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339


Vital signs and toxic syndromes

Chapter by: Goldfrank L; Flomenbaum N; Lewin N
in: Goldfrank's toxicologic emergencies by Goldfrank, Lewis R [Eds]
Stamford CT : Appleton & Lange, 1998
pp. 277-283
ISBN: 0838531482
CID: 4519

Managing the patient with an unknown overdose

Chapter by: Flomenbaum N; Goldfrank L; Lewin N
in: Goldfrank's toxicologic emergencies by Goldfrank, Lewis R [Eds]
Stamford CT : Appleton & Lange, 1998
pp. 515-540
ISBN: 0838531482
CID: 4521

Phencyclidine

Chapter by: Goldfrank L; Lewin N
in: Goldfrank's toxicologic emergencies by Goldfrank, Lewis R [Eds]
Stamford CT : Appleton & Lange, 1998
pp. 1105-1109
ISBN: 0838531482
CID: 4527

Goldfrank's toxicologic emergencies

Goldfrank LR; Flomenbaum NE; Lewin NA; Weisman RS; Howland MA; Hoffman RS
Stamford, CT : Appleton & Lange., 1998
Extent: 1917 p.
ISBN: 9780838531488
CID: 1133

Forward

Chapter by: Goldfrank LR
in: Clinical procedures in emergency medicine by Roberts JR; Hedges JR [Eds]
Philadelphia : Saunders, 1998
pp. ?-?
ISBN: 072166055x
CID: 3292

The effects of nutrition on plasma cholinesterase activity and cocaine toxicity in mice

Cahill-Morasco R; Hoffman RS; Goldfrank LR
BACKGROUND: Low plasma cholinesterase activity is associated with severe cocaine toxicity in human subjects and animal experiments. Exogenously enhanced plasma cholinesterase activity is protective against cocaine toxicity in animals. Cocaine users tend to have lower plasma cholinesterase activity than controls. Yet, when cocaine users are allowed to use cocaine in controlled settings without dietary restriction, their plasma cholinesterase activity increases. This study evaluates the influence of diet on plasma cholinesterase activity and cocaine toxicity. METHODS: Forty-five Swiss albino mice were maintained on a high (30%) protein diet for 3 weeks. They were then randomized into equal groups and given either the high protein diet, an isocaloric low protein diet, or a protein and calorie deficient diet which consisted of reduced intake of the high protein diet. Body weights and plasma cholinesterase activities were measured after a 21-day study period. All animals then received a fixed dose of intraperitoneal cocaine and were observed for seizures and death. RESULTS: Body weights and plasma cholinesterase activities of the high protein animals remained stable. Weights for the low protein and reduced intake animals fell by 5% and 15%, respectively (p < 0.05 for both vs baseline). Similarly, plasma cholinesterase activities for the low protein and reduced intake animals fell by 4% and 10%, respectively (p = 0.06 for low protein and < 0.05 for reduced intake vs baseline). Cocaine caused seizures in 67% of the high protein animals as compared to 93% and 100% of the low protein and reduced intake animals, respectively (p < 0.05 for high protein vs reduced intake). None of the high protein animals died as compared to 20% and 100% of the low protein and reduced intake animals, respectively (p < 0.05 for high protein vs reduced intake). CONCLUSION: Protein and calorie malnutrition is associated with a reduction in plasma cholinesterase activity and enhanced cocaine toxicity in mice. Further study is needed to determine if dietary factors are partially responsible for variations in plasma cholinesterase activity and cocaine susceptibility in humans
PMID: 9865234
ISSN: 0731-3810
CID: 44362

How dangerous is the unintentional use of the word accident in our literature? [Editorial]

Hung OL; Hoffman RS; Goldfrank LR
PMID: 9541033
ISSN: 0731-3810
CID: 44366

A milestone for emergency medicine in Europe [Editorial]

Goldfrank LR; Warnod V
ORIGINAL:0004759
ISSN: 1054-0725
CID: 44413

1998 Matthew Ellenhorn Award Lecture - Medical toxicology: past, present, and future [Lecture]

Goldfrank LR
ORIGINAL:0004784
ISSN: 1523-5130
CID: 44438

Cocaine related chest pain

Lee CC; Goldfrank LR
ORIGINAL:0004777
ISSN: 1082-6173
CID: 44431