colleagues  showed that 5-HT3 receptor antagonists had anti-inflammatory effects and due to this property they could have a role in decreasing pain following surgical incision pain. Also, they founded that 5-HT3 receptor antagonists could acted as supplement or replacement for local administration of corticosteroids. Not only ondansetron but the other 5-HT3 antagonists such as tropisetron and alosetron have analgesic effect. ,,
Färber and et al. colleagues  showed that tropisetron have analgesic effect in patients with fibromyalgia pain. Also, the analgesic effect of alosetron in female patients with diarrhea predominant irritable bowel syndrome was reported by Camilleri et al.,  and Muller et al.,  showed that local administration of 5-HT3 antagonists had rapid analgesic effect in various rheumatic diseases. It was reported that this local anesthetic effect lasts significantly longer compared with local anesthetics but was comparable with local injection of local anesthetics combined with corticosteroids.
One of important limiting factor in duration of IVRA is tourniquet pain. Neuropathic pain caused by nerve compression is considered as an important etiology for tourniquet pain.  Pain due to nerve compression is mediated by unmyelinated, slow conduction C-fiber.  It was shown by Mc clean et al.,  that ondansetron as a 5 HT3 receptor antagonist has potential benefit in neuropathic pain. 5-HT3 receptor antagonists decrease serotonin-induced release of substance P from C-fiber.  It has been shown that when the drugs with local anesthetic properties such as meperidine,  clonidine  or nitroglycerine , added to the local anesthetic solution in IVRG, they can reduce tourniquet and postoperative pain. As it was shown by Ye J and colleagues,  ondansetron has potent local anesthetic properties. More studies must be de designed to evaluate the efficacy of different dosage of ondansetron and the other 5-HT3 receptor antagonists in various types of orthopedic surgeries with different techniques of regional anesthesia.
In conclusion, adding ondansetron 8 mg to lidocaine for IVRA reduced intraoperative and post-operative analgesic use till 24 h, decreased onset of sensory and motor block, increased duration of sensory and motor block, decreased tourniquet induced pain, prolonged the rescue time for analgesic use, and finally improved the patients' and surgeons' satisfaction without causing significant adverse effects. Our study showed that ondansetron has local anesthesia properties. As our results showed, it seems ondansetron has no systemic analgesic effect but further studies must be performed before final conclusion can be elucidated.
| Acknowledgment|| |
The authors wish to sincerely thank the support of all the colleagues in Kashani Hospital Medical Center affiliated to Isfahan University of Medical Sciences in Isfahan, Iran. Furthermore, our special thanks go to the patients, who wholeheartedly and actively assisted us to carry out this research. No conflict of interest existed. This prospective randomized observational study was approved by the Ethics Committee of our university, (Isfahan University of Medical Sciences) and all patients gave written, informed consent.
This clinical trial study is registered in www.irct.ir with the code of: IRCT201207122410N10
| References|| |
|1.||Choyce A, Peng P. A systematic review of adjuncts for intravenous regional anesthesia for surgical procedure. Can J Anaesth 2002;49:32-45. |
|2.||Yurtlu S, Hanci V, Kargi E, Erdoðan G, Köksal BG, Gül Þ, et al. The analgesic effect of dexketoprofen when added to lidocaine for intravenous regional anaesthesia: A prospective, randomized, placebo-controlled study. J Int Med Res 2011;39:1923-31. |
|3.||Sørensen AM, Dalsgaard J, Hansen TB. Local anaesthesia versus intravenous regional anaesthesia in endoscopic carpal tunnel release: A randomized controlled trial. J Hand Surg Eur Vol 2012. [In Press]. |
|4.||Memis D, Turan A, Karamanlioglu B, Pamukcu Z, Kurt I. Adding dexmedetomidine to lidocaine for intravenous regional anaesthesia. Anesth Analg 2004;98:835-40. |
|5.||Esmaoglu A, Akin A, Mizrak A, Turk Y, Boyaci A. Addition of cisatracurium to lidocaine for intravenous regional anesthesia. J Clin Anesth 2006;18:194-7. |
|6.||Tramèr MR, Reynolds DJ, Stoner NS, Moore RA, McQuay HJ. Efficacy of 5-HT3 receptor antagonists in radiotherapy-induced nausea and vomiting: A quantitative systematic review. Eur J Cancer 1998;34:1836-44. |
|7.||Glaum SR, Proudfit HK, Anderson EG. Reversal of the antinociceptive effects of intrathecally administered serotonin in the rat by a selective 5-HT3 receptor antagonist. Neurosci Lett 1988;19:313-7. |
|8.||Ye JH, Mui WC, Ren J, Hunt EE. Ondansetron exhibits the Properties of a local anesthetic. Anesth Analg 1997;85:1116-21. |
|9.||Gregory RE, Ettinger DS. 5-HT3 receptor antagonists for the prevention of chemotherapy-induced nausea and vomiting. A comparison of their pharmacology and clinical efficacy. Drugs 1998;55:173-89. |
|10.||Farouk S. Ondansetron added to lidocaine for intravenous regional anaesthesia. Eur J Anaesthesiol 2009;26:1032-6. |
|11.||Raj PP, Garcia CE, Burleson JW, Jenkins MT. The site of action of intravenous regional anesthesia. Anesth Analg 1972;51:776-86. |
|12.||Rosenberg PH. Intravenous regional anesthesia: Nerve block by multiple mechanisms. Reg Anesth 1993;18:1-5. |
|13.||Deegan R. Ondansetron: Pharmacology of a specific 5HT3-receptor antagonist. Am J Med Sci 1992;304:373-8. |
|14.||Ambesh SP, Dubey PK, Sinha PK. Ondansetron pretreatment to alleviate pain on propofol injection: A randomized, controlled, double-blinded study. Anesth Analg 1999;89:197-9. |
|15.||Reddy MS, Chen FG, Ng HP. Effect of ondansetron pretreatment on pain after rocuronium and propofol injection: A randomised, double-blind controlled comparison with lidocaine. Anaesthesia 2001;56:902-5. |
|16.||Richardson BP, Bucheit KH. The pharmacology, distribution and function of 5-HT3 receptors. In: Osborne NN, Hamon M, editors. Neuronal serotonin. Chichester: John Wiley and Sons; 1988. p. 465-506. |
|17.||Kidd EJ, Laporte AM, Langlois X, Fattaccini CM, Doyen C, Lombard MC, et al. 5-HT3 receptors in the rat central nervous system are mainly located on nerve fibres and terminals. Brain Res 1993;612:289-98. |
|18.||Fassoulaki A, Melemeni A, Zotou M, Sarantopoulos C. Systemic ondansetron antagonizes the sensory block produced by intrathecal lidocaine. Anesth Analg 2005;100:1817-21. |
|19.||Cui M, Feng Y, McAdoo DJ, Willis WD. Periaqueductal gray stimulation-induced inhibition of nociceptive dorsal horn neurons in rats is associated with the release of norepinephrine, serotonin, and amino acids. J Pharmacol Exp Ther 1999;289:868-76. |
|20.||Arcioni R, della Rocca M, Romanò S, Romano R, Pietropaoli P, Gasparetto A. Ondansetron inhibits the analgesic effects of tramadol: A possible 5-HT (3) spinal receptor involvement in acute pain in humans. Anesth Analg 2002;94:1553-7. |
|21.||Murphy RM, Zemlan FP. Selective serotonin 1A/1B agonists differentially affect spinal nociceptive reflexes. Neuropharmacology 1990;29:463-8. |
|22.||Alhaider AA, Lei SZ, Wilcox GL. Spinal 5-HT3 receptor-mediated antinociception: Possible release of GABA. J Neurosci 1991;11:1881-8. |
|23.||Zeitz KP, Guy N, Malmberg AB, Dirajlal S, Martin WJ, Sun L, et al. The 5-HT3 subtype of serotonin receptor contributes to nociceptive processing via a novel subset of myelinated and unmyelinated nociceptors. J Neurosci 2002;22:1010-9. |
|24.||Stratz T, Müller W. The use of 5-HT3 receptor antagonists in various rheumatic diseases-a clue to the mechanism of action of these agents in fibromyalgia. Scand J Rheumatol Suppl 2000;113:66-71. |
|25.||Färber L, Stratz TH, Brückle W, Späth M, Pongratz D, Lautenschläger J, et al. German Fibromyalgia Study Group. Short-term treatment of primary fibromyalgia with the 5-HT3-receptor antagonist tropisetron. Results of a randomized, double-blind, placebo-controlled multicenter trial in 418 patients. Int J Clin Pharmacol Res 2001;21:1-13. |
|26.||Färber L, Stratz T, Brückle W, Späth M, Pongratz D, Lautenschläger J, et al. Efficacy and tolerability of tropisetron in primary fibromyalgia-a highly selective and competitive 5-HT3 receptor antagonist. German Fibromyalgia Study Group. Scand J Rheumatol Suppl 2000;113:49-54. |
|27.||Camilleri M, Mayer EA, Drossman DA, Heath A, Dukes GE, McSorley D, et al. Improvement in pain and bowel function in female irritable bowel patients with alosetron, a 5-HT3 receptor antagonist. Aliment Pharmacol Ther 1999;13:1149-59. |
|28.||Müller W, Fiebich BL, Stratz T. 5-HT3 receptor antagonist als analgetics in rheumatic diseases. Z Rheumatol 2006;65:546, 548-52. |
|29.||Gielen MJ, Stienstra R. Tourniquet hypertension and its prevention: A review. Reg Anesth 1991;16:191-4. |
|30.||McCleane GJ, Suzuki R, Dickenson AH. Does a single intravenous injection of the 5HT3 receptor antagonist ondansetron have an analgesic effect in neuropathic pain? A double-blinded, placebo-controlled cross-over study. Anesth Analg 2003;97:1474-8. |
|31.||Wolf H. Preclinical and clinical pharmacology of the 5-HT3 receptor antagonists. Scand J Rheumatol Suppl 2000;113:37-45. |
|32.||Reuben SS, Steinberg RB, Lurie SD, Gibson CS. A dose-response study of intravenous regional anesthesia with meperidine. Anesth Analg 1999;88:831-5. |
|33.||Gentili M, Bernard JM, Bonnet F. Adding clonidine to lidocaine for intravenous regional anesthesia prevents tourniquet pain. Anesth Analg 1999;88:1327-30. |
|34.||De Marzo C, Crovace A, De Monte V, Grimaldi D, Iarussi F, Staffieri F. Comparison of intra-operative analgesia provided by intravenous regional anesthesia or brachial plexus block for pancarpal arthrodesis in dogs. Res Vet Sci 2012. |
|35.||Honarmand A, Safavi M, Fatemy A. The analgesic effect of three different doses of nitroglycerine when added to lidocaine for intravenous regional anesthesia in trauma patients. Ulus Travma Acil Cerrahi Derg 2011;17:497-503. |
[Figure 1], [Figure 2], [Figure 3], [Figure 4]
[Table 1], [Table 2], [Table 3]