Literature DB >> 18400776

A randomised controlled trial of intramuscular vs. intravenous antivenom for latrodectism--the RAVE study.

G K Isbister1, S G A Brown, M Miller, A Tankel, E Macdonald, B Stokes, R Ellis, Y Nagree, G J Wilkes, R James, A Short, A Holdgate.   

Abstract

BACKGROUND: Widow spider-bite causes latrodectism and is associated with significant morbidity worldwide. Antivenom is given by both the intravenous (IV) and intramuscular (IM) routes and it is unclear which is more effective. AIM: To compare the effectiveness of IV vs. IM redback spider antivenom.
DESIGN: Randomized controlled trial.
METHODS: Patients with latrodectism were given either IV or IM antivenom according to a randomized double-dummy, double-blind protocol. The first antivenom treatment was followed by another identical treatment after two hours if required. The primary outcome was a clinically significant reduction in pain two hours after the last treatment. A fully Bayesian analysis was used to estimate the probability of the desired treatment effect, predetermined as an absolute difference of 20%.
RESULTS: We randomly allocated 126 patients to receive antivenom IV (64) and IM (62). After antivenom treatment pain improved in 40/64(62%) in the IV group vs. 33/62(53%) in the IM group (+9%; 95% Credible Interval [CrI]: -8% to +26%). The probability of a difference greater than zero (IV superior) was 85% but the probability of a difference >20% was only 10%. In 55 patients with systemic effects, these improved in 58% after IV antivenom vs. 65% after IM antivenom (-8%; 95% CrI: -32% to +17%). Twenty-four hours after antivenom pain had improved in 84% in the IV group vs. 71% in the IM group (+13%; 95% CrI: -2% to +27%). A meta-analysis including data from a previous trial found no difference in the primary outcome between IV and IM administration. DISCUSSION: The difference between IV and IM routes of administration of widow spider antivenom is, at best, small and does not justify routinely choosing one route over the other. Furthermore, antivenom may provide no benefit over placebo.

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Year:  2008        PMID: 18400776     DOI: 10.1093/qjmed/hcn048

Source DB:  PubMed          Journal:  QJM        ISSN: 1460-2393


  4 in total

1.  Therapeutics in clinical toxicology: in the absence of strong evidence how do we choose between antidotes, supportive care and masterful inactivity.

Authors:  Geoffrey K Isbister; Nicholas A Buckley
Journal:  Br J Clin Pharmacol       Date:  2016-03       Impact factor: 4.335

2.  An irritable infant and the runaway redback: an instructive case.

Authors:  Thomas R Ward; James A Falconer; John A Craven
Journal:  Case Rep Emerg Med       Date:  2011-09-28

3.  Low Health System Performance, Indigenous Status and Antivenom Underdosage Correlate with Spider Envenoming Severity in the Remote Brazilian Amazon.

Authors:  Vanderson Souza Sampaio; André Alexandre Gomes; Iran Mendonça Silva; Jacqueline Sachett; Luiz Carlos Lima Ferreira; Sâmella Oliveira; Meritxell Sabidò; Hipócrates Chalkidis; Maria Graças Vale Barbosa Guerra; Jorge Luis Salinas; Fan Hui Wen; Marcus Vinícius Guimarães Lacerda; Wuelton Marcelo Monteiro
Journal:  PLoS One       Date:  2016-05-26       Impact factor: 3.240

Review 4.  Treatments for Latrodectism-A Systematic Review on Their Clinical Effectiveness.

Authors:  Nicole M Ryan; Nicholas A Buckley; Andis Graudins
Journal:  Toxins (Basel)       Date:  2017-04-21       Impact factor: 4.546

  4 in total

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