Evidence map›Paper›PMID 36544617›Full record

ArticleHealth science reports2023

Retrospective multicenter registry for endovascular treatment with newer devices in over 25-cm femoropopliteal artery disease: A retrospective observational study.

Kazunori Horie, Mitsuyoshi Takahara, Tatsuya Nakama, Akiko Tanaka, Kazuki Tobita, Naoki Hayakawa, Shinsuke Mori, Yo Iwata, Kenji Suzuki

Open access · goldAbstract read
In one paragraph

Article in Health science reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 29% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Article
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

9 authors at 8 institutions in 1 country.

Kazunori HorieDepartment of Cardiovascular Medicine Sendai Kousei Hospital Miyagi Japan.ORCID 0000-0002-8614-7729
Mitsuyoshi TakaharaDepartment of Metabolic Medicine Osaka University Graduate School of Medicine Osaka Japan.ORCID 0000-0001-5105-041X
Tatsuya NakamaDepartment of Cardiology Tokyobay UrayasuIchikawa Medical Center Chiba Japan.ORCID 0000-0001-9107-6438
Akiko TanakaDepartment of Cardiovascular Medicine Sendai Kousei Hospital Miyagi Japan.
Kazuki TobitaDepartment of Cardiology Shonan Kamakura General Hospital Kanagawa Japan.ORCID 0000-0002-1913-6894
Naoki HayakawaDepartment of Cardiovascular Medicine Asahi General Hospital Chiba Japan.ORCID 0000-0002-4168-2808
Shinsuke MoriDepartment of Cardiology Saiseikai Yokohama City Eastern Hospital Kanagawa Japan.ORCID 0000-0001-9037-867X
Yo IwataDepartment of Cardiology Funabashi Municipal Medical Center Chiba Japan.
Kenji SuzukiDepartment of Cardiology Tokyo Saiseikai Central Hospital Tokyo Japan.
Sendai Kousei Hospital · JPAsahi General Hospital · JPFunabashi Municipal Medical Center · JPJuntendo University Urayasu Hospital · JPSaiseikai Central Hospital · JPSaiseikai Yokohama Eastern Hospital · JPShonan Kamakura General Hospital · JPThe University of Osaka · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Aims: Endovascular therapy (EVT) is recommended in femoropopliteal (FP) lesions shorter than 25 cm by current guidelines; however, diffuse FP lesions remains challenging for EVT. The aim of this study was to investigate the efficacy of EVT with the latest devices for FP lesions longer than 25 cm. Methods: This retrospective multicenter registry analyzed patients presented peripheral artery disease (PAD) having FP lesions longer than 25 cm who underwent EVT using the latest devices between 2017 and 2021. The primary outcome was restenosis 1 year after EVT. Results: The present study enrolled a total of 504 PAD patients with 614 lesions undergoing EVT for diffuse FP lesions. The Kaplan-Meier analysis showed that the rates of freedom from restenosis and clinically-driven target lesion revascularization were 79.3% and 82.4% 1 year after EVT, respectively. The multivariate Cox proportional hazards regression analysis showed that clinical features associated independently with restenosis risk were cilostazol use (adjusted hazard ratio, 0.49 [0.32-0.74]; Conclusion: In the current EVT era, the primary patency at 1 year was acceptable at 79.3% in patients with FP lesions longer than 25 cm. A small vessel and P3 segment involvement might be associated with a poor 1-year patency rate after EVT, whereas cilostazol administration might contribute to reducing restenosis.

Indexed as

angioplastydrug eluting stentsendovascular graftinginfrainguinal endovascularstentingvascular centers

Identifiers

PMID36544617
PMCPMC9764405
OpenAlexW4312113176

What OpenQuestion holds

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Registered trials

None linked

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 OpenQuestion graph.