In the operating room by a surgeon or pediatric gastroenterologist
Usually your child is in the operating room for 1 to 2 hours
What will happen after surgery?
Your child will have nothing to eat or drink for up to 24 hours after surgery but will have fluids through an IV
Your child may feel sore for a day or two and the area may be swollen
We will give your child medications for pain
There may be some sutures near the G-tube
You will start to learn about caring for the G-tube right away
We will clean the skin around the tube with saline and gauze or cotton tip applicators at first
The new site may have some drainage until it heals
A tract connecting the stomach to the outside skin develops around the tube as the stoma heals
Your child may only have sponge baths for the first 2 weeks
Your child’s nurses will help you learn and practice how to care for the G-tube. We want you to feel comfortable with these new skills before you go home. The case manager will arrange for the tube feeding supplies you need.
If you are worried about how the G-tube looks or is working, call the pediatric gastroenterologist or surgeon
When to call the surgeon or pediatric gastroenterologist:
If the G-tube falls out and it is less than 2 months since surgery
If the G-tube falls out before the first tube change (follow the instructions for the emergency tube and call the surgeon)
If the G-tube falls out and you are not able to get a new tube back in or if the hole has closed
If there is any bleeding or lots of redness around the G-tube
If there are any large bumps under the skin around the G-tub
For gastrostomy tubes placed by pediatric surgery: Call the pediatric surgery clinic during clinic hours. After hours, call the hospital operator (916-734-2011) and ask for the pediatric surgeon on call.
For gastrostomy tubes placed by pediatric gastroenterology: Call the pediatric gastroenterology advice line. After hours, call the hospital operator (916-734-2011) and ask for the pediatric gastroenterologist on call.
There are several types of gastrostomy tubes. The doctor will choose the best one for your child. It may be necessary to change the type or size of the G-tube as your child grows and his/her medical needs change.
Low Profile Device (such as MIC-KEY or Mini-One Buttons)
This is a skin level device
It is inserted into the stomach through the abdominal wall
There is an inflatable balloon at the end of the tube inside the stomach that is filled with water to hold the G-tube in place
The balloon port is the little opening labeled “BAL” on the side of the G-tube
An extension set is attached to the key shaped opening to give fluids and feedings
When not in use, the feeding port is covered with an attached cap
An anti-reflux valve is located inside the G-tube to help prevent the stomach contents from leaking out of the G-tube.
The extension set will open the valve.
Flush thoroughly with water to keep the valve clean and working properly.
A small opening is made in the skin of the abdomen. Another small opening is made in the stomach wall. The tube is passed through the openings into the stomach. This heals as a tract somewhat like the tract that forms with a pierced ear. When the tract has healed, the G-tube can be removed and replaced easily. However, the tract will close quickly if the G-tube falls out and is not replaced.
Post-op care
The area around the gastrostomy may be tender for several days. Discomfort usually can be treated with pain medications
A small amount of drainage around the G-tube is normal
There may be a dressing under the G-tube to prevent tube movement
Do not turn the G-tube until it is healed
Sponge bathe for the first two weeks after placement
Home Care
Keep the G-tube and the stoma (the skin around the tube) clean and dry
Clean the skin around the G-tube 1 to 2 times each day with soap and water
The G-tube is replaced about every 3 months.
At your follow-up appointment, the clinic staff will teach you how to change the G-tube at home, and how and when to check the water in the balloon.
A dressing under the extension set can help stabilize and prevent movement, but is not required.
Extension sets
Remove extension set from GT when not in use
If your child is receiving feedings over more than an hour, secure the extension set to the skin with tape to prevent pulling on the G-tube
Extensions sets are disposable and should be changed every week
The supply company providing your G-tube supplies should send you 4 to 5 sets every month
Clean the extension set with soap and water after every use
Do not use if clogged or dirty
The extension set may be available in different lengths (12 or 24 inch)
The most commonly used extension for feeding has a right angle connector and a y-port
The straight bolus extension set is useful for venting the G-tube or for large volume bolus
How to attach the extension set:
Align the black line of the extension set with the black line on the feeding port.
This tube is usually placed by a pediatric gastroenterologist or interventional radiologist
The PEG tube is changed after about 3 months by the specialist and replaced with another type of G-tube (usually a MIC-KEY)
Inside the stomach is a dome-shaped bumper that sits against the stomach wall to hold the tube in place
On the outside against the skin is a retention ring that keeps the PEG tube in place
Post-op care
The area around the gastrostomy may be tender for several Discomfort usually can be treated with pain medications
A small amount of drainage around the PEG tube is normal
There is usually no dressing under the retention ring
The PEG tube is turned two times a day
The centimeter marking at the skin is checked every day (see picture)
Sponge bathe for the first two weeks after placement
Home care
Clean the skin under the retention ring 1 to 2 times a day with soap and water
Do not use any dressings or gauze under the retention ring
Make sure the retention ring sits on the skin without indentations from the ring
Secure the PEG tube at all times to the abdomen with tape about 2 to 3 inches away from the insertion You may use a gauze bolster to support the tube if needed.
Every day, check the centimeter marking on the PEG tube where it enters the skin. The marking should be the same every day
If the centimeter marking at the skin is a bigger number, gently pull the PEG tube back to the proper marking and adjust the retention ring
If the centimeter marking at the skin is a smaller number, the PEG tube may be out of Call your specialist or go to the Emergency Room. Do not give anything through the tube.
Place your child in a comfortable position during feedings.
You may:
Hold your child
Place your child in a car seat, stroller, wheelchair, chair or high chair
Have a second person help you with the feeding
Place your child so his/her head is higher than the rest of the body
You and your child’s healthcare team will come up with a feeding plan that meets your child’s nutritional needs and is also most appropriate for his/ her medical condition.
Feedings usually begin the day after surgery. The initial feed will be a small amount to make sure your child’s stomach is ready for feeds.
Then, the amount of formula is gradually increased to what will be given at home.
Although formula contains water, it is usually not enough for your child’s needs. The feeding plan will include additional water to be given either before, after or in between feedings.
It is also recommended to flush the G-tube/extension set with 5 to 10 mLs of water before and after feedings to keep tube from clogging.
There are three ways that tube feedings may be given:
Bolus by gravity with a syringe
Bolus by gravity with a feeding bag
Bolus, continuous or cycled by pump with a feeding bag
With this method, a machine pumps formula from a bag through the G-tube into the stomach. Teaching about the pump will be arranged with the enteral supply company before your child is discharged from the hospital.
There are multiple ways of giving feedings with a pump:
Bolus: Feeding given over 30 minutes to several hours
Continuous: Feedings given over a longer time period, for example, overnight or 24 hours per day
Cycled: Feedings given over a longer time period with breaks in between
Supplies:
Formula (remember to rinse off the top of the unopened can)
Water
Pump and feeding bag
5 or 10 mL syringe for water flush
Extension set (if used)
Steps for feeding with pump:
Wash hands
Fill feeding bag with formula
Connect feeding bag to pump and prime according to pump instructions
Program pump settings as instructed
Attach extension set (if used) to G-tube and flush with water
Attach pump tubing to G-tube or extension set
Unclamp G-tube or extension set
Start pump and watch to make sure feeding has started properly
For bolus or overnight feeding:
At the end of the feeding, flush G-tube/extension set with water
Disconnect and wash extension set, and allow to air dry
The enteral supply company will instruct you on how to care for the feeding bag
Use a new feeding bag every 24 hours
For continuous or cycled feedings:
The enteral supply company will instruct you on how to care for the feeding bag
Use a new feeding bag every 24 hours
Disconnect and wash the extension set (if used) every day before setting up a new feeding bag
Change extension set (if used) weekly
Refrigerate any unused formula and use within 24 hours
Attach syringe (without plunger) to clamped feeding tube or extension set
Hold syringe above the level of your child’s stomach
Unclamp tube or extension set
Press lightly on the stomach or lift the legs
Excess gas will bubble up into the syringe. It is normal for formula/stomach contents to rise into the syringe
If liquid is seen in the syringe, allow it to flow back by gravity before clamping the tube/extension set and removing the syringe
“Venting”
Your child may get uncomfortable due to excess air or gas in his/her stomach. Venting allows air to escape from the stomach. Some children may need venting more frequently and/or during feedings. Your healthcare team may also recommend use of a Farrell Bag System.
The feeding plan you start with will change over time
The healthcare team will work with you to develop a plan that fits your family’s needs and fits with your child’s school, appointment, and sleep schedule
Activity- most activities including tummy time are allowed
Ask your team what to do if your child misses a feed. They can help determine where is the best place to fit it in
Be prepared: always make sure you have enough formula and supplies
If your child is not taking food by mouth, it is still important to keep the mouth clean
Brush 2 times per day
Floss 1 time per day
For infants, wipe the mouth and teeth with a soft moist cloth at least once a day
Your child needs to keep the connection between the mouth being used and the stomach getting full. If your child is allowed to have food or liquids by mouth, it is important to offer an oral feeding each time your child gets a tube feeding. If your child is not able to eat by mouth, oral stimulation (or a pacifier for infants) can be offered during tube feedings
Talk to your healthcare team about other ways to provide for your child’s oral development
Preventing Infection:
Wash your hands every time you handle the tube, formula, or supplies
Wash out the bag or place it in the refrigerator between feeds as instructed by your enteral supply company
Use a new bag every day
Good oral hygiene prevents bacteria from moving down the airway and causing pneumonia
Raise the head of the child’s bed to prevent reflux
The opening will start to close within 2 hours, and may be completely closed by 24 hours, so it is important to have a kit ready to use.
What to do if the G-tube falls out:
Don’t panic. Call the doctor immediately.
If the G-tube is newly placed, and you have notyet been seen in the pediatric gastroenterology (GI) clinic, call pediatric surgery 916-734-7844. After 5 p.m. or on weekends or holidays, call the Hospital Operator at 916-734-2011and ask for the on-call pediatric surgery to be paged.
If you have been seen by a pediatric gastroenterologist, but have not yet learned how to replace the G-tube, call the pediatric GI clinic at 916-734-5912. After 5 p.m. or on weekends or holidays, call the Hospital Operator at 916-734-2011and ask for the on-call pediatric gastroenterologist to be paged.
If you are unable to reach the doctor by phone, go the nearest emergency room.
Do Not Give Feedings or Medications Through the Emergency Tube
2 replacement emergency tubes will be in your emergency kit.
One tube is the same size as your child’s gastrostomy tube and the other tube is one size smaller.
The emergency tube is inserted to keep the stoma and gastrostomy tract open
Always carry the kit with your child
Never force the tube into the stoma. Try the smaller size tube if needed.
Do not take more than 10–15 minutes to try to insert the Emergency tube
Do not inflate the balloon on the emergency tube
Supplies:
2 tubes, 1 the size of current G-Tube and 1 a size smaller (this tube is often called a Foley)
Water soluble lubricating jelly
Tape
Catheter plug
Steps:
Do not panic!
Wash your hands
Put a small amount of water soluble lubricating jelly on the end of the emergency tube
Gently insert the emergency tube 2-3 inches into the stoma\
Tape the tube to the skin so that it won’t fall out
Do not give ANYTHING (formula, water, or medications) through the emergency tube
Call the doctor or go to the nearest emergency room