Evidence map›Paper›PMID 42458134›Full record

ArticleCVIR endovascular2026

Clinical feasibility of primary retrograde endovascular therapy via trans-ankle intervention: a retrospective single-center study.

Hiromi Miwa, Naoki Hayakawa, Toshiki Tsurumaki, Yasuyuki Tsuchida, Masanao Inoue, Shinya Ichihara, Shunichi Kushida

Abstract read
In one paragraph

Article in CVIR endovascular, 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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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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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Hiromi MiwaDepartment of Cardiovascular Medicine, Asahi General Hospital, Chiba, Japan. hiromi.n.saito@gmail.com.ORCID http://orcid.org/0009-0005-4785-7452
Naoki HayakawaDepartment of Cardiovascular Medicine, Asahi General Hospital, Chiba, Japan.
Toshiki TsurumakiDepartment of Cardiovascular Medicine, Asahi General Hospital, Chiba, Japan.
Yasuyuki TsuchidaDepartment of Cardiovascular Medicine, Asahi General Hospital, Chiba, Japan.
Masanao InoueDepartment of Cardiovascular Medicine, Asahi General Hospital, Chiba, Japan.
Shinya IchiharaDepartment of Cardiovascular Medicine, Asahi General Hospital, Chiba, Japan.
Shunichi KushidaDepartment of Cardiovascular Medicine, Asahi General Hospital, Chiba, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTrans-ankle intervention (TAI) through retrograde distal access via below-the-knee and below-the-ankle arteries has been increasingly reported as an alternative approach for the treatment of femoropopliteal (FP) lesions. Although previous studies have described the procedural success of this strategy, its clinical feasibility and post-procedural outcomes remain insufficiently characterized.

methodsIn this retrospective single-center study, the data from 33 patients with 36 FP lesions who underwent endovascular therapy (EVT) between January 2024 and January 2025 were analyzed. The primary endpoint was procedural success. The secondary endpoints were clinical worsening of lower-limb ischemia within 30 days, 1-year freedom from clinically driven target lesion revascularization (CD-TLR), and procedural complications. The risk of post-procedure access vessel occlusion was also investigated.

resultsTAI was performed via access sites ranging from the anterior tibial artery (ATA) to the dorsalis pedis artery in all patients. Procedural success was achieved in all cases, and the rate of 1-year freedom from CD-TLR was 91.8%. All patients had FP lesions, including three cases up to the iliac artery. Forty-two percent was chronic total occlusion, and EVT of the ATA was required in 42% of the cases to establish the access route. Ten cases (27.8%) were approached via the occluded pre-ATA, and 15 (41.7%) required intervention to approach the vessel. The average number of pre-procedural and post-procedural below-the-knee artery runoff vessels was 2.4 and 2.75, respectively. No patients showed clinical worsening within 30 days. The risk factors for ATA occlusion were hemodialysis, ATA intervention, and approach via the occluded ATA.

conclusionsTAI may represent a feasible result, especially for selected FP lesions. Although no clinical worsening was observed, an increased risk of postoperative ATA occlusion existed in patients on hemodialysis and those with access site atherosclerosis requiring ATA intervention. However, in these high-risk populations, this limitation may potentially be overcome by an approach through the occluded ATA.

Indexed as

Endovascular therapyFemoropopliteal arteryTibial arteryTrans-ankle intervention

Identifiers

PMID42458134
PMCPMC13373098

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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.