IBS Diagnosis and Management
Making the Diagnosis
IBS should be diagnosed as a positive, symptom-based diagnosis—not a diagnosis of exclusion—when patients meet Rome IV criteria and lack alarm features. 1
Core Diagnostic Criteria
The diagnosis requires recurrent abdominal pain at least 1 day per week in the last 3 months, associated with two or more of the following: 1
- Pain relieved by defecation
- Pain associated with change in stool frequency
- Pain associated with change in stool consistency
Symptoms must have onset at least 6 months prior to diagnosis. 1
Essential History Elements
Cardinal symptoms to confirm: 1
- Relationship between abdominal pain and bowel habit changes (this is the defining feature)
- Stool pattern using Bristol stool chart on days when stools are abnormal
- Presence of bloating (highly suggestive when present, though not required)
Additional supportive features that strengthen the diagnosis: 1
- Female sex, age <45 years
- Symptom duration >2 years
- Frequent past consultations for non-gastrointestinal symptoms
- Patient reports stress aggravates symptoms
- Extraintestinal symptoms: back pain, urological symptoms, gynecological symptoms, fibromyalgia, tension headache, chronic fatigue
- History of postinfectious onset, recurrent antibiotic use, or acute/chronic stress
Alarm Features Requiring Further Investigation
Immediately refer for colonoscopy or imaging if any of these are present: 1
- Age >50 years with new onset symptoms
- Unintentional weight loss
- Rectal bleeding or bloody diarrhea
- Nocturnal diarrhea or abdominal pain
- Anemia
- Family history of colon cancer or inflammatory bowel disease
- Short symptom duration (<6 months)
- Recent antibiotic use (raises concern for infection)
Baseline Investigations
Required for all patients in primary care or at first secondary care appointment: 1
- Full blood count
- C-reactive protein or erythrocyte sedimentation rate
- Coeliac serology
- Faecal calprotectin (if diarrhea present AND age <45 years)
Interpreting Faecal Calprotectin
- If ≥250 μg/g: High suspicion for IBD, proceed directly to colonoscopy
- If 100-249 μg/g: Repeat test off NSAIDs and proton pump inhibitors; refer for colonoscopy if remains elevated
- If normal: Proceed with IBS diagnosis
When to Consider Additional Testing
For IBS-D with atypical features (nocturnal diarrhea, prior cholecystectomy): 1
- SeHCAT scanning or serum 7α-hydroxy-4-cholesten-3-one to exclude bile acid diarrhea
- Between 25-33% of suspected IBS-D patients have abnormal bile acid retention
- Response to bile acid sequestrants is higher with retention <10% or <5%
For IBS-D to exclude microscopic colitis, consider colonoscopy with biopsies if: 1
- Female sex
- Age ≥50 years
- Coexistent autoimmune disease
- Nocturnal or severe watery diarrhea
- Duration of diarrhea <12 months
- Weight loss
- Use of NSAIDs, PPIs, SSRIs, or statins
Colonoscopy has extremely low yield otherwise and provides no reassurance benefit to patients. 1
Subtype Classification
Based solely on stool consistency using Bristol stool chart: 1
- IBS-C (constipation): Hard stools >25% of the time AND loose stools <25% of the time
- IBS-D (diarrhea): Loose stools >25% of the time AND hard stools <25% of the time
- IBS-M (mixed): Both hard and loose stools >25% of the time
- IBS-U (unclassified): Neither loose nor hard stools >25% of the time
Communicating the Diagnosis
After completing the clinical assessment, confidently communicate a positive diagnosis of IBS based on symptoms. 1
Key Educational Points to Convey
- IBS is a disorder of gut-brain interaction involving visceral hypersensitivity
- It is a chronic condition with fluctuating symptoms triggered by stress, illness, drugs, and eating
- IBS does not increase risk of cancer or mortality
- Quality of life impairment equals that of organic diseases like IBD
- Cure is unlikely, but substantial improvement in symptoms and quality of life is achievable
- Treatment targets the gut-brain axis through dietary, pharmacological, and psychological approaches
Initial Treatment Approach
First-Line Management for All Patients
Lifestyle modifications: 2
- Regular physical exercise (benefits last up to 5 years)
- Establish regular times for defecation
- Implement proper sleep hygiene
Dietary interventions: 2
- Provide standard first-line dietary advice
- Start soluble fiber supplementation (ispaghula 3-4g/day, gradually increase)
- Avoid insoluble fiber (wheat bran) as it may worsen symptoms
- Consider low FODMAP diet as second-line under dietitian supervision
Symptom-Directed Pharmacotherapy
For IBS-D (diarrhea-predominant): 1, 2
- First-line: Loperamide 2-4 mg up to four times daily, carefully titrated
- Second-line: Rifaximin 550 mg three times daily for 14 days (47% response rate vs 39% placebo for combined pain and stool improvement)
- Alternatives: Ondansetron or ramosetron
For IBS-C (constipation-predominant): 1
- Increase dietary fiber to 25 g/day
- Osmotic laxatives if fiber insufficient
- First-line: Antispasmodics (anticholinergics) or peppermint oil, particularly when meal-related
- Second-line: Low-dose tricyclic antidepressants if antispasmodics fail (provides dual benefit for pain and sleep)
For IBS-M (mixed type): 2
- Antispasmodics for pain relief
- SSRIs for global symptom improvement
- Consider psychological therapy early
Severe IBS-D: Alosetron Considerations
Alosetron is indicated ONLY for women with severe diarrhea-predominant IBS who have: 3
- Chronic symptoms (≥6 months duration)
- Excluded anatomic/biochemical GI abnormalities
- Failed conventional therapy
- Severe IBS defined as diarrhea PLUS ≥1 of: frequent/severe abdominal pain, frequent urgency/fecal incontinence, or disability restricting daily activities
Dosing: 3
- Start 0.5 mg twice daily
- May increase to 1 mg twice daily after 4 weeks if well-tolerated but inadequate control
- Discontinue if no adequate control after 4 weeks at 1 mg twice daily
Critical safety warnings: 3
- Contraindicated if constipation present at baseline, history of chronic/severe constipation, ischemic colitis, impaired intestinal circulation, severe hepatic impairment, or concomitant fluvoxamine use
- Discontinue immediately if constipation develops (29% incidence at 1 mg twice daily)
- Discontinue immediately if signs of ischemic colitis occur (rectal bleeding, bloody diarrhea, new/worsening abdominal pain)
- Serious complications include obstruction, ileus, impaction, toxic megacolon, perforation, and death
- Risk increased in elderly, debilitated patients, or those on medications decreasing bowel motility
Psychological Interventions
Consider early in treatment algorithm, particularly with psychological comorbidity: 2
- Cognitive behavioral therapy
- Gut-directed hypnotherapy
- Mindfulness-based stress reduction
- Brain-gut behavioral therapies improve quality of life by 32-39% compared to controls
For frequent or severe pain, or comorbid depression/anxiety: 1, 2
- Tricyclic antidepressants at low doses
- SSRIs at therapeutic doses for those with established mood disorders
Follow-Up and Monitoring
Reassess after 4-6 weeks of initial treatment: 2
- Evaluate both gastrointestinal and psychological symptoms
- Adjust treatment based on symptom evolution
- If no improvement with first-line therapies, consider testing for specific dysfunctions (rectal evacuation disorder, abnormal colonic transit, bile acid diarrhea)
Common Pitfalls to Avoid
- Treating IBS as diagnosis of exclusion rather than positive symptom-based diagnosis
- Ordering colonoscopy in patients without alarm features (provides no benefit)
- Focusing only on GI symptoms while neglecting psychological factors
- Overreliance on medications without addressing lifestyle and dietary factors
- Implementing restrictive diets without proper dietitian supervision
- Using low-dose TCAs as monotherapy in patients with established mood disorders
- Failing to recognize that up to 80% of IBS patients report at least one alarm symptom (modest diagnostic performance)