Envenoming by a captive Inland Taipan, Oxyuranus microlepidotus (McCoy, 1879), Elapidae. A case report, observations on clinical efficacy of expired antivenom and review of O. microlepidotus envenoming.

IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Scott A Weinstein, Daniel E Keyler, J P Jensen, Ryan Sawyers, Hunter Steward, Jack Facente, Diana Dean
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引用次数: 0

Abstract

The clinical evolution and management of a 22-yr-old male envenomed by a captive female inland taipan, Oxyuranus microlepidotus (McCoy, 1879), Elapidae, at a public educational reptile exhibit (Florida, USA) is reported. The patient was bitten (quick 'bite and release') in the right hand between digits #3 and 4 while performing captive maintenance. The victim did not attempt any first aid, but urgently presented to the local hospital within 25 mins post-bite. The patient had an unremarkable medical/surgical history including no previous envenoming/treatment with antivenom. Within approximately 5 mins post-bite he reported experiencing transient loss of consciousness/syncope, altered sensorium, nausea, dull headache, weakness, and "severe" bite site pain. Laboratory investigations revealed profound defibrinating coagulopathy including thrombocytopenia; there was only mildly elevated creatine kinase and renal function remained within normal limits. The patient's clinical evolution included cranial nerve palsies manifested as dysconjugate gaze, persistent, but minor, bite site bleeding, asthenia and reported myalgia as well as prolonged intense bite site pain. He was successfully and uneventfully treated with four vials of Australian polyvalent antivenom and one vial of taipan monovalent; all were expired products with expiration dates ranging from one month to 38 years. Effective antivenom therapy might have been achieved with only 2, possibly 3 vials; however, concerns about reduced efficacy of the long-expired antivenom (4/5 vials were expired 18-38 years) and persistent bite site bleeding/pain contributed to the provision of the additional vials. The patient recovered sufficiently for discharge in 48 h; there were no sequelae. There have been approximately 12 formally documented cases of O. microlepidotus envenoming and selected, detailed examples of these are briefly considered and compared with the clinical evolution of our patient; patient-centred recommendations for management of Oxyuranus spp. envenoming are discussed. The need for advanced preparedness and an action plan for any institution/collection that contains non-native, medically significant venomous species is emphasised, and a general recommended approach is outlined.

人工饲养的内陆大班蛇(Oxyuranus microlepidotus (McCoy, 1879), Elapidae)引起的蛇毒中毒。病例报告、对过期抗蛇毒血清临床疗效的观察以及对小鳞大班蛇(Oxyuranus microlepidotus)蛇毒中毒的回顾。
报告了一名 22 岁男性在美国佛罗里达州的一个公共教育爬行动物展览中被一只圈养的雌性内陆奚攀(Oxyuranus microlepidotus (McCoy, 1879),Elapidae)咬伤的临床演变和处理过程。患者是在进行圈养维护时被咬伤的(快速 "咬伤后松开"),咬伤部位在右手第 3 和第 4 指之间。受害者没有尝试任何急救措施,而是在被咬后 25 分钟内紧急送往当地医院。患者的病史和外科病史均无异常,也没有被咬伤或接受过抗蛇毒血清治疗的经历。在被咬后约 5 分钟内,他报告说出现了短暂的意识丧失/晕厥、感觉改变、恶心、钝性头痛、虚弱和 "严重 "的咬伤部位疼痛。实验室检查显示,患者出现了包括血小板减少在内的深度去纤维化凝血病;肌酸激酶轻度升高,肾功能保持在正常范围内。患者的临床表现包括颅神经麻痹(表现为凝视障碍)、持续但轻微的咬伤部位出血、气喘、肌痛以及咬伤部位长时间剧烈疼痛。他接受了四瓶澳大利亚多价抗蛇毒血清和一瓶大班单价抗蛇毒血清的成功治疗,治疗过程并无大碍;所有抗蛇毒血清均为过期产品,有效期从一个月到 38 年不等。本来只需两瓶(也可能是三瓶)抗蛇毒血清就能达到有效治疗的目的;但是,由于担心长期过期的抗蛇毒血清(4/5 瓶的过期时间为 18-38 年)会降低疗效,而且咬伤部位持续出血/疼痛,因此又追加了几瓶抗蛇毒血清。患者在 48 小时内康复出院,没有留下后遗症。目前约有 12 例有正式记录的小尾寒羊咬伤病例,本文简要介绍了这些病例的详细情况,并将其与我们患者的临床演变情况进行了比较;还讨论了以患者为中心的小尾寒羊咬伤处理建议。强调了任何机构/收藏馆如果收藏了非本地的、在医学上具有重要意义的毒蛇物种,都需要提前做好准备并制定行动计划,并概述了建议采用的一般方法。
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来源期刊
Toxicon
Toxicon 医学-毒理学
CiteScore
4.80
自引率
10.70%
发文量
358
审稿时长
68 days
期刊介绍: Toxicon has an open access mirror Toxicon: X, sharing the same aims and scope, editorial team, submission system and rigorous peer review. An introductory offer Toxicon: X - full waiver of the Open Access fee. Toxicon''s "aims and scope" are to publish: -articles containing the results of original research on problems related to toxins derived from animals, plants and microorganisms -papers on novel findings related to the chemical, pharmacological, toxicological, and immunological properties of natural toxins -molecular biological studies of toxins and other genes from poisonous and venomous organisms that advance understanding of the role or function of toxins -clinical observations on poisoning and envenoming where a new therapeutic principle has been proposed or a decidedly superior clinical result has been obtained. -material on the use of toxins as tools in studying biological processes and material on subjects related to venom and antivenom problems. -articles on the translational application of toxins, for example as drugs and insecticides -epidemiological studies on envenoming or poisoning, so long as they highlight a previously unrecognised medical problem or provide insight into the prevention or medical treatment of envenoming or poisoning. Retrospective surveys of hospital records, especially those lacking species identification, will not be considered for publication. Properly designed prospective community-based surveys are strongly encouraged. -articles describing well-known activities of venoms, such as antibacterial, anticancer, and analgesic activities of arachnid venoms, without any attempt to define the mechanism of action or purify the active component, will not be considered for publication in Toxicon. -review articles on problems related to toxinology. To encourage the exchange of ideas, sections of the journal may be devoted to Short Communications, Letters to the Editor and activities of the affiliated societies.
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