Multi-capillary column-ion mobility spectrometry (MCC-IMS) as a new method for the quantification of occupational exposure to sevoflurane in anaesthesia workplaces: an observational feasibility study
© Kunze et al.; licensee BioMed Central. 2015
Received: 1 November 2014
Accepted: 17 March 2015
Published: 27 March 2015
Occupational exposure to sevoflurane has the potential to cause health damage in hospital personnel. Workplace contamination with the substance mostly is assessed by using photoacoustic infrared spectrometry with detection limits of 10 ppbv. Multi-capillary column-ion mobility spectrometry (MCC-IMS) could be an alternative technology for the quantification of sevoflurane in the room air and could be even more accurate because of potentially lower detection limits. The aim of this study was to test the hypothesis that MCC-IMS is able to detect and monitor very low concentrations of sevoflurane (<10 ppbv) and to evaluate the exposure of hospital personnel to sevoflurane during paediatric anaesthesia and in the post anaesthesia care unit (PACU).
A MCC-IMS device was calibrated to several concentrations of sevoflurane and limits of detection (LOD) and quantification (LOQ) were calculated. Sevoflurane exposure of hospital personnel was measured at two anaesthesia workplaces and time-weighted average (TWA) values were calculated.
The LOD was 0.0068 ppbv and the LOQ was 0.0189 ppbv. During paediatric anaesthesia the mean sevoflurane concentration was 46.9 ppbv (8.0 - 314.7 ppbv) with TWA values between 5.8 and 45.7 ppbv. In the PACU the mean sevoflurane concentration was 27.9 ppbv (8.0 – 170.2 ppbv) and TWA values reached from 8.3 to 45.1 ppbv.
MCC-IMS shows a significantly lower LOD and LOQ than comparable methods. It is a reliable technology for monitoring sevoflurane concentrations at anaesthesia workplaces and has a particular strength in quantifying low-level contaminations of sevoflurane. The exposure of the personnel working in these areas did not exceed recommended limits and therefore adverse health effects are unlikely.
KeywordsSevoflurane Occupational exposure Volatile anaesthetics Ion mobility spectrometry Room air analyses Limit of detection
Chronic occupational exposure to the volatile anaesthetic sevoflurane has been discussed to have negative influence on the health of hospital personnel since it was introduced into clinical use in the 1990’s [1,2]. However, evidence on the adverse effects of low-level exposure to volatile anaesthetics stays inconclusive . Governmental organisations of most countries defined occupational exposure limits (OEL) for the first generation of volatile anaesthetics (N2O, Halothane). To our knowledge only the Netherlands with 18,700 parts per billion by volume (ppbv) defined an OEL for sevoflurane, by means of a time-weighted average over an 8-hour working day (TWA-S) . For the whole group of halogenated inhaled anaesthetics different countries recommended different TWA-S values between 2,000 and 50,000 ppbv [5,6]. Regarding the potential health damage caused by chronic occupational exposure to sevoflurane the National Institute for Occupational Safety and Health (NIOSH) of the United States recommended a ceiling value of 2,000 ppbv for health care workers .
The contamination of workplaces by sevoflurane has been assessed previously. Most authors used photoacoustic infrared spectrometry (PIS) and lower detection limits were indicated in a range between 9 ppbv and 20 ppbv [4,8-11]. Other authors used proton transfer reaction-mass spectrometry (PTR-MS) for measuring sevoflurane [12-14]. When coupled with a time-of-flight analysis (PTR-ToF-MS), the limits of detection (LOD) and quantification (LOQ) of the method were indicated as 19.86 ppbv and 27.58 ppbv .
With this present study we would like to introduce multi-capillary column-ion mobility spectrometry (MCC-IMS) as a fast and reliable method for monitoring the occupational exposure of hospital personnel to sevoflurane. The technology of ion mobility spectrometry (IMS) is widely used by security services and by the military for the detection of illegal substances and explosives . Coupling the IMS device with a multi-capillary column for pre-separation allows the analysis of complex and humid gas samples with substance specific detection limits down to parts per trillion (ppt). MCC-IMS technology has been used for a multitude of analytical questions in a medical surrounding, including breath gas analyses for diagnostic purposes, pharmacological monitoring or in-vitro analyses for the differentiation of human pathogenic microbes [16-20]. MCC-IMS provides direct and very fast detection (within seconds) and is able to detect more than one substance at once.
With our present study we want to answer the question if MCC-IMS is a suitable analytical tool for the quantification of workplace concentrations of sevoflurane. Therefore, we calibrated a MCC-IMS device to several sevoflurane concentrations and calculated the LOD and the LOQ of the method. To give an example of the performance of the MCC-IMS in quantifying sevoflurane and to answer the question if there is a relevant exposure to sevoflurane in our institution, we performed room air measurements during paediatric anaesthesia and in the PACU of our University Medical Centre. Both anaesthesia workplaces are at risk for higher sevoflurane exposures, by means of sevoflurane concentrations and TWA (−S) values above international recommendations [13,14,21]. Therefore these areas seemed of particular interest for occupational health research and were chosen for our measurements.
According to the regulations of the University Medical Centre of Göttingen no approval from the ethical committee was needed, as this study did not include any of our patient’s data or any medical interventions. However, the ethical committee of the Faculty of Medicine of the University of Göttingen has been informed about the study protocol.
Specifications of the MCC-IMS used for the study
Non-commercial, ISAS, Dortmund, Germany
Multi-capillary column OV-5 (length 20 cm), Multichrom Ltd., Novosibirsk, Russia
Teflon, volume 8 ml
Electric field strength
Shutter opening time
Drift and carrier gas
Synthetic air, Air Liquide AG, Düsseldorf, Germany
Drift gas flow
Carrier gas flow
Room air measurements were performed during 12 paediatric anaesthesia procedures for minor dental surgery during five measurement days between June 19th 2012 and August 7th 2012. All children had general anaesthesia. After mask induction with sevoflurane an intravenous cannula was placed and propofol (B. Braun AG, Melsungen, Germany) was used for the deepening of anaesthesia. Children were intubated using cuffed endotracheal tubes and anaesthesia was maintained by continuous intravenous application of propofol and remifentanil (Ultiva®, GlaxoSmithKline GmbH & Co. KG, Munich, Germany). A commercially available anaesthesia machine with a semi-closed breathing circuit (Cato® edition, Dräger AG, Lübeck, Germany) was used in this study. The anaesthesia machine was connected to the anaesthesia waste gas scavenging system with an air flow of 40 l/min.
Air samples were taken via a 1/8′′ PTFE suction line of 2 m length (Bohlender GmbH, Grünsfeld, Germany) that was attached to the anaesthesia machine in the height of the eyes of the anaesthetist. The first MCC-IMS measurement was started at the beginning of each mask induction. Sampling duration was 30 sec and samples were drawn with 350 ml/min. As sevoflurane was detected at only 7 sec retention time, we performed measurements of 200 s. During the remaining time of the surgical procedure every 13 – 14 minutes another room air measurement was started (up to 70 minutes procedure time). Each measurement was followed by one blank measurement of humid synthetic air in scientific quality (Air Liquid AG, Düsseldorf, Germany) for cleaning the sample loop of the IMS and for controlling the IMS for contaminations. All measurements were performed in two identically constructed operating theatres with room volumes of 95 m3 each and air conditioning systems producing air change rates of 3,600 m3 per hour.
In addition to our measurements during paediatric anaesthesia we performed room air measurements in the PACU. This central recovery area for all anaesthesia workplaces in our university hospital has a room volume of 715 m3 and can take up to 20 patients at once. Air condition is working 24 hours producing air change rates of 3,600 m3 per hour. The MCC-IMS was placed in the centre of the PACU and one measurement was performed each hour from October 27th 2009, 10 am until October 29th 2009, 4 pm. Again, each measurement was followed by one blank measurement of humid synthetic air.
Whereas TWA-S is the time-weighted average during an 8-hour shift (ppbv) and texp is the actual exposure time during the working day of 8 hours.
LOD and LOQ
Comparison of LOD and LOQ of the different analytical methods used for the quantification of sevoflurane in the room air
Results of the sevoflurane calibration: mean signal intensities (SI), standard deviations (SD) and relative standard deviation (RSD%) for the measured sevoflurane concentrations
Sevoflurane concentration [ppbv]
Mean SI [V]
TWA and TWA-S values for hospital personnel working in the paediatric dental surgical theatre
No. of mask inductions
TWA-S [ppbv] (8 hours)
June 19th 2012
July 3rd 2012
July 10th 2012
July 17th 2012
August 7th 2012
TWA-S values for hospital personnel working in the PACU. The time of measurement included two morning shifts (06:00 am – 02:00 pm), two evening shifts (02:00 pm – 10:00 pm) and two night shifts (10:00 pm – 06:00 am)
October 27th 2009
October 27th 2009
October 28th 2009
October 28th 2009
October 28th 2009
October 29th 2009
In our present study we focused on the use of the MCC-IMS technology for the detection and quantification of the volatile anaesthetic agent sevoflurane. Chronic occupational exposure to low concentrations of sevoflurane has been discussed to have adverse effects on the health of health care workers . Even though evidence is not clear on that issue occupational exposure limits and other ceiling value recommendations were published by governmental and health care organizations [4-7]. To answer the question if MCC-IMS could be a fast and reliable alternative to other analytical methods we calibrated the device to sevoflurane concentrations of 10 – 250 ppbv.
We were able to detect sevoflurane in the mode for the detection of negative ions and found a correlation between peak intensity in the MCC-IMS plots and sevoflurane air concentrations. The calibration of the MCC-IMS showed very low LOD and LOQ. Previously, PIS, PTR-MS and PTR-ToF-MS were used for assessing sevoflurane room air concentrations [4,8,9,12,13]. In our study MCC-IMS showed detection limits lower than all these methods – even when compared to PTR-ToF-MS . The LOQ of the MCC-IMS was found to be 0.0189 ppbv and therewith was very low as well. We were not able to find a LOQ for PIS in the literature. Because of very low detection limits MCC-IMS could be a feasible alternative to other methods, especially when low-level contamination with sevoflurane is expected.
To give an example on the performance of MCC-IMS in quantifying sevoflurane, we performed room air measurements during paediatric anaesthesia and in the PACU. In all children general anaesthesia was induced by sevoflurane mask inhalation and was continued as TIVA. We therefore expected the peak concentrations during this procedure and also expected sevoflurane concentrations to decrease in the following measurements. Our results confirmed these expectations. In all 12 patients we found the highest sevoflurane room air concentrations during mask induction with decreasing concentrations over the following measurements up to 70 minutes time of surgery (see Figure 3).
We also monitored the room air of the PACU for 54 hours. As expected our results showed higher concentrations during the evening shifts than during the night shifts or the morning shifts (see Table 5). These findings reflect the number of patients attending the PACU and being discharged from it (see Figure 4). Sevoflurane concentrations in both anaesthesia workplaces clearly did not exceed recommended exposure values [4-7].
Our results partly differ from findings of previous studies. Most authors using PIS for assessing the exposure of hospital personnel to sevoflurane described higher sevoflurane concentrations and TWA-S values. For instance Hoerauf et al. and Schiewe-Langgartner et al. described TWA-S values between 20 ppbv and 2,240 ppbv when sevoflurane was used as the only volatile anaesthetic agent during general anaesthesia [10,11]. On the other hand our results closely match the findings of Rieder et al. and Trefz et al. who assessed sevoflurane concentrations in the PACU using PTR-MS and PTR-ToF-MS. Both authors describe mean room air concentrations of the substance in a low ppbv-range with maxima between 300 and 1,000 ppbv, depending on the number of patients attending the PACU [13,14]. However, room air concentrations monitored with PIS might be overestimated due to the higher detection limits and results should be controlled by using more sensitive technologies, such as MCC-IMS or PTR-(ToF)-MS.
The calibration of the MCC-IMS using a calibration gas generator is a strength of the study. We found a linear correlation for concentrations between 25 and 175 ppbv. However, the upper end of the calibration range did not show a linear correlation anymore, but we expected higher concentrations in the workplace measurements. We decided to use the polynomial correlation to extrapolate the correlation for the higher concentrations, which is a limitation of our study. For the same reason we were not able to describe an upper detection limit of the method, which could be relevant for very high sevoflurane concentrations. However, to our knowledge for none of the other analytical methods an upper detection limit has been described. The assessment of the MCC-IMS’s performance in assessing much higher concentrations of sevoflurane in the room air should be part of future studies. As another limitation we did not use a different analytical method in parallel to the MCC-IMS. Future studies on the performance of PIS, PTR-MS and MCC-IMS should be compared by parallel measurements.
MCC-IMS allowed us to assess very low concentrations of sevoflurane. Compared to PIS the MCC-IMS device used in this study showed a very low LOD and our results showed a significantly lower exposure to sevoflurane than described by authors that used PIS for their measurements at anaesthesia workplaces. The performance of the MCC-IMS device in our study was similar to PTR-MS and PTR-ToF-MS devices used for the detection and quantification of sevoflurane. Both technologies provide very low detection limits and enable assessment of a minimal exposure to volatile anaesthetics. Due to the suitability to miniaturization and the possibility to detect more than one substance at once (e.g. when more than one anaesthetic agent is used in a workplace), MCC-IMS might be a preferable technology for a hospital setting. However, more investigation is needed to assess the performance of MCC-IMS in the quantification of different volatile anaesthetics, the combination of volatile anaesthetics and nitrous oxygen and the combination of several substances.
Our findings show that MCC-IMS is a reliable alternative method for the quantification of sevoflurane in the room air. MCC-IMS shows significant lower detection limits than comparable methods and has a particular strength in quantifying low-level contaminations of sevoflurane. The results of our room air measurements reflected the logical implications of the study protocol regarding the trends of sevoflurane concentrations in both anaesthesia workplaces. The exposure of the personnel working in these areas did not exceed recommended limitations.
We would like to thank Luzia Seifert of the ISAS in Dortmund, Germany for her help and support during the calibration of the MCC-IMS.
- Wiesner G, Schiewe-Langgartner F, Lindner R, Gruber M. Increased formation of sister chromatid exchanges, but not of micronuclei, in anaesthetists exposed to low levels of sevoflurane. Anaesthesia. 2008;63:861–4.View ArticlePubMedGoogle Scholar
- Ozer M, Baris S, Karakaya D, Kocamanoglu S, Tur A. Behavioural effects of chronic exposure to subanesthetic concentrations of halothane, sevoflurane and desflurane in rats. Canadian J Anaesthesia J Canadien d’anesthesie. 2006;53:653–8.View ArticleGoogle Scholar
- Nilsson R, Bjordal C, Andersson M, Bjordal J, Nyberg A, Welin B, et al. Health risks and occupational exposure to volatile anaesthetics–a review with a systematic approach. J Clin Nurs. 2005;14:173–86.View ArticlePubMedGoogle Scholar
- Blokker-Veldhuis MJ, Rutten PM, De Hert SG. Occupational exposure to sevoflurane during cardiopulmonary bypass. Perfusion. 2011;26:383–9.View ArticlePubMedGoogle Scholar
- Hoerauf KH, Koller C, Taeger K, Hobbhahn J. Occupational exposure to sevoflurane and nitrous oxide in operating room personnel. Int Arch Occup Environ Health. 1997;69:134–8.View ArticlePubMedGoogle Scholar
- Heijbel H, Bjurstom R, Jakobsson JG. Personnel breathing zone sevoflurane concentration adherence to occupational exposure limits in conjunction with filling of vaporisers. Acta Anaesthesiol Scand. 2010;54:1117–20.View ArticlePubMedGoogle Scholar
- NIOSH NIfOSaH. Criteria for a recommended standard: occupational exposure to waste anesthetic gases and vapors. US Department of Health, Education and Welfare, NIOSH, Cincinnati; 1977. 77–140.Google Scholar
- Byhahn C, Heller K, Lischke V, Westphal K. Surgeon’s occupational exposure to nitrous oxide and sevoflurane during pediatric surgery. World J Surg. 2001;25:1109–12.View ArticlePubMedGoogle Scholar
- Hoerauf KH, Wallner T, Akca O, Taslimi R, Sessler DI. Exposure to sevoflurane and nitrous oxide during four different methods of anesthetic induction. Anesth Analg. 1999;88:925–9.PubMedGoogle Scholar
- Schiewe-Langgartner F, Wiesner G, Gruber M, Hobbhahn J. [Exposure of hospital personnel to sevoflurane]. Anaesthesist. 2005;54:667–72.View ArticlePubMedGoogle Scholar
- Hoerauf KH, Hartmann T, Zavrski A, Adel S, Burger HJ, Koinig H, et al. Occupational exposure to sevoflurane during sedation of adult patients. Int Arch Occup Environ Health. 1999;72:174–7.View ArticlePubMedGoogle Scholar
- Summer G, Lirk P, Hoerauf K, Riccabona U, Bodrogi F, Raifer H, et al. Sevoflurane in exhaled air of operating room personnel. Anesth Analg. 2003;97:1070–3.View ArticlePubMedGoogle Scholar
- Trefz P, Schmidt M, Oertel P, Obermeier J, Brock B, Kamysek S, et al. Continuous real time breath gas monitoring in the clinical environment by proton-transfer-reaction-time-of-flight-mass spectrometry. Anal Chem. 2013;85:10321–9.View ArticlePubMedGoogle Scholar
- Rieder J, Prazeller P, Boehler M, Lirk P, Lindinger W, Amann A. Online monitoring of air quality at the postanesthetic care unit by proton-transfer-reaction mass spectrometry. Anesth Analg. 2001;92:389–92.View ArticlePubMedGoogle Scholar
- Eiceman GA, Karpas Z, Hill HH. Ion mobility spectrometry. 3rd ed. London: CRC Press; 2013.Google Scholar
- Perl T, Carstens E, Hirn A, Quintel M, Vautz W, Nolte J, et al. Determination of serum propofol concentrations by breath analysis using ion mobility spectrometry. Br J Anaesth. 2009;103:822–7.View ArticlePubMedGoogle Scholar
- Kunze N, Gopel J, Kuhns M, Junger M, Quintel M, Perl T. Detection and validation of volatile metabolic patterns over different strains of two human pathogenic bacteria during their growth in a complex medium using multi-capillary column-ion mobility spectrometry (MCC-IMS). Appl Microbiol Biotechnol. 2013;97:3665–76.View ArticlePubMed CentralPubMedGoogle Scholar
- Perl T, Junger M, Vautz W, Nolte J, Kuhns M, Borg-Von Zepelin M, et al. Detection of characteristic metabolites of Aspergillus fumigatus and Candida species using ion mobility spectrometry-metabolic profiling by volatile organic compounds. Mycoses. 2011;54:e828–37.View ArticlePubMedGoogle Scholar
- Junger M, Vautz W, Kuhns M, Hofmann L, Ulbricht S, Baumbach JI, et al. Ion mobility spectrometry for microbial volatile organic compounds: a new identification tool for human pathogenic bacteria. Appl Microbiol Biotechnol. 2012;93:2603–14.View ArticlePubMed CentralPubMedGoogle Scholar
- Pagonas N, Vautz W, Seifert L, Slodzinski R, Jankowski J, Zidek W, et al. Volatile organic compounds in uremia. PLoS One. 2012;7:e46258.View ArticlePubMed CentralPubMedGoogle Scholar
- Kurrek MM, Dain SL, Kiss A. Technical communication: the effect of the double mask on anesthetic waste gas levels during pediatric mask inductions in dental offices. Anesth Analg. 2013;117:43–6.View ArticlePubMedGoogle Scholar
- Vautz W, Bödeker B, Baumbach JI, Bader S, Westhoff M, Perl T. An implementable approach to obtain reproducible reduced ion mobility. Int J Ion Mobil Spectrom. 2009;12:47–57.View ArticleGoogle Scholar
- Vautz W, Schmäh M. HovaCAL®—a generator for multi-component humid calibration gases. Int J Ion Mobil Spectrom. 2009;12:139–47.View ArticleGoogle Scholar
- MacDougall D, Crummett WB. Guidelines for data acquisition and data quality evaluation in environmental chemistry. Anal Chem. 1980;52:2242–9.View ArticleGoogle Scholar
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