TY - JOUR
T1 - Phase II collaborative pilot study
T2 - Preliminary analysis of central neural effects from exposure to volatile anesthetics in the PACU
AU - Cope, Keary A.
AU - Merritt, William T.
AU - Krenzischek, Dina A.
AU - Schaefer, John
AU - Bukowski, James
AU - Foster, W. Michael
AU - Bernacki, Edward
AU - Dorman, Todd
AU - Risby, Terence H.
N1 - Funding Information:
Supported by an NIEHS training grant (T32 ES 07141) to K.A.C., and partially supported by grants from the US Air Force (F49620-98-1-0403) and NHLBI (HL56091).
Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 2002
Y1 - 2002
N2 - Nurses working in the PACU are occupationally exposed to volatile anesthetics that are exhaled by patients. Few studies have quantified this exposure using breath analysis or have characterized biological effects associated with this exposure. Isoflurane is a widely used anesthetic and is a strong respiratory depressant. Exposure to isoflurane has been shown to cause changes in breathing patterns at low doses. However, biological effects of isoflurane exposure have never been addressed in the occupational setting. This study investigates whether occupational exposure to anesthetic gases has a depressive effect on central neural control of breathing. In this study, concentrations of halogenated anesthetics were quantified in pre- and postshift breath samples of nurses working in the PACU on a Friday and the following Monday. After each breath sample was collected, an occlusion pressure measurement was taken as an indicator of central inspiratory drive. Cumulative nitrous oxide and halogenated anesthetics exposure was measured each day using personal sampling monitors placed close to the nurse's mouth. Exposure to nitrous oxide and isoflurane was significantly higher on Monday than on Friday (P < .001). Monday breath isoflurane concentrations (mean ± SD) increased significantly from 43 ± 30 parts per billion (ppb) in preshift breath samples to 124 ± 57 ppb in postshift breath samples (P < .002). On Monday, there was a significant decrease in occlusion pressure from 1.2 ± 0.37 cm H2O in preshift samples to 0.85 ± 0.43 cm H2O in postshift samples (P = .05). There was no statistical difference in pre- versus postbreath isoflurane or occlusion pressure on Friday. These data indicate that after increased exposure to isoflurane, central neurorespiratory activity was depressed.
AB - Nurses working in the PACU are occupationally exposed to volatile anesthetics that are exhaled by patients. Few studies have quantified this exposure using breath analysis or have characterized biological effects associated with this exposure. Isoflurane is a widely used anesthetic and is a strong respiratory depressant. Exposure to isoflurane has been shown to cause changes in breathing patterns at low doses. However, biological effects of isoflurane exposure have never been addressed in the occupational setting. This study investigates whether occupational exposure to anesthetic gases has a depressive effect on central neural control of breathing. In this study, concentrations of halogenated anesthetics were quantified in pre- and postshift breath samples of nurses working in the PACU on a Friday and the following Monday. After each breath sample was collected, an occlusion pressure measurement was taken as an indicator of central inspiratory drive. Cumulative nitrous oxide and halogenated anesthetics exposure was measured each day using personal sampling monitors placed close to the nurse's mouth. Exposure to nitrous oxide and isoflurane was significantly higher on Monday than on Friday (P < .001). Monday breath isoflurane concentrations (mean ± SD) increased significantly from 43 ± 30 parts per billion (ppb) in preshift breath samples to 124 ± 57 ppb in postshift breath samples (P < .002). On Monday, there was a significant decrease in occlusion pressure from 1.2 ± 0.37 cm H2O in preshift samples to 0.85 ± 0.43 cm H2O in postshift samples (P = .05). There was no statistical difference in pre- versus postbreath isoflurane or occlusion pressure on Friday. These data indicate that after increased exposure to isoflurane, central neurorespiratory activity was depressed.
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U2 - 10.1053/jpan.2002.34167
DO - 10.1053/jpan.2002.34167
M3 - Article
C2 - 12173155
AN - SCOPUS:0036689581
SN - 1089-9472
VL - 17
SP - 240
EP - 250
JO - Journal of Perianesthesia Nursing
JF - Journal of Perianesthesia Nursing
IS - 4
ER -