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Case studies in Toxicology Mind the Gap An 8-month-old infant with a history of presented to the ED with fever and poor oral intake.

Daniel Repplinger, MD, Lewis S. Nelson, MD

An 8-month-old boy with a history of hypotonia, developmental delay, and seizure disorder refractory to multiple medications was brought to the ED with a two-week history of intermittent fever and poor oral intake. His current medications included (185 mg bid, orally) for his seizure disorder.

n physical examination, the boy ap- peared small for his age, with diffuse Ohypotonia and diminished reflexes. He was able to track with his eyes but was otherwise unresponsive. No rash was present. Results of initial laboratory studies were sodium, 144 mEq/L; pletely balanced. The AG therefore refers to this dif- , 4.8 mEq/L; , 179 mEq/L; bicar- ference (ie, AG = Na – [Cl + HCO3]). bonate, 21 mEq/L; urea , 6 mg/dL; Of course, electroneutrality exists in vivo and is creatinine, 0.1 mg/dL; and glucose, 63 mg/dL. His accomplished by the presence of unmeasured an- (AG) was −56. (UA; eg, lactate and ) and unmea- sured cations (UC; eg, potassium and ) not What does accounted for in the AG (ie, AG = UA – UC). In other the anion gap represent? words, the sum of measured plus unmeasured an- The AG is a valuable clinical calculation derived from ions must equal the sum of the measured plus un- the measured extracellular and provides measured cations. an index of acid-base status.1 Due to the necessity of electroneutrality, the sum of positive charges (cat- What causes ions) in the must be balanced a low or negative anion gap? exactly with the sum of negative charges (anions). While most health care providers are well versed in However, to routinely measure all of the cations and the clinical significance of an elevated AG (eg, MUD- anions in the serum would be time-consuming and PILES [, uremia, diabetic , is also unnecessary. Because most clinical labora- propylene glycol or phenformin, iron or isoniazid, tories commonly only measure one relevant cation lactate, glycol, salicylates]), the meaning of (sodium) and two anions (chloride and bicarbon- a low or negative AG is underappreciated. There are ate), the positive and negative sums are not com- several scenarios that could potentially yield a low or negative AG, including decreased concentration of Daniel Repplinger is a medical toxicology fellow in the Depart- ment of Emergency Medicine at New York University Langone UA, increased concentrations of nonsodium cations Medical Center. Lewis S. Nelson is a professor in the Department (UC), and overestimation of serum chloride. of Emergency Medicine and Director of the Medical Toxicology Fel- Decreased concentration of unmeasured an- lowship Program at the New York University School of Medicine and the New York City Poison Control Center. This article originally ions. This most commonly occurs by two mecha- appeared in Emergency Medicine (2015;47[5]:216, 219-220). nisms: dilution of the extracellular fluid or hypoalbu-

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minemia. The addition of water to the extracellular tentially result in a falsely elevated value. However, fluid will cause a proportionate dilution of all the the degree of pseudohyperchloremia will depend on measured electrolytes. Since the concentration of the specific assay used for measurement. The - measured cations is higher than that of the mea- selective electrode method used by many common sured anions, there is a small and relatively insignifi- laboratory analyzers appears to have the greatest in- cant decrease in the AG. terference on chloride measurement in the presence Alternatively, hypoalbuminemia results in a low of bromide. This is simply due to the molecular simi- AG due to the change in UA; albumin is negatively larity of bromide and chloride. charged. At physiologic pH, the overwhelming ma- Conversely, the coulometry method, often used jority of serum proteins are anionic and counter- as a reference standard, has the least interference balanced by the positive charge of sodium. Albumin, of current laboratory methods.3 This is because the most abundant serum protein, accounts for ap- coulometry does not completely rely on molecular proximately 75% of the normal AG. Hypoalbumin- structure to measure concentration; rather, it mea- emic states, such as cirrhosis or nephrotic syndrome, sures the amount of energy produced or consumed can therefore cause low AG due to the retention of in an electrolysis reaction. Iodide, another halide chloride to replace the lost negative charge. The al- compound, has also been described as a cause of bumin concentration can be corrected to calculate pseudohyperchloremia, whereas fluoride does not the AG.2 seem to have significant interference.4 Nonsodium cations. There are a number of clini- cal conditions that result in the retention of non- How are patients exposed sodium cations. For example, the excess positively to bromide salts? charged paraproteins associated with IgG myeloma Bromide salts, specifically sodium bromide, are raise the UC concentration, resulting in a low AG. infrequently used to treat seizure disorders but Similarly, elevations of unmeasured cationic electro- are generally reserved for patients with epilepsy lytes, such as calcium and magnesium, may also re- refractory to other, less toxic anticonvulsant medi- sult in a lower AG. Significant changes in AG, though, cations. During the era when bromide salts were are caused only by profound (and often life-threat- more commonly used to treat epilepsy, bromide ening) hypercalcemia or hypermagnesemia. intoxication, or bromism, was frequently ob- Overestimation of serum chloride. Overestima- served. tion of serum chloride most commonly occurs in Bromism may manifest as a constellation of non- the clinical scenario of bromide exposure. In nor- specific neurologic and psychiatric symptoms. These mal physiologic conditions, chloride is the only ha- most commonly include , , agita- lide present in the extracellular fluid. With intake of tion, , and . In more severe brominated products, chloride may be partially re- cases of bromism, and may occur.3,5 placed by bromide. As there is greater renal tubular Although bromide salts are no longer commonly avidity for bromide, chronic ingestion of bromide prescribed, a number of products still contain bro- results in a gradual rise in serum bromide concen- minated ingredients. Symptoms of bromide intoxi- trations with a proportional fall in chloride. cation can occur with chronic use of a cough syrup However, and more importantly, bromide inter- containing dextromethorphan hydrobromide, as feres with a number of laboratory techniques mea- well as the brominated vegetable oils found in some suring chloride concentrations, resulting in a spuri- soft drinks.5 ously elevated chloride, or pseudohyperchloremia. Because the measured sodium and How is bromism treated? concentrations will remain unchanged, this falsely The treatment of bromism involves preventing- fur elevated chloride measurement will result in a nega- ther exposure to bromide and promoting bromide tive AG. excretion. Bromide has a long half-life (10 to 12 days), but in patients with normal renal function, it What causes is possible to reduce this half-life to approximately the falsely elevated chloride? three days with hydration and with sodium All of the current laboratory techniques for mea- chloride.3 surement of serum chloride concentration can po- Alternatively, in patients with impaired renal

26 Clinician Reviews • JULY 2015 clinicianreviews.com RadiologyReview

>> continued from page 20 Answer The radiograph shows that the distal fe- mur is medially dislocated relative to the tibial plateau. In addition, the patella is laterally dislocated. No obvious fractures are evident. Such injuries are typically associated with significant injuries, espe- cially of the medial collateral ligament (MCL), lateral collateral ligament (LCL), and anterior cruciate ligament (ACL). Or- thopedics was consulted for reduction of the dislocation, as well as further workup (including MRI of the knee). CR

Case Studies in Toxicology function or severe intoxication, has References been used effectively.5 1. Emmett M, Narins RG. Clinical use of the anion gap. Medicine (Balti- more). 1977;56(1):38-54. 2. Figge J, Jabor A, Kazda A, Fencl V. Anion gap and hypoalbumin- Case Conclusion emia. Crit Care Med. 1998;26(11):1807-1810. The patient was admitted for observation and treat- 3. Vasuyattakul S, Lertpattanasuwan N, Vareesangthip K, et al. A negative ed with IV . After consultation with anion gap as a clue to diagnose bromide intoxication. . his neurologist, he was discharged home in the care 1995;69(3):311-313. of his parents, who were advised to continue him 4. Yamamoto K, Kobayashi H, Kobayashi T, Murakami S. False hyperchlo- remia in bromism. J Anesth. 1991;5(1):88-91. on sodium bromide (185 mg bid, orally) since his 5. Ng YY, Lin WL, Chen TW. Spurious and decreased were refractory to other anticonvulsant med- anion gap in a patient with dextromethorphan bromide. Am J Nephrol. ications. CR 1992;12(4):268-270.

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