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SMALL ANIMALS/ EXOTIC Infusion of a lipid emulsion to treat lidocaine intoxication in a cat Taylor Q. O’Brien, dvm; Stuart C. Clark-Price, dvm, ms, dacvim, dacva; Erika E. Evans, dvm; Renata Di Fazio, dvm; Maureen A. McMichael, dvm, dacvecc Case Description—A 5-year-old castrated male domestic shorthair cat was examined because of presumptive lidocaine intoxication. Thirty minutes earlier, the cat had received an SC injection of approximately 140 mg of lidocaine hydrochloride (20 mg/kg [9.1 mg/lb]) to facilitate closure of a wound on the left pelvic limb. Clinical Findings—Initial physical examination revealed severe lethargy and respiratory distress; erratic, poor-quality pulses with severe hypotension; and pulmonary edema. Treatment and Outcome—Initial supportive treatment included administration of oxygen and IV administration of lactated Ringer’s solution. Additional treatment with a 20% lipid emulsion (1.5 mL/kg [0.68 mL/lb], IV) delivered over a 30-minute period resulted in dramatic improvement in cardiovascular and behavioral variables. No adverse effects from lipid emulsion were detected on routine hematologic evaluation, thoracic radiography, or computed tomography. Clinical Relevance—IV administration of a lipid emulsion was used in the treatment of lidocaine intoxication in a cat. Rapid infusion of a lipid emulsion may be a therapeutic option for veterinary patients with toxicosis attributable to local anesthetics or other lipid-soluble drugs. (J Am Vet Med Assoc 2010;237:1455–1458) A 5-year-old 6.8-kg (15.0-lb) castrated male domestic shorthair cat was examined at the Small Animal Emergency Service of the University of Illinois Veterinary Teaching Hospital because of severe lethargy and respiratory distress. Thirty minutes before admission, the cat had received an SC injection of approximately 140 mg of lidocaine hydrochloride (20 mg/kg [9.1 mg/ lb]) to aid debridement and repair of a 5-cm circumferential wound on the lateral aspect of the proximal portion of the left pelvic limb. Physical examination revealed that the cat was severely lethargic, unresponsive to stimuli, and unable to support itself in sternal recumbency. Rectal temperature was 38.3°C (101.0°F). The cat had an irregular pulse rate that varied from 60 to 200 beats/min; a rapid, gasping, open-mouth breathing pattern; dark red mucous membranes; and a prolonged capillary refill time of > 3 seconds. Pulse quality was poor. Thoracic auscultation revealed an irregular heart rhythm consistent with the pulse findings and bilateral crackles throughout all lung fields. An attempt was made to measure systolic blood pressure via Doppler oscillometry, but it was unsuccessful. Venous blood samples were collected for a CBC, serum biochemical analysis, and venous blood gas analysis. An attempt was made to obtain an arterial sample for blood gas analysis, but it was unsuccessful. Results of the CBC revealed leukopenia (3.87 X 103 cells/µL; reference range, 5.50 X 103 cells/µL to 19.50 From the Department of Veterinary Clinical Medicine, College of Veterinary Medicine, University of Illinois, Urbana, IL 61802. Dr. O’Brien’s present address is Animal Emergency and Referral Center, 1810 Skokie Blvd, Northbrook, IL 60062. Dr. O’Brien was a fourthyear veterinary student at the time of this report. Address correspondence to Dr. Clark-Price ([email protected]). JAVMA, Vol 237, No. 12, December 15, 2010 X 103 cells/µL) and lymphopenia (0.66 X 103 cells/µL; reference range, 1.70 X 103 cells/µL to 7.00 X 103 cells/µL). Results of the serum biochemical analysis revealed hypokalemia (3.54 mmol/L; reference range, 3.7 to 4.91 mmol/L), hypocalcemia (1.10 mmol/L; reference range, 1.17 to 1.37 mmol/L), hypernatremia (152.2 mmol/L; reference range, 144 to 152 mmol/L), and hyperchloremia (121.4 mmol/L; reference range, 110.04 to 117.96 mmol/L). Venous blood gas analysis revealed a mild decrease in bicarbonate concentration (16.6 mmol/L; reference range, 17.08 to 24.64 mmol/L); however, pH, partial pressure of oxygen (venous), partial pressure of carbon dioxide (venous), and lactate concentration were all within the respective reference ranges. On the basis of the medical history and clinical signs, a presumptive diagnosis of acute intoxication attributable to a local anesthetic was made. The cat was admitted to the intensive care unit for treatment. Supportive treatment (administration of oxygen via a facemask) was initiated. Attempts were made to place catheters in a jugular and cephalic vein, but ultimately they were unsuccessful. Thirty minutes after admission (15 minutes after instituting oxygen administration), the cat was less lethargic and able to remain in sternal recumbency without support but remained unable to support its head. Pulse quality had improved. A catheter was placed in a medial saphenous vein. Systolic blood pressure was measured (190 mm Hg). The cat was placed in an oxygen cage (fraction of inspired oxygen, 40%), and lactated Ringer’s solution was administered at a rate of 80 mL/kg/d (36.4 mg/lb/d). At that time, the cat received an IV infusion of a 20% lipid emulsiona for specific treatment of lidocaine toxicosis. A dose (3 mL/kg [1.4 mL/lb]) delivered over a Scientific Reports 1455 SMALL ANIMALS/ EXOTIC 30-minute period was selected for treatment; this treatment was extrapolated from a case report for a human.1 However, because of concerns about fluid overload and lack of reports on the use of this treatment in cats, the treatment was reduced to infusion of a 20% lipid emulsion (1.5 mL/kg [0.68 mL/lb]) over a 30-minute period with a second equivalent dose to be administered over an additional 30-minute period, if necessary. Fifteen minutes after initiation of the lipid emulsion, the cat was more responsive to stimuli (ie, could be more easily aroused) and was able to hold its head up without assistance. At the conclusion of the infusion, the cat appeared to be aware of its surroundings and began grooming behaviors; therefore, the second infusion of the lipid emulsion was not administered. The cat was kept in the oxygen cage overnight; it was continuously monitored for any decline in mental status, including seizure activity. The following morning, the cat appeared to be bright, alert, and responsive. Physical examination findings were within anticipated limits. The oxygen concentration in the cage was gradually reduced over a 2-hour period until the cat was breathing only room air; no adverse effects were observed. Results of a CBC and serum biochemical analysis revealed no abnormalities. Additionally, because of concerns about oxidative damage to the cat’s RBCs resulting from lidocaine intoxication, the methemoglobin concentration was measured. However, the methemoglobin concentration was within the reference range (0.3%; reference range, < 1%). Thoracic radiography and computed tomography were performed to assess pulmonary edema or pulmonary lipid deposition. Results revealed clear lung fields; however, there was an incidental finding of spondylosis deformans at T11-12. Blood samples obtained at admission and again the following morning were submitted for determination of plasma lidocaine concentration. The value was 6.3 µg/mL for the pretreatment sample, and lidocaine was not detected in the posttreatment sample. Therapeutic and toxic concentrations of plasma lidocaine have not been determined for cats; however, the reported2 range for antiarrhythmic treatment in humans is 2 to 5 µg/mL, with signs attributable to toxic effects evident at plasma concentrations of 5 to 10 µg of lidocaine/mL. The wound on the pelvic limb of the cat was cleaned and bandaged, and buprenorphine (0.02 mg/kg [0.009 mg/lb], IV) was administered for analgesia. The cat was discharged to the owner with instructions for continued care of the wound. Two days later, the owner reported that the cat was doing well with no residual effects from the lidocaine intoxication. Discussion Lidocaine is one of the most commonly used local anesthetics in human and veterinary medicine. It exerts local anesthetic effects by reversibly binding to sodium channels and preventing impulse conduction through nervous tissue.3 Lidocaine has a rapid onset of action with a duration of 60 to 120 minutes, which makes it suitable for use in procedures for which a short duration of action is desired.2 Lidocaine can also be administered IV as a treatment for ventricular arrhythmias, to 1456 Scientific Reports provide systemic analgesia, and to reduce the minimum alveolar concentration of inhalant anesthetics needed for anesthesia.4–6 Mepivacaine and bupivacaine are other local anesthetics that have been used in veterinary medicine. Both have a longer duration of action than does lidocaine, with the effects of mepivacaine lasting 90 to 180 minutes and the effects of bupivacaine lasting 240 to 480 minutes.7 Similar to other local anesthetics, toxic effects of lidocaine are related to excessive plasma and tissue concentrations. Some of the more serious toxic effects result from effects on the CNS and the cardiovascular system. Clinically, these can be evident as lethargy, unconsciousness, coma, convulsions, seizures, hypotension, bradycardia, and cardiovascular collapse and can result in death.2 Several of these signs were observed in the cat described here. At admission, the cat was lethargic, and severe hypotension was evident as an inability to obtain an initial blood pressure measurement and difficulty in inserting a catheter in a vein. The dosages of local anesthetics that cause CNS toxicosis are less than the dosages that cause signs of cardiovascular toxicosis.7 The reported plasma concentration of lidocaine in humans at which signs of CNS toxicosis are apparent is 5 to 10 µg/mL, whereas plasma concentrations > 25 µg/mL are associated with cardiovascular toxicosis.2 Lidocaine intoxication of the CNS often manifests initially as twitching and weakness of skeletal muscles and progresses to drowsiness and then seizures. In severe cases, CNS depression and coma can follow seizures. There is evidence that the plasma concentration at which CNS toxicosis develops may be more a function of the rate of administration and subsequent increase in the plasma concentration, rather than a function of the total amount of drug administered.8 Cardiovascular effects of toxic dosages of lidocaine may be evident as refractory hypotension from direct vasodilatory effects on vascular smooth muscle and reduced cardiac output from myocardial depression.2 Electrocardiographic findings from local anesthetic–induced cardiovascular toxicosis include a prolonged PR interval and widening of the QRS complex.2 Lidocaine and other local anesthetics generate methemoglobin, which typically comprises < 1% of the total blood hemoglobin content, from oxidation of hemoglobin, thereby potentially reducing the ability of RBCs to carry oxygen. Heinz bodies, which can result in RBC lysis, can also form as a result of oxidative damage to RBCs from toxic concentrations of local anesthetics.7 In domestic cats, lidocaine is commonly used to provide local analgesia and anesthesia for routine procedures, such as dental extractions, onychectomy, wound debridment, and epidural anesthesia.7 Although relatively free of adverse effects when proper dosages are used, excessive or IV administration of lidocaine can result in toxic effects similar to those seen in human patients. These toxic effects can develop as the dosage of lidocaine approaches 6 mg/kg (2.7 mg/lb) in cats. Seizure activity can be elicited in cats via IV administration of lidocaine at a dosage of 11.7 ± 4.6 mg/kg (5.3 ± 2.1 mg/lb).9 Therefore, it is recommended that the dosage of lidocaine used for local anesthesia in cats should not exceed 3 to 4 mg/kg (1.4 to 1.8 mg/ lb).10 The cat described here received an approximate JAVMA, Vol 237, No. 12, December 15, 2010 JAVMA, Vol 237, No. 12, December 15, 2010 to cyclic antidepressants, verapamil, β-adrenoceptor blockers, and clomipramine.21,24–26 A lipid emulsion has been used to treat moxidectin toxicosis in a puppy.27 Treatment with a lipid emulsion is not without potential complications. These emulsions can promote bacterial growth, which requires that aseptic procedures be used during administration to prevent contamination and possible sepsis. Intravenous administration of a lipid emulsion may cause immunosuppression through immune-cell dysfunction.28 Other potential effects include phlebitis, thrombosis, hypertriglyceridemia, and hepatic lipidosis.28 The dosage of a 20% lipid infusion has varied in human clinical case reports. The dosage used in the cat described here was extrapolated from a single human case report1 in which the authors reported success with a dosage of 3 mL/kg. In the cat of our case report, dramatic clinical response was achieved with a dosage of 1.5 mL/kg delivered over a 30-minute period, and at least in this cat, administration of an additional 1.5 mL/ kg dose was not necessary. After resolution of the condition in the cat reported here, a review of the use of lipid emulsion as a treatment for lidocaine intoxication in humans was published.21 The authors of that report made a recommendation for administration of a 20% lipid emulsion at a dosage of 1.5 mL/kg at infusion rates of 0.25 to 0.5 mL/kg/min (0.11 to 0.23 mL/lb/min), which could be repeated up to 3 times. On the basis of the findings in the cat described here, this recommendation may also be applicable to veterinary patients. It is important to mention that although lidocaine was not detected in the second plasma sample obtained from the cat described here, this may not have been a result of the use of the lipid emulsion. The half-life of lidocaine in cats is approximately 1.7 hours,29 and a lack of lidocaine in the second sample was most likely the result of typical elimination of the drug. The present case report confirmed the IV administration of a lipid emulsion for treatment of local anesthetic–induced toxicosis in a veterinary patient. The authors recognize the limitations of this report in that it represents only a single cat and that findings were based on subjective assessment of the cat. Further investigation into the use of lipid emulsions for the treatment of toxicosis attributable to local anesthetics is warranted. In this cat, no adverse effects from the lipid infusion were detected. Additionally, rapid infusion of a lipid emulsion may be a treatment option for patients with toxicosis attributable to other lipid-soluble drugs. a. Liposyn II, Hospira Inc, Lake Forest, Ill. References 1. Warren JA, Thoma RB, Georgescu A, et al. Intravenous lipid infusion in the successful resuscitation of local anestheticinduced cardiovascular collapse after supraclavicular brachial plexus block. Anesth Analg 2008;106:1578–1580. 2. Stoelting RK, Hillier SC. Local anesthetics. In: Stoelting RK, Hillier SC, eds. Pharmacology & physiology in anesthetic practice. Philadelphia: Lippincott Williams & Wilkins, 2006;179–207. 3. Butterworth JF, Strichartz GR. Molecular mechanisms of local anesthesia: a review. Anesthesiology 1990;72:711–734. 4. Pariaut R. Ventricular tachyarrhythmias. In: Silverstein DC, Hopper K, eds. Small animal critical care medicine. St Louis: Elsevier Inc, 2009;200–203. Scientific Reports 1457 SMALL ANIMALS/ EXOTIC dosage of 20 mg/kg. Lidocaine infusions for analgesia or reduction in the minimum alveolar concentration of inhalant anesthetics are not recommended in cats.11 It is postulated that cats are more susceptible to the toxic effects of amide local anesthetics (such as lidocaine), compared with the susceptibility of other species, because of a reduced ability for glucuronide metabolism of drugs in the liver.12 Treatment of intoxication attributable to a local anesthetic has traditionally been limited to palliative care. This includes administration of benzodiazepine drugs to control seizures, fluid administration and dobutamine infusions to correct hypotension and hypovolemia, anticholinergic drugs for bradyarrhythmias, oxygen insufflation, N-acetylcysteine to treat dyspnea and prevent reperfusion injury, and methylene blue or vitamin C to treat methemoglobinemia.7 If cardiac arrest occurs, prolonged cardiopulmonary cerebral resuscitation may be necessary, particularly for animals with intoxication attributable to long-acting local anesthetics. Lipid emulsions have been used successfully for the treatment of humans with acute intoxication attributable to local anesthetics,1,13–16 prompting the Association of Anaesthetists of Great Britain to develop and adopt guidelines that lipid emulsions be immediately available for all patients given potentially cardiotoxic doses of local anesthetic drugs.17 Lipid emulsions are most commonly used for IV administration to provide nutrients (ie, parenteral nutrition) as well as serving as a delivery vehicle for hydrophobic drugs, such as propofol.18 The lipid component of these emulsions forms chylomicrons, which aids in their ability to be rapidly and widely distributed.19 The exact mechanism of action for lipid emulsions in the treatment of intoxication attributable to local anesthetics is unknown. However, 3 theories have been postulated as to why lipid infusions appear to be clinically beneficial. First, a new pharmacokinetic equilibrium within an expanded plasma lipid base is achieved, which reduces the toxic effects by reducing the free drug concentration. Therapeutically, because of a high binding capacity of these emulsions, lipids are thought to exert an effect on local anesthetics by physically binding and trapping circulating local anesthetic molecules, thus rendering them inactive.20 It is probable that the high lipid solubility of local anesthetics and the high binding capacity of the lipid emulsions explain their clinical efficacy.20 Second, because fatty acids can increase calcium concentrations in cardiomyocytes, exogenously delivered lipids may cause an increase in inotropy that overcomes the depressive effects of the intoxication. Third, local anesthetics inhibit carnitine acyltransferase, which is necessary to transport fatty acids across myocardial mitochondrial membranes for oxidative phosphorylation. Bolus administration of a lipid emulsion may overcome the decreased fatty acid transport via mass action or an unknown mechanism.21 Studies22,23 in laboratory animals have confirmed the efficacy of lipid emulsions for countering the cardiovascular effects of toxic doses of local anesthetics. In addition to treatment of intoxication induced by local anesthetics, lipid infusions have been used as a treatment for various intoxications in humans and domestic animals, including intoxication attributable SMALL ANIMALS/ EXOTIC 5. 6. 7. 8. 9. 10. 11. 12. 13. 14. 15. 16. 17. Quandt J, Lee JA. Analgesia and constant rate infusions. In: Silverstein DC, Hopper K, eds. Small animal critical care medicine. St Louis: Elsevier Inc, 2009;710–716. Valverde A, Doherty TJ, Hernandez J, et al. Effect of lidocaine on the minimum alveolar concentration of isoflurane in dogs. Vet Anaesth Analg 2004;31:264–271. Skarda RT, Tranquilli WJ. Local anesthetics. In: Tranquilli WJ, Thurmon JC, Grimm KA, eds. Lumb & Jones’ veterinary anesthesia and analgesia. Ames, Iowa: Blackwell Publishing, 2007;395–418. Tucker GT, Mather LE. Clinical pharmacokinetics of local anaesthetics. Clin Pharmacokinet 1979;4:241–278. Chadwick HS. Toxicity and resuscitation in lidocaine or bupivacaine infused cats. Anesthesiology 1985;63:385–390. Carroll GL. Local anesthetic and analgesic techniques. In: Carroll GL, ed. Small animal anesthesia and analgesia. Ames, Iowa: Blackwell Publishing, 2008;107–122. Pypendop BH, Ilkiw JE. Assessment of the hemodynamic effects of lidocaine administered IV in isoflurane-anesthetized cats. Am J Vet Res 2005;66:661–668. Steffey EP, Booth NH. Local anesthetics. In: Adams HR, ed. Veterinary pharmacology and therapeutics. 7th ed. Ames, Iowa: Iowa State University Press, 1995;358–371. Litz RJ, Roessel T, Heller AR, et al. Reversal of central nervous system and cardiac toxicity after local anesthetic intoxication by lipid emulsion injection. Anesth Analg 2008;106:1575–1577. Ludot H, Tharin JY, Belouadah M, et al. Successful resuscitation after ropivacaine and lidocaine-induced ventricular arrhythmia following posterior lumbar plexus block in a child. Anesth Analg 2008;106:1572–1574. Rosenblatt MA, Abel M, Fischer GW, et al. Successful use of a 20% lipid emulsion to resuscitate a patient after a presumed bupivacaine related cardiac arrest. Anesthesiology 2006;105:217–218. Litz RJ, Popp M, Stehr SN, et al. Successful resuscitation of a patient with ropivacaine-induced asystole after axillary plexus block using lipid infusion. Anaesthesia 2006;61:800–801. Picard J, Ward SC, Zumpe R, et al. Guidelines and the adoption of “lipid rescue” therapy for local anaesthetic toxicity. Anaesthesia 2009;64:122–125. 1458 Scientific Reports 18. Han J, Davis SS, Washington C. Physical properties and stability of two emulsion formulations of propofol. Int J Pharm 2001;215:207–220. 19. Park Y, Damron BD, Miles JM, et al. Measurement of human chylomicron triglyceride clearance with a labeled commercial lipid emulsion. Lipids 2001;36:115–120. 20. Mazoit JX, Guen RL, Beloeil H, et al. Binding of long-lasting local anesthetics to lipid emulsions. Anesthesiology 2009;110:380–386. 21. Cave G, Harvey M. Intravenous lipid emulsion as antidote beyond local anesthetic toxicity: a systematic review. Acad Emerg Med 2009;16:815–824. 22. Weinberg GL, VadeBoncouer T, Ramaraju GA, et al. Pretreatment or resuscitation with a lipid infusion shifts the doseresponse to bupivacaine-induced asystole in rats. Anesthesiology 1998;88:1071–1075. 23. Cave G, Harvey MG, Winterbottom T. Evaluation of the Association of Anaesthetists of Great Britain and Ireland lipid infusion protocol in bupivacaine induced cardiac arrest in rabbits. Anaesthesia 2009;64:732–737. 24. Tebbutt S, Harvey M, Nicholson T, et al. Intralipid prolongs survival in a rat model of verapamil toxicity. Acad Emerg Med 2006;13:134–139. 25. Cave G, Harvey MG, Castle CD. The role of fat emulsion therapy in a rodent model of propranolol toxicity: a preliminary study. J Med Toxicol 2006;2:4–7. 26. Harvey M, Cave G. Intralipid outperforms sodium bicarbonate in a rabbit model of clomipramine toxicity. Ann Emerg Med 2007;49:178–185. 27. Crandell DE, Weinberg GL. Moxidectin toxicosis in a puppy successfully treated with intravenous lipids. J Vet Emerg Crit Care (San Antonio) 2009;19:181–186. 28. Freeman LM, Chan DL. Total parenteral nutrition. In: Dibartola SP, ed. Fluid, electrolyte, and acid-base disorders in small animal practice. St Louis: Elsevier Inc, 2006;584–601. 29. Thomasy SM, Pypendop BH, Ilkiw JE, et al. Pharmacokinetics of lidocaine and its active metabolite, monoethylglycinexylidide, after intravenous administration of lidocaine to awake and isoflurane-anesthetized cats. Am J Vet Res 2005;66:1162–1166. JAVMA, Vol 237, No. 12, December 15, 2010