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1.
Acad Emerg Med ; 6(9): 895-9, 1999 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-10490250

RESUMEN

OBJECTIVE: To compare the palatabilities of two activated charcoal formulations in patients with potentially toxic ingestions. METHODS: Prospective double-blinded randomized controlled trial comparing the palatability of standard charcoal [LiquiChar (LC)] with that of a superactivated granulated form [(CharcoAid G (CA)]. Alert adult patients with known or suspected toxic ingestions requiring activated charcoal were randomly assigned to receive 60 g of either LC or CA diluted in a cola beverage to a volume of 340 mL. Standardized forms were used to collect data on patient demographics, time required to drink the charcoal, the remaining volume of activated charcoal, and any adverse reactions. Patients rated the palatability of the activated charcoal on a 100-mm visual analog scale (VAS) with 100 indicating "best imaginable beverage." Telephone follow-up was obtained to identify complications. Student's t-tests or Mann-Whitney U tests were used to compare continuous variables (e.g., VAS, time, age). Fisher's exact tests were used to compare categorical variables. This study had a power of 0.9 to detect a 20-mm difference in the VAS, alpha = 0.05. RESULTS: There were 60 patients enrolled; 29 drank LC, 31 drank CA. Mean age was 34 years; 68% were female. The groups were similar for age, time from ingestion, ingested agents, time required to drink charcoal, and remaining volume. There were more females in the LC group. Patients receiving CA had significantly higher palatability scores than those receiving LC [35.9 (95% CI = 22.5 to 49.3 mm) vs 19.0 mm (95% CI = 9.3 to 28.6 mm) p = 0.04]. None of the patients aspirated. Of seven patients who vomited, five were given LC (p = 0.25). CONCLUSIONS: CharcoAid is more palatable to patients with toxic ingestions than the standard nongranulated form. Use of the granular charcoal may improve patient compliance.


Asunto(s)
Antídotos/uso terapéutico , Carbón Orgánico/administración & dosificación , Satisfacción del Paciente , Intoxicación/tratamiento farmacológico , Administración Oral , Adulto , Antídotos/química , Carbón Orgánico/química , Química Farmacéutica , Intervalos de Confianza , Método Doble Ciego , Femenino , Humanos , Masculino , Persona de Mediana Edad , Probabilidad , Estudios Prospectivos , Gusto
2.
Ann Emerg Med ; 24(5): 972-4, 1994 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-7526752

RESUMEN

A case of lindane toxicity in a 24-year-old woman who used lindane shampoo for treatment of an alleged case of lice infestation is described. The patient experienced uncontrolled motor activity that began approximately 2 hours after treatment and resolved approximately 48 hours later. A review of the literature revealed that most cases of acute lindane toxicity resulting from topical application have occurred in the pediatric and geriatric populations and are manifested by grand mal seizures. No case of acute lindane toxicity resulting from topical use was found in the emergency medicine literature. This case illustrates the toxic, neurologic effects of lindane in a young adult.


Asunto(s)
Atetosis/inducido químicamente , Alucinaciones/inducido químicamente , Hexaclorociclohexano/envenenamiento , Infestaciones por Piojos/tratamiento farmacológico , Dermatosis del Cuero Cabelludo/tratamiento farmacológico , Enfermedad Aguda , Administración Cutánea , Adulto , Atetosis/diagnóstico , Atetosis/terapia , Femenino , Alucinaciones/diagnóstico , Alucinaciones/terapia , Humanos , Jabones
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