Please use this identifier to cite or link to this item: https://dora.health.qld.gov.au/qldresearchjspui/handle/1/566
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dc.contributor.authorWhyte, I.en
dc.contributor.authorCurrie, B.en
dc.contributor.authorIrelan, G.en
dc.contributor.authorMill, K.en
dc.contributor.authorO'Leary, M. A.en
dc.contributor.authorMcCoubrie, D.en
dc.contributor.authorBrow, S.en
dc.contributor.authorBaile, P.en
dc.contributor.authorKer, F.en
dc.contributor.authorTreston, G.en
dc.contributor.authorWebb, M.en
dc.contributor.authorAlfred, S.en
dc.contributor.authorGray, T.en
dc.contributor.authorCurran, S.en
dc.contributor.authorHoldgate, A.en
dc.contributor.authorIsbister, G. K.en
dc.contributor.authorWard, D.en
dc.contributor.authorRyan, N.en
dc.contributor.authorTankel, A.en
dc.contributor.authorEllis, R.en
dc.contributor.authorGhen, T.en
dc.contributor.authorTaylor, M.en
dc.contributor.authorPorges, K.en
dc.contributor.authorDowne, M.en
dc.contributor.authorPascui, O.en
dc.contributor.authorGunj, N.en
dc.contributor.authorCoulson, A.en
dc.contributor.authorMcGregor, K.en
dc.contributor.authorCurrie, B. J.en
dc.contributor.authorDowsett, R.en
dc.contributor.authorGan, M.en
dc.contributor.authorIsbiste, G.en
dc.contributor.authorGaul, A.en
dc.contributor.authorWhitake, R.en
dc.contributor.authorJohnston, C. I.en
dc.contributor.authorBonni, R.en
dc.contributor.authorGreenberg, R.en
dc.contributor.authorChan, B.en
dc.contributor.authorMiller, M.en
dc.contributor.authorSpai, D.en
dc.contributor.authorWilliam, V.en
dc.contributor.authorPag, C.en
dc.contributor.authorMead, H.en
dc.contributor.authorParkin, A.en
dc.contributor.authorWhite, J.en
dc.contributor.authorFraser, T.en
dc.contributor.authorMacrokanis, C.en
dc.contributor.authorBitmea, D.en
dc.contributor.authorDawson, A.en
dc.contributor.authorMiller, P.en
dc.contributor.authorBrown, S. G. A.en
dc.contributor.authorThompso, P.en
dc.contributor.authorWilke, G.en
dc.contributor.authorBuckle, N.en
dc.contributor.authorGarre, P.en
dc.contributor.authorLittl, M.en
dc.contributor.authorHalkidis, L.en
dc.contributor.authorTay, K.en
dc.contributor.authorClose, B.en
dc.contributor.authorGreene, S.en
dc.contributor.authorYeun, J.en
dc.contributor.authorJus, S.en
dc.contributor.authorNagree, Y.en
dc.contributor.authorGraudins, A.en
dc.contributor.authorWhitaker, R.en
dc.contributor.authorBarnes, C.en
dc.contributor.authorGavaghan, C.en
dc.contributor.authorVlad, I.en
dc.date.accessioned2018-06-16T20:35:38Z-
dc.date.available2018-06-16T20:35:38Z-
dc.date.issued2012en
dc.identifier.citationSeptember 6, (9), 2012en
dc.identifier.otherRISen
dc.identifier.urihttp://dora.health.qld.gov.au/qldresearchjspui/handle/1/566-
dc.description.abstractBackground: 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.<br />en
dc.languageenen
dc.relation.ispartofPLoS Neglected Tropical Diseasesen
dc.titleDeath Adder Envenoming Causes Neurotoxicity Not Reversed by Antivenom - Australian Snakebite Project (ASP-16)en
dc.typeArticleen
dc.identifier.doihttp://dx.doi.org/10.1371/journal.pntd.0001841en
dc.subject.keywordsacanthophis antarcticusadolescenten
dc.subject.keywordsadulten
dc.subject.keywordsageden
dc.subject.keywordsanaphylaxis/si [Side Effect]en
dc.subject.keywordsarticleen
dc.subject.keywordsartificial ventilationen
dc.subject.keywordsAustraliaen
dc.subject.keywordsbolus injectionen
dc.subject.keywordsbulbar paralysisen
dc.subject.keywordschest tightness/si [Side Effect]en
dc.subject.keywordschilden
dc.subject.keywordsclinical articleen
dc.subject.keywordsclinical trialen
dc.subject.keywordscohort analysisen
dc.subject.keywordscontrolled studyen
dc.subject.keywordsdiplopiaen
dc.subject.keywordsdyspnea/si [Side Effect]en
dc.subject.keywordsenvenomation/dt [Drug Therapy]en
dc.subject.keywordsenzyme immunoassayen
dc.subject.keywordsfemaleen
dc.subject.keywordshumanen
dc.subject.keywordshypersensitivity/si [Side Effect]en
dc.subject.keywordsintubationen
dc.subject.keywordsleukocyte counten
dc.subject.keywordslimb weaknessen
dc.subject.keywordslymph node painen
dc.subject.keywordslymphocyte counten
dc.subject.keywordsmaleen
dc.subject.keywordsmulticenter studyen
dc.subject.keywordsmuscle weaknessen
dc.subject.keywordsneurotoxicity/dt [Drug Therapy]en
dc.subject.keywordsneutrophil counten
dc.subject.keywordsnonhumanen
dc.subject.keywordspainen
dc.subject.keywordspartial thromboplastin timeen
dc.subject.keywordspreschool childen
dc.subject.keywordsprospective studyen
dc.subject.keywordsptosisen
dc.subject.keywordsschool childen
dc.subject.keywordsskin bruisingen
dc.subject.keywordssnakeen
dc.subject.keywordssnakebite/dt [Drug Therapy]en
dc.subject.keywordsswellingen
dc.subject.keywordsurticaria/si [Side Effect]en
dc.subject.keywordswheezing/si [Side Effect]en
dc.subject.keywordsatropine/cb [Drug Combination]en
dc.subject.keywordsatropine/dt [Drug Therapy]en
dc.subject.keywordsneostigmine/cb [Drug Combination]en
dc.subject.keywordsneostigmine/dt [Drug Therapy]en
dc.subject.keywordssnake venom/to [Drug Toxicity]en
dc.subject.keywordssnake venom antiserum/ae [Adverse Drug Reaction]en
dc.subject.keywordssnake venom antiserum/ct [Clinical Trial]en
dc.subject.keywordssnake venom antiserum/dt [Drug Therapy]en
dc.relation.urlhttp://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=2012579262en
dc.identifier.risid504en
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.openairetypeArticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
Appears in Sites:Queensland Health Publications
Sunshine Coast HHS Publications
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