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"Random" gentamicin concentrations do not predict trough levels in neonates receiving once daily fixed dose regimens

BACKGROUND: Monitoring plasma gentamicin concentrations in neonates 24 hours after a once daily dose (4 mg/kg) often necessitates additional blood sampling. In adults a nomogram has been developed enabling evaluation of gentamicin doses by sampling concentrations with other blood tests, 4 – 16 hours...

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Autores principales: Boyle, Elaine M, Brookes, Isobel, Nye, Kathy, Watkinson, Mike, Riordan, F Andrew I
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1440860/
https://www.ncbi.nlm.nih.gov/pubmed/16545135
http://dx.doi.org/10.1186/1471-2431-6-8
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author Boyle, Elaine M
Brookes, Isobel
Nye, Kathy
Watkinson, Mike
Riordan, F Andrew I
author_facet Boyle, Elaine M
Brookes, Isobel
Nye, Kathy
Watkinson, Mike
Riordan, F Andrew I
author_sort Boyle, Elaine M
collection PubMed
description BACKGROUND: Monitoring plasma gentamicin concentrations in neonates 24 hours after a once daily dose (4 mg/kg) often necessitates additional blood sampling. In adults a nomogram has been developed enabling evaluation of gentamicin doses by sampling concentrations with other blood tests, 4 – 16 hours after administration. We attempted to develop a similar nomogram for neonates. METHODS: In addition to standard 24 hour sampling to monitor trough concentrations, one additional "random" gentamicin concentration was measured in each of 50 neonates <4 days of age (median gestation 33 weeks [28–41]), when other blood samples were clinically necessary, 4 – 20 hours after gentamicin administration. 24 hour concentrations of >1 mg/L were considered high, and an indication to extend the dosing interval. RESULTS: Highest correlation (r(2 )= 0.51) of plasma gentamicin concentration against time (4 to 20 hours) was with logarithmic regression. A line drawn 0.5 mg/L below the true regression line resulted in all babies with 24 hr gentamicin concentrations >1 mg/L having the additional "random" test result above that line, i.e. 100% sensitivity for 24 hour concentrations>1 mg/L, though only 58% specificity. Having created the nomogram, 39 further babies (median gestation 34 weeks [28–41]), were studied and results tested against the nomogram. In this validation group, sensitivity of the nomogram for 24 hr concentrations >1 mg/L was 92%; specificity 14%, positive predictive value 66%, and negative predictive value 50%. Prematurity (≤ 37 weeks) was a more sensitive (94%) and specific (61%) indicator of high 24-hour concentrations. 62 (87%) of 71 preterm babies had high 24-hour concentrations. CONCLUSION: It was not possible to construct a nomogram to predict gentamicin concentrations at 24 hours in neonates with a variety of gestational ages. Dosage tailored to gestation with monitoring of trough concentrations remains management of choice.
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spelling pubmed-14408602006-04-20 "Random" gentamicin concentrations do not predict trough levels in neonates receiving once daily fixed dose regimens Boyle, Elaine M Brookes, Isobel Nye, Kathy Watkinson, Mike Riordan, F Andrew I BMC Pediatr Research Article BACKGROUND: Monitoring plasma gentamicin concentrations in neonates 24 hours after a once daily dose (4 mg/kg) often necessitates additional blood sampling. In adults a nomogram has been developed enabling evaluation of gentamicin doses by sampling concentrations with other blood tests, 4 – 16 hours after administration. We attempted to develop a similar nomogram for neonates. METHODS: In addition to standard 24 hour sampling to monitor trough concentrations, one additional "random" gentamicin concentration was measured in each of 50 neonates <4 days of age (median gestation 33 weeks [28–41]), when other blood samples were clinically necessary, 4 – 20 hours after gentamicin administration. 24 hour concentrations of >1 mg/L were considered high, and an indication to extend the dosing interval. RESULTS: Highest correlation (r(2 )= 0.51) of plasma gentamicin concentration against time (4 to 20 hours) was with logarithmic regression. A line drawn 0.5 mg/L below the true regression line resulted in all babies with 24 hr gentamicin concentrations >1 mg/L having the additional "random" test result above that line, i.e. 100% sensitivity for 24 hour concentrations>1 mg/L, though only 58% specificity. Having created the nomogram, 39 further babies (median gestation 34 weeks [28–41]), were studied and results tested against the nomogram. In this validation group, sensitivity of the nomogram for 24 hr concentrations >1 mg/L was 92%; specificity 14%, positive predictive value 66%, and negative predictive value 50%. Prematurity (≤ 37 weeks) was a more sensitive (94%) and specific (61%) indicator of high 24-hour concentrations. 62 (87%) of 71 preterm babies had high 24-hour concentrations. CONCLUSION: It was not possible to construct a nomogram to predict gentamicin concentrations at 24 hours in neonates with a variety of gestational ages. Dosage tailored to gestation with monitoring of trough concentrations remains management of choice. BioMed Central 2006-03-17 /pmc/articles/PMC1440860/ /pubmed/16545135 http://dx.doi.org/10.1186/1471-2431-6-8 Text en Copyright © 2006 Boyle et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Boyle, Elaine M
Brookes, Isobel
Nye, Kathy
Watkinson, Mike
Riordan, F Andrew I
"Random" gentamicin concentrations do not predict trough levels in neonates receiving once daily fixed dose regimens
title "Random" gentamicin concentrations do not predict trough levels in neonates receiving once daily fixed dose regimens
title_full "Random" gentamicin concentrations do not predict trough levels in neonates receiving once daily fixed dose regimens
title_fullStr "Random" gentamicin concentrations do not predict trough levels in neonates receiving once daily fixed dose regimens
title_full_unstemmed "Random" gentamicin concentrations do not predict trough levels in neonates receiving once daily fixed dose regimens
title_short "Random" gentamicin concentrations do not predict trough levels in neonates receiving once daily fixed dose regimens
title_sort "random" gentamicin concentrations do not predict trough levels in neonates receiving once daily fixed dose regimens
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1440860/
https://www.ncbi.nlm.nih.gov/pubmed/16545135
http://dx.doi.org/10.1186/1471-2431-6-8
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