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...
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Veröffentlicht in: | Pediatric blood & cancer 2024-09, Vol.71 (9), p.e30942 |
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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 |
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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 <0.2 unit/mL in 53% of patients with BMI > 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.</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 & 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</subject><ispartof>Pediatric blood & 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 & 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 <0.2 unit/mL in 53% of patients with BMI > 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.</description><subject>Adolescent</subject><subject>Anticoagulants - administration & dosage</subject><subject>Anticoagulants - pharmacokinetics</subject><subject>Anticoagulants - therapeutic use</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Dosage</subject><subject>Enoxaparin - administration & dosage</subject><subject>Enoxaparin - pharmacokinetics</subject><subject>Enoxaparin - therapeutic use</subject><subject>Factor Xa Inhibitors - administration & 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 & 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 & dosage</topic><topic>Anticoagulants - pharmacokinetics</topic><topic>Anticoagulants - therapeutic use</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Dosage</topic><topic>Enoxaparin - administration & dosage</topic><topic>Enoxaparin - pharmacokinetics</topic><topic>Enoxaparin - therapeutic use</topic><topic>Factor Xa Inhibitors - administration & 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 & 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 & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Pediatric blood & 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 & 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 <0.2 unit/mL in 53% of patients with BMI > 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.</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> |
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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 |
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