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Items 1 - 7 of 7 |
One page. |
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Poison bottles.
Kravetz RE.
Archives Committee, American College of Gastroenterology.
PMID: 15447743 [PubMed - in process]
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Status epilepticus after a massive intravenous N-acetylcysteine overdose leading to intracranial hypertension and death.
Bailey B, Blais R, Letarte A.
Section of Emergency Medicine, Department of Pediatrics, Hopital Ste-Justine, Montreal, Quebec, Canada. baileyb@umontreal.ca
Cases of N-acetylcysteine overdose have been reported before. In some cases, these overdoses have led to death if an anaphylactoid reaction was present. A healthy 30-month-old girl allegedly ingested acetaminophen at 418 mg/kg. Because the emergency physician feared the time of ingestion might not be accurate, he decided to start the 20.5-hour intravenous N-acetylcysteine protocol 8 hours after ingestion. He mistakenly prescribed the maximum milliliter-per-kilogram volume of the dextrose 5% diluent for the milliliter-per-kilogram volume of N-acetylcysteine 20% to be administered. Five hours after the error was detected (19.5 hours postingestion), the patient started developing myoclonus on the left side of her body, with left eye deviation. This condition persisted intermittently for 3 hours despite treatment with diazepam, lorazepam, and phenytoin. A first computed tomographic scan result was normal. A few hours later, she sustained shorter recurrences of the myoclonus. At 30 hours after ingestion, she started to have irregular breathing and became unresponsive to pain. A repeated computed tomographic scan showed diffuse cerebral edema. A postmortem examination showed the presence of acute anoxic encephalopathy with marked cerebral edema and the beginning of uncal herniation that confirmed the clinical diagnosis of intracranial hypertension and brain death. A cumulative intravenous dose of 2,450 mg/kg of N -acetylcysteine was associated with status epilepticus, intracranial hypertension, and death in a child.
PMID: 15459624 [PubMed - in process]
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The benign clinical course following a large pediatric montelukast ingestion.
Cantrell FL, Farson-Collier M.
Publication Types:
PMID: 15362605 [PubMed - indexed for MEDLINE]
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Effectiveness of delayed use of crotalidae polyvalent immune Fab (ovine) antivenom.
Bebarta V, Dart RC.
Rocky Mountain Poison and Drug Center, Denver Health Medical Center, University of Colorado Health Sciences Center, Denver, Colorado 80204, USA.
Traditionally, horse-serum-based antivenom has been used in the United States for North American crotaline snake evenomation. Crotalidae polyvalent immune Fab (ovine) was approved in 2000 for use in mild to moderate envenomations. The manufacture recommends use within 6 h of envenomation. Published postmarketing retrospective reports describe its use up to 9 h after envenomation. We describe a case of effective use of FabAV 52 h after envenomation with resultant correction of coagulopathy and mild improvement of local symptoms.
Publication Types:
PMID: 15362603 [PubMed - indexed for MEDLINE]
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Acute renal failure following ingestion of manganese-containing fertilizer.
Huang WH, Lin JL.
Department of Nephrology, Poison Center and Division of Nephrology, Chang Gung Memorial Hospital, Taipei, Taiwan, ROC.
Fertilizers are used to promote the survival and growth of plants and crops and have a good safety record when used properly. The basic elements in fertilizer include phosphorus, nitrite, and potassium. In addition, there are additive agents that vary for different crops and which may include some metals. Acute intoxication by ingesting fertilizer includes damage to various organ systems as well as severe cardiovascular or respiratory distress. We report the case of a 64-year-old man who ingested about 700 mL of fertilizer and suffered acute renal failure, hyperkalemia, and mild methemoglobinemia. After supportive care and emergent hemodialysis for hemodynamic instability due to hyperkalemia, the renal function of the patient recovered in four days.
Publication Types:
PMID: 15362599 [PubMed - indexed for MEDLINE]
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Frequency and nature of recorded childhood immunization-related errors in Greece.
Petridou E, Kouri N, Vadala H, Dalamaga M, Sege R.
Department of Hygiene and Epidemiology, Center for Research and Prevention of Injuries among the Young, Athens University Medical School, Athens, Greece. epetrid@med.uoa.gr
BACKGROUND: While routine immunizations are very safe, their administration to healthy children requires minimization of immunization programmatic errors. In order to estimate the incidence and ascertain the nature of reported immunization errors in the Greek childhood population, we have undertaken a study using data from the National Poison Information Center in Greece, which also has the responsibility to address medication-induced errors. METHODS: All immunization errors concerning children and reported to the National Poison Information Center during the 2-yr period 1999-2000 were retrieved and the conditions of their occurrence were examined. The incidence of reported errors was calculated under the assumption that during each year 100,000 children are born in Greece, and during their childhood they receive a total of about 20 immunization doses of all childhood immunizations. RESULTS: There were 40 immunization errors reported, corresponding to a reported incidence of about 11 per million immunization doses. Of these errors, 20 concerned OPV, 13 DTP, 5 MMR, 1 Haemophilus influenza and 1 Hepatitis B immunizations. In 12 instances an erroneous route was used (out of which 11 concerned OPV), whereas overdose was documented in 13 instances (out of which 8 concerned OPV). The third most common error was administration of DTP instead of the recommended Td vaccine. No adverse patient outcomes were reported. CONCLUSIONS: In Greece, reported errors in immunization practice are relatively rare. Packaging modifications (about one in three errors in this study) of the OPV and DTP could further reduce their incidence.
PMID: 15362594 [PubMed - indexed for MEDLINE]
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Position paper: cathartics.
[No authors listed]
The administration of a cathartic alone has no role in the management of the poisoned patient and is not recommended as a method of gut decontamination. Experimental data are conflicting regarding the use of cathartics in combination with activated charcoal. No clinical studies have been published to investigate the ability of a cathartic, with or without activated charcoal, to reduce the bioavailability of drugs or to improve the outcome of poisoned patients. Based on available data, the routine use of a cathartic in combination with activated charcoal is not endorsed. If a cathartic is used, it should be limited to a single dose in order to minimize adverse effects of the cathartic. A review of the literature since the preparation of the 1997 Cathartics Position Statement revealed no new evidence that would require a revision of the conclusions of the Statement.
Publication Types:
PMID: 15362590 [PubMed - indexed for MEDLINE]
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