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Small-Volume Blood Collection Tubes to Reduce Transfusions in Intensive Care: The STRATUS Randomized Clinical Trial.
Siegal, Deborah M; Belley-Côté, Emilie P; Lee, Shun Fu; Hill, Stephen; D'Aragon, Frédérick; Zarychanski, Ryan; Rochwerg, Bram; Chassé, Michaël; Binnie, Alexandra; Honarmand, Kimia; Lauzier, François; Ball, Ian; Al-Hazzani, Waleed; Archambault, Patrick; Duan, Erick; Khwaja, Kosar; Lellouche, François; Lysecki, Paul; Marquis, François; Naud, Jean-François; Shahin, Jason; Shea, Jennifer; Tsang, Jennifer L Y; Wang, Han Ting; Crowther, Mark; Arnold, Donald M; Di Sante, Emily; Marfo, Gladys; Kovalova, Tanya; Fonguh, Sylvanus; Vincent, Jessica; Connolly, Stuart J.
Afiliação
  • Siegal DM; Population Health Research Institute, McMaster University, Hamilton, Ontario, Canada.
  • Belley-Côté EP; Department of Medicine, McMaster University, Hamilton, Ontario, Canada.
  • Lee SF; Department of Medicine, University of Ottawa, Ottawa, Ontario, Canada.
  • Hill S; Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
  • D'Aragon F; Population Health Research Institute, McMaster University, Hamilton, Ontario, Canada.
  • Zarychanski R; Department of Medicine, McMaster University, Hamilton, Ontario, Canada.
  • Rochwerg B; Department of Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, Ontario, Canada.
  • Chassé M; Population Health Research Institute, McMaster University, Hamilton, Ontario, Canada.
  • Binnie A; Department of Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, Ontario, Canada.
  • Honarmand K; Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario, Canada.
  • Lauzier F; Department of Anesthesiology, Université de Sherbrooke, Sherbrooke, Québec, Canada.
  • Ball I; Department of Internal Medicine, University of Manitoba, Winnipeg, Manitoba, Canada.
  • Al-Hazzani W; Department of Medicine, McMaster University, Hamilton, Ontario, Canada.
  • Archambault P; Department of Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, Ontario, Canada.
  • Duan E; Centre Hospitalier de l'Université de Montréal, Department of Medicine, Université de Montréal, Montréal, Québec, Canada.
  • Khwaja K; William Osler Health System - Brampton Civic and Etobicoke General, Brampton, Ontario, Canada.
  • Lellouche F; London Health Sciences Centre - CCTC and University Hospital, Department of Medicine, Western University, London, Ontario, Canada.
  • Lysecki P; Centre Hospitalier Universitaire de Québec - Enfant-Jésus and Hôtel-Dieu, Department of Medicine, Department of Anesthesiology, Université Laval, Québec, Canada.
  • Marquis F; London Health Sciences Centre - CCTC and University Hospital, Department of Medicine, Western University, London, Ontario, Canada.
  • Naud JF; Department of Medicine, McMaster University, Hamilton, Ontario, Canada.
  • Shahin J; St. Joseph's Healthcare Hamilton, Hamilton, Ontario, Canada.
  • Shea J; Hôtel-Dieu de Lévis, Department of Family Medicine and Urgent Care, Université Laval, Québec, Canada.
  • Tsang JLY; Department of Medicine, McMaster University, Hamilton, Ontario, Canada.
  • Wang HT; Niagara Health - St. Catharine's General Hospital, St. Catharine's, Ontario, Canada.
  • Crowther M; Montreal General Hospital, Departments of Surgery and Critical Care Medicine, McGill University, Montréal, Québec, Canada.
  • Arnold DM; Institut Universitaire de Cardiologie et de Pneumologie de Québec, Department of Medicine, Université Laval, Québec, Canada.
  • Di Sante E; Joseph Brant Hospital, Department of Surgery, McMaster University, Hamilton, Ontario, Canada.
  • Marfo G; Maisonneuve-Rosemont, Department of Medicine, Université de Montréal, Montréal, Québec, Canada.
  • Kovalova T; Centre intégré universitaire de santé et de services sociaux de la Mauricie-et-du-Centre-du-Québec-CHAUR, Trois-Rivières, Québec, Canada.
  • Fonguh S; Royal Victoria Hospital, Department of Critical Care, McGill University, Montréal, Québec, Canada.
  • Vincent J; Saint John Regional Hospital, Department of Medicine, Memorial University, St. John, New Brunswick, Canada.
  • Connolly SJ; Department of Medicine, McMaster University, Hamilton, Ontario, Canada.
JAMA ; 330(19): 1872-1881, 2023 11 21.
Article em En | MEDLINE | ID: mdl-37824152
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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transfusão de Sangue / Coleta de Amostras Sanguíneas / Anemia Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transfusão de Sangue / Coleta de Amostras Sanguíneas / Anemia Idioma: En Ano de publicação: 2023 Tipo de documento: Article