Evidence map›Paper›PMID 42530849›Full record

ArticleCVIR endovascular2026

Contemporary outcomes of a DCB-based strategy with selective stent implantation for femoropopliteal artery lesions: results from the REAL-LEAD registry.

Takafumi Fujita, Makoto Sugihara, Kaori Mine, Kenji Ogata, Shinya Kobata, Shotaro Furukawa, Takumi Yoshiga, Yuta Ishizaki, Kensuke Oe, Atsushi Kakazu and 8 more

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.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

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

18 authors.

Takafumi FujitaDepartment of Cardiology, Fukuoka University School of Medicine, 7-54-1 Jonan, Fukuoka, 814-0180, Japan. bcfit85142@gmail.com.ORCID http://orcid.org/0009-0007-2059-0166
Makoto SugiharaDepartment of Cardiology, Fukuoka University School of Medicine, 7-54-1 Jonan, Fukuoka, 814-0180, Japan.
Kaori MineDepartment of Cardiology, Fukuoka University School of Medicine, 7-54-1 Jonan, Fukuoka, 814-0180, Japan.
Kenji OgataDepartment of Cardiology, Miyazaki Medical Association Hospital, 1173 Arita, Miyazaki, 880-2102, Japan.
Shinya KobataDepartment of Cardiology, Fukuoka University School of Medicine, 7-54-1 Jonan, Fukuoka, 814-0180, Japan.
Shotaro FurukawaDepartment of Cardiology, Kumamoto Rosai Hospital, 1670 Takehara-machi Yatushiro, Kumamoto, 866-0826, Japan.
Takumi YoshigaDepartment of Internal Medicine, Division of Cardiovascular Medicine, Kurume University School of Medicine, 67 Asahi-Machi, Kurume, 830-0011, Japan.
Yuta IshizakiDepartment of Internal Medicine, Division of Cardiovascular Medicine, Kurume University School of Medicine, 67 Asahi-Machi, Kurume, 830-0011, Japan.
Kensuke OeDepartment of Cardiology, St. Mary's Hospital, 422 Kurume, Fukuoka, 830-8543, Japan.
Atsushi KakazuDepartment of Cardiology, Yuuai Medical Center, 50-5 Yone, Tomigusuku-City, , Okinawa, 901-0224, Japan.
Ryosuke YanariDepartment of Cardiology, Fukuoka Seisyukai Hospital, 4-11-8 Kasuya, Fukuoka, 811-2316, Japan.
Ryoichi KyuragiDepartment of Surgery, Saiseikai Karatsu Hospital, 817 Motohata, Karatsu, Saga, 847-0852, Japan.
Shoichiro FurukawaDepartment of Cardiology, Aso Iizuka Hospital, 3-83 Iizuka, Fukuoka, 820-0018, Japan.
Saburo KusumotoDepartment of Cardiology, Nagasaki Harbor Medical Center, 6-39 Shinchi-Machi, Nagasaki, 850-8555, Japan.
Ryohei AkashiDepartment of Cardiovascular Medicine, Nagasaki University Graduate School of Biomedical Sciences, 1-7-1 Sakamoto, Nagasaki, 852-8501, Japan.
Eiji KarashimaDepartment of Cardiology, Shimonoseki City Hospital, 1-13-1 Shimonoseki, Yamaguchi, 750-8520, Japan.
Hideki DoiDepartment of Cardiology, Kumamoto Rosai Hospital, 1670 Takehara-machi Yatushiro, Kumamoto, 866-0826, Japan.
Shin-Ichiro MiuraDepartment of Cardiology, Fukuoka University School of Medicine, 7-54-1 Jonan, Fukuoka, 814-0180, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundA drug-coated balloon (DCB)-based "leave-nothing-behind" strategy has become a predominant approach for femoropopliteal artery (FPA) lesions in contemporary clinical practice. However, despite the intention to complete procedures with DCB alone, stent implantation is frequently required because of severe dissection, elastic recoil, or suboptimal lesion preparation. Whether DCB angioplasty combined with selective stent implantation compromises 1-year primary patency compared with DCB monotherapy remains uncertain.

methodsIn this prospective multicenter registry, 310 limbs in 277 patients undergoing endovascular therapy for FPA lesions between September 2021 and December 2022 were enrolled. Thirty-seven limbs were excluded if they had isolated common femoral artery lesions (n = 8), were treated with bare nitinol stents or stent grafts (n = 25), or were treated with plain old balloon angioplasty alone (n = 4). A total of 273 limbs in 254 cases were included in the primary outcome analysis. Patients were categorized into three groups: the DCB group (balloon angioplasty with DCB alone), the drug-eluting stent (DES) group (implantation of Eluvia™ or Zilver PTX™), and the Combination group (DCB angioplasty combined with DES). The primary endpoint was 1-year primary patency. Secondary endpoints included freedom from clinically driven target lesion revascularization (CD-TLR) and clinically driven target vessel revascularization (CD-TVR), which were assessed using Kaplan-Meier analysis. Factors associated with loss of primary patency were evaluated using Cox regression analysis.

resultsDCB monotherapy was performed in 78.3% of cases, DESs in 10.9%, and combination therapy in 10.6%. The overall 1-year primary patency rate was 84.0%, with no significant differences among strategies (DCB: 84.1%, DES: 84.6%, Combination: 82.8%; log-rank p value = 0.91). Freedom from CD-TLR and CD-TVR at 1 year was 88.7% and 93.8%, respectively. Chronic limb-threatening ischemia and history of revascularization were independently associated with loss of primary patency. Combination therapy was not associated with an increased risk of loss of primary patency.

conclusionA DCB-based strategy with selective scaffolding may achieve acceptable patency outcomes.

Indexed as

Drug-coated balloon (DCB)Endovascular treatment (EVT)Femoropopliteal artery lesions (FPA lesions)Lower extremity arterial disease (LEAD)

Identifiers

PMID42530849
PMCPMC13424274

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.