Neuromuscular Effects of Common Krait (Bungarus caeruleus) Envenoming in Sri Lanka
| Field | Value | Language |
| dc.contributor.author | Silva, Anjana | |
| dc.contributor.author | Maduwage, Kalana | |
| dc.contributor.author | Sedgwick, Michael | |
| dc.contributor.author | Pilapitiya, Senaka | |
| dc.contributor.author | Weerawansa, Prasanna | |
| dc.contributor.author | Dahanayaka, Niroshana J. | |
| dc.contributor.author | Buckley, Nicholas A. | |
| dc.contributor.author | Johnston, Christopher | |
| dc.contributor.author | Siribaddana, Sisira | |
| dc.contributor.author | Isbister, Geoffrey K. | |
| dc.date.accessioned | 2016-05-06 | |
| dc.date.available | 2016-05-06 | |
| dc.date.issued | 2016-02-01 | |
| dc.identifier.citation | Silva A, Maduwage K, Sedgwick M, Pilapitiya S, Weerawansa P, Dahanayaka NJ, et al. (2016) Neuromuscular Effects of Common Krait (Bungarus caeruleus) Envenoming in Sri Lanka. PLoS Negl Trop Dis 10(2): e0004368. doi:10.1371/ journal.pntd.0004368 | en |
| dc.identifier.uri | http://hdl.handle.net/2123/14874 | |
| dc.description.abstract | Objective We aimed to investigate neurophysiological and clinical effects of common krait envenoming, including the time course and treatment response. Methodology Patients with definite common krait (Bungarus caeruleus) bites were recruited from a Sri Lankan hospital. All patients had serial neurological examinations and stimulated concentric needle single-fibre electromyography (sfEMG) of orbicularis oculi in hospital at 6wk and 6–9mth post-bite. Principal Findings There were 33 patients enrolled (median age 35y; 24 males). Eight did not develop neurotoxicity and had normal sfEMG. Eight had mild neurotoxicity with ptosis, normal sfEMG; six received antivenom and all recovered within 20–32h. Seventeen patients developed severe neurotoxicity with rapidly descending paralysis, from ptosis to complete ophthalmoplegia, facial, bulbar and neck weakness. All 17 received Indian polyvalent antivenom a median 3.5h post-bite (2.8–7.2h), which cleared unbound venom from blood. Despite this, the paralysis worsened requiring intubation and ventilation within 7h post-bite. sfEMG showed markedly increased jitter and neuromuscular blocks within 12h. sfEMG abnormalities gradually improved over 24h, corresponding with clinical recovery. Muscle recovery occurred in ascending order. Myotoxicity was not evident, clinically or biochemically, in any of the patients. Patients were extubated a median 96h post-bite (54–216h). On discharge, median 8 days (4–12days) post-bite, patients were clinically normal but had mild sfEMG abnormalities which persisted at 6wk post-bite. There were no clinical or neurophysiological abnormalities at 6–9mth. Conclusions Common krait envenoming causes rapid onset severe neuromuscular paralysis which takes days to recover clinically consistent with sfEMG. Subclinical neuromuscular dysfunction lasts weeks but was not permanent. Antivenom effectively cleared venom but did not prevent worsening or reverse neuromuscular paralysis. | en |
| dc.description.sponsorship | This work was supported by an Australian National Health and Medical Research Council Project Grant (ID1030069). GKI is supported by a National Health and Medical Research Council Senior Research Fellowship ID1061041. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. | en |
| dc.language.iso | en_AU | en |
| dc.publisher | PLoS Neglected Tropical Diseases | en |
| dc.relation | NHMRC 1030069 | en |
| dc.relation | http://purl.org/au-research/grants/nhmrc/1030069 | en |
| dc.rights | Other | en |
| dc.title | Neuromuscular Effects of Common Krait (Bungarus caeruleus) Envenoming in Sri Lanka | en |
| dc.type | Article | en |
| dc.identifier.doi | 10.1371/journal.pntd.0004368 | |
| dc.type.pubtype | Publisher's version | en |
| dc.rights.other | Copyright: © 2016 Silva et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Data Availability Statement: The data is freely available from the University of Newcastle, Australia, data repository. Data is available at URL http://hdl. handle.net/1959.13/1309398. | en |
| usyd.faculty | Faculty of Medicine and Health, School of Medical Sciences | en |
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