The risks, timing and safety of anticoagulation therapy following intracranial surgery: a systematic review and meta-analysis
The timing, safety, and efficacy of prophylactic anticoagulation following craniotomy are well established in the literature. However, anticoagulation therapy (ACT) remains a controversial topic, and the literature on the subject is extremely scarce, preventing robust conclusions about its risks and...
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Published in | Neurosurgical review Vol. 48; no. 1; p. 453 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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Springer Berlin Heidelberg
29.05.2025
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Abstract | The timing, safety, and efficacy of prophylactic anticoagulation following craniotomy are well established in the literature. However, anticoagulation therapy (ACT) remains a controversial topic, and the literature on the subject is extremely scarce, preventing robust conclusions about its risks and safety. Our study aims to identify the risks and the best time to start ACT following intracranial surgery. A systematic review was conducted using Embase, PubMed, and Cochrane databases. The primary outcome was intracranial hemorrhage (ICH). Secondary outcomes were mortality and surgical reintervention. Statistical analyses were performed using RStudio 2024.09.0 + 375. Sensitivity analysis was performed using subgroup analysis, and leave-one-out test. The risk of bias was assessed using ROBINS-I. Of 800 potential articles, seven met our inclusion criteria, encompassing a total of 304 patients. The mean age was 56 years and 46% of the patients were male. The main reasons for intracranial surgery were intracranial tumor (48%) and vascular surgery (18%). Intra-axial surgery and starting ACT before the first 48 h were factors associated with higher odds of ICH. The mean interval between the start of ACT and surgery was 5 days, and the mean time from initiation of ACT to ICH was 6.8 days. The ICH rate due to ACT use was 7.96% (95% CI 1.90%-16.86%) between 0 and 30 days after surgery, 11.61% (95% CI 0.98%-29.09%) between 0 and 10 days, and 9.15% (95% CI 3.03%-17.47%) between 10 and 30 days. The mortality rate due to ICH secondary to ACT was 0.70% (95% CI 0.00%-3.22%). The surgical reintervention rate due to ICH secondary to ACT was 1.06% (95% CI 0.00%-5.36%). Our results suggest that the risk of ICH and mortality due to early ACT (< 10 days) following intracranial surgery might be overestimated, and this management could be a viable strategy, especially if started 48 h after surgery and in patients who have undergone extra-axial surgery. Nevertheless, it is important to consider the various limitations that may impact these observations, and controlled prospective studies are needed to provide more robust conclusions.
Clinical trial number: Not applicable.
Graphical abstract |
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AbstractList | The timing, safety, and efficacy of prophylactic anticoagulation following craniotomy are well established in the literature. However, anticoagulation therapy (ACT) remains a controversial topic, and the literature on the subject is extremely scarce, preventing robust conclusions about its risks and safety. Our study aims to identify the risks and the best time to start ACT following intracranial surgery. A systematic review was conducted using Embase, PubMed, and Cochrane databases. The primary outcome was intracranial hemorrhage (ICH). Secondary outcomes were mortality and surgical reintervention. Statistical analyses were performed using RStudio 2024.09.0 + 375. Sensitivity analysis was performed using subgroup analysis, and leave-one-out test. The risk of bias was assessed using ROBINS-I. Of 800 potential articles, seven met our inclusion criteria, encompassing a total of 304 patients. The mean age was 56 years and 46% of the patients were male. The main reasons for intracranial surgery were intracranial tumor (48%) and vascular surgery (18%). Intra-axial surgery and starting ACT before the first 48 h were factors associated with higher odds of ICH. The mean interval between the start of ACT and surgery was 5 days, and the mean time from initiation of ACT to ICH was 6.8 days. The ICH rate due to ACT use was 7.96% (95% CI 1.90%-16.86%) between 0 and 30 days after surgery, 11.61% (95% CI 0.98%-29.09%) between 0 and 10 days, and 9.15% (95% CI 3.03%-17.47%) between 10 and 30 days. The mortality rate due to ICH secondary to ACT was 0.70% (95% CI 0.00%-3.22%). The surgical reintervention rate due to ICH secondary to ACT was 1.06% (95% CI 0.00%-5.36%). Our results suggest that the risk of ICH and mortality due to early ACT (< 10 days) following intracranial surgery might be overestimated, and this management could be a viable strategy, especially if started 48 h after surgery and in patients who have undergone extra-axial surgery. Nevertheless, it is important to consider the various limitations that may impact these observations, and controlled prospective studies are needed to provide more robust conclusions. Clinical trial number: Not applicable. The timing, safety, and efficacy of prophylactic anticoagulation following craniotomy are well established in the literature. However, anticoagulation therapy (ACT) remains a controversial topic, and the literature on the subject is extremely scarce, preventing robust conclusions about its risks and safety. Our study aims to identify the risks and the best time to start ACT following intracranial surgery. A systematic review was conducted using Embase, PubMed, and Cochrane databases. The primary outcome was intracranial hemorrhage (ICH). Secondary outcomes were mortality and surgical reintervention. Statistical analyses were performed using RStudio 2024.09.0 + 375. Sensitivity analysis was performed using subgroup analysis, and leave-one-out test. The risk of bias was assessed using ROBINS-I. Of 800 potential articles, seven met our inclusion criteria, encompassing a total of 304 patients. The mean age was 56 years and 46% of the patients were male. The main reasons for intracranial surgery were intracranial tumor (48%) and vascular surgery (18%). Intra-axial surgery and starting ACT before the first 48 h were factors associated with higher odds of ICH. The mean interval between the start of ACT and surgery was 5 days, and the mean time from initiation of ACT to ICH was 6.8 days. The ICH rate due to ACT use was 7.96% (95% CI 1.90%-16.86%) between 0 and 30 days after surgery, 11.61% (95% CI 0.98%-29.09%) between 0 and 10 days, and 9.15% (95% CI 3.03%-17.47%) between 10 and 30 days. The mortality rate due to ICH secondary to ACT was 0.70% (95% CI 0.00%-3.22%). The surgical reintervention rate due to ICH secondary to ACT was 1.06% (95% CI 0.00%-5.36%). Our results suggest that the risk of ICH and mortality due to early ACT (< 10 days) following intracranial surgery might be overestimated, and this management could be a viable strategy, especially if started 48 h after surgery and in patients who have undergone extra-axial surgery. Nevertheless, it is important to consider the various limitations that may impact these observations, and controlled prospective studies are needed to provide more robust conclusions. Clinical trial number: Not applicable.The timing, safety, and efficacy of prophylactic anticoagulation following craniotomy are well established in the literature. However, anticoagulation therapy (ACT) remains a controversial topic, and the literature on the subject is extremely scarce, preventing robust conclusions about its risks and safety. Our study aims to identify the risks and the best time to start ACT following intracranial surgery. A systematic review was conducted using Embase, PubMed, and Cochrane databases. The primary outcome was intracranial hemorrhage (ICH). Secondary outcomes were mortality and surgical reintervention. Statistical analyses were performed using RStudio 2024.09.0 + 375. Sensitivity analysis was performed using subgroup analysis, and leave-one-out test. The risk of bias was assessed using ROBINS-I. Of 800 potential articles, seven met our inclusion criteria, encompassing a total of 304 patients. The mean age was 56 years and 46% of the patients were male. The main reasons for intracranial surgery were intracranial tumor (48%) and vascular surgery (18%). Intra-axial surgery and starting ACT before the first 48 h were factors associated with higher odds of ICH. The mean interval between the start of ACT and surgery was 5 days, and the mean time from initiation of ACT to ICH was 6.8 days. The ICH rate due to ACT use was 7.96% (95% CI 1.90%-16.86%) between 0 and 30 days after surgery, 11.61% (95% CI 0.98%-29.09%) between 0 and 10 days, and 9.15% (95% CI 3.03%-17.47%) between 10 and 30 days. The mortality rate due to ICH secondary to ACT was 0.70% (95% CI 0.00%-3.22%). The surgical reintervention rate due to ICH secondary to ACT was 1.06% (95% CI 0.00%-5.36%). Our results suggest that the risk of ICH and mortality due to early ACT (< 10 days) following intracranial surgery might be overestimated, and this management could be a viable strategy, especially if started 48 h after surgery and in patients who have undergone extra-axial surgery. Nevertheless, it is important to consider the various limitations that may impact these observations, and controlled prospective studies are needed to provide more robust conclusions. Clinical trial number: Not applicable. The timing, safety, and efficacy of prophylactic anticoagulation following craniotomy are well established in the literature. However, anticoagulation therapy (ACT) remains a controversial topic, and the literature on the subject is extremely scarce, preventing robust conclusions about its risks and safety. Our study aims to identify the risks and the best time to start ACT following intracranial surgery. A systematic review was conducted using Embase, PubMed, and Cochrane databases. The primary outcome was intracranial hemorrhage (ICH). Secondary outcomes were mortality and surgical reintervention. Statistical analyses were performed using RStudio 2024.09.0 + 375. Sensitivity analysis was performed using subgroup analysis, and leave-one-out test. The risk of bias was assessed using ROBINS-I. Of 800 potential articles, seven met our inclusion criteria, encompassing a total of 304 patients. The mean age was 56 years and 46% of the patients were male. The main reasons for intracranial surgery were intracranial tumor (48%) and vascular surgery (18%). Intra-axial surgery and starting ACT before the first 48 h were factors associated with higher odds of ICH. The mean interval between the start of ACT and surgery was 5 days, and the mean time from initiation of ACT to ICH was 6.8 days. The ICH rate due to ACT use was 7.96% (95% CI 1.90%-16.86%) between 0 and 30 days after surgery, 11.61% (95% CI 0.98%-29.09%) between 0 and 10 days, and 9.15% (95% CI 3.03%-17.47%) between 10 and 30 days. The mortality rate due to ICH secondary to ACT was 0.70% (95% CI 0.00%-3.22%). The surgical reintervention rate due to ICH secondary to ACT was 1.06% (95% CI 0.00%-5.36%). Our results suggest that the risk of ICH and mortality due to early ACT (< 10 days) following intracranial surgery might be overestimated, and this management could be a viable strategy, especially if started 48 h after surgery and in patients who have undergone extra-axial surgery. Nevertheless, it is important to consider the various limitations that may impact these observations, and controlled prospective studies are needed to provide more robust conclusions. Clinical trial number: Not applicable. Graphical abstract |
ArticleNumber | 453 |
Author | Gago, Guilherme Vial, Antônio Delacy Martini Silva, Pedro Lorenzo Neves da Nascimento, Anderson Worm, Paulo Valdeci Fin, Manuella Giusti Lindner, Rafaela Jucá Andrade, Erion Junior Kraemer, Jorge Luiz Feltrin, Rafael Henrique Santos Gibbon, Frederico de Lima Schuster, Marcelo Neutzling |
Author_xml | – sequence: 1 givenname: Frederico de Lima orcidid: 0000-0002-5060-7850 surname: Gibbon fullname: Gibbon, Frederico de Lima email: fredericogibbon@hotmail.com organization: Department of Neurosurgery, Santa Casa de Porto Alegre, Postgraduate Program in Medicine: Surgical Sciences, Universidade Federal do Rio Grande do Sul – sequence: 2 givenname: Rafaela Jucá surname: Lindner fullname: Lindner, Rafaela Jucá organization: Department of Medical School, Universidade do Vale do Rio dos Sinos – sequence: 3 givenname: Pedro Lorenzo Neves da surname: Silva fullname: Silva, Pedro Lorenzo Neves da organization: Department of Medical School, Universidade Federal de Ciências da Saúde de Porto Alegre – sequence: 4 givenname: Manuella Giusti surname: Fin fullname: Fin, Manuella Giusti organization: Department of Medical School, Universidade Luterana do Brasil – sequence: 5 givenname: Anderson surname: Nascimento fullname: Nascimento, Anderson organization: Department of Medical School, Universidade Federal de Ciências da Saúde de Porto Alegre – sequence: 6 givenname: Rafael Henrique Santos surname: Feltrin fullname: Feltrin, Rafael Henrique Santos organization: Department of Medical School, Universidade Federal de Ciências da Saúde de Porto Alegre – sequence: 7 givenname: Guilherme surname: Gago fullname: Gago, Guilherme organization: Postgraduate Program in Medicine: Surgical Sciences, Universidade Federal do Rio Grande do Sul, Department of Neurological Surgery, Université Laval – sequence: 8 givenname: Antônio Delacy Martini surname: Vial fullname: Vial, Antônio Delacy Martini organization: Department of Neurosurgery, Santa Casa de Porto Alegre – sequence: 9 givenname: Erion Junior surname: Andrade fullname: Andrade, Erion Junior organization: Department of Neurosurgery, Santa Casa de Porto Alegre – sequence: 10 givenname: Marcelo Neutzling surname: Schuster fullname: Schuster, Marcelo Neutzling organization: Department of Neurosurgery, Santa Casa de Porto Alegre – sequence: 11 givenname: Jorge Luiz surname: Kraemer fullname: Kraemer, Jorge Luiz organization: Department of Neurosurgery, Santa Casa de Porto Alegre – sequence: 12 givenname: Paulo Valdeci surname: Worm fullname: Worm, Paulo Valdeci organization: Department of Neurosurgery, Santa Casa de Porto Alegre |
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Keywords | Craniotomy Systematic review Anticoagulation therapy Intracranial surgery Meta-analysis |
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Snippet | The timing, safety, and efficacy of prophylactic anticoagulation following craniotomy are well established in the literature. However, anticoagulation therapy... |
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SubjectTerms | Anticoagulants - administration & dosage Anticoagulants - adverse effects Anticoagulants - therapeutic use Craniotomy - adverse effects Humans Intracranial Hemorrhages Medicine Medicine & Public Health Neurosurgery Neurosurgical Procedures - adverse effects Postoperative Complications - prevention & control Review Time Factors |
Title | The risks, timing and safety of anticoagulation therapy following intracranial surgery: a systematic review and meta-analysis |
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