Literature DB >> 9158355

Rehydration of desiccated Baralyme prevents carbon monoxide formation from desflurane in an anesthesia machine.

P J Baxter1, E D Kharasch.   

Abstract

BACKGROUND: Desiccated carbon dioxide absorbents degrade desflurane, enflurane, and isoflurane to carbon monoxide (CO) in vitro and in anesthesia machines, which can result in significant clinical CO exposure. Carbon monoxide formation is highest from desflurane, and greater with Baralyme than with soda lime. Degradation is inversely related to absorbent water content, and thus the greatest CO concentrations occur with desflurane and fully desiccated Baralyme. This investigation tested the hypothesis that rehydrating desiccated absorbent can diminish CO formation.
METHODS: Baralyme was dried to constant weight. Carbon monoxide formation from desflurane and desiccated Baralyme was determined in sealed 20.7-ml vials without adding water, after adding 10% of the normal water content (1.3% water), and after adding 100% of the normal water content (13% water) to the dry absorbent. Similar measurements were made using an anesthesia machine and circle system. Carbon monoxide was measured by gas chromatography-mass spectrometry.
RESULTS: Carbon monoxide formation from desflurane in vitro was decreased from 10,700 ppm with desiccated Baralyme to 715 ppm and less than 100 ppm, respectively, when 1.3% and 13% water were added. Complete rehydration also decreased CO formation from enflurane and isoflurane to undetectable concentrations. Desflurane degradation in an anesthesia machine produced 2,500 ppm CO in the circuit, which was reduced to less than 180 ppm when the full complement of water (13%) was added to the dried absorbent.
CONCLUSIONS: Desflurane is degraded by desiccated Baralyme in an anesthesia machine, resulting in CO formation. Adding water to dried Baralyme is an effective means of reducing CO formation and the risk of intraoperative CO poisoning. Although demonstrated specifically for desflurane and Baralyme, rehydration is also applicable to enflurane and isoflurane, and to soda lime.

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Year:  1997        PMID: 9158355     DOI: 10.1097/00000542-199705000-00009

Source DB:  PubMed          Journal:  Anesthesiology        ISSN: 0003-3022            Impact factor:   7.892


  5 in total

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Authors:  Sang Yoong Park; Chan Jong Chung; Jung Hoon Jang; Jae Young Bae; So Ron Choi
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Review 2.  Anesthesia-Related Carbon Monoxide Exposure: Toxicity and Potential Therapy.

Authors:  Richard J Levy
Journal:  Anesth Analg       Date:  2016-09       Impact factor: 5.108

3.  Performance of an electrochemical carbon monoxide monitor in the presence of anesthetic gases.

Authors:  M Dunning; H J Woehlck
Journal:  J Clin Monit       Date:  1997-11

Review 4.  Sevoflurance: approaching the ideal inhalational anesthetic. a pharmacologic, pharmacoeconomic, and clinical review.

Authors:  L Delgado-Herrera; R D Ostroff; S A Rogers
Journal:  CNS Drug Rev       Date:  2001

Review 5.  Carbon monoxide and anesthesia-induced neurotoxicity.

Authors:  Richard J Levy
Journal:  Neurotoxicol Teratol       Date:  2016-09-09       Impact factor: 3.763

  5 in total

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