Tag Archive for: Ostomy Leaks

Navigating the world of ostomy products and supplies can feel overwhelming, but finding the right system and products are crucial for comfort and security.

The appropriate pouch is determined by a number of factors says certified ostomy nurse Linda Coulter. “First the pouch must be appropriate for the type of stoma and

A nurse selects ostomy product samples donated by a wide variety of manufacturers for the stoma clinic at UOAA’s 9th National Conference.

output (e.g. don’t use a urostomy pouch for a colostomy/ileostomy and vice-versa). Stoma characteristics such as size, protrusion, and surrounding contour (e.g. scars, creases, bulges, etc.) also affect pouch choice.”

Other factors, such as an individual’s lifestyle and dexterity play a role.

Here’s some helpful tips whether you are just out of the hospital or you’re having new issues and wondering if you should try something new.

Get Professional Help and Sample Supplies

  • Always consult with an ostomy nurse first for information and recommendations tailored to your body and stoma type. If you’re having trouble with your current system, such as skin irritation or recurrent leaks, ask them to help you find a solution and assist in getting it prescribed. Find an ostomy nurse available in-person or virtually or an Outpatient Ostomy Clinic near you.
  • Remember that every person is different, and you need to find what works best for you. People in online discussions don’t always say their ostomy type ileostomy, colostomy, urostomy and that is key to know what type of supplies to use.
  • Expect some trial and error. It’s common to try several types of products until you find what works best. You can request product samples from manufacturers or a supplier that works with your insurance company. Talk with members of a UOAA Affiliated Support Group, many have a supply closet where members share excess supplies.

Picking an Ostomy Pouching System

You’ll hear the terms appliance, ostomy pouch system, ostomy pouch, or ostomy bag. They are all just referring to a device consisting of pouch and a skin barrier (wafer, baseplate or faceplate) that sticks to and protects the skin around the stoma.

Understanding the terminology will help you communicate your needs effectively. “When possible, patient preference is taken into account for things like 1-piece vs 2-piece systems, clear vs opaque pouches, and pouch brand,” says Linda Coulter, BSN, RN, CWOCN.

Types of ostomy bags or pouches ileostomy

  •  One-piece system: The skin barrier/wafer and pouch are pre-attached. When you change the pouch, you change the whole thing (including the barrier).
    Why people choose it: Simple application and use, low profile under clothing, hernia or bulge near stoma, affordability.
  • Two-piece pouching system: A two-piece system lets you change the pouch while keeping the skin barrier/wafer in place. The pouch attaches to the barrier through a flange/coupling (often a snap-style ring or possibly an adhesive connection).Why people choose it: Versatility. Can easily switch between higher capacity or shorter pouch. Allows pouch to be changed more frequently than the skin barrier. Skin barrier stays in place while pouch is changed, best for higher stoma output, skin sensitivities, fast pouch changing.

Types of Urostomy Pouches

Pouch Closures

  • Drainable (open-ended): You can empty these while they are still attached. Colostomy or ileostomy pouches: use tail closures or separate plastic
    Colostomy Bag One-Piece

    Colostomy Pouch One-Piece Closed End

    clamps/clips. Urostomy pouches (urine): use a valve or “tap closure”. As the name implies, high-output pouches are designed to hold larger volume ileostomy output (rarely colostomy) and have tap closures.
    Why people may choose it: Have output throughout the day requiring pouch to be emptied 3 or more times per day, quick and easy to empty.

  • Closed-end: These are sealed at the bottom and typically discarded after one use. They are most commonly used by colostomates who have regular elimination patterns or can irrigate. Insurance usually covers up to 2-closed pouches per day.
    Why people may choose it: Can remove and throw it away, no draining or clamps.

Other Pouch Choices

Pouch options can include filtered (for automatic gas release and odor) or unfiltered (best with thick stool). Clear pouches are available to monitor output or color and opaque pouches for those who prefer not to see it. A variety of sizes are available depending on output and lifestyle. Urostomates often attach their pouch to an additional drainage bag or container at nighttime.

Skin Barriers

Picking the best skin barrier is critical since it protects the skin around the stoma and enables a secure seal and fit. Your choice depends on your stoma, output, and other factors, such as sensitivity. Frequent changers may ask about gentle adhesion options while those with liquid output may require a stronger adhesion. If your stoma size is changing or oval you may want to get cut-to-fit or moldable skin barriers while, if it is stable and round, pre-sized are a convenient option.

  • Flat: Flat barriers sit level on the skin. Why people may choose it: When the stoma sticks out, pouching with hernia or creases.
  • Convex: Refers to a curved skin barrier (or a system/insert that creates this curve) which helps press inward on the skin next to the stoma. This can help the stoma protrude outward, which helps output go into the pouch instead of leaking under the barrier. There are a variety of depths and flexibilities available.
    Why people may choose it: When the stoma does not stick out enough, or soft tissue, skin folds/creases.

Ostomy Accessories

Depending on the person and stoma type, accessories include products such as cleaning wipes, adhesive removers, stoma powder (pectin-based, non-medicated), stoma paste or barrier ring (provides a seal around the stoma), stoma belt, scissors, wafer extenders, skin protectant wipes, and lubricating deodorant. These products can improve wear time, skin condition, and overall pouching experience.

Ask an ostomy nurse what may be helpful for you.

Keeping Track of it All

Know Your Ostomy Supplies Checklist

Know your ostomy pouching system and supplies. Once you’ve found the supplies working best for you be sure to keep track of the names, sizes and order numbers. Download the UOAA Know Your Ostomy Supplies Checklist tool to have handy as you work with your ostomy nurse, doctor, supplier or insurance to get the ostomy pouching system and accessories you need.

 

 Blog by Ed Pfueller, UOAA Director of Strategic Communications with medical review by Linda Coulter, BSN, RN, CWOCN

It happens…Speaking with Ostomates in many stages of their Ostomy journey is the best part of my role at Ostomysecrets®. A frequent topic, and cause for concern, is the dreaded LEAK. My answer is always the same, they happen to all of us; however, they should be few and far between.

Well, it happened to me. I have had my Ostomy for over twenty years, I measure time in between leaks in years at this point, not months, days or weeks. My record is five years, and I had been on a streak of almost two years.

I live in Southern California, and my husband’s side of the family lives in Las Vegas, NV. When I was first recovering from surgery, I worked very hard with my home health nurse to independently manage my ostomy so that we could make the drive to Vegas for my first Thanksgiving as an Ostomate. I reached that goal, and we had a successful trip.

We make this journey 2-3 times a year, up the Cajon Pass, across the Mojave and into the shining city of neon in the middle of the desert. I have never had any issues with my ostomy during these travels, and we’ve had so many fun adventures through the years: swimming in fancy hotel pools, attending shows and concerts, hiking, dining, stargazing and maybe a bit of gambling too.

Last week, we made the drive to Las Vegas again. I typically get 5 days wear time, so I changed my pouch the day before we left. My plan was to change my pouch again before heading back to California. In Barstow, CA – the halfway point of the journey – we stopped for a quick dinner planning to quickly get back on the road to Las Vegas. Then our plans changed.

Something did not feel right, and I discovered that my pouch had leaked. All my ostomy confidence drained from me. I tried not to panic and to focus on finding a solution. This was not an optimal situation, but Barstow is a crossroads town featuring a number of Truck Stops. I love a road trip, and something I know to be true about Truck Stops is they have showers! We happened to be right in front of one of these truck stops, so I walked in, paid my $18 and waited my turn.

My husband helped me get my suitcase, and my trusty me+ Starter Kit that I always carry my supplies in when I travel anywhere overnight. I will always be a better safe than sorry girl, and I would never leave home overnight without my supplies.

In that moment, standing in the Truck Stop shower waiting area, I was feeling very vulnerable and had tears in my eyes. I let the attendant know I was having a medical issue, and that my husband would be coming in with me to help. She immediately opened a shower for me, and got us extra towels. I was so comforted by the kindness of strangers and their willingness to make it a little easier for me.

I showered, completed my pouch change, got myself together and we got back on the road. I was rattled and feeling all of the emotions of what had just happened. The story I share, and what I know to be true, is that my Ostomy saved my life. Even in this low moment, that truth remains. When I was battling my Ulcerative Colitis diagnosis, at my worst moment, I was going to bathroom 45 times a day. Travel, road trips and adventure were just not possible; I was just too sick.

As we finished the drive through the desert, I felt doubt and anxiety creeping in. We had a big family pool party the next day, and I was worried that the remaining supplies that I had would not be enough. Would I ruin my family’s trip?

I had to quiet those thoughts. Why would this trip be any different that the countless other trips? Why would I have pouching issues? My Convatec pouching system has served me well all these years. It helps me to feel freedom and confidence to complete the adventures I so enjoy.

We ended up having a wonderful weekend! I slept soundly in our hotel bed, I swam with all of the cousins at our family BBQ, we dined out and explored The Vegas Strip. My pouch held up, working as expected and intended, and I achieved my typical five-day wear time – even with the 110 degree desert heat and pool time.

Our ostomies don’t just save our lives; they enable us to live full and happy lives. We thrive because of our ostomies and the pouching systems we rely on, not in spite of them.

My comment still stands: leaks happen to all of us, sometimes. If you are experiencing frequent leaks, please call our Convatec me + team and certified ostomy nurses. They are available to you by phone at 1-800-422-8811.

Editor’s note: This blog is from a UOAA digital sponsor, Convatec. Sponsor support along with donations from readers like you help to maintain our website and the free trusted resources of UOAA, a 501(c)(3) nonprofit organization.

Why they Happen and What to do

Elaine O’Rourke and Ostomy Nurse and Phoenix Magazine columnist Anita Prinz discuss ostomy leaks, reasons why they happen, what to do and how to help with skin breakdown. There is lots of valuable information in this interview for even those who have had their ostomies for many years. Elaine has had her ileostomy since 2005 due to Crohn’s disease and has had her fair share of leaks over the years until finding the right pouching system for her. If you are having persistent leaks then you should always consult with an ostomy nurse who can help find a solution for you.

You can find Elaine on Facebook and her “3 simple ways to overcome fears about your Ostomy” program at www.ElaineOrourke.com/ostomyprograms/