Clinical management of snakebite envenoming: Future perspectives

IF 3.6 Q2 TOXICOLOGY Toxicon: X Pub Date : 2021-09-01 DOI:10.1016/j.toxcx.2021.100079
Muhammad Hamza , Cecilie Knudsen , Christeine Ariaranee Gnanathasan , Wuelton Monteiro , Matthew R. Lewin , Andreas H. Laustsen , Abdulrazaq G. Habib
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引用次数: 19

Abstract

Snakebite envenoming is a major cause of morbidity and mortality in rural communities throughout the tropics. Generally, the main clinical features of snakebites are local swelling, tissue necrosis, shock, spontaneous systemic hemorrhage, incoagulable blood, paralysis, rhabdomyolysis, and acute kidney injury. These clinical manifestations result from complex biochemical venom constituents comprising of cytotoxins, hemotoxins, neurotoxins, myotoxins, and other substances. Timely diagnosis of envenoming and identification of the responsible snake species is clinically challenging in many parts of the world and necessitates prompt and thorough clinical assessment, which could be supported by the development of reliable, affordable, widely-accessible, point-of-care tests. Conventional antivenoms based on polyclonal antibodies derived from animals remain the mainstay of therapy along with supportive medical and surgical care. However, while antivenoms save countless lives, they are associated with adverse reactions, limited potency, and are relatively inefficacious against presynaptic neurotoxicity and in preventing necrosis. Nevertheless, major scientific and technological advances are facilitating the development of new molecular and immunologic diagnostic tests, as well as a new generation of antivenoms comprising human monoclonal antibodies with broader and more potent neutralization capacity and less immunogenicity. Repurposed pharmaceuticals based on small molecule inhibitors (e.g., marimastat and varespladib) used alone and in combination against enzymatic toxins, such as metalloproteases and phospholipase A2s, have shown promise in animal studies. These orally bioavailable molecules could serve as early interventions in the out-of-hospital setting if confirmed to be safe and efficacious in clinical studies. Antivenom access can be improved by the usage of drones and ensuring constant antivenom supply in remote endemic rural areas. Overall, the improvement of clinical management of snakebite envenoming requires sustained, coordinated, and multifaceted efforts involving basic and applied sciences, new technology, product development, effective clinical training, implementation of existing guidelines and therapeutic approaches, supported by improved supply of existing antivenoms.

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蛇咬伤的临床处理:未来展望。
蛇咬伤是整个热带地区农村社区发病率和死亡率的主要原因。一般来说,毒蛇咬伤的主要临床特征是局部肿胀、组织坏死、休克、自发性全身出血、血液不凝、瘫痪、横纹肌溶解症和急性肾损伤。这些临床表现源于复杂的生化毒液成分,包括细胞毒素、血液毒素、神经毒素、肌肉毒素和其他物质。在世界许多地方,及时诊断环境感染和识别责任蛇物种在临床上具有挑战性,需要及时彻底的临床评估,这可以通过开发可靠、负担得起、可广泛获得的护理点测试来支持。基于源自动物的多克隆抗体的常规抗蛇毒血清仍然是治疗以及支持性医疗和外科护理的支柱。然而,尽管抗蛇毒血清挽救了无数人的生命,但它们与不良反应有关,效力有限,对突触前神经毒性和预防坏死相对无效。尽管如此,重大的科学和技术进步正在促进新的分子和免疫诊断测试的发展,以及新一代的抗蛇毒血清,该血清包含具有更广泛、更有效中和能力和更低免疫原性的人类单克隆抗体。基于小分子抑制剂(如marimastat和varespladib)的再利用药物,单独或联合使用对抗酶毒素,如金属蛋白酶和磷脂酶A2,在动物研究中显示出了前景。如果在临床研究中被证实是安全有效的,这些口服生物可利用分子可以作为院外环境的早期干预措施。通过使用无人机和确保偏远流行农村地区持续供应抗蛇毒血清,可以改善抗蛇毒血清的获取。总的来说,改善蛇咬伤环境的临床管理需要持续、协调和多方面的努力,包括基础科学和应用科学、新技术、产品开发、有效的临床培训、现有指南和治疗方法的实施,并辅以现有抗蛇毒药的供应。
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来源期刊
Toxicon: X
Toxicon: X Pharmacology, Toxicology and Pharmaceutics-Toxicology
CiteScore
6.50
自引率
0.00%
发文量
33
审稿时长
14 weeks
期刊最新文献
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