Hoffmann Ulrich, Papendorf Thomas
Ernst-Moritz-Arndt University Greifswald, Institute of Pharmacology, Friedrich-Loeffler-Strasse 23d, 17487, Greifswald, Germany.
Intensive Care Med. 2006 Mar;32(3):464-8. doi: 10.1007/s00134-005-0051-z. Epub 2006 Feb 15.
Organophosphate toxicity is the leading cause of morbidity and death in poisoning by insecticides. The clinical symptoms of pesticide toxicity range from the classic cholinergic syndrome to flaccid paralysis and intractable seizures. The mainstays of therapy are atropine, oximes, benzodiazepines and supportive care. The toxicokinetics vary not only with the extent of exposure, but also with the chemical structure of the agent.
We report two cases of poisoning with parathion-ethyl and dimethoate. The patients developed a cholinergic syndrome immediately, accompanied by bradycardia and hypotension.
The patients were admitted to the intensive care unit (ICU) a few hours after ingestion. Atropine was administered according to the cholinergic symptoms. The patients recovered in the ICU after 10-12 days and were discharged after 3 and 4 weeks.
Organophosphate blood and urine levels were determined on admission and during hospitalisation. The pesticides were rapidly distributed and slow elimination rate of the poisons was documented. In the case of parathion-ethyl the distribution half-life estimated was t(1/2alpha) = 3.1h while the terminal half-life was t(1/2beta) = 17.9 h. Using a one-compartment model for dimethoate the elimination half-life was t(1/2beta) = 30.4 h in plasma and 23.8 h in urine. The serum pseudo-cholinesterase activity was below the limit of detection at admission and recovered during the following 3weeks.
有机磷中毒是杀虫剂中毒导致发病和死亡的主要原因。农药中毒的临床症状从典型的胆碱能综合征到弛缓性麻痹和顽固性癫痫不等。治疗的主要方法是使用阿托品、肟类、苯二氮䓬类药物及支持治疗。毒物动力学不仅随接触程度而变化,还随药物的化学结构而变化。
我们报告了两例对硫磷和乐果中毒的病例。患者立即出现胆碱能综合征,伴有心动过缓和低血压。
患者在摄入毒物数小时后被收入重症监护病房(ICU)。根据胆碱能症状给予阿托品治疗。患者在ICU治疗10 - 12天后康复,并于3周和4周后出院。
入院时及住院期间测定了有机磷在血液和尿液中的水平。记录到农药迅速分布且毒物消除速率缓慢。对于对硫磷,估计分布半衰期为t(1/2α)= 3.1小时,而终末半衰期为t(1/2β)= 17.9小时。对于乐果,采用一室模型,其在血浆中的消除半衰期为t(1/2β)= 30.4小时,在尿液中为23.8小时。入院时血清假性胆碱酯酶活性低于检测限,并在接下来的3周内恢复。