Gastrointestinal Devices, Procedures, and Imaging

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46 Gastrointestinal Devices, Procedures, and Imaging

Nasogastric Tubes

The Salem Sump tube is the most commonly used nasogastric tube (NGT) in the emergency department (ED). The Salem Sump is a double-lumen tube with multiple distal suction eyes. The second lumen allows venting during suction, which prevents invagination and subsequent gastric injury. Indications for its use include gastric evacuation or decompression, diagnostic aspiration of gastric contents, and infusion of therapeutic agents. Intermittent suction may be set at a pressure of less than 120 mm Hg.1 A Levin tube is a single-lumen tube with multiple distal openings for suction, referred to as “eyes.” The Levin tube’s relatively large internal diameter makes it ideal for rapid decompression or drug infusion. Intermittent suction may be set at a level lower than 40 mm Hg. A Levin tube has the same uses as the Salem tube except that it may not be used for long-term gastric evacuation.1

Insertion Procedure

Inserting an NGT may cause the patient to cough, vomit, retch, or sneeze. Because traumatic epistaxis is common, protective apparel should be worn when placing an NGT—gloves, gown, and mask. The patient should be placed in either an upright or Fowler position.

2 Nares Patency Check, Anesthesia, and Vasoconstriction

Patency of the nares should be checked before placing an NGT. This can be done by direct visualization or by having the patient sniff or blow out of each nostril with the other naris occluded. Topical anesthetic spray or ointment should be used to decrease the discomfort and gagging associated with tube placement. The more patent nostril should be used for the procedure.

Pretreatment Medications

Placement of an NGT is one of the most painful routine procedures performed in the ED. In nonemergency situations it is best practice to treat the patient with nasal vasoconstrictors and anesthetics before placing the tube.4

Vasoconstrictors may be used 3 to 5 minutes before the procedure to decrease traumatic bleeding. Phenylephrine (Neo-Synephrine 0.5%) or oxymetazoline (Afrin 0.05%) is typically used. Vasoconstrictors must be used with caution in hypertensive patients.

Application of lidocaine before inserting an NGT has been shown to significantly decrease pain during the procedure.57 Lidocaine can be delivered as viscous, nebulized, or atomized preparations. Application of viscous lidocaine to the nasal passage combined with lidocaine spray applied to the posterior pharynx has been shown to be superior to other forms of anesthetics when placing an NGT or transnasal bronchoscope.6,8 However, no definitive study or review article has determined the best concentration, form, or dose of lidocaine to use.7

4 Insertion of the Tube

The tube is inserted into the naris along the floor of the nose inferior to the lower turbinates. The tube should be inserted at close to a 90-degree angle with the face and directed parallel to the floor of the nose (posteriorly), not cephalad (Fig. 46.2). Gentle pressure should be used to advance the tube past the nasopharynx and into the oropharynx. Once the tube is in the posterior pharynx, the patient is asked to swallow or take a sip of water to aid in smooth passage of the tube into the esophagus. The tube is then quickly advanced to the premeasured length to minimize discomfort. Care should be taken to not use excessive force when placing an NGT to avoid mucosal injury.

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Fig. 46.2 The nasogastric tube is passed parallel to the floor of the nose posteriorly and usually passes inferior to the inferior turbinate. The tube should not be directed cephalad.

(From Samuels LE. Nasogastric and feeding tube placement. In: Roberts JR, Hedges JR, editors. Clinical procedures in emergency medicine. 4th ed. Philadelphia: Saunders; 2004. pp. 794-816.)

Transabdominal Feeding Tubes

Feeding tubes are placed to provide long-term nutritional support. They are classified both by the location of their terminal lumen and by the method of placement. Gastrostomy tubes have a terminal lumen located within the stomach and are now typically placed via a percutaneous endoscopic technique; they are thus called PEG (percutaneous, endoscopically placed gastrostomy) tubes (Fig. 46.4). Several manufacturers make various types of PEG tubes. The other most frequently encountered feeding tube is a J tube, or jejunostomy tube. Such tubes are longer, smaller-caliber tubes that terminate in the jejunum. Unlike a gastrostomy tube, a J tube does not have an inflated balloon on its terminal end.

The classic open surgical gastrostomy procedure is less commonly performed than the percutaneous techniques. Percutaneous tubes can be placed by a gastroenterologist via endoscopy or by a radiologist via fluoroscopy. Fewer complications are seen with radiographically placed tubes than with tubes placed either by an open technique or endoscopically (Fig. 46.5).17,18

Replacing a Tube

Transabdominal feeding tubes must be replaced (Fig. 46.6) for many reasons, including expulsion, malfunction, leakage, tube deterioration resulting in cracks or fissures, and aneurysmal dilations of the tube. It is important that a patient’s tube be correctly identified with respect to type, size, and manufacturer before an attempt at replacement. A dislodged tube should be replaced as quickly as possible to maintain patency of the feeding tube tract. When replacing a feeding a tube it is important to clarify whether the terminal end was in the stomach versus the jejunum. After placement, the anchoring balloon in the replacement tube should be inflated in G tubes but never in J tubes.

Removing a Nonfunctional Tube

If the nonfunctioning PEG tube was placed under fluoroscopic guidance by a radiologist, it can usually be removed by deflation of the balloon and gentle retraction. Some devices have a flange rather than a balloon, and these flanges usually collapse with slow, gentle traction. If the tube was placed by a gastroenterologist or a surgeon, it may have an anchoring device or an internal component that prevents the tube from becoming dislodged from the gastrostomy tract. Such a tube cannot be removed by gentle traction alone; the internal component must be removed endoscopically. If resistance is met when attempting removal, a gastroenterologist, interventional radiologist, or surgeon should be consulted.

As an alternative method, the tube is lifted off the abdominal wall skin to allow the tube to be cut as close to the skin as possible. The internal component is then pushed into the GI tract so that it is free to pass through the intestines and be eliminated rectally. Most internal components pass within 2 weeks. There have, however, been reported cases of intestinal obstruction, perforation, and rarely death with this method.24,25 The internal component is less likely to pass without complications in children than in adults.26 If this technique is used, reliable patient follow-up is needed for serial abdominal radiographs. Radiographs should be taken within 1 week to monitor the progress of the component through the GI tract. If the internal component has not passed within 1 to 2 weeks, impaction has probably occurred, and endoscopic removal should be considered. Primary endoscopic removal is also advised in patients with intestinal obstruction, pseudoobstruction, pyloric stenosis, intestinal stricture, history of irradiation, and inflammatory bowel disease.27

Foley Catheters Versus Commercial Feeding Tube Products as Replacements

Both commercially available feeding tubes and Foley catheters can be used to replace a dislodged feeding tube. Commercial feeding tubes are more expensive than Foley catheters. Studies have found that a silicone Foley catheter with a retention disk and ring has the same efficacy and complication rate as a commercially available replacement gastrostomy tube. The retention disk and ring are used to prevent distal migration of the tube into the GI tract.28 However, many institutions do not stock silicone Foley catheters.

Foley Catheters Used as Replacement Feeding Tubes

A few simple modifications to a standard Foley catheter can maximize its longevity as a feeding tube, as well as reduce the chance of complications. When using a Foley catheter to replace a feeding tube, an external bolster, or anchor, is fashioned to prevent ingress of the tube into the ostomy and distal migration into the GI tract. An external bolster may be constructed by cutting a 3-cm section from a large rubber catheter. The outer bolster should be secured approximately 1 cm from the skin to prevent trapping of moisture and maceration.29 Its construction is as follows:

Verifying Tube Location

No standard method for verifying tube placement has been established. The safest and best practice is to obtain radiographic confirmation when a feeding tube is replaced.31 Radiographic confirmation should be obtained in the following circumstances:

Radiographic confirmation can be accomplished with fluoroscopy or by injection of water-soluble contrast material into the tube followed by plain radiography. Typically, 20 to 30 mL of contrast material is injected into the tube via a catheter tip syringe. An abdominal film should be obtained within 1 to 2 minutes. Generally, a flat-plate abdominal view is sufficient to verify tube placement. If insertion of the tube was very difficult or malposition is suspected, a two-view abdominal film may be required to ensure proper tube location. Proper location of the replaced tube is indicated by (1) ease of injection of the contrast material and (2) visualization of the gastric and intestinal walls as they are outlined by the contrast material. If extravasation of the dye is seen outside the stomach or intestine, tube malposition is verified.

Recently, two newer verification techniques have been described in small studies. The first uses air insufflation through the replacement tube to verify proper placement. Once the tube is replaced, a total of 240 mL of air is insufflated through the tube with a 60-mL syringe. The tube is considered properly replaced if it can be seen clearly within an air-distended stomach on a plain radiograph.32 The second technique was described in a small study with 10 subjects. Ultrasound was used to visualize the new tube as it was placed in the established tract. After insertion, color Doppler was applied over the catheter tip while it was gently oscillated to enhance visualization11 (Fig. 46.8).

Clogged Feeding Tubes

Larger-diameter feeding tubes are less likely than smaller tubes to become clogged. A tube can become obstructed if kinking occurs or the lumen is clogged with debris. A recently placed or reinserted tube is prone to kinking. A kink can be treated by withdrawing the tube a few centimeters and then advancing it again. Contrast-enhanced radiographs should be obtained whenever significant tube manipulation has occurred to evaluate for patency and proper location. A persistently clogged tube needs to be removed and replaced.

If a feeding tube is clogged by debris, the following approaches can be used to unclog the tube:

Instrumentation of the tube with either a Fogarty arterial embolectomy catheter or a nasal foreign body catheter can also be attempted. The length of the feeding tube external to the abdomen should be measured and the Fogarty catheter inserted only to this length. An instrument should never be inserted past the abdominal wall skin. The balloon on the catheter can be inflated in the tube if an obstruction is encountered and then further advanced to probe the entire length of the external tube. The catheter should not be withdrawn with the balloon inflated because this action might cause removal of the feeding tube. In a 10 French (10F) or 12F tube, a No. 4 embolectomy catheter should be used; a 14F tube requires a No. 5 embolectomy catheter.33

If a feeding tube has been unclogged by force or instrumentation, water-soluble contrast–enhanced radiographs should be obtained to verify proper tube placement, as well as to evaluate for tube perforation.

Gastroesophageal Balloon Tamponade

Variceal bleeding is a leading cause of significant morbidity and mortality in patients with cirrhosis. Sengstaken and Blakemore first described the use of a double-balloon tamponade system to control variceal bleeding in 1950. Sengstaken-Blakemore (SB) tubes are not advocated as primary or secondary therapy for cirrhotic patients; they are used as rescue therapy for life-threatening variceal bleeding.

Two gastroesophageal balloon tubes are in general use. The SB tubes have three lumens—a gastric balloon, an esophageal balloon, and a gastric aspiration port. The Minnesota tube has a fourth lumen for esophageal aspiration.

The indication for gastroesophageal balloon tamponade (GEBT) is severe, acute variceal bleeding that is refractory to available first-line interventions such as sclerotherapy and vasoconstrictor therapy. Relative contraindications are esophageal strictures, recent esophageal surgery, and decreased level of consciousness without airway protection. A patient with a decreased level of consciousness should always be intubated before insertion of an SB tube.

Procedure

The following equipment is needed:

The procedure is as follows2:

1. If needed, intubate the patient before placement of the tube.

2. Check the balloons for patency and leaks before use: use 100-mL increments of air to inflate the gastric balloon, and check the pressure with a sphygmomanometer after each increment. These pressure measurements should be recorded for each 100-mL increment of air and will be used to compare pressure readings once the tube has been inserted (step 12). The pressure in the gastric balloon should not increase more than 15 mm Hg with insufflation of each 100 mL of air.

3. If an NGT is to be inserted, tie a suture around it and the GEBT tube to secure them together. The tip of the NGT should be located 3 to 4 cm proximal to the esophageal balloon.

4. Lubricate the tube or tubes with a water-soluble lubricant.

5. Position the patient either upright angled at 45 degrees or in the left lateral decubitus position.

6. Anesthetize the posterior pharynx or nasopharynx with topical anesthetic spray or nebulized lidocaine (or both; see previous discussion on NGT insertion).

7. Place an NGT and evacuate the stomach before placing a GEBT tube to decrease the chance of emesis and aspiration. Once the gastric contents have been evacuated, remove the NGT.

8. Deflate all balloons and either clamp the ends of the tubes or place plugs in each lumen if provided by the manufacturer.

9. Pass the tube to a minimum level of 50 cm as marked on the tube.

10. Connect suction to the gastric and esophageal lumens to check for contents and to decrease the likelihood of aspiration.

11. Confirm proper tube placement with radiographs even if gastric contents or blood is evacuated. The tip of the tube or balloon should be located below the diaphragm if properly placed.

12. Remove the clamps or plugs and inflate the gastric balloon slowly with 100-mL increments of air. Check the pressure of the gastric balloon after each injection; with each 100 mL of air insufflated, the pressure should not be more than 15 mm Hg higher than the pressure measurements previously obtained for the same volume of air (step 2). If the pressure rises by more than 15 mm Hg, the balloon may be located in the esophagus and not in the stomach. If this occurs, deflate the balloon and obtain another radiograph to ensure proper tube location before resuming air insufflation. Generally, 400 to 500 mL of air must be insufflated to obtain the proper pressure; check the manufacturer’s recommendation for the tube being used.

13. Once proper pressure is obtained, clamp or plug the lumens of the gastric balloon and the air inlet.

14. Gently pull back on the GEBT tube until it snugs up against the diaphragm and applies pressure at the gastroesophageal junction.

15. Secure the GEBT tube to the traction device to be used while applying a small amount of tension to the GEBT tube to keep constant pressure on the lower esophageal sphincter. The traction devices may be an orthopedic trapeze apparatus or another device provided by the manufacturer.

16. If the tube was passed nasally, place the sponge rubber cuffs provided by the manufacturer into each nostril or pad the nostrils with gauze to prevent pressure ulcers.

17. Once the tube is properly placed and secured, lavage the stomach with room-temperature water to assess for active bleeding. Attach the gastric lumen to high-pressure, intermittent suction.

18. If blood continues to be aspirated from the gastric lumen, the esophageal balloon can be inflated to a minimum pressure level to control the bleeding or to the maximum pressure advised by the manufacturer (typically 30 to 45 mm Hg). Clamp or plug the lumen of the esophageal balloon once a desired pressure level is obtained.

19. Frequent manometer readings of the esophageal balloon should be obtained to decrease the risk for complications.

20. If bleeding continues, the most likely source is gastric; tension on the gastric balloon may be increased gradually to help control the bleeding.

21. Obtain radiographs any time that the position of the tube comes into question.

22. Once the bleeding is controlled, attempts should be made to decrease the pressure in the esophageal balloon by increments of 5 mm Hg every 3 hours until a pressure of 25 mm Hg is reached (or as recommended by the manufacturer). Typically, a pressure of 25 mm Hg can be maintained for 12 to 24 hours if the bleeding is controlled.

23. If the esophageal balloon requires inflation at pressures greater than 30 mm Hg, the balloon should be deflated every 6 hours for 5-minute intervals to prevent complications such as mucosal ischemia and necrosis.

24. To prevent vomiting and aspiration, the esophagus must be emptied continuously even if the esophageal balloon is not inflated. The gastric balloon will preclude passage of secretions into the stomach. Aspirate with either an esophageal aspiration port in a Minnesota tube or an NGT with its tip located in the esophagus next to the GEBT tube. The volume of oral and esophageal secretions can total up to 1500 mL/day.

25. Once the GEBT tube is properly inserted and bleeding has been controlled, the tube should not be disturbed for 12 to 24 hours.

26. If bleeding cannot be controlled, further therapies are indicated, such as emergency surgery, endoscopic interventions, or angiographic embolization.

References

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