Introduction
Impaired drainage of the main pancreatic duct (MPD) either from a stenosed pancreaticoenteral
tract anastomosis (PEA) after a pancreatoduodenectomy, pancreatic duct strictures
in chronic pancreatitis or in patients with disconnected pancreatic duct syndrome
(DPDS) after necrotizing pancreatitis, may cause recurrent acute or chronic pancreatitis
in the upstream gland [1]
[2]. All surgical approaches for management are associated with significant morbidity.
Surgical pancreaticojejunostomy is often not feasible with small ducts and surgical
resection of the upstream pancreas may result in diabetes [3]
[4]. Endoscopic pancreatic ductal drainage was introduced as an alternative in the 1980 s,
especially in poor surgical candidates. Endoscopic retrograde cholangiopancreatography
(ERCP) with pancreatic endotherapy including dilation and stenting is an option [5]
[6]
[7] but may not be possible [8]
[9]
[10] in 3 % to 10 % of cases [11] due to complete obstruction and/or disconnected duct after necrotizing pancreatitis
[11]
[12]
[13]. Endoscopic ultrasound (EUS)-guided interventions can be considered as an alternative
to surgical PD drainage when ERCP is not technically feasible [14]
[15]
[16]
[17].
EUS allows antegrade access to the MPD for creation of a pancreaticogastrostomy (PG).
The technique was first described in a case series of four patients in 2002 [14]. Since then, there have been case reports and case series [12]
[15]
[18]
[19]
[20]
[21] describing slight variations in technique for formation of a pancreaticogastrostomy.
All series have included only patients with dilated main pancreatic ducts, which occur
inconsistently in patients with chronic obstructive pancreatitis, and have involved
needle-knife cautery [12]
[14]
[22] bougie dilation [21] or a stent extraction screw along with standard balloon dilators [23] to allow stent passage across the muscular gastric wall and pancreatic parenchyma
into the MPD. These techniques are associated with significant trauma to the pancreatic
tissue and can result in complications such as bleeding, perforation, peri-gastric
collections or acute pancreatitis [12]
[21]
[22]
[23]. Standard balloon dilators commonly used have a shaft diameter of 5 to 6 Fr and
there is a substantial resultant risk of duct leak if the access to MPD is lost after
initial entry.
We hypothesized that EUS-guided pancreaticogastrostomy utilizing very-small-caliber
needles, wires, angioplasty balloons, and stents could be achieved relatively atraumatically,
and would be feasible in patients with small pancreatic ducts. We report our center’s
initial experience with this approach in patients with all diameters of MPD including
some with relatively small duct diameters.
Patients and methods
This was a retrospective study conducted at the University of Minnesota Medical Center
in Minneapolis, Minnesota. The study was approved by the institutional review board.
Consecutive patients who underwent EUS-guided MPD access between August 2013 and August
2018 were identified via a prospectively maintained database. Patients were included
if they were older than 18 years of age and underwent EUS-guided antegrade drainage
of MPD via small-shaft-diameter angioplasty balloon-assisted PG creation. Patient
were excluded if the PG creation was done using techniques other than small shaft
diameter angioplasty balloon such as needle knife cautery, stent extraction screw
or standard balloon dilators. EUS guided PG was offered to the patients when conventional
ERCP and/or EUS-guided rendezvous access to drain the pancreatic duct either failed
or was deemed unfeasible by a team of advanced endoscopists (MLF, JSM, SKA, GT). Clinical
data were retrospectively obtained from their electronic medical records including
demographics, hospitalization status (inpatient versus outpatient), any prior gastrointestinal
tract surgeries, indication for the pancreatic duct drainage procedure, reason for
failure or prior ERCP or EUS-guided rendezvous access if any, technical information
about the procedure (including type and diameter of wire used to gain access to MPD,
location of MPD puncture, diameter of the angioplasty balloon used to dilate the pancreaticogastrostomy
tract and length & diameter of the plastic endoprosthesis placed across the pancreaticogastrostomy
tract), any immediate complications related to the procedure or anesthesia. Complications
were defined using standardized consensus criteria within 30 days of the endoscopic
therapy as originally described by Cotton et al [24]. Clinical response was graded as poor, transient or complete. Duration of follow-up
was defined as extending until the last contact with the patient by clinic visit or
telephone.
Endoscopic techniques
All endoscopic and interventional procedures were performed by two of the authors
(JSM and MLF) under fluoroscopic guidance and general anesthesia. Please see the video
with this article for a step by step approach for creation of an EUS guided PG ([Video 1]). A linear echoendoscope (GF-UCT 180, Olympus America, Center Valley, Pennsylvania,
United States) was used to identify the MPD; color Doppler was then employed to ensure
there were no vascular structures between the MPD and the gastrointestinal tract.
The initial duct puncture was performed with a 19- or a 22-gauge needle. A 22-gauge
needle is the preferred first choice if the initial intent is EUS-guided PG but a
19-gauge needle was used in some instances in our case series where the original intent
of the procedure was an EUS-guided rendezvous access to the pancreatic duct since
it allows for more wire options. Contrast pancreatogram was performed, and a 0.018-inch
guidewire (Roadrunner, Cook Medical, Bloomington Indiana, United States) was passed
through the needle into the duct and either across the papilla, the anastomotic stricture
or coiled into the duct lumen. After removal of the needle over the guidewire, a small-diameter
(4 Fr) angioplasty balloon (Sterling, Boston Scientific, Marlborough MA) was passed
over the wire through the pancreaticogastric fistula in to the MPD and the balloon
was dilated (2 – 4 mm). A 3 Fr single pigtail endoprosthesis was passed pigtail first
as far as the initial guidewire could be passed. In patients where the guidewire passed
through the stricture or anastomosis, the pigtail was curled in the lumen of the bowel.
In patients with disconnected duct, or impassable stricture or anastomosis, the pigtail
of the stent was deployed inside the duct, usually curling only partway, limited by
the small diameter of the duct. The length of the plastic endoprosthesis was determined
at the time of procedure based on the anatomy and distance wire could be passed, varying
from 8 to 12 cm. The straight end of the stent was left extending at least 3 to 4 cm
into the gastric lumen. [Fig. 1a] depicts the relative size comparison of the devices used in our procedures. [Fig. 1b] shows a computed tomography (CT) scan demonstrating pigtail first placement of the
3F stent in the main pancreatic duct. In the first several cases, attempts were made
to reaccess the duct alongside the initial indwelling 3F stent but this was not possible,
likely due to edema in the tract. Subsequentlplacement of a second tandem stent was
not attempted until a repeat procedure. Patients were observed for 4 hours post-procedure,
with routine check of lipase and amylase levels at 2 hours; patients were admitted
for observation only if they complained of increased abdominal pain or had significant
(> 3 times upper limit of normal) enzyme levels. Patients were routinely brought back
for repeat procedures, at between 2 to 8 weeks once the tract had matured. Standard
duodenoscope and accessories were used to access the MPD through the PG alongside
the 3F stent, the tract was re-dilated and placement of a second 3Fr or larger stent
next to the first stent was performed. Stents were left in place indefinitely to maintain
the fistula, rather than to serve as hollow conduits.
Video 1 A case of endoscopic ultrasound guided pancreaticogastrostomy creation using cross-platform
small caliber devices (as detailed in text).
Fig. 1 a Relative size comparison of different devices used in our study (Top to bottom: Single
pigtail plastic stent, Angioplasty balloon, 0.018 platinum-tipped wire, 19-gauge needle).
b CT scan showing reverse placement of a single pig-tail plastic stent which anchors
by curling inside the pancreatic duct
Statistics
Data were analyzed using SPSS Version 23.0 (IBM Corp, Armonk, New York, United States).
All continuous variables are expressed as mean along with standard deviation and all
skewed variable are reported as median along with an interquartile range. Relative
proportions (%) are used for categorical variables.
Results
Patient characteristics
A total of 12 patients were identified from the prospectively maintained database
that had undergone a pancreaticogastrostomy between August 2013 and September 2018. Eight
patients were included in the final analysis group and 4 patients were excluded as
detailed in [Fig. 2]. Baseline characteristics of the patients are summarized in [Table 1]. Indications for duct drainage were disconnected pancreatic duct syndrome after
necrotizing pancreatitis (n = 4), stenotic pancreaticoenteral anastomosis after pancreaticoduodenectomy
(n = 3) and painful chronic pancreatitis with obstructed MPD (n = 1). Median MPD diameter
was 6.75 mm [IQR 2.8 – 7.6]. Only one of eight patients was hospitalized at the time
of the procedure for acute worsening of chronic symptoms. All other procedures were
scheduled on an outpatient basis. Five patients had presented with recurrent acute
pancreatitis (4 had disconnected pancreatic duct syndrome and 1 had a stenotic PDA)
and the other three cases had chronic abdominal pain as their presenting complaint
(1 patient with chronic pancreatitis and 2 patients with stenotic PDA).
Fig. 2 Flow diagram of all patients included in the study.
Table 1
Demographics, diagnostic findings and therapeutic first interventions in patients
requiring pancreatic duct drainage.
|
Patient
|
Age/sex
|
Anatomy
|
Indication for drainage
|
MPD diameter on EUS (mm)
|
Patient status (Outpatient vs inpatient)
|
Hospitalization post-procedure
|
|
1
|
75/F
|
Whipple
|
Stenotic PEA
|
8.0
|
O
|
N
|
|
2
|
70/F
|
Whipple
|
Stenotic PEA
|
1.1
|
O
|
N
|
|
3
|
47/M
|
Normal
|
DPDS
|
3.1
|
O
|
N
|
|
4
|
65/M
|
Normal
|
DPDS
|
7.2
|
O
|
Y
|
|
5
|
35/M
|
Normal
|
DPDS
|
7.0
|
O
|
N
|
|
6
|
68/F
|
Normal
|
Stenosed minor papillotomy,CP
|
11.0
|
O
|
Y
|
|
7
|
54/M
|
Normal
|
DPDS
|
2.5
|
O
|
N
|
|
8
|
57/F
|
Whipple
|
Stenotic PEA
|
6.5
|
I
|
NA
|
M, male; F, female; PEA, pancreaticoenteral tract anastomosis; DPDS, disconnected
pancreatic duct syndrome; CP, chronic pancreatitis; MPD, main pancreatic duct; O,
outpatient; I, inpatient; Y, yes; N, no; NA, not applicable
Procedure outcomes and complications
Procedure details and outcomes are detailed in [Table 2] and [Table 3], respectively. Technical success was achieved in seven of eight cases (88 %). The
one unsuccessful procedure was due to inability to pass the angioplasty balloon across
the pancreatic parenchyma after needle and wire access to the MPD had been obtained.
The 4F angioplasty balloon passed over the guidewire without noticeable resistance
in all other cases. Six patients had stents placed terminating inside into MPD while
one patient had a stent placed across the pancreaticoenteral anastomosis into the
jejunum. There was only one complication consisting of a small duct leak, which occurred
after the technically failed procedure. The patient had no worsening of clinic symptoms
or pancreatitis and the duct leak resolved without intervention. Five of seven patients
who had their procedure done as an outpatient were discharged on the same day as the
procedure. Two of seven patients were admitted for observation due to the complex
nature of their procedures and were discharged within 24 hours of their admission.
There were no late procedure-related complications documented in our patients.
Table 2
Procedure details.
|
Patient
|
Needle gauge
|
Wire diameter
|
Site of puncture in the MPD
|
Maximal inflation of angioplasty balloon (mm)
|
Stent
|
Drainage
|
Technical success
|
|
1
|
19
|
0.018
|
Body
|
2
|
3 Fr 9 cm
|
MPD-PG
|
Y
|
|
2
|
19
|
0.018
|
Body
|
3
|
3 Fr 7 cm
|
MPD-PEA
|
Y
|
|
3
|
22
|
0.018
|
Tail
|
3.5
|
3 Fr 8 cm
|
MPD-PG
|
Y
|
|
4
|
22
|
0.018
|
Body
|
4
|
3 Fr 12 cm
|
MPD-PG
|
Y
|
|
5
|
22
|
0.018
|
Body
|
4
|
3 Fr 7 cm
|
MPD-PG
|
Y
|
|
6
|
19
|
0.018
|
Body
|
3.5
|
3 Fr 11 cm
|
MPD-PG
|
Y
|
|
7
|
19
|
0.018
|
Body
|
3
|
3 Fr 8 cm
|
MPD-PG
|
Y
|
|
8
|
22
|
0.018
|
Body
|
3.5
|
NA
|
NA
|
N
|
Fr, French; MPD-PG, main pancreatic duct drained through pancreaticogastrostomy; MPD-PEA,
main pancreatic duct drained through pancreaticoenteral anastomosis; Y, yes; N, no
Table 3
Procedure-related outcomes.
|
Patient
|
Immediate complications
|
Late complications
|
Symptom control
|
Repeat intervention
|
Type of repeat intervention
|
Follow-up period (months)
|
|
1
|
N
|
N
|
Complete
|
Y
|
Two failed attempts at side by side stent placement. ERCP successful on 3rd attempt with side by side 3 Fr stent placement across PEA into jejunum
|
19
|
|
2
|
N
|
N
|
Complete
|
Y
|
ERCP in 6 weeks for 2nd 3 Fr stent placement side by side into MPD tail, parallel to 1st stent that was placed across PEA.
|
6
|
|
3
|
N
|
N
|
Complete
|
Y
|
ERCP in 2 weeks for a side by side 3 Fr 2nd stent placement
|
7
|
|
4[1]
|
N
|
N
|
Complete
|
Y
|
No repeat procedure done due to complete symptom improvement
|
5
|
|
5
|
N
|
N
|
Complete
|
Y
|
ERCP in 2 weeks for a side by side 3 Fr 2nd stent placement
|
16
|
|
6
|
N
|
N
|
Transient
|
Y
|
ERCP in 4 weeks for a side by side 4 Fr stent placement.
|
7
|
|
7
|
N
|
N
|
N
|
Y
|
ERCP in 8 weeks for a side by side 2nd 3 Fr stent placement. Continued to be symptomatic. Required a 3rd ERCP and EUS 16 weeks later due to persistent symptoms with placement of additional
trangastric stents in to pancreatic pseudocyst.
|
8
|
|
8
|
Contained duct leak
|
N
|
N
|
Y
|
Failed initial PG creation.[1]
|
6
|
N, no; Y, yes; Fr, French; ERCP, endoscopic retrograde cholangiopancreatography; PEA,
pancreaticoenteral anastomosis; EUS, endoscopic ultrasound; PG, pancreaticogastrostomy
1 Procedure converted to EUS-guided rendezvous with successful placement of trans-papillary
stent across PEA.
Follow-up for stent-related complications and stent replacement
Follow-up details and repeat interventions are detailed in [Table 3]. Mean duration of follow-up was around 9 months. All patients with successful drainage
underwent at least one repeat procedure 2 to 8 weeks after their index procedure.
There were no stent-related complications such as obstructive pancreatitis. At the
planned repeat procedure, placement of a second side-by-side stent was accomplished
in all patients. Overall clinical success was complete in five of eight patients with
successful procedures (62.5 %). Relief was transient in one patient after initial
placement of a single stent; a second parallel stent did not result in sustained improvement
and both stents eventually spontaneously migrated out of the pancreatic duct (not
visualized on most recent imaging). The patient is currently being considered for
surgical decompression or pancreatectomy with islet auto-transplantation. Three patients
had no initial or sustained relief of symptoms despite technical success.
Discussion
Therapeutic EUS for main pancreatic duct decompression has continued to evolve and
is now employed as salvage treatment after unsuccessful endoscopic retrograde access
to the MPD. EUS-guided pancreaticogastrostomy, initially described in 2002 by Francois
et al [14], has been used for MPD decompression in patients with native as well as surgically
altered anatomy [12]
[20]
[21]
[23]. Prior reports have been limited to patients with relatively dilated pancreatic
ducts, and have utilized relatively traumatic techniques to access the duct, included
electrocautery, bougie and screw dilation. In the current paper we report a less aggressive
method of accessing, dilating and stenting pancreatic ducts, including short segments
of non-dilated ducts in patients with disconnected duct syndrome presenting with recurrent
acute and/or chronic pancreatitis in the isolated tail.
The current technique utilizes readily available accessories including a small caliber
peripheral angioplasty balloon that is designed for use in peripheral vascular disease.
The common factor limiting cross-platform use of angioplasty devices for endoscopy
is the extra length needed to pass through an EUS or ERCP scope. The length of the
angioplasty balloon (150 cm) used in this series is just long enough to extend beyond
the tip of an echoendoscope or duodenoscope and cross a PG tract. The caliber of the
angioplasty balloon (4 Fr) is substantially smaller than currently available and marketed
endoscopic accessories. It allows relatively easy passage through the gastric wall
and pancreatic parenchyma without resorting to potentially traumatic maneuvers previously
reported. This balloon can only accommodate an 0.018-inch wire. The 0.018-inch wires
designed for ERCP use are platinum-tipped with a very flexible end and tend to knuckle
inside the pancreatic duct, even when restricted to a short distance by the blind
end of a disconnected duct. These 0.018-inch wires paradoxically remain relatively
stable during device exchanges and manipulation.
The technical failure rate of 12 % (1/8) in our study is similar to or less than reported
in previous reports, which has ranged from 0 to 40 % [12]
[21]
[22]. In contrast to other reported cases or series, we attempted drainage regardless
of the diameter of the pancreatic ducts. One of our patients with recurrent acute
pancreatitis after Whipple pancreaticoduodenectomy had a duct diameter of 1.1 and
had responded to EUS-guided rendezvous access and dilation in the past, but in that
individual, trans-anastomotic pancreaticojejunostomy stents repeatedly fell out [25]. The decision to place a trans-gastric pancreaticogastrostomy stent was intended
to leave a permanent indwelling stent to simultaneously maintain patency of the anastomosis
and provide a second drainage fistula back into the stomach. Interestingly, the one
technical failure in our study happened in the only patient with severe calcific chronic
pancreatitis in our study and was likely a result of markedly fibrotic pancreatic
parenchyma hindering passage of the angioplasty balloon. Clinical success occurred
in 62.5 % of patients, which is comparable to prior studies with EUS-guided pancreaticogastrostomy
[12]
[23]. The lack of response likely resulted from the fact that pain in chronic pancreatitis
is multifactorial and only partially related to ductal hypertension [26]. The technical feasibility and utility of this technique in patients with severe
calcific chronic pancreatitis will need to be further investigated in larger studies.
Previously employed techniques for creating a fistulous tract across the muscular
gastric wall, pancreatic parenchyma and in to the PD have used needle-knife cautery
[12]
[14]
[22], bougie dilation [21] or standard balloon dilators [23]. Such techniques are associated with significant trauma especially to the pancreatic
parenchyma and complications such as bleeding, perforation, perigastric collections
or acute pancreatitis have all been reported as a result. As mentioned earlier, the
technique proposed in our study uses small-shaft-diameter angioplasty balloons that
pass through the gastric wall and the pancreatic parenchyma with mild resistance and
importantly, with less trauma to the tissue and duct wall. So far, there have been
no serious complications of bleeding, perforation or acute pancreatitis. There was
only minor complication of contained duct leak, in the single case of unsuccessful
stent placement, which resolved without clinical consequences and did not require
any interventions.
Stent dysfunction from stent occlusion or migration has been a concern in previous
series of pancreaticogastrostomies and has been reported in 50 % to 55 % of cases
[12]
[23]. Outward migration of stents was seen in only one patient in our series and occurred
6 weeks after the initial EUS and 2 weeks after the repeat procedure for upsizing,
dilation and placement of a second side by side stent. There were no cases with inward
migration of stents. We hypothesize that unlike larger 5- to 7-Fr stents, as mostly
used in other studies, which provide through-the-stent drainage, but ultimately occlude,
the presence of 3-Fr stents, with long segments protruding into gastric lumen, act
as a wick to keep the pancreaticogastric fistula open rather than to maintain luminal
drainage. Placement of two small side-by-side stents is intended to allow separate
motion of the stents by gastric peristalsis, and create space for flow between the
stents [12]
[27].
Conclusion
The current paper is subject to the limitations inherent in all smaller, retrospective
studies but is meant to be hypothesis-generating. Randomized controlled trials with
larger series involving multiple centers would be ideal to achieve sufficient sample
size for comparison of outcomes between different approaches that are mentioned earlier
in our discussion. Nevertheless, use of very-small-caliber devices that are readily
available across other platforms, in this case peripheral angiography balloons, can
allow endoscopists to be therapeutically successful when traditional larger-caliber
pancreaticobiliary devices are inadequate even with standard ERCP [28].