Abstract

BackgroundPatients at risk of malignant hyperthermia need trigger-free anesthesia. Therefore, anesthesia machines prepared for safe use in predisposed patients should be free of volatile anesthetics. The washout time depends on the composition of rubber and plastic in the anesthesia machine. Therefore, new anesthesia machines should be evaluated regarding the safe preparation for trigger-free anesthesia. This study investigates wash out procedures of volatile anesthetics for two new anesthetic workstations: Dräger Atlan A350 and General Electric Healthcare (GE) Carestation 650 and compare it with preparation using activated charcoal filters (ACF).MethodsA Dräger Atlan and a Carestation 650 were contaminated with 4% sevoflurane for 90 min. The machines were decontaminated with method (M1): using ACF, method 2 (M2): a wash out method that included exchange of internal parts, breathing circuits and soda lime canister followed by ventilating a test lung using a preliminary protocol provided by Dräger or method 3 (M3): a universal wash out instruction of GE, method 4 (M4): M3 plus exchange of breathing system and bellows. Decontamination was followed by a simulated trigger-free ventilation. All experiments were repeated with 8% desflurane contaminated machines. Volatile anesthetics were detected with a closed gas loop high-resolution ion mobility spectrometer with gas chromatographic pre-separation attached to the bacterial filter of the breathing circuits. Primary outcome was time until < 5 ppm of volatile anesthetics and total preparation time.ResultsTime to < 5 ppm for the Atlan was 17 min (desflurane) and 50 min (sevoflurane), wash out continued for a total of 60 min according to protocol resulting in a total preparation time of 96-122 min. The Carestation needed 66 min (desflurane) and 24 min (sevoflurane) which could be abbreviated to 24 min (desflurane) if breathing system and bellows were changed. Total preparation time was 30-73 min. When using active charcoal filters time to < 5 ppm was 0 min for both machines, and total preparation time < 5 min.ConclusionBoth wash out protocols resulted in a significant reduction of trace gas concentrations. However, due to the complexity of the protocols and prolonged total preparation time, feasibility in clinical practice remains questionable. Especially when time is limited preparation of the anesthetic machines using ACF remain superior.

Highlights

  • Malignant hyperthermia (MH) is an inherited pharmaco-genetic disorder in which affected individuals are at risk to develop life-threatening metabolic crises when in contact to volatile anesthetics and/or succinylcholine

  • The European Malignant Hyperthermia Group (EMHG) guidelines provide an overview of the known wash out times for most anesthesia machines, but data is missing for the newest generation devices

  • This study showed that a preliminary washout procedure of Dräger meet the requirements of trigger-free anesthesia for the Atlan A350 in this study

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Summary

Introduction

Malignant hyperthermia (MH) is an inherited pharmaco-genetic disorder in which affected individuals are at risk to develop life-threatening metabolic crises when in contact to volatile anesthetics and/or succinylcholine. Whenever patients with a known susceptibility to malignant hyperthermia (MHS), or patients with MH associated myopathies (central core disease, KingDenborough syndrome and some other rare muscle disorders) need anesthesia, either regional or so called “trigger-free” general anesthesia is recommended. This includes, that the anesthetic machine should be clean of residual volatile anesthetics. This study investigates wash out procedures of volatile anesthetics for two new anesthetic workstations: Dräger Atlan A350 and General Electric Healthcare (GE) Carestation 650 and compare it with preparation using activated charcoal filters (ACF)

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