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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...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2006
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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. |
format | Text |
id | pubmed-1440860 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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