Enteral Nutrition Administration, Monitoring, and Clinical Issues Flashcards

1
Q

Which of the following is true regarding infectious complications associated with enteral feedings?

1: Bacterial contamination may originate from the patient’s throat, lung, and stomach
2: Exceeding manufacture hang-time guidelines is not a risk for bacterial contamination
3: Open systems have less exogenous bacterial contamination
4: The enteral tube site should be routinely cultured

A

1: Bacterial contamination may originate from the patient’s throat, lung, and stomach

Bacterial contamination may occur both exogenously through the feeding equipment and endogenously through retrograde contamination of the feeding apparatus from the patient’s own infected secretions. There is a correlation between prolonged length of enteral product hang time and bacterial contamination. Open systems provide more opportunity for contamination due to nursing manipulation when adding more formula to the bag. There is no need for routine cultures in the uncomplicated enterally-fed patient.

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2
Q

A male patient suffered from a stroke two weeks ago and has significant dysphagia. An isotonic enteral formula has been infusing continuously at goal rate for two days along with an ordered 30 mL water flush per hour. The patient begins to complain of bloating and is mildly distended (to 4 cm from baseline) upon examination. He denies nausea, abdominal cramping or abdominal pain. His last 2 gastric residual volume checks were measured at 100mLs. Which of the following interventions would be the best initial strategy to reduce his unpleasant symptoms?

1: Determine last bowel movement and initiate a bowel regimen if constipation suspected
2: Hold enteral nutrition
3: Initiate a pain reliever
4: Switch to a semi-elemental formula

A

1: Determine last bowel movement and initiate a bowel regimen if constipation suspected

Abdominal distention upon enteral tube feeding may result from many different reasons: rapid administration of feeding (i.e. bolus feeds); use of hyperosmolar solution (i.e. concentrated formulas); medications that slow peristalsis (i.e. pain relievers, anticholinergics); excess air in the stomach or intestines; tube migration from stomach to small intestine; infection; cold formula; inadequate fluid provision leading to constipation; bacterial contamination; and, fat, fiber or lactose intolerance. Aggressive bowel regimens need to be considered in these patients to reduce distention and prevent impaction. Holding enteral feedings is generally not indicated unless abdominal girth exceeds the baseline measurement by at least 8 to 10 cm. Agents such as narcotics or diphenhydramine have well documented anticholinergic effects often resulting in constipation. Fiber may help to promote regular bowel movements in patients receiving enteral nutrition, but may also lead to excess gas production and increased abdominal distention. Providing additional free water flushes may help to decrease constipation.

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3
Q

A terminally ill patient at home on hospice complains of nausea during enteral feedings. A decision is made to discontinue enteral feeding. Which of the following is true regarding the dying patient?

1: Intravenous hydration should be used to reduce symptoms of nausea, vomiting, diarrhea and respiratory distress
2: Dehydration, starvation, and ketosis produces a euphoric state that enhances the perception of hunger
3: The most common symptom when nutrition and hydration are withheld is dry mouth
4: Electrolyte imbalance should be expected and may produce a degree of analgesia

A

3: The most common symptom when nutrition and hydration are withheld is dry mouth

Enteral feeding and hydration do not always ensure comfort. During starvation, the body begins to use fat as the predominant energy source leading to increased ketone production with a resulting euphoria. Feeding even small amounts can prevent ketonemia and prolong the sense of hunger. The most common symptom when feeding or fluids are witheld is dry mouth, which is easily alleviated with good mouth care. Intravenous hydration in the terminal patient can raise the risk of patient discomfort and respiratory distress.

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4
Q

One method of minimizing the complications associated with refeeding syndrome is to initiate an electrolyte replacement protocol before nutrition therapy begins. Which of the following is true regarding such a plan?

1: Potassium, magnesium, and calcium are the most important electrolytes to closely monitor
2: Patients considered not-at-risk should also be included in the protocol
3: The protocol should replete all electrolytes ONLY via the feeding tube
4: Feeding should be delayed until the risk of electrolyte imbalance is eliminated

A

1: Potassium, magnesium, and calcium are the most important electrolytes to closely monitor

Refeeding syndrome describes the occurrence of electrolyte disturbances when attempting to initially feed the undernourished patient. Although hypokalemia, hypomagnesemia, and hypocalcemia may occur in refeeding syndrome, hypophosphatemia is more prevalent. Patients considered not-at-risk should also be included since methods for screening “at-risk” are inadequate. The protocol should replete all electrolytes via the intravenous, oral or feeding tube route depending on the condition of the patient and ability to tolerate PO repletion. Feeding should not be delayed but instead initiated slowly and then advanced based on electrolyte levels and clinical response.

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5
Q

Which is a benefit of using an electromagnetic placement device for nasogastric tube placement?

1: pH can be monitored
2: Checks the tip position relative to the pylorus
3: Provides a 3-dimensional localization
4: Shows a time-delayed perspective of the tube tip location

A

3: Provides a 3-dimensional localization

The display shows a real-time perspective of the tube tip location with a 3-dimensional localization. pH is not monitored in this placement technique. The receiver is placed on the patient at the xiphoid process, therefore the magnet follows the tip placement relative to the lower esophageal sphincter, not the pylorus

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6
Q

In a patient with a newly placed gastrostomy or jejunostomy tube, observation of which of the following conditions at the tube exit site would signal concern for infection?

1: Serosanguineous drainage
2: Foul-smelling drainage
3: Coffee-ground drainage
4: Bile-colored drainage

A

2: Foul-smelling drainage

Peristomal infection is the most common complication following gastrostomy placement. Foul-smelling drainage around the tube exit site is a sign of infection. Early recognition and treatment of exit site infections reduces morbidity and mortality. Leakage around the gastrostomy site is another common complication. Exit site care, proper outer bumper placement and prevention of tension on the tube help reduce gastrostomy exit site leakage.

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7
Q

Which of the following feeding schedules would be most appropriate for a critically ill patient with poorly controlled blood glucose?

1: Bolus
2: Continuous
3: Gravity drip
4: Nocturnal infusion

A

2: Continuous

Continuous infusions of enteral feeding and insulin may facilitate more steady and predictable blood glucose concentrations in critically ill patients. Intermittent feeding schedules, such as bolus, gravity drip, or nocturnal infusion may cause fluctuations in blood glucose concentrations, placing patients at risk for hypoglycemic and hyperglycemic complications.

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8
Q

Which of the following is a major risk factor for aspiration in critically ill patients?

1: Gastric residual volume <150 mL
2: Decreased level of consciousness
3: Age
4: Small diameter feeding tube

A

2: Decreased level of consciousness

Decreased level of consciousness is a major risk factor for aspiration. Other major risk factors include documented previous aspiration, vomiting, tracheal intubation, neuromuscular disease, persistent high gastric residual volumes, and prolonged supine positioning. An association between gastric residual volume amounts and aspiration remains a controversial topic. Age is an additional factor that can increase risk but it is not a major factor in identifying the risk of aspiration. A large diameter feeding tube is also a factor that may increase the risk of aspiration.

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9
Q

Which is considered appropriate management of hypergranulation around the PEG site?

1: Keeping the area dry
2: Using a tube stabilizing device
3: Applying an occlusive dressing
4: Cauterization with silver nitrate

A

4: Cauterization with silver nitrate

Granulation tissue often forms within the tract and may grow out onto the surface of the skin around the PEG tube. Although this does not usually cause excessive exudate and drainage, it is a source of moisture underneath the bolster, which can lead to breakdown of the skin. The hypergranulation tissue may be trimmed with scissors and then treated with silver nitrate sticks or any other cautery device.

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10
Q

Which of the following tube feeding orders best reflects the use of an intermittent schedule?

1: 240 mL administered over 45 minutes, five times per day
2: 50 mL/hr over 24 hours
3: 100 mL/hr over 12 hours
4: 120 mL administered over 15 minutes every other hour

A

1: 240 mL administered over 45 minutes, five times per day

Intermittent feedings are generally an amount of 240-480 mL administered over 45 minutes several times daily with or without feeding pump, whereas continuous feedings are delivered at a prescribed rate without interruption. Cyclic feedings are generally administered over 8-16 hours per day, depending on the patient’s volume tolerance. Bolus feedings are generally an amount of 240-480 mL delivered by gravity or a syringe over 15 minutes into the stomach.

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11
Q

Which of the following patients is at lowest risk of pulmonary injury from small bore feeding tube misplacement?

1: A patient status post stroke on the inpatient medical unit
2: A patient who is alert and cooperative
3: A patient with head and neck trauma admitted to the ICU
4: A patient status post Roux-en-Y gastric bypass

A

2: A patient who is alert and cooperative

The selection of enteral access device depends on the patient’s disease state, anatomy, and expected duration of therapy. An oral or nasoenteric small bore feeding tube is usually indicated when duration of EN therapy is anticipated to be less than 4 weeks. Passage of a feeding tube may be facilitated by concurrent patient swallowing thus decreasing the risk of feeding tube placement into the respiratory system. The procedure is difficult in uncooperative patients, in patients with anatomic abnormalities, and in critically ill patients in which swallowing is inhibited.

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12
Q

A patient with oral cancer, who has gained 10 pounds since starting home bolus enteral feedings via gastrostomy tube complains of pain and pressure on the " inside of his stomach" but no redness or drainage at the exterior gastrostomy site. Which of the following is the most appropriate response for the clinician?

1: Tell the patient to take over the counter pain medication and rotate the G tube 180 degrees each day.
2: Refer the patient to the gastroenterologist or enterostomal nurse.
3: Decrease the infusion volume of the formula in half to avoid excessive distention of the stomach.
4: Change to a slower tube feed infusion by using a gravity bag for feedings.

A

2: Refer the patient to the gastroenterologist or enterostomal nurse

Tube complications can be serious if not managed in a timely manner. Any new occurrence of pain at or near the tube site should be promptly evaluated by the patient’s gastroenterologist or enterostomal nurse. Buried bumper syndrome results from erosion of the internal bolster into the gastric mucosa and/or wall and occurs in 0.3%–2.4% of patients. Excessive traction on the internal bolster slowly pulls it into the gastric wall as the mucosa grows over it. Pain may indicate the presence of infection or pressure necrosis. Weight gain after tube placement places a patient at greater risk for pressure necrosis and ulceration at the tube site due to increase in abdominal girth.

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13
Q

Constipation in the enterally fed patient may be associated with all of the following EXCEPT

1: rapid or bolus infusion.
2: obstruction.
3: lack of adequate hydration.
4: prolonged bed rest.

A

1: rapid or bolus infusion.

Constipation is a gastrointestinal complication associated with enteral nutrition and may be caused by lack of adequate hydration, long-term fiber-free feedings, prolonged bedrest, impaction, obstruction and narcotics.

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14
Q

Which of the following is the most likely cause of watery diarrhea and bloating in the enterally fed adult patient?

1: lactose content of the enteral formula.
2: sorbitol content of liquid medications
3: sorbitol content of the enteral formula
4: lactose content of liquid medications

A

2: sorbitol content of liquid medications

Although lactose intolerance is well known to result in watery diarrhea and bloating, the vast majority of adult enteral products are lactose free and the lactose content of most individual dosage forms of medication is too small to result in significant problems. Sorbitol is not an ingredient of enteral products but the cumulative daily dose of sorbitol from liquid medication can easily equal purgative dosages.

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15
Q

An enterally fed patient reports nausea and vomiting. If delayed gastric emptying is suspected as the causative factor, which of the following is LEAST likely to improve the patient’s symptoms?

1: Reduce or discontinue narcotic medications
2: Switch to a low fat enteral formula
3: Reduce the rate of enteral nutrition infusion
4: Use a more concentrated enteral formula

A

4: Use a more concentrated enteral formula

Although the etiology of nausea and vomiting is multifactorial, delayed gastric emptying is a common source of tube feeding intolerance. Reduction or discontinuation of narcotic meds, use of low fat formulas, administering enteral formula at room temperature and reducing the rate and/or volume of tube feeding infusion may all improve gastric emptying and reduce the symptoms of nausea and vomiting. Concentrated enteral solutions generally contain more fat and can further contribute to enteral intolerance by presenting a higher osmotic load to the GI tract.

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16
Q

The initiation of enteral tube feeding should be delayed when the patient is

1: hemodynamically unstable.
2: at a decreased level of consciousness.
3: without bowel sounds.
4: at risk for refeeding syndrome.

A

1: hemodynamically unstable.

EN initiation should be delayed until the patient is fully volume resuscitated and hemodynamically stable to reduce the risk of intestinal ischemia. Evidence of bowel function, including bowel sounds, is not required prior to the initiation of enteral nutrition. Patients at risk for developing refeeding risk should be identified prior to initiation of nutrition support, but the risk of refeeding should not delay EN initiation. A patient thought to be at refeeding risk should be advanced slowly to goal regimen with frequent monitoring of electrolytes.

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17
Q

When initiating and advancing enteral feedings in the hospitalized patient, which of the following is most appropriate?

1: 1/2 strength formula at 25 mL/hr, advance to goal rate at full strength over 5-7 days
2: 240 mL bolus feedings of full strength hypertonic formulas every 4 hours
3: full strength formula at 10-40 mL/hr and advance to goal rate within 1 -2 days
4: 1/4 strength formula at goal rate. Advance to full strength over 3-5 days

A

3: full strength formula at 10-40 mL/hr and advance to goal rate within 1 -2 days

Currently, it is recommended that feedings in adults and children be initiated with full strength formulas at a slow rate and steadily advanced. This approach allows goal rates to be achieved earlier and reduces the risk for microbial contamination by minimizing the number of times the formulas is manipulated. This regimen has been noted to be well tolerated.

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18
Q

While a patient is receiving speech therapy, oral foods are provided during the daytime hours. To meet the patient’s nutritional requirements, polymeric tube feeding is required during the night at a rate of 75 mL per hour over 10 hours. The night feeding is an example of

1: bolus feeding.
2: intermittent feeding.
3: cyclic feeding.
4: continuous feeding.

A

3: cyclic feeding.

Cyclic feeding provides feedings by pump in less than a 24-hour time period. They are generally administered over 8-20 hours per day, depending on the patient’s tolerance. Cyclic feedings during the night are frequently used as patients are transitioning from enteral feeds to oral intake. Time off of tube feeding during the day often increases appetite.

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19
Q

Which of the following individuals would best benefit from cyclic tube feeding?

1: Status post cerebrovascular accident (CVA) who has initiated oral foods during the day
2: Critically ill motorcycle accident victim in the ICU
3: Critically ill patients with diabetes and hyperglycemia
4: Post-operative bowel surgery patient who has an ileus

A

1: Status post cerebrovascular accident (CVA) who has initiated oral foods during the day

Cyclic feedings are generally administered over 8-20 hours. Nocturnal feeds are frequently used to supplement oral intake and promote unobstructed activity during the day. A patient status post CVA, who is transitioning from tube feeding to an oral diet and will likely begin a rigorous therapy program can benefit from the use of cyclic nocturnal feeding. Critically ill patients are more likely to require continuous feeding, and the post-op individual with an ileus may require parenteral nutrition depending upon the length of time without enteral support.

20
Q

Which type of insulin should be used when initiating enteral nutrition in a hospitalized diabetic patient?

1: Premixed NPH/Regular insulin
2: Regular Insulin
3: NPH Insulin
4: Insulin glargine

A

2: Regular Insulin

When initiating enteral nutrition, use of short-acting insulin (regular insulin) is typically used as tolerance and titration may be unpredictable. This type of insulin may minimize the risk of hypoglycemia resulting from continued absorption of insulin from an intermediate (premixed NPH/regular insulin, NPH insulin) or long-acting (insulin glargine) insulin product in the event that enteral nutrition is interrupted for any reason. Once enteral nutrition administration is stable, use of a basal/bolus insulin regimen is recommended to achieve safe, effective glucose control.

21
Q

An 82 year old woman s/p CVA with dysphagia and subsequent PEG tube placement weighing 45kg is initiated on tube feeds which provide 1500kcal and 63gm protein per liter. The team added a modular protein supplement providing 15gm additional protein per day. She’s discharging to home and will be taken care of by family. During tube feeding education what is important to discuss with the family to prevent tube feeding syndrome?

1: The importance of checking weekly weights
2: The importance of providing goal volume of formula each day
3: The importance of providing adequate free water each day
4: The importance of ensuring adequate bowel movements

A

3: The importance of providing adequate free water each day

Tube feeding syndrome is related to the use of high-protein tube feedings without adequate fluid provision. Inadequate fluid delivery results in an inability to sufficiently excrete the solute load which can lead to the development of azotemia, hypernatremia, and dehydration. Prevention and treatment requires the provisions of adequate fluid (30-40ml/kg/day meets fluid requirements for the average adult). A reduction in protein may be necessary if the ability to excrete byproducts of protein metabolism during adequate fluid provision is compromised.

22
Q

Most enteral formulas designed for oral consumption are composed primarily of

1: carbohydrates.
2: protein.
3: fat.
4: vitamins.

A

1: carbohydrates.

Generally, enteral products designed for oral use contain more sucrose to improve palatability. This translates into a higher carbohydrate to protein and fat ratio. Most enteral products for oral use provide approximately 40% to 60% of total calories from carbohydrate, 15% to 25% from protein, and 15% to 35% from fat. The daily recommended intake (DRIs) for vitamins and minerals may be met by ingesting a portion of oral supplements daily. A blend of soluble and insoluble fibers are also typically found in the oral formulas.

23
Q

Which of the following best describes the addition of blue dye to enteral feedings?

1: It prevents aspiration of enteral formula
2: Its use in detection of aspiration is highly sensitive
3: It should be added only in small amounts
4: It is no longer recommended for the detection of aspiration of enteral formula

A

4: It is no longer recommended for the detection of aspiration of enteral formula

The addition of blue dye to enteral feedings was common practice in the past to help detect aspiration of formula. The use of blue dye in detecting aspiration of formula has a low sensitivity. Several cases of systemic toxicity, some resulting in death, have been reported. As a result the U.S. Food and Drug Administration removed FD&C Blue #1 from the market in 2003. Other blue dyes such as methylene blue and FD&C Blue #2 may have similar or greater toxicity than Blue #1 and are not suitable alternatives.

24
Q

Which enteral feeding method provides 240mL of formula via a syringe over as few as 4-10 minutes, three to six times daily?

1: Intermittent feeding
2: Cyclic feeding
3: Bolus feeding
4: Continuous feeding

A

3: Bolus feeding

Bolus feedings provide a set volume of formula at specified time intervals. Feedings are infused over a short period of time, over as few as 4-10 minutes, 3 to 6 times daily. Intermittent feedings are commonly delivered by enteral pump or gravity drip method over a period of 20-60 minutes, 4 to 6 times daily. Bolus and intermittent feedings may mimic normal meal times, provide additional flexibility, and be administered at home. Continuous feedings deliver formula via a pump-assisted continuous drip infusion. This is the preferred method for critically ill or mechanically ventilated patients. Cyclic feedings are similar to continuous feedings except the formula delivery rate ranges from 8 hours to < 24 hours. This type of feeding may be used to transition a patient from continuous feedings, or to increase the patient’s volitional intake.

25
Q

Which of the following types of feeding delivery methods is most appropriate for patients with a jejunostomy?

1: Bolus
2: Gravity
3: Intermittent
4: Continuous pump

A

4: Continuous pump

Jejunal feeding is usually delivered by a continuous pump to minimize diarrhea, abdominal bloating, and due to limited volume capacity. Gastric feeding can be given by the bolus or intermittent gravity methods. The stomach serves as a reservoir thus delaying the rapid emptying of formula into the small bowel.

26
Q

Which of the following methods of enteral nutrition (EN) delivery is preferred for critically ill patients?

1: Bolus
2: Cyclic
3: Intermittent
4: Continuous infusion

A

4: Continuous infusion

There are several factors related to the favorable use of continuous infusion feeding in critically ill patients. These include accessibility of enteral pumps to control the rate and volume of formula delivered to the patient, better EN tolerance with fewer gastric complaints, and possible lowered risk of aspiration by prevention of gastric distention.

27
Q

Which of the following is a best practice recommendation in enteral nutrition (EN) formula safety?

1: Mix or reconstitute enteral formulations at the bedside
2: Change the enteral feeding administration set every 24 hours with open systems
3: Limit hang time of closed-system EN formulas to no more than 12 hours
4: Store powdered formulas reconstituted in advance at room temperature for up to 24 hours

A

2: Change the enteral feeding administration set every 24 hours with open systems

When possible, enteral formulas should be mixed, reconstituted, or diluted in a sterile centralized location, such as an enteral formulary room or pharmacy, to minimize risk of contamination. The feeding administration set should be changed every 24 hours and disposable feeding administration sets should not be reused. Exceptions include administration sets for human breast milk (change every 4 hours) and closed enteral feeding systems (per manufacturer recommendations). Only an 8 to 12-hour supply of formula should be poured into an open administration set. Hang time of canned, ready-to-use formulas should be no longer than 12 hours. Closed-system EN formulas can be safely used for 24-48 hours after opening, depending on manufacturer’s guidelines. Powdered formulas reconstituted in advance should be refrigerated immediately after preparation and discarded within 24 hours of preparation if not used; they should also be exposed to room temperature for no longer than 4 hours. Use of purified water in formula reconstitution minimizes the potential of tap water as a source of contamination. Adding fresh formula to formula already hanging in the administration set should be avoided. To avoid contamination, hands should be washed thoroughly and gloved before touching any component of the tube feeding system and formula should be transferred without touching the component of the feeding set that comes in contact with the formula

28
Q

Which of the following is a benefit of closed enteral feeding systems?

1: Decreased risk for microbial contamination
2: Maximum hang time of 8-12 hours
3: Packaging amenable to addition of medication or modular
4: Decreased incidence of gastric intolerance

A

1: Decreased risk for microbial contamination

Closed enteral feeding systems are purchased as bags or rigid containers pre-filled with 1 Liter of sterile enteral nutrition formula. Due to the container design, minimal manipulation is required prior to administration and additions or changes to the formula are not easily accomplished, both decreasing the risk of microbial contamination. Closed system enteral feeding systems also have a longer hang time (24-48 hours compared to 8-12 hours for open feeding systems) and require less nursing time for administration.

29
Q

When transitioning from enteral to oral feeding, tube feeding may be discontinued when adequacy of oral intake meets at least

1: 33% of nutrient needs.
2: 50% of nutrient needs.
3: 66% of nutrient needs.
4: 90% of nutrient needs.

A

3: 66% of nutrient needs.

While there are no clinically proven points at which tube feeding should be discontinued with adequacy of oral intake, a general guideline is that oral intake should meet at least two-thirds to three-quarters of nutrient needs.

30
Q

Which of the following should always appear on the label of an enteral feeding product given to a patient in the hospital?

1: Product name, rate, volume, additives, caloric density, date and time the formula was prepared and hung
2: Patient identification, product name, administration method, route, access device, date and time the formula was prepared and hung
3: Patient’s name, product name, rate, strength, osmolality, date and time the formula was prepared and hung
4: Patient’s name, room number, strength, additives, volume, date and time the formula was prepared and hung

A

2: Patient identification, product name, administration method, route, access device, date and time the formula was prepared and hung

The EN formula label should reflect the four elements of the EN order form and therefore contain the following elements: patient identifiers, product name, enteral access delivery site, administration method, and time/date the formula was prepared and hung. The importance of providing this information ensures the patient is receiving the formula ordered and that the infusing formula is not expired or exceeding the recommended hang time.

31
Q

When administering multiple medications via enteral feeding tubes, medications should be

1: administered separately, followed by a 15-30 mL water flush.
2: mixed together in a 30 mL slurry and administered together.
3: delivered in liquid form without water flushes.
4: mixed directly into the feeding formulations for administration.

A

1: administered separately, followed by a 15-30 mL water flush.

Once an enteral feeding tube is placed, conversion of intravenous medications to the enteral route may be undertaken. Many factors dictate whether it is appropriate to administer medications enterally and include: tube size, tube tip location, and site of medication absorption. Each medication should be given separately flushing with at least 15-30 mL of water prior to, between, and after administration. There is a potential for drug-drug interaction if two or more drugs are crushed and/or diluted together. Medications should not be mixed into the feeding formulation or given through the tube without proper flushing in order to avoid tube obstruction and drug-nutrient interactions. Enteric-coated, controlled-release, and sustained release medications should not be crushed and given through feeding tube.

32
Q

Which of the following tubes requires immediate replacement if it becomes dislodged?

1: Jejunostomy tube
2: Nasogastric tube
3: Nasojejunal tube
4: Nasoduodenal tube

A

1: Jejunostomy tube

It should be a priority to replace any feeding tube that becomes dislodged so that the patient can continue to receive nutrition support. However, the jejunostomy tube requires immediate replacement since the tract for the jejunostomy tube can close quickly. Replacement of a jejunostomy tube requires radiographic verification with contrast medium. The first replacement of a gastrostomy or percutaneous endoscopic gastrostomy tube should be performed by the physician who inserted the tube. After that, it is appropriate for trained nurses to replace these tubes. A nasogastric or nasoduodenal tube can be replaced by a physician, physician assistant, nurse practitioner, or appropriately trained healthcare provider.

33
Q

Which formula is most likely to cause an occluded feeding tube?

1: Low fat formula
2: Low fiber formula
3: Peptide based formula
4: Calorically dense formula

A

4: Calorically dense formula

The viscosity of a formula depends on the concentration and characteristics of the macronutrients and fiber. An increase in the accumulation of formula sediment in the inner lumen of the feeding tube is seen more often with a calorically dense or high fiber formula decreasing tube patency.

34
Q

Which intervention assists with maintaining feeding tube patency in the adult patient?

1: Administer medications through feeding tube with 5 mL of water
2: Use a 20mL or smaller syringe to flush small-bore feeding tubes
3: Flush feeding tube with 30 mL of water every 4 hours during continuous feeding
4: Change feeding tube every 72 hours

A

3: Flush feeding tube with 30 mL of water every 4 hours during continuous feeding

Feeding tubes are prone to clogging. Water is the preferred flush solution to maintain tube patency. Tubes should be flushed with 30 mL of water every 4 hours during continuous feeds, before and after intermittent feedings, and after gastric residual volume measurements. Tubes should be flushed with 15 mL before, between, and after medication administration in the adult patient. Increased pressure exerted by a small syringe may cause feeding tube rupture. Short term feeding tubes should be changed every 4-6 weeks.

35
Q

Which of the following is NOT a research-based method used to restore patency to clogged feeding tubes?

1: Water flush
2: Cranberry juice flush
3: Mechanical declogging devices
4: Pancreatic enzyme mixed with sodium bicarbonate

A

2: Cranberry juice flush

Proper tube feeding administration and handling should minimize the incidence of tube clogging. Water was found to be superior to cranberry juice as an irrigant to maintain feeding tube patency in several clinical trials. Pancreatic enzyme with sodium bicarbonate and mechanical declogging device are two research based methods utilized to restore patency to clogged feeding tubes

36
Q

You receive a consult for a patient on EN with abdominal distention, nausea, and vomiting. Monitoring of GRV have been ordered as part of the treatment plan. What intervention can be utilized to prevent feeding tube occlusion associated with GRV assessment in the adult patient?

1: Feeding tube should be flushed with 30mL of water following GRV assessment
2: Place the patient in reverse Trendelenberg position prior to GRV assessment
3: Hold enteral feedings one hour prior to GRV assessment
4: Instill 60 mL of air into the tube prior to GRV assessment

A

1: Feeding tube should be flushed with 30mL of water following GRV assessment

The Society of Critical Care Medicine (SCCM)/ASPEN 2016 guidelines suggest that gastric residual volume (GRV) should not be used as part of routine care to monitor EN. Gastric tubes are reported to clog more frequently than small bowel tubes secondary to intact protein formulas coming in contact with acidic gastric fluid. Flushing feeding tubes with 30 mL of free water following GRV measurement in adult patients is recommended to prevent tube occlusion associated with GRV measurement. The reverse Trendelenberg position is used when elevated backrest is contraindicated to elevate HOB (head of bed). The instilling of air into gastric feeding tubes is useful for increasing negative pressure when drawing GRV from small bore feeding tubes.

37
Q

Which of the following interventions has NOT been proven effective in reducing the risk of aspiration associated with enteral tube feeding in adult patients?

1: Oral care twice a day
2: Motility agents for patients demonstrating intolerance to feeds
3: Post-pyloric tube placement for patients with high risk of aspiration
4: Check of gastric residuals every shift

A

4: Check of gastric residuals every shift

Research indicates that one key to preventing aspiration in all patients (including those fed enterally) is good oral hygiene, such as brushing teeth and rinsing with mouthwash daily. The ASPEN/SCCM guidelines state “We recommend that the level of infusion be diverted lower in the GI tract in those critically ill patients at high risk for aspiration (see section D4) or those who have shown intolerance to gastric EN.” Maintaining the head of bed at 30 - 45 degree elevation is desired to reduce the risk of aspiration.

38
Q

Which of the following is most likely to improve tolerance of enteral feeding in a postoperative patient with documented high gastric residual volume (GRV) receiving bolus tube feedings?

1: Provide intermittent feeding
2: Provide continuous enteral feeding
3: Starting the patient on levofloxacin to aid with motility
4: Putting the patient in a prone position

A

2: Provide continuous enteral feeding

Recovery of gastric emptying may be slower than return of small bowel motility in post-operative patients. Small bowel feeding may increase the amount of feeding delivered in patients with high GRVs. Continuous feeding is the preferred method as bolus and gravity feeding are poorly tolerated in the small bowel. Holding of feedings should be avoided when possible to optimize meeting calorie and protein needs. Prone positioning in a patient with elevated GRVs may increase the risk of aspiration. Prokinetic agents such as metoclopramide and erythromycin are used to increase motility and may be of benefit in this situation. Levofloxacin is an antibiotic and does not help with GI motility.

39
Q

Which of the following is a primary cause of oozing stools in a tube fed patient?

1: Fecal impaction
2: Fluid restriction
3: Physical inactivity
4: Narcotic usage

A

1: Fecal impaction

Impaction can be manifested by symptoms of diarrhea. Passage or secretion of fluid around the impaction may be responsible for the loose stool. The patient may intermittently pass small volumes of liquid stool and experience abdominal distention and cramping. Fluid restriction, physical inactivity and narcotic usage lead to constipation.

40
Q

A home enteral nutrition patient recently treated for pneumonia is noted to have new onset diarrhea. Of the following, the first intervention should be to

1: change to an elemental feeding.
2: obtain an order for a bile-sequestering agent.
3: obtain a Clostridium difficile toxin stool assay.
4: obtain an order for an antidiarrheal medication.

A

3: obtain a Clostridium difficile toxin stool assay.

There are many causes of diarrhea in the tube-fed patient including the patient’s underlying medical condition, tube-feeding intolerance, medication effects, and infectious causes including bacterial contamination of enteral tube feeding formula or equipment and Clostridium difficile. Clostridium difficile should be ruled out in any patient recently receiving antibiotic therapy. This should be done prior to ordering antidiarrheal medication since antidiarrheal medications are not indicated in those with Clostridium difficile. There is no need to change to an elemental formula if there are no other indications for an elemental diet.

41
Q

A patient with short bowel and an end-jejunostomy requires the use of an oral rehydration solution (ORS) to help prevent dehydration. Which best describes the preferred composition of the ORS?

1: An iso-osmolar solution such as juice diluted with 50% water
2: A hyper-osmolar solution such as fruit juice or Kool-aid
3: A hypo-osmolar solution such as water
4: A hyper-osmolar solution such as commercially available sports drink

A

1: An iso-osmolar solution such as juice diluted with 50% water

Use of oral rehydration solutions (ORS) may help to prevent dehydration in patients with short bowel syndrome (SBS) and an End-jejunostomy. Glucose is an important component in ORS as it promotes salt and water absorption. The optimal sodium concentration of ORS to promote jejunal absorption is in the range of 90-120 mEq/L. Hyper- or hypo-tonic solutions are not well absorbed and may increase osmotic diarrhea in patients with SBS. Commercial sports drinks are considerably lower in sodium and higher in carbohydrate content than ORS.

42
Q

What is the optimal sodium concentration of an oral rehydration solution for patients with short bowel syndrome?

1: 54 - 80 mmol/L
2: 90 - 120 mmol/L
3: 134 - 160 mmol/L
4: 170 - 190 mmol/L

A

2: 90 - 120 mmol/L

The ideal sodium concentration for oral rehydration solutions depends on the segment of bowel function lost, e.g. jejunum, ileum, colon. The sodium concentration of homemade or commercial oral rehydration solutions ranges from 90 - 120 mmol/L. This amount of sodium promotes jejunal absorption

43
Q

In critically ill patients receiving early enteral nutrition (EN), which is most likely to increase success in achieving goal feeding rate?

1: Use of small bowel feeding
2: Use of a standard EN feeding protocol
3: Use of gastric feeding
4: Use of a volume-based EN feeding protocol

A

4: Use of a volume-based EN feeding protocol

Volume-based EN feeding protocols prescribe EN in terms of the goal per day vs. goal per hour. The use of such protocols, including FEED ME (FeedEarly Enteral Diet Adequately for Maximum Effect? And PEP uP (Enhanced Protein-Energy Provision via the Enteral Route Feeding Protocol) have been found to significantly improve delivery of nutrients. Standard EN protocols begin EN full strength at an hourly rate and advance to goal within 24 to 48 hours. Effective use of a nutrition support protocol requires support from all medical disciplines involved.

44
Q

What is the maximum hang time for human breast milk (HBM)?

1: 4 hours
2: 8 hours
3: 12 hours
4: 24 hours

A

1: 4 hours

Human breast milk (HBM) should have a hang time of no longer than 4 hours. In addition, administration sets used for HBM should be di(2-ethylhexyl) phthalate (DEHP) free and the tubing and syringe should be changed every 4 hours. HBM for hospitalized neonates, infants, and children should be prepared in a clean environment using aseptic technique by specially trained personnel. Current recommendations also support the use of gloves during HBM administration.

45
Q

Your patient is showing outward signs of tube feeding intolerance including nausea and abdominal distention. The nurse checks gastric residuals and the last three measurements are 265 mL, 250 mL, and 330 mL. What is the most appropriate recommendation?

1: Consider adding a promotility agent
2: Change to a lower fat formula
3: Change to a more concentrated formula
4: Use a smaller bore feeding tube

A

1: Consider adding a promotility agent

The significance of GRV is controversial due to the lack of well-powered studies. Because of this, the relationship of GRV and aspiration PNA can’t be clarified. The measurement of GRV can be affected by the type of feeding tube, body position, and the location of the tip of the feeding tube. Checking gastric residuals as part of routine care in ICU patients is not recommended. If a patient is showing outward signs of intolerance gastric residuals can be measured. Gastric residual volumes between 250-500 mL should lead to implementation of measures to reduce the risk of aspiration including adding a promotility agent.