Y Ports For G Tubes

Y Connectors For Peg Tube
Y Ports For G Tubes

Connector Styles: bolus (one port only) and Y-port (two ports) Tip Styles: straight and right angle; AMT MiniONE and MIC-KEY Extensions are compatible for the AMT MiniONE G-tube button and the MIC-KEY G-tube and GJ-tube buttons.

Nasal feeding tubes have no restrictions on swimming, other than making sure the tube is closed, clamped, and not hooked up to a feeding pump. Ocean water and well-maintained private pools are. Gastrostomy Feeding Tube with Y Ports Kangaroo™ 16 Fr. Silicone Sterile The feeding port is incompatible with luer lock or IV connections, red Available with safe enteral connections to address the 2006 JCAHO Tubi The replaceable Y-port allows you to change the port rather than the e. Y Port Feed Adapter 20Fr for G-Tube Applied Medical 42020- 1 Each; For Capsule Dome G-Tube and Capsule Monarch G-Tube. Y-port with right angle feeding set is used for continuous feeding. Catheter tip syringe fits into the bolus port of the bolus feeding set and the feeding port of the right angle feeding set.

The feeding port is incompatible with luer lock or IV connections, reducing the risk of accidental connection or infusion. Available with safe enteral connections to address the 2006 JCAHO Tubing Misconnections Sentinel Event alert. The Kangaroo™ gastrostomy tube is constructed of a durable silicone that allows for optimal performance and longevity. The replaceable Y-port allows you to change the port rather than the entire tube.

Feeding ports are incompatible with luer lock or IV connectors, therefore, reducing the risk of accidental connection or infusion
Indicates nutritional port – not IV access
Durability and tube longevity
Tube stability
Allows for easy stoma depth measurement
Seals off the internal stoma to prevent fluid leakage
Provides optimal tube performance
Allows for simple Y-port replacement when port becomes stretched
20 mL

Catalogue Number	Size	Unit Measurement
SHER8884720163	16 FR/CH (5.3 mm)	Case/5 Each
SHER8884720189	18 FR/CH (6.0 mm)	Case/5 Each
SHER8884720221	22 FR/CH (7.3 mm)	Case/5 Each
SHER8884720247	24 FR/CH (8.0 mm)	Case/5 Each

WHAT YOU NEED TO KNOW:

What do I need to know about a percutaneous endoscopic gastrostomy (PEG) tube?

A PEG tube is a soft, plastic feeding tube that goes into your stomach. Healthcare providers will teach you how to put liquid food and certain medicines through the tube. You will also be taught how to care for the PEG tube and the skin where the tube enters your body.

How do I use a PEG tube for feedings?

Your healthcare provider will tell you when and how often to use your PEG tube for feedings. A bolus feeding means nutrition is given over a short period of time. An intermittent feeding is scheduled for certain times throughout the day. Continuous feedings run all the time. The following are types of PEG tube systems:

A feeding syringe helps liquid food to flow steadily into the PEG tube. The syringe is connected to the end of the PEG tube. You will pour the liquid into the syringe and hold it up high. The syringe plunger may be used to gently push the last of the liquid through the PEG tube.
A gravity drip bag allows liquid food to drip more slowly into the PEG tube. The tubing from the gravity drip bag is connected to the end of the PEG tube. You will pour the liquid into the bag. The bag hangs on a medical pole or similar device. You can adjust the flow rate on the tubing according to your healthcare provider's instructions.
An electric feeding pump controls the flow of the liquid food into your PEG tube. Your healthcare provider will teach you how to set up and use the pump.

How do I care for my PEG tube?

Always wash your hands before and after each use. This helps prevent infections. Use soap and water to wash your hands.
Always flush your PEG tube before and after each use. This helps prevent blockage from formula or medicine. Use at least 30 milliliters (mL) of water to flush the tube. Follow directions for flushing your PEG tube.
If your PEG tube becomes clogged, try to unclog it as soon as you can. Flush your PEG tube with a 60 mL syringe filled with warm water. Never use a wire to unclog the tube. A wire can poke a hole in the tube. Your healthcare provider may have you use a medicine or a plastic brush to help unclog your tube.
Check the PEG tube daily:
- Check the length of the tube from the end to where it goes into your body. If it gets longer, it may be at risk for coming out. If it gets shorter, let your healthcare provider know right away.
- Check the bumper. The bumper is a piece that goes around the tube, next to your skin. It should be snug against your skin. Tell your healthcare provider if the bumper seems too tight or too loose.
Use an alcohol pad to clean the end of your PEG tube. Clean before you connect tubing or a syringe to your PEG tube and after you remove it. Do not let the end of the PEG tube touch anything.

How do I care for the skin around my PEG tube?

Do not remove the stitches or medical tape. Stitches or medical tape hold your PEG tube in place when you first get it. Your healthcare provider will take them off once the skin around your tube heals. Leave clean bandages over the tube area for the first 24 hours after the tube is put in. You may not need to use bandages after 24 hours if the skin around the tube looks dry. Ask when you can shower or bathe.
Routine skin care:
- Clean the skin around your tube 1 to 2 times each day. Ask your healthcare provider what you should use to clean your skin. Check for redness, swelling, or pus in the area where the tube goes into your body. Check for fluid draining from your stoma (the hole where the tube was put in).
- Gently turn your tube daily after your stitches come out. This may decrease pressure on your skin under the bumper. It may also help prevent an infection.
- Keep the skin around your PEG tube dry. This will help prevent skin irritation and infection.
Use topical medicines as directed. You may need to put antibiotic cream on the skin around your tube after you are done cleaning it.

Y Connectors For Peg Tube

What else do I need to know about a PEG tube?

Keep a record of liquids you have each day. You may also need to keep a record of how much you urinate and how many times you have a bowel movement each day. Bring this record to your follow-up visits.
Check your weight as directed. Keep a record of your weights and bring it to your follow-up visits. Your healthcare provider may need to change your feedings if your weight changes too quickly.
Take your medicines as directed. Learn which of your medicines can be crushed, mixed with water, and given through the PEG tube. Certain medicines should not be crushed or may clog the PEG tube.
Go to all follow-up appointments. You may need to have blood tests and other tests when you see your healthcare provider.

When should I call my doctor?

You start coughing or vomiting during or after a feeding.
You have severe abdominal pain.
Blood or tube feeding fluid leaks from the PEG tube site.
Your PEG tube is shorter than it was when it was put in.
Your PEG tube comes out.
Your mouth feels dry, your heart feels like it is beating too fast, or you feel weak.
You have nausea, diarrhea, or abdominal bloating or discomfort.
You have stomach pain after each feeding or when you move around.
You have discomfort or pain around your PEG tube site.
The skin around your PEG tube is red, swollen, or draining pus.
You weigh less than your healthcare provider says you should.
Your PEG tube is longer than it was when it was put in.
You have questions or concerns about your condition or care.

Care Agreement

You have the right to help plan your care. Learn about your health condition and how it may be treated. Discuss treatment options with your healthcare providers to decide what care you want to receive. You always have the right to refuse treatment. The above information is an educational aid only. It is not intended as medical advice for individual conditions or treatments. Talk to your doctor, nurse or pharmacist before following any medical regimen to see if it is safe and effective for you.

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