Guidelines for Nasogastric Tube Insertion
Guidelines for Nasogastric Tube Insertion
DEFINITION
PURPOSES
ASSESSMENT
PLANNING
EQUIPMENT
IMPLEMENTATION
3. Prior to performing the insertion, introduce Identifying the patient ensures the right patient
yourself and verify the client’s identity using receives the intervention and helps prevent errors.
two patient's identifiers,(i.g., name and date
of birth.) Explain to the client what you are Explanation facilitates patient cooperation
going to do, why it is necessary, and how
he or she can participate. The passage of a
gastric tube is unpleasant because the gag
reflex is activated during insertion. Establish
a method for the client to indicate distress
and a desire for you to pause the insertion.
Raising a finger or a hand is often used for
this.
4. Perform hand hygiene and observe other Hand hygiene and PPE prevent the spread of
appropriate infection control procedures microorganisms
5. Provide for client privacy Closing the door or pulling the curtain is the client's
right to privacy
● If a large bore- tube (e.g Salem sump tube) ● This allows the tubing to become more
is being used, place the tube in a basin of pliable and flexible. However, if the
warm water, while preparing the client softened tube becomes difficult to control, it
may be helpful to place the distal end in a
basin of ice water to help it hold its shape.
● Insert the tube, with its natural curve toward ● Hyperextension of the neck reduces the
client, into the selected nostril. Ask the curvature of the nasopharyngeal junction.
client to hyperextend the neck, and gently
advance the tube toward the nasopharynx
● Direct the tube along the floor of the nostril ● Directing the tube along the floor avoids the
and toward the ear on that side projections (turbinate) along the lateral wall.
● Almost all nasogastric tubes are ● The stylet is sharp and could pierce the
radiopaque, and position can be confirmed tube and injure the client or cut off the tube
by x-ray. Check agency policy. If a small- end.
bore tube is used, leave the stylet or
guidewire in place until the correct position
is verified by x-ray. If the stylet has been
removed, never reinsert it while the tube is
in place
● Place a stethoscope over a client’s
epigastrium and inject 10-30 ml of air into ● This method does not guarantee tube
the tube while listening for a whooshing position
sound. Although still one of the methods
used, do not use this method as the primary
method for determining placement of the
feeding tube.
● If the signs indicate placement in the lung,
remove the tube and begin again
● If the signs do not indicate placement in the
lungs or stomach, advance the tube
5cm(2in), and repeat the tests
EVALUATION
DEFINITION
PURPOSES
ASSESSMENT
PLANNING
EQUIPMENT
IMPLEMENTATION
1. Perform hand hygiene and put on PPE, if Hand hygiene and PPE prevent the spread of
indicated. microorganisms. PPE is required based on
transmission precautions.
2. Identify the patient by using two identifiers Identifying the patient ensures the right patient
(patient full name and date of birth) and receives the intervention and helps prevent errors.
greet him/her by name
3. Explain the procedure to the patient and Explanation facilitates patient cooperation.
why this intervention is needed. Answer
any questions as needed.
4. Close the patient’s bedside curtain or Closing curtains or door provides for patient privacy.
door. Raise the bed to a comfortable Having the bed at the proper height prevents back
working position, usually elbow height of and muscle strain. Due to changes in the patient’s
the caregiver. Perform key abdominal condition, assessment is vital before initiating the
assessments as described above. intervention.
5. Gather equipment. Check amount, This provides for an organized approach to the task.
concentration, type, and frequency of tube Checking ensures that correct feeding will be
feeding in the patient’s medical record. administered. Outdated formulas may be
Check formula expiration date. contaminated.
7. Position the patient with head of bed This position minimizes possibility of aspiration into
(HOB) elevated at least 30 to 45 degrees the trachea. Patients who are considered at high risk
or as near normal position for eating as for aspiration should be assisted to at least a 45-
possible. degree position.
8. Put on gloves. Unpin the tube from the Gloves prevent contact with blood and body fluids.
patient’s gown. Verify the position of the The tube should be marked with an indelible marker
marking on the tube at the nostril. at the nostril. This marking should be assessed each
Measure length of exposed tube and time the tube is used to ensure the tube has not
compare with the documented length. become displaced. Tube length should be checked
and compared with this initial measurement, in
conjunction with pH measurement and visual
assessment of aspirate. An increase in the length of
the exposed tube may indicate dislodgement.
9. Attach a syringe to the end of the tube and The tube is in the stomach if its contents can be
aspirate a small amount of stomach aspirated: pH of aspirate can then be tested to
contents. determine gastric placement. If unable to obtain a
specimen, reposition the patient and flush the tube
with 30 mL of air. This action may be necessary
several times. Current literature recommends that
the nurse ensures proper placement of the NG tube
by relying on multiple methods and not on one
method alone.
11. Visualize aspirated contents, checking for Gastric fluid can be green, with particles, off-white,
color and consistency. or brown if old blood is present. Intestinal aspirate
tends to look clear or straw-colored to a deep golden
yellow color. Also, intestinal aspirate may be
greenish-brown if stained with bile. Respiratory or
tracheobronchial fluid is usually off-white to tan and
may be tinged with mucus. A small amount of blood-
tinged fluid may be seen immediately after NG
insertion.
12. If it is not possible to aspirate contents; The x-ray is considered the most reliable method for
assessments to check placement are identifying the position of the NG tube.
inconclusive; the exposed tube length has
changed; or there are any other
indications that the tube is not in place,
check placement by x-ray.
13. After multiple steps have been taken to Checking for residual before each feeding or every 4
ensure that the feeding tube is located in to 6 hours during a continuous feeding according to
the stomach or small intestine, aspirate all institutional policy is implemented to identify delayed
gastric contents with the syringe and gastric emptying. High gastric residual volumes
measure to check for gastric residual—the (200 to 250 mL or greater) can be associated with
amount of feeding remaining in the high risk for aspiration and aspiration-related
stomach. Return the residual based on pneumonia. Some experts now recommend that the
facility policy. Proceed with feeding if patient’s pattern of residual is more important than
amount of residual does not exceed the amount. Feedings should be held if residual
agency policy or the limit indicated in the volumes exceed 200 mL on two successive
medical record. assessments (ASPEN). Research findings are
inconclusive on the benefit of returning gastric
volumes to the stomach or intestine to avoid fluid or
electrolyte imbalance, which has been accepted
practice. Consult facility policy concerning this
practice
14. Flush tube with 30 mL of water for Flushing tube prevents occlusion. Capping the tube
irrigation. Disconnect syringe from tubing deters the entry of microorganisms and prevents
and cap end of tubing while preparing the leakage onto the bed linens.
formula feeding equipment. Remove
gloves.
15. Put on gloves before preparing, Gloves prevent contact with blood and body fluids
assembling, and handling any part of the and deter transmission of contaminants to feeding
feeding system. equipment and/or formula.
16.1.2 Check the expiration date of the Cleansing container top with alcohol minimizes risk
formula. Cleanse the top of the feeding for contaminants entering the feeding bag. Formula
container with a disinfectant before displaces air in tubing.
opening it. Pour formula into the feeding
bag and allow the solution to run through
tubing. Close clamp.
16.1.3 Attach feeding setup to feeding Introducing formula at a slow, regular rate allows the
tube, open clamp, and regulate drip stomach to accommodate the feeding and
according to the medical order, or allow decreases GI distress.
feeding to run in over 30 minutes.
16.1.4 Add 30 to 60 mL (1 to 2 oz.) of Water rinses the feeding from the tube and helps to
water for irrigation to feeding bag when keep it patent
feeding is almost completed and allow it to
run through the tube.
16.1.5 Clamp tubing immediately after Clamping the tube prevents air from entering the
water has been instilled. Disconnect stomach. Capping the tube deters entry of
feeding setup from feeding tube. Clamp microorganisms and covering end of tube protects
tube and cover end with cap. patient and linens from fluid leakage from tube.
16.2.2 Attach syringe to feeding tube, The higher the syringe is held, the faster the formula
pour pre measured amount of tube flows.
feeding formula into syringe, open clamp,
and allow food to enter tube. Regulate
rate, fast or slow, by height of the syringe.
Do not push formula with a syringe
plunger.
16.2.3 Add 30 to 60 mL (1 to 2 oz.) of Water rinses the feeding from the tube and helps to
water for irrigation to the syringe when keep it patent.
feeding is almost completed, and allow it
to run through the tube.
16.2.4 When the syringe has emptied, By holding syringe high, the formula will not
hold the syringe high and disconnect it backflow out of tube and onto patient. Clamping the
from the tube. Clamp tube and cover end tube prevents air from entering the stomach.
with cap. Capping end of tube deters entry of microorganisms.
Covering the end protects the patient and linens
from fluid leakage from the tube.
16.3 When Using an Enteral Feeding Closing clamp prevents formula from moving
Pump: through tubing until nurse is ready. Labeling date
16.3.1 Close flow-regulator clamp on and time of first use allows for disposal within 24
tubing and fill feeding bag with prescribed hours, to deter growth of microorganisms.
formula. Amount used depends on agency
policy. Place a label on the container with
the patient's name, date, and time the
feeding was hung.
16.3.2 Hang feeding container on IV pole. This prevents air from being forced into the stomach
Allow the solution to flow through tubing. or intestines.
16.3.3 Connect to the feeding pump Feeding pumps vary. Some of the newer pumps
following manufacturer’s directions. Set have built-in safeguards that protect the patient from
rate. Maintain the patient in the upright complications. Safety features include cassettes that
position throughout the feeding. If the prevent free-flow of formula, automatic tube flush,
patient needs to lie flat temporarily, pause safety tips that prevent accidental attachment to an
the feeding. Resume the feeding after the IV setup, and various audible and visible alarms.
patient’s position has been changed back Feedings are started at full strength rather than
to at least 30 to 45 degrees. diluted, which was recommended previously. A
smaller volume, 10 to 40 mL, of feeding infused per
hour and gradually increased has been shown to be
more easily tolerated by patients.
17. Observe the patient’s response during and Pain or nausea may indicate stomach distention,
after tube feeding and assess the which may lead to vomiting. Physical signs, such as
abdomen at least once a shift. abdominal distention and firmness or regurgitation of
tube feeding, may indicate intolerance.
18. Have the patient remain in an upright This position minimizes risk for backflow and
position for at least 1 hour after feeding. discourages aspiration, if any reflux or vomiting
should occur.
19. Remove equipment and return the patient Promotes patient comfort and safety. Removing
to a position of comfort. Remove gloves. gloves properly reduces the risk for infection
Raise the side rail and lower bed. transmission and contamination of other items.
20. Put on gloves. Wash and clean equipment This prevents contamination and deters spread of
or replace according to agency policy. microorganisms. Reusable systems are cleansed
Remove gloves. with soap and water with each use and replaced
every 24 hours.
21. Remove additional PPE, if used. Perform Removing PPE properly reduces the risk for
hand hygiene infection transmission and contamination of other
items. Hand hygiene prevents transmission of
microorganisms.
EVALUATION
DEFINITION
PURPOSES
ASSESSMENT
PLANNING
EQUIPMENT
IMPLEMENTATION
1. Perform hand hygiene and put on PPE, if Hand hygiene and PPE prevent the spread of
indicated. microorganisms. PPE is required based on
transmission precautions.
2. Identify the patient using two identifiers. Identifying the patient ensures the right patient
receives the intervention and helps prevent errors.
3. Explain the procedure to the patient and Explanation facilitates patient cooperation.
why this intervention is needed. Answer any
questions, as needed.
4. Pull the patient’s bedside curtain. Raise bed Provide for privacy. Appropriate working height
to a comfortable working position, usually facilitates comfort and proper body mechanics for
elbow height of the caregiver. Assist the nurse. This position minimizes risk for
patient to 30- to 45-degree position, unless aspiration. Preparing the irrigation provides for an
this is contraindicated. Pour the irrigating organized approach to the task.
solution into the container.
5. Gather equipment. Verify the medical order Assembling equipment provides for an organized
or facility policy and procedure regarding approach to the task. Verification ensures the
frequency of irrigation, solution type, and patient receives the correct intervention. Facility
amount of irrigant. Check expiration dates policy dictates safe intervals for reuse of
on irrigating solutions and irrigation sets. equipment.
7. Put on gloves. Place a waterproof pad on Gloves prevent contact with body fluids.
the patient’s chest, under the nasogastric Waterproof pad protects the patient's clothing and
tube and suction tubing. bed linens from accidental leakage of gastric fluid.
8. Check placement of the NG tube. Checking placement before the instillation of fluid is
Auscultation of air insufflated through the necessary to prevent accidental instillation into the
feeding tube ('whoosh' test). respiratory tract if the tube has become dislodged.
8.1 Attach a syringe to the end of the tube The tube is in the stomach if its contents can be
and aspirate a small amount of stomach aspirated: pH of aspirate can then be tested to
contents. determine gastric placement. If unable to obtain a
specimen, reposition the patient and flush the tube
with 30 mL of air. This action may be necessary
several times. Current literature recommends that
the nurse ensures proper placement of the NG
tube by relying on multiple methods and not on one
method alone.
8.3 Visualize aspirated contents, checking Gastric fluid can be green, with particles, off-white,
for color and consistency. or brown if old blood is present. Intestinal aspirate
tends to look clear or straw-colored to a deep
golden yellow color. Also, intestinal aspirate may
be greenish-brown if stained with bile. Respiratory
or tracheobronchial fluid is usually off-white to tan
and may be tinged with mucus. A small amount of
blood-tinged fluid may be seen immediately after
NG insertion.
8.4 If it is not possible to aspirate contents; The x-ray is considered the most reliable method
assessments to check placement are for identifying the position of the NG tube.
inconclusive; the exposed tube length has
changed; or there are any other indications
that the tube is not in place, check
placement by x-ray.
10. Place the tip of the syringe in the tube. Hold Gentle insertion of saline solution (or gravity
the syringe upright and gently insert the insertion) is less traumatic to gastric mucosa.
irrigant (or allow solution to flow in by
gravity if facility policy or medical order
indicates). Do not force the solution into the
tube.
11. If unable to irrigate the tube, reposition the Tube may be positioned against gastric mucosa,
patient and attempt irrigation again. Inject making it difficult to irrigate. Injection of air may
10 to 20 mL of air and aspirate again. If reposition the end of the tube.
repeated attempts to irrigate a tube fail,
consult with a physician.
12. After the irrigant has been installed, hold Return flow may be collected in an irrigating tray or
the end of NGT over the irrigation tray or other available container and measured. This
emesis basin. Observe the return flow of amount will need to be subtracted from the irrigant
NG drainage into available containers. to record the true NG drainage. A second method
involves subtracting the total irrigant from the shift
from the total NG drainage emptied over the entire
shift, to find the true NG drainage. Check agency
policy for guidelines.
13. Remove gloves. Lower the bed and raise Lowering the bed and assisting the patient to a
side rails, as necessary. Assist the comfortable position promotes safety and comfort.
patient to a position of comfort. Perform
hand hygiene.
14. Put on gloves. Measure returned solution, if Gloves prevent contact with blood and body fluids.
collected outside of suction apparatus. Irrigant placed in the tube is considered intake;
Rinse equipment if it will be reused. Label solution returned is recorded as output. Record on
with the date, patient’s name, room number, the intake and output record. Rinsing promotes
and purpose (for NGT/ irrigation). cleanliness, infection control, and prepares
equipment for next irrigation.
15. Remove gloves and additional PPE, if Removing PPE properly reduces the risk for
used. Perform hand hygiene. infection transmission and contamination of other
items. Hand hygiene prevents transmission of
microorganisms.
EVALUATION
BLOOD TRANSFUSION
DEFINITION
ASSESSMENT
PLANNING
EQUIPMENT
IMPLEMENTATION
1. Verify the medical order for transfusion of a Verification of order ensures the right patient
blood product. Verify the completion of informed receives the correct intervention.
consent documentation in the medical record. Premedication is sometimes administered to
Verify any medical order for pretransfusion decrease the risk for allergic and febrile
medication. If ordered, administer medication at reactions for patients who have received
least 30 minutes before initiating transfusion. multiple previous transfusions.
3. Perform hand hygiene and put on PPE, if Hand hygiene and PPE prevent the spread of
indicated. microorganisms. PPE is required based on
transmission precautions.
4. Verify patient using 2 identifiers —such as a Identifying the patient ensures the right patient
patient's full name, date of birth and/or medical receives the intervention and helps prevent
identification (ID) number—be used for every errors.
patient encounter.
5. Close the curtains around the bed and close the This ensures the patient’s privacy. Explanation
door to the room, if possible. Explain what you relieves anxiety and facilitates cooperation.
are going to do and why you are going to do it to Previous reactions may increase the risk for
the patient. Ask the patient about previous reaction to this transfusion. Any reaction to the
experience with a transfusion and any reactions. transfusion necessitates stopping the
Advise the patient to report any chills, itching, transfusion immediately and evaluating the
rash, or unusual symptoms. situation.
6. Prime blood administration set with the normal Normal saline is the solution of choice for
saline IV fluid. blood product administration. Solutions with
dextrose may lead to clumping of red blood
cells and hemolysis.
7. Put on gloves. If a patient does not have a Gloves prevent contact with blood and body
venous access in place, initiate peripheral fluids. Infusion of fluid via venous access
venous access. Connect the administration set maintains patency until the blood product is
to the venous access device via the extension administered. Start an IV before obtaining the
tubing. Infuse the normal saline per facility blood product in case the initiation takes
policy. longer than 30 minutes. Blood must be stored
at a carefully controlled temperature (4°C) and
transfusion must begin within 30 minutes of
release from the blood bank.
8. Obtain blood product from blood bank according Bar codes on blood products are currently
to agency policy. Scan for bar codes on blood being implemented in some agencies to
products if required. identify, track, and assign data to transfusions
as an additional safety measure.
9. Two nurses compare and validate the following Most states/agencies require two registered
information with the medical record, patient nurses to verify the following information: unit
identification band, and the label of the blood numbers match; ABO group and Rh type are
product: the same; expiration date (after 35 days, red
blood cells begin to deteriorate). Blood is
9.1 Medical order for transfusion of blood never administered to a patient without an
product identification band. If clots or signs of
contamination (clumping, gas bubbles) are
9.2 Informed consent present, return blood to the blood bank.
9.3 Patient identification numberImage result
for blood bag label
10. Obtain baseline set of vital signs before Any change in vital signs during the
beginning the transfusion. transfusion may indicate a reaction.
11. Put on gloves. If using an electronic infusion Gloves prevent contact with blood and body
device, put the device on “hold.” Close the roller fluids. Stopping the infusion prevents blood
clamp closest to the drip chamber on the saline from infusing to the patient before completion
side of the administration set. Close the roller of preparations. Closing the clamp to saline
clamp on the administration set below the allows blood product to be infused via
infusion device. Alternately, if infusing via electronic infusion device.
gravity, close the roller clamp on the
administration set.
12. Close the roller clamp closest to the drip Filling the drip chamber prevents air from
chamber on the blood product side of the entering the administration set. The filter in the
administration set. Remove the protective cap blood administration set removes particulate
from the access port on the blood container. material formed during storage of blood. If the
Remove the cap from the access spike on the administration set becomes contaminated, the
administration set. Using a pushing and twisting entire set would have to be discarded and
motion, insert the spike into the access port on replaced.
the blood container, taking care not to
contaminate the spike. Hang the blood container
on the IV pole. Open the roller clamp on the
blood side of the administration set. Squeeze
drip chamber until the in-line filter is saturated.
Remove gloves.
14. Observe the patient for flushing, dyspnea, These signs and symptoms may be an early
itching, hives or rash, or any unusual comments. indication of a transfusion reaction.
15. After the observation period (5 to 15 minutes) If no adverse effects occurred during this time,
increase the infusion rate to the calculated rate the infusion rate is increased. If complications
to complete the infusion within the prescribed occur, they can be observed and the
time frame, no more than 4 hours. transfusion can be stopped immediately.
Verifying the rate and device settings ensures
the patient receives the correct volume of
solution. Transfusion must be completed
within 4 hours due to potential for bacterial
growth in blood product at room temperature.
16. Reassess vital signs after 15 minutes. Obtain Vital signs must be assessed as part of
vital signs thereafter according to facility policy monitoring for possible adverse reaction.
and nursing assessment. Facility policy and nursing judgment will
dictate frequency.
17. Maintain the prescribed flow rate as ordered or Rate must be carefully controlled, and the
as deemed appropriate based on the patient’s patient’s reaction must be monitored
overall condition, keeping in mind the outer frequently.
limits for safe administration. Ongoing
monitoring is crucial throughout the entire
duration of the blood transfusion for early
identification of any adverse reactions.
18. During transfusion, assess frequently for If a transfusion reaction is suspected, the
transfusion reaction. Stop blood transfusion if blood must be stopped. Do not infuse the
you suspect a reaction. Quickly replace the normal saline through the blood tubing
blood tubing with a new administration set because you would be allowing more of the
primed with normal saline for IV infusion. Initiate blood into the patient’s body, which could
an infusion of normal saline for IV at an open complicate a reaction. Besides a serious life-
rate, usually 40 mL/hour. Obtain vital signs. threatening blood transfusion reaction, the
Notify primary care providers and blood banks. potential for fluid–volume overload exists in
older patients and patients with decreased
cardiac function.
19. When transfusion is complete, close the roller Saline prevents hemolysis of red blood cells
clamp on the blood side of the administration set and clears the remainder of blood in the IV
and open the roller clamp on the normal saline line.
side of the administration set. Initiate infusion of
normal saline. When all of the blood has infused Proper disposal of equipment reduces
into the patient, clamp the administration set. transmission of microorganisms and potential
Obtain vital signs. Put on gloves. Cap access contact with blood and body fluids.
site or resume previous IV infusion. Dispose of
blood- transfusion equipment or return to blood
bank, according to facility policy.
20. Remove equipment. Ensure patient’s comfort. Promotes patient comfort and safety.
Remove gloves. Lower bed, if not in lowest Removing gloves properly reduces the risk for
position. infection transmission and contamination of
other items.
21. Remove additional PPE, if used. Perform Removing PPE properly reduces the risk for
hand hygiene. infection transmission and contamination of
other items. Hand hygiene prevents
transmission of microorganisms.
22. Monitor and assess the patient for one hour Ensures early detection and prompt
after the transfusion for signs and symptoms of intervention. Delayed transfusion reactions
delayed transfusion reaction. Provide patient can occur one to several days after
education about signs and symptoms of delayed transfusion.
transfusion reactions.
EVALUATION
2. Platelets
● Used to treat thrombocytopenia and platelet dysfunctions.
● Infusion time: 15 to 30 minutes
● Crossmatching is not required.
● An increase of 5000-10,000 cells/mm3 is expected for each unit of platelets
administered after 18-24 hours transfusion
3. Fresh Frozen Plasma
● Used to treat thrombocytopenia and platelet dysfunctions.
● Infusion time: 15 to 30 minutes
● Crossmatching is not required.
● An increase of 5000-10,000 cells/mm3 is expected for each unit of platelets
administered after 18-24 hours transfusion
4. Cryoprecipitate
● Prepared from fresh-frozen plasma.
● Can be stored for 1 year.
● Once thawed, the product must be used.
● Infusion time: 15-30 minutes
● Used to replace factor VII and fibrinogen
5. Granulocytes
● Used to treat a client with sepsis or a neutropenic client with an infection that
is unresponsive to antibiotics.
● Assessed by monitoring the white blood cell and differential counts.
Compatibility
● To determine compatibility, crossmatching is done.
● The universal RBC donor is O(-); the universal recipient is AB(+).
● Client with Rh(+) blood can receive Rh(-) donor if necessary
● RH(-) should not receive Rh(+)
● Type A: can receive from type A or O
● Type B: can receive from type B or OT
● Type AB: can receive from type A, B, AB or O
● Type O: only from type O
Complications
1. Transfusion reactions
An adverse reaction that happens as a result of receiving a blood transfusion.
TYPES:
● Hemolytic
● Allergic,
● Febrile,
● Bacterial
2. Circulatory overload
3. Septicemia
4. Iron Overload
5. Disease Transmission
6. Hypocalcemia
7. Hyperkalemia
8. Citrate toxicity
PLANNING:
ASSESSMENT:
CRITERIA RATIONALE
[Link] your hands. Wear gloves and follow standard Washing your hands and taking standard
precautions if contact with blood or body fluids cannot precautions prevent the spread of infections.
be avoided. (Carter, 2012)
2. Identify the person using two identifiers (age and Identifying the person ensures that the procedure is
date of birth), and greet him or her by name. being done on the correct patient or resident.
Greeting the person by name is being courteous.
(Carter, 2012)
3. Explain the procedure and encourage the person Helps the person know what to expect and helps him
to participate as appropriate. understand how he can help. (Carter, 2012)
4. Provide privacy by showing any visitor where they Asking visitors to leave the room, and closing the
should wait, if necessary, until you have completed door and curtain protect the person’s right to privacy.
the procedure. Close the door and the curtain. (Carter, 2012)
6. Place the side rail on the opposite side of the bed. Successful catheter insertion requires a nurse to
assume a comfortable position with all equipment
easily accessible. (Perry, 2013)
9. Drape patient. Drape the upper trunk with a bath This promotes client’s safety. (Perry, 2013)
blanket and cover lower extremities with bed sheets
exposing only genitalia.
10. When inserting an indwelling catheter, open the Prevents soiling of bed linen. (Perry, 2013)
package containing the drainage system. Place the
drainage bag over the edge of the bottom bed frame.
Bring drainage tube up between side rail and
mattress.
11. Open catheterization kit according to directions, This position relaxes abdominal and perineal
using aseptic technique. Place the waste receptacle muscles. (Smith, 2011)
in an accessible place.
12. Don sterile gloves. This avoids unnecessary exposure of body parts
and maintains client’s comfort. (Perry, 2013)
14. Nurses may want to ensure that an inflatable Placement of equipment near the work site
balloon of indwelling catheter is intact by inserting increases efficiency. Sterile technique protects the
syringe tip through valve of intake lumen and injecting patient and prevents the spread of microorganisms.
sterile fluid until balloon inflates. Then aspirate all fluid (Taylor, 2014)
out of the inflated lumen.
15. Apply sterile drape. Apply drape over thighs just This allows nurses to handle sterile supplies without
below penis. Pick up fenestrated sterile drape, allow contamination. (Perry, 2013)
it to unfold, and drape it over penis with a fenestrated
slit resting over penis.
[Link] that the catheter tip is properly It is necessary to open all supplies and prepare for
lubricated. Male 12.5-17.5 cm (5-7 inches). the procedure while both hands are sterile. (Taylor,
2014)
19. Pickup catheter with gloved dominant hand 7.5- This checks the integrity of the balloon. Do not use
10 cm (3-4 inches) from catheter tip. Hold end of the catheter if the balloon does not inflate or leaks.
catheter loosely coiled in palm of dominant hand. Checking the balloon in this way may stretch the
Place distal end of catheter in urine tray specimen. balloon and cause increased trauma on insertion.
(Perry, 2013)
20.2 Ask the patient to bear down as if to void and This provides easy access to supplies during
slowly insert a catheter through the meatus. catheter insertion. (Perry, 2013)
20.3 Advance catheter 17.5-22.5 cm (7-9 inches) in This eases insertion of the catheter through the
adults and 5- 7.5 cm (2-3 inches) in young children urethral canal. (Perry, 2013)
or until urine flows out of the catheter's end. If
resistance is felt, withdraw the catheter and do not
force it through urethra. When urine appears,
advance the catheter another 5 cm (2 inches).
20.4 Lower penis and hold catheter securely in The hand touching the penis becomes
nondominant hand. Place the end of the catheter in contaminated. Cleansing the area around the
the urine tray receptacle. meatus and under the foreskin in the uncircumcised
male patient helps prevent infection. (Taylor, 2014)
21.1 With a nondominant hand, carefully retract the Moving from the meatus toward the base of the
labia to fully expose urethra meatus. Maintain position penis prevents bringing organisms to meatus.
of nondominant hand throughout the procedure (Taylor, 2014)
22. Pick up catheter with gloved dominant hand 7.5- Hold catheter near tip because it allows
10 cm (3-4 inches) from catheter tip. Hold the end of easier manipulation during insertion into
the catheter loosely coiled in the palm of the dominant urethral meatus and prevents distal end
hand. Place distal end of catheter in urine tray from striking contaminated surface.
specimen.
23. Insert catheter This movement straightens the urethra for easier
23.1 Ask patient to bear down as if to void and slowly insertion of catheter. (Smith, 2011) Bearing down
insert catheter through meatus. eases the passage of the catheter through the
urethra. (Taylor, 2014)
Deep breaths or slight twisting of the catheter bay
23.2 Advance catheter 5-7.5 cm (2-3 inches) in adults ease the catheter past resistance at sphincters.
and 2.5 cm (1 inch) in young child or until urine flows Advancing an indwelling catheter facilitates inflation
out of the catheter's end. When urine appears, of the balloon without damaging the urethra. (Taylor,
advance the catheter up to another 5cm (2 inches). 2014)
Do not force against resistance.
23.3 Release labia and hold the catheter securely This allows sterile specimen to be obtained for
with a nondominant hand. culture analysis. (Perry, 2013)
24. Collect urine specimen as needed: fill specimen This allows sterile specimen to be obtained for
cup to desired level (20-30 mL) by holding the end of culture analysis. (Perry, 2013)
catheter with the dominant hand over the cup. With
dominant hand, pinch catheter to stop urine flow
temporarily. Release catheter to allow remaining
urine in bladder to drain in the collection tray. Cover
the specimen cup and set aside for labeling.
25. Allow bladder to empty full (750-1000 mL) unless Retained urine may serve as reservoir for growth of
institution policy restricts maximal volume of urine to microorganisms. (Perry, 2013)
drain with each catheterization.
25.1 For straight, single use catheter, pinch catheter This causes less discomfort to the patient. (Taylor,
and remove slowly but smoothly when urine ceases 2014)
to flow.
25.2 For indwelling catheter, inflate balloon of the The balloon anchors the catheter in place in the
indwelling catheter. bladder. Sterile water is used to inflate the balloon
as a precaution in case the balloon ruptures. (Taylor,
2014)
25.3 While holding catheter with your thumb and little
finger of the nondominant hand at meatus, take end
of catheter and place it between first two fingers of
nondominant hand.
25.4 With free dominant hand, attach syringe to
injection port at the end of catheter.
25.5 Slowly inject total amount of solution. If client
complains of sudden pain, aspirate back solution and
advance catheter further.
25.6 After inflating the balloon fully, release catheter Improper inflation can cause patient’s discomfort
with the nondominant hand and pull it gently if there and malpositioning of catheter. (Taylor, 2014)
is resistance.
26. Attach end of catheter to the collecting tube of To facilitate drainage of urine by gravity. Raising bag
drainage system. Drainage bag must be below level on side rail will cause backflow of urine into bladder.
of bladder. (Perry, 2013)
27. Tape catheter tubing on top of thigh or lower Closed drainage system minimizes the risk of
abdomen. Allow slack in catheter so movement does organisms being introduced into the bladder.
not create tension on catheter. (Taylor, 2014)
28. Be sure that there are no obstructions or kinks in Anchoring catheter to lower abdomen reduces
tubing. Inspect all that may lead to obstruction in the pressure on urethra at junction of penis and
flow of the urine from the catheter to the drainage bag. scrotum, thus reducing the possibility of tissue injury
at this area. (Perry, 2013)
29. Remove gloves and dispose of equipment, drapes
and urine in proper receptacle.
[Link] client to comfortable position. Wash dry
perineal area as needed.
[Link] patient on ways to lie in bed with catheter. This facilitates drainage of urine and prevents the
Side lying facing drainage system with catheter and backflow of urine. (Taylor, 2014)
tubing draped over thigh and side lying facing away
from the system, catheter and tubing extended
between legs.
32. Caution patient against pulling the catheter. It maintains comfort and security. (Perry, 2013)
33. Wash hands thoroughly. It reduces transmission of microorganisms. (Perry,
2013)
EVALUATION
1. Palpate bladder and ask if patient remains uncomfortable.
2. Determine if there is no urine leaking from catheter or tubing connections.
3. Record time of procedure, characteristics and amount of urine in drainage system.
4. Observe for signs of obstruction (e.g., decreased urine in collection bag, voiding
around the catheter, abdominal discomfort and bladder distention).
NURSING CONSIDERATIONS
DEFINITION
A urine specimen is collected from an indwelling catheter when a urinary tract infection is
suspected and a sterile urine specimen is needed for a urine culture and sensitivity test. The
specimen must be obtained aseptically, so as not contaminate the closed drainage system or
contaminate the specimen. A registered nurse (RN) or licensed practical nurse (LPN) may
collect the specimen from the indwelling catheter.
ASSESSMENT:
MATERIALS:
➔ 3 mL syringe with 1inch needle (21-25 gauge) for culture or 20 mL syringe with 1inch
needle (21-25 gauge) for routine urinalysis
➔ Metal clamp or rubber band
➔ Alcohol, povidone-iodine, or other disinfectant swab
➔ Specimen container: non-sterile for routine urinalysis, sterile for culture
➔ Specimen label
➔ Completed laboratory requisition with patient’s name, date and time of collection
➔ Clean, disposable gloves
Implementation:
Criteria Rationale
1. Wash your hands. Wear gloves and follow Washing your hands and taking standard precautions
standard precautions if contact with blood or body prevent the spread of infections. (Carter, 2012)
fluids cannot be avoided.
2. Identify the person, and greet him or her by Identifying the person ensures that the procedure is
name. being done on the correct patient or resident. Greeting
the person by name is being courteous. (Carter, 2012)
3. Explain the procedure and encourage the Helps the person know what to expect and helps him
person to participate as appropriate. understand how he can help. (Carter, 2012)
4. Provide privacy by showing any visitor where Asking visitors to leave the room, and closing the door
they should wait, if necessary, until you have and curtain protects the person’s right to privacy.
completed the procedure. Close the door and the (Carter, 2012)
curtain.
5. Clamp the drainage tubing with clamp or rubber This ensures that the urine specimen is adequate.
band for 30 minutes. (Smith, 2011)
6. Return to room and inform patient that the This promotes cooperation. (Perry, 2013)
procedure to collect specimen from the catheter
will begin.
7. Wash hands again or an alcohol and don Handwashing deters the spread of microorganisms.
gloves. Gloves protects the nurse from exposure to
microorganisms in the urine. (Taylor, 2014)
8. Cleanse entry port for needle with disinfectant This prevents the transmission of microorganisms.
swab. (Taylor, 2014)
9. Insert the needle at 30-degree angle just above This facilitates sealing of the rubber in the port following
where the catheter is attached to drainage tube or removal of the needle. This allows urine to accumulate
built-in sampling port. in the tubing. (Smith, 2011)
13. Unclamp catheter and allow urine to flow into This facilitates drainage of urine and prevents the
drainage bag. backflow of urine. (Taylor, 2014)
14. Secure attached properly completed
identification label and laboratory requisition
specimen.
16. Dispose of soiled supplies and wash hands. This reduces transmission of microorganisms. (Perry,
2013)
EVALUATION
2. Record collection of specimen on nurse’s notes; note time and date, appearance and odor.
BLOOD GLUCOSE MONITORING
Children and young people < 18 years old Adults ≥ 18 years of age
Preprandial blood glucose levels 4–8 mmol/L Preprandial blood glucose levels 4–7 mmol/L
Postprandial blood glucose levels of less than Postprandial blood glucose levels of less than
10 mmol/L 9 mmol/L
Essential Equipment
● Blood glucose monitor
● Test strips
● Control solution
● Single-use safety lancets
● Non-sterile gloves
● Cotton wool/low-linting gauze
● Sharps box
Implementation
PRE-PROCEDURE
Action Rationale
1. Turn the machine on and ensure the correct date To ensure accuracy in the result record and
and time patient safety (Roche Diagnostics 2013, C).
are presented on screen, and that there is adequate
battery
life. Where applicable, enter or scan operator
number, e.g.
number or bar code on name badge, as per
manufacturer’s
guidelines.
2. Check the unit of measure and ensure that it is Units of measure may change from mmol/L to
reading in mmol/L prior to each use. mg/dL, which could result in the meter user
thinking that the blood glucose level is higher than
it actually is (MHRA 2011, C).
4. Identify the patient, i.e. verbally and against their The patient should give consent to the procedure.
hospital identity band, and explain the procedure. Explanation may allay any fear or anxieties
5. Select a site that is warm, pink and free of any It is important to avoid previous punctures by
calluses, burns, cuts, scars, bruises or rashes. rotating the site lanced to avoid fngertip soreness
Avoid skin areas that have evidence of previous and reduce callus formation (WHO 2010, C).
punctures. The usual site for lancing is the palmar Fingers on the non-dominant hand and the index
surface of the distal segment of the third or fourth fnger are generally less calloused. The index fnger
finger, ideally of the non-dominant hand as they are is also potentially more sensitive to pain due to
usually less calloused. additional nerve endings. The thumb also may be
calloused and has a pulse, indicating arterial
presence, and the distance between the skin
surface and the bone in the ffth fnger also makes
it unsuitable for puncture (WHO 2010, C). Tips and
pads of fngers should be avoided as they are
denser with nerve supply and can be more painful
PROCEDURE
6. Ask patient to sit or lie down. To ensure the patient’s safety and minimize the
risks if they feel faint when blood is taken
7. Ask the patient to wash their hands with soap and To avoid sample contamination (CDC 2013, C).
water and dry thoroughly with low-linting gauze Not washing hands can lead to a diference in the
glucose concentration, especially with fngers
exposed to fruit or a sugar-containing product
8. Wash your hands and put on gloves. To minimize the risk of cross-infection and
contamination
9. Take a single-use lancet and, if it has depth To minimize the risk of cross-infection and
settings, ensure the correct setting is used (most accidental needlestick injury. The correct depth
commonly middle one). setting will ensure patient comfort
10. Activate the single-use, auto-disabling In settings where assisted monitoring of blood
fngerstick device/ lancet or reusable device, as per glucose is performed, single-use, auto-disabling
manufacturer’s guidelines, at the chosen site, e.g. fngerstick devices should be used. Although
the side of the fnger. Ensure the site of piercing is reusable devices may be used in the patient’s own
rotated, avoiding frequent use of index fnger and environment, they should never be used for more
thumb. Other areas may be used if fnger or palm of than one person due to the risk of bloodborne
hand are unusable. The fngertip may need ‘milking’ viruses (CDC 2013, C). The side of the fnger is
from palm of hand towards fnger to gain a large less painful and easier to obtain a hanging droplet
enough droplet of blood but avoid milking the fnger of blood. Sites are rotated to avoid infection from
alone. multiple stabbings, area becoming toughened and
to reduce pain (Roche Diagnostics 2013, C).
Milking the fnger can cause tissue fuid
contamination and a false low reading (Hortensius
et al. 2011, R1b), cause haemolysis and impede
blood fow.
11. Activate safety-engineered medical device A cost-efective way to reduce the risk of
(where applicable and if not automated), dispose of needlestick injury
lancet and testing strip in a sharps container.
12. Insert testing strip into blood glucose monitor To ensure accurate results, the window on the test
and apply the frst drop of blood to the testing strip. strip needs to be adequately flled as per
Some strips are hydrophilic and are dosed/flled manufacturer’s guidelines
from the side instead of dropping blood directly onto
the strip. Ensure that the window on the test strip is
entirely covered with blood
13. Place gauze over puncture site, apply from To ensure patient safety (Wallymahmed 2007, E)
pressure and monitor for excess bleeding. and to stop the bleeding
14. Remove gloves, place in clinical waste and To prevent healthcare-associated infections and
perform hand hygiene again. spread of antimicrobial resistance (WHO 2013, C).
POST-PROCEDURE
15. Once result is obtained (see Action fgure 15), To ensure accuracy in record keeping
document and sign.
16. Where applicable, dock machine. To ensure centralized records are maintained
17. Report any unexpected results To ensure appropriate treatment and obtain
optimal blood glucose range