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Research Article | Open Access

The pharmacological landscape of chronic subdural hematoma: a systematic review and network meta-analysis of randomized and non-randomized controlled studies

Tao Liu† , Zhihao Zhao†, Mingqi Liu† , Shuo An, Meng Nie, Xuanhui Liu, Yu Qian, Ye Tian, Jianning Zhang( ), Rongcai Jiang ( )
Department of Neurosurgery, Tianjin Neurological Institute, State Key Laboratory of Experimental Hematology, Key Laboratory of Post‐Neuroinjury Neurorepair and Regeneration in Central Nervous System Tianjin & Ministry of Education, Tianjin Medical University General Hospital, 154 Anshan Road, Tianjin 300052, China

†Tao Liu, Zhihao Zhao and Mingqi Liu contributed equally to this work.

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Highlights

• The inaugural network meta-analysis aimed at appraising the efficacy and safety of various traditional and emerging non-surgical interventions for the treatment of CSDH.

• Statins + glucocorticoids may be the most effective pharmacological intervention in preventing recurrence, improving prognosis and facilitating hematoma absorption.

• Tranexamic acid emerges as a promising option for CSDH recurrence prevention, ranking second in effectiveness, suggesting its potential adjunct role in treatment strategies.

• Statins are favored for lowering mortality and adverse events in CSDH patients, emphasizing their significance in treatment. Conversely, antithrombotic agents show inferior outcomes, urging careful treatment selection.

Abstract

Background

There are various treatment modalities for chronic subdural hematoma (CSDH) and there is extensive debate surrounding pharmaceutical interventions. There is no consensus regarding the relative efficacy and safety of multiple treatment modalities. This study aims to investigate this issue and offer potential clinical recommendations.

Methods

We searched PubMed, Web of Science, Embase and the Cochrane Library from January 2000 to May 2023 to identify randomized and nonrandomized controlled studies reporting one or more outcomes associated with the pharmacologic management of CSDH. The primary outcomes of interest included recurrence, favorable prognosis and adverse events, while the secondary outcomes included a reduction in hematoma volume and mortality. Pooled estimates, credible intervals and odds ratios were calculated for all outcomes using a fixed effects model. Confidence in network meta-analysis judgments were employed to stratify the evidential quality. This study was registered with PROSPERO: CRD42023406599.

Results

The search strategy yielded 656 references; ultimately, 36 studies involving 8082 patients fulfilled our predefined inclusion criteria. The findings suggested that statins + glucocorticoids (GCs) ranked highest for preventing recurrence, improving prognosis and facilitating hematoma absorption. Tranexamic acid ranked second highest for preventing recurrence. Statins were found to be the preferred drug intervention for decreasing mortality and preventing adverse events. Antithrombotic agents ranked lowest in terms of decreasing mortality and improving prognosis.

Conclusions

Our findings indicate that statins + GCs may be the most effective treatment modality for preventing recurrence, improving patient prognosis and facilitating hematoma absorption. In terms of reducing mortality and preventing adverse events, statins may be superior to other pharmacological interventions. Routine use of GCs is not suggested for patients with CSDH. Further prospective research is needed to directly compare the efficacy and superiority of various pharmaceutical interventions targeting CSDH to reinforce and validate our findings.

References

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Burns & Trauma
Article number: tkae034

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Cite this article:
Liu T, Zhao Z, Liu M, et al. The pharmacological landscape of chronic subdural hematoma: a systematic review and network meta-analysis of randomized and non-randomized controlled studies. Burns & Trauma, 2024, 12: tkae034. https://doi.org/10.1093/burnst/tkae034

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Received: 22 March 2024
Revised: 21 May 2024
Accepted: 22 May 2024
Published: 10 October 2026
© The Author(s) 2024. Published by Oxford University Press.

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com