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Published on: October 23, 2018
Derivation of an occupational exposure limit for an inhalation analgesic methoxyflurane (Penthrox(®))
John Frangos1, Antti Mikkonen1, Christin Down1
1Golder Associates, 570 - 588 Swan Street, Richmond, Victoria, 3121, Australia.
Abstract:
Methoxyflurane (MOF) a haloether, is an inhalation analgesic agent for emergency relief of pain by self administration in conscious patients with trauma and associated pain. It is administered under supervision of personnel trained in its use. As a consequence of supervised use, intermittent occupational exposure can occur. An occupational exposure limit has not been established for methoxyflurane. Human clinical and toxicity data have been reviewed and used to derive an occupational exposure limit (referred to as a maximum exposure level, MEL) according to modern principles. The data set for methoxyflurane is complex given its historical use as anaesthetic. Distinguishing clinical investigations of adverse health effects following high and prolonged exposure during anaesthesia to assess relatively low and intermittent exposure during occupational exposure requires an evidence based approach to the toxicity assessment and determination of a critical effect and point of departure. The principal target organs are the kidney and the central nervous system and there have been rare reports of hepatotoxicity, too. Methoxyflurane is not genotoxic based on in vitro bacterial mutation and in vivo micronucleus tests and it is not classifiable (IARC) as a carcinogenic hazard to humans. The critical effect chosen for development of a MEL is kidney toxicity. The point of departure (POD) was derived from the concentration response relationship for kidney toxicity using the benchmark dose method. A MEL of 15 ppm (expressed as an 8 h time weighted average (TWA)) was derived. The derived MEL is at least 50 times higher than the mean observed TWA (0.23 ppm) for ambulance workers and medical staff involved in supervising use of Penthrox. In typical treatment environments (ambulances and treatment rooms) that meet ventilation requirements the derived MEL is at least 10 times higher than the modelled TWA (1.5 ppm or less) and the estimated short term peak concentrations are within the MEL. The odour threshold for MOF of 0.13-0.19 ppm indicates that the odour is detectable well below the MEL. Given the above considerations the proposed MEL is health protective.
Insights
Methoxyflurane (MOF), an inhalation analgesic, has a new occupational exposure limit (MEL) of 15 ppm. This limit is health-protective, considering kidney toxicity as the critical effect for healthcare workers exposed to MOF.
Area of Science:
- Occupational Health
- Toxicology
- Pharmacology
Background:
- Methoxyflurane (MOF) is an inhalation analgesic used for emergency pain relief.
- Occupational exposure to MOF can occur during its supervised use.
- No established occupational exposure limit existed for methoxyflurane previously.
Purpose of the Study:
- To derive an occupational exposure limit (Maximum Exposure Level, MEL) for methoxyflurane.
- To assess the health risks associated with intermittent occupational exposure to methoxyflurane.
- To establish a health-protective exposure limit based on toxicity data.
Main Methods:
- Reviewed human clinical and toxicity data for methoxyflurane.
- Identified kidney toxicity as the critical effect.
- Utilized benchmark dose method to determine the point of departure (POD) for kidney toxicity.
Main Results:
- A Maximum Exposure Level (MEL) of 15 ppm (8-hour time-weighted average) was derived for methoxyflurane.
- The derived MEL is significantly higher than observed and modeled occupational exposure levels.
- Methoxyflurane is not genotoxic or carcinogenic.
Conclusions:
- The derived MEL of 15 ppm is considered health-protective for occupational exposure.
- The odor threshold of methoxyflurane is well below the derived MEL.
- The established MEL provides a safety margin for healthcare workers using methoxyflurane.
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