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340


Thallium poisoning from maliciously contaminated food [Case Report]

Meggs WJ; Hoffman RS; Shih RD; Weisman RS; Goldfrank LR
Four young adults presented two days after one of them had received marzipan balls packaged in a box from an expensive candy manufacturer. Two ate one candy ball, while two others shared a third. The next day, variable gastrointestinal symptoms developed. On the third day, two patients developed painful paresthesiae of the hands and feet, an early but nonspecific clinical marker of thallium poisoning. A tentative diagnosis of thallium poisoning was made based on symptoms, and treatment was initiated. The remaining candies were radiographed. Metallic densities in the candies supported the diagnosis, and atomic absorption spectroscopy was used to quantitate thallium content. Each candy contained a potentially fatal dose. Five to seven days later, hypertension and tachycardia developed in the two patients who had ingested an entire candy. All patients developed alopecia but recovered without overt neurologic or other sequelae. While the diagnosis of thallium poisoning is often delayed until alopecia develops, an early diagnosis favors an effective treatment strategy
PMID: 7966530
ISSN: 0731-3810
CID: 44382

General management of the poisoned or overdosed patient

Chapter by: Flomenbaum N; Goldfrank L; Weisman R; Howland MA; Lewin N
in: Goldfrank's toxicologic emergencies by Goldfrank, Lewis R [Eds]
Norwalk CT : Appleton & Lange, 1994
pp. 25-41
ISBN: 0838531466
CID: 4508

Cocaine

Chapter by: Lewin N; Goldfrank L; Hoffman R
in: Goldfrank's toxicologic emergencies by Goldfrank, Lewis R [Eds]
Norwalk CT : Appleton & Lange, 1994
pp. 847-880
ISBN: 0838531466
CID: 4515

Phencyclidine

Chapter by: Lewin N; Goldfrank L; Osborn H
in: Goldfrank's toxicologic emergencies by Goldfrank, Lewis R [Eds]
Norwalk CT : Appleton & Lange, 1994
pp. 875-880
ISBN: 0838531466
CID: 4516

Data, epidemiology, and the future strength of emergency medicine [Comment]

Goldfrank LR
PMID: 8239108
ISSN: 0196-0644
CID: 44383

Prevalence of sorbitol in multiple-dose activated charcoal regimens in emergency departments

Wax PM; Wang RY; Hoffman RS; Mercurio M; Howland MA; Goldfrank LR
STUDY OBJECTIVES: To determine the availability and use of premixed activated charcoal in sorbitol preparations during multiple-dose activated charcoal therapy in the emergency department. DESIGN AND SETTING: A prospective telephone survey of all 911 receiving hospitals within the catchment area of one poison center. TYPE OF PARTICIPANTS: Hospital pharmacy supervisors and ED charge nurses. INTERVENTION: Hospital pharmacy supervisors were surveyed about the available preparations of activated charcoal on their hospital's formulary, and ED charge nurses in these same hospitals were surveyed about the prevalence of sorbitol use in multiple-dose activated charcoal regimens. MEASUREMENTS AND MAIN RESULTS: Eleven hospitals (16%) stocked only activated charcoal in sorbitol preparations. Twenty-one hospitals (31%) had both activated charcoal in sorbitol preparations and activated charcoal without sorbitol preparations, and 35 hospitals (52%) had only activated charcoal without sorbitol preparations. Repeat dosing of sorbitol during multiple-dose activated charcoal therapy occurred in 33 of 67 (49%) of the EDs surveyed. CONCLUSION: Sorbitol dosing is often repeated with activated charcoal during multiple-dose activated charcoal therapy in the ED because of the ready availability (and sometimes exclusive availability) of premixed activated charcoal in sorbitol preparations
PMID: 8239100
ISSN: 0196-0644
CID: 44384

Tetracaine protects against cocaine lethality in mice

Grant SA; Hoffman RS; Goldfrank LR
STUDY HYPOTHESIS: Tetracaine will enhance cocaine toxicity. STUDY POPULATION: Two hundred forty female Swiss albino mice weighing 27 to 45 g. METHODS: Intraperitoneal injections of tetracaine and cocaine were given to groups of ten mice each in a controlled, blinded fashion. Either tetracaine or an equal volume of normal saline was given five minutes before one of six incremental doses of cocaine, ranging from 60 to 110 mg/kg. The experiment was repeated twice using two different doses of tetracaine: either an LD10 (40 mg/kg determined from preliminary studies), or one-twentieth of the dose of cocaine (which approximates the ratio used in tetracaine, epinephrine, and cocaine). Lethality was recorded at 24 hours. Lethality between groups was compared with a Wilcoxon sign-rank test. RESULTS: Tetracaine reduced cocaine lethality at all doses. This reduction in lethality was statistically significant at both tetracaine doses (P < .05). CONCLUSION: In the mouse, pretreatment with tetracaine significantly decreases cocaine lethality
PMID: 8239098
ISSN: 0196-0644
CID: 44385

Initial management of the multiply injured or intoxicated patient

Chapter by: Delaney KA; Goldfrank LR
in: Head injury by Cooper PR [Eds]
Baltimore : Williams & Wilkins, 1993
pp. 43-64
ISBN: 0683021087
CID: 3296

Poisioning and overdose

Chapter by: Henry GC; Goldfrank LR
in: Shock and reuscitation by Geller ER [Eds]
New York : McGraw-Hill Health Professionals, 1993
pp. 527-560
ISBN: 0070235007
CID: 3298

Osmol gaps revisited: normal values and limitations

Hoffman RS; Smilkstein MJ; Howland MA; Goldfrank LR
A study was designed to define the osmol gap in patients whose serum ethanol concentrations are known, to reevaluate several accepted equations for calculating osmolarity, and to apply the results to the theoretical clinical scenario of a toxic alcohol ingestion. The design for the study used consecutive, prospective enrollment of all patients presenting to a large inner city hospital who clinically required determination of their serum ethanol and electrolytes. Three hundred and twenty one consecutive adult patients were enrolled in the study, sixteen were excluded from the final analysis. A stepwise multiple linear regression analysis was performed to determine the best coefficients for sodium, blood urea nitrogen, and ethanol from the data set. Osmolarity was then calculated using these coefficients and traditional models. The osmol gap (measured osmolality minus calculated osmolarity [2*Na + BUN/2.8 + Glu/18 + Etoh/4.6]) was -2 +/- 6 mOsm. Although different equations produced different osmol gaps (ranging from -5 to + 15 mOsm) the standard deviations and correlation coefficients were similar. Large variations exist in the range of osmol gaps. Absolute values are very dependent on the equations used to calculate osmolarity. Because of the larger range of values, small osmol gaps should not be used to eliminate the possibility of toxic alcohol ingestion
PMID: 8433417
ISSN: 0731-3810
CID: 44386