Risk of venous and arterial thrombosis in non-surgical patients receiving systemic tranexamic acid: A systematic review and meta-analysis
Antifibrinolytic agents such as tranexamic acid (TXA) are commonly used as adjunctive therapies to prevent and treat excessive bleeding. In non-surgical settings, TXA is known to reduce bleeding related mortality. However, impact of TXA use on thrombosis is uncertain. We systematically searched the...
Gespeichert in:
Veröffentlicht in: | Thrombosis research 2019-07, Vol.179, p.81-86 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 86 |
---|---|
container_issue | |
container_start_page | 81 |
container_title | Thrombosis research |
container_volume | 179 |
creator | Chornenki, Nicholas L. Jackson Um, Kevin J. Mendoza, Pablo A. Samienezhad, Ashkan Swarup, Vidushi Chai-Adisaksopha, Chatree Siegal, Deborah M. |
description | Antifibrinolytic agents such as tranexamic acid (TXA) are commonly used as adjunctive therapies to prevent and treat excessive bleeding. In non-surgical settings, TXA is known to reduce bleeding related mortality. However, impact of TXA use on thrombosis is uncertain.
We systematically searched the MEDLINE, EMBASE, and CENTRAL databases from January 1985 to August 2018. Studies with the following characteristics were included: (i) RCT design; (ii) compared systemic (oral or intravenous) TXA for prevention or treatment of bleeding for non-surgical indications and placebo or no TXA, and (iii) reported thrombotic events or mortality. A Mantel-Haenzel, random-effects model was used to calculate risk ratios, and risk of bias was assessed using the Cochrane risk of bias tool.
Our search identified 22 studies representing 49,538 patients. Those receiving TXA had a significantly lower risk of death from any cause (RR = 0.92; 95% CI = 0.87–0.98; I2 = 0%). There was no significant increase in the risk of stroke (RR = 1.10; 95% CI = 0.68–1.78; I2 = 31%), myocardial infarction (RR = 0.88; 95% CI = 0.43–1.84; I2 = 46%), pulmonary embolism (RR = 0.97; 95% CI = 0.75–1.26; I2 = 0%), or deep vein thrombosis (RR = 0.99; 95% CI = 0.70–1.41; I2 = 0%) from use of TXA. The results were similar when restricted to studies at low risk of bias.
In our systematic review and meta-analysis, the use of tranexamic acid reduced all-cause mortality without increased risk of venous or arterial thrombotic complications.
•Among non-surgical patients systemic Tranexamic Acid (TXA) usage was associated with an 8% reduction in all-cause mortality.•There was no increase in venous or arterial thrombotic events with the use of TXA.•These results persisted when restricted to studies at low risk of bias. |
doi_str_mv | 10.1016/j.thromres.2019.05.003 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2231858436</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0049384819302312</els_id><sourcerecordid>2231858436</sourcerecordid><originalsourceid>FETCH-LOGICAL-c368t-82b04c0c8a0b66caa5280371fd965c5860b8d7443bd218211412431ebb5d45c83</originalsourceid><addsrcrecordid>eNqFkc1uEzEUhS0EoqHwCpWXbGa4_h0PK6qKP6kSEoK15fHcFIcZT7CdlDwCb43TpGxZ2dI9x-f6O4RcMWgZMP1m05YfaZkT5pYD61tQLYB4QlbMdH3DZcefkhWA7BthpLkgL3LeALCO9eo5uRCMAWjBV-TP15B_0mVN9xiXXaYujtSlgim4iT5EDEsOmYZI4xKbvEt3wdfR1pWAsWSa0GPYh3hH8yEXnIOnJbmIv93x6nwY39Lr86x6fDXsA94_BM1YXOOimw414iV5tnZTxlfn85J8__D-282n5vbLx88317eNF9qUxvABpAdvHAxae-cUNyA6th57rbwyGgYzdlKKYeTMcMYk41IwHAY1SuWNuCSvT-9u0_Jrh7nYOWSP01SXrgQs54IZZaTQVapPUp-WnBOu7TaF2aWDZWCPNdiNfazBHmuwoGytoRqvzhm7Ycbxn-2RexW8Owmw_rTySDb7ytPjGCrQYscl_C_jL5YZnyc</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2231858436</pqid></control><display><type>article</type><title>Risk of venous and arterial thrombosis in non-surgical patients receiving systemic tranexamic acid: A systematic review and meta-analysis</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Chornenki, Nicholas L. Jackson ; Um, Kevin J. ; Mendoza, Pablo A. ; Samienezhad, Ashkan ; Swarup, Vidushi ; Chai-Adisaksopha, Chatree ; Siegal, Deborah M.</creator><creatorcontrib>Chornenki, Nicholas L. Jackson ; Um, Kevin J. ; Mendoza, Pablo A. ; Samienezhad, Ashkan ; Swarup, Vidushi ; Chai-Adisaksopha, Chatree ; Siegal, Deborah M.</creatorcontrib><description>Antifibrinolytic agents such as tranexamic acid (TXA) are commonly used as adjunctive therapies to prevent and treat excessive bleeding. In non-surgical settings, TXA is known to reduce bleeding related mortality. However, impact of TXA use on thrombosis is uncertain.
We systematically searched the MEDLINE, EMBASE, and CENTRAL databases from January 1985 to August 2018. Studies with the following characteristics were included: (i) RCT design; (ii) compared systemic (oral or intravenous) TXA for prevention or treatment of bleeding for non-surgical indications and placebo or no TXA, and (iii) reported thrombotic events or mortality. A Mantel-Haenzel, random-effects model was used to calculate risk ratios, and risk of bias was assessed using the Cochrane risk of bias tool.
Our search identified 22 studies representing 49,538 patients. Those receiving TXA had a significantly lower risk of death from any cause (RR = 0.92; 95% CI = 0.87–0.98; I2 = 0%). There was no significant increase in the risk of stroke (RR = 1.10; 95% CI = 0.68–1.78; I2 = 31%), myocardial infarction (RR = 0.88; 95% CI = 0.43–1.84; I2 = 46%), pulmonary embolism (RR = 0.97; 95% CI = 0.75–1.26; I2 = 0%), or deep vein thrombosis (RR = 0.99; 95% CI = 0.70–1.41; I2 = 0%) from use of TXA. The results were similar when restricted to studies at low risk of bias.
In our systematic review and meta-analysis, the use of tranexamic acid reduced all-cause mortality without increased risk of venous or arterial thrombotic complications.
•Among non-surgical patients systemic Tranexamic Acid (TXA) usage was associated with an 8% reduction in all-cause mortality.•There was no increase in venous or arterial thrombotic events with the use of TXA.•These results persisted when restricted to studies at low risk of bias.</description><identifier>ISSN: 0049-3848</identifier><identifier>EISSN: 1879-2472</identifier><identifier>DOI: 10.1016/j.thromres.2019.05.003</identifier><identifier>PMID: 31100632</identifier><language>eng</language><publisher>United States: Elsevier Ltd</publisher><subject>Bleeding ; Hemostasis ; Humans ; Thrombosis ; Thrombosis - chemically induced ; Thrombosis - pathology ; Tranexamic Acid - adverse effects ; TXA</subject><ispartof>Thrombosis research, 2019-07, Vol.179, p.81-86</ispartof><rights>2019 Elsevier Ltd</rights><rights>Copyright © 2019 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c368t-82b04c0c8a0b66caa5280371fd965c5860b8d7443bd218211412431ebb5d45c83</citedby><cites>FETCH-LOGICAL-c368t-82b04c0c8a0b66caa5280371fd965c5860b8d7443bd218211412431ebb5d45c83</cites><orcidid>0000-0002-4013-0956</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0049384819302312$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31100632$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chornenki, Nicholas L. Jackson</creatorcontrib><creatorcontrib>Um, Kevin J.</creatorcontrib><creatorcontrib>Mendoza, Pablo A.</creatorcontrib><creatorcontrib>Samienezhad, Ashkan</creatorcontrib><creatorcontrib>Swarup, Vidushi</creatorcontrib><creatorcontrib>Chai-Adisaksopha, Chatree</creatorcontrib><creatorcontrib>Siegal, Deborah M.</creatorcontrib><title>Risk of venous and arterial thrombosis in non-surgical patients receiving systemic tranexamic acid: A systematic review and meta-analysis</title><title>Thrombosis research</title><addtitle>Thromb Res</addtitle><description>Antifibrinolytic agents such as tranexamic acid (TXA) are commonly used as adjunctive therapies to prevent and treat excessive bleeding. In non-surgical settings, TXA is known to reduce bleeding related mortality. However, impact of TXA use on thrombosis is uncertain.
We systematically searched the MEDLINE, EMBASE, and CENTRAL databases from January 1985 to August 2018. Studies with the following characteristics were included: (i) RCT design; (ii) compared systemic (oral or intravenous) TXA for prevention or treatment of bleeding for non-surgical indications and placebo or no TXA, and (iii) reported thrombotic events or mortality. A Mantel-Haenzel, random-effects model was used to calculate risk ratios, and risk of bias was assessed using the Cochrane risk of bias tool.
Our search identified 22 studies representing 49,538 patients. Those receiving TXA had a significantly lower risk of death from any cause (RR = 0.92; 95% CI = 0.87–0.98; I2 = 0%). There was no significant increase in the risk of stroke (RR = 1.10; 95% CI = 0.68–1.78; I2 = 31%), myocardial infarction (RR = 0.88; 95% CI = 0.43–1.84; I2 = 46%), pulmonary embolism (RR = 0.97; 95% CI = 0.75–1.26; I2 = 0%), or deep vein thrombosis (RR = 0.99; 95% CI = 0.70–1.41; I2 = 0%) from use of TXA. The results were similar when restricted to studies at low risk of bias.
In our systematic review and meta-analysis, the use of tranexamic acid reduced all-cause mortality without increased risk of venous or arterial thrombotic complications.
•Among non-surgical patients systemic Tranexamic Acid (TXA) usage was associated with an 8% reduction in all-cause mortality.•There was no increase in venous or arterial thrombotic events with the use of TXA.•These results persisted when restricted to studies at low risk of bias.</description><subject>Bleeding</subject><subject>Hemostasis</subject><subject>Humans</subject><subject>Thrombosis</subject><subject>Thrombosis - chemically induced</subject><subject>Thrombosis - pathology</subject><subject>Tranexamic Acid - adverse effects</subject><subject>TXA</subject><issn>0049-3848</issn><issn>1879-2472</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1uEzEUhS0EoqHwCpWXbGa4_h0PK6qKP6kSEoK15fHcFIcZT7CdlDwCb43TpGxZ2dI9x-f6O4RcMWgZMP1m05YfaZkT5pYD61tQLYB4QlbMdH3DZcefkhWA7BthpLkgL3LeALCO9eo5uRCMAWjBV-TP15B_0mVN9xiXXaYujtSlgim4iT5EDEsOmYZI4xKbvEt3wdfR1pWAsWSa0GPYh3hH8yEXnIOnJbmIv93x6nwY39Lr86x6fDXsA94_BM1YXOOimw414iV5tnZTxlfn85J8__D-282n5vbLx88317eNF9qUxvABpAdvHAxae-cUNyA6th57rbwyGgYzdlKKYeTMcMYk41IwHAY1SuWNuCSvT-9u0_Jrh7nYOWSP01SXrgQs54IZZaTQVapPUp-WnBOu7TaF2aWDZWCPNdiNfazBHmuwoGytoRqvzhm7Ycbxn-2RexW8Owmw_rTySDb7ytPjGCrQYscl_C_jL5YZnyc</recordid><startdate>201907</startdate><enddate>201907</enddate><creator>Chornenki, Nicholas L. Jackson</creator><creator>Um, Kevin J.</creator><creator>Mendoza, Pablo A.</creator><creator>Samienezhad, Ashkan</creator><creator>Swarup, Vidushi</creator><creator>Chai-Adisaksopha, Chatree</creator><creator>Siegal, Deborah M.</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-4013-0956</orcidid></search><sort><creationdate>201907</creationdate><title>Risk of venous and arterial thrombosis in non-surgical patients receiving systemic tranexamic acid: A systematic review and meta-analysis</title><author>Chornenki, Nicholas L. Jackson ; Um, Kevin J. ; Mendoza, Pablo A. ; Samienezhad, Ashkan ; Swarup, Vidushi ; Chai-Adisaksopha, Chatree ; Siegal, Deborah M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c368t-82b04c0c8a0b66caa5280371fd965c5860b8d7443bd218211412431ebb5d45c83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Bleeding</topic><topic>Hemostasis</topic><topic>Humans</topic><topic>Thrombosis</topic><topic>Thrombosis - chemically induced</topic><topic>Thrombosis - pathology</topic><topic>Tranexamic Acid - adverse effects</topic><topic>TXA</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chornenki, Nicholas L. Jackson</creatorcontrib><creatorcontrib>Um, Kevin J.</creatorcontrib><creatorcontrib>Mendoza, Pablo A.</creatorcontrib><creatorcontrib>Samienezhad, Ashkan</creatorcontrib><creatorcontrib>Swarup, Vidushi</creatorcontrib><creatorcontrib>Chai-Adisaksopha, Chatree</creatorcontrib><creatorcontrib>Siegal, Deborah M.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Thrombosis research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chornenki, Nicholas L. Jackson</au><au>Um, Kevin J.</au><au>Mendoza, Pablo A.</au><au>Samienezhad, Ashkan</au><au>Swarup, Vidushi</au><au>Chai-Adisaksopha, Chatree</au><au>Siegal, Deborah M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Risk of venous and arterial thrombosis in non-surgical patients receiving systemic tranexamic acid: A systematic review and meta-analysis</atitle><jtitle>Thrombosis research</jtitle><addtitle>Thromb Res</addtitle><date>2019-07</date><risdate>2019</risdate><volume>179</volume><spage>81</spage><epage>86</epage><pages>81-86</pages><issn>0049-3848</issn><eissn>1879-2472</eissn><abstract>Antifibrinolytic agents such as tranexamic acid (TXA) are commonly used as adjunctive therapies to prevent and treat excessive bleeding. In non-surgical settings, TXA is known to reduce bleeding related mortality. However, impact of TXA use on thrombosis is uncertain.
We systematically searched the MEDLINE, EMBASE, and CENTRAL databases from January 1985 to August 2018. Studies with the following characteristics were included: (i) RCT design; (ii) compared systemic (oral or intravenous) TXA for prevention or treatment of bleeding for non-surgical indications and placebo or no TXA, and (iii) reported thrombotic events or mortality. A Mantel-Haenzel, random-effects model was used to calculate risk ratios, and risk of bias was assessed using the Cochrane risk of bias tool.
Our search identified 22 studies representing 49,538 patients. Those receiving TXA had a significantly lower risk of death from any cause (RR = 0.92; 95% CI = 0.87–0.98; I2 = 0%). There was no significant increase in the risk of stroke (RR = 1.10; 95% CI = 0.68–1.78; I2 = 31%), myocardial infarction (RR = 0.88; 95% CI = 0.43–1.84; I2 = 46%), pulmonary embolism (RR = 0.97; 95% CI = 0.75–1.26; I2 = 0%), or deep vein thrombosis (RR = 0.99; 95% CI = 0.70–1.41; I2 = 0%) from use of TXA. The results were similar when restricted to studies at low risk of bias.
In our systematic review and meta-analysis, the use of tranexamic acid reduced all-cause mortality without increased risk of venous or arterial thrombotic complications.
•Among non-surgical patients systemic Tranexamic Acid (TXA) usage was associated with an 8% reduction in all-cause mortality.•There was no increase in venous or arterial thrombotic events with the use of TXA.•These results persisted when restricted to studies at low risk of bias.</abstract><cop>United States</cop><pub>Elsevier Ltd</pub><pmid>31100632</pmid><doi>10.1016/j.thromres.2019.05.003</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0002-4013-0956</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0049-3848 |
ispartof | Thrombosis research, 2019-07, Vol.179, p.81-86 |
issn | 0049-3848 1879-2472 |
language | eng |
recordid | cdi_proquest_miscellaneous_2231858436 |
source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | Bleeding Hemostasis Humans Thrombosis Thrombosis - chemically induced Thrombosis - pathology Tranexamic Acid - adverse effects TXA |
title | Risk of venous and arterial thrombosis in non-surgical patients receiving systemic tranexamic acid: A systematic review and meta-analysis |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-03T07%3A05%3A26IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Risk%20of%20venous%20and%20arterial%20thrombosis%20in%20non-surgical%20patients%20receiving%20systemic%20tranexamic%20acid:%20A%20systematic%20review%20and%20meta-analysis&rft.jtitle=Thrombosis%20research&rft.au=Chornenki,%20Nicholas%20L.%20Jackson&rft.date=2019-07&rft.volume=179&rft.spage=81&rft.epage=86&rft.pages=81-86&rft.issn=0049-3848&rft.eissn=1879-2472&rft_id=info:doi/10.1016/j.thromres.2019.05.003&rft_dat=%3Cproquest_cross%3E2231858436%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2231858436&rft_id=info:pmid/31100632&rft_els_id=S0049384819302312&rfr_iscdi=true |