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Tranexamic acid versus placebo to reduce perioperative blood transfusion in patients undergoing liver resection: protocol for the haemorrhage during liver resection tranexamic acid (HeLiX) randomised controlled trial.
Karanicolas, Paul Jack; Lin, Yulia; McCluskey, Stuart; Roke, Rachel; Tarshis, Jordan; Thorpe, Kevin E; Ball, Chad G; Chaudhury, Prosanto; Cleary, Sean P; Dixon, Elijah; Eeson, Gareth; Moulton, Carol-Anne; Nanji, Sulaiman; Porter, Geoff; Ruo, Leyo; Skaro, Anton I; Tsang, Melanie; Wei, Alice C; Guyatt, Gordon.
Afiliação
  • Karanicolas PJ; Department of Surgery, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada paul.karanicolas@sunnybrook.ca.
  • Lin Y; Department of Surgery, University of Toronto, Toronto, Ontario, Canada.
  • McCluskey S; Department of Laboratory Medicine and Molecular Diagnostics, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada.
  • Roke R; Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada.
  • Tarshis J; Department of Anesthesia and Pain Management, University Health Network, Toronto, Ontario, Canada.
  • Thorpe KE; Department of Anesthesia, University of Toronto, Toronto, Ontario, Canada.
  • Ball CG; Department of Evaluative Clinical Sciences, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada.
  • Chaudhury P; Institute of Health Policy, Management and Evaluation, University of Toronto, Toronto, Ontario, Canada.
  • Cleary SP; Department of Anesthesia, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada.
  • Dixon E; Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.
  • Eeson G; Department of Surgery, Foothills Medical Centre, Calgary, Alberta, Canada.
  • Moulton CA; Department of Medicine, University of Calgary, Calgary, Alberta, Canada.
  • Nanji S; Department of Surgery, McGill University Health Centre, Montreal, Québec, Canada.
  • Porter G; Department of Surgery, Mayo Clinic, Rochester, Minnesota, USA.
  • Ruo L; Department of Surgery, Foothills Medical Centre, Calgary, Alberta, Canada.
  • Skaro AI; Department of Surgery, University of Calgary, Calgary, Alberta, Canada.
  • Tsang M; Department of Surgery, Kelowna General Hospital, Kelowna, British Columbia, Canada.
  • Wei AC; Department of Surgery, University of British Columbia, Vancouver, British Columbia, Canada.
  • Guyatt G; Department of Surgery, University of Toronto, Toronto, Ontario, Canada.
BMJ Open ; 12(2): e058850, 2022 Feb 24.
Article em En | MEDLINE | ID: mdl-35210348
ABSTRACT

INTRODUCTION:

Despite use of operative and non-operative interventions to reduce blood loss during liver resection, 20%-40% of patients receive a perioperative blood transfusion. Extensive intraoperative blood loss is a major risk factor for postoperative morbidity and mortality and receipt of blood transfusion is associated with serious risks including an association with long-term cancer recurrence and overall survival. In addition, blood products are scarce and associated with appreciable expense; decreasing blood transfusion requirements would therefore have health system benefits. Tranexamic acid (TXA), an antifibrinolytic, has been shown to reduce the probability of receiving a blood transfusion by one-third for patients undergoing cardiac or orthopaedic surgery. However, its applicability in liver resection has not been widely researched. METHODS AND

ANALYSIS:

This protocol describes a prospective, blinded, randomised controlled trial being conducted at 10 sites in Canada and 1 in the USA. 1230 eligible and consenting participants will be randomised to one of two parallel groups experimental (2 g of intravenous TXA) or placebo (saline) administered intraoperatively. The primary endpoint is receipt of blood transfusion within 7 days of surgery. Secondary outcomes include blood loss, postoperative complications, quality of life and 5-year disease-free and overall survival. ETHICS AND DISSEMINATION This trial has been approved by the research ethics boards at participating centres and Health Canada (parent control number 177992) and is currently enrolling participants. All participants will provide written informed consent. Results will be distributed widely through local and international meetings, presentation, publication and ClinicalTrials.gov. TRIAL REGISTRATION NUMBER NCT02261415.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ácido Tranexâmico / Antifibrinolíticos Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Ácido Tranexâmico / Antifibrinolíticos Idioma: En Ano de publicação: 2022 Tipo de documento: Article