Small-Volume Blood Collection Tubes to Reduce Transfusions in Intensive Care

Deborah Siegal(University of Ottawa), Emilie P. Belley‐Côté(Population Health Research Institute), Shun Fu Lee(Population Health Research Institute), Stephen Hill(McMaster University), Frédérick D’Aragon(Université de Sherbrooke), Ryan Zarychanski(University of Manitoba), Bram Rochwerg(Impact), Michaël Chassé(Centre Hospitalier de l’Université de Montréal), Alexandra Binnie(William Osler Health System), Kimia Honarmand(Western University), François Lauzier(Centre hospitalier universitaire de Québec), Ian Ball(Western University), Waleed Alhazzani(St. Joseph’s Healthcare Hamilton), Patrick Archambault(Hôtel-Dieu de Québec), Erick Duan(Niagara Health System), Kosar Khwaja(Montreal General Hospital), François Lellouche(Institut universitaire de cardiologie et de pneumologie de Québec), Paul Lysecki(Joseph Brant Hospital), François Marquis(Hôpital Maisonneuve-Rosemont), Jean-François Naud(Centre intégré universitaire de santé et de services sociaux de la Mauricie-et-du-Centre-du-Québec), Jason Shahin(Royal Victoria Hospital), Jennifer Shea(Memorial University of Newfoundland), Jennifer Tsang(Niagara Health System), Han Ting Wang(Hôpital Maisonneuve-Rosemont), Mark Crowther(St. Joseph’s Healthcare Hamilton), Donald M. Arnold(McMaster University), Emily Di Sante(Population Health Research Institute), Gladys Marfo(Population Health Research Institute), Tanya Kovalova(Population Health Research Institute), Sylvanus Fonguh(Population Health Research Institute), Jessica Vincent(Population Health Research Institute), Stuart J. Connolly(Population Health Research Institute)
JAMA
October 12, 2023
Cited by 41Open Access
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Abstract

Importance: Blood collection for laboratory testing in intensive care unit (ICU) patients is a modifiable contributor to anemia and red blood cell (RBC) transfusion. Most blood withdrawn is not required for analysis and is discarded. Objective: To determine whether transitioning from standard-volume to small-volume vacuum tubes for blood collection in ICUs reduces RBC transfusion without compromising laboratory testing procedures. Design, Setting, and Participants: Stepped-wedge cluster randomized trial in 25 adult medical-surgical ICUs in Canada (February 5, 2019 to January 21, 2021). Interventions: ICUs were randomized to transition from standard-volume (n = 10 940) to small-volume tubes (n = 10 261) for laboratory testing. Main Outcomes and Measures: The primary outcome was RBC transfusion (units per patient per ICU stay). Secondary outcomes were patients receiving at least 1 RBC transfusion, hemoglobin decrease during ICU stay (adjusted for RBC transfusion), specimens with insufficient volume for testing, length of stay in the ICU and hospital, and mortality in the ICU and hospital. The primary analysis included patients admitted for 48 hours or more, excluding those admitted during a 5.5-month COVID-19-related trial hiatus. Results: In the primary analysis of 21 201 patients (mean age, 63.5 years; 39.9% female), which excluded 6210 patients admitted during the early COVID-19 pandemic, there was no significant difference in RBC units per patient per ICU stay (relative risk [RR], 0.91 [95% CI, 0.79 to 1.05]; P = .19; absolute reduction of 7.24 RBC units/100 patients per ICU stay [95% CI, -3.28 to 19.44]). In a prespecified secondary analysis (n = 27 411 patients), RBC units per patient per ICU stay decreased after transition from standard-volume to small-volume tubes (RR, 0.88 [95% CI, 0.77 to 1.00]; P = .04; absolute reduction of 9.84 RBC units/100 patients per ICU stay [95% CI, 0.24 to 20.76]). Median decrease in transfusion-adjusted hemoglobin was not statistically different in the primary population (mean difference, 0.10 g/dL [95% CI, -0.04 to 0.23]) and lower in the secondary population (mean difference, 0.17 g/dL [95% CI, 0.05 to 0.29]). Specimens with insufficient quantity for analysis were rare (≤0.03%) before and after transition. Conclusions and Relevance: Use of small-volume blood collection tubes in the ICU may decrease RBC transfusions without affecting laboratory analysis. Trial Registration: ClinicalTrials.gov Identifier: NCT03578419.


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