Feeding tube patients: What's your experience?
I have a G tube in my stomach and am curious about what you tube feed, problems incurred, everything that has worked.. My tube is a permanent part of me and been keeping me alive since mid October last year. It is no different to me than my mouth, throat, esophagus except it doesn't get cancer. It is a Godsend.
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My only experience: any inflammation around j-tube site needs to be taken seriously.
Yes, our experiences are very similar - also a J-tube and also the overwhelming nausea worsened by the sight or smell of food, fear of vomiting, also have the goal of 2,000 calories a day plus water 6 times a day. Is your pump detachable and have a rechargeable battery where you can put it in a backpack and have mobility? When my husband was at 4 cartons it was at 76 mL/hr going from 7 pm to 7 am. I assume the Boost is by mouth, correct? If your husband does better getting the tube feeding during the day, then the ability to move around should help keep the formula moving through his gut. We chose to remain free of being hooked up during the day. He also has been sleeping on a recliner chair since diagnosis, that helps a lot. We are a little bit ahead of you in that his tube will be removed next week, he has met the goal of intake by mouth as laid out by the Mayo nutritionist. He still has no appetite, eating is a job and every intake is written down with calorie content, foods are chosen to be bland and fairly similar from day to day. The nausea is finally gone but it persisted for months with some help from Ondasedron 8 mg. Since your husband already tapes the tube to prevent gravity pull, I have no further suggestions on that issue, sorry.
First of all, congratulations to your hubby. The reason, I believe, that the sight or smell of food, etc., that your husband was experiencing is because during this type of operation, the vagus nerve is severed—so you no longer feel full nor hungry.
Yes, our pump is detachable and rechargeable and he does have the backpack (although he hasn't chosen to use it yet). Formula overnight would be the best solution but it causes nausea. As I said, we break it up. Yes, the Boost is by mouth and it's worth 530 calories. He does take Ondansetron, as well as Prochlorperazine, both of which offer minimum relief of nausea.
After his first session with the hypnotherapist he had an entire yogurt by mouth (usually he'd have one spoonful and that would be it for him. He also ate about 80% of both a scrambled and one piece of bacon—all without nausea. I feel that we've finally turned a corner but it's going to be a while yet until we can talk about getting his tube removed.
Thank you for all your suggestions and congratulations and best of luck to your husband.
Thank you! My husband did not have the surgery, he is stage 2 and 82 yrs old. He chose to do chemo/radiation only and had a very hard time at that. Upcoming PET in 2 weeks will tell whether foregoing surgery is wise.....or not. The Ondansedron offered minimum relief here too and I vetoed using Prochlorperazine after trying it for 3 days with no relief because it is a mind altering drug and he was on a substantial dose of Fentanyl patches which is also mind altering. Last thing, I would suggest you experiment with trying the speed of mL/hr to be 2 hours per carton. We are all trying our best to make this journey a little easier for our hubbies but it is a tough journey! Warm wishes to you both!
My husband has a G tube, though not permanent as of yet, but it has kinda changed in appearance. Towards the top near the stoma it looks like it has melted because it is so warpped. How does he go about having a new tube line put in?
This is all awesome, thank you. What should my husband do or who does he need to talk to about his tube connected to the stoma is all warpped looking? It looks like it has melted in some areas towards the top near the stoma.
pic included so you can see what I'm talking about.
My Husband is on osmolite 1.5 and does 6 a day by 12 hour continous feed at 120 ml per hour, then does chicken broth by mouth to keep his sodium up. He was doing 8 boxes of Osmolite a day. He was 175lbs when Diagnosed with stage 4 esophageal cancer 1/31/24 and is now up to 188lbs as of last week. Still having issues with low iron. He has iron infusions, Immunotherapy, and Chemo every other week, but his iron is still extremely low. Had to have 5 bags of blood transfused to get his hemoglobin up from 7.1 to 9.0
From the image you provided, the G-tube does appear to be somewhat deformed. It still appears to be patent. Is your husband still able to receive infusions through the tube? If so, what is the diameter of French (Fr) measurement of the tube?
It appears that the tube deformities apparent in your picture are consistent with repeated physical deformation of the tube, perhaps related to folding, pinching or kinking the tube or the use of a metal hemostat or clamp to stop outflow of infused fluids while switching between catheter tipped syringes or feeding bags.
Where and how often do you or your husband clamp the G-tube when you need to perform infusions? You should use a plastic hemostat to clamp off the tube as it will not damage or deform the soft tubing.
Of course it could be that the current tube inserted is defective but I doubt that they would place a defective tube.
If the tube continues to deteriorate becomes occluded or has reduced flow, it should be replaced.
My husband pinches it daily to try to break the food up at the opening. We flush it with 100 ml of water every 4 hours, He's on a 12 hour continuous feed, but he has his chemo, iron infusions, and Immunotherapy done at City Medical Dallas. It's still working fine. Thank you for your help.