Digoxin and tube feeding
Common Questions and Answers about Digoxin and tube feeding
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s first poo) asperation. He was on a feeding tube for about 2 weeks because it was too much work for him to eat and breath at the same time. It's a little bit different with your grandson, but I would imagine the tube would be to make sure he gets enough to grow stronger to where he can tolerate a feeding without getting too tired that he can't finish. I hope this helps a little and that your grandson gains and grows well so he can go home. Please keep me updated on how things go!
My Dad has been on a feeding tube for almost a year. He had esophagus cancer and they removed it and he is now cancer free. My question is why he is so tired all the time ? and what kind of quality of life he can have? He does not have much interest in the things he used to enjoy.It makes me very sad to hear him like this. He lives in another state, so I do not get to see him.
I just logged on. No experience there, but malnutrition is such a problem. I hope Hector logs on soon. There are many good people on this site.
My grandson has the G tube and Nissan and I think this has been the worst thing that a doctor has ever done to him. They convinced my son that he needed to have this surgery for his son to be able to feed. He also was 3 months early and had severe reflux. It did stop the reflux but his life and health iare so messed up because of this tube and Nissan that I wish they would have waited and sought another option.
Our daughter had her echo repeat this past Friday (12 weeks old) and they advised that her ASD has gotten smaller, but that her VSD is still approx. 6 mm. He said it has a very strong shunt of 67mmHg, which he seemed to feel meant that the hole might be getting smaller? Is it possible the strong pressure means it's getting smaller?
I do not have a feeding tube, but many POTSies who have feeding tubes have a GI disorder called gastroparesis. This is when the intestines and stomach move food too slowly and in severe cases the stomach can actually be paralyzed. The other reason I have heard for POTSies to get feeding tubes is because of extremely severe nausea and/or vomiting to the point where malnutrition sets in and severe weight loss occurs. Hope this helps!
My son was born at 34weeks and 5days and he was eating slow. They used a feeding tube on him for 2 days and than he was off of it.
The caloric density can also be increased to as much as 30 kilocalories per ounce (normal formula as well as breast milk has a density of only 20 kilocalories per ounce). At times, a nasogastric feeding tube can also be put in to help ensure that adequate calories are delivered for growth. If she is hospitalized, sometimes physicians will give her a blood transfusion to get her hematocrit over at least 45%.
Our DD was born with a moderate/large VSD and ASD, only she was in heart failure by 10 days old, was placed on Lasix, Digoxin and Spironolactone and NG tube by 6 weeks. She was in very significant heart failure. She is now 3.5 years old, and surgery free. Both defects improved enough that surgery ended up not being warranted. She is still small, at 3 years, 7 months she is still only 28.5 lbs, but she is perfectly healthy!
If a patient has a jejunostomy and is being fed continuous artifital nutrition, should placement be checked and should residual be checked?
During the first week I fed her water, food, and meds through her feeding tube and the vet decided to pull after a week due to the fact the feeding tube was causing her discomfort and that she started drinking water on her own. Although since the feeding tube was pulled she has not been able to eat on her own and I have been feeding her about every two hours with about 5-6 ml per session resulting in 20 ml a day as mentioned above.
By bolus feeding him before meals he will feel full and not want regular food. Recommend feeding at night with a tube feed pump, higher calorie tube feed (2.0 calorie), and see a Registered Dietitian (RD) to help guide you. To find an RD in your area, go to the American Dietetic Association website, www.eatright.org.
How do you tell if Afib converted on its own or if the medication did the conversion or if the medication was causing the Afib? I have been to the Primary doctor and Emergency room both said I was not in afib currently. Another words, when do you know when to stop taking the medications? In Nov 2013, I have Aortic heart valve replacement and a maze procedure. My old cardiologist wanted to do a cardioversion but I didn't want it, so I had to change Cardiologist.
re that little) a feeding tube, and formula. When you tube feed, you take the feeding tube and hold it along the outside of the puppy so that the tip of the tube touches the puppy's side right in the flank area. You then mark the tube where it touches the puppy's muzzle. Normally you will have about a 5 or 6" length of tube marked off for newborn puppies, but giant breeds, of course, will be larger.
Finally after he started vomiting, I demanded a neurologist see him, who immediately diagnosed the stroke and moved him to ICU where he stayed for 2 weeks, on the vent and feeding tube. After 2 weeks he was moved to the rehab floor with a trach and feeding tube. He receive inpatient OT, PT and Speech therapy for 3 months. He is now taking outpatient PT and Speech therapy. He still has numbness and really bad tingling of the right side. The left side is week as well.
My husband and I would like to start trying for a baby but i'm on Betablockers for a tachycardia that no-one can find a reason for! i'm only on 1.25mg of bisoprolol, and would like to know what risks there are. I'm currently on a waiting list to see cardiology and find out what their opinion is but would like a bit of advice.
And I am glad she arrived well and safe. Feeding issues can be so overwhelming and distressing. When Hunter was born, he was so sleepy that he didn't want to eat. It took him a bit to get it, we had to feed him with a nursing tube attached to my breast, but he was a smarty from birth, figured out how to spit out my breast and just drink from the nursing tube! Crazy.
This landed us at the hospital for dehydration , for tests like endoscopy, swallow studies aso and now he is on a feeding tube. We went from a normal eating kid (picky, but I d KILL for picky at this point) to a kid who needs round the clock feedings and is hooked up to a pump all night, just to keep up with his calorie needs at 5 foot 10, 200 pounds. We started him back on anxiety meds, and are working with our speech therapist to start feeding therapy.
My doctors finally agreed that I need a feeding tube, but the problem is I've been kind of obsessed with them for 4 years now prior to my current issues. I have a lot of GI issues and a lot of sensory issues with food. I prefer blended and pureed food and liquids. However with MCAS (mast cell activation syndrome), most of the foods I like to have are high histamines.
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