
Efficacy and Safety of Tropical Use of Tranexamic Acid during Off-Pump Coronary Artery Bypass Surgery: A Randomized Control Trial
Author(s) -
Asraful Hoque,
Tasmin Rubayath,
Romena Rahman,
Md. Tanvir Hossain,
Abu Shadat Mohammad Saem Khan,
Monzur Hossain,
Muhammad Asif Ahsan Chowdhury,
Imran Ahmed,
Wahida Salam
Publication year - 2022
Publication title -
journal of national institute of neurosciences bangladesh
Language(s) - English
Resource type - Journals
eISSN - 2518-6612
pISSN - 2410-8030
DOI - 10.3329/jninb.v7i2.58109
Subject(s) - medicine , tranexamic acid , surgery , anesthesia , saline , randomized controlled trial , placebo , off pump coronary artery bypass , blood transfusion , artery , bypass grafting , blood loss , alternative medicine , pathology
Background: Postoperative mediastinal bleeding in patients undergoing cardiac surgery is still one of the most common complications.
Objective: This study was intended to investigate the efficacy of topical tranexamic acid in reducing postoperative bleeding after post-operative cardiovascular surgery.
Methodology: In this non-randomized, double blinded, clinical trial, patients undergoing Off-Pump Coronary Artery Bypass (OPCAB) surgery in NICVD, Dhaka, Bangladesh during January 2014 to December 2015 and fulfilling inclusion and exclusion criteria were recruited. They were assigned in two groups- 30 patients in tranexamic acid group (Group 1) and 30 patients in placebo group (Group 2). On completion of the grafting, before closure of the sternum tranexamic acid (2.5 g/25 mL) or placebo (25 mL of saline) diluted in 100 mL of warm saline (370 C) was instilled into the pericardial cavity including the mediastinal tissues and left for 5 minutes. Then it was cleared out by wall sucker and sternum was closed.
Results: There was no significant difference in baseline demographic data, basic clinical characteristics and preoperative coagulation profile between the 2 groups (P > 0.05). Total mediastinal bleeding in group 1 and group 2 patients were421.67±70.32 vs 593.33±77.38ml, p<0.001. In case of, whole blood transfusion in group 1 and group 2 patients were 0.87±0.0.73 units and1.77±0.57 units respectively, p<0.001.
Conclusion: No patient required reoperation for bleeding and there was no incidence of prolonged ventilation, MI, thromboembolism, DVT or CVA in any of the patients in either group.
Journal of National Institute of Neurosciences Bangladesh, July 2021, Vol. 7, No. 2, pp. 142-146