<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>15</volume><submitter>Hahn RG</submitter><pubmed_abstract>&lt;h4>Introduction&lt;/h4>The interstitial space harbours two fluid compartments linked serially to the plasma. This study explores conditions that lead to fluid accumulation in the most secluded compartment, termed the "third space".&lt;h4>Methods&lt;/h4>Retrospective data was collected from 326 experiments in which intravenous crystalloid fluid was administered to conscious volunteers as well as a small group of anaesthetized patients. The urinary excretion and plasma dilution derived from haemoglobin served as input variables in nine population volume kinetic analyses representing subtly different settings.&lt;h4>Results&lt;/h4>An infusion of 250-500 mL of Ringer's solution expanded only the central fluid space (plasma), whereas the infusion of 500-1,000 mL extended into a rapidly exchanging interstitial fluid space. When more than 1 L was infused over 30 min, it was distributed across plasma and both interstitial fluid compartments. The remote space, characterized by slow turnover, abruptly accommodated fluid upon accumulation of 700-800 mL in the rapidly exchanging space, equivalent to an 11%-13% volume increase. However, larger expansion was necessary to trigger this event in a perioperative setting. The plasma half-life of crystalloid fluid was 25 times longer when 2,000-2,700 mL expanded all three fluid compartments compared to when only 250-500 mL expanded the central space (14 h versus 30 min).&lt;h4>Conclusion&lt;/h4>As the volume of crystalloid fluid increases, it apparently occupies a larger proportion of the interstitial space. When more than 1 L is administered at a high rate, there is expansion of a remote "third space", which considerably extends the intravascular half-life.</pubmed_abstract><journal>Frontiers in physiology</journal><pagination>1439035</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11387178</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Sequential recruitment of body fluid spaces for increasing volumes of crystalloid fluid.</pubmed_title><pmcid>PMC11387178</pmcid><pubmed_authors>Hahn RG</pubmed_authors></additional><is_claimable>false</is_claimable><name>Sequential recruitment of body fluid spaces for increasing volumes of crystalloid fluid.</name><description>&lt;h4>Introduction&lt;/h4>The interstitial space harbours two fluid compartments linked serially to the plasma. This study explores conditions that lead to fluid accumulation in the most secluded compartment, termed the "third space".&lt;h4>Methods&lt;/h4>Retrospective data was collected from 326 experiments in which intravenous crystalloid fluid was administered to conscious volunteers as well as a small group of anaesthetized patients. The urinary excretion and plasma dilution derived from haemoglobin served as input variables in nine population volume kinetic analyses representing subtly different settings.&lt;h4>Results&lt;/h4>An infusion of 250-500 mL of Ringer's solution expanded only the central fluid space (plasma), whereas the infusion of 500-1,000 mL extended into a rapidly exchanging interstitial fluid space. When more than 1 L was infused over 30 min, it was distributed across plasma and both interstitial fluid compartments. The remote space, characterized by slow turnover, abruptly accommodated fluid upon accumulation of 700-800 mL in the rapidly exchanging space, equivalent to an 11%-13% volume increase. However, larger expansion was necessary to trigger this event in a perioperative setting. The plasma half-life of crystalloid fluid was 25 times longer when 2,000-2,700 mL expanded all three fluid compartments compared to when only 250-500 mL expanded the central space (14 h versus 30 min).&lt;h4>Conclusion&lt;/h4>As the volume of crystalloid fluid increases, it apparently occupies a larger proportion of the interstitial space. When more than 1 L is administered at a high rate, there is expansion of a remote "third space", which considerably extends the intravascular half-life.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024</publication><modification>2026-06-02T23:38:26.793Z</modification><creation>2025-04-05T18:43:07.117Z</creation></dates><accession>S-EPMC11387178</accession><cross_references><pubmed>39263627</pubmed><doi>10.3389/fphys.2024.1439035</doi></cross_references></HashMap>