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of requirement for further re-intervention following the deployment of FET, which is significantly high and
these question the safety of recommending a 100 mm vs. 130-160 mm graft length in their “idea” of using
the FET graft.
We all know that using the FET device offers many solutions to acute and chronic pathologies of thoracic
aorta and it has undoubtedly saved many lives. However, the FET is not a benign addition to the
conventional elephant trunk; we believe caution should be taken in patients with borderline indication,
where the sole purpose is an endovascular platform for distal diseases that are not requiring treatment
immediately. Using FET in patients who are not “ideal” candidates can result in incremental and, perhaps,
unnecessary risks of paraplegia, quadriplegia, distal stent-graft induced entry tear, endoluminal thrombosis,
[4]
endoleaks and pressurization from false lumen . Also, the risks associated with chronic dissection flaps
such as sizing issues and stent coarctation should not be ignored. In our opinion, careful patient selection
with favorable anatomy and available multidisciplinary expertise is an ideal approach to minimizing the risk
of avoidable complications at the initial procedure.
DECLARATIONS
Authors’ contributions
Reviewed and approved final form of the letter to editor: Harky A, Othman A, Field M
All authors contributed equally to this paper.
Availability of data and materials
Not applicable.
Financial support and sponsorship
None.
Conflicts of interest
All authors declared that there are no conflicts of interest.
Ethical approval and consent to participate
Not applicable.
Consent for publication
Not applicable.
Copyright
© The Author(s) 2021.
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