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44 Patient Selection forEndovascular AAA Repair
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Wallaert JB, etal. Designation as “unt for open repair” is associated with poor outcomes after endovascular aortic aneurysm repair.
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33. Pane B, Spinella G, Signori A, Musio D, Perfumo MG, Lucertini
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34. Sobocinski J, Maurel B, Delsart P, d’Elia P, Guillou M, Maioli F,
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35. Timaran CH, Veith FJ, Rosero EB, Modrall JG, Arko FR, Clagett
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36. Bush RL, Johnson ML, Hedayati N, Henderson WG, Lin PH,
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Aulivola B, Cho JS.Outcomes of endovascular abdominal aortic
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38. Kontopodis N, Galanakis N, Charalambous S, Matsagkas M,
Giannoukas AD, Tsetis D, Ioannou CV, Antoniou GA. Editor’s
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39. Truijers M, Resch T, Van Den Berg JC, Blankensteijn JD, Lonn
L.Endovascular aneurysm repair: state-of-art imaging techniques
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40. Picel AC, Kansal N.Essentials of endovascular abdominal aortic
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41. Saida T, Mori K, Sato F, etal. Prospective intraindividual comparison of unenhanced magnetic resonance imaging vs contrastenhanced computed tomography for the planning of endovascular
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42. Keefer A, Hislop S, Singh MJ, Gillespie D, Illig KA.The inuence
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46. Linsen MA, Jongkind V, Nio D, Hoksbergen AW, Wisselink
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49. DeRubertis BG, Quinones-Baldrich WJ, Greenberg JI, Jimenez
JC, Lee JT. Results of a doublebarrel technique with commercially available devices for hypogastric preservation during aortoiliac endovascular abdominal aortic aneurysm repair. J Vasc Surg.
2012;56:1252–9.
50. Bosanquet DC, Wilcox C, Whitehurst L, Cox A, Williams IM,
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51. Papazoglou KO, Sfyroeras GS, Zambas N, Konstantinidis K,
Kakkos SK, Mitka M.Outcomes of endovascular aneurysm repair
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54. Parodi JC, Ferreira M.Relocation of the iliac artery bifurcation to
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Preprocedural Planning
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andMeasurements forEVAR
TheodosiosBisdas
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Background
The endovascular repair (EVAR) of non-complex infrarenal abdominal aortic aneurysms (AAA) is the standard of
care in the majority of health systems worldwide [1]. At
present, there is a plethora of endovascular devices with
different characteristics and features; however, the principles of planning and measurement remain the same [2]. It
is crucial for the nal outcome that the physician is able to
make his/her own measurements and select the most
appropriate device. The rule of “6Ps” (prior proper plan-
ning prevents poor performance) reects that the preoperative planning is equally important to the intervention
itself. In this chapter, we present the basic principles of
planning and measurements which can be applied to all
standard AAAs and devices.
Preoperative Clinical Assessment
The rst important step is to assess the clinical status of the
patient. The examination includes palpation of the abdomen
and the peripheral pulses, measurement of the ankle-brachial
index, duplex ultrasound of both carotid and popliteal arteries, and exclusion of any skin infection at the level of the
groin.
Assessment oftheComputed Tomography
Angiography (CTA): Drawing
oftheAneurysm
The CTA should be maximum 6months old, at least 1mm
in thickness, and should cover the renovisceral segment up
to the proximal part of the supercial femoral artery at both
sides. During the rst brief assessment, the physician looks
for possible co-existing aneurysms in the aorta (e.g., visceral arteries) or other pathological ndings from the
scanned area. The next step is to upload the CTA in a dedicated software for EVAR (e.g., Endosize, 3Mensio) or to
perform the measurements manually through OsiriX or
RadiAnt DICOM Viewer. After the upload, we strongly recommend drawing the AAA on a sheet of paper (Fig.45.1),
which will include all important details for both patient and
CTA. Such details are:
1. Name of the patient, date of birth
2. Date of CTA, thickness
3. Morphology of the AAA, all relevant diameters and
lengths
4. All relevant anatomic characteristics, which can cause
problems during the intervention (e.g., patchplasty of the
common femoral artery, hostile abdomen, calcication,
stenosis, femoral bifurcation above the inguinal ligament,
dissection of the arteries, stenosis of the renal arteries,
inferior mesenteric artery with >3mm diameter)
T. Bisdas (*)
Clinic for Vascular Surgery, Athens Medical Center,
Athens, Greece
© The Author(s), under exclusive license to Springer Nature Switzerland AG 2024
G. Geroulakos et al. (eds.), Mastering Endovascular Techniques, https://doi.org/10.1007/978-3-031-42735-0_45
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Fig. 45.1 Example of drawing an infrarenal aortic aneurysm on a sheet
of paper and all relevant information needed for a successful endovascular aortic repair
Creating theCenterline: Step-by-Step
Measurement
During the measurements, it is crucial to create automatically or manually the centerline. The centerline essentially
represents the position of the stiff guidewire through which
the device will be delivered. It is obvious that two centerlines
should be created, one for each iliac axis and one for the
abdominal aorta. In case of angulated infrarenal neck and/or
elongated iliac arteries, any calculation of the lengths will be
wrong with the risk of a poor nal outcome or the need for
more devices (Fig.45.2).
After the creation of the centerline, the physician should
follow the next steps:
Step 1: The rst measurement is the diameter of the infra-
renal aorta just below the lowest renal artery. It is important
Fig. 45.2 Measurement of the aneurysm length by (a) adding the
length of each slide of a CT angiography and (b) using the centerline
to mention which is the lowest renal artery in your drawing.
Moreover, you have to assess from which view you will see
precisely the origin of the lowest renal artery and the least
parallax of the proximal markers. This calculation will lead
to lower administration of contrast agent and use of radiation. However, it is feasible mainly in dedicated software for
EVAR planning. According to the instructions for use (IFU),
you have to measure the diameter of the aorta 15–20mm
below the lowest renal artery. We recommend measuring the
aorta at three different points, level of the lowest renal artery,
10mm below it, and 20mm below it, and selecting the diameter of the device according to the rst two diameters. The
main reason for this strategy is that the proximal sealing of
the stent graft is based mainly on the rst stent of the devices
which is 10 mm in length in the majority of the EVAR
devices. In specic cases of hostile proximal neck (bulged,
reversed tapered, tapered), the diameter of the aorta at 20mm
should be taken into consideration for the diameter of the
EVAR device. In such cases, the operator should know that
the implantation might be outside the IFUs and inform the
patient accordingly.
All manufacturers recommend 20% oversizing of the
EVAR device and we strongly agree with this recommendation. However, in angulated necks, the centerline does not
always represent the real position of the guidewire during the

LL L
=
−
LL L
=−−or
LL L
=
−
45 Preprocedural Planning andMeasurements forEVAR
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gate through the common femoral artery, and thus the physician has to change the entry site of the main body. This
maneuver will facilitate the cannulation of the contralateral
limb having the sac at the opposite site of the gate.
Step 3: The last step is to measure the diameter and the
length of the common iliac arteries. In general, it is suggested to measure the distance up to the iliac bifurcation and
to cover it with the iliac limb accordingly. However, this
strategy is not always necessary in long common iliac
arteries. In any case, the physician should dene a distal
landing zone of at least 20mm (in some devices 15mm) and
measure the proximal and distal diameter or the common
iliac artery. The length and the diameter of the limb will be
selected accordingly and always taking into consideration
the IFUs of the manufacturer.
The physician should calculate the length of the iliac limb
using the following formula:
Fig. 45.3 Diameter of the aorta in angulated neck based on the centerline (red line, 27mm) and the real landing zone of the device (yellow
line, 29mm). The device was selected with a diameter of 36mm
intervention. Thus, and according to our experience, our
common practice in angulated necks is to perform a 30%
instead of 20% oversizing (Fig.45.3). In any case, we recommend always ordering an aortic extension in angulated
necks in case you identify a type Ia endoleak
intraoperatively.
Step 2: The next step is to assess the distance between the
lowest renal artery and the bifurcation. This measurement is
important in order to ensure that the contralateral gate of the
bifurcated endograft will open adequately inside the aneurysm sac. Thus, we recommend measuring the distance from
the lowest renal artery up to 0.5–1cm above the bifurcation
in order to be sure that the contralateral limb will be adequately opened and catheterized during the intervention.
During this step, it is important to assess and highlight in
your drawing any important anatomic challenges regarding
the morphology of the aneurysm sac (Fig.45.1). For instance,
opening the contralateral limb in saccular aneurysms may
lead to a challenging or even impossible cannulation of the
where L
limblowerRA IliacBif MBTube
length of the iliac limb, L
limb
−
lower RA–Iliac Bif
length
between the lowest renal artery and the distal landing point
above the iliac bifurcation, and L
length between cra-
MB Tube
nial graft edge and bifurcation of the graft.
In case the company does not include the overlapping
zone in the provided length of the limbs (e.g., Zenith Spiral
Z, COOK Medical), the formula changes to the following:
where L
limblowerRA IliacBif MBcontralat
limblowerRA IliacBif MBipsilat
length of the iliac limb, L
limb
−
lower RA–Iliac Bif
length
between the lowest renal artery and the distal landing point
above the iliac bifurcation, and L
MB contralat
cranial graft edge and end of the contralateral limb or L
length between cranial graft edge and end of the ipsilat-
ipsilat
length between
MB
eral limb.
There are a few devices where the iliac leg should not
necessarily overlap the total length of the ipsilateral or contralateral limb (in situ measurement). We recommend always
using total overlapping length. There are two scenarios
where this option is useful: (1) in case of the tortuous iliac
arteries where the selected limb is shorter than initially considered and (2) if the required length for the iliac leg is not
represented in the available limbs of the manufacturer (e.g.,
length to cover: 134 mm, available device 124 mm or
156mm in length).
Take-Home Messages
• Draw the aneurysm on a sheet of paper.
• Be aware of all relevant issues (stenosis, tortuosity, dis-
section, thrombus, etc.) that may inuence your interven-
tion—notice all issues in your drawing.

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• Plan your intervention according to the respective IFU of
each manufacturer.
• Identify the right landing zone, especially in case of angulated necks.
• Oversize adequately.
• Learn all features and sizes of the endograft you use.
• Start with one endograft until you build your own learning curve.
References
1. Donas KP, Torsello G, Bisdas T.New EVAR devices: pros and cons.
J Cardiovasc Surg (Torino). 2012;53(5):559–69.
2. Bisdas T, Weiss K, Eisenack M, Austermann M, Torsello G,
Donas KP.Durability of the endurant stent-graft in patients undergoing endovascular abdominal aortic aneurysm. J Vasc Surg.
2014;60(5):1125–31.

Introduction toEndografts
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forInfrarenal AAAs
AndreasM.Lazaris
History
The history of endovascular treatment of aortic aneurysm
diseases began about four decades ago. It was May 4, 1985,
when a Ukrainian (USSR) cardiovascular surgeon, Professor
Nikolai Leontyevich Volodos (Fig.46.1), implanted the rst
hand-made endograft into iliac arteries. His patient had presented with lower limb gangrene secondary to multi-level
peripheral arterial occlusive disease. The patient was treated
by inserting a stent graft into the iliac arteries, followed by a
femorotibial venous bypass graft [1]. In March 1987, following extensive preclinical work in models and cadavers,
Volodos and his team implanted the rst aortic stent graft in
history. The patient had presented with a false aneurysm of
the descending thoracic aorta [1]. The patient survived
18 years after the aneurysm exclusion with this rst-ever
stent graft. In 1986, Volodos published his rst report about
the use of “self-xing synthetic blood vessel endoprosthesis”
[2]. It probably did not receive wide acceptance because it
was written in Russian. In 1989, Volodos and his colleagues
tried to treat an abdominal aortic aneurysm (AAA) with a
stent graft using a unibody bifurcated endoprosthesis.
Unfortunately, the unsupported contralateral limb twisted,
and the endovascular procedure was converted to open surgery [3].
At the same time, Juan Parodi, a vascular surgeon from
Argentina, then a clinical fellow at the Cleveland Clinic in
Ohio, USA, conceived his idea for a stent graft to treat AAA.
Parodi proved that his early concept of stent grafts, based on
zigzag stents in combination with polyurethane, was workable in dogs. However, he never published his work [3]. In
1988, when he met Julio Palmaz, and through him obtained
the balloon-expandable Palmaz stent, he was able to use the
combination of his straight tubular polyester stent graft with
a Palmaz stent as a proximal xation to treat his rst patient
with an AAA on September 7, 1990, with great success
A. M. Lazaris (*)
Vascular Surgery Department, Attikon University Hospital,
National and Kapodistrian University of Athens, Athens, Greece
46
Fig. 46.1 Nicolai Leontievich Volodos was a Soviet and Ukrainian
cardiovascular surgeon and scientist. Volodos developed and introduced
the world’s rst endovascular stent graft into clinical practice for treating stenotic and aneurysmal diseases of the arterial system
(Fig.46.2). In 1991, Parodi published the details of the rst
ve patients, all treated successfully with straight tubular
endografts (Fig.46.3) [4].
Following these two pioneers, the endovascular treatment
of aortic aneurysm disease exploded. The concept of stent
graft treatment for aortic aneurysms rapidly spread to the
USA, Australia, and Europe. Geoff White, Jim May, Michael
© The Author(s), under exclusive license to Springer Nature Switzerland AG 2024
G. Geroulakos et al. (eds.), Mastering Endovascular Techniques, https://doi.org/10.1007/978-3-031-42735-0_46
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Fig. 46.2 Illustration of the
rst custom-made endografts.
The surgeons created the
endografts on the operating
theater’s back table.
Balloon-expandable stents
anchor the graft onto the
aortic wall [4]
A. M. Lazaris

46 Introduction toEndografts forInfrarenal AAAs
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489
The invention of endovascular aortic repair (EVAR) took
place almost in the same period, in multiple locations around
the world, on a simultaneous invention concept of invention
and discovery, found in other elds of development such as
aviation and automotive vehicle manufacturing. Like other
elds of medicine, Vascular Surgery owes a great deal to its
development in biology and engineering evolution. The
growth and expansion of EVAR sprang from a simple common idea of a small group of inventive radiological and surgical visionaries, ourished almost simultaneously in
industrial laboratories and hospital operating rooms, and
became one of the most signicant discoveries in the history
of medicine.
Fig. 46.3 Endovascular grafts composed from commercially available
materials, used for the repair of aortic and peripheral artery aneurysms,
arterial occlusions, and traumatic vascular injuries [5]
Lawrence-Brown, and David Hartley in Australia contributed signicantly to developing aortic stent grafts and using
them to treat patients. In the 1990s, tubular aortic stent grafts
were the way to treat patients with aortic aneurysm disease.
However, it soon became apparent that common iliac arteries
and the abdominal aorta should be part of the treatment
option. Thus, the idea of using bifurcated or aorto-uni-iliac
endograft systems soon became necessary. Vascular surgeons such as Tim Chutter from the USA and Krassi Ivancev
from Sweden proposed their solutions to this concept. The
involvement of industry and vascular surgery pioneers inevitably boosted the design and development of the stent- graft
philosophy. Cook Inc. (Bloomington, Indiana, USA) was an
example, working closely with a signicant number of vascular surgeons, such as Michale Lawrence Brown and David
Hartley in Perth (Australia), Krassi Invacev in Malmoe
(Sweden), Brian Hopkinson in Nottingham (England), Tim
Chutter in Cornell (USA), Wof Stelter in Frankfurt
(Germany), and Eric Verhoeven in Groningen (Netherlands).
Soon, other companies followed, such as Gore (W.L. Gore
& Associates, Incorporated, Flagstaff, Arizona), Medtronic
(Medtronic Vascular, Santa Rosa, California), and many others in the following years. Famous worldwide vascular surgeons, well known for their open aortic surgery skills, made
a signicant shift in their careers, embracing with enthusiasm the new technology. Frank Veith in NewYork (USA),
Edward “Ted” Dietrich in Phoenix (USA), Peter Bell in
Leicester (UK), and Roger Greenhalgh in London (UK)
were some of them.
The need to preserve the normal anatomy led to the development of fenestrations and directional branches. Marcel Goodman
in Perth (Australia), Wolf Stelter in Frankfurt (Germany), and
Tim Chuter and Roy Greenberg in the USA proposed and implemented fenestrations for splanchnic vessels.
Design andCharacteristics ofAortic
Endografts
The evolution of endografts has undergone multiple changes
over time. Numerous generations of technological advancements based on physician and engineering feedback have
addressed areas of clinical need, improved deliverability,
decreased prole, and promoted better conformability to tortuous anatomy. Nevertheless, a similar general philosophy
exists for all endografts. Every aortic endograft is comprised
of two distinct components: the sheath with the delivery system and the endograft.
Sheath andDelivery System
The sheath is a necessary component of the aortic endograft
device, ensuring the device’s safe insertion into the arterial
system. In most devices, the endograft and the sheath are
combined into one single sheath-endograft unity. An exception to this general concept is the Gore endograft delivered
through a separately provided sheath. The delivery system
and the endograft are loaded in an over-the-wire fashion and
brought into the arterial system.
The sheaths and delivery systems of all modern endograft
devices have some common general characteristics:
1. Hydrophilic coating. The sheath is covered by a hydro-
philic cover which reduces the friction resistance.
Hydrophilic coating permits easy insertion and removal
of the sheath, minimizing the risk of artery spasm.
2. Conical tip. The tip of the sheath is conical, allowing
easy and safe insertion into the arterial system.
3. Low prole. First- and second-generation delivery sys-
tems were bulky, blunt-ended, and stiff. The advances in
engineering allowed the development of narrow delivery
systems, reducing the rate of iliac artery trauma, and
allowing endovascular treatment in patients with small

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A. M. Lazaris
iliofemoral access arteries, like those with severe calcication or those with iliac vessels of small caliber, for
example women.
4. Controlled deployment. Most delivery systems allow a
controlled endograft deployment, increasing the accuracy
of positioning inside the aorta. The existence of gradual
stent-graft-releasing mechanisms in endograft devices
accomplishes this.
Endograft
The endograft is usually preloaded in the sheath, except for
the Gore device, where the sheath and endograft are distinct
components. There is a wide availability of different devices
today (Fig.46.4), with plenty of similarities but also some
unique differences:
• Endograft coating. Endografts are made of polyester
(Dacron) or polytetrauorethylene (PTFE).
• Metallic skeleton. A metallic frame (skeleton) supports
the endograft. In the rst generations of endografts the
skeleton was made of stainless steel, which is rarely used
nowadays. Most endografts frames today are made of
nitinol, an alloy of nickel and titanium. The skeleton lies
either outside the graft (exoskeleton) or, more rarely,
inside the graft (endoskeleton), and it is secured on the
graft with tiny non-absorbable sutures. The conguration
of the skeleton can be either circular or, more often, in a
Z-stent fashion.
• Endograft packing. The endograft is packed in a collapsed state inside the sheath of the delivery system. In
the Gore device, in contrast to other devices, the endograft is brought as a separate unit; it is collapsed around
the delivery system and is inserted into the sheath by the
surgeon during the surgical procedure.
• Fixation systems. The xation of the endograft on the
healthy proximal aorta is necessary to minimize the possibility of distal migration and is achieved in various ways.
On the top end of the endograft there are various types of
anchoring adjuncts like hooks, barbs, and anchors that
embed into the aortic wall. Fixation is also enhanced by
the radial force of the metallic frame produced by the
stents of the skeleton (Z-stent or circular). The endograft
oversizing, as compared to the size of the native proximal
aortic neck, is necessary to achieve an adequate radial
force increasing the endograft stabilization on the healthy
aortic neck. In some grafts, a longitudinal metallic wire
along the endograft enhances the xation of the endograft
by increasing its columnar strength. Finally, most endografts carry a line of triangular-shaped are metal stents on
their top end, which contributes to the stabilization and
xation of the endograft on the suprarenal aorta. A unique
idea for endograft stabilization exists in the Endologix
AFX Powerlink graft. Its unibody bifurcated design allows
the positioning of the endograft over the aortic bifurcation,
eliminating the possibility of distal migration.
• Endograft repositioning. After the endograft is extracted
from the sheath, it cannot be reloaded back on the sheath.
However, most modern endografts are repositionable,
Fig. 46.4 Various types of endografts

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meaning that the user can reposition the graft inside the
arterial system, as long as the endograft remains partially
deployed.
• Modular concept. Abdominal aortic endografts are usually modular grafts. They consist of two or three different
endograft components that are united inside the human
body. An adequate overlap between the adjacent components is necessary to minimize the possibility of blood
leakage between them (type III endoleak), An exception
to the modular design of most endografts, is the Endologix
AFX Powerlink device, which is delivered on a unibody
conguration.
• Bifurcated conguration. Abdominal aortic endografts
are bifurcated grafts. Aorto-uni-iliac tube grafts are rarely
used today in the usual treatment of AAA disease. Aortouni- iliac endografts are used today for specic clinical
cases, such as when there is a narrow distal aortic neck or
when there is an occlusion of one iliac axis not allowing
intraluminal access from both iliac arteries and the accommodation of a bifurcated graft.
• Radiopaque markers. All endografts have x-ray radi-
opaque markers on specic positions, such as the top end
of the endograft in the graft bifurcation, on the entry gate
of the contralateral limb. Radiopaque markers assist graft
orientation and correct alignment inside the human body.
• Self-expanding property. Endografts are self-expanding
straight after their deployment outside their sheath.
Ballooning is usually necessary to improve proximal and
distal apposition on the landing zones of the endograft, on
the healthy aorta, and on the iliac arteries.
Principles andConcepts ofEndograft
Deployment
For the deployment of each different endograft, there are
specic steps that need to be followed. These steps are
always explained in detail in each endograft instructions for
use (IFU). However, certain steps are common in most cases.
The typical steps that need to be followed for all endografts
are the following:
1. Choice of the iliac axis for the insertion of the main
body’s delivery system. The iliac axis should be wide
enough to accommodate the large prole main body
device. Additionally, it should be as free of calcication
as possible. If both iliac axes are suitable in terms of size
for the main body delivery system, it is a prudent choice
to prefer the most tortuous iliac artery, and leave the less
tortuous iliac artery for the contralateral limb. This way,
catheterizing the contralateral gate can be a relatively
easy task. In contrast, when the most tortuous iliac artery
is left for the contralateral limb, the catheterization of the
contralateral gate of the main body could become a difcult task for both the patient and the performing
physician.
2. Access in both femoral arteries. After deciding which
iliac axis is suitable for the main body delivery system,
access to the femoral arteries follows. Usually, this is
done through small incisions on both groins, although the
availability of closure devices and the low-prole endografts may occasionally permit percutaneous ultrasoundguided access. Using the Seldinger technique, a standard
J wire is inserted into the femoral artery through which
the main body will be advanced. The wire is supported by
a short 11cm-long, 6 Fr sheath, and it is advanced to the
aortic arch and the ascending aorta together with a soft
catheter. The same procedure is performed on the contralateral side, which will be used to insert the angiographic
catheter.
3. Insertion of the angiographic catheter. A pigtail angiographic catheter or a large bore 8 Fr, 45cm long sheath
can be used for the diagnostic angiography. The large
bore sheath allows a good-quality angiogram even when
done without an injector, simply by manual contrast
injection. The angiographic catheter or sheath is advanced
at the level of renal arteries orices, usually at the level of
L1–L2 vertebrae.
4. Insertion of main body delivery system. Based on the
preoperative CT investigation, the main body is inserted
over an extra stiff guidewire approximately at the level
where it should be, usually between L1 and L2 vertebrae
levels.
5. Angiography. From the angiographic catheter or sheath,
an angiogram is performed. The patient needs to be as
still as possible. This can be accomplished by asking the
patient not to breathe if the procedure is performed under
local anesthesia or by asking the anesthetist to hold the
patient’s breath for a while. To better view the proximal
neck, the two renal arteries need to be visualized. This
can be achieved by putting the C-arm intensier perpendicular to the aorta onto the area of interest.
6. Deployment of the main body of the endograft.
Usually, the ipsilateral limb is partially deployed until the
contralateral gate has been cannulated.
7. Catheterization of the contralateral gate. By using a
hydrophilic guidewire with a half J tip from the ipsilateral
iliac axis, the contralateral gate is catheterized with the
support of a catheter. Occasionally, this can prove a timeconsuming task, and the vascular surgeon/interventionist
needs to be as patient as possible to complete it. If catheterization is not successful from the iliac axis, other
options should be considered such as catheterization from
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