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Preoperative Embolization of Collateral Side Branches: A Valid Means to Reduce Type II Endoleaks After Endovascular AAA Repair

Authors:

Abstract

To report the results of preprocedural embolization of collateral branches arising from abdominal aortic aneurysms (AAA) scheduled for endovascular repair. Twenty-three consecutive AAA patients (all men; mean age 73 years, range 56-82) had coil embolization of patent lumbar and inferior mesenteric arteries (IMA) in a staged procedure prior to endovascular repair. Embolization with microcoils was attempted in 37 of the 52 identified lumbar arteries and 14 of 15 inferior mesenteric arteries. Follow-up included biplanar abdominal radiography, spiral computed tomography, and duplex ultrasonography at 1, 30, 90, and 180 days after the stent-graft procedure and at 6-month intervals thereafter. Successful embolization was obtained in 24 (65%) of lumbar arteries, while all 14 (100%) IMAs were occluded with coils. No complication was associated with embolotherapy. Over a mean 17-month follow-up of 22 patients (1 intraoperative death), there was only 1 (4.5%) type II endoleak from a patent lumbar artery, with no sac expansion after 2 years. There were 4 (18%) type I and 1 (4.5%) type III endoleaks. The embolization of side branches arising from an infrarenal aortic aneurysm before endovascular repair is feasible, with a high success rate; this maneuver may play a relevant role in reducing the rate of type II endoleak, improving long-term outcome.
J ENDOVASC THER
2003;10:227–232
227
Q2003 by the I
NTERNATIONAL
S
OCIETY OF
E
NDOVASCULAR
S
PECIALISTS
Available at www.jevt.org
l
CLINICAL INVESTIGATION
l
Preoperative Embolization of Collateral Side
Branches: A Valid Means to Reduce Type II
Endoleaks After Endovascular AAA Repair
Robert Bonvini, MD
1
; Mario Alerci, MD
2
; Francesco Antonucci, MD
2
;
Paolo Tutta, MD
1
; Rolf Wyttenbach, MD
4
; Marcel Bogen, MD
3
;
Angelo Pelloni, MD
3
; Ludwig von Segesser, MD
5
; and Augusto Gallino, MD
1
Departments of
1
Vascular Medicine,
2
Interventional Radiology,
3
Surgery, and
4
Radiology, Ospedale Regionale Bellinzona e Valli, Bellinzona, Switzerland; and
5
Division of Cardiovascular Surgery, CHUV, Lausanne, Switzerland
l
l
Purpose:
To report the results of preprocedural embolization of collateral branches arising
from abdominal aortic aneurysms (AAA) scheduled for endovascular repair.
Methods:
Twenty-three consecutive AAA patients (all men; mean age 73 years, range 56–
82) had coil embolization of patent lumbar and inferior mesenteric arteries (IMA) in a
staged procedure prior to endovascular repair. Embolization with microcoils was attempted
in 37 of the 52 identified lumbar arteries and 14 of 15 inferior mesenteric arteries. Follow-
up included biplanar abdominal radiography, spiral computed tomography, and duplex
ultrasonography at 1, 30, 90, and 180 days after the stent-graft procedure and at 6-month
intervals thereafter.
Results:
Successful embolization was obtained in 24 (65%) of lumbar arteries, while all 14
(100%) IMAs were occluded with coils. No complication was associated with embolother-
apy. Over a mean 17-month follow-up of 22 patients (1 intraoperative death), there was
only 1 (4.5%) type II endoleak from a patent lumbar artery, with no sac expansion after 2
years. There were 4 (18%) type I and 1 (4.5%) type III endoleaks.
Conclusions:
The embolization of side branches arising from an infrarenal aortic aneurysm
before endovascular repair is feasible, with a high success rate; this maneuver may play
a relevant role in reducing the rate of type II endoleak, improving long-term outcome.
J Endovasc Ther 2003;10:227–232
Key words:
abdominal aortic aneurysm, endovascular repair, stent-graft, complication, en-
doleak, lumbar artery, inferior mesenteric artery, coil embolization
l
l
Drs. Bonvini and Alerci contributed equally to the paper.
Address for correspondence and reprints: Prof. Dr. Augusto Gallino, Department of Cardiovascular
Medicine, Ospedale Regionale Bellinzona e Valli, CH-6500 Bellinzona, Switzerland. Fax: 41-91-811-91-
69; E-mail:
agallino@bluewin.ch
The most frequent mid and long-term com-
plications observed after endovascular repair
of abdominal aortic aneurysms (AAA) are en-
doleaks,
1–5
which occur in up to 45%
3
of cas-
es. Patients with aortic endografts require
regular surveillance with computed tomog-
raphy (CT), duplex ultrasonography, or mag-
netic resonance imaging (MRI).
6–8
When en-
doleaks are found, additional endovascular
interventions or even conversion to open re-
pair may be needed,
4,9
which drives up the
overall costs of AAA treatment.
White and colleagues
10–12
in Australia first
categorized endoleaks as types I through IV,
228 PRE-ENDOGRAFT SIDE BRANCH EMBOLIZATION
Bonvini et al.
J ENDOVASC THER
2003;10:227–232
but the focus of our report is on type II, which
refers to retrograde perfusion through collat-
eral branches. Although type II leaks may re-
solve spontaneously,
13
they may also lead to
further expansion of the aneurysm sac, per-
petuating the risk of rupture.
3,6,14–16
Type II en-
doleaks can transmit pressure to the aneu-
rysm sac,
17,18
and several authors have noted
that even a minor type II endoleak inhibits sac
shrinkage.
8,14,19,20
On the other hand, we were
able to find only 2 patients with type II en-
doleak who died after sac rupture.
21–24
Development of a type II endoleak after en-
dovascular aneurysm repair (EVAR) seems to
be correlated with the number of collateral
branches present before the operation,
13,15,25
although this explanation is not unanimously
accepted.
7,26,27
We conducted a study to ex-
amine the hypothesis that meticulous preop-
erative microcoil embolization of patent col-
lateral branches in endograft candidates
could significantly reduce the postoperative
incidence of type II endoleaks.
METHODS
Under a protocol approved by our ethical
committee, we obtained informed consent to
embolize patent side branches from 23 con-
secutive AAA patients (all men; mean age 73
years, range 56–82) undergoing EVAR be-
tween March 1999 and December 2001. The
patients’ cardiovascular risk factors and co-
morbidities included hypertension (13, 56%),
hyperlipidemia (9, 39%), diabetes (4, 17%),
coronary artery disease (9, 39%), peripheral
arterial disease (8, 35%), mild renal failure (11,
48%), and mild to severe pulmonary disease
(5, 22%). The aneurysms were categorized ac-
cording to the EUROSTAR classification
28
as
type A (4, 17%), type B (18, 78%), and type D
(1, 4%).
Preoperative spiral CT was performed with
a Tomoscan Advantage scanner (Phillips
Medical Systems, Best, The Netherlands) at 5-
mm slice thickness, 10-mm table speed, with
5-mm reconstruction intervals during bolus
injection of 150 mL of Optiray 300 (Guerbet,
Paris, France) at a 3-mL/s flow rate and scan
delay of 30 seconds. Postprocessing was per-
formed with an Easy Vision satellite worksta-
tion (Philips Medical Systems) to obtain mul-
tiplanar reconstructions (MPR) and maximum
intensity projections (MIP) of the entire aorta.
Digital subtraction angiography was per-
formed with a standard angiography unit (In-
tegris V 3000; Philips Medical Systems). A 5-
F calibrated pigtail catheter (PBM Medicals,
Stenloese, Denmark) was positioned in the
abdominal aorta, and examinations of the
aorta and pelvic arteries were made in an-
teroposterior, left and right anterior oblique,
and lateral views with multiple 20-mL injec-
tions of Hexabrix 300 (Guerbet) at a flow rate
of 20 mL/s. The total amount of contrast me-
dium varied from 120 to 150 mL.
According to the study plan, all patent in-
ferior mesenteric arteries (IMA) were to un-
dergo coil embolization in a staged procedure
prior to EVAR. The threshold for treating pat-
ent lumbar arteries (LA) was an arteriograph-
ically-measured diameter .2.5 mm or .2.0
mm without ostium stenosis; LAs with a di-
ameter ,2.0 mm were not treated, nor were
LAs arising from the proximal or distal neck
in the event they would be covered by the
prosthesis.
The preoperative examinations identified
52 patent LAs arising from the aneurysm sac
in 16 patients, but only 37 met the diameter
criterion. Fifteen patent IMAs were found in
15 patients. One patent IMA arose distal to the
aneurysm sac and therefore was not embo-
lized because it would be covered by the
prosthesis. In 7 cases, there was no patent LA,
and 8 patients had an occluded IMA.
Embolization was performed in a separate
session ;15 days before endovascular AAA
repair. The coaxial catheterization technique
employed a microcatheter (Transit, Cordis,
Johnson and Johnson AG, Spreitenbach,
Switzerland; or Turbo Tracker, Boston Scien-
tific, Solothurn, Switzerland) and a 4 or 5-F
diagnostic catheter as the guiding catheter
(Sim1, Sim2, C1, C2, C3; Cordis or Cook, Sur-
see, Switzerland) for direct injection of micro-
coils (Vortex, Boston Scientific; Trufill, Cordis).
The time for the procedure varied from 0.75
to 2.5 hours depending on the number of the
vessels to be embolized (Figure).
For subsequent aneurysm exclusion, 19 bi-
furcated stent-grafts (14 Talent [Medtronic
World Medical, Sunrise, FL, USA] and 5 Ex-
cluder [W.L. Gore and Associates, Flagstaff,
J ENDOVASC THER
2003;10:227–232
PRE-ENDOGRAFT SIDE BRANCH EMBOLIZATION
Bonvini et al.
229
AZ, USA]) were used in addition to 2 aorto-
monoiliac prostheses (Talent) with crossover
bypass and 2 tube endografts (Talent). Biplan-
ar abdominal radiograms, duplex ultrasound
scans, and abdominal spiral CT scans were
performed at 1, 30, 90, and 180 days after the
procedure and at 6-month intervals thereafter.
The same operator (P.T.) always performed
the duplex studies using a Sequoia 256 scan-
ner (Acuson, Mountain View, CA, USA) to
identify endoleak and measure the diameters
of the aneurysm sac. The CT scan was per-
formed at 5-mm thickness, 10-mm table
speed, pitch 1:2, and 3-mm reconstruction in-
tervals using a triphasic technique: before
and then during contrast injection (150 mL of
Hexabrix 300 at a 3-mL/s flow rate and a scan
delay of 30 seconds) and 2 minutes after in-
jection. If sac shrinkage was documented af-
ter the first year, then only duplex imaging
and abdominal radiography were done at the
6-month examinations.
RESULTS
In embolization sessions performed 2 to 21
days before stent-graft implantation, 24 (65%)
of 37 LAs identified for embolized were suc-
cessfully occluded. The 13 failures were due
to an inability to catheterize the vessel. All 14
(100%) patent IMAs were successfully embo-
lized. This produced complete collateral
branch embolization in 9 (39%) of 23 patients;
another 9 (39%) had only partial branch oc-
clusion owing to procedural failure in 5 (22%)
or to small LAs in 4 (17%). The other 5 (22%)
patients presented with spontaneous occlu-
sion of the LA and IMA. No complications oc-
curred during or after the embolization pro-
cedures.
There was 1 (4.3%) death related to the
EVAR procedure; the patient sustained an iliac
artery rupture and died of multiorgan failure
subsequent to hemorrhage shock. The re-
maining 22 patients were followed for a mean
17 months (range 3–36). There were 4 (18%)
type I endoleaks, 3 detected immediately after
EVAR and 1 diagnosed a year later. According
to the guidelines proposed by Go¨ rich et al.,
3
2 of these type I endoleaks originated from
the proximal anastomosis (type IA, one early
and one late), 1 at the distal anastomosis
(type IB, early), and the fourth from the iliac
artery occluder (type IC, early). At the 3-
month CT scan, 2 (early IA and IC) had sealed
spontaneously. The other 2 (late IA, early IB)
were still present at 3 months and so were
treated with transcatheter embolization. How-
ever, despite embolization, the aneurysm with
the type IB endoleak showed continuous ex-
pansion, and a second bifurcated stent-graft
was implanted. A type III endoleak was found
in this patient 1 year later.
Only 1 (4.5%) type II endoleak was seen on
the 1-day postprocedural CT scan; the mini-
mal posterior contrast enhancement indicated
a lumbar artery etiology. This patient had only
partial preprocedural branch embolization
(IMA successful, but only 3 of 6 LAs embo-
lized). This type II endoleak was treated con-
servatively since there was no evidence of sac
expansion during the 2-year follow-up.
In 8 (36%) AAAs, the sac reduced in diam-
eter from an average of 64 361 mm preop-
eratively to 51 353 mm postoperatively; the
remaining 13 (59%) AAAs demonstrated no
significant change in diameter. Among the 8
patients with sac shrinkage, 4 had complete
collateral occlusion (3 embolized, 1 with spon-
taneous occlusion). Three had only partial
embolization due to technical failure, and 1
had no embolization because of a small LA.
The only instance of sac expansion was the
patient mentioned above who underwent a
secondary stent-graft procedure after embo-
lization failed to resolve a type IB endoleak.
DISCUSSION
The incidence of type II endoleaks persisting
beyond 6 months is reported in the range of
3.5% to 28%,
2,3,6,7,15,29
and it may be respon-
sible for increased EVAR-related morbidity
with potential risk of rupture.
3,6,14,15,16
This po-
tential risk, in association with sac expansion,
is equivalent to procedural failure and is of
major concern.
8,19,23,24,30–33
Some authors re-
ported sac expansion or rupture in the face of
a type II endoleak.
23,24,31
Others advised an
aggressive attitude be assumed in cases of
sac expansion even without evidence of en-
doleak
32
or stated that sac shrinkage is the
only parameter that indicates successful
EVAR.
8
For this reason, many authors have
230 PRE-ENDOGRAFT SIDE BRANCH EMBOLIZATION
Bonvini et al.
J ENDOVASC THER
2003;10:227–232
Figure
l
(A) A preoperative right anterior oblique abdominal angiogram indicates patent lum-
bar (arrowhead) and inferior mesenteric (arrow) arteries arising from the aneurysm sac in a
patient with a type B aortic aneurysm. (B) The same patient after successful coil embolization.
used a variety of percutaneous procedures to
treat these postoperative endoleaks, includ-
ing sac embolization with coils, glue, or
thrombin, or retrograde catheterization to oc-
clude the IMA or LA.
The best treatment modality, however, is
still a question of debate. Furthermore, all
these techniques are often time-consuming
and are not uniformly successful.
9,13,15,33–35
Recently, the translumbar approach has been
proposed by some authors as the first choice
treatment strategy for type II endoleaks.
34
Other authors suggest that LA occlusion by
injection of gelatin sponge in the aneurysm
sac during the EVAR may reduce the devel-
opment of side branch–related endoleaks.
36
However, Gould et al.
7
suggested that pre-
operative embolization of collateral branches
had no beneficial effect on type II endoleaks.
Their incidence of early type II endoleaks in
patients with or without preoperative embo-
lization was 20% and 23%, respectively, with
similar results at 6 months (10% incidence of
type II for both groups). On the other hand,
Parry et al.
8
performed preoperative emboli-
zation of the sac feeders (IMA and LA). They
found no type II endoleak among 13 patients
who had occluded side branches at baseline
or 14 patients who underwent successful IMA
or LA embolization. Conversely, 8 of 13 pa-
tients with patent LAs developed a type II
lumbar endoleak.
To avoid or at least to reduce the occur-
rence of endoleaks, we prospectively per-
formed meticulous preoperative microcoil
embolization of patent collateral branches in
a consecutive series of EVAR candidates. Ev-
ery patent IMA arising from the aneurysm sac
was embolized, whereas the decision on
which LAs required embolization was at the
discretion of the interventionist. Arbitrary cri-
teria (.25-mm diameter or .20 mm if no os-
tial stenosis existed) were established be-
cause large LAs are easier to catheterize and
embolize; microcoil embolization was at-
tempted even in the presence of a thrombotic
corona in the aneurysm sac.
This approach proved feasible in our rela-
tively small prospective series, achieving a
high success rate. In follow-up, we observed
only a single (4.5%) type II endoleak, which
we believe supports the hypothesis that pre-
operative embolization of collateral branches
can reduce the number of type II endo-
J ENDOVASC THER
2003;10:227–232
PRE-ENDOGRAFT SIDE BRANCH EMBOLIZATION
Bonvini et al.
231
leaks.
13,15,25
To our knowledge, only Hovsepi-
an et al.
29
have reported a lower incidence of
this complication (3.5%).
Type I endoleaks were found more fre-
quently than type II in our series, but half of
these sealed spontaneously within a 3-month
period, which may mean that type I endoleak
is also associated with patent collateral
branches present preoperatively, as recently
reported by Fan et al.
15
Major limitations of our study are the rela-
tively small patient population and a midterm
follow-up averaging 17 months. This short
observation period could explain why only a
relatively small percentage of patients had
significant sac shrinkage. Moreover, endo-
leaks may occur even beyond 1 year after
EVAR, especially in cases where preoperative
side branch embolization has not been per-
formed.
7
Another shortcoming to the study
was the absence of a control group without
preoperative embolization.
Despite these limitations, the 4.5% inci-
dence of type II endoleak is very low com-
pared to previous reports
1–3,6,7,15
and may
support our preventive strategy if corroborat-
ed by further studies with a larger number of
patients. We believe that preoperative side
branch embolization is safe and easier to per-
form preoperatively than after the EVAR pro-
cedure. This maneuver may contribute to a
reduction in the rate of type II endoleak and
improve the long-term outcome after EVAR.
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... 19) Therefore, a patent IMA is thought to be an important cause of T2EL. Many studies 10,16,[20][21][22][23][24][25][26][27] have reported preoperative or intraoperative embolization attempts for the IMA and the success rate has been reported as ranged from 88.7%-100%. In these reports, embolization was attempted for 457 IMAs in total, with a remarkably high success rate of 95.8% has been reported. ...
... However, T2EL from LA may occur when only IMA embolization is performed and T2EL from LA occurs in 14%-34% cases in these reports. In studies embolizing both the IMA and LA, 10,16,20,23,24) the success rate of LA embolization was 62%-92%. However, for studies that showed the actual number of vessels with embolization attempts, 10,16,20,24) the success rate was 69.0% for 116 attempts. ...
... In studies embolizing both the IMA and LA, 10,16,20,23,24) the success rate of LA embolization was 62%-92%. However, for studies that showed the actual number of vessels with embolization attempts, 10,16,20,24) the success rate was 69.0% for 116 attempts. The frequency of T2EL after IMA and LA embolization reported in these studies was extremely low, with values of 0%-4.5%. ...
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Objective: Coil embolization of aortic side branches has been additionally performed to prevent type II endoleak during EVAR in our institute. In this study, we evaluated the predictive factors of the possibility for coil embolization of the inferior mesenteric artery (IMA) and lumbar artery (LA) during EVAR. Methods: Seventy-four EVAR patients during June 2015 and April 2019 were included in the study. The coil embolization procedural time for one vessel is limited to 10 min. Aortic side branches were selected with 4 Fr Shepherd hook type catheter (Medikit, Tokyo, Japan) and were embolized with Interlock (Boston Scientific, MA, USA) via microcatheter. As predictive factors, internal diameter of aortic side branches and the aortic diameter perpendicular to the origin of LA (aortic diameter) were evaluated. Results: Coil embolization was tried for 52 patent IMAs and all IMAs except two IMAs with ostial stenosis were successfully coil embolized (96.2%). Totally 190 LAs were patent and coil embolization was tried for 144 LAs. Among 144 LAs, 106 LAs (73.6%) were successfully coil embolized and the diameter was significantly longer (2.30±0.51 mm vs. 2.04±0.41 mm, p=0.007) and aortic dimeter was significantly shorter (30.0±8.1 mm vs. 40.5±11.6 mm, p<0.001) in successfully embolized LAs. Cut off value of successful LA coil embolization was 2.06 mm for internal diameter and 36.1 mm for aortic diameter by receiver operating characteristic curve analysis. Successful coil embolization rate for LAs with internal diameter longer than 2.0 mm and aortic diameter less than 36.2 mm was 90% (72 among 80 LAs). Conclusion: Coil embolization during EVAR for IMA was highly successful, if there was no calcified ostial stenosis. LA embolization was feasible especially for LAs with internal diameter ≥2.0 mm and aortic diameter ≤36.1 mm. This information would be useful to select the target vessel for aortic side branches coil embolization during EVAR. (This is a translation of Jpn J Vasc Surg 2019; 28: 389–396.)
... AMI sola, logrando una disminución de la presencia de endofugas, que se redujo del 3,6 % al 47,8 % en el grupo control. Sin embargo, el grupo de Alerci(14,16) informó de que la embolización de las AL fue técnicamente difícil debido a su diámetro pequeño, así como a la tortuosidad que presentan, lo que requirió un tiempo de procedimiento más prolongado y una tasa de éxito menor (alrededor del 60 %). En aquellos casos en los que se realizó embolización de la AMI, pero no fue posible la embolización de todas las AL, no se objetivó un crecimiento del saco aneurismático.Otro estudio publicado recientemente recomienda la embolización de las AL previa al EVAR cuando presenten un diámetro interno ≥ 2,0 mm y un diámetro máximo de la luz aórtica sin trombo ≤ 36,1 mm, ya que es más factible la canulación de las AL cuanto menor sea el diámetro aórtico. ...
... 1,2 Accordingly, it has been postulated that pre-EVAR IMA embolization reduces the incidence of type II endoleaks. [3][4][5][6] However, the cohort of patients and their respective risk factors for whom this intervention will yield maximum benefit is yet to be clearly defined. One of the factors proposed to increase the risk of type II endoleak development is increasing IMA ostium size. ...
Article
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Purpose: This study aims to evaluate the relationship between inferior mesenteric artery (IMA) diameter and risk of type II endoleak. Subjects and Methods: A retrospective study design to review all EVARs performed over a 4-year period at a tertiary care center. Out of the total cohort of 400 patients who underwent EVAR, 41 patients (10.3%) developed type II endoleak. The mean IMA ostial diameter for patients with type II endoleak secondary to IMA contributories was 4mm, while the mean IMA diameter for patients with lumbar arteries contributing to the type II endoleak was 3.7mm. Results: Statistical analysis using a paired t-test did not show a statistically significant difference in the IMA ostial diameter between the two groups. Conclusion: There is no significant correlation between preprocedural IMA ostium diameter and type II endoleak development and hence, preprocedural IMA embolization is not an appropriate prophylactic management strategy.
... Preoperative coil embolization of side branches has been an effective option to reduce EIIs and increase shrinkage of the aneurysm sac. 6,7 Moreover, intraoperative sac embolization during EVAR has been performed to decrease the EII and reintervention rates, 8,9 but no systematic review has investigated this topic. Hence, this analysis sought to determine if these embolization techniques are safe and more effective in preventing EIIs as compared with no embolization. ...
Article
Purpose:To investigate the efficacy and safety of preoperative side branch embolization or intraoperative sac embolization for preventing type II endoleaks after endovascular aneurysm repair (EVAR). Materials and Methods: A systematic literature search of MEDLINE and EMBASE was performed to identify studies that evaluated the outcomes of sac embolization vs no embolization or side branch embolization vs no embolization in patients who received EVAR. Among the 904 studies screened, 17 studies with 2084 participants were included in this review. Outcome measures included the type II endoleak rate, the reintervention rate for type II endoleaks, the incidence of types I/III endoleaks, and the rate of complications. Fixed (no heterogeneity) or random effects models were constructed for each outcome; the results are presented as the odds ratio (OR) with 95% confidence interval (CI). Results: The sac embolization group had significantly lower type II endoleak (OR 0.21, 95% CI 0.13 to 0.34, p<0.001) and reintervention (OR 0.15, 95% CI 0.07 to 0.33, p<0.001) rates than the no embolization group. No significant differences between the 2 groups were found for the type I/III endoleak rate (OR 0.57, 95% CI 0.23 to 1.37, p=0.21) or complication rate (OR 1.22, 95% CI 0.32 to 4.70, p=0.77). Compared with no embolization, side branch embolization was also associated with a decrease in type II endoleak (OR 0.35, 95% CI 0.21 to 0.60, p<0.001) and reinterventions (OR 0.10, 95% CI 0.04 to 0.27, p<0.001). One severe procedure-related complication (fatal colon ischemia) was reported in the side branch embolization group. Conclusion: Sac embolization and side branch embolization are safe and effective in preventing type II endoleaks. Further randomized trials are needed to directly compare the clinical outcomes of these procedures.
... Some Authors have assessed models to predict high risk for T2E at the time of initial procedure using anatomic features, number and size of patent feeding arteries, and other factors. These groups have then looked at pre-emptive coil embolization to prevent T2E [27,[29][30][31][32][33][34], but a strong and definitive benefit failed has to be proved. ...
Article
Background: Endovascular aneurysm repair (EVAR) has revolutionized the treatment of abdominal aortic aneurysm (AAA) disease. However, the survival advantage is lost in the long term due the occurrence of endoleaks affecting the late rupture of aneurism sac. Few data are available on the role of blood pressure control in affecting the incidence of type 2 endoleaks in patients undergoing EVAR. Objective: Aim of this study was to evaluated whether tight systolic blood pressure (SBP) control to target 130 mm Hg reached after preoperative cardiology consultant might decrease the incidence of type II endoleak(T2E), sac expansion and related aortic reintervention after elective endovascular aneurysm repair(EVAR). Methods: We analysed 386 patients undergoing EVAR between 2008 and 2016. The primary endpoints were T2E, sac expansion and related aortic re-intervention or sac shrinkage during a median follow-up of 24 months (12-48). The secondary endpoint was every cause of vascular or cardiac morbidity and mortality. Results: The SBP value of 130 mmHg at the time of EVAR resulted, at ROC curve analysis, the most sensitive and specific for all the analysed endpoints (T2E, n=74; sac expansion n=19; re-intervention,n=10, sac shrinkage,n=72). The combination antihypertensive therapy showed a significant inverse relationship with T2E occurrence. The incidence of primary endpoints was significantly higher (p<0.001) in patients with SBP≥130 mmHg. Cardiovascular death was significantly more prevalent (p<0,001) in patients with SBP ≥130 mmHg. These findings were confirmed at the multivariable Cox regression analysis [primary endpoint HR=0.09(0.06-0.15),p<0.001; cardiovascular death HR=0.33(0.12-0.85), p=0.023]. Conclusions: Tight SBP control at the target of 130 mmHg at the time of elective EVAR significantly decreases TE2 occurrence, need of re-intervention and cardiovascular death in a prolonged follow-up of a large sample of patients.
... More recently, several attempts have been proposed to treat or prevent endoleaks by using coils and/or polymeric embolizing agents that include ethylene vinyl alcohol copolymer (Onyx V R ) [22,23] , n-butyl cyanoacrylate (NBCA or Histoacryl) [24,25] , fibrin glue [26] combined or not with coils [27] , and alginate [28] . However, the frequent recurrence was reported for the most abovementioned agents [22][23][24][25][26][29][30][31][32][33][34] . For type II endoleaks, these agents were used to perform either trans-arterial embolization of collateral vessels or to fill the leak area in the aneurysm after direct puncture of the sac [34] , the latter approach probably being more efficient when liquid embolizing agents are used [24,34] . ...
Article
Persistent perfusion of the space between the stent-graft and the aneurysm wall (endoleak) is the most common failure mode of endovascular aneurysm repair. In this respect, several embolizing agents have been proposed for embolization of abdominal aortic aneurysms to avoid endoleaks. Among these, a chitosan-based embolizing hydrogel agent has been proposed and it is under investigation. This radiopaque hydrogel, which gels in situ and it is trackable in vivo, showed a great potential as embolizing agent for endovascular aneurysm repair and other endovascular therapies.
Article
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Objective Previous reports have revealed a high incidence of type II endoleak (T2EL) after endovascular aneurysm repair (EVAR). The incidence of T2EL after EVAR is reduced by pre-emptive embolization of aneurysm sac side branches (ASSB) and aneurysm sac coil embolization (ASCE). This study aimed to investigate whether different preventive interventions for T2EL were correlated with suppression of aneurysm sac expansion and reduction of the re-intervention rate. Methods The PubMed, Web of Science, MEDLINE and Embase databases, and conference proceedings were searched to identify articles on EVAR with or without embolization. The study was developed in line with the Participants, Interventions, Comparisons, Outcomes, and Study design principles and was conducted and reported in accordance with the Preferred Reporting Items for Systematic reviews and Meta-Analyses guidelines. We used network meta-analysis based on multivariate random-effects meta-analysis to indirectly compare outcomes of different strategies for embolization during EVAR. Results A total of 31 studies met all inclusion criteria and were included in the qualitative and quantitative syntheses. The included studies were published between 2001 and 2022 and analyzed a total of 18,542 patients, including 1,882 patients who received prophylactic embolization treatment during EVAR (experimental group) and 16,660 who did not receive prophylactic embolization during EVAR (control group). The effect of pre-emptive embolization of the inferior mesenteric artery (IMA) (IMA-ASSB) in preventing T2EL was similar (relative risk [RR] 1.01, 95% confidence interval [CI] 0.38–2.63) to the effects of non-selective embolization of ASSB (NS-ASSB) and ASCE (RR 0.88, 95% CI 0.40–1.96). IMA-ASSB showed a better clinical effect in suppressing the aneurysm sac expansion (RR 0.27, 95% CI 0.09–2.25 compared with NS-ASSB; RR 0.93, 95% CI 0.16–5.56 compared with ASCE) and reducing the re-intervention rate (RR 0.34, 95% CI 0.08–1.53 compared with NS-ASSB; RR 0.66, 95% CI 0.19–2.22 compared with ASCE). All prophylactic embolization strategies improved the clinical outcomes of EVAR. Conclusion Prophylactic embolization during EVAR effectively prevents T2EL, suppresses the aneurysm sac expansion, and reduces the re-intervention rate. IMA embolization demonstrated benefits in achieving long-term aneurysm sac stability and lowering the risk of secondary surgery. NS-ASSB more effectively reduces the incidence of T2EL, while IMA embolization alone or in combination with ASCE enhances the clinical benefits of EVAR. In addition, as network meta-analysis is still an indirect method based on a refinement of existing data, more studies and evidence are still needed in the future to establish more credible conclusions.
Article
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Introduction Although the preoperative risk factors associated with the occurrence of type II endoleak (ETII) after endovascular aortic repair (EVAR) have gradually become more evident, the preoperative risk factors associated with aneurysm sac enlargement caused by ETII remain unclear. This study aimed to determine the preoperative risk factors associated with aneurysm sac enlargement caused by ETII after EVAR. Methods This retrospective cohort study reviewed 519 EVARs performed for true abdominal aortic aneurysm between January 2006 and December 2018 at our institution. EVARs using commercially available bifurcated devices with no type I or III endoleaks during follow-up and with ≧12 months follow-up were included. A total of 320 patients were enrolled in the study. To identify the preoperative risk factors of sac enlargement after EVAR, Cox regression analysis was used to assess preoperative data. Results The median follow-up period was 60.8 months. Overall, 135 of 320 patients (42%) had ETII during follow-up, and 47 of 135 patients (35%) developed aneurysm sac enlargement. Multivariate analysis revealed that chronic kidney disease (CKD) stage ≧4 (hazard ratio [HR], 4.65; 95% confidence interval [CI], 2.13–10.15; p =0.001), patent inferior mesenteric artery (IMA) (HR, 17.85; 95% CI, 2.46–129.73; p <0.001), and number of patent lumbar arteries (LAs) (HR, 1.37; 95% CI, 1.13–1.68; p =0.002) were risk factors of aneurysm sac enlargement caused by ETII. Conclusion CKD stage ≧4, patent IMA, and number of patent LAs were independent risk factors for aneurysm sac enlargement after EVAR. In particular, patent IMA had the highest HR and seemed to have the greatest impact on long-term aneurysm sac enlargement. Hence, taking preoperative measures to address a patent IMA appears to be important in reducing the incidence of sac enlargement.
Article
Type 2 endoleaks are a potential complication of endovascular aortic repair for abdominal aortic aneurysms. They are caused by vessels that have been excluded from the aorta lumen, but may still fill the aneurysm sac due to collateral filling. Type 2 endoleaks may lead to increased morbidity and need for additional procedures. Being able to identify patients at risk for Type 2 endoleaks and prevent them is important for any physician who is performing endovascular aortic repair.
Article
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EUROSTAR(EUROpean collaborators on Stent-graft Techniques for abdominal aortic Aneurysm Repair) was established for the purpose of combining and studying data on endovascular abdominal aortic aneurysm (AAA) repair. EUROSTAR is independent of any commercial interest and has as its ultimate goal an independent, scientifically reliable assessment of endovascular AAA grafting. A standardized case record form is used for data collection and transmission, and the database is maintained in a central registry office. A comprehensive set of clinical, imaging, technical, and laboratory data obtained at initial admission and follow-up are recorded; these data are analyzed periodically and reports generated on the collated experience. As a first priority, an observational study without controls was initiated in July 1996 to address the issues of procedural safety, device durability, and long-term effect upon the aneurysms. Several ancillary studies have been initiated, including a “Retrieval and Analysis Study” for the evaluation of explanted devices. While a randomized study does not seem feasible at present, this may be organized at the appropriate time when the devices and techniques become more standardized.
Article
Full-text available
EUROSTAR (EUROpean collaborators on Stent-graft Techniques for abdominal aortic Aneurysm Repair) was established for the purpose of combining and studying data on endovascular abdominal aortic aneurysm (AAA) repair, EUROSTAR is independent of any commercial interest and has as its ultimate goal an independent, scientifically reliable assessment of endovascular AAA grafting. A standardized case record form is used for data collection and transmission, and the database is maintained in a central registry office. A comprehensive set of clinical, imaging, technical, and laboratory data obtained at initial admission and follow-up are recorded; these data are analyzed periodically and reports generated on the collated experience. As a first priority, an observational study without controls was initiated in July 1996 to address the issues of procedural safety, device durability, and long-term effect upon the aneurysms. Several ancillary studies have been initiated, including a "Retrieval and Analysis Study" for the evaluation of explanted devices. While a randomized study does not seem feasible at present, this may be organized at the appropriate time when the devices and techniques become more standardized.
Conference Paper
Objective: The exact significance of collateral endoleaks is unknown and a topic of great debate, Because of this uncertainty, some physicians choose to watch and wait while others aggressively treat these leaks. The purpose of this investigation was the evaluation of the efficacy of the two techniques used in the treatment of collateral endoleaks that occur after endovascular aneurysm repair. Methods: Patients with 33 angiographically proven type 2 endoleaks underwent treatment with either transarterial inferior mesenteric artery embolization (n = 20) or direct translumbar embolization (n = 13) during an 18-month period. Embolization success was defined as resolution of endoleak on all subsequent computed tomography angiogram results. The likelihood of embolization failure between the two treatments was expressed as a risk ratio and was compared with Fisher exact test. Results. Sixteen of 20 transarterial inferior mesenteric artery embolizations (80%) failed with recanalization of the original endoleak cavity over time. A single failure (8%) in the direct translumbar embolization group occurred in a patient in whom a new attachment site leak developed. The remaining 12 translumbar endoleak embolizations (92%) were successful and durable, with a median follow-up period of 254 days. The patients who underwent transarterial inferior mesenteric artery embolization were significantly more Likely to have persistent endoleak than were the patients who underwent treatment with direct translumbar embolization (risk ratio, 4.6; 95% confidence interval, 1.9 to 11.2; P = .0001). Conclusion: The transarterial embolization of inferior mesenteric arteries for the repair of type 2 endoleaks is ineffective and should not be performed. Direct translumbar embolization of the endoleak is effective in the elimination of type 2 leaks and should be the therapy of choice when aggressive endoleak management is indicated.
Article
Persistent aneurysm perfusion represents failure of endovascular repair. The leak may occur around either end of the prosthesis or through a collateral route. Most cases can be treated by endovascular means. Stents can be rotated, the prosthesis can be lengthened at either end, and collateral pathways can be occluded, all without recourse to open repair. This report describes the management of persistent aneurysm perfusion in five patients from a total experience of 32 cases of endovascular aneurysm repair.
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The treatment of aortic aneurysms with endovascular stents or stent-graft prostheses is receiving increasing attention as an alternative to major abdominal surgery. To define the clinical value of this technique, we prospectively studied the use of stent-graft endoprostheses made of nitinol and covered with polyester fabric for the treatment of infrarenal abdominal aortic aneurysms. We treated a total of 154 patients at three academic hospitals. Twenty-one patients with aortic aneurysms not involving the aortic bifurcation received straight stent-grafts, and 133 patients with aortic aneurysms involving the bifurcation and the common iliac arteries received bifurcated stent-grafts. After a unilateral surgical arteriotomy, the endoprostheses were advanced through the femoral arteries and placed under fluoroscopic guidance. Computed tomography and intraarterial angiography were performed during an average follow-up of 12.5 months. The primary success rate, defined as complete exclusion of the abdominal aortic aneurysm from the circulation, was 86 percent in the group receiving straight grafts and 87 percent in the group receiving bifurcated grafts. In three patients the procedure had to be converted to an open surgical operation. Minor (n=13) or major (n=3) complications associated with the procedure (including 1 death) occurred in 10 percent of the patients. All patients had a postimplantation syndrome, with leukocytosis and elevated C-reactive protein levels. Our results suggest that endovascular treatment of infrarenal abdominal aortic aneurysms is technically feasible and can effectively exclude abdominal aortic aneurysms from the circulation. With further refinement, endoluminal repair may emerge as an interventional strategy to treat infrarenal aortic aneurysms, especially in patients at high surgical risk.
Article
To relate changing abdominal aortic aneurysm (AAA) morphology after endovascular grafting to the presence of leakage, collateral perfusion, and other factors. Thirty-five patients who underwent successful AAA endovascular grafting were evaluated. Self-expanding Z-stents and Dacron grafts were applied in bifurcated and aortomonoiliac systems. Postoperative diameter changes were calculated from repeated spiral computed tomographic scans, angiograms, and ultrasonic phase-locked echo-tracking scans during a median 6-month follow-up (interquartile range [IQR] 3 to 12). At 12 months, the diameters of completely excluded aneurysms had decreased 6 mm (IQR 2 to 11; p = 0.006). The proximal graft-anchoring stents had dilated 2 mm (IQR 0.5 to 3.3; p = 0.01). The aortic diameters immediately below the renal arteries but above the stents had not changed. Endoleakage and collateral perfusion (n = 13) were each associated with preserved aneurysm size and a 12 times higher risk of aneurysm dilation. After the leakage or the collateral perfusion had been treated, the aneurysm size decreased. Aneurysms with extensive intraluminal thrombi presented a reduced risk of leakage or perfusion. The diameters of endovascularly excluded AAAs decrease, except in cases of leakage or perfusion. Careful follow-up of patients with aortic endografts is necessary.
Article
The inability to obtain or maintain a secure seal between a vessel wall and a transluminally implanted intra-aneurysmal graft is a complication unique to the evolving technique of endovascular aneurysm exclusion. Because the term “leak” has long been associated with aneurysm rupture, the term “endoleak” is proposed as a more definitive description of this phenomenon. Embracing both persistent blood flow into the aneurysmal sac from within or around the graft (graft related) and from patent collateral arteries (nongraft related), endoleak can be classified as primary or secondary depending on the time of occurrence (within 30 days of implantation or following apparent initial seal, respectively). Diagnostic techniques to detect endoleak include arteriography, intraprocedural pressure monitoring, contrast-enhanced computed tomography, abdominal X ray, and duplex scanning. Management strategies for endoleak range from observation with periodic imaging surveillance to correction by additional endoluminal or surgical procedures. Standardization of the terminology describing this important sequela to endovascular aneurysm exclusion should facilitate uniform reporting of clinical trial data vital to the evaluation of this emerging technique.
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We describe a case of abdominal aortic aneurysm (AAA) with rupture 16 months after treatment by an endograft. A 76-year-old patient on Coumadin after aortic valve replacement had initially successful exclusion by stentgraft. There was no evidence of an endoleak seven months after stentgraft repair, although a computed tomography scan detected an enlargement of the aneurysm sac. Sixteen months after initial endograft surgery, rupture of the aneurysm occurred and we performed open emergency surgery. We treated the aneurysm by conventional technique, and the patient survived the rupture. This case emphasized the fact that patients after endograft AAA repair require a close follow-up. An expansion of the aneurysm sac after the procedure should signal failed exclusion, even if a computed tomography scan does not demonstrate an endoleak. Anticoagulation can be an important factor in failure after endoluminal graft treatment. Supravisceral aortic cross clamping is helpful in dealing with a stented aorta.
Article
Endoleakage is a fairly common problem after endovascular repair of abdominal aortic aneurysm and may prevent successful exclusion of the aneurysm. The consequences of endoleakage in terms of pressure in the aneurysmal sac are not exactly known. Moreover, the diagnosis of endoleakage is a problem because visualization of endoleaks can be difficult. With an ex vivo model of circulation with an artificial aneurysm managed by means of a tube graft, studies were performed to evaluate precisely known diameters of endoleaks with both imaging techniques (computed tomography and digital subtraction angiography) and pressure measurements of the aneurysmal sac. The experiments were performed without endoleak (controls) and with 1.231-French (0.410 mm), 3-French (1 mm), and 7-French (2.33 mm) endoleaks. Pressure and imaging were evaluated in the absence and presence of a simulated open lumbar artery. The pressure in the prosthesis and in the aneurysmal sac were recorded simultaneously. Digital subtraction angiography with and without a Lucite acrylic plate, computed tomographic angiography, and delayed computed tomographic angiography were performed. For the first experiments, the aneurysmal sac was filled with starch solution. All tests were repeated with fresh thrombus in the aneurysmal sac. Each endoleak was associated with a diastolic pressure in the aneurysmal sac that was identical to diastolic systemic pressure, although the pressure curve was damped. At digital subtraction angiography without a Lucite acrylic plate, the 1.231-French (0.410 mm) endoleak was visualized without an open lumbar artery. When a Lucite acrylic plate was added, the endoleak was not visible until a lumbar artery was opened. In the presence of thrombus within the aneurysmal sac, all endoleaks were not visualized at digital subtraction angiography. At computed tomographic angiography, all endoleaks were not visualized in the absence of a thrombus mass in the aneurysmal sac. In the presence of thrombus within the aneurysmal sac, the 1.231-French (0.410 mm) endoleak became visible after opening of a simulated lumbar artery. At delayed computed tomographic angiography, all endoleaks were visualized without and with thrombus. Every endoleak, even a very small one, caused pressure greater than systemic diastolic pressure within the aneurysmal sac. However, small endoleaks were not visualized with digital subtraction angiography and computed tomographic angiography, whereas all endoleaks were visualized with a delayed computed tomographic angiography protocol. We believe that follow-up examinations after stent graft placement for aortic aneurysms should focus on pressure measurements, but until this is clinically feasible, delayed computed tomographic angiography should be performed.