Department of Child Health; and Department of Medicine, Division of Medical Toxicology and Precision Medicine, University of Arizona College of Medicine - Phoenix, Phoenix, AZ, USA.
Department of Medical Toxicology, Banner - University Medical Center Phoenix, Phoenix, AZ, USA.
J Med Toxicol. 2020 Jan;16(1):24-32. doi: 10.1007/s13181-019-00729-8. Epub 2019 Aug 12.
Hematologic effects of North American rattlesnake envenomation can include fibrinogenolysis and thrombocytopenia, depending on species, geography, and other variables. During treatment, these effects are routinely monitored through assessment of fibrinogen concentrations and platelet counts. However, these tests provide no information about fibrinolysis or platelet dysfunction, both of which can also occur with venom from some species.
This was a retrospective chart review of patients admitted to a quaternary care academic hospital (Banner - University Medical Center Phoenix) in the southwestern United States for treatment of rattlesnake envenomation, over an approximately 1-year period from March 2017 through April 2018. Patients who had thromboelastography with platelet studies (TEG® with PlateletMapping®) during their care were included.
Twelve patients were identified for this study. Four patients exhibited inhibition of ADP-induced platelet activation: one had normal fibrinogen and platelet count, two had concurrent hypofibrinogenemia, and one had concurrent thrombocytopenia. Crotalidae polyvalent immune Fab (ovine) reversed platelet inhibition in the single patient for whom serial thromboelastographs were available. Fibrinolysis was present in seven patients and resolved in the two patients with serial thromboelastographs.
Inhibition of ADP-induced platelet aggregation and fibrinolysis occurred independent of hypofibrinogenemia and thrombocytopenia, indicating fibrinogen concentration (or protime) and platelet count monitoring alone is insufficient to assess the extent of hematologic toxicity in rattlesnake envenomation. Crotalidae polyvalent immune Fab (ovine) reversed platelet inhibition in one case, suggesting platelet inhibition could also be used in treatment decisions. Fibrinolysis could also be reversed, although the timing to antivenom administration was less clear.
北美的响尾蛇咬伤可导致血液学效应,包括纤维蛋白原溶解和血小板减少,具体取决于物种、地理位置和其他变量。在治疗过程中,通常通过评估纤维蛋白原浓度和血小板计数来监测这些影响。然而,这些测试无法提供有关纤维蛋白溶解或血小板功能障碍的信息,这些问题也可能发生在某些蛇种的毒液中。
这是对 2017 年 3 月至 2018 年 4 月期间在美国西南部一家四级护理学术医院(Banner - University Medical Center Phoenix)因响尾蛇咬伤住院的患者进行的回顾性图表审查。包括在治疗过程中进行血栓弹性图伴血小板研究(TEG® with PlateletMapping®)的患者。
本研究共确定了 12 名患者。4 名患者表现出 ADP 诱导的血小板活化抑制:1 名患者纤维蛋白原和血小板计数正常,2 名患者同时伴有低纤维蛋白原血症,1 名患者同时伴有血小板减少症。在有连续血栓弹性图的患者中,抗蛇毒血清逆转了单例患者的血小板抑制。7 名患者存在纤维蛋白溶解,在有连续血栓弹性图的 2 名患者中得到缓解。
ADP 诱导的血小板聚集和纤维蛋白溶解的抑制与低纤维蛋白原血症和血小板减少无关,表明单独监测纤维蛋白原浓度(或凝血酶原时间)和血小板计数不足以评估响尾蛇咬伤的血液毒性程度。抗蛇毒血清在 1 例患者中逆转了血小板抑制,这表明血小板抑制也可用于治疗决策。纤维蛋白溶解也可以逆转,尽管抗蛇毒血清给药的时间不太明确。