Alfi Surgery /English edition
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From Clinic to Recovery · First Edition

Chapter 14 — Colorectal Surgery and Living with a Stoma

Dr. Tamer Rushdy Elalfy · 20 min read

In this chapter
  1. 14.1 Common reasons for bowel surgery
  2. 14.2 Explaining a stoma
  3. 14.3 The psychological journey
  4. 14.4 Supporting adjustment
  5. 14.5 Faith and the stoma
  6. 14.6 Intimacy and relationships
  7. 14.7 Before the operation
  8. 14.8 After the operation
  9. 14.9 Reversal and bowel function afterward
  10. 14.10 Material risks
  11. 14.11 Consent checklist
  12. 14.12 Warning signs
  13. References

Bowel surgery is performed for cancer, diverticular disease, inflammatory bowel disease, and emergencies such as obstruction or perforation. For many patients the operation itself is not what they fear most. It is the possibility of a stoma: an opening of the bowel on the abdomen, with a pouch to collect waste. A stoma touches body image, intimacy, cleanliness, religious practice, work, and how a person believes others see them. Most people adapt well with good preparation and support, but depressive symptoms affect almost half of patients after stoma surgery [1]. This chapter covers the counseling for colorectal surgery, with particular emphasis on the psychological care of the person with a stoma.

Learning objectives

After reading this chapter you should be able to:

  • Explain bowel surgery and the reasons for a temporary or permanent stoma in plain language.

  • Describe the emotional journey of a person with a stoma and the support that helps at each stage.

  • Prepare patients before surgery with stoma nurse counseling, site marking, and involvement of family as the patient wishes.

  • Address body image, intimacy, work, and faith, including prayer, ablution, and fasting, with sensitivity.

  • Screen for low mood and act on it, and teach the physical warning signs of stoma problems.

Table 14.1. Colorectal surgery and stomas at a glance.

At a glance
Common operationsRight or left colectomy; anterior resection of the rectum; abdominoperineal resection; emergency resection (Hartmann’s procedure)
When a stoma is madeTo protect a low join (temporary ileostomy); when a join is unsafe (temporary colostomy); when the anus is removed (permanent colostomy)
Hospital stayUsually 3 to 7 days with enhanced recovery
Risks every patient should hearLeak from the join, infection, ileus, stoma problems, dehydration, change in bowel function after reversal, and low mood
The key counseling message“A stoma changes how your body works, not who you are. Most people return to work, family life, prayer, and travel, and we will support you every step.”

STEP 1 Explaining the operation and the stoma

14.1 Common reasons for bowel surgery

For bowel cancer, the operation is planned by the multidisciplinary team and may follow or precede chemotherapy or radiotherapy; breaking the news is covered in Section 1.7. For diverticulitis, the decision about elective resection is individualized according to the patient’s symptoms, complications, and quality of life, rather than the number of past episodes [2]. Inflammatory bowel disease and emergency operations raise the possibility of a stoma with little warning. All planned operations follow the enhanced recovery principles of Chapter 2, and preoperative education, including stoma education, shortens recovery [3].

14.2 Explaining a stoma

Explain what a stoma is, why it may be needed, which type is likely, and whether it is expected to be temporary or permanent (Figure 14.1). When a stoma is possible rather than certain, say so, and prepare the patient as though it will be made. Patients woken from an emergency operation with an unexpected stoma find adjustment much harder.

[Figure — diagram omitted in this text edition; see the figure caption below and the Word chapter file for the image]

Figure 14.1. Ileostomy and colostomy compared, for use with patients.

Script: explaining a stoma

What it is. “A stoma is where the end of the bowel is brought out through a small opening on your tummy. It looks pink and moist, like the inside of your mouth. It has no feeling. A soft pouch sticks to the skin around it and collects what would normally pass from your back passage.”

Why. “In your case, we may need a stoma to let the join in your bowel heal safely. We expect it to be temporary, and to close it in a smaller operation, usually after a few months.”

What it means for daily life. “Modern pouches are flat, discreet, and odor-proof. People with stomas work, pray, travel, swim, and have intimate relationships. Our stoma nurse will meet you before the operation, mark the best place for it, and teach you everything you need.”

Feelings. “Many people feel shocked or upset at first. That is normal, and it usually gets easier. Please tell us how you are feeling, because we can help with that too.”

14.3 The psychological journey

Adjustment to a stoma follows a recognizable path (Figure 14.2). Before surgery, patients fear disfigurement, smell, and rejection. The first sight of the stoma can cause shock, disgust, or grief, and some patients refuse to look at it or touch it for days. In the first weeks at home, leaks, noise, and fear of odor lead some people to withdraw from family, work, and the mosque. Most adapt over months, but a substantial minority remain anxious, low, or isolated. In a meta-analysis, depressive symptoms were present in almost half of patients after stoma surgery, more often than in comparable patients without a stoma [1].

[Figure — diagram omitted in this text edition; see the figure caption below and the Word chapter file for the image]

Figure 14.2. The emotional journey with a stoma, and what helps at each stage.

Several factors make adjustment harder: an unexpected or emergency stoma, a permanent stoma, a poorly sited stoma that leaks, lack of confidence in self-care, an unsupportive partner, and cultural or religious concern about cleanliness. Several things make it easier: preoperative counseling and site marking, early hands-on teaching, a peer who has lived with a stoma, and a partner or family member who is involved and accepting.

14.4 Supporting adjustment

  • Before surgery. Every patient who may need a stoma should see a stoma nurse for counseling and marking of the stoma site, which improves outcomes and quality of life [4]. Offer a meeting with a trained volunteer who has a stoma.
  • Family. Ask the patient whom they want involved. A spouse who learns stoma care alongside the patient, and who is not shocked by it, is one of the strongest supports. Respect a patient who prefers to keep it private.

  • The first look. Plan the first look with the nurse, at a time the patient chooses. Staff should keep calm, neutral expressions while handling the stoma; patients watch faces closely.

  • Self-care. Aim for independence in emptying and changing the pouch before discharge. Confidence in self-care is closely linked to adjustment.

  • Practical fixes for fears. Odor filters and deodorants, emptying before outings, pouch covers, high-waisted underwear, and a small kit for travel address the commonest worries.

  • Screening. Ask about mood at every visit, using simple questions or a validated tool, and refer for psychological support when needed.

Words that help and words that hurt

Avoid: “bag” said with distaste; “dirty”; “disabled”; a visible reaction to smell or appearance; “you will get used to it.”

Prefer: “pouch” or “appliance”; “your stoma looks healthy”; “many people feel like this at first”; “what worries you most about it?”

Ask, do not assume: “How are you feeling about your stoma?” “Has it changed how you go out or see people?” “Is there anything you have stopped doing because of it?”

Caution: screening for low mood and self-harm

Ask at every follow-up: “Over the last two weeks, have you often felt down, depressed, or hopeless? Have you lost interest or pleasure in doing things?” If the answer is yes, ask more, and refer for psychological assessment. If a patient expresses thoughts of self-harm or that life is not worth living, do not leave it for the next appointment: arrange same-day assessment according to your hospital’s policy.

14.5 Faith and the stoma

For Muslim patients, the stoma raises immediate questions about ritual purity, prayer, fasting, and pilgrimage, and these concerns are a major reason for lower quality of life after stoma surgery [5]. Many patients are reluctant to ask, and many clinicians do not raise the subject. Reviews of Islamic scholarly opinion conclude that a person with a stoma can perform ablution and pray, attend the mosque, and perform Hajj and Umrah, and may fast when it is medically safe; the stoma is generally treated like other continuous conditions, so ablution is performed for each prayer time [5]. Religion-specific counseling before and after surgery improves quality of life [5].

Practical guidance for prayer and fasting

  • Empty the pouch and clean around it before ablution; then perform ablution and pray. A fresh pouch or a pouch cover gives confidence.

  • Keep a clean set of prayer clothes available, and a small kit when going to the mosque.

  • Colostomy: fasting is usually possible once recovered. Ileostomy: fasting carries a real risk of dehydration; plan fluids and salt between iftar and suhoor, and stop fasting if dizzy or output is high.

  • Hajj and Umrah: take extra supplies, carry them in hand luggage, and plan for heat and dehydration.

  • Refer patients to a religious adviser or imam when they wish, and use resources from Muslim ostomy associations where available.

14.6 Intimacy and relationships

Fear of rejection by a spouse is one of the deepest worries, and one that patients rarely raise. Ask gently, with the patient alone, and offer practical advice: emptying the pouch beforehand, using a small or opaque pouch or a cover, and choosing positions that avoid pressure on the stoma. Rectal surgery can affect the pelvic nerves, causing erectile or ejaculatory problems in men and pain or dryness in women; discuss this before surgery and offer referral if it occurs. Pregnancy is possible with a stoma, with specialist support.

STEP 2 Preparation, medicines, and recovery

14.7 Before the operation

  • Stoma counseling and site marking by the stoma nurse, with the patient sitting, standing, and bending, and with their usual clothes and belt line in mind [4].

  • Bowel preparation and antibiotics according to the unit protocol.

  • Enhanced recovery as in Chapter 2: carbohydrate and fluid advice, early mobilization, and early feeding.

  • Medicines. Blood thinners, diabetes medicines, and weight-loss injections need individual plans (Chapters 18, 22, and 23).

  • Supplies. Make sure the patient knows how to obtain stoma supplies after discharge, including in other cities or when traveling.

14.8 After the operation

The stoma is swollen at first and shrinks over about six weeks, so the pouch size needs adjusting. An ileostomy produces liquid output, and high output can cause dehydration and kidney injury; teach patients to measure output, drink oral rehydration solution rather than only plain water, add salt, and seek help if output is high or they feel dizzy. Before discharge, the patient or a family member should be able to empty and change the pouch, and should know how to contact the stoma nurse.

14.9 Reversal and bowel function afterward

A temporary stoma is usually closed after the join has healed, often after a few months or after chemotherapy. Not every temporary stoma is reversed, because of complications, further treatment, or the patient’s health, and patients should know this [unit data]. After reversal of a stoma that protected a low rectal join, bowel function often changes, with urgency, frequency, clustering, or incontinence, known as low anterior resection syndrome. Major symptoms affect about 41 in 100 patients [6]. They often improve over the first one to two years, and treatments are available. Some patients with severe symptoms prefer to keep or return to a stoma.

Table 14.2. Typical recovery after bowel surgery with a stoma.

ActivityUsually fromNotes
WalkingThe first dayWalk several times a day
ShoweringDay 2You can shower with or without the pouch on
DrivingAbout 3 to 4 weeksWhen you can brake firmly without pain
Office workAbout 4 to 6 weeksLonger if chemotherapy follows
LiftingLight from the start; heavy after about 3 monthsA support belt may help reduce the risk of a hernia around the stoma
SwimmingAfter about 6 weeksModern pouches are waterproof
PrayerFrom the first dayEmpty the pouch and clean the area before ablution
Ramadan fastingAfter recoveryUsually possible with a colostomy; take care with an ileostomy because of dehydration
IntimacyWhen you feel readyEmpty the pouch first; a cover or smaller pouch may help

STEP 3 Questions patients ask

“Will people be able to smell it?”

No. Modern pouches are sealed and have odor filters. You will notice a smell only when emptying or changing it, as with going to the toilet.

“Will my husband or wife still find me attractive?”

Most couples adjust well, especially when the partner is involved from the start. Many people find their partner is more accepting than they feared. If you would like, we can talk with both of you together.

“Can I still pray?”

Yes. Scholars agree that you can perform ablution and pray, and go to the mosque. Empty the pouch and clean around it before ablution, and perform ablution for each prayer time [5].

“Can I fast in Ramadan or go for Umrah or Hajj?”

Many people do. With a colostomy, fasting is usually possible once you have recovered. With an ileostomy, there is a risk of dehydration, so plan with us first. For pilgrimage, take plenty of supplies and plan for the heat [5].

“Can I wear normal clothes, swim, and exercise?”

Yes. Most people wear their usual clothes. Pouches are waterproof, and you can swim and exercise once recovered.

“Will I be able to work?”

Most people return to their usual work. If your work involves heavy lifting, we will discuss a support belt and a gradual return.

“I cannot look at it. Is something wrong with me?”

No. Many people feel this way at first. We will go at your pace, and most people find it gets easier within days or weeks.

“Should I tell people about it?”

That is your choice. Some people tell only close family; others are open. There is no right answer.

“Will my stoma definitely be reversed?”

We plan to reverse a temporary stoma, but not every one is closed, sometimes because of other treatment or health problems. We will review this with you.

“What will my bowels be like after reversal?”

After surgery low in the rectum, many people have frequent or urgent bowel movements at first. About 4 in 10 have major symptoms [6], which often improve over a year or two, and there are treatments.

“Can I have children?”

Yes. Pregnancy is possible with a stoma. Tell your team early so that we can support you.

STEP 4 Risks, warning signs, and consent

14.10 Material risks

Table 14.3. Material risks of colorectal surgery and stomas. Square brackets mark figures to replace with unit data.

BandRiskTypical frequencyExample wording
CommonDepressive symptoms after stoma surgeryAlmost half of patients [1]“Many people feel low after a stoma. Please tell us, because help is available.”
CommonSore skin around the stoma; pouch leaks[unit data]“Sore skin is the most common stoma problem. The nurse can usually fix it quickly.”
CommonChange in bowel function after reversal of a low joinMajor symptoms in about 41 in 100 [6]“About 4 in 10 have major bowel symptoms after reversal, often improving with time.”
Less commonLeak from the bowel join[unit data]“Rarely, the join leaks and needs a drain or another operation.”
Less commonHigh output and dehydration with an ileostomy[unit data]“If the output is very high, you can become dry and need fluids.”
Less commonHernia around the stoma, prolapse, or narrowing[unit data]“A bulge can develop around the stoma over time.”
Less commonTemporary stoma not reversed[unit data]“Not every temporary stoma is closed.”
Rare but seriousPoor blood supply to the stoma; bleeding; blood clots; death[unit data]“Rarely, the stoma loses its blood supply and needs urgent surgery.”

Before the patient signs

☐ Operation explained, including whether a stoma is planned, possible, temporary, or permanent.

☐ Stoma nurse counseling and site marking done; peer visitor offered.

☐ Psychological effects discussed openly, with permission to talk about feelings.

☐ Faith concerns asked about and addressed: prayer, ablution, fasting, and pilgrimage.

☐ Intimacy and possible nerve effects discussed privately.

☐ Risks from Table 14.3 explained, including leak, dehydration, reversal, and bowel function afterward.

☐ Family involvement agreed according to the patient’s wishes.

☐ Who will perform the operation, including trainee involvement under supervision.

☐ Teach-back done; patient guide and stoma supplies plan given.

14.12 Warning signs

Table 14.4. Green, amber, and red warning signs after bowel surgery and with a stoma.

LevelSigns after bowel surgery or with a stomaWhat to do
Green

A swollen stoma in the first weeks, shrinking gradually

Small spots of blood when cleaning the stoma

Feeling emotional or tearful in the first weeks

Expected. Follow the guide and talk to your stoma nurse.
Amber

Sore, red, or broken skin around the stoma, or frequent leaks

Ileostomy output above about 1.5 liters a day, or very watery

A bulge around the stoma

Feeling low most days, or avoiding people

Call the stoma nurse or clinic the same day.
Red

A stoma that turns dark red, purple, or black

No output for 24 hours with pain, bloating, or vomiting

Dizziness, little urine, or confusion with high output

Fever with increasing tummy pain

Thoughts of harming yourself

Go to the emergency department now, or call for urgent help.

Key points

  • Prepare every patient who may need a stoma, with stoma nurse counseling and site marking, even when the stoma is only possible.

  • Expect strong feelings: depressive symptoms affect almost half of patients after stoma surgery. Ask about mood at every visit.

  • Involve the partner or family as the patient wishes; staff reactions during the first look matter.

  • Address faith directly: patients can pray, attend the mosque, perform pilgrimage, and fast when medically safe.

  • Teach ileostomy patients to recognize and prevent dehydration.

  • Before reversal, explain that bowel function may change, with major symptoms in about 4 in 10 after low rectal surgery.

STEP 5 Patient education guide

The following pages may be photocopied and given to patients. Tick the type of stoma, and add your unit’s name, the stoma nurse’s phone number, and the review date before use.

PATIENT GUIDE

Living with Your Stoma

For you and your family. Your stoma nurse will go through it with you.

Your stoma

☐ Ileostomy (small bowel)

☐ Colostomy (large bowel)

☐ Temporary: we plan to close it in about ______ months

☐ Permanent

Your feelings are normal

  • Many people feel shocked, sad, angry, or embarrassed at first. This usually gets easier with time.

  • Take your time to look at and touch your stoma. Your nurse will help you.

  • Talk to someone you trust: your spouse, a family member, your nurse, or someone who has a stoma.

  • If you feel low most days, lose interest in things, or avoid people, tell us. Help is available.

  • If you have thoughts of harming yourself, get help the same day.

1. Looking after your stoma

  • Empty the pouch when it is one-third to half full.

  • Change it as your nurse showed you. Measure the stoma for the first weeks, because it shrinks.

  • Clean the skin with warm water and dry it well. Do not use soap or cream unless your nurse advises.

  • Order supplies before you run out. Supplier: ______________________

2. Food and drink

  • Eat small, regular meals and chew well.

  • Ileostomy: drink at least 1.5 to 2 liters a day, including oral rehydration drinks, and add a little salt to food. Measure your output if asked.

  • Some foods cause gas or odor, such as onions, eggs, and fizzy drinks. Try foods one at a time.

3. Prayer, fasting, and pilgrimage

  • You can perform ablution and pray, and go to the mosque.

  • Empty the pouch and clean around it before ablution. Keep clean prayer clothes ready.

  • Ask us before fasting, especially with an ileostomy.

  • For Umrah or Hajj, take extra supplies in your hand luggage and drink plenty.

  • You can talk to an imam or religious adviser if you wish.

4. Clothes, intimacy, and daily life

  • Most people wear their usual clothes.

  • Before intimacy, empty the pouch. A cover or smaller pouch may help you feel more confident.

  • You can shower, swim, exercise, and travel once recovered.

5. Getting back to normal

ActivityUsually from
WalkingThe first day. Walk more each day.
DrivingAbout 3 to 4 weeks
Office workAbout 4 to 6 weeks
Heavy liftingAfter about 3 months. Ask about a support belt.
SwimmingAfter about 6 weeks
PrayerFrom the first day

6. Follow-up

  • Your stoma nurse appointment: ______________________

  • Your surgeon appointment: ______________________

  • Support group or stoma visitor: ______________________

7. Warning signs: when to get help

LevelWhat you noticeWhat to do
GREENSwollen stoma in the first weeks; small spots of blood when cleaning; feeling emotionalThis is normal. Talk to your stoma nurse.
AMBERSore or broken skin; frequent leaks; very watery or high output; a bulge around the stoma; feeling low most daysCall your stoma nurse today.
REDStoma turns dark, purple, or black; no output for 24 hours with pain or vomiting; dizzy with little urine; fever with tummy pain; thoughts of harming yourselfGo to the emergency department now, or call for urgent help.

My contacts

Stoma nurse: ______________________ Hours: ______________

Out of hours: ______________________

My questions: ____________________________________________________________

[Unit name] [Guide version and review date]

References

1. Kovoor JG, Jacobsen JHW, Stretton B, et al. Depression after stoma surgery: a systematic review and meta-analysis. BMC Psychiatry. 2023;23:352.

2. Hall J, Hardiman K, Lee S, et al. The American Society of Colon and Rectal Surgeons clinical practice guidelines for the treatment of left-sided colonic diverticulitis. Dis Colon Rectum. 2020;63(6):728-747.

3. Gustafsson UO, Rockall TA, Wexner S, et al. Guidelines for perioperative care in elective colorectal surgery: Enhanced Recovery After Surgery (ERAS) Society recommendations 2025. Surgery. 2025;184:109397. doi:10.1016/j.surg.2025.109397

4. Hendren S, Hammond K, Glasgow SC, et al. Clinical practice guidelines for ostomy surgery. Dis Colon Rectum. 2015;58(4):375-387.

5. Iqbal F, Kujan O, Bowley DM, Keighley MRB, Vaizey CJ. Quality of life after ostomy surgery in Muslim patients: a systematic review of the literature and suggestions for clinical practice. J Wound Ostomy Continence Nurs. 2016;43(4):385-391.

6. Croese AD, Lonie JM, Trollope AF, Vangaveti VN, Ho YH. A meta-analysis of the prevalence of low anterior resection syndrome and systematic review of risk factors. Int J Surg. 2018;56:234-241.

Note: references are numbered within this chapter for the pilot. Items marked in square brackets are collected in the Author Fill-in and Verification Log.