<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>89(5)</volume><submitter>Romano LGR</submitter><pubmed_abstract>&lt;h4>Aims&lt;/h4>Nadroparin is administered to COVID-19 intensive care unit (ICU) patients as thromboprophylaxis. Despite existing population pharmacokinetic (PK) models for nadroparin in literature, the population PK of nadroparin in COVID-19 ICU patients is unknown. Moreover, optimal dosing regimens achieving anti-Xa target levels (0.3-0.7 IU/mL) are unknown. Therefore, a population PK analysis was conducted to investigate different dosing regimens of nadroparin in COVID-19 ICU patients.&lt;h4>Methods&lt;/h4>Anti-Xa levels (n = 280) from COVID-19 ICU patients (n = 65) receiving twice daily (BID) 5700 IU of subcutaneous nadroparin were collected to perform a population PK analysis with NONMEM v7.4.1. Using Monte Carlo simulations (n = 1000), predefined dosing regimens were evaluated.&lt;h4>Results&lt;/h4</pubmed_abstract><journal>British journal of clinical pharmacology</journal><pagination>1617-1628</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9878197</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Population pharmacokinetics of nadroparin for thromboprophylaxis in COVID-19 intensive care unit patients.</pubmed_title><pmcid>PMC9878197</pmcid><pubmed_authors>Endeman H</pubmed_authors><pubmed_authors>Romano LGR</pubmed_authors><pubmed_authors>Hunfeld NGM</pubmed_authors><pubmed_authors>Kruip MJHA</pubmed_authors><pubmed_authors>Preijers T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Population pharmacokinetics of nadroparin for thromboprophylaxis in COVID-19 intensive care unit patients.</name><description>&lt;h4>Aims&lt;/h4>Nadroparin is administered to COVID-19 intensive care unit (ICU) patients as thromboprophylaxis. Despite existing population pharmacokinetic (PK) models for nadroparin in literature, the population PK of nadroparin in COVID-19 ICU patients is unknown. Moreover, optimal dosing regimens achieving anti-Xa target levels (0.3-0.7 IU/mL) are unknown. Therefore, a population PK analysis was conducted to investigate different dosing regimens of nadroparin in COVID-19 ICU patients.&lt;h4>Methods&lt;/h4>Anti-Xa levels (n = 280) from COVID-19 ICU patients (n = 65) receiving twice daily (BID) 5700 IU of subcutaneous nadroparin were collected to perform a population PK analysis with NONMEM v7.4.1. Using Monte Carlo simulations (n = 1000), predefined dosing regimens were evaluated.&lt;h4>Results&lt;/h4</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 May</publication><modification>2025-04-18T14:06:06.694Z</modification><creation>2025-04-06T23:59:56.451Z</creation></dates><accession>S-EPMC9878197</accession><cross_references><pubmed>36495312</pubmed><doi>10.1111/bcp.15634</doi></cross_references></HashMap>