Comparing Efficacy and Safety of Different Anticoagulants in Cerebral Venous Thrombosis: A Systematic Review and Network Meta-Analysis
Research article published in Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis (2026)
Abstract
BackgroundCerebral venous thrombosis (CVT) is a rare but severe type of stroke, typically treated with vitamin K antagonists (VKAs). This study compares different direct oral anticoagulants (DOACs) with VKAs for the management of CVT.MethodsPubMed, Cochrane Central, and ScienceDirect were searched up to May 2025. A network meta-analysis using a frequentist approach was performed in RStudio version 4.3.3. P-scores were used to rank treatments. The evaluated outcomes included full recanalization, recurrent venous thromboembolism (VTE), major hemorrhage, intracranial hemorrhage (ICH), and mortality. The Cochrane Risk of Bias (RoB 2.0) tool and the Newcastle-Ottawa Scale (NOS) were employed to assess the quality of randomized controlled trials (RCTs) and observational studies.ResultsOur analysis included 16 studies involving 1403 patients. We found that various DOACs, including apixaban, dabigatran, and rivaroxaban, had rates of full recanalization, VTE recurrence, major hemorrhage, ICH, and mortality comparable to those of VKAs. VKAs showed the highest likelihood of full recanalization, with a P-score of 0.70, whereas apixaban had the lowest, with a P-score of 0.04. For reducing recurrent VTE rates, apixaban was the most effective (P-score = 0.83), and dabigatran the least (P-score = 0.04). Apixaban also led to the greatest reduction in ICH risk (P-score = 0.70), while rivaroxaban had the lowest likelihood (P-score = 0.29). Regarding major hemorrhage, apixaban had the highest probability of reduction (P-score = 0.81), with VKAs performing worst (P-score = 0.26). Lastly, apixaban ranked highest for reducing mortality (P-score = 0.78), whereas VKAs ranked lowest (P-score = 0.39).ConclusionDOACs showed no significant differences in rates of full recanalization, VTE recurrence, major hemorrhage, ICH, or mortality compared with VKAs. Apixaban had the highest probability of reducing VTE recurrence, mortality, and hemorrhagic events, whereas VKAs had the highest probability of achieving full recanalization.
Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.
Zusammenfassung
Peer-reviewed clinical and outcomes research relevant to medicinal leech therapy and its biology. Indexed in PubMed and verified against the NCBI record.
Warum dies für die Hirudotherapie relevant ist
Diese systematische Übersichtsarbeit und frequentistische Netzwerk-Metaanalyse (16 Studien, 1.403 Patienten) verglich DOAC mit Vitamin-K-Antagonisten bei zerebraler Venenthrombose und fand keine signifikanten Unterschiede bei vollständiger Rekanalisation, rezidivierender VTE, schwerer Blutung, intrakranieller Blutung oder Mortalität; gemäß der P-Score-Rangfolge erreichten Vitamin-K-Antagonisten am wahrscheinlichsten eine vollständige Rekanalisation, während apixaban bei der Reduktion von VTE-Rezidiven, Mortalität und hämorrhagischen Ereignissen am höchsten rangierte. Ihre Relevanz für die Hirudotherapie ist indirekt und auf Klassenebene: dabigatran, einer der verglichenen direkten Thrombininhibitoren, wirkt auf dasselbe Ziel wie das Blutegelpeptid hirudin, sodass die Analyse diese Wirkstoffklasse in die Evidenz zu einer schweren thrombotischen Erkrankung einordnet. Einschränkung: Diese Evidenzsynthese poolt heterogene RCT und Beobachtungsstudien synthetischer Antikoagulanzien (keine Blutegeltherapie), die Gesamtzahl der Patienten ist für eine seltene Erkrankung gering, und die P-Score-Rangfolgen geben Wahrscheinlichkeiten und keine direkte Überlegenheit im Kopf-an-Kopf-Vergleich an.
Zitation
Comparing Efficacy and Safety of Different Anticoagulants in Cerebral Venous Thrombosis: A Systematic Review and Network Meta-Analysis.
Waseem et al. · Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis, 2026
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