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Pain assessment by pupil dilation reflex in response to noxious stimulation in anaesthetized adults

BACKGROUND: In response to noxious stimulation, pupillary dilation reflex (PDR) occurs even in anaesthetized patients. The aim of the study was to evaluate the ability of pupillometry with an automated increasing stimulus intensity to monitor intraoperative opioid administration. METHODS: Thirty‐fou...

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Autores principales: Wildemeersch, D., Peeters, N., Saldien, V., Vercauteren, M., Hans, G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099429/
https://www.ncbi.nlm.nih.gov/pubmed/29671874
http://dx.doi.org/10.1111/aas.13129
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author Wildemeersch, D.
Peeters, N.
Saldien, V.
Vercauteren, M.
Hans, G.
author_facet Wildemeersch, D.
Peeters, N.
Saldien, V.
Vercauteren, M.
Hans, G.
author_sort Wildemeersch, D.
collection PubMed
description BACKGROUND: In response to noxious stimulation, pupillary dilation reflex (PDR) occurs even in anaesthetized patients. The aim of the study was to evaluate the ability of pupillometry with an automated increasing stimulus intensity to monitor intraoperative opioid administration. METHODS: Thirty‐four patients undergoing elective surgery were enrolled. Induction by propofol anaesthesia was increased progressively until the sedation depth criteria (SeD) were attained. Subsequently, a first dynamic pupil measurement was performed by applying standardized nociceptive stimulation (SNS). A second PDR evaluation was performed when remifentanil reached a target effect‐site concentration. Automated infrared pupillometry was used to determine PDR during nociceptive stimulations generating a unique pupillary pain index (PPI). Vital signs were measured. RESULTS: After opioid administration, anaesthetized patients required a higher stimulation intensity (57.43 mA vs 32.29 mA, P < .0005). Pupil variation in response to the nociceptive stimulations was significantly reduced after opioid administration (8 mm vs 28 mm, P < .0005). The PPI score decreased after analgesic treatment (8 vs 2, P < .0005), corresponding to a 30% decrease. The elicitation of PDR by nociceptive stimulation was performed without changes in vital signs before (HR 76 vs 74/min, P = .09; SBP 123 vs 113 mm Hg, P = .001) and after opioid administration (HR 63 vs 62/min, P = .4; SBP 98.66 vs 93.77 mm Hg, P = .032). CONCLUSIONS: During propofol anaesthesia, pupillometry with the possibility of low‐intensity standardized noxious stimulation via PPI protocol can be used for PDR assessment in response to remifentanil administration.
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spelling pubmed-60994292018-08-24 Pain assessment by pupil dilation reflex in response to noxious stimulation in anaesthetized adults Wildemeersch, D. Peeters, N. Saldien, V. Vercauteren, M. Hans, G. Acta Anaesthesiol Scand General Anaesthesia BACKGROUND: In response to noxious stimulation, pupillary dilation reflex (PDR) occurs even in anaesthetized patients. The aim of the study was to evaluate the ability of pupillometry with an automated increasing stimulus intensity to monitor intraoperative opioid administration. METHODS: Thirty‐four patients undergoing elective surgery were enrolled. Induction by propofol anaesthesia was increased progressively until the sedation depth criteria (SeD) were attained. Subsequently, a first dynamic pupil measurement was performed by applying standardized nociceptive stimulation (SNS). A second PDR evaluation was performed when remifentanil reached a target effect‐site concentration. Automated infrared pupillometry was used to determine PDR during nociceptive stimulations generating a unique pupillary pain index (PPI). Vital signs were measured. RESULTS: After opioid administration, anaesthetized patients required a higher stimulation intensity (57.43 mA vs 32.29 mA, P < .0005). Pupil variation in response to the nociceptive stimulations was significantly reduced after opioid administration (8 mm vs 28 mm, P < .0005). The PPI score decreased after analgesic treatment (8 vs 2, P < .0005), corresponding to a 30% decrease. The elicitation of PDR by nociceptive stimulation was performed without changes in vital signs before (HR 76 vs 74/min, P = .09; SBP 123 vs 113 mm Hg, P = .001) and after opioid administration (HR 63 vs 62/min, P = .4; SBP 98.66 vs 93.77 mm Hg, P = .032). CONCLUSIONS: During propofol anaesthesia, pupillometry with the possibility of low‐intensity standardized noxious stimulation via PPI protocol can be used for PDR assessment in response to remifentanil administration. John Wiley and Sons Inc. 2018-04-19 2018-09 /pmc/articles/PMC6099429/ /pubmed/29671874 http://dx.doi.org/10.1111/aas.13129 Text en © The Authors. Acta Anaesthesiologica Scandinavica published by John Wiley & Sons Ltd on behalf of Acta Anaesthesiologica Scandinavica Foundation. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle General Anaesthesia
Wildemeersch, D.
Peeters, N.
Saldien, V.
Vercauteren, M.
Hans, G.
Pain assessment by pupil dilation reflex in response to noxious stimulation in anaesthetized adults
title Pain assessment by pupil dilation reflex in response to noxious stimulation in anaesthetized adults
title_full Pain assessment by pupil dilation reflex in response to noxious stimulation in anaesthetized adults
title_fullStr Pain assessment by pupil dilation reflex in response to noxious stimulation in anaesthetized adults
title_full_unstemmed Pain assessment by pupil dilation reflex in response to noxious stimulation in anaesthetized adults
title_short Pain assessment by pupil dilation reflex in response to noxious stimulation in anaesthetized adults
title_sort pain assessment by pupil dilation reflex in response to noxious stimulation in anaesthetized adults
topic General Anaesthesia
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099429/
https://www.ncbi.nlm.nih.gov/pubmed/29671874
http://dx.doi.org/10.1111/aas.13129
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