Publication: Blood volume and hemodynamics during treatment of major hemorrhage with Ringer solution, 5% albumin, and 20% albumin: a single-center randomized controlled trial.
cris.virtual.author-orcid | 0000-0003-3704-6785 | |
cris.virtualsource.author-orcid | 52b7226f-2364-460d-8d21-27e5c55084f9 | |
cris.virtualsource.author-orcid | 428fdfe2-e714-4592-94eb-a31812cd897f | |
cris.virtualsource.author-orcid | 50a86e7d-5976-4036-9fec-e4a47a512a94 | |
cris.virtualsource.author-orcid | 9c7eeb76-1ae3-42a5-b32b-21add6c6a297 | |
datacite.rights | open.access | |
dc.contributor.author | Jardot, François Sébastien | |
dc.contributor.author | Hahn, Robert G | |
dc.contributor.author | Engel, Dominique | |
dc.contributor.author | Beilstein, Christian | |
dc.contributor.author | Wüthrich, Patrick Yves | |
dc.date.accessioned | 2024-10-26T17:13:40Z | |
dc.date.available | 2024-10-26T17:13:40Z | |
dc.date.issued | 2024-02-05 | |
dc.description.abstract | BACKGROUND Volume replacement with crystalloid fluid is the conventional treatment of hemorrhage. We challenged whether a standardized amount of 5% or 20% albumin could be a viable option to maintain the blood volume during surgery associated with major hemorrhage. Therefore, the aim of this study was to quantify and compare the plasma volume expansion properties of 5% albumin, 20% albumin, and Ringer-lactate, when infused during major surgery. METHODS In this single-center randomized controlled trial, fluid replacement therapy to combat hypovolemia during the hemorrhagic phase of cystectomy was randomly allocated in 42 patients to receive either 5% albumin (12 mL/kg) or 20% albumin (3 mL/kg) over 30 min at the beginning of the hemorrhagic phase, both completed by a Ringer-lactate replacing blood loss in a 1:1 ratio, or Ringer-lactate alone to replace blood loss in a 3:1 ratio. Measurements of blood hemoglobin over 5 h were used to estimate the effectiveness of each fluid to expand the blood volume using the following regression equation: blood loss plus blood volume expansion = factor + volume of infused albumin + volume of infused Ringer-lactate. RESULTS The median hemorrhage was 848 mL [IQR: 615-1145]. The regression equation showed that the Ringer-lactate solution expanded the plasma volume by 0.18 times the infused volume while the corresponding power of 5% and 20% albumin was 0.74 and 2.09, respectively. The Ringer-lactate only fluid program resulted in slight hypovolemia (mean, - 313 mL). The 5% and 20% albumin programs were more effective in filling the vascular system; this was evidenced by blood volume changes of only + 63 mL and - 44 mL, respectively, by long-lasting plasma volume expansion with median half time of 5.5 h and 4.8 h, respectively, and by an increase in the central venous pressure. CONCLUSION The power to expand the plasma volume was 4 and almost 12 times greater for 5% albumin and 20% albumin than for Ringer-lactate, and the effect was sustained over 5 h. The clinical efficacy of albumin during major hemorrhage was quite similar to previous studies with no hemorrhage. TRIAL REGISTRATION ClinicalTrials.gov NCT05391607, date of registration May 26, 2022. | |
dc.description.sponsorship | Universitätsklinik für Anästhesiologie und Schmerztherapie | |
dc.description.sponsorship | Universitätsklinik für Anästhesiologie und Schmerztherapie | |
dc.identifier.doi | 10.48350/192620 | |
dc.identifier.pmid | 38317178 | |
dc.identifier.publisherDOI | 10.1186/s13054-024-04821-6 | |
dc.identifier.uri | https://boris-portal.unibe.ch/handle/20.500.12422/174205 | |
dc.language.iso | en | |
dc.publisher | BioMed Central | |
dc.relation.ispartof | Critical care | |
dc.relation.issn | 1364-8535 | |
dc.relation.organization | 318E781798EC6684E053980C5C821B39 | |
dc.relation.organization | DCD5A442BADCE17DE0405C82790C4DE2 | |
dc.subject | 20% albumin 5% albumin Fluid therapy Hemorrhage Plasma volume expansion Ringer-lactate | |
dc.subject.ddc | 600 - Technology::610 - Medicine & health | |
dc.title | Blood volume and hemodynamics during treatment of major hemorrhage with Ringer solution, 5% albumin, and 20% albumin: a single-center randomized controlled trial. | |
dc.type | article | |
dspace.entity.type | Publication | |
dspace.file.type | text | |
oaire.citation.issue | 39 | |
oaire.citation.volume | 28 | |
oairecerif.author.affiliation | Universitätsklinik für Anästhesiologie und Schmerztherapie | |
oairecerif.author.affiliation | Universitätsklinik für Anästhesiologie und Schmerztherapie | |
oairecerif.author.affiliation | Universitätsklinik für Anästhesiologie und Schmerztherapie | |
oairecerif.author.affiliation | Universitätsklinik für Anästhesiologie und Schmerztherapie | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.date.licenseChanged | 2024-02-07 07:45:09 | |
unibe.description.ispublished | pub | |
unibe.eprints.legacyId | 192620 | |
unibe.journal.abbrevTitle | CRIT CARE | |
unibe.refereed | true | |
unibe.subtype.article | journal |
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