Evidence map›Paper›PMID 32547765›Full record

ArticleSAGE open medical case reports2020

Dual alternate access sites for the treatment of an ostial left common iliac artery chronic total occlusion.

Mohan Satish, Sanjum S Sethi, Sahil Parikh, Philip Green, Justin Ratcliffe

Abstract readCase Reports
In one paragraph

Article in SAGE open medical case reports, 2020. 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

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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

5 authors.

Mohan SatishCenter for Interventional Vascular Therapy, Columbia University Irving Medical Center/New York Presbyterian Hospital, New York, NY, USA.ORCID https://orcid.org/0000-0003-3567-8877
Sanjum S SethiCenter for Interventional Vascular Therapy, Columbia University Irving Medical Center/New York Presbyterian Hospital, New York, NY, USA.
Sahil ParikhCenter for Interventional Vascular Therapy, Columbia University Irving Medical Center/New York Presbyterian Hospital, New York, NY, USA.
Philip GreenCenter for Interventional Vascular Therapy, Columbia University Irving Medical Center/New York Presbyterian Hospital, New York, NY, USA.
Justin RatcliffeCenter for Interventional Vascular Therapy, Columbia University Irving Medical Center/New York Presbyterian Hospital, New York, NY, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Growing endovascular strategies with TASC D lesions in aortoiliac disease reflect increasing technical success with evidenced safety and efficacy. In cases of failed transfemoral access, revascularization of iliac chronic total occlusions has prompted the utilization of other alternate access sites (e.g. transradial and transbrachial approaches) as important options in aortoiliac TASC D lesions. We describe a case of successful revascularization of an occluded ostial left common iliac artery in an 81-year-old man using a dual ulnar and tibioperoneal approach (absent radial artery). A Controlled Antegrade and Retrograde Tracking technique was performed where a balloon was advanced from the peroneal artery into the distal cap of the chronic total occlusion in the proximal common femoral artery. Balloon inflation was performed and a glidewire from transulnar access was advanced and re-entered into the true lumen in the common femoral artery. The wire was then snared and externalized out the transpedal access site creating a continuous true lumen from the ulnar artery to the peroneal artery. To reconstruct the aortic bifurcation, kissing balloon inflations were performed from the peroneal as well as the ulnar artery approaches. A 10 mm × 59 mm balloon expandable stent was placed in the ostial left common iliac artery and a 8 mm × 60 mm self-expanding stent was placed in the left external iliac artery successfully.

Indexed as

alternate access siteCardiovascularchronic total occlusioniliac artery stenosisperipheral artery diseasesurgerytranspedal interventiontransradial intervention

Identifiers

PMID32547765
PMCPMC7273553

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