Radiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Abstract Freely available
Right arrow Figures Only
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Mauro, M. A.
Right arrow Articles by Baron, T. H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Mauro, M. A.
Right arrow Articles by Baron, T. H.
(Radiology. 2000;215:659-669.)
© RSNA, 2000


State of the Art

Advances in Gastrointestinal Intervention: The Treatment of Gastroduodenal and Colorectal Obstructions with Metallic Stents1

Matthew A. Mauro, MD, Robert E. Koehler, MD and Todd H. Baron, MD

1 From the Departments of Radiology and Surgery, University of North Carolina School of Medicine, Chapel Hill, NC 27599 (M.A.M.); the Department of Radiology, University of Alabama School of Medicine, Birmingham (R.E.K.); and the Division of Gastroenterology and Hepatology, Mayo School of Medicine, Rochester, Minn (T.H.B.). Received April 1, 1999; revision requested June 14; revision received July 12; accepted July 30. Address correspondence to M.A.M.

Abstract

Metallic stents are currently an established component of the endoluminal treatment of stenoses within the blood vessels, bile ducts, esophagus, trachea, and bronchi. With the development of newer stent designs and delivery systems and the general momentum toward minimally invasive therapies, metallic stent placement has expanded into the nonsurgical therapy for gastroduodenal and colorectal obstructions. The use of metallic stents within the stomach, duodenum, or colon is intended not to be curative but to provide nonsurgical palliation for the symptoms of gastric or colonic obstruction. This palliation may be intended for the life of the patient in the case of unresectable disease or as a temporizing procedure prior to a definitive surgical procedure. In the latter clinical scenario, the benefits of a minimally invasive intestinal decompression procedure include (a) quick and noninvasive relief of the intestinal obstruction in an acutely ill patient that obviates a more extensive procedure; (b) allowance of time to improve a patient's overall medical condition and thus to allow a patient to better tolerate the definitive surgical procedure; and (c) reduction of the complexity of the definitive procedure by eliminating the need for staged procedures and allowing the definitive procedure to be performed at one setting.

Index terms: Gastrointestinal tract, abnormalities, 72.30, 73.30, 73.723, 75.30, 75.725 • Gastrointestinal tract, interventional procedures, 72.126, 73.126, 75.126 • State of the Art

The use of expandable metallic stents in the treatment of gastric or colonic obstruction is a direct extension of their established utility in treating obstruction within the biliary tree, tracheobronchial tree, vascular system, and esophagus. Within the esophagus, stent placement has been used effectively in the treatment of malignant dysphagia and is now a well-established procedure (16). Technical success approaches 100%, and improvement in the dysphagia score ranges from 83% to 100% (13). As with the esophagus, metallic stents used within the stomach, duodenum, and colon are intended not to be curative but rather as nonsurgical palliation of the symptoms of obstruction. Unlike treatment in the esophagus, the treatment of gastroduodenal and colorectal obstructions with metallic stents is not yet well established, to our knowledge. Increased familiarity with the available devices, indications, and techniques will be needed before widespread acceptance can be achieved. Innovations in stent design also promise to increase the use of this treatment method in the future.

Unlike plastic tubes or catheters, flexible metallic stents have a high ratio of deployed (expanded) diameter to introduction diameter. That is, they have a relatively small-caliber introduction system that allows safe and atraumatic placement via the mouth or anus; yet when deployed, they expand to a diameter large enough to relieve the obstruction. Some of these devices will even pass through the working channel of a therapeutic endoscope.

STENT TECHNOLOGY

Despite the recent advances in stent technology, the search for the ideal enteral stent continues. Enteral stents should be flexible enough to allow placement but should remain in position once deployed. They should have an internal diameter large enough to relieve obstructive symptoms and restore normal eating and bowel habits. They should have sufficient radial force to expand slowly within areas of fibrosis or neoplasm. They should also prevent obstruction due to tumor ingrowth or reactive hyperplasia. Covered stents have the advantage of resisting tumor ingrowth but tend to be less stable and more rigid, require larger delivery systems, and are more likely to migrate. They are thus more difficult to deploy at distant locations through a tortuous delivery path (7). Uncovered stents are more flexible, and at least one variety can be passed through the working channel of an endoscope. However, when used for long-term palliation of malignant obstruction, they are subject to tumor ingrowth and resultant obstruction.

Until recently, stents used in the stomach and colon were those designed for esophageal, tracheobronchial, or vascular use. Commercially available esophageal stents that have been used in the stomach or colon include the Gianturco Z-stent (Wilson-Cook, Winston-Salem, NC), Wallstent (Boston Scientific, Natick, Mass), Ultraflex nitinol mesh stent (Microinvasive, Natick, Mass), and Esophacoil (IntraTherapeutics, Eden Prairie, Minn) (Fig 1). Tracheobronchial stents that have been used in other anatomic areas include the Gianturco Z tracheobronchial tree stent and the Wallstent tracheobronchial endoprosthesis. A Wallstent enteral endoprosthesis is now available in the United States specifically for the treatment of gastroduodenal and colonic obstructions (Fig 2).



View larger version (68K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 1a. Photographs of esophageal stents used in the gastroduodenal and colorectal regions. (a) Deployment systems. Top: Ultraflex knitted nitinol stent delivered with a 24-F-outer diameter delivery system. Middle: Covered Gianturco Z-stent delivered with a 28-F-outer diameter delivery system. Bottom: Covered Wallstent II delivered with an 18-F-outer diameter delivery system. (b) Deployed stents. Top: Uncovered Ultraflex nitinol stent. Middle: Covered Gianturco Z-stent. Bottom: Covered Wallstent II with bare metal ends.

 


View larger version (95K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 1b. Photographs of esophageal stents used in the gastroduodenal and colorectal regions. (a) Deployment systems. Top: Ultraflex knitted nitinol stent delivered with a 24-F-outer diameter delivery system. Middle: Covered Gianturco Z-stent delivered with a 28-F-outer diameter delivery system. Bottom: Covered Wallstent II delivered with an 18-F-outer diameter delivery system. (b) Deployed stents. Top: Uncovered Ultraflex nitinol stent. Middle: Covered Gianturco Z-stent. Bottom: Covered Wallstent II with bare metal ends.

 


View larger version (42K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 2a. Photographs of the enteral Wallstent. (a) Deployment system: 10-F-outer diameter stent delivery system. The self-expanding stent is deployed by withdrawing the enveloping membrane. The stent delivery assembly fits through the 3.5-mm working channel of the endoscope. (b) The deployed stent expands to a predetermined diameter. The bare metal edges help prevent stent migration.

 


View larger version (55K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 2b. Photographs of the enteral Wallstent. (a) Deployment system: 10-F-outer diameter stent delivery system. The self-expanding stent is deployed by withdrawing the enveloping membrane. The stent delivery assembly fits through the 3.5-mm working channel of the endoscope. (b) The deployed stent expands to a predetermined diameter. The bare metal edges help prevent stent migration.

 
The Gianturco Z-stent is available in uncovered and polyethylene-covered varieties. The covered esophageal Z-stent is designed with flared ends to provide stability and reduce migration (Fig 1). It has an outer diameter of 18 mm in its midportion (16-mm middle inner diameter) and an outer diameter of 25 mm at each end (8,9). The device is inserted via a 24-F (inner diameter), 28-F (outer diameter) sheath. The uncovered tracheobronchial Z-stents are cylindric and are available in diameters of 15, 20, 25, and 30 mm.

The Wallstent is also available in covered and uncovered varieties. There are two silicone-covered esophageal Wallstents. Wallstent I has a dog-bone configuration with an 18-mm luminal diameter and is placed with a 38-F delivery system. Wallstent II has a more gradual flare at each end and is introduced with an 18-F delivery system (Fig 1). The Wallstent esophageal endoprosthesis has a length of uncovered wire at each end to allow tissue ingrowth and stabilization (10). The uncovered Wallstent endoprostheses (tracheobronchial or enteral) are available in a wide range of diameters; the largest expands to 24 mm. The enteral endoprosthesis is deployed from a 10-F delivery system that can fit through a 3.5-mm working channel of an endoscope (Fig 2).

The original Ultraflex nitinol mesh stent is an uncovered stent knitted with elastic alloy wire that slowly expands when deployed at body temperature. It has a lower radial expansile force than the other stents, but its flexibility allows it to be placed across acutely angled stenoses (10,11). The body is 18 mm in diameter and is introduced via a 24-F (outer diameter) sheath (Fig 1). The Ultraflex II is now available in both covered and uncovered varieties and is enclosed within a weave that is released during deployment.

The Esophacoil is an uncovered nitinol coiled stent delivered through a 32-F introduction system.

STOMACH AND DUODENUM

Clinical Factors and Alternative Treatments
Malignant obstruction of the stomach or duodenum causes nausea, vomiting, esophagitis, electrolyte imbalance, poor nutrition, and severe dehydration (12). Causes include primary tumors of the stomach and duodenum, malignant infiltration by neoplasms from adjacent organs (eg, pancreas), and compression by malignant regional lymphadenopathy. Curative resection is not possible in 40% of patients with gastric cancer and 80%–95% of patients with pancreatic cancer (13,14). Palliative gastrojejunostomy with or without gastric resection is commonly performed to relieve obstructive symptoms (1316). However, in patients with extensive malignant disease and a poor short-term prognosis, surgery may not be possible or desirable (17). Nonsurgical palliative endoluminal techniques such as endoluminal irradiation, laser ablation, and chemical injection have been performed, predominantly in the esophagus. They tend to be useful only in cases of bulky exophytic tumors, often require multiple sessions, and can be accompanied by clinically important complications (1828).

Nonsurgical palliation can also be accomplished by means of nasogastric intubation or the placement of a gastrostomy or a gastrojejunostomy tube. Prolonged nasogastric intubation is very uncomfortable. A dual-lumen gastrojejunostomy tube will allow gastric decompression and direct jejunal enteral feedings. The gastrojejunostomy tube will not, however, allow the oral intake of solid food (29).

Indications
Expandable metallic stents offer another nonsurgical alternative. They are most useful in poor surgical candidates with malignant obstruction of the gastric outlet. These patients may be medically unable to undergo a surgical procedure or may have a limited life expectancy, which makes the more durable surgical procedure unwarranted. The ability to treat duodenal obstruction secondary to extrinsic compression from pancreatic cancer further expands the spectrum of indications of metallic stent placement for primary nonsurgical palliation. Patients who are able to undergo a more extensive procedure and who have a reasonable life expectancy will continue to benefit from conventional surgical treatment, even when palliative. Metallic stents have also been used in patients with benign gastroduodenal strictures when conventional surgical resection or bypass was not possible or wanted (2946). In patients with benign disease, coexistent morbid factors involving the cardiopulmonary systems may limit surgical options, which makes the use of metallic stents more attractive. In all cases, intestinal perforation remains the primary contraindication to metallic stent placement.

Technical Considerations
Both covered and uncovered stents have been deployed in the gastroduodenal segment (2932,42). The primary advantage of covered stents is the prevention of tissue ingrowth (tumor or mucosal hyperplasia) that leads to recurrent obstruction (42,47). This advantage is often outweighed by the stent's increased rigidity and tendency to migrate. Uncovered stents are more flexible and therefore easier to deploy (2938). The enteral Wallstent can be deployed through the working channel of a therapeutic endoscope (39). Tumor ingrowth through the interstices of the uncovered stent has not been a clinically important disadvantage because of the limited life expectancy of patients with extensive malignancy (29,31,39).

Expandable metallic stents can be placed with fluoroscopic guidance, endoscopic guidance, or a combination of both (2944). The techniques used will often depend on local political and utilization issues. In programs with a strong and aggressive interventional gastroenterology division, stent insertion with endoscopic or combined endoscopic-fluoroscopic guidance will likely be performed. In areas where an interventional gastroenterologist is not present, is unavailable, or is uninterested or where a direct referral pattern has been established from a surgeon to an interventional radiologist, fluoroscopically guided stent insertion will be performed. Fluoroscopic monitoring is extremely helpful in accurately deploying the stent and ensuring that the lesion is adequately covered.

Fluoroscopic guidance.—All patients should undergo a preprocedural contrast radiologic study of the affected segment of the gut for an anatomic overview. A nasogastric tube is placed and the stomach is decompressed overnight prior to the procedure. The procedure can be performed with the patient under conscious sedation on a conventional fluoroscopic table or within a vascular-interventional suite.

The nasogastric tube is exchanged for a steerable angiographic catheter, which is passed via the nose or mouth (Fig 3). It is often helpful to place a long sheath that extends to the midesophagus to reduce trauma to the oral and hypopharynx during catheter exchanges. Iodinated contrast material is injected with the catheter in the stomach to identify the proximal extent of the stricture. The catheter is manipulated through the obstruction by using standard catheter and guide wire techniques. This is the most technically challenging portion of the procedure, as torque control is often poor when the catheter buckles within a capacious stomach (29,32,38,42,43). Gastric decompression for several days before the procedure can minimize this problem.



View larger version (69K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 3. Diagrams demonstrate gastroduodenal stent deployment with fluoroscopic guidance. An obstructive lesion is present within the proximal duodenum and is depicted with darker shading. A, A diagnostic angiographic catheter is passed via the nose or mouth and is manipulated past the obstructive lesion under fluoroscopic guidance. B, Contrast material is injected to confirm an intraluminal position and to critically delineate the distal aspect of the obstructive lesion. C, A stiff exchange length stiff guide wire is placed distally into the jejunum, and the diagnostic catheter is removed and replaced with the stent assembly. D, The stent is deployed, and it is ensured that the lesion is adequately covered, which thus relieves the obstruction.

 
Alternatively, access to the stomach can be achieved with percutaneous gastrostomy by using standard techniques (29). This access allows the placement of a stiff sheath through which the steerable catheter and guide wire can be placed. This more direct access provides greater catheter control and allows successful catheterization in virtually all cases.

Once a catheter has been passed beyond the lesion, contrast material is injected again to demonstrate the distal margin of the stenosis. The catheter is manipulated into the proximal jejunum, and an exchange length stiff guide wire is placed. Preplacement balloon dilation is usually not necessary for device deployment. However, gentle balloon dilation may be used to better determine the exact dimensions and location of the proximal and distal aspects of the stenosis when they are not clearly delineated with intraluminal contrast material. These areas can be marked on the fluoroscopic screen or on the patient.

A stent of adequate diameter (at least 16 mm) and length should be chosen to traverse the entire stenosis, with allowance of 1–2 cm extending proximally and distally after expansion. If multiple stents are required, the distal stent should be placed initially, with confirmation that it extends well beyond the lesion. At least 1–2 cm of the stents should overlap to prevent migration.

Postdeployment balloon dilation is usually not necessary, as most stents will self-expand over time. A postinsertion contrast material–enhanced radiographic study is performed through a guiding catheter to assess positioning and to evaluate the need for additional stents. A study with oral contrast material enhancement is performed prior to discharge (Fig 4), and the patient receives instructions relating to eating habits in an attempt to minimize episodes of solid food bolus obstruction (29,30,32,38,42,43). If the procedure was performed via a gastrostomy access, the gastrostomy tube is left in place until there has been adequate adhesion of the stomach to the abdominal wall. At a later time, the gastrostomy tube can be removed if deemed necessary by the patient (29).



View larger version (153K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 4. Anteroposterior radiograph obtained after oral administration of contrast material in a 31-year-old patient with duodenal carcinoma. Wallstents have been placed in the common bile duct (short arrows) and the duodenum (long arrows).

 
Endoscopic-fluoroscopic guidance.—The combination of endoscopic and fluoroscopic guidance adds increased control, which facilitates both catheterization of the stenosis and accurate device deployment (30,31,3437,39,44). The stricture is first identified endoscopically; then, the lesion is traversed with a guide wire and the catheter is passed through the endoscope. In this way, the endoscope functions as a long guiding catheter to provide stability within the capacious stomach and increased catheter torque control. The catheterization is also monitored fluoroscopically. Contrast material is injected to confirm successful traversal of the stenosis. The length of the lesion can then be measured by placing a clamp on the guide wire when its tip is at the distal aspect and then at the proximal aspect of the obstructive lesion. A stent should be chosen that has a length when fully expanded that is at least 2 cm longer than the stricture.

If the endoscope can be passed through the lesion, a submucosal injection of iodinated contrast material can be performed to mark the distal end of the stenosis (39). An extra-long exchange length stiff guide wire is placed well beyond the lesion. The endoscope is then removed and the stent is deployed over the guide wire. The enteral Wallstent can be deployed through the accessory channel of the endoscope (39). Other larger devices require removal of the scope prior to placing the device over the wire. In these cases, the endoscope can be reinserted adjacent to the device.

By using fluoroscopic markers, the device is deployed while making sure that at least 1–2 cm is distal to the lesion. The proximal location of the stent can be monitored fluoroscopically and can be directly seen with the endoscope within the stomach. Additional stents are deployed if necessary. The final adequacy of stent placement is assessed both endoscopically and fluoroscopically (30,31,3437,39,44). A final contrast-enhanced radiographic examination is performed following the procedure (Fig 4).

Results and Complications
Soetikno et al (39) reported the results of a prospective study in which enteral Wallstents were placed through an endoscope in 12 patients with malignant gastric outlet obstruction. They used stents ranging from 16 to 22 mm in diameter and 60 to 90 mm in length. Eleven of their patients presented with nausea and vomiting and were unable to take in adequate oral nutrition. One patient with pancreatic cancer and outlet obstruction had recurrence of cholangitis due to food impaction in a biliary Wallstent placed through a choledochoduodenostomy.

All stents were successfully placed. Three patients were treated entirely as outpatients. Following stent placement, six patients were able to eat a regular diet, and three were able to eat a soft pureed diet. Three patients had no relief of symptoms. One of these had multiple distal small-bowel strictures, and two had malpositioned stents. Follow-up ranged from 2 to 40 weeks, during which time nine died of cancer. Complications included three recurrent obstructions—one in a patient with distal migration 2 weeks after implantation treated with repeat stent placement, one in a patient with tumor ingrowth at 21 weeks treated with repeat stent placement, and one in a patient with proximal migration treated supportively. No perforations were reported.

Feretis et al (32) used 22-mm-diameter Wallstents placed with endoscopic-fluoroscopic guidance but not passed through the endoscope in 12 patients. There was complete relief of symptoms in 11 patients. One patient had partial tumor ingrowth; by 6 months after stent insertion, only two patients were still alive.

Binkert et al (31) placed 16-mm-diameter Wallstents with combined endoscopic-fluoroscopic guidance in nine patients, seven with malignant disease and two with chronic ulcer disease. Technical success was achieved in eight (89%) patients. During the follow-up, which ranged from 1 to 52 weeks or until death, there were no signs of stent obstruction. Seven patients had clearly improved quality of life with relief of vomiting and restoration of oral food intake.

Nevitt et al (37) used endoscopic-fluoroscopic guidance to insert four stent designs in eight patients with malignant obstruction. All patients had the distal and proximal aspects of the lesion marked with an intramural injection of contrast material through the endoscope. All stents were deployed successfully. Seven patients had immediate relief of obstructive symptoms. Two had recurrent symptoms due to tumor ingrowth, which was treated with percutaneous gastrostomy in one patient and gastrojejunostomy in the other patient.

De Baere et al (29) reported on fluoroscopically guided insertion of 16-mm-diameter Wallstents without endoscopic assistance in 10 patients. Seven patients had successful peroral insertion of the device. In one, the stricture could not be catheterized via the mouth, and in two, the available stent delivery catheter was not long enough to reach the strictured area via the mouth. These three patients then underwent successful stent placement via percutaneous gastrostomy access. All three patients had a 9-F Foley catheter that was left in place and then removed 10 days after stent insertion. Peroral cannulation required a mean of 17 minutes (range, 3–40 minutes) in the seven patients with successful treatment. In the one patient with treatment failure, oral cannulation was attempted for 45 minutes before reverting to a gastrostomy access. Cannulation then required less than 5 minutes.

Eight of De Baere et al's 10 patients had an immediate benefit from the procedure. In the two without benefit, an examination performed with oral contrast material demonstrated multiple unsuspected small-bowel stenoses that had been previously overlooked because of the severe duodenal stenosis. The stents were beneficial until death (at 25–168 days after implantation) in six patients and remained beneficial in two patients at 55 and 76 days after implantation. The mean hospital stay was 3 days (29). The flexible small-caliber Wallstent delivery system was critical for the successful peroral deployment without endoscopic assistance.

Pinto (38) also reported experience with fluoroscopically guided metallic stent implantation in six patients with malignant gastric outlet obstruction. Five of the six had successful peroral stent placement, and one required gastrostomy access. Wallstents (16 or 20 mm) were used, and all patients were relieved of their presenting symptoms. One had an ascitic leak from the gastrostomy site and died 1 week after the procedure. Three patients had stent obstruction within 2 months of placement. Two patients with stent obstruction were treated with additional stent placement, with relief of symptoms. By 20 weeks, only one patient remained alive. In one patient with recurrent obstruction, endoscopy revealed chronic inflammatory tissue ingrowth without malignant tumor.

Yates et al (30) used a variety of stents (Wallstent, Ultraflex, Esophacoil) to palliatively treat gastric or small-intestinal obstruction in 11 patients, with combined endoscopic-fluoroscopic guidance. Both technical and clinical success was achieved in 10 of the 11 patients (91%). The one failure was due to severe anastomotic angulation and distal luminal obstruction. Five patients had subsequent stent occlusion due to tumor ingrowth at 81/2, 31/2, 4, 11, or 7 weeks after implantation. There was no evidence of perforation, bleeding, or infection.

Summary
Combining the reported cases in 11 series, 91 patients with inoperable gastric outlet obstruction were treated with expandable metallic stents (Table 1) (2932,34,3639,48,49). There was immediate clinical benefit in 81 patients (89%). Five of the 10 patients with no clinical benefit were subsequently found to have additional unsuspected stenoses of the small intestine. These synchronous small-intestinal lesions are easy to overlook because of the difficulty in evaluating the small bowel in patients with gastric obstruction. Seventeen patients (21% of the group with an initially successful procedure; 19% of the entire group) had recurrent obstructive symptoms. Stent occlusion secondary to tumor growth and stent migration were the causes of recurrent symptoms in 14 (15%) and three (3%) patients, respectively.


View this table:
[in this window]
[in a new window]

 
TABLE 1. Expandable Metallic Stents in Gastroduodenal Obstruction
 
COLON AND RECTUM

Clinical Factors and Alternative Treatments
Malignant tumors of the colon and rectum account for more than 150,000 deaths yearly worldwide (50). Of all patients with colorectal malignancy, 10%–30% have large-intestinal obstruction at presentation (51,52). Furthermore, even in those patients who undergo successful resection, recurrent disease may lead to recurrence of intestinal obstruction.

Acute colonic obstruction is considered a surgical emergency. Failure to treat the obstruction expeditiously predisposes the patient to perforation, metabolic and electrolyte disturbances, intestinal ischemia, and sepsis. The majority of malignant colonic obstructions occur in the descending or sigmoid colon or in the rectum (53,54). Elective resection of a properly cleansed and antibiotically prepared colon is associated with a mortality rate of less than 5%. Emergent colectomy, on the other hand, especially for left-sided malignant obstruction, is associated with much higher mortality (23%) and morbidity (approaching 50%) rates (53,55). The poorer outcomes are largely due to inadequate colonic preparation and other complications associated with emergent surgery. In addition to a higher surgical complication rate, urgent colonic resection without preoperative preparation or adjuvant therapy is associated with a decrease in the overall survival rate (56).

Emergent surgery for colonic obstruction alters the surgical approach to the tumor. The traditional selective approach involves segmental resection of the tumor and drainage of lymph nodes, with primary anastomosis in a single operation. This is ill-advised in patients with poorly prepared colons and markedly dilated proximal intestines. In acutely ill patients, a diverting colostomy may be the best surgical option. In less ill patients, a two-stage operation (Hartmann procedure) is performed. This entails primary tumor resection and end colostomy, with colostomy closure performed as a second, subsequent procedure (51,57). Nearly 25% of patients never undergo the colostomy closure (51). Furthermore, colostomy closure is associated with substantial morbidity and mortality rates, as high as 37% and 7%, respectively (51).

A number of alternative approaches have been advocated to treat patients with malignant colonic obstruction without performing diverting colostomy and multiple operations. Some use percutaneous decompression with irrigation of the bowel. Others advocate a single surgical procedure consisting of segmental resection with on-table lavage followed by primary resection and anastomosis, with an intracolonic bypass tube used to protect the anastomosis (5861) from breakdown or leakage. Each of these approaches adds complexity to the operation.

Patients with unresectable primary or recurrent malignant colonic obstruction at presentation represent an even greater dilemma. They have limited life expectancy and would clearly benefit from a safe, effective, and nonsurgical alternative to relieve their obstructive symptoms.

The primary goal of a nonsurgical approach for treating acute colonic obstruction is to eliminate the need for emergent surgical treatment of the inadequately prepared colon in an insufficiently stabilized patient (54). Endoscopic laser therapy has been used to maintain luminal patency (62,63). This approach requires a substantial investment in equipment. Because of the risk of perforation and tumor seeding, it is limited to those patients with unresectable tumors. An endoluminal stent with a plastic tube placed transanally via an endoscope has also been used (6466). Lesions above the rectum require long flexible tubes that have limited internal diameters (65).

Indications
The placement of flexible expandable metallic stents across obstructive lesions of the colon is a new nonsurgical alternative for reestablishing luminal patency (6780). These devices, already covered, have the large internal diameters needed in the colon. The primary indications for endoluminal metallic stent placement in the colon and rectum are (a) for temporary colonic decompression in patients with an acute potentially resectable malignant colonic obstruction to allow laxative preparation and a single-stage surgical resection and (b) for long-term colonic decompression in patients with unresectable malignant obstruction of the colon or rectum. Patients with diverticulitis and obstruction can also be treated with metallic stents to permit elective colon cleansing prior to resection. It is often difficult to distinguish diverticulitis from tumor as the cause of the obstruction. The presence of tumor does not necessarily need to be established before decompression. Clinical or radiologic evidence of perforation is a contraindication to the procedure. Tumors that are too long or kinked or that are too proximal within the colon are unable to be treated.

Technical Considerations
Stent technology is rapidly evolving, and devices are now being developed specifically for colorectal applications. A variety of stents have been used effectively in the colon, including the enteral Wallstent, Ultraflex stent, Esophacoil, Gianturco-Rosch stent (Cook, Bloomington, Ind), and Memotherm stent (Bard, Covington, Ga) (6780). Stent placement in distal colonic and rectal lesions can be guided with fluoroscopy or endoscopy alone. Because of the difficulty in accessing more proximal portions of the colon because of sigmoid colon tortuosity, these lesions are best handled with combined endoscopic-fluoroscopic guidance.

A radiologic water-soluble enema (one part 76% contrast material with two parts water) examination is performed to localize and characterize the length and caliber of the obstructive lesion. The enema is also useful for determining the best position in which to place the patient to display the lesion such that the stricture is perpendicular to the beam. This position facilitates visualization of the stricture during stent placement. On the basis of the length of the stricture and its distance from the anus, the appropriate device and delivery system are selected.

Fluoroscopic guidance.—With the patient placed in a good position to visualize the obstructive lesion, an angiographic catheter or guiding catheter is placed into the colon. High-torque, 70–100-cm-long catheters are often needed. The colonic segments are negotiated with the catheter–guide wire combination. Conventional or hydrophilic 0.035- or 0.038-inch wires are used.

Following successful catheterization past the obstructive lesion, contrast material is injected through the diagnostic angiographic catheter to better define the lesion (length, location, optimal position) and to rule out a perforation. The location of the lesion is marked and noted. An exchange length stiff guide wire is advanced well beyond the lesion. When using Wallstents, the tracheobronchial system has a working length of 110 cm, as compared with 240 cm for the enteral system, and may be easier to deploy. A stent with an adequate length and diameter (20–24 mm) is advanced under fluoroscopic guidance and deployed such that the middle of the stent covers the lesion with 1–2 cm of the stent extending beyond both the proximal and distal margins of the lesion (Fig 5). Long lesions may require two stents (69,7578) (Fig 5).



View larger version (47K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 5. Diagrams demonstrate colorectal stent deployment with fluoroscopic guidance. An obstructive lesion is present within the sigmoid colon and is depicted with darker shading. A, A diagnostic angiographic catheter is manipulated past the obstructive lesion with fluoroscopic guidance. B, Contrast material is injected to confirm an intraluminal position and to delineate the proximal aspect of the obstructive lesion. C, An exchange length stiff guide wire is placed proximally into the colon, and the diagnostic catheter is removed and exchanged for the stent assembly. D, The stent is appropriately positioned and deployed by withdrawing the enveloping membrane with fluoroscopic control to ensure that the lesion is adequately covered, which thus relieves the obstruction.

 
Endoscopic-fluoroscopic guidance.—An upper endoscope or colonoscope (depending on distance from anus) is placed at the distal portion of the lesion (Fig 6b). The distal end of the lesion is noted fluoroscopically (by using bony landmarks or opaque clamps). A 0.035- or 0.038-inch guide wire is passed through the lesion via the endoscope. A hydrophilic wire has been successfully used to traverse the lesions. If the contrast material enema did not adequately opacify the part of the colon proximal to the lesion, a 5-F catheter is placed and contrast material is injected to opacify the proximal aspect of the lesion and to rule out a perforation (Fig 7b). The 5-F catheter is then replaced with an exchange length stiff guide wire. The stent apparatus is passed over the guide wire and through the lesion until it is past the proximal aspect of the stricture. If the stent apparatus will not fit through the working channel of the endoscope, a super stiff wire must be placed through the stricture and the endoscope must be removed. The endoscope is reinserted alongside the stent assembly.



View larger version (149K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 6a. Anteroposterior radiographs obtained in a 53-year-old patient with colonic obstruction due to unresectable adenocarcinoma of the sigmoid colon. (a) Barium enema radiograph shows the classic apple core lesion (arrow) in the sigmoid colon. (b) Guide wire (arrow) and catheter are passed through the lesion with a colonoscope. (c) Deployed stents. The first stent (curved arrows) was deployed too proximally, and the second stent (straight solid arrows) was needed. Note the waist (open arrow) in the stents at the level of the tumor. (d) Radiograph obtained after a water-soluble enema the day after a-c were obtained shows that the stents have expanded to provide an adequate lumen.

 


View larger version (147K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 6b. Anteroposterior radiographs obtained in a 53-year-old patient with colonic obstruction due to unresectable adenocarcinoma of the sigmoid colon. (a) Barium enema radiograph shows the classic apple core lesion (arrow) in the sigmoid colon. (b) Guide wire (arrow) and catheter are passed through the lesion with a colonoscope. (c) Deployed stents. The first stent (curved arrows) was deployed too proximally, and the second stent (straight solid arrows) was needed. Note the waist (open arrow) in the stents at the level of the tumor. (d) Radiograph obtained after a water-soluble enema the day after a-c were obtained shows that the stents have expanded to provide an adequate lumen.

 


View larger version (152K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 6c. Anteroposterior radiographs obtained in a 53-year-old patient with colonic obstruction due to unresectable adenocarcinoma of the sigmoid colon. (a) Barium enema radiograph shows the classic apple core lesion (arrow) in the sigmoid colon. (b) Guide wire (arrow) and catheter are passed through the lesion with a colonoscope. (c) Deployed stents. The first stent (curved arrows) was deployed too proximally, and the second stent (straight solid arrows) was needed. Note the waist (open arrow) in the stents at the level of the tumor. (d) Radiograph obtained after a water-soluble enema the day after a-c were obtained shows that the stents have expanded to provide an adequate lumen.

 


View larger version (138K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 6d. Anteroposterior radiographs obtained in a 53-year-old patient with colonic obstruction due to unresectable adenocarcinoma of the sigmoid colon. (a) Barium enema radiograph shows the classic apple core lesion (arrow) in the sigmoid colon. (b) Guide wire (arrow) and catheter are passed through the lesion with a colonoscope. (c) Deployed stents. The first stent (curved arrows) was deployed too proximally, and the second stent (straight solid arrows) was needed. Note the waist (open arrow) in the stents at the level of the tumor. (d) Radiograph obtained after a water-soluble enema the day after a-c were obtained shows that the stents have expanded to provide an adequate lumen.

 


View larger version (99K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 7a. Oblique radiographs obtained in a patient with rectosigmoid carcinoma. (a) Barium enema radiograph shows total obstruction to retrograde flow. (b) A colonoscope could not pass the tumor, but a catheter (curved arrow) could pass into the lumen inside the tumor. The injected contrast material opacifies a long irregular segment of colonic narrowing (straight arrows). (c) A guide wire was manipulated through the tumor, and a Wallstent was deployed. (d) Radiograph obtained after a water-soluble enema following stent deployment on the same day as a-c shows a patent lumen and no leak.

 


View larger version (148K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 7b. Oblique radiographs obtained in a patient with rectosigmoid carcinoma. (a) Barium enema radiograph shows total obstruction to retrograde flow. (b) A colonoscope could not pass the tumor, but a catheter (curved arrow) could pass into the lumen inside the tumor. The injected contrast material opacifies a long irregular segment of colonic narrowing (straight arrows). (c) A guide wire was manipulated through the tumor, and a Wallstent was deployed. (d) Radiograph obtained after a water-soluble enema following stent deployment on the same day as a-c shows a patent lumen and no leak.

 


View larger version (148K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 7c. Oblique radiographs obtained in a patient with rectosigmoid carcinoma. (a) Barium enema radiograph shows total obstruction to retrograde flow. (b) A colonoscope could not pass the tumor, but a catheter (curved arrow) could pass into the lumen inside the tumor. The injected contrast material opacifies a long irregular segment of colonic narrowing (straight arrows). (c) A guide wire was manipulated through the tumor, and a Wallstent was deployed. (d) Radiograph obtained after a water-soluble enema following stent deployment on the same day as a-c shows a patent lumen and no leak.

 


View larger version (144K):
[in this window]
[in a new window]
[Download PPT slide]
 
Figure 7d. Oblique radiographs obtained in a patient with rectosigmoid carcinoma. (a) Barium enema radiograph shows total obstruction to retrograde flow. (b) A colonoscope could not pass the tumor, but a catheter (curved arrow) could pass into the lumen inside the tumor. The injected contrast material opacifies a long irregular segment of colonic narrowing (straight arrows). (c) A guide wire was manipulated through the tumor, and a Wallstent was deployed. (d) Radiograph obtained after a water-soluble enema following stent deployment on the same day as a-c shows a patent lumen and no leak.

 
The stent is deployed and adjusted with constant fluoroscopic and visual monitoring to ensure it has crossed the lesion (Figs 6c, 7c). If the lesion was not successfully or totally covered by the stent, an additional stent is placed (Fig 6c). Balloon dilation following stent placement is not recommended.

A water-soluble enema examination is performed immediately after the procedure or the following day to check for patency and leakage (Figs 6d, 7d)(7073). Patients who are candidates for resection are treated medically, and a bowel-cleaning preparation is instituted for subsequent surgery. Patients with unresectable disease who receive stents only for palliation are placed on a low-residue diet and receive mineral oil to lessen the likelihood of stent obstruction. Follow-up radiographs are obtained in symptomatic patients if needed to check for stent migration, perforation, or colonic obstruction.

Results and Complications
Fluoroscopic guidance, endoscopic guidance, and combined endoscopic-fluoroscopic guidance have all been successfully used to deploy metallic stents within the colon and rectum (6780). Technical success in deploying the device has ranged from 80% to 100%. Clinical or medical success (relief of obstructive symptoms) has been reported in 80%–92% (Table 2). A higher rate of successful stent placement can be achieved with more distal lesions.


View this table:
[in this window]
[in a new window]

 
TABLE 2. Expandable Metallic Stents in Colorectal Obstruction
 
Baron et al (72) treated 25 patients, with obstructive colorectal carcinoma in 11, anastomotic tumor recurrence in six, other malignant neoplasms in five, and benign causes in three patients. Ten patients received stents preoperatively; the remaining 15 patients had metallic stents placed for palliative colonic decompression. Lesions were located in the transverse colon (n = 2), splenic flexure (n = 2), descending colon (n = 5), sigmoid colon (n = 13), and rectum (n = 3). Combined endoscopic-fluoroscopic guidance was used to place uncovered metallic stents. Stent placement was successful in nine (90%) of the 10 patients with preoperative colon cleansing. Two of these patients were ultimately found to have unresectable disease, and their stents were left in place for palliative decompression. Of the 15 patients who underwent stent placement for palliative decompression, 12 (80%) had successful relief of obstruction for 2–64 weeks.

Binkert et al (73) reported the results of colonic stent placement in 13 patients with a combined endoscopic-fluoroscopic guidance technique. Eleven of the 13 had lesions in the rectosigmoid region; one patient each had a lesion that was successfully treated with stent placement in the hepatic flexure or descending colon. Uncovered, 16-mm, vascular Wallstents were used with 92% (12 of 13 patients) technical and clinical success rates.

DeGregorio et al (75) reported the results of a prospective multiinstitutional colon stent trial in Europe in which the use of metallic stents for only palliative purposes in patients with acute colorectal obstruction was studied. Twenty-four patients were treated with uncovered stents by using only fluoroscopic guidance. The 22-mm Wallstent was used in 22 patients. One 25-mm Memotherm stent and one covered 18-mm Z-stent were also implanted in one patient each. The technical success rate with fluoroscopic guidance alone was 100% (24 of 24 patients). Twenty-three patients had lesions in the rectosigmoid area, and only one patient had a lesion within the proximal descending colon. Resolution of bowel obstruction was achieved within 24 hours in 96% (23 of 24) of patients. The high success rate can partly be explained by the predominance of distal lesions.

Mainar et al (76) reported the results of the use of metallic stents in the treatment of acute colorectal obstruction prior to surgical resection. In 71 patients, lesions were located in the transverse colon in one patient, descending colon in 22 patients, and rectosigmoid region in 48 patients. All stents were placed within 24 hours of diagnosis of the acute obstruction. Of the 71 patients, 64 (90%) were able to have stents placed in the proper location. In two patients, stents could not be deployed because of the proximal location (transverse colon) in one patient and because of a tortuous rectosigmoid colon in the other. The longer delivery systems now available and the use of endoscopic assistance may have allowed these obstacles to be overcome. In five patients, stents were poorly positioned; three patients required additional stents. Overall, 60 (85%) of the 71 patients had immediate relief of symptoms and of radiographic signs of colonic obstruction within 24 hours of stent deployment. Six other patients were relieved in 24–96 hours. Three (4%) experienced no relief despite apparent proper stent placement and required emergent surgery.

Perforation, stent migration, and restenosis are the major complications encountered with colonic stent placement. Perforation has been reported in 0%–16% of cases (6779) (Table 2). Baron et al (72) reported colonic perforation in four patients, which was associated with balloon dilation of the stricture at the time of stent placement in three of the patients. Balloon dilation is no longer recommended, and stents are allowed to slowly self-expand. Without balloon dilation, perforation rates may fall below 5%. Perforation should be suspected in patients who complain of abdominal pain during or immediately after the procedure.

Stent migration has been reported to occur in as many as 40% of cases and is usually detected on follow-up radiographs within 1 week of insertion. The displaced stent can be removed endoscopically and another (larger) stent can be placed. Migrations tend to occur with stents too narrow in diameter and/or too short in length for the stricture they are placed in. Stent migration should also decrease substantially in the future with the wider availability of larger-diameter (20–24-mm) stents and flared stents and with increased experience with proper stent positioning.

Choo et al (74) used two covered flexible stents in the colon. One had bulbous ends and was completely covered with polyurethane. This stent migrated in four (50%) of eight patients. The stent was redesigned with the proximal bulbous end left uncovered. There were no cases of stent migration when the redesigned stent was used in subsequent patients.

Restenosis has been reported in up to 25% of cases and is usually due to tumor ingrowth through the open interstices of the stent (6779). Tumor ingrowth is not a problem in those patients in whom short-term colonic stent placement is performed for preparation prior to definitive surgery. However, for palliative colonic decompression for a longer time, tumor ingrowth with restenosis can be problematic. Covered stents can help address the problem of tumor ingrowth but tend to be less flexible and more difficult to deploy in proximal locations and are associated with higher migration rates (74).

New stents need to be developed to provide long-term colonic decompression by balancing the need to prevent tumor ingrowth and the propensity for stent migration. The redesigned Choo stent (Samsung Biomedical Research Institute, Seoul, Korea) has addressed some of these issues but is not available in the United States. When restenosis due to tumor ingrowth does occur, a new stent can be placed coaxially within the original stent. Restenosis due to tumor overgrowth (extension of tumor above or below the stent) can also be treated with a second stent. It is best prevented by deploying the original stent 2–3 cm above or below the lesion when possible.

Minor complications, including mild abdominal pain and transient rectal bleeding, generally require no treatment. Bare stent wires do produce mucosal injury, but major gastrointestinal bleeding has to our knowledge been uncommon. Fecal impaction can certainly occur and is treated with a cleansing enema. Impactions can be made less likely by using a 20–24-mm-diameter stent and by prescribing a low-residue diet and a mineral oil supplement.

Summary
By combining the reported cases in 12 published articles (Table 2), 234 patients with colonic obstruction were treated with expandable metallic stents (6770,7279). The stents were placed with endoscopic, fluoroscopic, and combined endoscopic-fluoroscopic guidance in 25, 136, and 73 patients, respectively. The technical and clinical success rates achieved in this combined group were 93% (217 of 234 patients) and 90% (210 of 234 patients), respectively.

CONCLUSION

Early experience has shown the use of metallic stents within the upper and lower gastrointestinal tracts will provide appropriately selected patients palliation of their obstructive symptoms. In addition, the minimally invasive nature of these procedures will further benefit patients by allowing them to avoid more extensive and invasive surgical procedures. The indications for stent insertion within the gastrointestinal tract will continue to expand with improved stent design and physician ingenuity. Metallic stent placement within the alimentary tract has proved to be beneficial in patients who require palliation of their gastroduodenal or colorectal obstruction and should be a part of the interventionalist's armamentarium.

References

  1. Cwikiel W, Stridbeck H, Tranberg KG, et al. Malignant esophageal strictures: treatment with a self expanding nitinol stent. Radiology 1993; 187:661-665.[Abstract/Free Full Text]
  2. Saxon RR, Barton RE, Katon RM, et al. Treatment of malignant esophageal obstructions with covered metallic Z stents: long term results in 52 patients. J Vasc Intervent Radiol 1995; 6:747-754.[Medline]
  3. Song HY, Do YS, Young-Min H, et al. Covered, expandable esophageal metallic stent tubes: experiences in 119 patients. Radiology 1994; 193:689-695.[Abstract/Free Full Text]
  4. Gasparri G, Casalegno PA, Camadona M, et al. Endoscopic insertion of 248 prostheses in inoperable carcinoma of the esophagus and cardia: short-term and long-term results. Gastrointest Endosc 1987; 33:354-356.[Medline]
  5. Adam A, Ellul J, Watkinson AF, et al. Palliation of inoperable esophageal carcinoma: a prospective randomized trial of laser therapy and stent placement. Radiology 1997; 202:344-348.[Abstract/Free Full Text]
  6. Watkinson A, Ellul J, Entwistle K, et al. Plastic-covered metallic endoprostheses in the management of oesophageal perforation in patients with oesophageal carcinoma. Clin Radiol 1995; 50:304-309.[Medline]
  7. Adam A, Morgan R, Ellul J, Mason RC. A new design of the esophageal Wallstent endoprosthesis resistant to distal migration. AJR Am J Roentgenol 1998; 170:1477-1481.[Abstract/Free Full Text]
  8. Kozarek RA. Use of expandable stent for esophageal and biliary stenosis. Gastroenterologist 1994; 2:264-272.[Medline]
  9. Kozarek RA. Expandable endoprostheses for gastrointestinal stenosis. Gastrointest Endosc Clin North Am 1994; 4:279-295.[Medline]
  10. Nevitt AW, Kozarek RA, Kidd R. Expandable esophageal prostheses: recognition, insertion techniques, and positioning. AJR Am J Roentgenol 1996; 167:1009-1013.[Free Full Text]
  11. Klose KJ. Nitinol prostheses for the treatment of inoperable malignant esophageal obstruction. J Vasc Intervent Radiol 1994; 5:899-904.[Medline]
  12. Patton JT, Carter R. Endoscopic stenting for recurrent malignant gastric outlet obstruction. Br J Surg 1997; 84:865-866.[Medline]
  13. Kurtz RC, Sherlock P. Carcinoma of the stomach. In: Berk JE, Haubrich WS, Kalser MH, Roth JLA, Schaffner F, eds. Bockus gastroenterology. 4th ed. Philadelphia, Pa: Saunders, 1985; 1278-1304.
  14. Wade TP, Neuberger TJ, Swope TJ, et al. Pancreatic cancer palliation: using tumor stage to select appropriate operation. Am J Surg 1994; 167:208-213.[Medline]
  15. Monson JR, Donohue JH, McIlrath DC, et al. Total gastrectomy for advanced cancer: a worthwhile palliative procedure. Cancer 1991; 68:1863-1868.[Medline]
  16. Smith JW, Brennan MF. Surgical treatment of gastric cancer: proximal, mid and distal stomach. Surg Clin North Am 1992; 72:381-399.[Medline]
  17. Weaver D, Winczek R, Bowman D, et al. Gastrojejunostomy: is it helpful for patients with pancreatic cancer?. Surgery 1987; 25:608-613.
  18. Spinelli P, Cerrai FG, Dal Fante M. Endoscopic treatment of upper gastrointestinal tract malignancies. Endoscopy 1993; 25:675-678.[Medline]
  19. Marcon NE. The endoscopic management of esophageal cancer. Acta Gastroenterol Belg 1994; 57:143-154.[Medline]
  20. Lambert R. Endoscopic treatment of esophagogastric tumors. Endoscopy 1996; 28:27-37.
  21. Narayan S, Sivak M, Jr. Palliation of esophageal carcinoma: laser and photodynamic therapy. Chest Surg Clin North Am 1994; 4:347-367.[Medline]
  22. Overholt BF, Panjehpour M, DeNovo RC, et al. Photodynamic therapy for esophageal cancer using a 180° windowed esophageal balloon. Laser Surg Med 1994; 14:27-33.
  23. Heier SK, Rothman KA, Heier LM, et al. Photodynamic therapy for obstructing esophageal cancer: light dosimetry and randomized comparison with Nd:YAG laser therapy. Gastroenterology 1995; 109:63-72.[Medline]
  24. Rau BK, Harikrishnan KM, Krishna S. Oesophageal carcinoma: laser palliation in 231 cases. Ann Acad Med 1994; 23:32-34.
  25. Boarke MJ, Hope KL, Cha G. Laser palliation of inoperable malignant dysphagia: initial and at death. Gastrointest Endosc 1996; 43:29-32.[Medline]
  26. Lightdale CL, Heier SK, Marcon NE, et al. Photodynamic therapy with porfimer sodium versus thermal ablation therapy with Nd:YAG laser for palliation of esophageal cancer: a multicenter randomized trial. Gastrointest Endosc 1995; 42:507-512.[Medline]
  27. Payne-James JJ, Spiller R, Misiewicz JJ, et al. Use of ethanol-induced tumor necrosis to palliate dysphagia in patients with esophagogastric cancer. Gastrointest Endosc 1990; 36:43-46.[Medline]
  28. Wright RA, O'Connor KW. A pilot study of endoscopic injection chemo/sclerotherapy of esophageal carcinoma. Gastrointest Endosc 1990; 36:47-48.[Medline]
  29. de Baere T, Harry G, Ducreux M, et al. Self-expanding metallic stents as palliative treatment of malignant gastroduodenal stenosis. AJR Am J Roentgenol 1997; 169:1079-1083.[Abstract/Free Full Text]
  30. Yates MR, Morgan DE, Baron TH. Palliation of malignant and small intestinal strictures with self-expanding metal stents. Endoscopy 1998; 30:266-272.[Medline]
  31. Binkert CA, Jost R, Steiner A, et al. Benign and malignant stenoses of the stomach and duodenum: treatment with self-expanding metallic endoprostheses. Radiology 1996; 199:335-338.[Abstract/Free Full Text]
  32. Feretis C, Benakis P, Dimopoulos C, et al. Palliation of malignant gastric outlet obstruction with self-expanding metal stents. Endoscopy 1996; 28:225-228.[Medline]
  33. Freeman ML, Cas OW. Interlocking expandable metal stents for simultaneous treatment of malignant biliary and duodenal obstruction. Gastrointest Endosc 1996; 44:98-99.[Medline]
  34. Keymling M, Wagner JH, Vakil N, et al. Relief of malignant duodenal obstruction by percutaneous insertion of a metal stent. Gastrointest Endosc 1993; 39:439-441.[Medline]
  35. Kozarek RA, Ball TJ, Patterson DJ. Metallic self-expanding stent application in the upper gastrointestinal tract: caveats and concerns. Gastrointest Endosc 1992; 38:1-6.[Medline]
  36. Maetani I, Inoue H, Sato M, et al. Peroral insertion techniques of self-expanding metal stents for malignant gastric outlet and duodenal stenoses. Gastrointest Endosc 1996; 44:468-471.[Medline]
  37. Nevitt AW, Vida F, Kozarek RA, et al. Expandable metallic prostheses for malignant obstructions of gastric outlet and proximal small bowel. Gastrointest Endosc 1998; 47:271-276.[Medline]
  38. Pinto IT. Malignant gastric and duodenal stenosis: palliation by peroral implantation of a self-expanding metallic stent. Cardiovasc Intervent Radiol 1997; 20:431-434.[Medline]
  39. Soetikno RM, Lichtenstein DR, Vandervoort J, et al. Palliation of malignant gastric outlet obstruction using an endoscopically placed Wallstent. Gastrointest Endosc 1998; 47:267-270.[Medline]
  40. Solt J, Papp Z. Strecker stent implantation in malignant gastric outlet stenosis. Gastrointest Endosc 1993; 39:442-444.[Medline]
  41. Sommer A, Bethge N. Relief of malignant external gastric obstruction by endoscopic implantation of self-expanding metal stent. Endoscopy 1995; 27:210-211.[Medline]
  42. Song HY, Yang DH, Kuh JH, et al. Obstructing cancer of the gastric antrum: palliative treatment with covered metallic stents. Radiology 1993; 187:357-358.[Abstract/Free Full Text]
  43. Strecker EP, Boos I, Husfield KJ. Malignant duodenal stenosis: palliation with peroral implantation of a self-expanding nitinol stent. Radiology 1995; 196:349-351.[Abstract/Free Full Text]
  44. Topazin M, Ring E, Grendale J. Palliation of obstructing gastric cancer with steel mesh, self-expanding endoprostheses. Gastrointest Endosc 1992; 38:58-60.[Medline]
  45. Truong S, Bohndorf V, Geller H, et al. Self-expanding metal stents for palliation of malignant gastric outlet obstruction. Endoscopy 1992; 24:433-435.[Medline]
  46. Scott-Mackie P, Morgan R, Farrugia M, et al. The role of metallic stents in malignant duodenal obstruction. Br J Radiol 1997; 70:252-255.[Abstract]
  47. Bethge N, Sommer A, Gross U, et al. Human tissue responses to metal stents implanted in vivo for the palliation of malignant stenoses. Gastrointest Endosc 1996; 43:596-602.[Medline]
  48. Howell DA, Bosco JJ, Muggia RA, et al. Endoscopic double bypass: duodenal metal expandable stenting late in malignancy. Gastrointest Endosc 1994; 40:40A.
  49. Feretis C, Benakis P, Dimopoulos C, et al. Self-expanding endoprostheses for palliation of duodenal obstruction. Gastrointest Endosc 1997; 46:161-165.[Medline]
  50. Gordon PH. Malignant neoplasms of the colon. In: Gordon PH, Nivatvongs S, eds. Principles and practice of surgery for the colon, rectum and anus. St Louis, Mo: Quality Medical, 1992; 502-576.
  51. Deans GT, Krukowski ZH, Irwin ST. Malignant obstruction of the left colon. Br J Surg 1994; 81:1270-1276.[Medline]
  52. MacKenzie S, Thomson SR, Baker LW. Management options in malignant obstruction of the left colon. Surgery 1992; 174:337-345.
  53. Beuchter KJ, Boustany C, Caillouette R, et al. Surgical management of the acutely obstructed colon: a review of 127 cases. Am J Surg 1988; 156:163-168.[Medline]
  54. Leitman IM, Sullivan JD, Brams D, et al. Multivariate analysis of morbidity and mortality from the initial surgical management of obstructing carcinoma of the colon. Surg Gynecol Obstet 1992; 174:513-518.[Medline]
  55. Griffith RS. Preoperative evaluation: medical obstacles to surgery. Cancer 1992; 70:1333-1341.[Medline]
  56. Serpell JW, McDermott FT, Katrivesis H, et al. Obstructing carcinomas of the colon. Br J Surg 1989; 76:965-969.[Medline]
  57. The Subtotal Colectomy vs On-Table Irrigation and Anastomosis Study Group. Single-stage treatment for malignant left-sided colonic obstruction: a prospective randomized clinical trial comparing subtotal colectomy with segmental resection following intraoperative irrigation. Br J Surg 1995; 82:1622-1627.[Medline]
  58. Salim AS. Percutaneous decompression and irrigation for bowel obstruction. Dis Colon Rectum 1991; 34:973-980.[Medline]
  59. Stewart J, Diament RH, Brennan TG. Management of obstructing lesions of the left colon by resection, on-table lavage, and primary anastomosis. Surgery 1992; 114:502-505.
  60. Tan SG, Nambiar R, Rauf A, et al. Primary resection and anastomosis in obstructed descending colon due to cancer. Arch Surg 1991; 126:748-751.[Abstract]
  61. Rosati C, Smith L, Deitel M, et al. Primary colorectal anastomosis with the intracolonic bypass tube. Surgery 1992; 112:618-622.[Medline]
  62. Eckhauser ML, Mansour EG. Endoscopic laser therapy for obstructing and/or bleeding colorectal carcinoma. Am Surg 1992; 55:358-363.
  63. Tacke W, Paech S, Kruis W, et al. Comparison between endoscopic laser and different surgical treatments for palliation of advanced rectal cancer. Dis Colon Rectum 1993; 36:377-382.[Medline]
  64. Keen RR, Orsay CP. Rectosigmoid stent for obstructing colonic neoplasms. Dis Colon Rectum 1992; 35:912-913.[Medline]
  65. Lelcuk S, Ratan J, Klausner JM, et al. Endoscopic decompression of acute colonic obstruction. Ann Surg 1986; :292-294.
  66. Ruiz PL, Facciuto EM, Facciuto ME, et al. New intraluminal bypass tube for management of acutely obstructed left colon. Dis Colon Rectum 1995; 38:1108-1109.[Medline]
  67. Rey JF, Romanczyk T, Greff M. Metal stents for palliation of rectal carcinoma: a preliminary report of 12 patients. Endoscopy 1995; 27:501-504.[Medline]
  68. Spinelli P, Dal Fante M, Mancini A. Rectal metal stents for palliation of colorectal malignant stenosis. Bildgebung 1993; 60(suppl 1):48-50.
  69. Mainar A, Tejero E, Maynar M, et al. Colorectal obstruction: treatment with metallic stents. Radiology 1996; 198:761-764.[Abstract/Free Full Text]
  70. Saida Y, Sumiyama Y, Nagao J, et al. Stent endoprosthesis for obstructing colorectal cancers. Dis Colon Rectum 1996; 39:552-555.[Medline]
  71. Canon CL, Baron TH, Morgan DE, et al. Treatment of colonic obstruction with expandable metal stents: radiologic features. AJR Am J Roentgenol 1997; 168:199-205.[Abstract/Free Full Text]
  72. Baron TH, Dean PA, Yates MR, III, et al. Expandable metal stents for the treatment of colonic obstruction: techniques and outcomes. Gastrointest Endosc 1998; 47:277-286.[Medline]
  73. Binkert CA, Ledermann H, Jost R, et al. Acute colonic obstruction: clinical aspects and cost-effectiveness of preoperative and palliative treatment with self-expanding metallic stents—a preliminary report. Radiology 1998; 206:199-204.[Abstract/Free Full Text]
  74. Choo IW, Do SY, Chun H, et al. Malignant colorectal obstruction: treatment with a flexible covered stent. Radiology 1998; 206:415-421.[Abstract/Free Full Text]
  75. DeGregorio MA, Mainar A, Tejero E, et al. Acute colorectal obstruction: stent placement for palliative treatment—results of a multicenter study. Radiology 1998; 209:117-120.[Abstract/Free Full Text]
  76. Mainar A, Ariza M, Tejero H, et al. Acute colorectal obstruction: treatment with self-expandable metallic stents before scheduled surgery—results of a multicenter study. Radiology 1999; 210:65-69.[Abstract/Free Full Text]
  77. Diaz LP, Pabon PI, Lobato RF. Metallic stents as a palliative measure in obstructive colon cancer. J Intervent Radiol 1998; 13:24-30.
  78. Wholey MH, Levine EA, Ferral H, et al. Initial clinical experience with colonic stent placement. Am J Surg 1998; 175:194-197.[Medline]
  79. Wallis F, Campbell KL, Eremin O, et al. Self-expanding metal stents in the management of colorectal carcinoma: a preliminary report. Clin Radiol 1998; 53:251-254.[Medline]
  80. Turegano-Fuentes F, Echenagusia-Belda A, Simo-Muerza G, et al. Transanal self-expanding metal stents as an alternative to palliative colostomy in selected patients with malignant obstruction of the left colon. Br J Surg 1998; 85:232-235.[Medline]



This article has been cited by other articles:


Home page
Am. J. Roentgenol.Home page
J. H. Kim, H.-Y. Song, J. H. Shin, E. Choi, T. W. Kim, S. K. Lee, and B. S. Kim
Stent Collapse as a Delayed Complication of Placement of a Covered Gastroduodenal Stent
Am. J. Roentgenol., June 1, 2007; 188(6): 1495 - 1499.
[Abstract] [Full Text] [PDF]