RESUMO
Importance: Tranexamic acid reduces bleeding and blood transfusion in many types of surgery, but its effect in patients undergoing liver resection for a cancer-related indication remains unclear. Objective: To determine whether tranexamic acid reduces red blood cell transfusion within 7 days of liver resection. Design, Setting, and Participants: Multicenter randomized clinical trial of tranexamic acid vs placebo conducted from December 1, 2014, to November 8, 2022, at 10 hepatopancreaticobiliary sites in Canada and 1 site in the United States, with 90-day follow-up. Participants, clinicians, and data collectors were blinded to allocation. A volunteer sample of 1384 patients undergoing liver resection for a cancer-related indication met eligibility criteria and consented to randomization. Interventions: Tranexamic acid (1-g bolus followed by 1-g infusion over 8 hours; n = 619) or matching placebo (n = 626) beginning at induction of anesthesia. Main Outcomes and Measures: The primary outcome was receipt of red blood cell transfusion within 7 days of surgery. Results: The primary analysis included 1245 participants (mean age, 63.2 years; 39.8% female; 56.1% with a diagnosis of colorectal liver metastases). Perioperative characteristics were similar between groups. Red blood cell transfusion occurred in 16.3% of participants (n = 101) in the tranexamic acid group and 14.5% (n = 91) in the placebo group (odds ratio, 1.15 [95% CI, 0.84-1.56]; P = .38; absolute difference, 2% [95% CI, -2% to 6%]). Measured intraoperative blood loss (tranexamic acid, 817.3 mL; placebo, 836.7 mL; P = .75) and total estimated blood loss over 7 days (tranexamic acid, 1504.0 mL; placebo, 1551.2 mL; P = .38) were similar between groups. Participants receiving tranexamic acid experienced significantly more complications compared with placebo (odds ratio, 1.28 [95% CI, 1.02-1.60]; P = .03), with no significant difference in venous thromboembolism (odds ratio, 1.68 [95% CI, 0.95-3.07]; P = .08). Conclusions and Relevance: Among patients undergoing liver resection for a cancer-related indication, tranexamic acid did not reduce bleeding or blood transfusion but increased perioperative complications. Trial Registration: ClinicalTrials.gov Identifier: NCT02261415.
Assuntos
Antifibrinolíticos , Hepatectomia , Neoplasias Hepáticas , Complicações Pós-Operatórias , Ácido Tranexâmico , Idoso , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Antifibrinolíticos/administração & dosagem , Antifibrinolíticos/efeitos adversos , Perda Sanguínea Cirúrgica/prevenção & controle , Perda Sanguínea Cirúrgica/estatística & dados numéricos , Método Duplo-Cego , Transfusão de Eritrócitos/estatística & dados numéricos , Hepatectomia/efeitos adversos , Hepatectomia/estatística & dados numéricos , Neoplasias Hepáticas/cirurgia , Ácido Tranexâmico/administração & dosagem , Ácido Tranexâmico/efeitos adversos , Complicações Pós-Operatórias/epidemiologia , Complicações Pós-Operatórias/etiologia , Período Perioperatório/estatística & dados numéricosRESUMO
The practice of living donor liver transplantation in adults has developed rapidly over the past five years and brings with it a set of unique technical and ethical challenges. The evaluation of potential donors focuses on their health and motives, and the results of noninvasive imaging, with the objective of ensuring the best outcomes for both donors and recipients. Graft volume is critical to success, and venous outflow reconstruction is paramount, although there is no consensus on the preferred method. Biliary tract complications occur in 30% of recipients. Complications that may interfere with recovery or delay the return to well-being occur in one of every four or five donors. The precise risk of donor death cannot be stated with certainty because comprehensive data on all cases are not available. It is clear, however, that donation of the right lobe of the liver carries with it a much greater risk of mortality than kidney donation. The paucity of details reported on donors who have died make it impossible to determine to what extent the deaths were preventable. The option of living donation is an invitation to expand the criteria for recipient selection to include, for example, patients with tumours that exceed traditional transplant guidelines. The risk-benefit ratios for donors become especially problematic when post-transplant recipient survival is below current standards.
Assuntos
Transplante de Fígado/métodos , Doadores Vivos , Complicações Pós-Operatórias/epidemiologia , Adulto , Doenças Biliares/epidemiologia , Doenças Biliares/etiologia , Humanos , Transplante de Fígado/ética , Doadores Vivos/ética , Doadores Vivos/psicologia , Motivação , Seleção de Pacientes , Guias de Prática Clínica como Assunto , SobrevidaRESUMO
Doppler ultrasound (DUS) is able to measure parameters of blood flow within vessels of transplanted organs, and vascular complications are associated with abnormal values. We analyzed the findings of 51 consecutive patients who underwent DUS on 2 occasions in the first postoperative week following liver transplantation for cirrhosis to determine the range of values in patients following liver transplantation. Three patients developed early vascular thromboses that were detected by the absence of a Doppler signal. In patients making an uneventful recovery, the arterial velocity tended to increase and the resistive index (RI) to decrease during the first postoperative week. All recipients were shown to have high-velocity segments within the hepatic artery, without an increase in flow resistance. Assessment of the portal vein revealed narrowing at the anastomosis, associated with a segmental doubling of flow velocity, and the mean portal venous flow decreased by approximately 20% in the first postoperative week. In conclusion, a wide range of abnormalities occurs in the vessels of liver transplant recipients, which were not associated with the development of vascular complications or affect patient management.