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Lipid Emulsion for the Treatment of Local Anesthetic Toxicity: Patient Safety Implications

Brull, Sorin J., MD

doi: 10.1213/01.ane.0b013e31816b9415
Editorial: Editorial
Free
CME

From the Mayo Clinic, College of Medicine, Jacksonville, Florida.

Accepted for publication January 16, 2008.

Reprints will not be available from the author.

Address correspondence to Sorin J. Brull, MD, Anesthesia & Analgesia, Section Editor, Patient Safety, Professor of Anesthesiology, Mayo Clinic, College of Medicine, 4500 San Pablo Rd, Jacksonville, FL 32224. Address e-mail to Brull@APSF.org.

There is little question that the absolute, scientific “proof” of lipid emulsion’s efficacy in reversing local anesthetic-induced cardiac arrest is yet lacking. Such a proof would require prospective, double-blind, placebo-controlled studies in humans, and such studies will thankfully never be performed, for obvious ethical reasons. However, when deciding on the patient safety implications of a novel, potentially life-saving, therapy, one must consider the tenuous and often unknown balance between the purported benefits and potential risks.

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BENEFITS

On the one hand, it is obvious from the published case reports (including the three manuscripts in this issue of the journal),1–3 and the anecdotal “evidence” posted on the web at www.lipidrescue.org, that lipid emulsion (LE) has been used successfully to reverse local anesthetic toxicity. First, it should be noted that it is indeed reversal of “local anesthetic” cardiac toxicity, not just “bupivacaine”-induced cardiac toxicity that responds to LE treatment.4,5 In fact, there is also published evidence that overdoses with other lipid-soluble drugs (such as bupropion, lamotrigine, verapamil, and clomipramine) may respond equally well to LE therapy.6–8 Second, recent reports attest to the efficacy of LE therapy in reversing the central nervous system (CNS) toxicity.3,9 This finding may be equally significant, as the abolition of CNS symptoms may well prevent the progression of CNS toxicity to cardiac toxicity. This has obvious patient safety implications: the CNS toxicity (seizures) can be treated successfully with a number of drugs (benzodiazepines, barbiturates, and isopropylphenol), whereas cardiac toxicity is extremely refractory to most conventional resuscitative techniques and drugs, and previously, institution of cardiopulmonary bypass was the only known treatment. Despite the continued publication of new case reports, however, the ultimate “proof” of efficacy may require many years, if not decades, of LE therapy, given the relatively infrequent incidence of local anesthetic toxicity.

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RISKS

On the other hand, the side effects and/or toxicity of LE used as an antidote to local anesthetic-induced toxicity also must be considered. There are no reports suggesting that empiric treatment of local anesthetic toxicity with LE may render the patient less susceptible to advanced cardiac life support rescue. Thus, it may be that even if not directly effective in reversing the local anesthetic toxicity, the empiric use of LE does not appear to pose any acute risks (primum non nocere). And although LE is safe and well tolerated in routine clinical practice at doses of 1–2 g · kg−1 · d−1,10 administration of LE has been associated with several potential complications: LE infusions modulate cytokine production by mononuclear white cells in response to Candida yeast, suggesting an increased risk of infection11,12; LE infusions may produce thrombophlebitis during peripheral IV administration13; they may lead to impaired reticuloendothelial system function and altered inflammatory responses during long-term therapy14,15; they may induce allergic reactions, including anaphylaxis, especially if they contain soy bean oil16,17; they may result in pulmonary, splenic, placental, and cerebral fat emboli, especially if the emulsified fat particles are greater than 5 microns in diameter18,19; they may cause pulmonary hypertension if administered at rates larger than 100 mg · kg−1 · h−119; they may lead to warfarin resistance by facilitating warfarin binding to albumin20; they may interfere with extracorporeal membrane oxygenation circuits21; they may induce weakness, altered mental status, and seizures in children22; and they may induce an increase in the intracranial pressure after a severe traumatic brain injury.23 Because of the many possible side effects associated with LE administration, the multiple types and combinations of lipid preparations, the various free fatty acid concentrations, and the wide range of lipid globule sizes available, some experts have suggested the adoption of certain pharmaceutical requirements and standards.24–26 Of all these reported side effects, however, only allergic reactions are likely to arise after acute, short-term administration, such as would occur with administration of LE for rescue from local anesthetic toxicity.

Based on the available evidence, therefore, it would seem imprudent to withhold LE administration in local anesthetic-induced toxicity clinical settings while awaiting scientific proof. This recommendation is not to imply, however, that administration of LE should be the first step in such a clinical setting. Clearly, CNS symptoms such as loss of responsiveness, disorientation, tremors, or seizures must be treated conventionally by ensuring oxygenation and ventilation, securing the airway to protect aspiration of gastric contents in patients at risk, administering anticonvulsants, and instituting advanced cardiac life support protocols in the case of cardiac arrest. Once these conventional treatment modalities have begun, however, immediate IV administration of LE would seem very reasonable and desirable.

Finally, as anesthesiologists, we have always been trained to “prepare for most eventualities” and one of our guiding principles is “vigilance.” Based on the available data, it would seem reasonable to have a rescue kit available in any setting in which regional anesthesia is practiced—and in fact, in any location where local anesthetics are administered by any professional, by any route, and in almost any dose. Although cost may be mentioned by some as a consideration when preparing “lipid rescue kits” for all such locations, such concerns must necessarily be secondary to patient safety, and are in fact, trivial: the Intralipid in these kits may be returned to the hospital’s central pharmacy to be used for parenteral nutrition before the expiration date, and new Intralipid with a 1-yr shelf life can be restocked in the kit.

These are exciting times, and we may well be witnessing the birth of Panacea.

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REFERENCES

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