Impact of Increased Enoxaparin Dosing on Anti-Xa Levels for Venous Thromboembolism Prophylaxis in Trauma Patients
Introduction Venous thromboembolism (VTE) contributes to significant morbidity in trauma patients while increasing hospital costs and length of stay. Standard trauma prophylaxis dosing with enoxaparin 30 mg twice daily may be inadequate to prevent VTEs. The objective of this study was to compare sta...
Gespeichert in:
Veröffentlicht in: | The American surgeon 2022-09, Vol.88 (9), p.2158-2162 |
---|---|
Hauptverfasser: | , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 2162 |
---|---|
container_issue | 9 |
container_start_page | 2158 |
container_title | The American surgeon |
container_volume | 88 |
creator | Bellfi, Lillian T. Zimmerman, S. Anthony Boudreau, Ryan Mosier, Willard Smith, Alison Rueb, Nicole Hunt, John P. Stuke, Lance Greiffenstein, Patrick Schoen, Jonathan Marr, Alan |
description | Introduction
Venous thromboembolism (VTE) contributes to significant morbidity in trauma patients while increasing hospital costs and length of stay. Standard trauma prophylaxis dosing with enoxaparin 30 mg twice daily may be inadequate to prevent VTEs. The objective of this study was to compare standard dosing of enoxaparin to an increased dose of enoxaparin 40 mg twice daily for trauma patients. We hypothesized that increasing thromboprophylaxis dosing leads to an increase in therapeutic anti-Xa levels and reduced VTE rates.
Methods
A retrospective study was performed from January 2020 to June 2021 at a Level I trauma center, following implementation of an increased enoxaparin dosing strategy. Patients with increased enoxaparin dosing were compared with those who received standard dosing. The primary outcome evaluated was the incidence of subtherapeutic anti-Xa levels. Secondary outcomes evaluated VTE rates and clinically significant bleed.
Results
A total of 204 trauma patients were identified. Ninety-one patients received an increased enoxaparin dose compared to 113 who received standard dosing. The baseline demographics of both groups were similar (P > .05). Subtherapeutic levels were higher with standard dosing compared to the increased dose (50 vs 22%, P = .003). Higher VTE rates were observed with standard dosing compared to higher dosing (6.2 vs 3.3%) but with a lower incidence of major bleed (1.8 vs 4.4%). Overall annual VTE rates decreased from 1.6 to 1.3% after implementation of the increased dosing regimen.
Conclusions
This study demonstrated that an increased dosing strategy decreased rates of subtherapeutic anti-Xa levels and trended toward lower overall VTE rates in trauma. |
doi_str_mv | 10.1177/00031348221091935 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2691049595</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sage_id>10.1177_00031348221091935</sage_id><sourcerecordid>2691049595</sourcerecordid><originalsourceid>FETCH-LOGICAL-c345t-2f05b25d365531e7ccfc4d9467dc6b5b998986e164767782c5062477f7aca9823</originalsourceid><addsrcrecordid>eNp1kcFLwzAUxoMoOKd_gLeAFy-dSdqXNMcxpw4G7jDFW8nSdOtoky5pZfvv7ZggKB4ej8f7fR_f4yF0S8mIUiEeCCExjZOUMUoklTGcoQEFgEimLD5Hg-M-OgKX6CqEbT8mHOgA7WZ1o3SLXYFnVnujgsnx1Lq9apQvLX50obRr7Cwe27aMPhSem09TBVw4j9-NdV3Ay4139cqZvqoy1HjhXbM5VGpfBtxbLL3qaoUXqi2NbcM1uihUFczNdx-it6fpcvISzV-fZ5PxPNJxAm3ECgIrBnnMAWJqhNaFTnKZcJFrvoKVlKlMuaE8EVyIlGkgnCVCFEJpdTx6iO5Pvo13u86ENqvLoE1VKWv61BnjkpJEgoQevfuFbl3nbZ8uY4ICI8BB9hQ9Udq7ELwpssaXtfKHjJLs-ITszxN6zeikCWptflz_F3wBtPaFzw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2715205659</pqid></control><display><type>article</type><title>Impact of Increased Enoxaparin Dosing on Anti-Xa Levels for Venous Thromboembolism Prophylaxis in Trauma Patients</title><source>SAGE Complete A-Z List</source><creator>Bellfi, Lillian T. ; Zimmerman, S. Anthony ; Boudreau, Ryan ; Mosier, Willard ; Smith, Alison ; Rueb, Nicole ; Hunt, John P. ; Stuke, Lance ; Greiffenstein, Patrick ; Schoen, Jonathan ; Marr, Alan</creator><creatorcontrib>Bellfi, Lillian T. ; Zimmerman, S. Anthony ; Boudreau, Ryan ; Mosier, Willard ; Smith, Alison ; Rueb, Nicole ; Hunt, John P. ; Stuke, Lance ; Greiffenstein, Patrick ; Schoen, Jonathan ; Marr, Alan</creatorcontrib><description>Introduction
Venous thromboembolism (VTE) contributes to significant morbidity in trauma patients while increasing hospital costs and length of stay. Standard trauma prophylaxis dosing with enoxaparin 30 mg twice daily may be inadequate to prevent VTEs. The objective of this study was to compare standard dosing of enoxaparin to an increased dose of enoxaparin 40 mg twice daily for trauma patients. We hypothesized that increasing thromboprophylaxis dosing leads to an increase in therapeutic anti-Xa levels and reduced VTE rates.
Methods
A retrospective study was performed from January 2020 to June 2021 at a Level I trauma center, following implementation of an increased enoxaparin dosing strategy. Patients with increased enoxaparin dosing were compared with those who received standard dosing. The primary outcome evaluated was the incidence of subtherapeutic anti-Xa levels. Secondary outcomes evaluated VTE rates and clinically significant bleed.
Results
A total of 204 trauma patients were identified. Ninety-one patients received an increased enoxaparin dose compared to 113 who received standard dosing. The baseline demographics of both groups were similar (P > .05). Subtherapeutic levels were higher with standard dosing compared to the increased dose (50 vs 22%, P = .003). Higher VTE rates were observed with standard dosing compared to higher dosing (6.2 vs 3.3%) but with a lower incidence of major bleed (1.8 vs 4.4%). Overall annual VTE rates decreased from 1.6 to 1.3% after implementation of the increased dosing regimen.
Conclusions
This study demonstrated that an increased dosing strategy decreased rates of subtherapeutic anti-Xa levels and trended toward lower overall VTE rates in trauma.</description><identifier>ISSN: 0003-1348</identifier><identifier>EISSN: 1555-9823</identifier><identifier>DOI: 10.1177/00031348221091935</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>Body mass index ; Clinical outcomes ; Clinical trials ; Disease prevention ; Dosage ; Gender ; Injuries ; Morbidity ; Orthopedics ; Patients ; Prophylaxis ; Pulmonary embolisms ; Thromboembolism ; Thrombosis ; Trauma ; Veins & arteries</subject><ispartof>The American surgeon, 2022-09, Vol.88 (9), p.2158-2162</ispartof><rights>The Author(s) 2022</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c345t-2f05b25d365531e7ccfc4d9467dc6b5b998986e164767782c5062477f7aca9823</citedby><cites>FETCH-LOGICAL-c345t-2f05b25d365531e7ccfc4d9467dc6b5b998986e164767782c5062477f7aca9823</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/00031348221091935$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/00031348221091935$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>314,776,780,21799,27903,27904,43600,43601</link.rule.ids></links><search><creatorcontrib>Bellfi, Lillian T.</creatorcontrib><creatorcontrib>Zimmerman, S. Anthony</creatorcontrib><creatorcontrib>Boudreau, Ryan</creatorcontrib><creatorcontrib>Mosier, Willard</creatorcontrib><creatorcontrib>Smith, Alison</creatorcontrib><creatorcontrib>Rueb, Nicole</creatorcontrib><creatorcontrib>Hunt, John P.</creatorcontrib><creatorcontrib>Stuke, Lance</creatorcontrib><creatorcontrib>Greiffenstein, Patrick</creatorcontrib><creatorcontrib>Schoen, Jonathan</creatorcontrib><creatorcontrib>Marr, Alan</creatorcontrib><title>Impact of Increased Enoxaparin Dosing on Anti-Xa Levels for Venous Thromboembolism Prophylaxis in Trauma Patients</title><title>The American surgeon</title><description>Introduction
Venous thromboembolism (VTE) contributes to significant morbidity in trauma patients while increasing hospital costs and length of stay. Standard trauma prophylaxis dosing with enoxaparin 30 mg twice daily may be inadequate to prevent VTEs. The objective of this study was to compare standard dosing of enoxaparin to an increased dose of enoxaparin 40 mg twice daily for trauma patients. We hypothesized that increasing thromboprophylaxis dosing leads to an increase in therapeutic anti-Xa levels and reduced VTE rates.
Methods
A retrospective study was performed from January 2020 to June 2021 at a Level I trauma center, following implementation of an increased enoxaparin dosing strategy. Patients with increased enoxaparin dosing were compared with those who received standard dosing. The primary outcome evaluated was the incidence of subtherapeutic anti-Xa levels. Secondary outcomes evaluated VTE rates and clinically significant bleed.
Results
A total of 204 trauma patients were identified. Ninety-one patients received an increased enoxaparin dose compared to 113 who received standard dosing. The baseline demographics of both groups were similar (P > .05). Subtherapeutic levels were higher with standard dosing compared to the increased dose (50 vs 22%, P = .003). Higher VTE rates were observed with standard dosing compared to higher dosing (6.2 vs 3.3%) but with a lower incidence of major bleed (1.8 vs 4.4%). Overall annual VTE rates decreased from 1.6 to 1.3% after implementation of the increased dosing regimen.
Conclusions
This study demonstrated that an increased dosing strategy decreased rates of subtherapeutic anti-Xa levels and trended toward lower overall VTE rates in trauma.</description><subject>Body mass index</subject><subject>Clinical outcomes</subject><subject>Clinical trials</subject><subject>Disease prevention</subject><subject>Dosage</subject><subject>Gender</subject><subject>Injuries</subject><subject>Morbidity</subject><subject>Orthopedics</subject><subject>Patients</subject><subject>Prophylaxis</subject><subject>Pulmonary embolisms</subject><subject>Thromboembolism</subject><subject>Thrombosis</subject><subject>Trauma</subject><subject>Veins & arteries</subject><issn>0003-1348</issn><issn>1555-9823</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp1kcFLwzAUxoMoOKd_gLeAFy-dSdqXNMcxpw4G7jDFW8nSdOtoky5pZfvv7ZggKB4ej8f7fR_f4yF0S8mIUiEeCCExjZOUMUoklTGcoQEFgEimLD5Hg-M-OgKX6CqEbT8mHOgA7WZ1o3SLXYFnVnujgsnx1Lq9apQvLX50obRr7Cwe27aMPhSem09TBVw4j9-NdV3Ay4139cqZvqoy1HjhXbM5VGpfBtxbLL3qaoUXqi2NbcM1uihUFczNdx-it6fpcvISzV-fZ5PxPNJxAm3ECgIrBnnMAWJqhNaFTnKZcJFrvoKVlKlMuaE8EVyIlGkgnCVCFEJpdTx6iO5Pvo13u86ENqvLoE1VKWv61BnjkpJEgoQevfuFbl3nbZ8uY4ICI8BB9hQ9Udq7ELwpssaXtfKHjJLs-ITszxN6zeikCWptflz_F3wBtPaFzw</recordid><startdate>202209</startdate><enddate>202209</enddate><creator>Bellfi, Lillian T.</creator><creator>Zimmerman, S. Anthony</creator><creator>Boudreau, Ryan</creator><creator>Mosier, Willard</creator><creator>Smith, Alison</creator><creator>Rueb, Nicole</creator><creator>Hunt, John P.</creator><creator>Stuke, Lance</creator><creator>Greiffenstein, Patrick</creator><creator>Schoen, Jonathan</creator><creator>Marr, Alan</creator><general>SAGE Publications</general><general>SAGE PUBLICATIONS, INC</general><scope>AAYXX</scope><scope>CITATION</scope><scope>4T-</scope><scope>4U-</scope><scope>7QL</scope><scope>7T7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>NAPCQ</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>202209</creationdate><title>Impact of Increased Enoxaparin Dosing on Anti-Xa Levels for Venous Thromboembolism Prophylaxis in Trauma Patients</title><author>Bellfi, Lillian T. ; Zimmerman, S. Anthony ; Boudreau, Ryan ; Mosier, Willard ; Smith, Alison ; Rueb, Nicole ; Hunt, John P. ; Stuke, Lance ; Greiffenstein, Patrick ; Schoen, Jonathan ; Marr, Alan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c345t-2f05b25d365531e7ccfc4d9467dc6b5b998986e164767782c5062477f7aca9823</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Body mass index</topic><topic>Clinical outcomes</topic><topic>Clinical trials</topic><topic>Disease prevention</topic><topic>Dosage</topic><topic>Gender</topic><topic>Injuries</topic><topic>Morbidity</topic><topic>Orthopedics</topic><topic>Patients</topic><topic>Prophylaxis</topic><topic>Pulmonary embolisms</topic><topic>Thromboembolism</topic><topic>Thrombosis</topic><topic>Trauma</topic><topic>Veins & arteries</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bellfi, Lillian T.</creatorcontrib><creatorcontrib>Zimmerman, S. Anthony</creatorcontrib><creatorcontrib>Boudreau, Ryan</creatorcontrib><creatorcontrib>Mosier, Willard</creatorcontrib><creatorcontrib>Smith, Alison</creatorcontrib><creatorcontrib>Rueb, Nicole</creatorcontrib><creatorcontrib>Hunt, John P.</creatorcontrib><creatorcontrib>Stuke, Lance</creatorcontrib><creatorcontrib>Greiffenstein, Patrick</creatorcontrib><creatorcontrib>Schoen, Jonathan</creatorcontrib><creatorcontrib>Marr, Alan</creatorcontrib><collection>CrossRef</collection><collection>Docstoc</collection><collection>University Readers</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The American surgeon</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bellfi, Lillian T.</au><au>Zimmerman, S. Anthony</au><au>Boudreau, Ryan</au><au>Mosier, Willard</au><au>Smith, Alison</au><au>Rueb, Nicole</au><au>Hunt, John P.</au><au>Stuke, Lance</au><au>Greiffenstein, Patrick</au><au>Schoen, Jonathan</au><au>Marr, Alan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Impact of Increased Enoxaparin Dosing on Anti-Xa Levels for Venous Thromboembolism Prophylaxis in Trauma Patients</atitle><jtitle>The American surgeon</jtitle><date>2022-09</date><risdate>2022</risdate><volume>88</volume><issue>9</issue><spage>2158</spage><epage>2162</epage><pages>2158-2162</pages><issn>0003-1348</issn><eissn>1555-9823</eissn><abstract>Introduction
Venous thromboembolism (VTE) contributes to significant morbidity in trauma patients while increasing hospital costs and length of stay. Standard trauma prophylaxis dosing with enoxaparin 30 mg twice daily may be inadequate to prevent VTEs. The objective of this study was to compare standard dosing of enoxaparin to an increased dose of enoxaparin 40 mg twice daily for trauma patients. We hypothesized that increasing thromboprophylaxis dosing leads to an increase in therapeutic anti-Xa levels and reduced VTE rates.
Methods
A retrospective study was performed from January 2020 to June 2021 at a Level I trauma center, following implementation of an increased enoxaparin dosing strategy. Patients with increased enoxaparin dosing were compared with those who received standard dosing. The primary outcome evaluated was the incidence of subtherapeutic anti-Xa levels. Secondary outcomes evaluated VTE rates and clinically significant bleed.
Results
A total of 204 trauma patients were identified. Ninety-one patients received an increased enoxaparin dose compared to 113 who received standard dosing. The baseline demographics of both groups were similar (P > .05). Subtherapeutic levels were higher with standard dosing compared to the increased dose (50 vs 22%, P = .003). Higher VTE rates were observed with standard dosing compared to higher dosing (6.2 vs 3.3%) but with a lower incidence of major bleed (1.8 vs 4.4%). Overall annual VTE rates decreased from 1.6 to 1.3% after implementation of the increased dosing regimen.
Conclusions
This study demonstrated that an increased dosing strategy decreased rates of subtherapeutic anti-Xa levels and trended toward lower overall VTE rates in trauma.</abstract><cop>Los Angeles, CA</cop><pub>SAGE Publications</pub><doi>10.1177/00031348221091935</doi><tpages>5</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0003-1348 |
ispartof | The American surgeon, 2022-09, Vol.88 (9), p.2158-2162 |
issn | 0003-1348 1555-9823 |
language | eng |
recordid | cdi_proquest_miscellaneous_2691049595 |
source | SAGE Complete A-Z List |
subjects | Body mass index Clinical outcomes Clinical trials Disease prevention Dosage Gender Injuries Morbidity Orthopedics Patients Prophylaxis Pulmonary embolisms Thromboembolism Thrombosis Trauma Veins & arteries |
title | Impact of Increased Enoxaparin Dosing on Anti-Xa Levels for Venous Thromboembolism Prophylaxis in Trauma Patients |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-25T16%3A25%3A41IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Impact%20of%20Increased%20Enoxaparin%20Dosing%20on%20Anti-Xa%20Levels%20for%20Venous%20Thromboembolism%20Prophylaxis%20in%20Trauma%20Patients&rft.jtitle=The%20American%20surgeon&rft.au=Bellfi,%20Lillian%20T.&rft.date=2022-09&rft.volume=88&rft.issue=9&rft.spage=2158&rft.epage=2162&rft.pages=2158-2162&rft.issn=0003-1348&rft.eissn=1555-9823&rft_id=info:doi/10.1177/00031348221091935&rft_dat=%3Cproquest_cross%3E2691049595%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2715205659&rft_id=info:pmid/&rft_sage_id=10.1177_00031348221091935&rfr_iscdi=true |