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-orcid0000-0003-3704-6785
cris.virtualsource.author-orcid52b7226f-2364-460d-8d21-27e5c55084f9
cris.virtualsource.author-orcid428fdfe2-e714-4592-94eb-a31812cd897f
cris.virtualsource.author-orcid50a86e7d-5976-4036-9fec-e4a47a512a94
cris.virtualsource.author-orcid9c7eeb76-1ae3-42a5-b32b-21add6c6a297
datacite.rightsopen.access
dc.contributor.authorJardot, François Sébastien
dc.contributor.authorHahn, Robert G
dc.contributor.authorEngel, Dominique
dc.contributor.authorBeilstein, Christian
dc.contributor.authorWüthrich, Patrick Yves
dc.date.accessioned2024-10-26T17:13:40Z
dc.date.available2024-10-26T17:13:40Z
dc.date.issued2024-02-05
dc.description.abstractBACKGROUND 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.sponsorshipUniversitätsklinik für Anästhesiologie und Schmerztherapie
dc.description.sponsorshipUniversitätsklinik für Anästhesiologie und Schmerztherapie
dc.identifier.doi10.48350/192620
dc.identifier.pmid38317178
dc.identifier.publisherDOI10.1186/s13054-024-04821-6
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/174205
dc.language.isoen
dc.publisherBioMed Central
dc.relation.ispartofCritical care
dc.relation.issn1364-8535
dc.relation.organization318E781798EC6684E053980C5C821B39
dc.relation.organizationDCD5A442BADCE17DE0405C82790C4DE2
dc.subject20% albumin 5% albumin Fluid therapy Hemorrhage Plasma volume expansion Ringer-lactate
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.titleBlood volume and hemodynamics during treatment of major hemorrhage with Ringer solution, 5% albumin, and 20% albumin: a single-center randomized controlled trial.
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.issue39
oaire.citation.volume28
oairecerif.author.affiliationUniversitätsklinik für Anästhesiologie und Schmerztherapie
oairecerif.author.affiliationUniversitätsklinik für Anästhesiologie und Schmerztherapie
oairecerif.author.affiliationUniversitätsklinik für Anästhesiologie und Schmerztherapie
oairecerif.author.affiliationUniversitätsklinik für Anästhesiologie und Schmerztherapie
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
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unibe.date.licenseChanged2024-02-07 07:45:09
unibe.description.ispublishedpub
unibe.eprints.legacyId192620
unibe.journal.abbrevTitleCRIT CARE
unibe.refereedtrue
unibe.subtype.articlejournal

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