Sanders Taylor, Murphy Christine, Davis Greggory, Aspinwall Christina, Theriot Lauren, McVicker Christopher, Arnold Thomas
Emergency Medicine Residency Program, Louisiana State University Health Sciences Center School of Medicine - New Orleans, Baton Rouge Branch Campus, 5246 Brittany Drive, MEIC Building, 3rd Floor, Baton Rouge, LA, 70808, USA.
Department of Emergency Medicine, Division of Medical Toxicology, Atrium Health's Carolinas Medical Center, 1000 Blythe Blvd., Charlotte, NC, 28203, USA.
J Med Toxicol. 2025 Sep 2. doi: 10.1007/s13181-025-01093-6.
Copperheads and cottonmouths are responsible for most snake envenomations in Louisiana. While the United States Food and Drug Administration has approved both Crotalidae polyvalent immune Fab (FabAV) and Crotalidae immune F(ab') (Fab2AV) for Agkistrodon envenomations, data is limited comparing their efficacies for this indication.
This is a retrospective study comparing FabAV to Fab2AV in the treatment of suspected Agkistrodon envenomations in Louisiana between April 2017 and October 2024. Cases identifying rattlesnakes were excluded. The primary outcome was the need for additional antivenom doses to achieve control after the initial antivenom dose.
One hundred fifty-eight patients received FabAV or Fab2AV, with 100 cases meeting inclusion criteria. Fifty-seven patients received FabAV and 43 received Fab2AV. The snake was identified as copperhead in 48 cases, cottonmouth in 23, and unidentified in 29. In the FabAV cohort, the initial number of vials ranged from four to 12 with a median dose of four vials. Nine FabAV cases (16%) required additional vials for initial control after the first dose. In the Fab2AV cohort, all patients received 10 vials initially, with 24 cases (56%) requiring additional vials for initial control after the first dose. There was a significant difference in the percentage of patients requiring additional control vials between FabAV and Fab2AV.
In this cohort of suspected Agkistrodon envenomations, control with initial recommended dosing was more often achieved with FabAV compared to Fab2AV (84% vs. 44%). The results suggest potential benefit to hospitals stocking FabAV in Louisiana and possibly other Agkistrodon-predominant regions.
在路易斯安那州,大部分蛇咬伤中毒事件是由铜头蛇和水腹蛇造成的。虽然美国食品药品监督管理局已批准抗蛇毒血清(FabAV)和抗蛇毒血清F(ab')(Fab2AV)用于治疗蝮蛇咬伤中毒,但比较它们在该适应症上疗效的数据有限。
这是一项回顾性研究,比较了2017年4月至2024年10月期间在路易斯安那州治疗疑似蝮蛇咬伤中毒时FabAV和Fab2AV的疗效。排除了被确认为响尾蛇咬伤的病例。主要结局是在初始抗蛇毒血清剂量后,是否需要额外的抗蛇毒血清剂量来实现病情控制。
158名患者接受了FabAV或Fab2AV治疗,其中100例符合纳入标准。57例患者接受了FabAV治疗,43例接受了Fab2AV治疗。确定蛇种为铜头蛇的有48例,水腹蛇的有23例,未明确的有29例。在FabAV队列中,初始使用的药瓶数量为4至12瓶,中位剂量为4瓶。9例FabAV治疗的病例(16%)在首剂后需要额外的药瓶来进行初始控制。在Fab2AV队列中,所有患者最初均接受10瓶治疗,其中24例(56%)在首剂后需要额外的药瓶来进行初始控制。FabAV和Fab2AV之间需要额外控制药瓶的患者百分比存在显著差异。
在这一疑似蝮蛇咬伤中毒队列中,与Fab2AV相比,FabAV更常通过初始推荐剂量实现病情控制(84%对44%)。结果表明,路易斯安那州以及其他可能以蝮蛇为主的地区的医院储备FabAV可能有益。