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Transgastrostomal Observation and Management Using an Ultrathin Endoscope After Percutaneous Endoscopic Gastrostomy

Written By

Shinji Nishiwaki, Hiroo Hatakeyama, Masahide Iwashita and Hiroshi Araki

Submitted: 20 November 2010 Published: 22 September 2011

DOI: 10.5772/22564

From the Edited Volume

Therapeutic Gastrointestinal Endoscopy

Edited by Oliviu Pascu and Marcel Tantau

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1. Introduction

Recent developments have made ultrathin endoscopes available for routine esophagogastroduodenoscopy and also for unsedated transnasal observation (Shaker, 1994). Transnasal endoscopy is known to be less of a burden for patients (more tolerable) than transoral endoscopy and has benefits including fewer effects on respiratory and cardiovascular status and reduced recovery time after the procedure (Campo et al., 1998; Dumortier et al., 1999; Mori et al., 2008). Transnasal ultrathin endoscopy has also been applied for biliary drainage, insertion of a nasoenteral feeding tube or a long intestinal tube, and percutaneous endoscopic gastrostomy (PEG) (Fang et al., 2005; Itoi et al., 2008; Sato et al., 2008; Vitale et al., 2005). PEG has become the primary access for long term enteral feeding since its introduction in 1980 (Gauderer et al., 1980; Ponsky & Gauderer, 1981), being a very easy and rapid method compared with the previous surgical technique to place a gastrostomy tube.

The endoscopic approach from the gastrocutaneous tract was first described by Chaurasia, et al. for the insertion of a jejunal feeding tube through the PEG (PEG-J) tract (Chaurasia & Chang, 1995). Although they used a pediatric bronchoscope at that time, an ultrathin endoscope later took its place for this purpose (Adler et al., 2002). We have been employing an ultrathin endoscope through the gastrostomy tract for observation, diagnosis, and treatment of various digestive diseases from April 2003. We also investigated the usefulness of such transgastrostomal endoscopy (TGE) for management of patients who had undergone percutaneous endoscopic gastrostomy (PEG).

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2. Procedure of transgastrostomal endoscopy (TGE)

Patients with a mature gastrocutaneous tract are candidates for this procedure. Patients before the maturation of the fistula (2 to 4 weeks after the PEG) have higher risk of fistula disruption. If it is necessary to perform TGE in an earlier phase or at the PEG, tight affixation of the stomach to the abdominal wall using a gastropexy device (Rogers, 1989) allows TGE to be performed.

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2.1. Equipment

The endoscopes we used were GIF-XP240, GIF-XP260 and GIF-XP260N (Olympus Optical Co., Ltd., Tokyo, Japan) (Fig. 1). The diameters of these endoscopes were 7.7, 6.5, and 5.2 mm, respectively. The diameter of the working channel of these endoscopes was 2.0 mm. GIF-XP240, GIF-XP260, and GIF-XP260N allow insertion through more than 24, 20 and 18 F fistula tracts, respectively.

Figure 1.

Photograph of ultrathin endoscopes and gastrostomy tubes. a: GIF-XP260N, b: GIF-XP260, c: GIF-XP240 (Olympus Optical Co., Ltd., Tokyo, Japan), d: Ponsky NBR, 20F (Bard Access Systems, Inc., Salt Lake City, UT, USA ), e: Securi-T, 24F (Boston Scientific, Natick, MA, USA)

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2.2. Routine observation by TGE

The patient is usually infused with 500 ml of water instead of liquid feeds for several hours before the endoscopic examination to remove the gastric mucus. The patient is laid in the supine position and then the gastrostomy tube is removed. After applying lidocaine jelly around the stoma, an ultrathin endoscope is inserted through the fistural tract and proceeded into the gastric lumen (Fig. 2A). The endoscope is directed to the oral side and advanced to the esophagogastric junction (Fig. 2B). The junction can be observed in detail without disturbance, free from the shade of the endoscope. The endoscope is retrogradely inserted through the esophagus, and we can observe oral cavity as well as pharyngeal cavity if necessary. The endoscope is then withdrawn to the stomach and directed to the anal side. The endoscope is easily inserted up to the upper jejunum from the stoma (Fig. 2C). The endoscope is pulled back to the stomach and turned back to see around the stoma (Fig. 2D).

Figure 2.

A: Insertion of an ultrathin endoscope through the gastrostomy tract. B: Endoscopic view of esophagogastric junction (arrow) which is retrogradely observed from the stomach. C: Endoscopic view of upper jejunum. D: Endoscopic view of the stoma from the stomach. Arrow indicates the endoscope inserted through the stoma.

After the observation of the upper gastrointestinal tract, the endoscope is withdrawn from the stoma and a new gastrostomy tube is replaced via the skin incision.

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3. Diagnostic application of TGE

Since most of patients who undergo PEG are of advanced age and also have comorbid diseases, they usually do not undergo esophagogastroduodenoscopy after PEG. As TGE is a less invasive procedure to perform even for critically ill patients, we have routinely conducted TGE at the periodical replacement of gastrostomy tubes. We have found variety of newly developed lesions in the upper gastrointestinal tracts and were able to treat them at an early stage without symptoms.

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3.1. Cardiopulmonary tolerance during the procedure of TGE

TGE is a less invasive examination compared to transoral and transnasal endoscopy, because TGE does not pass through the pharynx. It requires neither local anesthesia of the pharynx or nasal tract nor conscious sedation before the procedure of TGE. We monitored blood pressure, heart rate, and percutaneous oxygen saturation concentration measurement of the arterial blood (SPO2) during TGE procedures in 20 consecutive patients. The values were compared to those for patients with the same clinical background during the examination of transoral endoscopy in routine esophagogastroduodenoscopy. Table 1 shows the comparison of cardiopulmonary effects during the procedures of TGE and transoral endoscopy. None of the TGE examinations required sedation, while the transoral examinations required 1 to 4 mg of intravenous administration of midazolam. There were no significant differences in the fluctuation of blood pressure and heart rate between TGE and transoral endoscopy. TGE displayed no effects on SPO2 during the procedure, while transoral endoscopy caused a decrease of SPO2 in 46% of the patients.

Transgastrostomal endoscopy (n=20) Transoral endoscopy (n=13) P value
Fluctuation of blood pressure (more than 20%) 5% (1/20) 23% (3/13) P = 0.157
Fluctuation of heart rate (more than 20%) 15% (3/20) 15% (2/13) P "/ 0.5
Decrease of SPO2
(more than 3%)
0% (0/20) 46% (6/13) P < 0.01

Table 1.

The effects of TGE and transoral endoscopy on blood pressure, heart rate, and SPO2

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3.2. Newly developed lesions in upper gastrointestinal tract after PEG

We have been conducting TGE for screening the upper gastrointestinal tract since April 2003. TGE was carried out 805 times in 245 PEG patients (Table 2) during routine replacement of gastrostomy tubes until November 2010. The demographic data are shown in Table 2. The mean age of the subjects was 80.8 years old, and the most frequent underlying disease was cerebrovascular disease. The endoscopic findings of TGE were compared to those at PEG placement. There were a variety of newly developed lesions after PEG.

Age (mean + SD) 80.8 + 8.9
Gender (male : female) 71 : 174
Underlying disease
Cerebrovascular disease
Dementia
Neuromuscular disease
Pneumonia
Malignant tumor
Others
143
42
23

20
6
11

Table 2.

Demographic data of patients who underwent TGE after PEG

Reflux esophagitis was found in 35 patients (14.2%), which was the most frequent lesion after PEG. Among the 35 patients, reflux esophagitis was absent at the PEG tube placement in the 30 patients. There were 5 severe cases with symptoms of hematemesis and this had subsequently led to stricture of the lower esophagus in 3 patients (Fig. 3A). Although in these 3 patients, we were unable to insert a transoral endoscope into the stomach, we were able to conduct endoscopic observation of the stomach by TGE (Fig. 3B).

Figure 3.

Endoscopic view of severe reflux esophagitis after PEG. A: Circumferential ulcer was observed by emergency transoral esophagoscopy after the symptom of hematemesis. B: The stricture of the lower esophagus after administration of proton pump inhibitor was observed from the stomach by TGE.

The next most frequent lesion after PEG was polypoid lesion around the stoma. We classified polypoid lesions into 3 types according to their location e.g.; basal bumper type, peri-bumper type and opposite-bumper type. The basal-bumper type polyp was communicated with the fistural tract and the pathology was inflammatory granulation (Fig. 4A). The peri-bumper type polyp was located around the stoma and often observed in cases with decompression by a mushroom type gastrostomy tube (Fig. 4B). Pathological examination revealed hyperplasia of the gastric mucosa. The opposite-bumper type polyp was located on the contra lateral wall of the stoma, probably caused by the contact of the top of the bumper or tube (Fig. 4C). The pathology was hyperplasia. Most of the polypoid lesion was not significantly changed in the subsequent observation by TGE. One case with haemorrhage from the basal-bumper type granuloma was resected by polypectomy using TGE.

Figure 4.

Endoscopic views of polypoid lesions around the stoma. A: basal-bumper type, B: peri-bumper type, C: opposite-bumper type.

Gastric ulcer was observed in 6 patients. All of their lesions were accidentally found at TGE, because they did not complain of symptoms due to their comorbid diseases. Among the 6 patients, the lesions of 3 patients were supposed to have been caused by direct contact with the bumper. These ulcers were characterized by their location on the contralateral side of the bumper (Fig. 5A). The remaining 3 patients were sporadic cases (Fig. 5B). We have also experienced additional 2 cases of symptomatic gastric ulcer which were detected by transoral endoscopy. For their initial symptoms of hematemesis and tarry stool, emergent esophagogastroduodenoscopy was performed (Nishiwaki et al., 2010b). Hemostasis was obtained by endoscopic hemoclips and coagulation, respectively. TGE was not available for such therapy, because the working channel of the ultrathin endoscope was too narrow to insert the devices to achieve hemostasis.

Figure 5.

A: Gastric ulcer was observed on the posterior wall of the lower body of the stomach, contralateral to the stoma. B: Peptic ulcer was observed on the lesser curvature of the upper body in the stomach.

Neoplastic lesions were also detected by TGE. We have experienced 3 cases of early gastric cancer and one case of carcinoid tumor that developed after PEG. One case was recurrence of early gastric cancer after endoscopic mucosal resection before the PEG. One case of early gastric cancer underwent coagulation therapy with argon plasma (Fig. 6A). The remaining two cancer (Fig. 6B) and one carcinoid tumor lesions were resected by endoscopic submucosal dissection assisted by TGE, the technique of which is described in section 4.2.1. The primary duodenal cancer was accidentally found by TGE at the first endoscopic examination 5 years after PEG.

Candida esophagitis was observed in 4 patients. All of the patients were administered proton pump inhibitor, which might have been involved in the development of the esophagitis.

Figure 6.

A: Indigocarmine sprayed endoscopic view of early gastric cancer. Superficial depressed lesion (IIc) was observed on the greater curvature of the antrum. The biopsy specimen of the lesion was well-differentiated tubular adenocarcinoma. B: Superficial elevated lesion (IIa) was observed on the lesser curvature of the upper body of the stomach. Pathological finding of the biopsy specimen was well-differentiated tubular adenocarcinoma.

Table 3 summarizes newly developed lesions after PEG. TGE was useful for the early detection and follow up of these lesions.

Pathological conditions Number of patients
Reflux esophagitis 30
Polypoid lesion around the stoma 28
Gastric ulcer 6
Neoplastic lesions
Early gastric cancer 3
Gastric carcinoid tumor 1
Primary duodenal cancer 1
Candida esophagitis 4
Total 73

Table 3.

Newly developed upper gastrointestinal lesions which were detected by TGE after PEG

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4. Therapeutic application of TGE

TGE also offers several advantages for endoscopic treatments compared with a transoral endoscope. TGE can easily access up to the upper jejunum with less patient discomfort. TGE covers treatments for lesions from the upper esophagus to upper jejunum. Table 4 shows the list of TGE we have conducted for therapeutic purposes..

No. of trial No. of success
Establishement of direct jejunal feeding access
Placement of jejunal feeding thorough the PEG (PEG-J) 27 27
Direct percutaneous endoscopic jejunostomy (DPEJ) 36 33
Resection of upper gastrointestinal tumors
TGE assisted endoscopic submucosal dissection (ESD) 5 5
Endoscopic mucosal resection 1 1
Polypectomy 1 1
Palliative therapy for gastrointestinal obstruction
Transgastrostomal gastroduodenal stenting 5 4
Placement of long intestinal decompression tube 2 2
Other usage for endoscopic treatments
Recovery of disrupted gastrocutaneous tract 5 5
Transgastrostomic biliary drainage 1 1

Table 4.

Reference chart of TGE for therapeutic purposes and their outcomes

4.1. Establishment of direct jejunal feeding access

Since the introduction of endoscopic placement of a gastrostomy tube, PEG has been the primary choice for long-term enteral access. However, there are some situations which postpyloric or jejunal feeding is preferable to gastric feeding. The indications for jejunal feeding include a high risk of aspiration, previous gastric resection, gastric pull-up, gastric outlet obstruction, an obstructed or nonfunctioning gastrojejunostomy, and gastric dysmotility (Shike & Latkany, 1998). The access for jejunal feeding was initially established as two methods, i.e.; transnasal insertion of a feeding tube and surgical placement of a jejunostomy tube. Alternative accesses methods for jejunal feeding have been developed; placement of a jejunal feeding tube through the PEG (PEG-J) and direct percutaneous endoscopic jejunostomy (DPEJ). We utilized TGE for the establishment of the two access methods.

4.1.1. Placement of a jejunal feeding tube through the PEG (PEG-J)

PEG-J was first described in 1984 (Ponsky & Aszodi, 1984). This technique was usually conducted for patients with high risk of aspiration due to gastroesophageal reflux of food after PEG (Nishiwaki et al., 2006). The tube is usually placed under fluoroscopic guidance. However, it is sometimes difficult to pass the feeding tube through the pyloric ring and duodenum using only fluoroscopy. A technique to assist the tube passage into the duodenum by transoral endoscopy has been reported (Duckworth et al., 1994; Leichus L et al., 1997). A transgastric technique using a pediatric bronchoscope or an ultrathin endoscope was described first in 1995 (Adler et al., 2002; Chaurasia & Chang, 1995).

We treated 27 patients using this technique with the following procedures: 1. Remove the gastrostomy tube. 2. Insert an endoscope through the gastrostomy and proceed up to the jejunum (Fig. 7A). 3. Insert a guidewire through the working channel of the endoscope. 4. Remove the endoscope retaining the guidewire (Fig. 7B). 5. Place a jejunal feeding tube over the guidewire through the PEG under fluoroscopic guidance (Figs. 7 C& D).

Figure 7.

Schematic procedure of PEG-J using TGE.

The jejunal feeding tubes (J-tube, Boston Scientific, Natick, MA, USA, or Jejunal Feeding Tube, Bard Access Systems, Inc., Salt Lake City, UT, USA) were successfully placed in all 27 patients. The duration of the procedure ranged from 4 to 20 minutes, which was remarkably quick compared with the procedure using only fluoroscopic guidance.

4.1.2. Direct percutaneous endoscopic jejunostomy (DPEJ)

Direct percutaneous placement of the jejunostomy tube was first described in 1987 (Shike et al., 1987). The first case series were for patients with previous gastric resection, and the technique was subsequently applied for patients with intact stomach. Becuase the length of the endoscope for the performance of DPEJ in the transoral route is 160 cm or longer, it requires the use of a long colonoscope or a small intestinal scope (Shike et al., 1991). However, the transgastrostomal approach facilitates access to the upper jejunum without difficulty. DPEJ using TGE was first described in 2002 (Baron, 2002). Although they successfully placed a jejunostomy tube through the mature gastrostomy tract, the gastrocutaneous tract was disrupted by passing through the bumper of the jejunostomy tube. We modified the procedure (Fig. 8) so that the jejunostomy tube does not pass the gastrostomy tract (Nishiwaki et al., 2009b).

After conscious sedation with intravenous administration of midazolam (1 to 2 mg) in most patients, an ultrathin endoscope was inserted through the gastrocutaneous tract immediately after the removal of the gastrostomy tube. The endoscope was inserted up to the jejunum and the site for placement was determined by transillumination to the abdominal wall and finger pressure against the jejunum (Fig. 8A). The abdominal skin surface of the placement area was cleansed with povidone-iodine, and local anesthesia was done administering 1% lidocaine. After test-puncturing with a 21-gauge needle, one or two point sutures were made using gastropexy devices (Create Medic Co., Ltd., Yokohama, Japan, or Easy Tie, Boston Scientific Japan K.K., Tokyo, Japan) to fix the jejunum against the abdominal wall. A 16- or 18-gauge Seldinger needle was inserted through the abdomen toward an open snare inserted through the TGE and a loop wire was passed through the outer sheath of the needle. The loop wire was grasped by the snare and pulled out through the gastrocutaneous tract with the endoscope (Fig. 8B). In most cases, the loop wire was then grasped in the stomach by biopsy forceps of an orally inserted endoscope (Fig. 8C) and pulled out via the mouth (Fig. 8D). In a few cases, the loop wire was directly brought out from the mouth by transgastrostomic endoscopy. Next, an jejunostomy tube was connected to the loop wire and the tube was placed in the jejunum by the pull-through technique (Fig. 8E). The systems to place the jejunostomy tube were One Step Button (Boston Scientific Co., Natick, MA, USA) or Bard Ponsky Pull PEG (Bard Access Systems, Inc., Salt Lake City, UT, USA)

Figure 8.

Schematic procedure of DPEJ using TGE.

Thirty six DPEJ procedures were attempted in 35 patients, with 33 (92%) successful placements. One unsuccessful placement was due to jejunum migration away from the abdominal wall during the puncture; this patient was maintained by feeding via the PEG-J. The other two failures were due to the lack of transillumination. The average + SD of duration of procedure, from insertion of the endoscope to the placement of the jejunostomy tube, was 29.6 + 13.1 (15 to 70) min.

Procedure-related complications consisted of 1 case each of pneumonia, colocutaneous fistula, and pneumoperitoneum. Of these, pneumonia and colocutaneous fistula were considered major complications. In the former case, placement of the jejunostomy tube took 50 min, and pneumonia occurred before administration of nutrients. The patient died 4 days after DPEJ due to respiratory failure. In the latter case, the fact that the jejunostomy tube had been placed penetrating through the colon was revealed at the second replacement of the jejunostomy tube. The colocutaneous fistula was naturally closed after removal of the replaced tube and DPEJ was successfully completed 28 days after the removal. Pneumoperitoneum, a minor complication, was observed in a severely obese patient.

4.2. Resection of upper gastrointestinal tumors

Endoscopic techniques to remove gastrointestinal tumors have been established as snare polypectomy and endoscopic mucosal resection (EMR). EMR allows the removal of flat lesions by injection with saline into the submucosal layer, but it is difficult to remove larger tumors. Recent development of the technique of endoscopic submucosal dissection (ESD) facilitates the removal of widely-spread neoplastic lesions compared to the EMR. We utilized TGE for these resection techniques of the upper gastrointestinal tumors.

4.2.1. TGE assisted endoscopic submucosal dissection (ESD)

ESD is a new technique for the resection of early gastric cancer (Ono et al., 2001). This technique allows en bloc resection even for larger lesions and allows for precise histological analyses. However, this method has a high incidence of complications such as bleeding and perforation, and the technique requires skill and a longer time for resection compared to conventional EMR (Gotoda 2006). One of the technical problems of ESD is the difficulty of maintaining a clear view of the submucosal layer of the gastric wall during submucosal dissection. We developed the technique of ESD assisted by TGE to dissolve the problem (Nishiwaki et al., 2009a).

Five patients previously established with PEG underwent TGE-assisted ESD (Table 5). ESD was carried out by a single-channel videoendoscope, GIF H260 (Olympus Optical Co., Ltd, Tokyo), attached with a short hood. The high-frequency electrosurgical unit was the Erbotom ICC 200 in Cases 1-3, and the VIO 300D in Cases 4 and 5 (ERBE Elektromedizin GmbH, Tubingen, Germany). After circumferential markings around the lesion, submucosal injection was carried out using a mixture of hyaluronic acid and glycerol containing indigocarmine, according to the method described by Fujishiro, et al (Fujishiro et al., 2006). Circumferential mucosal cutting and submucosal dissection were carried out using a needle knife, a Flex knife, an insulation-tipped (IT) knife, or a combination of the three. TGE was inserted through the mature gastrocutaneous tract and grasped the edge of the resecting specimen to achieve appropriate counter-traction during submucosal dissection (Figs. 9A-C). Hemostatic forceps were used when active bleeding took place during the procedure or to prevent bleeding from large vessels before cutting in soft coagulation mode. TGE also worked for additional submucosal injection, washing with water, aspiration of gastric fluid.

Case I.D. 1 2 3 4 5
Age/Gender 83/M 82/F 72/M 79/F 82/F
Pathology tub 1 tub 1 adenoma tub 1 carcinoid tumor
Location a.w. antrum l.c. body p.w. antrum g.c. body a.w. body
Dissection size (mm) 24 X 22 20 X 20 60 X 30 30 X 22 15 X 10
Operative duration (min) 21 18 105 55 80

Table 5.

ub 1: well differentiated tubular adenocarcinoma, a.w.: anterior wall, l.c.: lesser curvature, p.w.: posterior wall, g.c.: greater curvature

Table 5. Summary of the patients who underwent TGE-assisted ESD.

A laparoscopic port with a trocar is inserted into the gastric lumen percutaneously and assists in the ESD using an IT knife (Kondo et al., 2004). However these methods are thought to be limited for some tumor locations, as the assisting devices are not flexible. EMR assisted by a magnetic anchor has also been reported to create strong counter traction (Kobayashi et al., 2004). In our methods, an ultrathin endoscope is inserted through the gastrocutaneous tract after PEG, and assisted ESD is performed with an orally inserted videoendoscope. TGE can cover the whole stomach and esophagus and create appropriate counter traction for dissection of the lesion. Furthermore, TGE not only can provide traction control but can also support diverse procedures of ESD, such as marking, submucosal injection, washing out or aspiration of the intragastric contents. TGE facilitates ESD by this type of assistance, and the operation duration of TGE-assisted ESD has been found to be relatively short compared to the single-scope ESD in our hospital.

One of the problems of this method is light interference between the two endoscopes (Fig. 9D). When the two endoscopes faced each other, the position of the TGE had to be changed to eliminate the light interference. The other problem of this method is that it might be difficult to perform TGE before maturation of the gastrocutaneous tract. In the present case series, gastric tumors were found after PEG in three cases, but two tumors were found at the placement of PEG catheter. In general, it takes 3-4 weeks to complete the stoma. ESD was conducted in the two cases 3-4 weeks after PEG, after waiting for maturation of the gastrocutaneous tract. Pneumoperitoneum occurred after ESD in Case 3, although it recovered spontaneously. The use of gastropexy devices enabled us to fix the abdominal and gastric walls more tightly, such that pneumoperitoneum might be prevented even with prolonged endoscopic treatment. Narrowing of the ultrathin endoscope would be helpful for this method. Therefore, simultaneous PEG and TGE-assisted ESD using a gastropexy device and an ultrathin endoscope might be possible for large, difficult lesions.

Figure 9.

TGE-assisted ESD. A. Schematic illustration of ESD assisted by TGE. B. Endoscopic view from transoral endoscope in Case 4. A grasping forceps was inserted through the TGE and grasped the edge of the gastric tumor (arrow). C. Endoscopic view from transoral endoscope in Case 4. Counter traction of the exfoliating lesion by TGE facilitated the submucosal dissection by a Flex knife. D. Endoscopic view from transoral endoscope in Case 1. Light from the TGE impeded the procedure of ESD when the endoscope faces each other. The position of TGE should be changed so as not to disturb the procedure.

4.2.2. Endoscopic mucosal resection (EMR) and polypectomy

The performance of ESD by TGE alone is quite difficult because the working channel of the ultrathin endoscope is too narrow to insert the devices for ESD. However, TGE itself can be used for polypectomy and EMR by using an appropriate injection needle and snare for the ultrathin endoscope. We carried out resection of two benign polyps by TGE. One case was a hyperplastic polyp on the prepylorus, and the other was inflammatory granuloma on the gastric stoma (Fig. 4A). Both polyps showed a tendency to develop during the periodical observation by TGE. Transgastric resections were successfully conducted without conscious sedation.

4.3. Palliative therapy for gastrointestinal obstruction using TGE

One of the indications of PEG is decompression of gastrointestinal content in cases of obstruction of gastrointestinal tract. On the other hand, some cases develop gastrointestinal obstruction after PEG. TGE also facilitates the palliative therapy in such cases.

4.3.1. Transgastrostomal stenting on gastroduodenal outlet obstruction

Endoscopic deployment of stents for malignant gastroduodenal outlet obstruction has been reported as a less invasive palliative therapy compared to a surgical bypass operation (Yim et al., 2001). It is more difficult to place the stent across the postpyloric lesion compared to the esophagus, because the delivery system often forms a loop in the stomach before passing through the obstruction. When the gastrostomy site is adjacent to the obstructed lesion, a transgastric approach for stenting is easier than a transoral approach. Transgastrostomic stenting for malignant duodenal obstruction was first described in 1993 (Keymling et al., 1993).

The schematic procedure of transgastrostomal stenting is shown in Fig. 10. An ultrathin endoscope is inserted through the mature gastrocutaneous tract followed by removal of the gastrostomy tube. A guidewire is advanced through the stenosis (Fig. 10A). The endoscope is once removed from the gastrostomy keeping the position of the guidewire. A balloon catheter is inserted over the guidewire and the stenosis is dilated with the balloon catheter (Fig. 10B). The ultrathin endoscope is inserted after the removal of the balloon catheter and advanced to the upper jejunum (Fig. 10C). A guidewire is inserted deeply in the jejunum through the endoscope and the endoscope is removed again, retaining the guidewire. A stent is finally deployed over the guidewire across the obstructed lesion using a delivery device (Figs. 10D& E).

Figure 10.

Schematic procedure of the placement of an expandable metallic stent on the pyloric stenosis.

We tried this procedure for 5 patients in whom we had failed to place a stent by the transoral approach (Table 6). In 4 out of 5 patients, a non-covered expandable metallic stent was successfully deployed (Ultraflex, Boston Scientific Co., Natick, MA, USA). The one case (#5) of failure was changed to the placement of a jejunal feeding tube through the obstruction. The duodenal obstruction of this case was too severe to pass the delivery device but a 12F jejunal feeding tube was successfully inserted through the obstruction. All of the patients could successfully feed again after the procedure.

Case I.D. 1 2 3 4 5
Age/Gender 88/F 82/F 84/M 75/M 72/F
Tumors Stomach CBD Stomach CBD Gall bladder
Obstruction Pylorus Duodenum Pylorus Duodenum Duodenum
Operative duration (min) 20 27 15 45
Outcome Success Success Success Success Failure

Table 6.

BD: common bile duct

Summary of the cases with transgastrostomal stenting

4.3.2. Placement of long intestinal decompression tube

Placement of a long intestinal decompression tube was carried out for malignant lower intestinal obstructions. A series of radiographs of the procedure in the case with ascending colon cancer is shown in Fig. 11. The procedure was the same as for the placement of a PEG-J tube as described in 4.1.1. The benefit of this procedure is that it is more comfortable for the patient, especially in the prolonged period of decompression, compared to transnasal placement.

Figure 11.

Radiographs of the placement of a long intestinal decompression tube. A. An ultrathin endoscope was inserted into the stomach after removal of the gastrostomy tube. B. The endoscope was advanced to the upper jejunum. C. A guidewire was passed through the endoscope. D. A long intestinal decompression tube (CLINY Ileus Tube, Create Medic Co. Ltd., Yokohama, Japan) was placed over the guidewire.

4.4. Other usage for endoscopic treatments

We utilized TGE to treat other pathological conditions. The applications for pancreaticobiliary and esophageal diseases have been reported. Alternative possibilities for the usage of TGE are discussed in this section.

Figure 12.

Schematic illustrations of the recanalization of a disrupted fistula using TGE. A. Misplacement of a gastrostomy tube into the peritoneal cavity. B. Insertion of ultrathin endoscopy from the skin incision and looking for the gastric lumen. C. Successful insertion into the stomach. D. Passing the endoscope through the esophagus to the oral cavity. E. Insertion of a loop wire from the stoma out of mouth. F. A new gastrostomy tube is replaced by the pull-thorough technique.

4.4.1. Recovery of disrupted gastrocutaneous tract

Fistula disruption usually occurs upon early dislodgement of the gastrostomy tube or upon replacement of the tube. It might cause the serious complication of peritonitis due to leaking of gastric contents or feeding materials into the peritoneal cavity (Fang, 2007; McQuaid & Little, 1992; Romero et al., 1996). In order to place a new gastrostomy tube, a PEG procedure is often performed adjacent to the disrupted fistula (Galat et al., 1990). We employed TGE for recanalization of the disrupted fistula at the tube replacement (Nishiwaki et al., 2009 c). Schematic illustrations of the procedure are shown in Fig. 12.

We tried this technique for 5 patients with fistula disruption and in all of the patients, the disrupted fistula tract was successfully recovered. Before the introduction of this procedure, we inserted a guidewire to search for the gastric lumen from the skin incision under fluoroscopic guidance. However, in 2 out of 5 trials, we failed to reestablish a gastrocutaneous tract. The endoscopic view of TGE is helpful to locate the intragastric route from the skin incision.

4.4.2. Transgastrostomic biliary drainage

Endoscopic retrograde cholangiopancreatography from the gastrostomy have been reported (Baron & Vickers, 1998; Mori et al., 2007). Since all ultrathin endoscopes are forward-viewing, it is more difficult to insert a canula into a pancreatic or bile duct. Moreover, endoscopic treatment has limitations because of the limited availability of therapeutic devices. However, there is a benefit of direct access into the bile duct after sphincterotomy and the ability to conduct direct endoscopic observation of the bile tract (Larghi & Waxman, 2006).

We only experienced one case with transgastrostomal biliary drainage for obstructive jaundice in a patient with primary sclerosing cholangitis (Fig. 13). Placement of a transgastrostomal drain tube is more comfortable than that of a transnasal drain tube.

Figure 13.

Establishment of transgastrostomal biliary drainage. A. Endoscopically placed retrograde biliary drainage tube (FLEXIMA Single-Use Biliary Stent System, 6F, Boston Scientific, Maple Grove, MN, USA) was retrieved from the gastric stoma by TGE. B. The tube was passed through a 12F Jejunal Feeding Tube (Bard Access Systems, Inc., Salt Lake City, UT, USA). This procedure allowed the patient to continue to feed through the gastric decompression port of the tube.

4.4.3. Transstomal endoscopy other than gastrostomy

Transstomal endoscopy is also available via other routes than the gastrostomy tract. We experienced two cases of endoscopic placement of a jejunal extension tube through direct endoscopic jejunostomy. The first case had undergone DPEJ and showed repeated aspiration due to jejunoesophageal reflux of the feeding materials. We inserted the top of a feeding tube to 40 cm anal direction from the jejunostomy site using a transjejunostomal endoscope (Fig. 14). Another case was jejunal obstruction caused by inflammatory granuloma of the jejunostomy site (Nishiwaki et al., 2007). We could successfully place a feeding tube on the anal side of the obstruction by transjejunostomal endoscope. Although a similar procedure has previously reported under fluoroscopic guidance (Luttman et al., 2005), it might be easier to place a feeding tube using the transjejunostomal endoscope.

Figure 14.

Placement of an extension feeding tube through the DPEJ. A. An ultrathin endoscope was inserted through the jejunostomy site (arrow) and advanced to the anal side. B. A guidewire was placed through the endoscope. C. J-tube (Boston Scientific, Natick, MA, USA) was placed over the guidewire.

Figure 15.

Placement of an expandable metallic stent (Ultraflex, Boston Scientific, Natric MA, USA) across the obstructed ascending cancer. A. Insertion of an ultrathin endoscope through the cecostomy (arrow). Arrow heads indicate the location of the tumor. B. A guidewire was passed through the obstruction and inserted deeply along the anal side of the bowel under the guidance of fluoroscopy. C. Delivery system of the Ultraflex was inserted through the obstruction over the guidewire. D. Ultraflex was deployed across the tumor.

We additionally experienced one case of transcecostomal endoscopy for stent placement across the ascending colon cancer (Nishiwaki et al., 2010b). The patient was too critically ill to undergo surgical treatment, and we were also unable to place a colonic stent by colonoscopy. After establishment of ultrasonography-guided percutaneous cecostomy, transcecostomal endoscopy facilitated the passing of a guidewire thorough the obstruction. The procedure of the stent deployment is shown in Fig. 15.

4.4.4. Other applications

TGE was reported to be useful for the dilatation of radiation-induced complete esophageal obstruction (Maple et al., 2006). The rendezvous technique for the dilatation of esophageal stricture was conducted by cooperative use of transoral endoscope and TGE. The use of TGE made the procedure more safe and effective.

Recent developments in super ultrathin endoscopes allow for insertion through the gastrostomy tube. The endoscope is then utilized for verification of a replaced gastrostomy tube into the stomach.

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5. Conclusions

TGE offers a less invasive way to observe the upper gastrointestinal tract and allows for the detection of early stage gastrointestinal lesions. TGE also facilitates endoscopic treatments which might be more difficult by transoral endoscope. However, the narrow working channel of the ultrathin endoscope is a limitation of therapeutic TGE. Further improvements to the endoscope and applicable devices will be expected in the future.

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6. Acknowledgements

We express our appreciation to Dr. Saito, Nishimino Kosei Hospital, for generous advice on these procedures. We also appreciate the members of the endoscopy unit of Nishimino Kosei Hospital (Dr. Maeda, Dr. Hayashi, Dr. Tagami, and Dr. Takada) for their assistance with the endoscopic procedures.

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Written By

Shinji Nishiwaki, Hiroo Hatakeyama, Masahide Iwashita and Hiroshi Araki

Submitted: 20 November 2010 Published: 22 September 2011