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Intravenous lidocaine infusion as a component of multimodal analgesia for colorectal surgery—measurement of plasma levels

BACKGROUND: Growing evidence suggests that intravenous lidocaine as a component of multimodal analgesia improves recovery after major colorectal surgery. There is little published data regarding ideal dosing and target plasma concentration in this context, and we wanted to establish our dosing sched...

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Autores principales: Greenwood, E., Nimmo, S., Paterson, H., Homer, N., Foo, I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6390549/
https://www.ncbi.nlm.nih.gov/pubmed/30858969
http://dx.doi.org/10.1186/s13741-019-0112-4
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author Greenwood, E.
Nimmo, S.
Paterson, H.
Homer, N.
Foo, I.
author_facet Greenwood, E.
Nimmo, S.
Paterson, H.
Homer, N.
Foo, I.
author_sort Greenwood, E.
collection PubMed
description BACKGROUND: Growing evidence suggests that intravenous lidocaine as a component of multimodal analgesia improves recovery after major colorectal surgery. There is little published data regarding ideal dosing and target plasma concentration in this context, and we wanted to establish our dosing schedule was safe by measuring blood levels of lidocaine. METHODS: We measured the plasma lidocaine concentration of 32 patients at 30 min, 6 h and 12 h after starting intravenous lidocaine infusion for analgesia after major colorectal surgery. Patients received a bolus of 1.5 mg kg(−1) over 20 min at the time of induction of anaesthesia. This was followed by a continuous infusion of 2% w/v lidocaine at 3 ml hr(−1) (60 mg hr(−1)) for patients weighing up to 70 kg and 6 ml hr(−1) (120 mg hr(−1)) for patients weighing over 70 kg, using actual body weight. RESULTS: The overall mean plasma lidocaine concentration was 4.0 μg ml(−1) (range 0.6–12.3 μg ml(−1)). In patients treated with the higher infusion dose, the mean concentration was 4.6 μg ml(−1) compared to 3.2 μg ml(−1) in those patients on the lower dose. Mean levels were higher at 6 h than 30 min and higher again at 12 h. There were no adverse events or reports of symptoms of local anaesthetic toxicity. CONCLUSIONS: Whilst there were no signs or symptoms of lidocaine toxicity in our patients, there was a wide range of plasma concentrations including some over 10 μg ml(−1); a level above which symptoms of toxicity may be expected. We have changed our dosing protocol to using ideal rather than actual body weight based on these results.
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spelling pubmed-63905492019-03-11 Intravenous lidocaine infusion as a component of multimodal analgesia for colorectal surgery—measurement of plasma levels Greenwood, E. Nimmo, S. Paterson, H. Homer, N. Foo, I. Perioper Med (Lond) Research BACKGROUND: Growing evidence suggests that intravenous lidocaine as a component of multimodal analgesia improves recovery after major colorectal surgery. There is little published data regarding ideal dosing and target plasma concentration in this context, and we wanted to establish our dosing schedule was safe by measuring blood levels of lidocaine. METHODS: We measured the plasma lidocaine concentration of 32 patients at 30 min, 6 h and 12 h after starting intravenous lidocaine infusion for analgesia after major colorectal surgery. Patients received a bolus of 1.5 mg kg(−1) over 20 min at the time of induction of anaesthesia. This was followed by a continuous infusion of 2% w/v lidocaine at 3 ml hr(−1) (60 mg hr(−1)) for patients weighing up to 70 kg and 6 ml hr(−1) (120 mg hr(−1)) for patients weighing over 70 kg, using actual body weight. RESULTS: The overall mean plasma lidocaine concentration was 4.0 μg ml(−1) (range 0.6–12.3 μg ml(−1)). In patients treated with the higher infusion dose, the mean concentration was 4.6 μg ml(−1) compared to 3.2 μg ml(−1) in those patients on the lower dose. Mean levels were higher at 6 h than 30 min and higher again at 12 h. There were no adverse events or reports of symptoms of local anaesthetic toxicity. CONCLUSIONS: Whilst there were no signs or symptoms of lidocaine toxicity in our patients, there was a wide range of plasma concentrations including some over 10 μg ml(−1); a level above which symptoms of toxicity may be expected. We have changed our dosing protocol to using ideal rather than actual body weight based on these results. BioMed Central 2019-02-26 /pmc/articles/PMC6390549/ /pubmed/30858969 http://dx.doi.org/10.1186/s13741-019-0112-4 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Greenwood, E.
Nimmo, S.
Paterson, H.
Homer, N.
Foo, I.
Intravenous lidocaine infusion as a component of multimodal analgesia for colorectal surgery—measurement of plasma levels
title Intravenous lidocaine infusion as a component of multimodal analgesia for colorectal surgery—measurement of plasma levels
title_full Intravenous lidocaine infusion as a component of multimodal analgesia for colorectal surgery—measurement of plasma levels
title_fullStr Intravenous lidocaine infusion as a component of multimodal analgesia for colorectal surgery—measurement of plasma levels
title_full_unstemmed Intravenous lidocaine infusion as a component of multimodal analgesia for colorectal surgery—measurement of plasma levels
title_short Intravenous lidocaine infusion as a component of multimodal analgesia for colorectal surgery—measurement of plasma levels
title_sort intravenous lidocaine infusion as a component of multimodal analgesia for colorectal surgery—measurement of plasma levels
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6390549/
https://www.ncbi.nlm.nih.gov/pubmed/30858969
http://dx.doi.org/10.1186/s13741-019-0112-4
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