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Improvement in survival after paraquat ingestion following introduction of a new formulation in Sri Lanka

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dc.contributor.author Wilks, M.F. en
dc.contributor.author Fernando, R. en
dc.contributor.author Ariyananda, P.L. en
dc.contributor.author Eddleston, M. en
dc.contributor.author Berry, D.J. en
dc.contributor.author Tomenson, J.A. en
dc.contributor.author Buckley, N.A. en
dc.contributor.author Jayamanne, S. en
dc.contributor.author Gunnell, D. en
dc.contributor.author Dawson, A. en
dc.date.accessioned 2016-01-28T09:18:08Z en
dc.date.available 2016-01-28T09:18:08Z en
dc.date.issued 2008 en
dc.identifier.citation PLoS Medicine.2008;5(2):e49 en_US
dc.identifier.issn 1549-1277 (Print)
dc.identifier.issn 1549-1676 (Electronic)
dc.identifier.uri http://repository.kln.ac.lk/handle/123456789/11439
dc.description Indexed in MEDLINE en_US
dc.description.abstract BACKGROUND: Pesticide ingestion is a common method of self-harm in the rural developing world. In an attempt to reduce the high case fatality seen with the herbicide paraquat, a novel formulation (INTEON) has been developed containing an increased emetic concentration, a purgative, and an alginate that forms a gel under the acid conditions of the stomach, potentially slowing the absorption of paraquat and giving the emetic more time to be effective. We compared the outcome of paraquat self-poisoning with the standard formulation against the new INTEON formulation following itsintroduction into Sri Lanka. METHODS AND FINDINGS: Clinical data were prospectively collected on 586 patients with paraquat ingestion presenting to nine large hospitals across Sri Lanka with survival to 3 mo as the primary outcome. The identity of the formulation ingested after October 2004 was confirmed by assay of blood or urine samples for a marker compound present in INTEON. The proportion of known survivors increased from 76/297 with the standardformulation to 103/289 with INTEON ingestion, and estimated 3-mo survival improved from 27.1% to 36.7% (difference 9.5%; 95% confidence interval [CI] 2.0%-17.1%; p = 0.002, log rank test). Cox proportional hazards regression analyses showed an approximately 2-fold reduction in toxicity for INTEON compared to standard formulation. A higher proportion of patients ingesting INTEON vomited within 15 min (38% with the originalformulation to 55% with INTEON, p < 0.001). Median survival time increased from 2.3 d (95% CI 1.2-3.4 d) with the standard formulation to 6.9 d (95% CI 3.3-10.7 d) with INTEON ingestion (p = 0.002, log rank test); however, in patients who did not survive there was a comparatively smaller increase in median time to death from 0.9 d (interquartile range [IQR] 0.5-3.4) to 1.5 d (IQR 0.5-5.5); p = 0.02. CONCLUSIONS: The survey has shown that INTEON technology significantly reduces the mortality of patients following paraquat ingestion and increases survival time, most likely by reducing absorption. Comment in : New formulation of paraquat: a step forward but in the wrong direction. [PLoS Med. 2008] en_US
dc.language.iso en_US en_US
dc.publisher Public Library of Science en_US
dc.subject Improvement in survival en_US
dc.title Improvement in survival after paraquat ingestion following introduction of a new formulation in Sri Lanka en_US
dc.type Article en_US


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