Tranexamic Acid During Radical Cystectomy: A Randomized Clinical Trial.


Journal

JAMA surgery
ISSN: 2168-6262
Titre abrégé: JAMA Surg
Pays: United States
ID NLM: 101589553

Informations de publication

Date de publication:
02 Oct 2024
Historique:
medline: 2 10 2024
pubmed: 2 10 2024
entrez: 2 10 2024
Statut: aheadofprint

Résumé

Among cancer surgeries, patients requiring open radical cystectomy have the highest risk of red blood cell (RBC) transfusion. Prophylactic tranexamic acid (TXA) reduces blood loss during cardiac and orthopedic surgery, and it is possible that similar effects of TXA would be observed during radical cystectomy. To determine whether TXA, administered before incision and for the duration of radical cystectomy, reduced the number of RBC transfusions received by patients up to 30 days after surgery. The Tranexamic Acid During Cystectomy Trial (TACT) was a double-blind, placebo-controlled, randomized clinical trial with enrollment between June 2013 and January 2021. This multicenter trial was conducted in 10 academic centers. A consecutive sample of patients was eligible if the patients had a planned open radical cystectomy for the treatment of bladder cancer. Before incision, patients in the intervention arm received a loading dose of intravenous TXA, 10 mg/kg, followed by a maintenance infusion of 5 mg/kg per hour for the duration of the surgery. In the control arm, patients received indistinguishable matching placebo. The primary outcome was receipt of RBC transfusion up to 30 days after surgery. A total of 386 patients were assessed for eligibility, and 33 did not meet eligibility. Of 353 randomized patients (median [IQR] age, 69 [62-75] years; 263 male [74.5%]), 344 were included in the intention-to-treat analysis. RBC transfusion up to 30 days occurred in 64 of 173 patients (37.0%) in the TXA group and 64 of 171 patients (37.4%) in the placebo group (relative risk, 0.99; 95% CI, 0.83-1.18). There were no differences in secondary outcomes among the TXA group vs placebo group including mean (SD) number of RBC units transfused (0.9 [1.5] U vs 1.1 [1.8] U; P = .43), estimated blood loss (927 [733] mL vs 963 [624] mL; P = .52), intraoperative transfusion (28.3% [49 of 173] vs 24.0% [41 of 171]; P = .08), or venous thromboembolic events (3.5% [6 of 173] vs 2.9% [5 of 171]; P = .57). Non-transfusion-related adverse events were similar between groups. Results of this randomized clinical trial reveal that TXA did not reduce blood transfusion in patients undergoing open radical cystectomy for bladder cancer. Based on this trial, routine use of TXA during open radical cystectomy is not recommended. ClinicalTrials.gov Identifier: NCT01869413.

Identifiants

pubmed: 39356537
pii: 2824307
doi: 10.1001/jamasurg.2024.4183
doi:

Banques de données

ClinicalTrials.gov
['NCT01869413']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Rodney H Breau (RH)

Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.

Luke T Lavallée (LT)

Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.

Ilias Cagiannos (I)

Ottawa Hospital, Ottawa, Ontario, Canada.

Franco Momoli (F)

School of Epidemiology and Public Health, University of Ottawa, Ottawa, Ontario, Canada.

Gregory L Bryson (GL)

Departments of Anesthesiology and Pain Medicine, University of Ottawa, Ottawa, Ontario, Canada.

Salmaan Kanji (S)

Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.

Christopher Morash (C)

Ottawa Hospital, Ottawa, Ontario, Canada.

Alexis F Turgeon (AF)

Department of Anesthesiology and Critical Care Medicine, Division of Critical Care Medicine, Université Laval, Québec City, Québec, Canada.
Population Health and Optimal Health Practices Research Unit (Trauma-Emergency-Critical Care Medicine), CHU de Québec-Université Laval Research Center, Québec City, Québec, Canada.

Ryan Zarychanski (R)

Department of Internal Medicine, University of Manitoba, Winnipeg, Manitoba, Canada.
Department of Medical Oncology and Haematology, Cancercare Manitoba, Winnipeg, Manitoba, Canada.

Brett L Houston (BL)

Department of Internal Medicine, University of Manitoba, Winnipeg, Manitoba, Canada.
Department of Medical Oncology and Haematology, Cancercare Manitoba, Winnipeg, Manitoba, Canada.

Daniel I McIsaac (DI)

Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
Departments of Anesthesiology and Pain Medicine, University of Ottawa, Ottawa, Ontario, Canada.

Ranjeeta Mallick (R)

Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.

Greg A Knoll (GA)

Department of Medicine (Nephrology), The Ottawa Hospital, Ottawa, Ontario, Canada.

Girish Kulkarni (G)

Division of Urology, Department of Surgery, University of Toronto, Toronto, Ontario, Canada.

Jonathan Izawa (J)

Department of Surgery & Oncology, Division of Urology, Western University, London, Ontario, Canada.

Fred Saad (F)

University of Montreal Hospital Center (CHUM), Montreal Cancer Institute/CRCHUM, Montréal, Québec, Canada.

Wassim Kassouf (W)

Department of Surgery (Urology), McGill University Health Center, Montréal, Québec, Canada.

Vincent Fradet (V)

Department of Surgery (Urology), CHU de Québec - Université Laval, Québec City, Québec, Canada.

Ricardo Rendon (R)

Department of Urology, Dalhousie University and Nova Scotia Health Authority, Halifax, Nova Scotia, Canada.

Bobby Shayegan (B)

Division of Urology, McMaster University, Hamilton, Ontario, Canada.

Adrian Fairey (A)

Division of Urology, University of Alberta, Edmonton, Alberta, Canada.

Darrel E Drachenberg (DE)

Urologic Oncologist, Section of Urology, Department of Surgery, University of Manitoba, Winnipeg, Manitoba, Canada.

Dean Fergusson (D)

Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.

Classifications MeSH