Evidence map›Paper›PMID 41676274›Full record

ArticleAmerican journal of translational research2026

Clinical value of targeted arterial infusion of ginkgo biloba extract combined with urokinase in thromboangiitis obliterans.

Ziyuan Liu, Fang Zheng, Guanghui Lu

Abstract read
In one paragraph

Article in American journal of translational research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Ziyuan LiuCardiovascular Center, Liyuan Hospital, Tongji Medical College, Huazhong University of Science and Technology Wuhan 430061, Hubei, China.
Fang ZhengDepartment of Imaging, Army Xiamen Special Service Sanatorium Center Xiamen 361002, Fujian, China.
Guanghui LuDepartment of General Surgery, The Fifth Clinical Medical College of Henan University of Chinese Medicine (Zhengzhou People's Hospital) Zhengzhou 450003, Henan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo investigate the clinical efficacy and safety of targeted artery infusion of Ginkgo biloba extract (GBE) combined with urokinase (URK) for treatment of thromboangiitis obliterans (TAO), and to provide a reference for the optimized treatment of TAO.

methodsA total of 108 male TAO patients (December 2021-December 2023) were retrospectively enrolled and divided into a GBE group (54 cases, single GBE infusion) and a GBE-URK group (54 cases, GBE+URK infusion) after propensity score matching. Both groups received 72-hour continuous infusion, followed by standardized adjuvant therapy and 12-month follow-up. Key indices (pain, hemodynamics, inflammation) and safety/recurrence were compared.

resultsAt 90 days, the GBE-URK group had lower FPS-R scores (1.89±0.84 vs 2.74±0.48, P<0.001), intermittent claudication scores (1.00±0.55 vs 1.69±0.61, P<0.001), and higher pain relief rate (94.44% vs 70.37%, P = 0.001). At 30 days, it had a higher ABI (1.14±0.22 vs 0.82±0.16, P<0.001), TBI (1.09±0.30 vs 0.76±0.26, P<0.001) and lower TNF-α (29.99±4.27 vs 39.99±5.14 pg/mL, P<0.001), ET-1 (189.85±19.20 vs 268.17±37.44 pg/mL, P<0.001). Adverse reaction rates were 7.41% vs 14.81% (P = 0.221); 12-month recurrence-free survival was higher in GBE-URK group (Log-rank P = 0.009). This was confirmed to be an independent factor by multivariable regression (P<0.05).

conclusionsGBE-URK infusion improves pain, hemodynamics, and long-term prognosis in TAO, providing a safe, minimally invasive strategy.

Indexed as

clinical efficacyginkgo biloba extracttarget artery infusionThromboangiitis obliteransurokinase

Identifiers

PMID41676274
PMCPMC12886097

What Socratic holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.