Please use this identifier to cite or link to this item: https://dora.health.qld.gov.au/qldresearchjspui/handle/1/566
Title: Death Adder Envenoming Causes Neurotoxicity Not Reversed by Antivenom - Australian Snakebite Project (ASP-16)
Authors: Whyte, I.
Currie, B.
Irelan, G.
Mill, K.
O'Leary, M. A.
McCoubrie, D.
Brow, S.
Baile, P.
Ker, F.
Treston, G.
Webb, M.
Alfred, S.
Gray, T.
Curran, S.
Holdgate, A.
Isbister, G. K.
Ward, D.
Ryan, N.
Tankel, A.
Ellis, R.
Ghen, T.
Taylor, M.
Porges, K.
Downe, M.
Pascui, O.
Gunj, N.
Coulson, A.
McGregor, K.
Currie, B. J.
Dowsett, R.
Gan, M.
Isbiste, G.
Gaul, A.
Whitake, R.
Johnston, C. I.
Bonni, R.
Greenberg, R.
Chan, B.
Miller, M.
Spai, D.
William, V.
Pag, C.
Mead, H.
Parkin, A.
White, J.
Fraser, T.
Macrokanis, C.
Bitmea, D.
Dawson, A.
Miller, P.
Brown, S. G. A.
Thompso, P.
Wilke, G.
Buckle, N.
Garre, P.
Littl, M.
Halkidis, L.
Tay, K.
Close, B.
Greene, S.
Yeun, J.
Jus, S.
Nagree, Y.
Graudins, A.
Whitaker, R.
Barnes, C.
Gavaghan, C.
Vlad, I.
Issue Date: 2012
Source: September 6, (9), 2012
Journal: PLoS Neglected Tropical Diseases
Abstract: Background: Death adders (Acanthophis spp) are found in Australia, Papua New Guinea and parts of eastern Indonesia. This study aimed to investigate the clinical syndrome of death adder envenoming and response to antivenom treatment. Methodology/Principal Findings: Definite death adder bites were recruited from the Australian Snakebite Project (ASP) as defined by expert identification or detection of death adder venom in blood. Clinical effects and laboratory results were collected prospectively, including the time course of neurotoxicity and response to treatment. Enzyme immunoassay was used to measure venom concentrations. Twenty nine patients had definite death adder bites; median age 45 yr (5-74 yr); 25 were male. Envenoming occurred in 14 patients. Two further patients had allergic reactions without envenoming, both snake handlers with previous death adder bites. Of 14 envenomed patients, 12 developed neurotoxicity characterised by ptosis (12), diplopia (9), bulbar weakness (7), intercostal muscle weakness (2) and limb weakness (2). Intubation and mechanical ventilation were required for two patients for 17 and 83 hours. The median time to onset of neurotoxicity was 4 hours (0.5-15.5 hr). One patient bitten by a northern death adder developed myotoxicity and one patient only developed systemic symptoms without neurotoxicity. No patient developed venom induced consumption coagulopathy. Antivenom was administered to 13 patients, all receiving one vial initially. The median time for resolution of neurotoxicity post-antivenom was 21 hours (5-168). The median peak venom concentration in 13 envenomed patients with blood samples was 22 ng/mL (4.4-245 ng/mL). In eight patients where post-antivenom bloods were available, no venom was detected after one vial of antivenom. Conclusions/Significance: Death adder envenoming is characterised by neurotoxicity, which is mild in most cases. One vial of death adder antivenom was sufficient to bind all circulating venom. The persistent neurological effects despite antivenom, suggests that neurotoxicity is not reversed by antivenom. 2012 Johnston et al.
DOI: http://dx.doi.org/10.1371/journal.pntd.0001841
Resources: http://www.plosntds.org/article/fetchObjectAttachment.action?uri=info%3Adoi%2F10.1371%2Fjournal.pntd.0001841&representation=PDFhttp://ovidsp.ovid.com/ovidweb.cgi?T=JS&CSC=Y&NEWS=N&PAGE=fulltext&D=emed10&AN=2012579262
Keywords: acanthophis antarcticusadolescent;adult;aged;anaphylaxis/si [Side Effect];article;artificial ventilation;Australia;bolus injection;bulbar paralysis;chest tightness/si [Side Effect];child;clinical article;clinical trial;cohort analysis;controlled study;diplopia;dyspnea/si [Side Effect];envenomation/dt [Drug Therapy];enzyme immunoassay;female;human;hypersensitivity/si [Side Effect];intubation;leukocyte count;limb weakness;lymph node pain;lymphocyte count;male;multicenter study;muscle weakness;neurotoxicity/dt [Drug Therapy];neutrophil count;nonhuman;pain;partial thromboplastin time;preschool child;prospective study;ptosis;school child;skin bruising;snake;snakebite/dt [Drug Therapy];swelling;urticaria/si [Side Effect];wheezing/si [Side Effect];atropine/cb [Drug Combination];atropine/dt [Drug Therapy];neostigmine/cb [Drug Combination];neostigmine/dt [Drug Therapy];snake venom/to [Drug Toxicity];snake venom antiserum/ae [Adverse Drug Reaction];snake venom antiserum/ct [Clinical Trial];snake venom antiserum/dt [Drug Therapy]
Type: Article
Appears in Sites:Sunshine Coast HHS Publications

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