Application of a nomogram model for the prediction of 90-day poor outcomes following mechanical thrombectomy in patients with acute anterior circulation large-vessel occlusion.

Authors:
Li X; Li C; Liu AF; Jiang CC; Zhang YQ and 5 more

Journal:
Front Neurol

Publication Year: 2024

DOI:
10.3389/fneur.2024.1259973

PMCID:
PMC10836145

PMID:
38313559

Journal Information

Full Title: Front Neurol

Abbreviation: Front Neurol

Country: Unknown

Publisher: Unknown

Language: N/A

Publication Details

Subject Category: Clinical Neurology

Available in Europe PMC: Yes

Available in PMC: Yes

PDF Available: No

Transparency Score
4/6
66.7% Transparent
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Evidence found in paper:

"Conflict of interest The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest."

Evidence found in paper:

"The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This study was supported by the grants from the National Key Basic Research Program of China (973 program) (grant no. 2013CB733805), the National Natural Science Foundation of China (grant no. 81871464), and the Joint Project of Inner Mongolia Medical University (grant no. YKD2021LH085)."

Evidence found in paper:

"This study was a retrospective investigation of the prospectively collected data from the Jrecan trial between 1 March 2018 and 30 June 2019, which was named as the training set. The Jrecan trial was a prospective, multicenter, randomized, non-inferiority clinical trial comparing the efficacy and safety of two MT stents (the Jrecan revascularization device and the Solitaire device) in patients with AC-LVO stroke. The trial involved 16 comprehensive stroke centers in China. Each center handled more than 50 cases of MT annually, and each neuro-interventionalist performed at least 10 MT procedures per year. The Jrecan trial was approved by the ethics committees of the participating centers and was duly registered with the Chinese Clinical Trial Registry, http://www.chictr.org.cn/showproj.aspx?proj=23396, identifier ChiCTR-TOC-17013822. The patient data for the validation set were retrospectively collected from Baotou Center Hospital between January 2013 and December 2020 and approved by the ethics committee of Baotou Center Hospital. Informed consent was obtained from the participants or their legal representatives. The flowchart of the patient profile is shown in ."

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Last Updated: Aug 05, 2025