Impact of an Antimicrobial Stewardship Program on Patient Safety in Veterans Prescribed Vancomycin

Abstract Purpose This study aimed to determine the safety impact of an antimicrobial stewardship program (ASP) on vancomycin-associated nephrotoxicity and to examine risk factors contributing to the development of toxicity. Methods This was a retrospective chart review of data from 453 veterans rece...

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Veröffentlicht in:Clinical therapeutics 2016-03, Vol.38 (3), p.494-502
Hauptverfasser: Fodero, Kristen E., PharmD, BCPS, Horey, Amy L., PharmD, BCPS, Krajewski, Michael P., PharmD, MLS, Ruh, Christine A., PharmD, BCPS, Sellick, John A., DO, MS, Mergenhagen, Kari A., PharmD, BCPS, AQ-ID
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container_end_page 502
container_issue 3
container_start_page 494
container_title Clinical therapeutics
container_volume 38
creator Fodero, Kristen E., PharmD, BCPS
Horey, Amy L., PharmD, BCPS
Krajewski, Michael P., PharmD, MLS
Ruh, Christine A., PharmD, BCPS
Sellick, John A., DO, MS
Mergenhagen, Kari A., PharmD, BCPS, AQ-ID
description Abstract Purpose This study aimed to determine the safety impact of an antimicrobial stewardship program (ASP) on vancomycin-associated nephrotoxicity and to examine risk factors contributing to the development of toxicity. Methods This was a retrospective chart review of data from 453 veterans receiving vancomycin in the VA Western New York Healthcare System between October 2006 and July 2014. Nephrotoxicity was defined as an increase in serum creatinine of ≥0.5 mg/dL or by 50% of baseline for 2 consecutive days. Findings Patients receiving vancomycin after the implementation of the ASP were less likely to develop nephrotoxicity (odds ratio [OR] = 2.06; 95% CI, 1.02–4.28). Nephrotoxicity occurred in 6.84% of patients from the pre-ASP cohort and in 3.75% of patients after the implementation of the ASP. Predictors of nephrotoxicity included hospital service (surgical service, OR = 2.29; 95% CI, 1.13–4.64), elevated maximum trough concentration (unit OR = 1.15; 95% CI, 1.10–1.20), and concurrent piperacillin/tazobactam therapy (OR = 3.21; 95% CI, 1.43–7.96). The number of vancomycin trough concentration measurements per patient did not vary between the pre-ASP and ASP groups. Implications ASPs represent an important aspect of a patient-safety initiative in order to reduce vancomycin-associated nephrotoxicity. Concurrent piperacillin/tazobactam therapy, surgical service, and elevated maximum trough concentration were risk factors for nephrotoxicity.
doi_str_mv 10.1016/j.clinthera.2016.01.001
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Methods This was a retrospective chart review of data from 453 veterans receiving vancomycin in the VA Western New York Healthcare System between October 2006 and July 2014. Nephrotoxicity was defined as an increase in serum creatinine of ≥0.5 mg/dL or by 50% of baseline for 2 consecutive days. Findings Patients receiving vancomycin after the implementation of the ASP were less likely to develop nephrotoxicity (odds ratio [OR] = 2.06; 95% CI, 1.02–4.28). Nephrotoxicity occurred in 6.84% of patients from the pre-ASP cohort and in 3.75% of patients after the implementation of the ASP. Predictors of nephrotoxicity included hospital service (surgical service, OR = 2.29; 95% CI, 1.13–4.64), elevated maximum trough concentration (unit OR = 1.15; 95% CI, 1.10–1.20), and concurrent piperacillin/tazobactam therapy (OR = 3.21; 95% CI, 1.43–7.96). The number of vancomycin trough concentration measurements per patient did not vary between the pre-ASP and ASP groups. Implications ASPs represent an important aspect of a patient-safety initiative in order to reduce vancomycin-associated nephrotoxicity. Concurrent piperacillin/tazobactam therapy, surgical service, and elevated maximum trough concentration were risk factors for nephrotoxicity.</description><identifier>ISSN: 0149-2918</identifier><identifier>EISSN: 1879-114X</identifier><identifier>DOI: 10.1016/j.clinthera.2016.01.001</identifier><identifier>PMID: 26831569</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Acute Kidney Injury - blood ; Acute Kidney Injury - chemically induced ; Aged ; Aged, 80 and over ; Anti-Bacterial Agents - adverse effects ; Anti-Bacterial Agents - blood ; Anti-Bacterial Agents - therapeutic use ; antimicrobial stewardship ; Creatinine - blood ; Drug Therapy, Combination - adverse effects ; Female ; Hospital Departments - statistics &amp; numerical data ; Humans ; Internal Medicine ; Interrupted Time Series Analysis ; Male ; Medical Education ; Middle Aged ; nephrotoxicity ; Patient Safety ; Penicillanic Acid - adverse effects ; Penicillanic Acid - analogs &amp; derivatives ; Penicillanic Acid - therapeutic use ; Piperacillin - adverse effects ; Piperacillin - therapeutic use ; Retrospective Studies ; Risk Factors ; vancomycin ; Vancomycin - adverse effects ; Vancomycin - blood ; Vancomycin - therapeutic use ; Veterans</subject><ispartof>Clinical therapeutics, 2016-03, Vol.38 (3), p.494-502</ispartof><rights>2016</rights><rights>Published by Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c525t-d2f2279fe00012b5e707a0122d7f3df63ca55f399754e5d3e6c9cc031984223</citedby><cites>FETCH-LOGICAL-c525t-d2f2279fe00012b5e707a0122d7f3df63ca55f399754e5d3e6c9cc031984223</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0149291816000059$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26831569$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fodero, Kristen E., PharmD, BCPS</creatorcontrib><creatorcontrib>Horey, Amy L., PharmD, BCPS</creatorcontrib><creatorcontrib>Krajewski, Michael P., PharmD, MLS</creatorcontrib><creatorcontrib>Ruh, Christine A., PharmD, BCPS</creatorcontrib><creatorcontrib>Sellick, John A., DO, MS</creatorcontrib><creatorcontrib>Mergenhagen, Kari A., PharmD, BCPS, AQ-ID</creatorcontrib><title>Impact of an Antimicrobial Stewardship Program on Patient Safety in Veterans Prescribed Vancomycin</title><title>Clinical therapeutics</title><addtitle>Clin Ther</addtitle><description>Abstract Purpose This study aimed to determine the safety impact of an antimicrobial stewardship program (ASP) on vancomycin-associated nephrotoxicity and to examine risk factors contributing to the development of toxicity. Methods This was a retrospective chart review of data from 453 veterans receiving vancomycin in the VA Western New York Healthcare System between October 2006 and July 2014. Nephrotoxicity was defined as an increase in serum creatinine of ≥0.5 mg/dL or by 50% of baseline for 2 consecutive days. Findings Patients receiving vancomycin after the implementation of the ASP were less likely to develop nephrotoxicity (odds ratio [OR] = 2.06; 95% CI, 1.02–4.28). Nephrotoxicity occurred in 6.84% of patients from the pre-ASP cohort and in 3.75% of patients after the implementation of the ASP. Predictors of nephrotoxicity included hospital service (surgical service, OR = 2.29; 95% CI, 1.13–4.64), elevated maximum trough concentration (unit OR = 1.15; 95% CI, 1.10–1.20), and concurrent piperacillin/tazobactam therapy (OR = 3.21; 95% CI, 1.43–7.96). The number of vancomycin trough concentration measurements per patient did not vary between the pre-ASP and ASP groups. Implications ASPs represent an important aspect of a patient-safety initiative in order to reduce vancomycin-associated nephrotoxicity. 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derivatives</subject><subject>Penicillanic Acid - therapeutic use</subject><subject>Piperacillin - adverse effects</subject><subject>Piperacillin - therapeutic use</subject><subject>Retrospective Studies</subject><subject>Risk Factors</subject><subject>vancomycin</subject><subject>Vancomycin - adverse effects</subject><subject>Vancomycin - blood</subject><subject>Vancomycin - therapeutic use</subject><subject>Veterans</subject><issn>0149-2918</issn><issn>1879-114X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkk1v1DAQQC0EotvCXwAfuSR47DheX5BWVaGVKlFpUcXNcpwJ9ZI4i-0F7b_H0ZYeuMDJlvXmw2-GkLfAamDQvt_VbvQhP2C0NS8PNYOaMXhGVrBWugJovj4nKwaNrriG9Rk5T2nHGBNa8pfkjLdrAbLVK9LdTHvrMp0HagPdhOwn7-LceTvSbcZfNvbpwe_pXZy_RTvROdA7mz2GTLd2wHykPtB7zKWRkAqFyUXfYU_vbXDzdHQ-vCIvBjsmfP14XpDtx6svl9fV7edPN5eb28pJLnPV84FzpQcsbQLvJCqmbLnxXg2iH1rhrJSD0FrJBmUvsHXaOSZArxvOxQV5d8q6j_OPA6ZsJp8cjqMNOB-SAQ1at0IJ_W9UqUYK0YAqqDqhxUlKEQezj36y8WiAmWUSZmeeJmGWSRgGpnygRL55LHLoJuyf4v6oL8DmBGBx8tNjNMkVrw57H9Fl08_-P4p8-CvHwnlnx-94xLSbDzEU5QZM4oaZ7bIQyz5AWyQzqcVvVYSy5g</recordid><startdate>20160301</startdate><enddate>20160301</enddate><creator>Fodero, Kristen E., PharmD, BCPS</creator><creator>Horey, Amy L., PharmD, BCPS</creator><creator>Krajewski, Michael P., PharmD, MLS</creator><creator>Ruh, Christine A., PharmD, BCPS</creator><creator>Sellick, John A., DO, MS</creator><creator>Mergenhagen, Kari A., PharmD, BCPS, AQ-ID</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>20160301</creationdate><title>Impact of an Antimicrobial Stewardship Program on Patient Safety in Veterans Prescribed Vancomycin</title><author>Fodero, Kristen E., PharmD, BCPS ; Horey, Amy L., PharmD, BCPS ; Krajewski, Michael P., PharmD, MLS ; Ruh, Christine A., PharmD, BCPS ; Sellick, John A., DO, MS ; Mergenhagen, Kari A., PharmD, BCPS, AQ-ID</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c525t-d2f2279fe00012b5e707a0122d7f3df63ca55f399754e5d3e6c9cc031984223</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Acute Kidney Injury - blood</topic><topic>Acute Kidney Injury - chemically induced</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Anti-Bacterial Agents - adverse effects</topic><topic>Anti-Bacterial Agents - blood</topic><topic>Anti-Bacterial Agents - therapeutic use</topic><topic>antimicrobial stewardship</topic><topic>Creatinine - blood</topic><topic>Drug Therapy, Combination - adverse effects</topic><topic>Female</topic><topic>Hospital Departments - statistics &amp; numerical data</topic><topic>Humans</topic><topic>Internal Medicine</topic><topic>Interrupted Time Series Analysis</topic><topic>Male</topic><topic>Medical Education</topic><topic>Middle Aged</topic><topic>nephrotoxicity</topic><topic>Patient Safety</topic><topic>Penicillanic Acid - adverse effects</topic><topic>Penicillanic Acid - analogs &amp; derivatives</topic><topic>Penicillanic Acid - therapeutic use</topic><topic>Piperacillin - adverse effects</topic><topic>Piperacillin - therapeutic use</topic><topic>Retrospective Studies</topic><topic>Risk Factors</topic><topic>vancomycin</topic><topic>Vancomycin - adverse effects</topic><topic>Vancomycin - blood</topic><topic>Vancomycin - therapeutic use</topic><topic>Veterans</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fodero, Kristen E., PharmD, BCPS</creatorcontrib><creatorcontrib>Horey, Amy L., PharmD, BCPS</creatorcontrib><creatorcontrib>Krajewski, Michael P., PharmD, MLS</creatorcontrib><creatorcontrib>Ruh, Christine A., PharmD, BCPS</creatorcontrib><creatorcontrib>Sellick, John A., DO, MS</creatorcontrib><creatorcontrib>Mergenhagen, Kari A., PharmD, BCPS, AQ-ID</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Clinical therapeutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fodero, Kristen E., PharmD, BCPS</au><au>Horey, Amy L., PharmD, BCPS</au><au>Krajewski, Michael P., PharmD, MLS</au><au>Ruh, Christine A., PharmD, BCPS</au><au>Sellick, John A., DO, MS</au><au>Mergenhagen, Kari A., PharmD, BCPS, AQ-ID</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Impact of an Antimicrobial Stewardship Program on Patient Safety in Veterans Prescribed Vancomycin</atitle><jtitle>Clinical therapeutics</jtitle><addtitle>Clin Ther</addtitle><date>2016-03-01</date><risdate>2016</risdate><volume>38</volume><issue>3</issue><spage>494</spage><epage>502</epage><pages>494-502</pages><issn>0149-2918</issn><eissn>1879-114X</eissn><abstract>Abstract Purpose This study aimed to determine the safety impact of an antimicrobial stewardship program (ASP) on vancomycin-associated nephrotoxicity and to examine risk factors contributing to the development of toxicity. Methods This was a retrospective chart review of data from 453 veterans receiving vancomycin in the VA Western New York Healthcare System between October 2006 and July 2014. Nephrotoxicity was defined as an increase in serum creatinine of ≥0.5 mg/dL or by 50% of baseline for 2 consecutive days. Findings Patients receiving vancomycin after the implementation of the ASP were less likely to develop nephrotoxicity (odds ratio [OR] = 2.06; 95% CI, 1.02–4.28). Nephrotoxicity occurred in 6.84% of patients from the pre-ASP cohort and in 3.75% of patients after the implementation of the ASP. Predictors of nephrotoxicity included hospital service (surgical service, OR = 2.29; 95% CI, 1.13–4.64), elevated maximum trough concentration (unit OR = 1.15; 95% CI, 1.10–1.20), and concurrent piperacillin/tazobactam therapy (OR = 3.21; 95% CI, 1.43–7.96). The number of vancomycin trough concentration measurements per patient did not vary between the pre-ASP and ASP groups. Implications ASPs represent an important aspect of a patient-safety initiative in order to reduce vancomycin-associated nephrotoxicity. Concurrent piperacillin/tazobactam therapy, surgical service, and elevated maximum trough concentration were risk factors for nephrotoxicity.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>26831569</pmid><doi>10.1016/j.clinthera.2016.01.001</doi><tpages>9</tpages></addata></record>
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subjects Acute Kidney Injury - blood
Acute Kidney Injury - chemically induced
Aged
Aged, 80 and over
Anti-Bacterial Agents - adverse effects
Anti-Bacterial Agents - blood
Anti-Bacterial Agents - therapeutic use
antimicrobial stewardship
Creatinine - blood
Drug Therapy, Combination - adverse effects
Female
Hospital Departments - statistics & numerical data
Humans
Internal Medicine
Interrupted Time Series Analysis
Male
Medical Education
Middle Aged
nephrotoxicity
Patient Safety
Penicillanic Acid - adverse effects
Penicillanic Acid - analogs & derivatives
Penicillanic Acid - therapeutic use
Piperacillin - adverse effects
Piperacillin - therapeutic use
Retrospective Studies
Risk Factors
vancomycin
Vancomycin - adverse effects
Vancomycin - blood
Vancomycin - therapeutic use
Veterans
title Impact of an Antimicrobial Stewardship Program on Patient Safety in Veterans Prescribed Vancomycin
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