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      Can we use Tramadol as an anti-shivering agent?

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          Abstract

          Sir, Tramadol seems to have the best combination of anti-shivering and analgesic efficacy without causing too much sedation in the post-operative period. Seizures have been reported in patients receiving the drug in overdose and, rarely, at the recommended dose unless it is taken by the patients with history of epilepsy or taken with other drugs that reduce seizure threshold.[1] We report a case of a 45-year-old, ASA Grade I, female patient, weighing 52 kg electively posted for vaginal hysterectomy. The patient had no family history of epilepsy and was not on any other medication. Subarachnoid anaesthesia was instituted at the L3-4 interspace using hyperbaric 0.5% Bupivacaine. Towards the end of the procedure, the patient complained of shivering, and intravenous Tramadol 100 mg was administered slowly over 2–3 min. After 2 min, the patient had generalized tonic-clonic seizures. The patient was given 100% oxygenation using Bain's circuit, and intravenous Midazolam 2 mg was administered. The convulsions subsided. The patient was awake but confused and disoriented. She got better after 30 min. Other neurological examinations were normal. Serum electrolytes, blood sugar and computed tomography of the brain were normal. The patient was followed-up for the next 15 days, and there was no recurrence of seizure. After searching the literature, we found few Tramadol- induced seizure reports at therapeutic doses in non operative setting. Talaie and others concluded in their study that Tramadol intake does not differ between patients with and without seizures, and the most common dose range in those with seizures is 500–1000 mg, with the incidence of seizure with Tramadol not being dose-dependent.[2] Jick et al. found that there was no increased risk of idiopathic incident seizures associated with exposure to Tramadol alone. The seizures seem rarely attributable to the agent.[3] Gasse et al. also suggested that the risk of idiopathic seizures was elevated in each analgesic exposure category compared with non-users, suggesting that the risk for patients taking Tramadol was not increased compared with other analgesics.[4] Massoud Mehrpour reported two cases of intravenous Tramadol-induced seizure at therapeutic doses prescribed for headache, and opined that Tramadol can induce seizure and even status epilepticus, especially in intravenous prescription, which could be due to serotonergic effects.[5] In our case, administration of other epileptogenic drugs was ruled out and we ruled out all possible secondary causes like electrolyte imbalance, undiagnosed cerebral pathology, hypoglycemia etc. In conclusion, though intravenous Tramadol, in therapeutic doses, has proven antishivering as well as analgesic actions in the peri operative setting, utmost caution should be exercised while using the drug.

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          Dose-independent occurrence of seizure with tramadol.

          Tramadol, as a centrally-acting, opioid-like analgesic with serotonin reuptake inhibition property, is one of the most prescribed analgesics in the world. We assessed the incidence of seizure, as it is one of the most important adverse effects. In a cross-sectional study, 215 cases of tramadol users or abusers who were admitted to Loghman-Hakim Hospital Poisoning Center (LHHPC) in Tehran during a 5-month period, from April 2007 to September 2007, were assessed to evaluate the occurrence of seizure. Patients with positive history of co-ingestion of other drugs, addiction, convulsive disorders, renal diseases, or head trauma with abnormal electroencephalography (EEG) or computerized tomography (CT) scan of the brain were excluded, thus 132 patients were included in the study. For patients who had seizure, CT scan of the brain and EEG were performed, and frequency and type of seizure were identified. Mean tramadol dose was compared between patients with and without seizure. Among the patients, 97 (73.5%) were male. Seizure occurred in 61 patients (46.2%) within 24 hours after tramadol ingestion. The majority of patients who had seizure were male (male, 83.6% vs. female, 16.4%). Mean tramadol dose was lower among females than males (males, 2413 mg vs. females, 1706 mg), but the difference was not statistically significant. Of 35 patients with documented seizure type, all showed generalized tonic-clonic seizure and 12 patients had abnormal EEG (35.3%). No statistically significant difference was observed in mean tramadol intake between patients with or without seizure. Analysis of patients with seizure, according to tramadol intake, indicated that most patients used tramadol in the dose range of 500-1000 mg followed in occurrence by 1500-2000 mg, then 100-500 mg, 2500-3000 mg, and 3500-4000 mg. Mean tramadol intake does not differ between patients with and without seizure, and the most common dose range in those with seizure is 500-1000 mg. We thus conclude that the incidence of seizure with tramadol is not dose dependent.
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            Incidence of first-time idiopathic seizures in users of tramadol.

            To assess the risk of idiopathic incident seizures among patients who ever took tramadol. Nested case-control design. General Practice Research Database from November 1996-August 1998. Eleven thousand three hundred eighty-three patients. Comparison of risks of idiopathic incident seizures during exposed and unexposed times among patients who had ever taken tramadol and other analgesics with 90-day follow-up. Among the 11,383 subjects we identified 21 cases of idiopathic seizures, 10 of which were categorized as definite cases and 11 categorized as possible cases. Three patients were exposed to tramadol alone in the previous 90 days, 10 to opiates, three to both tramadol and opiates, one to other analgesics, and four to no analgesics. The risk of idiopathic seizures was similarly elevated in each analgesic exposure category compared with nonusers, suggesting that the risk for patients taking tramadol was not increased compared with other analgesics.
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              Seizures reported with tramadol.

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                Author and article information

                Journal
                Indian J Anaesth
                Indian J Anaesth
                IJA
                Indian Journal of Anaesthesia
                Medknow Publications & Media Pvt Ltd (India )
                0019-5049
                0976-2817
                Jan-Feb 2012
                : 56
                : 1
                : 91-92
                Affiliations
                [1]Department of Anaesthesiology, SN Medical College and HSK Hospital, Bagalkot, Karnataka, India
                Author notes
                Address for correspondence: Dr. Chhaya Joshi, Department of Anaesthesiology, SN Medical College and HSK Hospital, Bagalkot, Karnataka 587 101, India. E-mail: chhaya_joshi@ 123456yahoo.com
                Article
                IJA-56-91
                10.4103/0019-5049.93359
                3327088
                22529435
                2c962f53-c9cc-4593-ae62-4be7af60f268
                Copyright: © Indian Journal of Anaesthesia

                This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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                Anesthesiology & Pain management
                Anesthesiology & Pain management

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