Department of Medical Toxicology, Banner Good Samaritan Medical Center, Phoenix, AZ, United States.
Toxicon. 2011 Jan;57(1):53-9. doi: 10.1016/j.toxicon.2010.09.014. Epub 2010 Oct 8.
North American rattlesnake envenomations commonly produce defibrination, coagulopathy and/or thrombocytopenia, which may be reversed following treatment with Crotalidae Polyvalent Immune Fab Ovine (FabAV). Despite initial resolution with FabAV, late onset or recurrence of venom-induced hematologic effects may occur. Time at which onset of late hematotoxicity may first be detected is unknown. The purpose of this study was to identify the incidence and time of onset of recurrent or new late hypofibrinogenemia, coagulopathy, or thrombocytopenia in a cohort of rattlesnake envenomation patients seen in outpatient follow-up after treatment with FabAV, and to report hematologic outcomes in these patients.
Review of 66 charts of patients with rattlesnake envenomation who were treated with FabAV, and subsequently had outpatient follow-up evaluation at least 48 h after last FabAV, was performed. Demographic information, rattlesnake and bite characteristics, dose and timing of antivenom administration, adverse events, in-patient laboratory values, length of hospital stay, and follow-up laboratory values were collected. The primary outcome parameters were recurrent or delayed onset coagulopathy, hypofibrinogenemia, or thrombocytopenia identified no sooner than 48 h after last dose of FabAV.
Prior to control of the envenomation with FabAV, 42 patients (63.6%) experienced hematologic toxicity. At follow-up, 21 patients (32%) were found to have late coagulopathy, hypofibrinogenemia, or thrombocytopenia. Of twenty-three patients (35%) with more than one follow-up visit, fifteen had normal laboratory findings at the first follow-up visit. Five of these 15 patients (8% of total study group; 33% of this subgroup) with normal hematologic studies at first follow-up exhibited late hematologic toxicity at second follow-up. Severe late hematologic toxicity developed in five of 66 (8%) patients. One patient was retreated with FabAV for late severe thrombocytopenia.
Recurrent and delayed onset of hematologic toxicity in rattlesnake envenomation victims treated with FabAV is common. Follow-up more than three days after treatment is necessary to detect all cases of late hematologic toxicity.
北美的响尾蛇咬伤通常会导致纤维蛋白原分解、凝血功能障碍和/或血小板减少,这些症状在使用抗蛇毒血清 Crotalidae Polyvalent Immune Fab Ovine(FabAV)治疗后可能会逆转。尽管使用 FabAV 后最初得到缓解,但毒液引起的血液学效应可能会延迟发作或再次出现。目前尚不清楚何时会首次发现迟发性血液毒性发作。本研究的目的是确定在使用 FabAV 治疗后接受门诊随访的响尾蛇咬伤患者中,复发性或新的迟发性低纤维蛋白原血症、凝血功能障碍或血小板减少症的发生率和发作时间,并报告这些患者的血液学结局。
对 66 例接受 FabAV 治疗且在最后一次 FabAV 治疗后至少 48 小时进行门诊随访评估的响尾蛇咬伤患者的病历进行回顾性分析。收集患者的人口统计学信息、响尾蛇和咬伤特征、抗蛇毒血清的剂量和使用时间、不良反应、住院期间的实验室值、住院时间和随访期间的实验室值。主要结局参数为在最后一次 FabAV 给药后 48 小时内首次发现的复发性或延迟发作的凝血功能障碍、低纤维蛋白原血症或血小板减少症。
在使用 FabAV 控制蛇毒之前,42 名患者(63.6%)出现血液学毒性。在随访时,21 名患者(32%)出现迟发性凝血功能障碍、低纤维蛋白原血症或血小板减少症。在 23 名(35%)有不止一次随访就诊的患者中,15 名在第一次随访就诊时实验室检查结果正常。这 15 名患者中有 5 名(总研究组的 8%;该亚组的 33%)在第一次随访就诊时血液学检查正常,但在第二次随访就诊时出现迟发性血液学毒性。66 名患者中有 5 名(8%)出现严重迟发性血液学毒性。1 名患者因迟发性严重血小板减少症再次接受 FabAV 治疗。
在使用 FabAV 治疗的响尾蛇咬伤患者中,复发性和迟发性血液学毒性很常见。治疗后三天以上的随访是发现所有迟发性血液学毒性的必要条件。