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                                                   The Effect of TXA on Blood Loss during Laparoscopic Sleeve Gastrectomy
          intravenously during  induction. The second group  Postoperative Blood Loss
          included the remaining 25 patients in whom TXA was   Drain was kept for all patients who underwent lapa-
          not given and was considered as control group. Injection   roscopic sleeve gastrectomy. Most of the drains were
          TXA was administered in a dose of 10 mg/kg as bolus   removed within 72 hours. The fluid collected in the post-
          injection (treatment group) given intravenously over   operative drains was measured. In the treatment group,
          5 minutes. The heart rate, respiratory rate, and blood   20 patients out of 25 patients had blood drain below 100 ml
          pressure were checked and charted intraoperatively and   on 1st postoperative day. In the control group, 16 patients
          postoperatively.                                    out of 25 patients had drained blood more than 100 ml
             A single brand of TXA from a reputed firm was    on the 1st postoperative day (Table 3).
          used in all cases in order to minimize the brand-related
          bias and for standardization. Intraoperative blood loss         Table 3: Postoperative blood loss
          was calculated by galanometric method, weighing the               50–100 ml 100–150 ml 150–200 ml  Total
          sponges used and soiled by blood during surgery and   Treatment group 20   2          3         25
          measuring the amount of blood collected in suction   Control group  2      16         7         25
          apparatus used during the surgery. Postoperatively, the   Total   22       18         10        50
          drained fluid collected in the drain was measured till the
          drain was removed.                                  Change in Hemoglobin Level
             The hemoglobin level was assessed postopera-  In patients who had laparoscopic sleeve gastrectomy,
          tively and was compared with preoperative hemoglobin  23 patients out of 25 patients in the treatment group had
          level. The data were collected in an excel sheet. The  preoperative and postoperative hemoglobin difference
          patients were followed up till they were discharged  of less than 1 mg/dl. In the control group, 18 patients
          from the hospital and were followed up in outpatient  out of 25 patients had preoperative and postoperative
          department.                                         hemoglobin difference of more than 1 mg/dl (Table 4).

                                                                      Table 4: Measurement of hemoglobin level
          RESULTS
                                                              Preoperative hemoglobin  Treatment  Control  Total
          There were 50 patients in our study of whom 25      Less than 1            23         2
          (50%) patients who received TXA were in the treat-   1.1–2                 2          18
          ment group and remaining 25 (50%) patients who      2.1–3                  0          3
          did not receive the drug were in the control group     More than 3         0          2
          (Table 1).                                          Total                  25         25       50

                       Table 1: Distribution of patients      DISCUSSION
           Drug            Total           Percentage         Reduction of bleeding during laparoscopic sleeve
           Control         25              50                 gastrectomy is a major benefit for the operating surgeon.
           Treatment       25              50                 Tranexamic acid inhibits plasminogen activity and
           Total           50              100                fibrinolysis and thereby reduces capillary ooze. It thus
          There were 42 females and 8 males                   increases clot formation and decreases blood loss. The

                                                              added advantage is no postoperative alteration of patient’s
          Intraoperative Blood Loss
                                                              coagulation profile and absence of major side effects.
          In the treatment group, 20 patients out of 25 had blood   A randomized controlled trial (RCT) was conducted
          loss below 300 ml, and 2 patients had blood loss of more  in 274 hospitals in 40 countries. This RCT named clinical
          than 400 ml. In the control group, 5 patients out of 25 had  randomization of an antifibrinolytic in significant
          blood loss below 300 ml, and 20 patients had blood loss  hemorrhage-2 (CRASH-2) assessed the efficacy and safety
          of more than 400 ml (Table 2).                      of TXA by investigating 20,211 adult trauma patients
                                                              who had or were at risk of significant hemorrhage. In
                      Table 2: Intraoperative blood loss      the trial, the injured patients were randomly separated
                    Less than    300–   More than             into two groups within 8 hours of injury. One group
                    300 ml     400 ml  400 ml     Total       received an initial dose of 1 gm of TXA and a second
           Treatment  20       3       2          25 patients  dose of 1 gm as infusion over 8 hours. The other group
           Control  5          15      5          25 patients  received a matching placebo. A total of 10,096 patients
           Total                                  50 patients  received TXA and 10,115 received placebo; of these

          World Journal of Laparoscopic Surgery, January-April 2016;9(1):30-33                              31
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