The association of thromboembolic complications and the use of tranexamic acid during resection of intracranial meningiomas : systematic review and meta-analysis of randomized controlled trials
OBJECTIVE: Antifibrinolytics, such as tranexamic acid (TXA), have been shown to decrease intraoperative blood loss across multiple surgical disciplines. However, they carry the theoretical risk of thromboembolic events secondary to induced hypercoagulability. Therefore, the aim of this study was to systematically review the available literature and perform a meta-analysis on the use of TXA in meningioma resection to assess thromboembolic risks.
METHODS: The PubMed, Web of Science, and Google Scholar databases were reviewed for all randomized controlled trials presenting primary data on TXA use during resection of intracranial meningiomas. Data were gathered on operative duration, venous thromboembolic complications, deep venous thrombosis, use of allogeneic blood transfusion, estimated blood loss (EBL), and postoperative hemoglobin. Patients who received TXA were compared with controls who did not receive TXA intraoperatively using random-effects models.
RESULTS: A total of 508 unique articles were identified, of which 493 underwent full-text review. Ultimately, 6 studies with 381 total patients (190 receiving TXA) were included in the final analysis. All 6 trials were randomized, blinded, and placebo controlled with a TXA administration rate of a 20-mg/kg load followed by a 1-mg/kg/hr infusion. All studies were performed in lower-middle-income countries. There were no reported instances of venous thromboembolism (VTE) in the TXA and non-TXA cohorts. Patients receiving TXA exhibited fewer allogeneic transfusions (21.5% vs 41.6% [OR 0.26, 95% CI 0.09-0.77], p = 0.02) and lower EBL (MD -282.48 mL [95% CI -367.77 to -197.20 mL], p < 0.001) compared with patients who did not receive TXA, and they also had lower rates of perioperative complications (10.7% vs 19.9% [OR 0.47, 95% CI 0.2-0.95], p = 0.04).
CONCLUSIONS: Current literature suggests that TXA is not associated with increased risk for VTE when administered during resection of intracranial meningioma. TXA appears to decrease intraoperative blood loss and allogeneic transfusion requirements during meningioma resection and thus may improve the safety of surgical management of this pathology.
| Medienart: |
E-Artikel |
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| Erscheinungsjahr: |
2024 |
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| Erschienen: |
2024 |
| Enthalten in: |
Zur Gesamtaufnahme - volume:140 |
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| Enthalten in: |
Journal of neurosurgery - 140(2024), 4 vom: 01. Apr., Seite 1008-1018 |
| Sprache: |
Englisch |
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| Beteiligte Personen: |
Nguyen, Andrew [VerfasserIn] |
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| Links: |
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| Themen: |
6T84R30KC1 |
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| Anmerkungen: |
Date Completed 03.04.2024 Date Revised 03.04.2024 published: Electronic-Print Citation Status MEDLINE |
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| doi: |
10.3171/2023.7.JNS23849 |
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| funding: |
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| Förderinstitution / Projekttitel: |
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| PPN (Katalog-ID): |
NLM363488405 |
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| 100 | 1 | |a Nguyen, Andrew |e verfasserin |4 aut | |
| 245 | 1 | 4 | |a The association of thromboembolic complications and the use of tranexamic acid during resection of intracranial meningiomas |b systematic review and meta-analysis of randomized controlled trials |
| 264 | 1 | |c 2024 | |
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| 500 | |a Date Completed 03.04.2024 | ||
| 500 | |a Date Revised 03.04.2024 | ||
| 500 | |a published: Electronic-Print | ||
| 500 | |a Citation Status MEDLINE | ||
| 520 | |a OBJECTIVE: Antifibrinolytics, such as tranexamic acid (TXA), have been shown to decrease intraoperative blood loss across multiple surgical disciplines. However, they carry the theoretical risk of thromboembolic events secondary to induced hypercoagulability. Therefore, the aim of this study was to systematically review the available literature and perform a meta-analysis on the use of TXA in meningioma resection to assess thromboembolic risks | ||
| 520 | |a METHODS: The PubMed, Web of Science, and Google Scholar databases were reviewed for all randomized controlled trials presenting primary data on TXA use during resection of intracranial meningiomas. Data were gathered on operative duration, venous thromboembolic complications, deep venous thrombosis, use of allogeneic blood transfusion, estimated blood loss (EBL), and postoperative hemoglobin. Patients who received TXA were compared with controls who did not receive TXA intraoperatively using random-effects models | ||
| 520 | |a RESULTS: A total of 508 unique articles were identified, of which 493 underwent full-text review. Ultimately, 6 studies with 381 total patients (190 receiving TXA) were included in the final analysis. All 6 trials were randomized, blinded, and placebo controlled with a TXA administration rate of a 20-mg/kg load followed by a 1-mg/kg/hr infusion. All studies were performed in lower-middle-income countries. There were no reported instances of venous thromboembolism (VTE) in the TXA and non-TXA cohorts. Patients receiving TXA exhibited fewer allogeneic transfusions (21.5% vs 41.6% [OR 0.26, 95% CI 0.09-0.77], p = 0.02) and lower EBL (MD -282.48 mL [95% CI -367.77 to -197.20 mL], p < 0.001) compared with patients who did not receive TXA, and they also had lower rates of perioperative complications (10.7% vs 19.9% [OR 0.47, 95% CI 0.2-0.95], p = 0.04) | ||
| 520 | |a CONCLUSIONS: Current literature suggests that TXA is not associated with increased risk for VTE when administered during resection of intracranial meningioma. TXA appears to decrease intraoperative blood loss and allogeneic transfusion requirements during meningioma resection and thus may improve the safety of surgical management of this pathology | ||
| 650 | 4 | |a Meta-Analysis | |
| 650 | 4 | |a Systematic Review | |
| 650 | 4 | |a Journal Article | |
| 650 | 4 | |a complications | |
| 650 | 4 | |a deep venous thrombosis | |
| 650 | 4 | |a intracranial tumor | |
| 650 | 4 | |a meningioma | |
| 650 | 4 | |a thromboembolic | |
| 650 | 4 | |a tranexamic acid | |
| 650 | 7 | |a Tranexamic Acid |2 NLM | |
| 650 | 7 | |a 6T84R30KC1 |2 NLM | |
| 650 | 7 | |a Antifibrinolytic Agents |2 NLM | |
| 700 | 1 | |a Brown, Nolan J |e verfasserin |4 aut | |
| 700 | 1 | |a Gendreau, Julian |e verfasserin |4 aut | |
| 700 | 1 | |a Nguyen, Brandon A |e verfasserin |4 aut | |
| 700 | 1 | |a Pennington, Zach |e verfasserin |4 aut | |
| 700 | 1 | |a Zhang, Angie |e verfasserin |4 aut | |
| 700 | 1 | |a Harris, Mark H |e verfasserin |4 aut | |
| 700 | 1 | |a Chakravarti, Sachiv |e verfasserin |4 aut | |
| 700 | 1 | |a Douse, Dontre' M |e verfasserin |4 aut | |
| 700 | 1 | |a Van Gompel, Jamie J |e verfasserin |4 aut | |
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