Enoxaparin thromboprophylaxis in hospitalized obese pediatric patients

Enoxaparin is an anticoagulant used for pharmacologic thromboprophylaxis in pediatrics. Enoxaparin pharmacokinetics can be altered in the setting of obesity. Optimal enoxaparin dosing for thromboprophylaxis in children with obesity remains unclear. A retrospective review was conducted of pediatric p...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Pediatric blood & cancer 2024-09, Vol.71 (9), p.e30942
Hauptverfasser: Yim, Juwon, Jahan, Afrin, Braykov, Nikolay, Murphy, Nina D, Woods, Gary M
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue 9
container_start_page e30942
container_title Pediatric blood & cancer
container_volume 71
creator Yim, Juwon
Jahan, Afrin
Braykov, Nikolay
Murphy, Nina D
Woods, Gary M
description Enoxaparin is an anticoagulant used for pharmacologic thromboprophylaxis in pediatrics. Enoxaparin pharmacokinetics can be altered in the setting of obesity. Optimal enoxaparin dosing for thromboprophylaxis in children with obesity remains unclear. A retrospective review was conducted of pediatric patients who weighed ≥60 kg with BMI ≥ 95th percentile, received enoxaparin for thromboprophylaxis, and had at least one appropriately drawn anti-factor Xa (anti-Xa) from 2013 to 2022. Anti-Xa levels were reviewed for patients initially treated with enoxaparin 30 mg every 12 h. The average daily enoxaparin dose required to achieve an anti-Xa of 0.2-0.4 unit/mL, which was stratified by BMI percentile and weight, was calculated. Of 116 patients (median age 15.8 years) included for analysis, 106 patients were initially treated with enoxaparin 30 mg every 12 h. Anti-Xa levels were  99th percentile and 54% of patients >100 kg. Ninety-one patients had at least one anti-Xa 0.2-0.4 unit/mL with an average daily enoxaparin dosing of 66 mg. When stratified by severity of obesity, higher doses were required to attain an anti-Xa 0.2-0.4 unit/mL in patients with BMI > 99th percentile compared with those with 95th-99th percentile (67.8 ± 15.7 vs. 62 ± 5.6 mg/day, p = .01). Patients > 100 kg required significantly higher dose than those ≤100 kg (69.1 ± 15.5 vs 61.2 ± 7.3 mg/day, p = .002). Increased initial dosing and/or anti-Xa level monitoring should be considered in adolescents with severe obesity receiving enoxaparin thromboprophylaxis.
doi_str_mv 10.1002/pbc.30942
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2958296582</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2958296582</sourcerecordid><originalsourceid>FETCH-LOGICAL-c313t-ab5e814b597c3e0b84aca60350799f6ca6f76f8e76efded90aaa5c5e78d81fa63</originalsourceid><addsrcrecordid>eNpdkEFLwzAUx4Mobk4PfgEpeNFDZ9I0aXKUsakw8KLnkLavLKNtYtLC5qc3Ot3By3t_Hj_-PH4IXRM8JxhnD66s5hTLPDtBU8JyljJMitNjxnKCLkLYRpRjJs7RhIpccFyIKVote7vTTnvTJ8PG2660zlu32bd6Z0ISrxsbnBl0az6hTmwJARIHtdGDN1Xi9GCgH8IlOmt0G-Dqd8_Q-2r5tnhO169PL4vHdVpRQodUlwwEyUsmi4oCLkWuK80xZbiQsuExNwVvBBQcmhpqibXWrGJQiFqQRnM6Q3eH3vjkxwhhUJ0JFbSt7sGOQWWSiUzyOCJ6-w_d2tH38TtFscix4Dwjkbo_UJW3IXholPOm036vCFbfclWUq37kRvbmt3EsO6iP5J9N-gXZk3XB</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3084086621</pqid></control><display><type>article</type><title>Enoxaparin thromboprophylaxis in hospitalized obese pediatric patients</title><source>MEDLINE</source><source>Wiley Online Library All Journals</source><creator>Yim, Juwon ; Jahan, Afrin ; Braykov, Nikolay ; Murphy, Nina D ; Woods, Gary M</creator><creatorcontrib>Yim, Juwon ; Jahan, Afrin ; Braykov, Nikolay ; Murphy, Nina D ; Woods, Gary M</creatorcontrib><description>Enoxaparin is an anticoagulant used for pharmacologic thromboprophylaxis in pediatrics. Enoxaparin pharmacokinetics can be altered in the setting of obesity. Optimal enoxaparin dosing for thromboprophylaxis in children with obesity remains unclear. A retrospective review was conducted of pediatric patients who weighed ≥60 kg with BMI ≥ 95th percentile, received enoxaparin for thromboprophylaxis, and had at least one appropriately drawn anti-factor Xa (anti-Xa) from 2013 to 2022. Anti-Xa levels were reviewed for patients initially treated with enoxaparin 30 mg every 12 h. The average daily enoxaparin dose required to achieve an anti-Xa of 0.2-0.4 unit/mL, which was stratified by BMI percentile and weight, was calculated. Of 116 patients (median age 15.8 years) included for analysis, 106 patients were initially treated with enoxaparin 30 mg every 12 h. Anti-Xa levels were &lt;0.2 unit/mL in 53% of patients with BMI &gt; 99th percentile and 54% of patients &gt;100 kg. Ninety-one patients had at least one anti-Xa 0.2-0.4 unit/mL with an average daily enoxaparin dosing of 66 mg. When stratified by severity of obesity, higher doses were required to attain an anti-Xa 0.2-0.4 unit/mL in patients with BMI &gt; 99th percentile compared with those with 95th-99th percentile (67.8 ± 15.7 vs. 62 ± 5.6 mg/day, p = .01). Patients &gt; 100 kg required significantly higher dose than those ≤100 kg (69.1 ± 15.5 vs 61.2 ± 7.3 mg/day, p = .002). Increased initial dosing and/or anti-Xa level monitoring should be considered in adolescents with severe obesity receiving enoxaparin thromboprophylaxis.</description><identifier>ISSN: 1545-5009</identifier><identifier>ISSN: 1545-5017</identifier><identifier>EISSN: 1545-5017</identifier><identifier>DOI: 10.1002/pbc.30942</identifier><identifier>PMID: 38486078</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Adolescent ; Anticoagulants - administration &amp; dosage ; Anticoagulants - pharmacokinetics ; Anticoagulants - therapeutic use ; Child ; Child, Preschool ; Dosage ; Enoxaparin - administration &amp; dosage ; Enoxaparin - pharmacokinetics ; Enoxaparin - therapeutic use ; Factor Xa Inhibitors - administration &amp; dosage ; Factor Xa Inhibitors - pharmacokinetics ; Factor Xa Inhibitors - therapeutic use ; Female ; Follow-Up Studies ; Humans ; Male ; Obesity ; Obesity - complications ; Pediatric Obesity - complications ; Pediatrics ; Pharmacokinetics ; Retrospective Studies ; Venous Thromboembolism - drug therapy ; Venous Thromboembolism - etiology ; Venous Thromboembolism - prevention &amp; control</subject><ispartof>Pediatric blood &amp; cancer, 2024-09, Vol.71 (9), p.e30942</ispartof><rights>2024 Wiley Periodicals LLC.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c313t-ab5e814b597c3e0b84aca60350799f6ca6f76f8e76efded90aaa5c5e78d81fa63</citedby><cites>FETCH-LOGICAL-c313t-ab5e814b597c3e0b84aca60350799f6ca6f76f8e76efded90aaa5c5e78d81fa63</cites><orcidid>0000-0001-6653-2868 ; 0000-0002-0921-0974</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38486078$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yim, Juwon</creatorcontrib><creatorcontrib>Jahan, Afrin</creatorcontrib><creatorcontrib>Braykov, Nikolay</creatorcontrib><creatorcontrib>Murphy, Nina D</creatorcontrib><creatorcontrib>Woods, Gary M</creatorcontrib><title>Enoxaparin thromboprophylaxis in hospitalized obese pediatric patients</title><title>Pediatric blood &amp; cancer</title><addtitle>Pediatr Blood Cancer</addtitle><description>Enoxaparin is an anticoagulant used for pharmacologic thromboprophylaxis in pediatrics. Enoxaparin pharmacokinetics can be altered in the setting of obesity. Optimal enoxaparin dosing for thromboprophylaxis in children with obesity remains unclear. A retrospective review was conducted of pediatric patients who weighed ≥60 kg with BMI ≥ 95th percentile, received enoxaparin for thromboprophylaxis, and had at least one appropriately drawn anti-factor Xa (anti-Xa) from 2013 to 2022. Anti-Xa levels were reviewed for patients initially treated with enoxaparin 30 mg every 12 h. The average daily enoxaparin dose required to achieve an anti-Xa of 0.2-0.4 unit/mL, which was stratified by BMI percentile and weight, was calculated. Of 116 patients (median age 15.8 years) included for analysis, 106 patients were initially treated with enoxaparin 30 mg every 12 h. Anti-Xa levels were &lt;0.2 unit/mL in 53% of patients with BMI &gt; 99th percentile and 54% of patients &gt;100 kg. Ninety-one patients had at least one anti-Xa 0.2-0.4 unit/mL with an average daily enoxaparin dosing of 66 mg. When stratified by severity of obesity, higher doses were required to attain an anti-Xa 0.2-0.4 unit/mL in patients with BMI &gt; 99th percentile compared with those with 95th-99th percentile (67.8 ± 15.7 vs. 62 ± 5.6 mg/day, p = .01). Patients &gt; 100 kg required significantly higher dose than those ≤100 kg (69.1 ± 15.5 vs 61.2 ± 7.3 mg/day, p = .002). Increased initial dosing and/or anti-Xa level monitoring should be considered in adolescents with severe obesity receiving enoxaparin thromboprophylaxis.</description><subject>Adolescent</subject><subject>Anticoagulants - administration &amp; dosage</subject><subject>Anticoagulants - pharmacokinetics</subject><subject>Anticoagulants - therapeutic use</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Dosage</subject><subject>Enoxaparin - administration &amp; dosage</subject><subject>Enoxaparin - pharmacokinetics</subject><subject>Enoxaparin - therapeutic use</subject><subject>Factor Xa Inhibitors - administration &amp; dosage</subject><subject>Factor Xa Inhibitors - pharmacokinetics</subject><subject>Factor Xa Inhibitors - therapeutic use</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Male</subject><subject>Obesity</subject><subject>Obesity - complications</subject><subject>Pediatric Obesity - complications</subject><subject>Pediatrics</subject><subject>Pharmacokinetics</subject><subject>Retrospective Studies</subject><subject>Venous Thromboembolism - drug therapy</subject><subject>Venous Thromboembolism - etiology</subject><subject>Venous Thromboembolism - prevention &amp; control</subject><issn>1545-5009</issn><issn>1545-5017</issn><issn>1545-5017</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkEFLwzAUx4Mobk4PfgEpeNFDZ9I0aXKUsakw8KLnkLavLKNtYtLC5qc3Ot3By3t_Hj_-PH4IXRM8JxhnD66s5hTLPDtBU8JyljJMitNjxnKCLkLYRpRjJs7RhIpccFyIKVote7vTTnvTJ8PG2660zlu32bd6Z0ISrxsbnBl0az6hTmwJARIHtdGDN1Xi9GCgH8IlOmt0G-Dqd8_Q-2r5tnhO169PL4vHdVpRQodUlwwEyUsmi4oCLkWuK80xZbiQsuExNwVvBBQcmhpqibXWrGJQiFqQRnM6Q3eH3vjkxwhhUJ0JFbSt7sGOQWWSiUzyOCJ6-w_d2tH38TtFscix4Dwjkbo_UJW3IXholPOm036vCFbfclWUq37kRvbmt3EsO6iP5J9N-gXZk3XB</recordid><startdate>20240901</startdate><enddate>20240901</enddate><creator>Yim, Juwon</creator><creator>Jahan, Afrin</creator><creator>Braykov, Nikolay</creator><creator>Murphy, Nina D</creator><creator>Woods, Gary M</creator><general>Wiley Subscription Services, 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>7T5</scope><scope>7TK</scope><scope>7TO</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-6653-2868</orcidid><orcidid>https://orcid.org/0000-0002-0921-0974</orcidid></search><sort><creationdate>20240901</creationdate><title>Enoxaparin thromboprophylaxis in hospitalized obese pediatric patients</title><author>Yim, Juwon ; Jahan, Afrin ; Braykov, Nikolay ; Murphy, Nina D ; Woods, Gary M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c313t-ab5e814b597c3e0b84aca60350799f6ca6f76f8e76efded90aaa5c5e78d81fa63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adolescent</topic><topic>Anticoagulants - administration &amp; dosage</topic><topic>Anticoagulants - pharmacokinetics</topic><topic>Anticoagulants - therapeutic use</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Dosage</topic><topic>Enoxaparin - administration &amp; dosage</topic><topic>Enoxaparin - pharmacokinetics</topic><topic>Enoxaparin - therapeutic use</topic><topic>Factor Xa Inhibitors - administration &amp; dosage</topic><topic>Factor Xa Inhibitors - pharmacokinetics</topic><topic>Factor Xa Inhibitors - therapeutic use</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Male</topic><topic>Obesity</topic><topic>Obesity - complications</topic><topic>Pediatric Obesity - complications</topic><topic>Pediatrics</topic><topic>Pharmacokinetics</topic><topic>Retrospective Studies</topic><topic>Venous Thromboembolism - drug therapy</topic><topic>Venous Thromboembolism - etiology</topic><topic>Venous Thromboembolism - prevention &amp; control</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yim, Juwon</creatorcontrib><creatorcontrib>Jahan, Afrin</creatorcontrib><creatorcontrib>Braykov, Nikolay</creatorcontrib><creatorcontrib>Murphy, Nina D</creatorcontrib><creatorcontrib>Woods, Gary M</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Pediatric blood &amp; cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yim, Juwon</au><au>Jahan, Afrin</au><au>Braykov, Nikolay</au><au>Murphy, Nina D</au><au>Woods, Gary M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Enoxaparin thromboprophylaxis in hospitalized obese pediatric patients</atitle><jtitle>Pediatric blood &amp; cancer</jtitle><addtitle>Pediatr Blood Cancer</addtitle><date>2024-09-01</date><risdate>2024</risdate><volume>71</volume><issue>9</issue><spage>e30942</spage><pages>e30942-</pages><issn>1545-5009</issn><issn>1545-5017</issn><eissn>1545-5017</eissn><abstract>Enoxaparin is an anticoagulant used for pharmacologic thromboprophylaxis in pediatrics. Enoxaparin pharmacokinetics can be altered in the setting of obesity. Optimal enoxaparin dosing for thromboprophylaxis in children with obesity remains unclear. A retrospective review was conducted of pediatric patients who weighed ≥60 kg with BMI ≥ 95th percentile, received enoxaparin for thromboprophylaxis, and had at least one appropriately drawn anti-factor Xa (anti-Xa) from 2013 to 2022. Anti-Xa levels were reviewed for patients initially treated with enoxaparin 30 mg every 12 h. The average daily enoxaparin dose required to achieve an anti-Xa of 0.2-0.4 unit/mL, which was stratified by BMI percentile and weight, was calculated. Of 116 patients (median age 15.8 years) included for analysis, 106 patients were initially treated with enoxaparin 30 mg every 12 h. Anti-Xa levels were &lt;0.2 unit/mL in 53% of patients with BMI &gt; 99th percentile and 54% of patients &gt;100 kg. Ninety-one patients had at least one anti-Xa 0.2-0.4 unit/mL with an average daily enoxaparin dosing of 66 mg. When stratified by severity of obesity, higher doses were required to attain an anti-Xa 0.2-0.4 unit/mL in patients with BMI &gt; 99th percentile compared with those with 95th-99th percentile (67.8 ± 15.7 vs. 62 ± 5.6 mg/day, p = .01). Patients &gt; 100 kg required significantly higher dose than those ≤100 kg (69.1 ± 15.5 vs 61.2 ± 7.3 mg/day, p = .002). Increased initial dosing and/or anti-Xa level monitoring should be considered in adolescents with severe obesity receiving enoxaparin thromboprophylaxis.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>38486078</pmid><doi>10.1002/pbc.30942</doi><orcidid>https://orcid.org/0000-0001-6653-2868</orcidid><orcidid>https://orcid.org/0000-0002-0921-0974</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 1545-5009
ispartof Pediatric blood & cancer, 2024-09, Vol.71 (9), p.e30942
issn 1545-5009
1545-5017
1545-5017
language eng
recordid cdi_proquest_miscellaneous_2958296582
source MEDLINE; Wiley Online Library All Journals
subjects Adolescent
Anticoagulants - administration & dosage
Anticoagulants - pharmacokinetics
Anticoagulants - therapeutic use
Child
Child, Preschool
Dosage
Enoxaparin - administration & dosage
Enoxaparin - pharmacokinetics
Enoxaparin - therapeutic use
Factor Xa Inhibitors - administration & dosage
Factor Xa Inhibitors - pharmacokinetics
Factor Xa Inhibitors - therapeutic use
Female
Follow-Up Studies
Humans
Male
Obesity
Obesity - complications
Pediatric Obesity - complications
Pediatrics
Pharmacokinetics
Retrospective Studies
Venous Thromboembolism - drug therapy
Venous Thromboembolism - etiology
Venous Thromboembolism - prevention & control
title Enoxaparin thromboprophylaxis in hospitalized obese pediatric patients
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T08%3A09%3A07IST&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=Enoxaparin%20thromboprophylaxis%20in%20hospitalized%20obese%20pediatric%20patients&rft.jtitle=Pediatric%20blood%20&%20cancer&rft.au=Yim,%20Juwon&rft.date=2024-09-01&rft.volume=71&rft.issue=9&rft.spage=e30942&rft.pages=e30942-&rft.issn=1545-5009&rft.eissn=1545-5017&rft_id=info:doi/10.1002/pbc.30942&rft_dat=%3Cproquest_cross%3E2958296582%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=3084086621&rft_id=info:pmid/38486078&rfr_iscdi=true