A question I get asked often is, “How many times should I be emptying my ostomy bag?”.
Table of Contents
Introduction
Of course, just like with other questions about what’s normal when you have an ostomy, the answer may vary for each person.
In this post, I’ll go over various factors that can influence how often an ostomy bag may need to be emptied, as well as go over when to empty it.
If you are newly out of surgery, keep in mind that things will be a little crazy and your stoma may not be as consistent or predictable as it will eventually become with time.
Video
By playing the above video you agree to YouTube's Terms and Conditions and Privacy Policy
When Should You Empty Your Ostomy Bag?
Most ostomy nurses, supply manufacturers, and health websites will recommend that you empty your bag when it’s between 1/3 and 1/2 full.
I happen to agree, although I often get lazy and empty my bag when it’s more than 1/2 full. I don’t recommend waiting until your bag is too full because there are plenty of reasons why this could cause problems:
- It gets heavy. The weight of a full ostomy bag is unwieldy and uncomfortable.
- It gets bulky. Full ostomy bags are hard to keep concealed.
- Leaks are more likely to happen. Really full bags can cause leaks because of pressure and tugging.
- Emptying will be more difficult. I think most will agree that emptying 1/3 of a bag full is much easier than emptying 3/4 of a bag full!
- Pouch deodorants will fail to work. There’s only so much a few drops of liquid pouch deodorants will be able to do. If you’ve got a really full bag then expect more odor from it.
- Shit bombs aren’t fun! Ever have a two-pound bag of crap detach from your two-piece appliance and hit the floor? Let’s just say that it won’t be your proudest moment.
For me, the most difficult times to empty my bag are in the middle of the night because I can’t actively check my output while I’m asleep (no kidding, right?).
There are a few strategies to consider if you find yourself with a full bag at night or in the early morning.
- Don’t eat or drink too late at night. Some people swear by the, “don’t eat after 6 pm” rule, but the results will be different from person to person and it depends a lot on your “transit time” (the time for food to pass through your entire digestive system).
- Consider setting an alarm. Some ostomates will set an alarm to ring in the middle of the night so they can empty their bag before it gets too full. The disruption of your sleeping pattern may not be desirable.
- Wear a larger bag at night or use a night drainage bag.
- Consider medication to slow down your bowel movements. This should be discussed with your doctor, but you might be able to take something that will slow bowel movements for you at night.
Size Matters
Ostomy bags come in many different sizes, from teeny-tiny stoma caps (which really aren’t meant to hold any amount of output) to large, overnight drainage bags which are designed to hold several LITRES of output.

Obviously, the smaller the bag, the more often it’ll need to be emptied.
Many “large” bags (which are about 12″ in length) can hold about 650ml of liquid, but keep in mind that’s at maximum capacity. Smaller bags measuring 7″ may only hold 400 or 500ml of output at most, so at 1/3 full you’re looking at just over 130ml of output, which isn’t much.
I usually recommend wearing the largest size that’s comfortable to manage. That means if you’re only emptying your bag once or twice a day (i.e. you have a colostomy), there’s no reason to wear a large or XL-size bag. At the same time, if you find yourself constantly needing to empty your appliance, perhaps a small or medium bag is just not enough.
Type of Ostomy
Generally speaking, the higher up on your digestive tract your stoma is, the more output you should expect.
So someone with a jejunostomy would have more output than someone with an ileostomy. Likewise, someone with an ileostomy would have more output compared to someone who has a colostomy.
If you have a “short bowel” or have had a large part of your bowel resected, then your output frequency may be higher than normal.
Why does that happen? Well, mostly because fluids get absorbed further down (like the colon), so the more you’re missing the higher the volume of fluids will be passing through your stoma. This is why someone with an ileostomy or jejunostomy will usually have liquid output and a colostomate will often have a drier stool.
Some common expectations for various types of stomas follow below.
Colostomy
If you have a colostomy and irrigate your bowels, you might not need to empty your bag for a day or two! That’s pretty convenient! But if you aren’t irrigating your bowel then you may be emptying 1-3 times a day (or however often you would have been going to the bathroom before your surgery).
Ileostomy
Most ileostomates will empty their bag 4-10 times per day, but some may need to empty more often if they have liquid output. I find myself emptying around seven or more times per day, but I also let my bag fill up past the 1/3 mark.
Urostomy
A urostomy bag may need to be drained several times a day depending on the capacity. The volume of urine collected throughout the day should be closely matted with the volume of liquids you consume. A urostomate who drinks several liters of water should expect several liters of output in a 24h span.
Info: Visit my “What is an ostomy?” page for more information about types of ostomies.
What You Eat and How Often You Eat It
“What goes in must come out” is a nice adage that perfectly illustrates this point.
If you’re a coffee drinker, you may already notice that your stoma will be more active than when you aren’t drinking coffee. This may also true for people who drink red wine or fruit juice. Consider cutting back on foods and beverages that cause excess output if it’s something that worries you.
It also goes without saying that the greater the volume of food and beverage you consume the more output you will have. This is especially true if you’re eating fibrous, plant-based foods (like I do). If you find that eating plant-based foods cause your stoma to go wild, cut back on the amounts you’re eating in a single meal to help spread things out.
Some ileostomates and colostomates may change their diet a little to include more starch-based foods (i.e. potatoes, rice, etc.) to help slow down their bowel movements. This can be used as a long-term solution, provided you’re eating healthy foods and not only potato chips.
Info: For a list of foods that may increase your output, check out THIS article.
Other Factors
Several other factors could influence how often you’re emptying your appliance.
For example, if you are on antibiotics, you may notice that your bowel frequency is increased along with a change in the consistency of your output. This is considered a normal side-effect that often resolves itself after you’ve finished taking them.
I also tend to get a huge change in the frequency and consistency of my output when I have the flu or a cold.
Some, or all of these, may cause a change in your bowel habits:
- Stress.
- Cancer treatment.
- Antibiotic use.
- Food poisoning.
- Medication or supplement side effects.
- Active disease.
- Motility disorders.
Should You Worry?
There are a few instances where I would be concerned about the frequency of my output. Of course, always talk to your stoma nurse or doctor if you have any concerns.
Emptying Too Often
If you find yourself emptying your bag far more than have been in the past, check to see if your diet has changed recently. Even small changes in our diet can influence our bowel transit time – at least in the short-term.
If it hasn’t, I would generally wait to see if things settle down after a day or two. Sometimes, frequent stoma output tends to resolve itself without me even knowing the cause.
But if bowel movements have been increased over many days or weeks, I’d schedule a Dr’s appointment to investigate this further.
Not Emptying Enough
When I notice that I’m not emptying my bag as often as I should be in relation to the amount of food I’m consuming, the first thing I’ll do is make sure I’m getting enough fluids. Dehydration can slow things down considerably.
I’ll also try to note whether I have any pain or discomfort around my stoma, which often indicates a partial blockage.
Sudden Changes
Most short changes in bowel frequency aren’t usually a cause for concern, but if you notice any unusual or sudden changes that seem to be persistent then it’s important to monitor things more closely.
Always let your doctor or stoma nurse know of sudden changes to your bowel habits as it may indicate disease activity, which is something you’ll want to be addressed quickly.
Conclusion
As you can see, there are many factors that play a role in determining how often you’ll be emptying your ostomy bag.
While there are certain things that can make it more predictable, such as the volume of food you’re eating, expect to find your new normal after several months past surgery.
Question: What type of ostomy do you have and how often do you empty your ostomy bag?





Hello GiGi and welcome.All the thing Eric has suggested are ( of course) great ideas. This must be so frustrating. You need more help.I might suggest you also ask about nutritional support … I think its intravenous ?? Apparently more IBD patients are getting this prior to surgery now to maintain health and weight. Might not be long term solution, but worth asking about. My Primary Care doctor was surprised that I had not had this option when I was first diagnosed and lost 85 pounds in about four months. YIKES!Also, never underestimate the power of a spoonful ( or several) of peanut butter. Loaded with protein and goes down easy.All the best to you. Keep posting!
Hi I’m Gi Gi. I have a colostomy and I am very concerned about my weight. I’m petite in size and since my surgery July 2,2019 my weight is between 80 to 85 lbs. And I simply hate it!!!! My normal weight is 110/ 112lbs but I haven’t seen that in yrs. Now that I have a permanent colostomy I have been trying to find ways to gain my weight back but I empty so much. if there is someone out there that can help me please feel free to email me at godfavor777@aol.com I look fwd to it. What I’m taking now is lomotil and Imodium to slow things down but it’s not working. I also have purchased guar gum and tried it twice but havent figured out the right mixture or way to take it, need help with that. I’m just ready for a different plan, different solution. I also wanna know when will this thing slow down cause i m not getting any nutrients. It’s frustrating!!! And I hate looking like I’m some kinda drug head being skinny and all…… Thanks!
Just wanna get back to my life and living again. I workout but I think I’m hurting myself instead of helping due to lack of nutrient so I don’t do it as much. Thinking of trying casein protein. That’s something I stumbled on while searching the internet. Please help me someone!!!😥😢
@Gi Gi
Hi Gi Gi,
That sounds frustrating, but there’s always a solution.
Your history is unknown, so the slow weight gain could be a matter of not getting enough calories, or it could be health-related. You and your doctor should discuss this.
But in the meantime, consider a food diary so you can at least track your calories and nutrient intake. You’d be surprised by what you see, but it will at least point you in a direction where you may need to simply increase your caloric intake. I have an article about how I do it here: https://www.veganostomy.ca/track-nutrient-intake/
I don’t advocate for the use of products that slow down the bowel unless your doctor tells you to take it. I much prefer increasing my starch intake if I need to slow things down: potatoes, rice, pasta, etc.
Your bowels tend to adjust and slow down on their own with time, unless you have a short bowel (did you have more than your colon removed?). You are still pretty “fresh" out of surgery, so there’s still more that your body needs to adjust to.
I also suggest speaking with a registered dietitian, who can help you come up with a meal plan that satisfies your nutritional needs and also works for your stoma. This article may be helpful in finding one: https://www.veganostomy.ca/finding-registered-dietitian-ibdostomy-tips/
Best of luck!
@Gi GiHello Gigi and welcome. You are in a tough place right now, and weight loss to that extent makes you aware of just how hard furniture and the bed can really be not to mention the white circle. Please make a point of going back to your gastroenterologist and telling him also, what is going on with your bowel. GPS are good and they run interference for us sometimes but on occasion we need to go back to the GI doctor. If you have not done this already you need to go back and let him know that you are having these serious issues and how concerned you are. You are tiny to begin with so you will notice this weight loss all the more. About 12 years ago I went through my first bout of malnutrition from malabsorption and fortunately after some time, things began to improve. There are a few ways to get extra nutrition. If you can drink the nutritional drinks that you can purchase in the drugstore a good one and I’m not sure if it’s available where you live but the brand name boost is a good drink vanilla and chocolate flavour are nice try to drink them cold. Nutritional support through the doctor can come through TPN, the other is through a tube through your nose and into your stomach. Both ways have to be ordered through your doctor. Make a point of stressing to them how thin you are and how uncomfortable you are with what is happening to you. You have good reason to be concerned. Please keep us in the loop and let us know how you manage through this time. All the best Gigi try and keep your chin up. Linda
Linda—I have been drinking Boost drinks since leaving the hospital over a year ago. I was so incredibly malnourished and had a number of albumin iv’s before they would let me go and I needed to keep getting as much protein as possible and those drinks have 20g each. Plus they do taste good too. I alternate between the chocolate and the strawberry, though the strawberry is my favorite.
I too drink boost I started on them in the early 1990’s after having my first colostomy. They have been a god send and they will also help reverse some of the dreaded effects steroids have on our bones!
Hi Laurel, As far fetched as it might seem, I was just thinking this morning that I wish an ostomy nurse or even a doctor would get on this site and share their expertise with the community. Please, please consider registering an account and blessing us with your knowledge from a nursing standpoint.
Hello All, I am a certified ostomy nurse and think this site is WONDERFUL!!! I am wondering if I could have permission to reproduce your picture of when to empty the pouch. I love the color and think it would be great to use it with ostomates.
Hi Laurel,
Thanks for finding me!
Can you please email me about this request? My email address is @veganostomy.ca">info@veganostomy.ca
Regards,
Eric
Miriam, I just re-read you question. I want to add, that on occasion when Rose has a day or two off, this does happen. But, be aware of what you eat and when, and then also if what you passed before yours became quiet, has it been in the bag or not. Write it down if need be to keep track. I can tell this by colour usually. Milk will be creamy when had with a meal…V8 juice will be dark orange Beets will be pink or purple. Not to be mistaken for blood even in urine. If your bowel is on the empty side, it can take time to fill again and then work. But, also always be aware of a possible blockage. Eric has a video on blockages I believe. I get blockages a lot, and they are not fun. Painful, so it is good you are aware of what is going on. As soon as I notice a change I did not cause I try and keep track of my input, and output and also when she rolls again after a stop I caused. For me the first sign of a blockage is a quiet stoma, unless I have been out and caused it for more then one day especially if I have eaten less, or little to none. We flew to Hawaii five months after my stoma and I was terrified of the flight time. I did not want to wait in the washroom lineup at all. So I only ate once there, and very little the day ahead, but always drinking water or juice. It worked just great, but I really got things going again when on land. I am 60. Had Rose since 2008. Is this more what you need to know?Linda