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Using a Peg for nutrition following a stroke

jamazon

Newbie
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1
Can anyone offer any advice or experience please? my Dad has managed t2 diabetes for many years though had a stroke last year that rendered him unable to swallow. He now uses a peg feed overnight with bolus feeds during the day. He manages tiny amounts of fluid and food (also chews and spits food so that he can still enjoy mealtimes with the family).
It hasn't been easy and recently he's been losing weight, now into muscle weight loss. I understand the feed regime isn't really primarily designed for diabetes but is all we have. Has anyone else had experience of this and any positive news or advice please?

Thanks.
 
Hi.
Welcome to the Forum. Sorry to hear about the problems you are having with your Dad's Diabetes.

Firstly I don't think we actually have any members who use PEG feeding (Enteral Feeding) ? So doing a bit of searching I came up with this information which may be of benefit for him. I have put it as a quote as for some reason I am unable to link to it ! No idea why. :?

You really need to see a DSN (Diabetes Specialist Nurse) and also a Nutrition Nurse. It is not something that a plain old GP should be dealing with. I hope that you get a referral soon and get this sorted out. As you can see from the information the suggestion is that he should really be put onto Insulin to make things easier.

Please let us know how you get on..........

Patients with diabetes mellitus who are being considered for enteral feeding should be notified to the Diabetes Specialist Nurses. The Dietitian and Nutrition Nurse should already be involved.

If the patient is insulin-dependent then insulin will of course be required throughout the course of the tube feed. If the patient had tablet-controlled diabetes it is likely that poor glycaemic control will already have been recognised and the patient switched to subcutaneous insulin.

If however the patient's diabetes had previously been controlled by "diet alone" or oral agents, always assume that insulin will be necessary to cover enteral feeding.

The general principle is for the Dietitian and Nutrition Nurse to make decisions on the nutritional requirement of the patient and for the insulin to be fitted around the feeding regime. We should never be in the position of having to adjust the enteral feed because the patient is taking a particular insulin regime. Enteral feeding will usually begin with a slow infusion over 20 hours. Commence an intravenous insulin infusion, Humulin S 1 unit/ml in normal saline. Infuse at an initial rate of 1 unit/hr. For the first 48 hours of enteral feeding, two-hourly bedside capillary blood glucose measurements should be performed aiming for blood glucose levels of between 5 and 9 mmol/l. The insulin infusion rate can be adjusted in steps of ½ unit, 1 unit, 2 units, 3 units, 4 units, and 6 units/hr. If more than 6 units/hr are required obtain advice from the Diabetes Team. After 48 hours enteral feeding, consider switching to subcutaneous insulin. Use once daily glargine as background insulin. Use isophane insulin at the commencement of the cycle of feeding and halfway through the cycle. e.g. enteral feeding to run 09.00 to 05.00 the following day (20hours feeding). Give glargine insulin subcutaneously 10 units at 9.00 a.m. Give Humulin I insulin 8 units subcutaneously at 9.00 a.m. Give Humulin I insulin 8 units subcutaneously at 7.00 p.m. Continue to monitor blood glucose 2-hourly. Aim for blood glucose levels of between 5 and 9 mmol/l, be prepared to increase the insulin doses as necessary to achieve the target.

This is from one particular Hospital and may well be slightly different but the principle is the same.
 
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