Literature DB >> 12712036

Rapid atropine synthesis for the treatment of massive nerve agent exposure.

Richard J Kozak1, Scott Siegel, Jim Kuzma.   

Abstract

STUDY
OBJECTIVE: We developed and tested a protocol for compounding a large volume of injectable atropine from powder. The resulting protocol could be used by hospitals to rapidly use large amounts of stockpiled atropine.
METHODS: The protocol required 2 g of solid (powdered) atropine and 1 L of normal saline solution. The solution was filtered and mixed. One hundred syringes were filled by using a standard syringe-batching system. Modifications, including hand filling, were studied to reduce the time required to synthesize one hundred 3-mL syringes.
RESULTS: A single pharmacist was able to reconstitute one hundred 6-mg atropine syringes in 29 minutes using the batching system. The quickest method for a single pharmacist filling syringes by hand was 34 minutes. The cost to the hospital for 5 g of powdered atropine was 11 dollars versus 5,000 dollars for prefilled syringes.
CONCLUSION: Large quantities of atropine syringes can be compounded from a powdered form in a timely manner. Additionally, there is a significant cost advantage to using powdered atropine as a hospital stockpile.

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Year:  2003        PMID: 12712036     DOI: 10.1067/mem.2003.146

Source DB:  PubMed          Journal:  Ann Emerg Med        ISSN: 0196-0644            Impact factor:   5.721


  1 in total

1.  Nerve Agent Toxicity and Treatment.

Authors:  Christopher P Holstege; Stephen G Dobmeier
Journal:  Curr Treat Options Neurol       Date:  2005-03       Impact factor: 3.972

  1 in total

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