Goel Parul, Gupta Nidhi, Singh Surjit, Bhalla Ashish, Sharma Navneet, Gill K D
Department of Biochemistry, Postgraduate Institute of Medical Education and Research, Chandigarh, 160012 India.
Indian J Clin Biochem. 2012 Jan;27(1):34-9. doi: 10.1007/s12291-011-0152-0. Epub 2011 Aug 2.
Oximes such as pralidoxime chloride reactivate acetylcholinesterase. However their role in management of organophosphate poisoning is controversial. The study was carried out to find effectiveness of pralidoxime chloride (2-PAM) in regenerating red cell acetyl cholinesterase in first 24 h following administration of it in dose recommended by WHO. Eight patients with OPP [chlorpyriphos (3), phorate (3), dichlorvos (1) and monocrotophos (1) who fulfilled the criteria for inclusion were investigated. In addition to decontamination and atropine, all these patients were administered 30 mg/kg body wt of 2-PAM as bolus dose followed by 7.5 mg/kg body wt/h with maximum dose being 500 mg/h as continuous infusion till first 24 h. Red cell AChE activity was estimated every 15 min for first 4 h, one hourly for next 4 h and then 2 hourly till 24 h and subsequently without 2-PAM every 12 h till 7 days or discharge or death which ever earlier. In all the patients maximum increase in activity was observed in first 4 h following which rise was very slow despite continued 2-PAM infusion and reaching a steady state in 20 h in all the cases. The increase in red cell AChE activity observed in diethyl group at 24 h of 2-PAM infusion was 154% vs. 81% in dimethyl group. At 7 days the increase in activity was 215% vs. 118% respectively. However on multiple repeated ANOVA, no statistically significant difference was observed between diethyl and dimethyl groups at admission and discharge (P > 0.05). Similarly no significant difference was observed in three groups when patients were categorized according to WHO classification of organophosphates (P > 0.05). The maximum increase in red cell AChE activity occurs in first 4 h of 2-PAM administration followed by a slow increase despite 2-PAM infusion till 24 h.
氯解磷定等肟类药物可使乙酰胆碱酯酶重新活化。然而,它们在有机磷中毒治疗中的作用存在争议。本研究旨在探讨按照世界卫生组织推荐剂量给药后,氯解磷定(2 - 吡啶醛肟甲基氯化物)在前24小时内对红细胞乙酰胆碱酯酶再生的有效性。对8例符合纳入标准的有机磷中毒患者[毒死蜱(3例)、甲拌磷(3例)、敌敌畏(1例)和久效磷(1例)]进行了调查。除了进行去污处理和使用阿托品外,所有这些患者均给予30mg/kg体重的2 - 吡啶醛肟甲基氯化物作为静脉推注剂量,随后以7.5mg/kg体重/小时的速度持续输注,最大剂量为500mg/小时,持续至24小时。在最初4小时内每15分钟、接下来4小时内每小时、然后直至24小时每2小时估计红细胞乙酰胆碱酯酶活性,随后在停止使用2 - 吡啶醛肟甲基氯化物的情况下,每12小时估计一次,直至7天或出院或死亡(以先到者为准)。在所有患者中,给药后最初4小时内活性增加最大,此后尽管继续输注2 - 吡啶醛肟甲基氯化物,活性上升仍非常缓慢,所有病例在20小时达到稳定状态。在输注2 - 吡啶醛肟甲基氯化物24小时时,二乙基组红细胞乙酰胆碱酯酶活性增加154%,而二甲基组为81%。在7天时,活性增加分别为215%和118%。然而,经多次重复方差分析,入院时和出院时二乙基组和二甲基组之间未观察到统计学上的显著差异(P>0.05)。同样,当根据世界卫生组织对有机磷的分类对患者进行分组时,三组之间也未观察到显著差异(P>0.05)。红细胞乙酰胆碱酯酶活性的最大增加发生在给予2 - 吡啶醛肟甲基氯化物后的最初4小时内,此后尽管输注2 - 吡啶醛肟甲基氯化物直至24小时,活性增加仍很缓慢。