United Ostomy Association, Inc.
Evansville, Indiana Chapter
Re-Route

 
Contents:
WHAT CAN YOU DO?
PATCH vs. POUCH vs. PLUG
ALL POUCH WEARERS
THE FUNGUS AMONG US!
EXERCISES AFTER SURGERY
PAT YOURSELF ON THE BACK
PLAIN TEXT VERSION OF THIS NEWSLETTER

Re-Route Archive

Volume 33, Number 11  October, 2006



WHAT CAN YOU DO?
Via: The Innermost News, Monterey City & the G.B. News Review  
Your ultimate goal is to take personal charge and live a happier life—despite having ostomy surgery. Here are a few strategies that can help you to better handle your ostomy and improve your overall health, happiness and productivity. Be a person, not a patient. Make this the foundation of your thinking. You are a person who has had ostomy surgery, not an ill person. The only time you are a patient is when you’re in the doctor’s office or in the hospital. The way you see yourself living with an ostomy is an essential part of coping successfully.
Understand the unique way that your ostomy affects you and your life - Identify the ways that your ostomy causes problems for you. You’ll want to identify them and then determine how you’re going to deal with them.
Set overall goals for improving your life: Improve your ability to adapt to your situation. Improve your coping style. Set reasonable, realistic, achievable goals. Aim to regain control of your life. Do things that you like and spend less time with things you dislike. Enhance positive relationships. Improve participation in your social network. Improve your life satisfaction and quality of life.
Pinpoint what you need to help improve your life. Think about all the difficulties that you are having living with your ostomy. Write these down on the left side of a folded piece of paper. On the right side next to each item, write down things you can do to improve each one. Note as many alternatives as you can. Ask others for additional ideas, especially if you’re not sure what to do about certain things. Keep adding to your list and plan how you will use these ideas to improve your life.
Anticipate the negative. There are negative things that can happen during your life with an ostomy (leakage, skin irritation, depression, fear, sexual concerns) but some of these could also happen if you didn’t have an ostomy. The more you anticipate and prepare—the better you will cope.


PATCH vs. POUCH vs. PLUG
Via: Jacksonville, FL Mail Bag, Via: SW Arizona ICU Bulletin & S. Brevard FL Ostomy Newsletter
There has been much discussion over whether colostomates should wear a patch over their stomas, a pouch or the plug (a pouchless product). The controversy behind the three Ps dilemma is whether or not the person with a colostomy should irrigate. No two ostomies are alike and irrigating is not for everyone. The colostomy has to be in the descending or sigmoid colon to irrigate. A colostomy in the ascending or transverse colon will produce stool too watery for regulation. People who had a very unpredictable bowel schedule before surgery may continue to do so despite efforts to achieve regulation with irrigations. Some people have work schedules or lifestyles that don’t permit them to irrigate at a consistent time each day and this, too, can cause irrigations to be unsuccessful. Other people simply don’t like to irrigate. The thing you need to know is this: YOU DO NOT HAVE TO IRRIGATE YOUR COLOSTOMY FOR IT TO WORK. Your bowels will work anyway, irrigation or not. The purpose of irrigating is to achieve regulation of the bowel. The reason for regulating the bowel is for the individual’s comfort and convenience. If irrigating is not accomplishing regulation and if it is making you more uncomfortable trying to fit in your personal schedule, you should not be doing it. FIND OUT WHAT WORKS FOR YOU AND STICK TO IT.!


ALL POUCH WEARERS
Via: Coos Bay Oregon & Greater Cincinnati Ostomy Association
Avoid letting your appliance get too full, either of waste or gas. Although one of our members says he likes his pouch to “balloon up” because it makes him lighter on his feet, it’s not a good practice. Normally, you should empty your pouch when it becomes 1/3 to 1/2 full, and before trapped gas makes it feel firm. As the pouch becomes fuller, it places a greater strain on the snap fastener holding the pouch onto the flange, for two piece wearers and increases the tendency for the adhesive part of the appliance to pull away from the skin around a stoma for even a one-piece pouching system. If it is not convenient to empty a “filling” pouch, get somewhere you can discreetly “pop” the seal, releasing the gas pressure. This trick can buy you a little more time before emptying is absolutely necessary. Also, for ileostomates, if you know that you are going to be traveling or in a situation where easy access to a rest room is not available, adjust what you eat to avoid high residue food. Instead of eating two bran muffins and a bowl of Raisin Bran for breakfast, consider pancakes, which have much less residue. Be aware of how fast your body responds to eating. If you know that you can expect lots of stoma activity about two hours after eating, time your meal so that you won’t have to deal with a pouch approaching its capacity at an inopportune time. Similarly, urostomates may want to consider temporarily adjusting their rate of fluid intake for a short time. The caution here is that urostomates should consume plenty of fluids during the day. This technique is not advisable for periods of more than a couple of hours. Ostomates shouldn’t skip meals before going out socially. In general, the less an ostomate eats, the more gas, he or she will produce, with its attendant problems. Actually, a quick arm across the stoma will usually silence if it is operating at the wrong time.


THE FUNGUS AMONG US!
By Kathy Dahn, RN, Riverside HealthCare Via: Kankakee Ostomy Association
My patients frequently tell me how good it feels when I remove the ostomy appliance and bathe the skin around the stoma with warm soapy water. A bit of itchiness at that point is normal. What is not normal is to have severe itching under the appliance while you are still wearing it. There can be several reasons for this but one of the most common is a fungal infection. This is not a cause for panic!! Many people worry that having a fungal infection indicates they are not clean and that is simply not the case. Fungus thrives where it is warm and dark and moist—a great description of the environment under an ostomy appliance! The peristomal skin (the skin around the stoma) will usually be a “hot pink” or strawberry-red when a fungal infection is present. The skin may be intact or there may be places where the top layer of skin is missing, leaving an open wound which is red and moist (and tender). The fungal infection can be treated in different ways with the main difference being the use of a powder versus a cream product. Regardless of whether you use a powder or a cream, your appliance will probably not adhere for as long a period of time as you are used to, so beware! (My sixth grade teacher used to say, “Fore-warned is fore-armed”, so consider yourself warned!) Nystatin (Mycostatin) powder is a product that will combat the fungal infection. Powder is especially helpful when there are many areas which are open and moist. To use the powder, clean and dry the peristomal skin well, then apply a light “dusting” of the powder to the affected areas. You can place your appliance directly over the powder or you can apply a skin-prep over the powder to help achieve a tighter seal. Another method (which Karen and I frequently use) is to apply Lotrisone to the entire reddened area. Lotrisone is a combination product with clotrimazole to fight the fungus and betamethasone (steroid) to decrease the itching. By the time patients come to see us with a fungal infection, they are frequently so miserable with the constant itching that we elect to use the Lotrisone to give relief. At this point, I’m sure you’re probably thinking….but Lotrisone is a cream and the appliance will just slip right off...and you’re right! To help achieve a tighter seal, we then cover the Lotrisone with a “second skin” - Extra Thin Duoderm. Extra Thin Duoderm is just what it says it is—it is very thin and it adheres to the skin when the body heat softens the Duoderm. Skin prep can be applied over the Duoderm to increase adhesion, then the ostomy appliance can be placed in the usual fashion. The edges of the Duoderm can be secured with tape as needed. One little hint about using the Extra Thin Duoderm: if you are cutting a hole in the center to accommodate your stoma, you will need to cut the hole smaller than usual as the Duoderm tends to stretch somewhat when you remove the paper backing. There is no special amount of time that you will need to use the antifungal products. They can be discontinued once the peristomal skin looks and feels completely normal. If you have had your ostomy for years and never had a fungal infection before, you may wonder, why now? One reason is that our immune system becomes less efficient as we age. In addition, increased use of antibiotics not only kills the “bad germs” but wipes out our normal flora– the “good germs” that normally live in our body. Our normal flora help to keep the “bad germs” in check so when the normal flora is decreased; the fungus can take over—sort of a “when the cat is away, the mice will play” scenario And of course, summer heat can cause moisture under the appliance through perspiration. I hope this helps to clarify some of the confusion about “the fungus among us”.


EXERCISES AFTER SURGERY
by Barbara Hiser RNC, MBAs Via: S. Brevard FL & Heart of Iowa Support Group
When a patient has surgery, he becomes a candidate for several complications. The degree of risk depends upon the exact type of surgery, its location, how long the surgery lasted, how much pain the patient is having after surgery, how much movement the patient is able to perform after surgery, and other factors. Immediately after surgery, most patients don’t move about very much. This might be related to pain from the surgery, sleepiness from medications, the presence of tubes and dressings that make mobility difficult, and other factors. As a result, blood flow slows down, especially in the legs, and a blood clot can form. If not treated, the blood clot can become dislodged and travel to other parts of the body. Your nurses and doctors will be checking regularly for blood clots. Let them know immediately if you have any tenderness in your legs, especially in the calves. If a blood clot is suspected, special tests will be performed to confirm the diagnosis and special medications will be started to help reduce the size of the clot. This treatment complicates the hospital stay, delays the discharge, and adds additional discomfort to the patient. The following things will help to prevent blood clots. Each patient will benefit differently, depending upon the type of surgery.
1. Your doctor might order elastic stockings. The nursing staff will remove these daily for a short period of time, and then replace them.
2. Your doctor might order inflatable stockings or “booties”. They apply alternating pressure to the legs or feet to encourage blood flow. The nursing staff will remove these daily for a short period of time, then replace them.
3. You can help prevent blood clots by performing special exercises while in bed. Tighten and release the buttocks for several seconds frequently throughout the day. Move the feet up and down, as if working the gas pedal on a car. Pretend you are writing your name or leading an orchestra with your feet. Do this frequently throughout the day.
4. Call for assistance to get out of bed and walk as much as possible, and change position in bed.
Lung Complications
Immediately after surgery, most patients don’t breathe very deeply. This might be related to pain from the surgery, sleepiness from medications, the presence of tubes and dressings, all of which make breathing difficult, and other factors. As a result of slow, shallow breathing, lung complications can develop. If not treated, the lung complications can progress to pneumonia or a type of collapsed lung. Your nurses and doctors will be listening regularly to your lungs, measuring your breathing, and checking your temperature. Let them know right away if you have any trouble breathing, excess mucus, or pain in your lungs. If lung complications are suspected, special tests will be required to confirm the diagnosis and special medications will be started. This treatment complicates the hospital stay, delays discharge, and adds additional discomfort to the patient. The following things will help prevent lung complications by expanding your lungs and eliminating any after-effects of the anesthesia. Each person will benefit differently, depending upon the type of surgery:
1. The nurses will encourage you to take deep breaths every hour while you are awake, 5-10 times each.
2. The nurses will encourage you to cough several times after each series of deep breaths. Depending upon the location of your surgery, this may be uncomfortable. It will be made a bit easier by placing a pillow or folded blanket over the surgical incision and pressing gently during the cough. This is called “splinting” the incision.
3. You might be given a small plastic device to help you take deep breaths. The nurses will show you how to use it, and will encourage you to use it every hour while you are awake, 5-10 times each. Keep it near you at all times.
4. Call for assistance to get out of bed and walk as much as possible, and change position in in bed. This promotes deep breaths and allows any secretions in the lungs to be coughed up more easily.
Patient Reminders
1.
Practice your leg and foot exercises every hour while awake, 5-10 times each.
2. Practice your breathing exercises every hour while awake, 5-10 times each.
3. If you watch TV, an easy way to help you remember to do your lung and leg exercises is to practice them each time a commercial comes on!
4. If you are having pain, take your pain medication regularly, because if your pain is well-controlled you will be better able to do your exercises and move about.


PAT YOURSELF ON THE BACK
Via: Snohomish Cty Insight
Have you ever had the experience of having someone, learning about your ostomy for the first time, express amazement at your ability to live a normal life and admire your ability to carry on despite your “infirmity”? Then, have you asked yourself if you have really accomplished some miracles and overcome such difficult obstacles? We, who have been through trying times, sometimes do not realize our mettle was tested. So...lift up your chin with pride and give yourself a pat on the back once in a while. Those who have not been tested, wonder about their own ability to stand up under severe adversity, and so admire us. We have proven our ability, so we ought to occasionally take personal pride in this accomplishment.



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