{"title":"Superwarfarin (Long-Acting Anticoagulant Rodenticides) Poisoning: from Pathophysiology to Laboratory-Guided Clinical Management.","authors":"Yeow-Kuan Chong, Tony Wing-Lai Mak","doi":"10.33176/AACB-19-00029","DOIUrl":null,"url":null,"abstract":"<p><p>Superwarfarins are long-acting anticoagulant rodenticides developed from warfarin. The mechanism of action is by inhibition of vitamin K epoxide reductase, resulting in the inability of the body to recycle vitamin K. Deficiency of vitamin K thereafter leads to inability for the body to synthesise vitamin K-dependent coagulation factors, factor II, VII, IX, and X, leading to prolonged prothrombin time. Due to the bulky aromatic sidechains, superwarfarins have a much longer half-life when compared to warfarin, and exposure to superwarfarins results in a prolonged period of anticoagulation which can result in clinical bleeding. Diagnosis is straightforward in patients with known history of superwarfarin exposure but has proved difficult for patients who did not report superwarfarin intake. Superwarfarin poisoning should therefore be suspected in all patients with unexplained prolongation of prothrombin time, and can be confirmed by their detection in serum. Treatment for superwarfarin poisoning includes rapid correction of factor deficiencies with either 4-factor prothrombin complex concentrate or fresh frozen plasma in patients with active bleeding, and high dose vitamin K therapy given multiple times per day for a prolonged period of weeks to months.</p>","PeriodicalId":34924,"journal":{"name":"Clinical Biochemist Reviews","volume":"40 4","pages":"175-185"},"PeriodicalIF":0.0000,"publicationDate":"2019-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6892705/pdf/cbr-40-175.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical Biochemist Reviews","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.33176/AACB-19-00029","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 0
Abstract
Superwarfarins are long-acting anticoagulant rodenticides developed from warfarin. The mechanism of action is by inhibition of vitamin K epoxide reductase, resulting in the inability of the body to recycle vitamin K. Deficiency of vitamin K thereafter leads to inability for the body to synthesise vitamin K-dependent coagulation factors, factor II, VII, IX, and X, leading to prolonged prothrombin time. Due to the bulky aromatic sidechains, superwarfarins have a much longer half-life when compared to warfarin, and exposure to superwarfarins results in a prolonged period of anticoagulation which can result in clinical bleeding. Diagnosis is straightforward in patients with known history of superwarfarin exposure but has proved difficult for patients who did not report superwarfarin intake. Superwarfarin poisoning should therefore be suspected in all patients with unexplained prolongation of prothrombin time, and can be confirmed by their detection in serum. Treatment for superwarfarin poisoning includes rapid correction of factor deficiencies with either 4-factor prothrombin complex concentrate or fresh frozen plasma in patients with active bleeding, and high dose vitamin K therapy given multiple times per day for a prolonged period of weeks to months.
超华法林是从华法林发展而来的长效抗凝血灭鼠剂。其作用机制是通过抑制维生素 K 环氧化物还原酶,导致机体无法循环利用维生素 K。缺乏维生素 K 会导致机体无法合成依赖维生素 K 的凝血因子 II、VII、IX 和 X,从而导致凝血酶原时间延长。与华法林相比,超级华法林由于含有笨重的芳香族侧链,半衰期要长得多,接触超级华法林会导致抗凝时间延长,从而导致临床出血。对于已知有超华法林接触史的患者来说,诊断非常简单,但对于没有报告摄入超华法林的患者来说,诊断却很困难。因此,对于所有原因不明的凝血酶原时间延长的患者,都应怀疑超华素中毒,并可通过在血清中检测到超华素来确诊。治疗超华素中毒的方法包括用 4 因子凝血酶原复合物浓缩物或新鲜冰冻血浆快速纠正活动性出血患者的因子缺乏症,以及每天多次、持续数周至数月的大剂量维生素 K 治疗。