Efficacy and safety of tranexamic acid in acute upper gastrointestinal bleeding: meta-analysis of randomised controlled trials.

Tranexamic acid meta-analysis randomised controlled trials upper gastrointestinal bleeding

Journal

Scandinavian journal of gastroenterology
ISSN: 1502-7708
Titre abrégé: Scand J Gastroenterol
Pays: England
ID NLM: 0060105

Informations de publication

Date de publication:
Dec 2020
Historique:
pubmed: 29 10 2020
medline: 19 8 2021
entrez: 28 10 2020
Statut: ppublish

Résumé

Studies evaluating the role of tranexamic acid in acute upper GI bleeding (UGIB) have reported conflicting results. In this systematic review, we have evaluated the efficacy and safety of tranexamic acid in UGIB. We searched several databases from inception to June 6, 2020 to identify randomised controlled trials (RCTs) that compared tranexamic acid and placebo in UGIB. Our outcomes of interest were mortality, rebleeding, all thromboembolic events, venous thromboembolic events, need for transfusion, endoscopic intervention and surgery. Pooled risk ratios (RR) with 95% confidence intervals (CI) were calculated using fixed effect model. We used the Grading of Recommendations Assessment, Development and Evaluation (GRADE) framework to assess the certainty of evidence. We included 12 RCTs comprising 14,100 patients. We found no significant difference in mortality, pooled RR (95% CI) 0.87 (0.74-1.01), rebleeding, pooled RR (95% CI) 0.90 (0.79-1.02), need for surgery, pooled RR (95% CI) 0.86 (0.73-1.02), need for transfusion, pooled RR (95% CI) 1.00 (0.99-1.01) or thromboembolic events, RR (95% CI) 1.16 (0.87-1.56) between treatments. We found an increased risk of venous thromboembolic events with tranexamic acid, pooled RR (95% CI) 1.94 (1.23-3.05). Certainty of evidence based on the GRADE framework for the different outcomes ranged from low to very low. Tranexamic acid does not improve outcomes in UGIB and may increase the risk of venous thromboembolic events.

Sections du résumé

BACKGROUND BACKGROUND
Studies evaluating the role of tranexamic acid in acute upper GI bleeding (UGIB) have reported conflicting results. In this systematic review, we have evaluated the efficacy and safety of tranexamic acid in UGIB.
METHODS METHODS
We searched several databases from inception to June 6, 2020 to identify randomised controlled trials (RCTs) that compared tranexamic acid and placebo in UGIB. Our outcomes of interest were mortality, rebleeding, all thromboembolic events, venous thromboembolic events, need for transfusion, endoscopic intervention and surgery. Pooled risk ratios (RR) with 95% confidence intervals (CI) were calculated using fixed effect model. We used the Grading of Recommendations Assessment, Development and Evaluation (GRADE) framework to assess the certainty of evidence.
RESULTS RESULTS
We included 12 RCTs comprising 14,100 patients. We found no significant difference in mortality, pooled RR (95% CI) 0.87 (0.74-1.01), rebleeding, pooled RR (95% CI) 0.90 (0.79-1.02), need for surgery, pooled RR (95% CI) 0.86 (0.73-1.02), need for transfusion, pooled RR (95% CI) 1.00 (0.99-1.01) or thromboembolic events, RR (95% CI) 1.16 (0.87-1.56) between treatments. We found an increased risk of venous thromboembolic events with tranexamic acid, pooled RR (95% CI) 1.94 (1.23-3.05). Certainty of evidence based on the GRADE framework for the different outcomes ranged from low to very low.
CONCLUSIONS CONCLUSIONS
Tranexamic acid does not improve outcomes in UGIB and may increase the risk of venous thromboembolic events.

Identifiants

pubmed: 33112175
doi: 10.1080/00365521.2020.1839963
doi:

Substances chimiques

Tranexamic Acid 6T84R30KC1

Types de publication

Journal Article Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1390-1397

Auteurs

Faisal Kamal (F)

Division of Gastroenterology, University of Tennessee Health Science Center, Memphis, TN, USA.

Muhammad Ali Khan (MA)

Division of Gastroenterology, University of Alabama at Birmingham, Birmingham, AL, USA.

Wade Lee-Smith (W)

Mulford Medical Sciences Library, University of Toledo, Toledo, OH, USA.

Sachit Sharma (S)

Department of Medicine, University of Toledo, Toledo, OH, USA.

Zaid Imam (Z)

Division of Gastroenterology, William Beaumont Hospital, Royal Oak, MI, USA.

Dawit Jowhar (D)

Department of Medicine, University of Tennessee Health Science Center, Memphis, TN, USA.

Ellen Petryna (E)

Department of Medicine, University of Tennessee Health Science Center, Memphis, TN, USA.

Hemnishil K Marella (HK)

Division of Gastroenterology, University of Tennessee Health Science Center, Memphis, TN, USA.

Pavel Aksionav (P)

Department of Medicine, University of Tennessee Health Science Center, Memphis, TN, USA.

Umair Iqbal (U)

Division of Gastroenterology, Geisinger Medical Center, Danville, PA, USA.

Claudio Tombazzi (C)

Division of Gastroenterology, University of Tennessee Health Science Center, Memphis, TN, USA.

Colin W Howden (CW)

Division of Gastroenterology, University of Tennessee Health Science Center, Memphis, TN, USA.

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