a Pharmacology, Toxicology, and Therapeutics , University/BHF Centre for Cardiovascular Science, University of Edinburgh , Edinburgh , UK.
b Centre for Clinical Toxicology and Pharmacology , University Medical Centre Ljubljana , Ljubljana , Slovenia.
Clin Toxicol (Phila). 2018 Aug;56(8):725-736. doi: 10.1080/15563650.2018.1446532. Epub 2018 Mar 20.
Treatment of acute organophosphorus or carbamate insecticide self-poisoning is often ineffective, with tens of thousands of deaths occurring every year. Researchers have recommended the addition of magnesium sulfate or calcium channel blocking drugs to standard care to reduce acetylcholine release at cholinergic synapses.
We aimed to review systematically the evidence from preclinical studies in animals exposed to organophosphorus or carbamate insecticides concerning the efficacy of magnesium sulfate and calcium channel blocking drugs as therapy compared with placebo in reducing mortality or clinical features of poisoning. We also systematically reviewed the evidence from clinical studies in patients self-poisoned with organophosphorus or carbamate insecticides concerning the efficacy of magnesium sulfate and calcium channel blocking drugs as therapy compared with placebo, in addition to standard therapy, in reducing mortality, atropine requirement, need for intubation and ventilation, and intensive care unit and hospital stay.
We performed a systematic review for articles on magnesium sulfate and calcium channel blocking drugs in organophosphorus or carbamate insecticide poisoning using PubMed and China Academic Journals Full-text (Medicine/Hygiene Series) databases and keywords: "organophosphorus or organophosphate poisoning", "cholinesterase inhibitor poisoning" OR "carbamate poisoning" AND "magnesium", "calcium channel blocker", or generic names of different calcium channel blocking drugs. Review of titles and abstracts revealed 2262 papers of potential relevance. After review of the full papers, a total of 19 papers relevant to the question were identified: five preclinical studies, nine case reports or small case series, and five clinical studies and trials. We also obtained primary data from three unpublished clinical trials of magnesium sulfate, providing data from a total of eight clinical studies and trials for analysis. All studies were of organophosphorus insecticides; no studies of carbamates were found. No pre-clinical or clinical studies of calcium channel blocking drugs and magnesium sulfate in combination were found. We extracted data on study type, treatment regimens, outcome, and side effects. Pre-clinical studies: Two rodent studies indicated a benefit of calcium channel blocking drugs treatment on mortality if given before or soon after organophosphorus exposure, in addition to atropine and/or oxime. In poisoned minipigs, treatment with magnesium sulfate after organophosphorus insecticide poisoning reduced cholinergic stimulation and hypertension. Of note, magnesium sulfate further suppressed serum butyrylcholinesterase activity in one rat study. Observational clinical studies: Calcium channel blocking drugs and magnesium sulfate have been used to treat cardiac dysrhythmias and hypertonic uterine contractions in organophosphorus poisoned patients. A small neurophysiological study of magnesium sulfate reported reversion of neuromuscular junction effects of organophosphorus insecticide exposure. Comparative clinical studies: Only four of eight studies were randomized controlled trials; all studies were of magnesium sulfate, of small to modest size, and at substantial risk of bias. They included 441 patients, with 239 patients receiving magnesium sulfate and 202 control patients. The pooled odds ratios for magnesium sulfate for mortality and need for intubation and ventilation for all eight studies were 0.55 (95% confidence interval [CI] 0.32-0.94) and 0.52 (95% CI 0.34-0.79), respectively. However, there was heterogeneity in the results of higher quality phase III randomized controlled trials providing more conservative estimates. Although a small dose-escalation study suggested benefit from higher doses of magnesium sulfate, there was no evidence of a dose effect across the studies. Adverse effects were reported rarely, with 11.1% of patients in the randomized controlled trials receiving the highest dose of magnesium sulfate requiring their infusion to be stopped due to hypotension.
Both preclinical and clinical data suggest that magnesium sulfate and calcium channel blocking drugs might be promising adjunct treatments for acute organophosphorus insecticide poisoning. However, evidence is currently insufficient to recommend their use. Mechanistic and large multi-center randomized controlled trials testing calcium channel blocking drugs and magnesium sulfate are required to provide the necessary evidence, with careful identification of the insecticides ingested and measurement of surrogate markers of toxicity, including butyrylcholinesterase activity.
急性有机磷或氨基甲酸酯类杀虫剂中毒的治疗往往效果不佳,每年有成千上万的人因此死亡。研究人员建议在标准治疗中加入硫酸镁或钙通道阻滞剂,以减少胆碱能突触处乙酰胆碱的释放。
我们旨在系统回顾动物暴露于有机磷或氨基甲酸酯类杀虫剂的临床前研究证据,评估硫酸镁和钙通道阻滞剂作为治疗药物,与安慰剂相比,在降低死亡率或中毒临床特征方面的疗效。我们还系统回顾了有机磷或氨基甲酸酯类杀虫剂中毒患者的临床研究证据,评估硫酸镁和钙通道阻滞剂作为治疗药物,与安慰剂相比,在除标准治疗外,在降低死亡率、阿托品需求、需要插管和通气以及重症监护病房和住院时间方面的疗效。
我们使用 PubMed 和中国学术期刊全文数据库(医学/卫生系列)和关键词“有机磷或有机磷杀虫剂中毒”、“胆碱酯酶抑制剂中毒”或“氨基甲酸酯中毒”以及“镁”、“钙通道阻滞剂”或不同钙通道阻滞剂的通用名称,对硫酸镁和钙通道阻滞剂在有机磷或氨基甲酸酯类杀虫剂中毒中的应用进行了系统评价。标题和摘要的回顾显示了潜在相关的 2262 篇论文。在对全文进行审查后,共确定了 19 篇与问题相关的论文:5 篇临床前研究、9 篇病例报告或小病例系列、5 篇临床研究和试验。我们还从三项未发表的硫酸镁临床研究中获得了原始数据,为 8 项临床研究和试验提供了分析数据。所有研究均为有机磷杀虫剂;未发现有关氨基甲酸酯的研究。未发现钙通道阻滞剂和硫酸镁联合使用的临床前或临床研究。我们提取了研究类型、治疗方案、结局和副作用的数据。临床前研究:两项啮齿动物研究表明,钙通道阻滞剂在有机磷暴露前或暴露后不久与阿托品和/或肟联合使用,对死亡率有治疗作用。在中毒的小型猪中,有机磷杀虫剂中毒后使用硫酸镁可降低胆碱能刺激和高血压。值得注意的是,在一项大鼠研究中,硫酸镁进一步抑制了血清丁酰胆碱酯酶活性。观察性临床研究:钙通道阻滞剂和硫酸镁已被用于治疗有机磷中毒患者的心律失常和子宫收缩性高血压。一项关于硫酸镁的神经生理学小研究报告了有机磷杀虫剂暴露对神经肌肉接头作用的逆转。比较性临床研究:只有八项研究中的四项是随机对照试验;所有研究均为硫酸镁,规模较小,存在较大的偏倚风险。它们包括 441 名患者,其中 239 名患者接受硫酸镁治疗,202 名对照组患者。硫酸镁治疗死亡率和需要插管和通气的所有八项研究的汇总优势比分别为 0.55(95%置信区间[CI]0.32-0.94)和 0.52(95%CI0.34-0.79)。然而,高质量的三期随机对照试验的结果存在异质性,提供了更保守的估计。虽然一项小剂量递增研究表明高剂量硫酸镁有获益,但在这些研究中没有证据表明剂量效应。不良反应很少报道,在随机对照试验中,11.1%接受最高剂量硫酸镁治疗的患者因低血压需要停止输液。
临床前和临床数据均表明,硫酸镁和钙通道阻滞剂可能是急性有机磷杀虫剂中毒的有前途的辅助治疗方法。然而,目前的证据还不足以推荐其使用。需要进行机制和多中心大样本随机对照试验,以测试钙通道阻滞剂和硫酸镁,并谨慎确定摄入的杀虫剂种类,并测量包括丁酰胆碱酯酶活性在内的毒性替代标志物。