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Enteric Stents: Indications and Placement Techniques
Todd Baron
1 1
Self-expandable metal biliary stents (SEMS), fi rst used outside of the USA, became commer­cially available in the USA approximately 20 years ago because of their prolonged patency when compared to plastic biliary stents [ 1 ] . Esophageal SEMS were introduced soon after expandable biliary stents, and SEMS speci fi cally designed for gastroduodenal use were developed several years later. However, both esophageal and biliary SEMS have been used for relief of gastroduodenal obstruction. The indications and placement techniques for enteric stents, de fi ned as gastric and small bowel stents for the purposes of this chapter, will be reviewed.
Basic Concepts
Self-expandable stents placed for enteric use are composed of a variety of materials ranging from plastic to stainless steel to nitinol. Stents vary based upon type of material that they are composed of, lattice width (if any), con fi guration, length and diameter, and presence and degree of covering. More importantly, in order for precise placement to be achieved, the degree of shortening (if any) that occurs with expansion and the nuances of the delivery and release systems must be known. There are a number of stents available from a
T. Baron , M.D. () Department of Medicine , Mayo Clinic , 200 First Street SW , Rochester , MN 55905 , USA e-mail: baron.todd@mayo.edu
variety of manufacturers around the world. The principles of all expandable stents are similar, and the concepts presented here can be applied to all expandable stents.
It is extremely helpful to have nursing assistants who are comfortable with complex therapeutic endoscopic procedures to include expandable stent placement. Moreover, an under­standing of the complexities of stent placement will assure that complications are minimized [ 2 ] .
Indications for and Contraindications to Enteric Stent Placement
Indications
There are several indications for placement of enteric stents (Table into benign and malignant conditions, although indications for placement in malignant disease are much more common than for benign disease. In Table tion and type of disease process. Indications for enteric stent placement in benign diseases are generally due to postoperative complications that include strictures, leaks, and fi stula. Post-bariatric surgery, historically Roux-en-Y gastric bypass, and more recently, sleeve gastrectomy can be associated with postoperative leaks, fi stula, and strictures and can be managed using temporary stent placement [ 3– 11 ] (Fig. 11.1 ). Similarly, occasional patients who have had prior Billroth II operations and pancreaticoduodenectomy may
11.1 , indications are divided into loca-
11.1 ). These can be divided
R. Kozarek et al. (eds.), Self-Expandable Stents in the Gastrointestinal Tract, DOI 10.1007/978-1-4614-3746-8_11, © Springer Science+Business Media New York 2013
159
160
T. Baron
Table 11.1 Indications for placement of enteric stents
Benign
Gastric
Postoperative fi stula/leaks – gastric (sleeve gastrec­tomy) and gastrojejunal anastomosis (Roux-en-Y gastric bypass, post-Whipple and Billroth II)
Gastric stricture (sleeve gastrectomy)
Duodenal – stricture due to peptic ulcer disease; duodenal fi stula (rare)
Small bowel – postoperative strictures – anastomotic, Crohn’s disease (rare)
Malignant
Gastric obstruction
Primary and recurrent gastric cancer Gastrojejunal anastomosis (afferent and efferent limb
obstruction) Gastric stricture (sleeve gastrectomy)
Duodenal obstruction
Periampullary cancer Pancreatic cancer/metastatic disease to the head of
the pancreas Cholangiocarcinoma Gallbladder cancer Locally invasive tumors (colon cancer)
Small bowel – metastatic disease (particularly ligament of Treitz), distal terminal ileum (pelvic cancers, metastatic disease)
Other (uncommon)
Perforation of the duodenum or jejunal limbs of anastomoses (within reach of endoscope and stent delivery system)
Bridge to surgery Transgastric or transduodenal placement for drainage
or debridement of pancreatic necrosis
develop benign anastomotic complications that can be managed with stents [
12 ] . Crohn’s disease
with small bowel stricture is an uncommon indi­cation for stent placement, although recent data on the use of SEMS [ 13 ] , as well biodegradable stents [
14 ] , show promise for these patients. In
most patients with benign strictures, stent place­ment should only be considered after the patient has failed an adequate trial of serial endoscopic dilation.
Malignant disease is a much more common cause of luminal obstruction and needs palliative enteric stent placement. Rarely, enteric stents are placed as a bridge to surgery (e.g., primary small bowel lymphoma), although there are no published data for this indication.
Fig. 11.1 Use of a fully covered stent for treatment of complete gastric outlet obstruction due to a benign stricture following sleeve gastrectomy. ( a ) Endoscope is positioned above the predeployed stent. ( b ) Postdeployment upper gastrointestinal series shows persistent narrowing. The stent was removed 3 months later, and the patient remains well 5 years later
Before offering stent placement for relief of gastric outlet obstruction (GOO), the degree of oral intake should be assessed. A gastric outlet obstruction scoring system (GOOSS), adapted from the dysphagia scoring system, was intro­duced by Adler and Baron in 2002 [ 15 ] and has become accepted as a measure of oral intake (Table 11.2 ). Patients with GOOSS scores <2 are candidates for stent placement. Alternatively,
16111 Enteric Stents: Indications and Placement Techniques
palliative gastrojejunostomy, increasingly performed laparoscopically, should be considered an alternative to stent placement in patients with anticipated survival longer than 3–4 months [
16, 17 ] ,
potentially predictable by a WHO (World Health Organization) score. The WHO score is based upon a scale of 0–5, with 0 being healthy and 5 being dead. A recent study showed that patients
Table 11.2 Gastric outlet obstruction scoring system (GOOSS)
Level of oral intake Score No oral intake 0 Liquids only 1 Soft solids 2 Low-residue or full diet 3
with a WHO score of 0–1 may be managed with gastrojejunostomy, while those with a WHO score of 3–4 should be considered for stent place­ment [ 18 ] as a consequence of the longer survival and more durable duration of palliation in the surgical group. The type of malignancy that causes lumen obstruction (Table 11.1 ) varies throughout the world. For example, in the East, primary and recurrent gastric cancer with resultant GOO is more common, whereas in the West, pancre­atic cancer is the most common cause of GOO.
Occasional patients have distal small bowel obstruction that does not involve the colon, but only be reached retrograde via colonoscopy (Fig. 11.2 ). Free luminal perforation, usually iat- rogenic, is a rare indication for enteric stent placement [ 19 ] (Fig. 11.3 ).
Fig. 11.2 Placement of fully covered biliary stent for treatment of a benign postoperative distal ileal anastomotic stricture. ( a ) Colonoscope has been passed through the ileocecal valve to the site of obstruction. Injected contrast does not pass the obstruction. ( b ) After traversing the
stricture with a guidewire, the upstream dilated ileum is seen. ( c ) Note placement of a fully covered biliary stent and 10-Fr nasojejunal tube inserted for safety and decompression. The stent passed spontaneously 1 month after resolution of obstruction
162
T. Baron
Fig. 11.3 Closure of a large lateral wall duodenal perfo­ration during ERCP for obstructive jaundice. ( a ) The duodenoscope has been removed and a Savary wire advanced beyond the ligament of Treitz using a forward-
Contraindications
There are relatively few contraindications to plac­ing self-expandable, enteric metal stents. Free per­foration, although considered a contraindication to most endoscopic procedures, may, in fact, be an indication for perforation closure (Fig.
Peritoneal carcinomatosis is a relative con­traindication to enteric stent placement because many patients have multifocal areas of obstruc­tion and encasement of the small bowel and may not respond to stent placement for palliation of obstruction; moreover, if clinically successful, the improvement is often short-lived. Patients with peritoneal carcinomatosis are identi fi ed by the presence of underlying malignant ascites
11.3 ).
viewing endoscope. Free air outlines the kidney (K). ( b ) Immediately after placement of a covered non-TTS esophageal stent. ( c ) Upper GI 2 days later shows no leak
and/or peritoneal thickening on abdominal CT imaging. There are two morphologic types of peritoneal implants. Layered implants (higher grade, nonmucinous, and invasive lesions) conform to the normal shape of abdominal structures and are not well seen on computed tomography (CT), whereas nodular implants (lower grade, muci­nous, and noninvasive lesions) are more readily apparent (Fig.
11.4a ) [ 20 ] . In one recent study,
patients with peritoneal carcinomatosis were found to have similar results to those without [ 21 ] . This is in contrast to this author’s experi­ence, although I believe that selected patients with peritoneal carcinomatosis and what appears to be a single, dominant obstructive stricture with marked upstream dilation and a clear-cut
16311 Enteric Stents: Indications and Placement Techniques
Fig. 11.4 Peritoneal carcinomatosis in the setting of SEMS placement. ( a ) CT shows typical features with ascites and nodularity around the liver ( single arrow ) and nodules in the left upper quadrant adjacent to the colon ( double arrows ). Ascites (marked by A) is present
transition point on CT may respond to stent therapy (Fig. 11.4b ). In such cases, where stent placement is technically successful, yet clinically unsuccessful, placement of additional stents is usually futile and other means of palliation should be undertaken (such as nasogastric or decom­pressive gastrostomy tube placement).
Stent Selection
Selection of the appropriate stent is based upon the indication for placement and stent availabil­ity. For documented, unresectable disease, uncov­ered stents are most commonly used because of their low rate of migration compared to covered stents, although the latter are associated with a decrease in tumor ingrowth [ for enteric use are available outside of the USA. In the USA, the only available, dedicated enteric stents are uncovered [ 23 ] . The advantage of these dedicated stents is that their delivery systems are long enough and small enough in diameter to pass through the scope (TTS), including adult colonoscopes. The lack of removability, however, makes them unsuitable for treatment of benign disease or closure of fi stula. Thus, within the USA, stent options for benign disease and for
22 ] . Covered stents
throughout. ( b ) Upper gastrointestinal series in same patient shows high-grade lesion. Despite successful stent placement and patency con fi rmed by upper gastrointesti­nal series, the patient did not clinically improve, and distal lesions were identi fi ed
closure of fi stula are limited to the use of esopha­geal and biliary stents.
Esophageal stents are available as fully and partially covered self-expandable metal (SEMS) or plastic (SEPS) but are limited by their short, non-TTS delivery systems. The only available SEPS (see Chap.
3 ) has a particularly rigid
delivery system that limits their use to place­ment in lesions that are close to the mouth and are relatively straight in the projected pathway (e.g., treatment of a Roux-en-Y gastrojejunal anastomotic stricture or leak).
Esophageal SEMS are more fl exible, but their relatively short delivery systems generally limit transoral placement in patients with nonsurgically altered anatomy to the fi rst and second portion of the duodenum in best-case scenarios. However, novel placement techniques include placement through gastrostomy tracts – either after matura­tion [ 24 ] or through fresh tracts created with introducer systems (Fig. delivery systems [
25 ] , and use of overtubes [ 26 ] .
11.5 ), extension of
Biliary SEMS are available as partially and fully covered stents and are long enough to pass through a colonoscope and for benign strictures of the small bowel, either antegrade or retrograde. The disadvantage to these stents is a luminal diameter of 8–10 mm. However, side-by-side
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T. Baron
Fig. 11.5 Closure of a large duodenal fi stula (at site of percutaneous pigtail drain) using overlapping covered (partially and fully) esophageal stents. A gastrostomy sheath ( small arrows ) was placed percutaneously immedi- ately before stents were passed through the sheath. Note small-caliber endoscope ( large arrow ) could also be passed through sheath to assess stent position after deployment
placement is possible to achieve luminal diameters of 20 mm (Fig. 11.6 ).
Gastroduodenal Stent Placement
Preparation, Sedation, and Positioning
Obtaining a pre-procedural radiographic contrast study is not essential, and often not performed, although such imaging allows determination of the anatomy and stricture length (Figs.
11.6a ) and precludes need for passage of the
endoscope beyond the lesion to determine their length and angulation. It is most helpful if it is unclear whether the patient’s symptoms are due to obstruction or other cancer-related processes (neural invasion by tumor with delayed gastric emptying, peritoneal carcinomatosis). Most patients will have had a recent abdominal CT scan which provides information on degree of obstruction, location, length of stricture, and presence or absence of fi stula.
Before undertaking stent placement in patients with malignant gastroduodenal obstruction, it is important to fi rst assess the status of the biliary tree, since placement of an expandable stent across the papilla may make subsequent endo-
11.4 and
scopic access to the papilla dif fi cult, if not impossible. In addition, in patients with proximal duodenal strictures, the stent does not necessarily have to cross the papilla to achieve palliation. Thus, a stent should be chosen that is adequate to cross the lesion, but not excessively long so as to prevent access to the papilla, if potentially required in the future. A recent review of combined gastroduodenal and biliary obstruction has been published [ 27 ] , and a technical approach to combined obstruction will be discussed later in this chapter.
Not unexpectedly, patients with complete gastric outlet obstruction have retained liquids and/or solids and are at risk for aspiration during stent placement unless precautions are taken. Patients with complete obstruction are already nil per os, hospitalized, and often have nasogastric suction for decompression. Nonetheless, solid food may not be adequately evacuated and remain in place. Outpatients with subtotal obstruction should consume clear liquids for at least 24 h prior to their procedure, but may have retained solid food. Sedation with airway protection (endotracheal intubation), large-bore evacuation, type of endoscope, and patient positioning all play a role in the prevention of aspiration and optimization of endoscopic visualization. Large­bore evacuation tubes can be used, if necessary, to allow endoscopic visualization, but are best reserved for patients who have airway protection. Large working channel (6 mm) endoscopes, such as those designed for removal of blood clots during gastrointestinal bleeding, can be used to evacuate semisolid material.
Fluoroscopy, although not always necessary when stents are placed using endoscopic tech­niques, especially for nonobstructive indica­tions, should be readily available and is mandatory when stents are placed using inter­ventional radiologic techniques alone. Placing the patient in the left lateral decubitus position prevents aspiration, but the fl uoroscopic image is less than ideal for gastroduodenal stent place­ment. Thus, placement in the prone or supine position is preferred. When moderate or moni­tored anesthesia care is used, I place the patient in the left lateral decubitus position and remove all gastric contents, if possible. The patient is
16511 Enteric Stents: Indications and Placement Techniques
Fig. 11.6 Treatment of a benign duodenojejunal anasto­motic stricture with side-by-side covered biliary stents. ( a ) Upper GI contrast series showing stricture. ( b ) Two guidewires are passed alongside each other. The fi rst stent is predeployed in position across the stricture. ( c ) Radiograph
subsequently placed supine and the airway carefully monitored and suctioned with the head of the bed elevated (if possible). In addition, one may consider endotracheal intubation in these patients to prevent aspiration.
taken immediately after deployment of both stents. Contrast is injected through the inferior stent. ( d ) Endoscopic photo of side-by-side covered expandable metal biliary stents. ( e ) Follow-up upper gastrointestinal series after removal of both stents shows resolution of stricture
Choice of Endoscope
The choice of endoscope for gastroduodenal stent placement depends on the site of the lesion (stom­ach versus duodenum), type of stent, and whether
166
T. Baron
an ERCP will be done at the same setting. Small-caliber endoscopes (5.4-mm outer diame­ter or less) can be used for gastric lesions and those with a disease process at or near a gastroje­junal anastomosis. These endoscopes allow easy traversal of tight strictures for endoscopic inspec­tion and may obviate fl uoroscopy to determine stricture length. However, the working channel is small, suction capability is suboptimal, and the scopes do not permit passage of accessories (catheters), and essentially, only guidewires can be passed. However, once a guidewire is passed, the endoscope can be removed, and a therapeutic channel endoscope can be backloaded over the wire for TTS delivery [
28 ] .
Standard adult endoscopes are intermediate in terms of fl exibility and use of accessories, but the working channel does not allow TTS stent placement. Therapeutic channel endoscopes (working channel ³ 3.8 mm) are most often used when TTS stents with predeployment delivery systems of 10 Fr are placed.
Duodenoscopes also allow passage of TTS stents and are advantageous when ERCP with biliary stent placement and gastroduodenal stents are placed in the same session, precluding the need to change endoscopes. The side-viewing duodenoscope may be helpful in those patients in whom the stricture cannot be traversed with a forward endoscope and may allow an en face view of the stricture.
Upper endoscopes and duodenoscopes are usually limited to lesions proximal to the second duodenum in patients with GOO since the often dilated stomach creates looping that consumes the length of the endoscope. Thus, even for proximal duodenal lesions, it may be useful to use adult caliber colonoscopes for TTS placement. These scopes are essential for lesions beyond the second to third duodenum, to include the proxi­mal jejunum in patients with intact anatomy. Moreover, they are often used for patients with afferent limb obstructions far from the origin of the anastomoses.
Finally, balloon enteroscopes may be useful in selected cases, not only because of the ability to pass deep into the bowel but also because of their fl exibility. Following wire passage beyond the stenosis, the endoscope can either be removed
and a therapeutic endoscope backloaded over the wire, or the stent can be passed through the overtube [ been used with spiral overtubes [
29 ] . Similar placement techniques have
30 ] .
Insertion Techniques
Stents can be placed using endoscopic techniques with or without fl uoroscopy and can be TTS or non-TTS. Alternatively, stents can be placed using interventional radiologic techniques alone. TTS and non-TTS endoscopic techniques will be discussed separately, but the rate-limiting step that is common to all techniques for successful placement is passage of a guidewire across the intended site of placement. This can be techni­cally dif fi cult in patients whose primary problem is obstruction, particularly complete obstruction. Thus, techniques to traverse the lesion are espe­cially important. This chapter will focus primarily on endoscopic approaches.
Through-the-Scope Insertion
Since therapeutic channel endoscopes (working channel ³ 3.8 mm) are needed to place TTS stents and are large in caliber, it is frequently not possible to traverse the stricture with the endo­scope and is not necessary to achieve placement. Thus, aggressive dilation of the stricture in order to traverse it (unless a duodenoscope is needed to pass through the stricture to reach the papilla) should be avoided to minimize perforation risks. Occasionally, however, small-caliber endoscopes are useful to pass guidewires; however, the working channel only accepts 0.035–038″ guidewires and not standard diameter biliary catheters. This requires removal of the endoscope and back­loading of a therapeutic endoscope to place the stent in TTS fashion [ 28 ] , although at times, a second guidewire can be inserted through a thera­peutic scope alongside the initial wire without the need to backload the wire.
The usual approach is to pass the endoscope to the site of the lesion. In the presence of subtotal obstruction, water-soluble contrast can be injected through the working channel of the endoscope to de fi ne stricture characteristics and a fl exible
0.025–0.035″ long-length biliary wire passed
16711 Enteric Stents: Indications and Placement Techniques
through the stricture freehand or through a cathe- ter. The stent is passed through the lesion and deployed across the stricture. In complete obstruc­tion or more dif fi cult, tortuous strictures, a biliary occlusion (stone retrieval) balloon preloaded with a hydrophilic wire is in fl ated to 18 mm with its tip positioned against the lesion to provide pressure for injection across the stricture in an attempt to obtain a “strictureogram” (Fig.
11.7a ). If this is
unsuccessful, a biliary sphincterotome may be useful (Fig. 11.7b ) when an en face view of the stricture cannot be obtained since they can be bowed to change direction and orientation, espe­cially those that are rotatable. Once the stricture has been traversed with the catheter, contrast is injected to con fi rm bowel entry and to de fi ne the stricture length (Fig. 11.7c ). The stent length can be con fi rmed by in fl ating the occlusion balloon once it is beyond the stricture. The in fl ated balloon is pulled snugly against the distal end of the stric­ture. The catheter is grasped at the biopsy port, and the balloon is de fl ated and withdrawn until it is visible endoscopically on the proximal side of the stricture. The distance between the operators’ fi ngers and the biopsy cap corresponds to the length of the stricture.
A stent is chosen with a fi nal length after deployment about 4 cm longer than the mea­sured stricture. The stent is passed through the channel of the endoscope and across the lesion. Predeployment stent placement is rarely needed because of the small diameter delivery systems.
It is important to note that most gastroduode­nal stents foreshorten up to 40% during deploy­ment and all deploy from the distal end. Thus, a key to optimal stent placement is to position the endoscope about three to four centimeters proxi­mally from the proximal end of the stricture while endoscopically monitoring the proximal end. The stent will appear to move away from the tip of the endoscope as it is pushed out of the delivery system as it shortens during expansion; thus, the endoscopist usually needs to pull back on the delivery system during deployment. Most dedi­cated enteral stents are recapturable up to 70–80% of complete deployment, and thus, if the process is not progressing as planned, the stent can be recaptured and redeployed after appropriate adjustments are made.
After deployment of the stent, the delivery system is withdrawn, but the guidewire should not be removed until one is certain that the stric­ture has been adequately covered by the stent. In extremely tight strictures, the delivery system may not be easily withdrawn as it may be con­strained by the unexpanded stent. In addition, the WallFlex stent has a shelf on the distal end of the delivery system, which may catch on the wires. The assistant should place the stent in the prede­ployment position to match the sheath against the distal end of the stent and resolve this shelf. The endoscopist simultaneously needs to advance the delivery catheter as this maneuver tends to pull the distal nose proximally and may dislodge the stent proximally.
Proper positioning of the stent within the stricture is con fi rmed fl uoroscopically by a waist within the stent (Fig. 11.7d ). Contrast can be injected through the working channel and into the stent to assess complete patency. Leaving the wire in place allows additional stent(s) to be deployed in overlapping fashion, if needed or for postdeployment balloon dilation. If overlapping stents are required, it is essential to have at least 2 cm overlapping after deployment, since with further expansion after placement, the stents may shorten and separate. Balloon dilation is usually not needed as the stent will expand on its own and postdeployment dilation has been shown to induce perforation.
For strictures in the second duodenum, there is some debate about whether or not the proximal end of the stent should remain in the duodenum or in the gastric antrum because of the potential difference in functional result. Stent-induced per­foration may occur when the proximal end of a stent with sharp wires remains in the duodenum [ 19 ] . Newer stents with rounded edges may reduce this complication and allow for more physiologic gastric emptying.
Non-Through-the-Scope Stent Insertion
Non-TTS stent placement is most often used when placed by interventional radiologists and when endoscopists use stents that cannot be placed TTS (e.g., use of esophageal stents). The dif fi culty with non-TTS placement is the lack of mechanical advantage in lesions distal to the
168
T. Baron
Fig. 11.7 Palliation of malignant obstruction near the ligament of Treitz due to gastric cancer. ( a ) A colono- scope is in position at the lesion. An occlusion balloon is in fl ated and contrast injected under pressure. No con­trast passes. ( b ) A rotatable biliary sphincterotome with
small diameter hydrophilic wire is passed across the stricture. ( c ) Contrast is injected con fi rming passage into small bowel. ( d ) Radiographic image immediately after stent deployment. ( e ) Endoscopic photo of deployed stent