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Pediatric Vancomycin Use in 421 Hospitals in the United States, 2008
BACKGROUND: Recommendations to prevent the spread of vancomycin resistance have been in place since 1995 and include guidelines for inpatient pediatric use of vancomycin. The emergence of large databases allows us to describe variation in pediatric vancomycin across hospitals. We analyzed a database...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3420889/ https://www.ncbi.nlm.nih.gov/pubmed/22916234 http://dx.doi.org/10.1371/journal.pone.0043258 |
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author | Lasky, Tamar Greenspan, Jay Ernst, Frank R. Gonzalez, Liliana |
author_facet | Lasky, Tamar Greenspan, Jay Ernst, Frank R. Gonzalez, Liliana |
author_sort | Lasky, Tamar |
collection | PubMed |
description | BACKGROUND: Recommendations to prevent the spread of vancomycin resistance have been in place since 1995 and include guidelines for inpatient pediatric use of vancomycin. The emergence of large databases allows us to describe variation in pediatric vancomycin across hospitals. We analyzed a database with hospitalizations for children under 18 at 421 hospitals in 2008. METHODOLOGY/PRINCIPAL FINDINGS: The Premier hospital 2008 database, consisting of records for 877,201 pediatric hospitalizations in 421 hospitals, was analyzed. Stratified analyses and logistic mixed effects models were used to calculate the probability of vancomycin use while considering random effects of hospital variation, hospital fixed effects and patient effects, and the hierarchical structure of the data. Most hospitals (221) had fewer than 10 hospitalizations with vancomycin use in the study period, and 47 hospitals reported no vancomycin use in 17,271 pediatric hospitalizations. At the other end of the continuum, 21 hospitals (5.6% of hospitals) each had over 200 hospitalizations with vancomycin use, and together, accounted for more than 50% of the pediatric hospitalizations with vancomycin use. The mixed effects modeling showed hospital variation in the probability of vancomycin use that was statistically significant after controlling for teaching status, urban or rural location, size, region of the country, patient ethnic group, payor status, and APR-mortality and severity codes. CONCLUSIONS/SIGNIFICANCE: The number and percentage of pediatric hospitalizations with vancomycin use varied greatly across hospitals and was not explained by hospital or patient characteristics in our logistic models. Public health efforts to reduce vancomycin use should be intensified at hospitals with highest use. |
format | Online Article Text |
id | pubmed-3420889 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-34208892012-08-22 Pediatric Vancomycin Use in 421 Hospitals in the United States, 2008 Lasky, Tamar Greenspan, Jay Ernst, Frank R. Gonzalez, Liliana PLoS One Research Article BACKGROUND: Recommendations to prevent the spread of vancomycin resistance have been in place since 1995 and include guidelines for inpatient pediatric use of vancomycin. The emergence of large databases allows us to describe variation in pediatric vancomycin across hospitals. We analyzed a database with hospitalizations for children under 18 at 421 hospitals in 2008. METHODOLOGY/PRINCIPAL FINDINGS: The Premier hospital 2008 database, consisting of records for 877,201 pediatric hospitalizations in 421 hospitals, was analyzed. Stratified analyses and logistic mixed effects models were used to calculate the probability of vancomycin use while considering random effects of hospital variation, hospital fixed effects and patient effects, and the hierarchical structure of the data. Most hospitals (221) had fewer than 10 hospitalizations with vancomycin use in the study period, and 47 hospitals reported no vancomycin use in 17,271 pediatric hospitalizations. At the other end of the continuum, 21 hospitals (5.6% of hospitals) each had over 200 hospitalizations with vancomycin use, and together, accounted for more than 50% of the pediatric hospitalizations with vancomycin use. The mixed effects modeling showed hospital variation in the probability of vancomycin use that was statistically significant after controlling for teaching status, urban or rural location, size, region of the country, patient ethnic group, payor status, and APR-mortality and severity codes. CONCLUSIONS/SIGNIFICANCE: The number and percentage of pediatric hospitalizations with vancomycin use varied greatly across hospitals and was not explained by hospital or patient characteristics in our logistic models. Public health efforts to reduce vancomycin use should be intensified at hospitals with highest use. Public Library of Science 2012-08-16 /pmc/articles/PMC3420889/ /pubmed/22916234 http://dx.doi.org/10.1371/journal.pone.0043258 Text en © 2012 Lasky et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Lasky, Tamar Greenspan, Jay Ernst, Frank R. Gonzalez, Liliana Pediatric Vancomycin Use in 421 Hospitals in the United States, 2008 |
title | Pediatric Vancomycin Use in 421 Hospitals in the United States, 2008 |
title_full | Pediatric Vancomycin Use in 421 Hospitals in the United States, 2008 |
title_fullStr | Pediatric Vancomycin Use in 421 Hospitals in the United States, 2008 |
title_full_unstemmed | Pediatric Vancomycin Use in 421 Hospitals in the United States, 2008 |
title_short | Pediatric Vancomycin Use in 421 Hospitals in the United States, 2008 |
title_sort | pediatric vancomycin use in 421 hospitals in the united states, 2008 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3420889/ https://www.ncbi.nlm.nih.gov/pubmed/22916234 http://dx.doi.org/10.1371/journal.pone.0043258 |
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