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POISONINGS AND ANTIDOTES |
F Baud |
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| Frédéric J Baud1 | |||||
| 1Medical and Toxicological Critical Care Department. Assistance Publique–Hôpitaux de Paris ; Hôpital Lariboisière-Université Denis Diderot. Paris, France | |||||
| Abstract | |||||
| The treatment of poisoning includes supportive treatment, decontamination, and antidotes. | |||||
| This classification masks the duality of human poisoning involving the combination of toxicokinetic and toxicodynamic processes. | |||||
| All treatments used in toxicology can be classified within 8 categories including 5 modifying toxicokinetics and 3 modifying toxicodynamics of poisons. | |||||
| The 5 ways to modify toxicokinetics include: | |||||
| -1- decreasing the bioavailability of toxicants by non-specific (activated charcoal, skin or ocular washing, whole bowel irrigation) or specific agents (ex: calcium for fluoride, Prussian blue for Thallium) | |||||
| -2- promoting the extra-cellular redistribution of the toxicants: specific Fab fragments for cardiac glycosides, methemoglobin-forming agents or hydroxocobalamin for cyanide | |||||
| -3- promoting the elimination of the toxicant unchanged in the urine (alkaline dieresis for salicylates, phenobarbital, glyphosate; chelating agents for heavy metals) or in the breath (oxygen and carbon monoxide) | |||||
| -4- increasing the metabolism resulting in inactive metabolites: N-acetylcystein for paracetamol, sodium thiosulfate for cyanide, carboxypeptidase for methotrexate, L-carnithine for valproate | |||||
| -5- blocking a metabolism resulting in active metabolites: fomepizole for toxic alcohols | |||||
| The 3 ways modifying toxidynamics include: | |||||
| -6- non competitive (pralidoxime in organophosphates), or competitive antagonism (antagonists: naloxone, flumazénil, atropine, catecholamines, …) | |||||
| -7- by pass of the binding of the toxicant to the receptor/target (glucagon and beta-blockers, insulin and calcium channel inhibitors) | |||||
| -8- correcting the peripheral effects of the toxicants (dextrose for insulin, calcium to correct fluoride-induced hypocalcaemia, mechanical ventilation to support drug-induced respiratory failure, cardiovascular support in drug-induced cardiovascular shock) | |||||
| Decontamination aimed at decreasing the bioavailability of toxic substances; there are accumulating evidence of its efficiency during a very short period of time. | |||||
| Supportive treatment efficiently corrects the peripheral effects of the toxicants. | |||||
| Supportive treatment may correct failure of organ involved in the elimination of substances. | |||||
| In this condition, supportive treatment is also a toxicokinetic treatment. | |||||
| The number of antidotes obviating or decreasing the need for supportive therapy is progressively growing. | |||||
版权所有© 2006-2009,中国病理生理学会危重病医学专业委员会 Chinese Society of Critical Care Medicine
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