Abstract:The objective of this guideline is to assist poison center personnel in the appropriate out-of-hospital triage and initial management of patients with suspected ingestions of acetaminophen. An evidencebased expert consensus process was used to create this guideline. This guideline applies to ingestion of acetaminophen alone and is based on an assessment of current scientific and clinical information.
“…Based on a consensus guideline for out-of-hospital management of paracetamol overdose, evaluation at a medical facility is recommended if: (a) at least 10 g or 200 mg/kg (whichever is less) is ingested within an eight-hour period for single ingestion; (b) in the case of repeated supratherapeutic ingestion, at least 10 g or 200 mg/kg (whichever is less) is ingested within a 24-hour period; or (c) at least 6 g or 150 mg/kg (whichever is less) is ingested per 24-hour period for 48 hours or longer. (23) Bernal cited 7.5 g or 125 mg/kg as the minimum dose capable of causing hepatotoxicity. (24) Among the patients who developed severe hepatotoxicity in our study, the majority had ingested at least 10 g or 200 mg/kg within an eight-hour period.…”
“…Based on a consensus guideline for out-of-hospital management of paracetamol overdose, evaluation at a medical facility is recommended if: (a) at least 10 g or 200 mg/kg (whichever is less) is ingested within an eight-hour period for single ingestion; (b) in the case of repeated supratherapeutic ingestion, at least 10 g or 200 mg/kg (whichever is less) is ingested within a 24-hour period; or (c) at least 6 g or 150 mg/kg (whichever is less) is ingested per 24-hour period for 48 hours or longer. (23) Bernal cited 7.5 g or 125 mg/kg as the minimum dose capable of causing hepatotoxicity. (24) Among the patients who developed severe hepatotoxicity in our study, the majority had ingested at least 10 g or 200 mg/kg within an eight-hour period.…”
“…To reduce the tremendous variability in triage practices [15], 17 US national triage guidelines were published from 2003 to 2008, but address only 107 ingredients [18][19][20][21][22][23][24][25][26][27][28][29][30][31][32][33][34]. Most substances are not covered by national guidelines, and most poison centers have only a limited set of additional site-specific guidelines; thus, there is a high degree of triage variability both between and within centers and considerable time spent reassessing toxicity each time an exposure occurs.…”
webPOISONCONTROL augments traditional poison control services by providing automated, accurate online access to case-specific triage and first aid guidance for poison ingestions. It is safe, quick, and easy to use.
“…The serious outcome rate (portion of total cases with serious medical outcomes) was determined for selected variables that might be expected to influence the severity or management of a case based on triage guidelines published by the American Association of Poison Control Centers (AAPCC) for other substances (Dart et al, 2006;Caravati et al, 2005;Manoguerra et al, 2005;Olson et al, 2005;Wax et al, 2005). The threshold for dose variables included in this analysis was based on double the manufacturer's recommended maximum daily dose for children and adolescents of 1.4 mg/kg or 100 mg (Eli Lilly and Company, 2006).…”
Limited information exists on potentially adverse consequences following pediatric atomoxetine ingestions reported to poison control centers. Using pediatric atomoxetine ingestions reported to Texas poison control centers during 2003-2005, the proportion of cases involving serious outcomes (medical outcomes classified as moderate effects, major effects, death, or judged as potentially toxic exposures) was determined for selected variables and evaluated for statistical significance by calculating the rate ratio (RR) and 95% confidence interval (CI). Of 501 cases identified, 31 (6%) involved serious outcomes. Higher serious outcome rates were found with a maximum dose of >2.8 mg/kg or >200 mg or >4 tablets. Serious outcome rates were also higher if the exposure involved intentional self-harm or the patient was already at or en route to a health care facility when the poison control center was contacted or referred to a health care facility by the poison control center. The severity of the outcome associated with pediatric atomoxetine ingestions was dependent upon the dose and the circumstances of the ingestion (whether intentional self-harm was involved). The management of patients with serious outcomes was more likely to involve health care facilities. This information is useful for creating triage guidelines for the management of pediatric atomoxetine ingestions.
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