Diagnosis, Work-Up, and Management of Constipation-Predominant Irritable Bowel Syndrome
IBS-C is a positive clinical diagnosis based on Rome III criteria—recurrent abdominal pain for ≥12 weeks in the past year with at least two features: pain relief with defecation, onset associated with change in stool frequency, or onset associated with change in stool form—combined with hard stools >25% of the time and loose stools <25% of the time. 1
Diagnostic Criteria
Rome III Classification for IBS-C
- Abdominal pain is mandatory—patients with painless constipation have "functional constipation," not IBS-C. 1
- Symptoms must be present for at least 6 months before diagnosis, with criteria fulfilled for the past 3 months. 2
- Stool consistency defines the subtype: hard stools (Bristol 1-2) >25% of the time and loose stools (Bristol 6-7) <25% of the time. 1
Supportive Clinical Features
- Female sex, age <45 years, symptom duration >2 years, and frequent consultations for non-gastrointestinal complaints (lethargy, fibromyalgia, backache, urinary frequency, dyspareunia) increase diagnostic likelihood. 1
- Patients report that stress aggravates symptoms. 1
- Symptoms occur intermittently with flares lasting 2-4 days followed by remission. 1
Work-Up Algorithm
Step 1: Screen for Alarm Features
Any of the following mandates extended investigation (typically colonoscopy):
- Age ≥50 years at symptom onset 1, 3
- Unintentional weight loss 1, 3
- Rectal bleeding not attributable to hemorrhoids or anal fissures 1, 3
- Iron-deficiency anemia 1, 3
- Nocturnal diarrhea or pain that awakens the patient 1, 3
- Family history of colon cancer, inflammatory bowel disease, or celiac disease 1, 3
- Recent antibiotic use 1
- Male sex (lower threshold for investigation) 1
- Short history of symptoms 1
Step 2: Baseline Laboratory Testing (All Patients)
Perform these tests in every patient with suspected IBS-C:
- Complete blood count (CBC) to exclude anemia and inflammatory changes 1, 3, 4
- C-reactive protein (CRP) or ESR—but note that ≈20% of active Crohn's disease patients have normal CRP, so normal results do not exclude IBD. 3, 5
- Celiac serology: IgA tissue transglutaminase (IgA-tTG) plus total IgA level; if IgA-deficient, use IgG-based testing (IgG-deamidated gliadin peptide or IgG-tTG). 1, 3, 4
- Fecal calprotectin in patients <45 years with diarrhea-predominant symptoms to exclude IBD (cutoff >50 μg/g has 100% sensitivity and 97% specificity). 3, 5
- Stool testing for Giardia 1, 3
- Fecal occult blood test 1, 3
Step 3: Tests NOT Recommended
- Colonoscopy in patients <45 years with typical IBS-C symptoms and no alarm features is not cost-effective. 1, 3, 5
- Ultrasound detects incidental findings unrelated to symptoms. 3
- Hydrogen breath testing for small intestinal bacterial overgrowth is not indicated. 3
- CRP or ESR alone should not be used to screen for IBD (conditional recommendation against). 3
- Ova and parasite testing (other than Giardia) unless travel history to or recent immigration from high-risk areas. 3
- Serologic tests for IBS diagnosis have <50% sensitivity and cannot rule out IBS. 3
Step 4: When to Perform Colonoscopy
Colonoscopy is indicated when:
- Age ≥50 years (some guidelines use ≥45 years) 1, 3, 5
- Any alarm feature is present 1, 3, 5
- Family history of colorectal cancer or IBD 1, 3, 5
- Atypical or short-duration symptoms 3, 5
During colonoscopy, take biopsies from both abnormal-appearing and normal-appearing mucosa; in diarrhea-predominant patients, biopsies are essential to detect microscopic colitis even if mucosa appears normal. 3, 5
Management of IBS-C
Step 1: Patient Education and Reassurance
- Provide a clear, positive diagnosis using Rome III criteria—IBS-C is not merely a diagnosis of exclusion. 1, 3
- Explain that IBS-C is a chronic functional disorder with no increased mortality or cancer risk. 5
- Detailed explanation improves outcomes and reduces unnecessary repeat testing. 1, 3
Step 2: Dietary and Lifestyle Modifications
- Identify and eliminate common food triggers: wheat, dairy products, coffee, potatoes, corn, onions. 1, 3
- Lactose restriction only if the patient consumes >0.5 pint (≈280 mL) milk daily and has a positive lactose breath test. 1, 3
- Soluble fiber supplementation may decrease symptoms, though individual response varies. 3
- Low-FODMAP diet may reduce symptom severity. 3
Step 3: First-Line Pharmacologic Therapy
For abdominal pain:
- Antispasmodic agents (e.g., hyoscyamine, dicyclomine) 3
For constipation:
Step 4: FDA-Approved Prescription Therapies for IBS-C
If first-line therapies fail after 3-6 weeks, consider:
- Linaclotide 1, 6, 7
- Plecanatide 1, 8, 6, 7
- Lubiprostone 1, 6, 7
- Tenapanor 1, 7
- Tegaserod (reintroduced) 1, 6
These agents improve both constipation and abdominal pain and are generally well tolerated. 7
Step 5: Neuromodulators and Behavioral Therapy
For persistent abdominal pain or psychological symptoms:
- Tricyclic antidepressants (TCAs) 1
- Selective serotonin reuptake inhibitors (SSRIs) 1
- Brain-gut behavioral therapy 7
Step 6: Follow-Up and Reassessment
- Review patients 4-6 weeks after initiating therapy to assess response. 3
- Refer to gastroenterology if symptoms persist despite optimized first-line treatment (3-6 weeks), if atypical or severe symptoms develop, or if new alarm features appear. 3
- Reassess if the patient reaches ≥45-50 years with ongoing symptoms. 3
Common Pitfalls to Avoid
- Over-testing young patients (<45 years) with typical IBS-C symptoms—colonoscopy without alarm features delays appropriate care and is not cost-effective. 1, 3
- Serial repetitive testing increases anxiety and provides little diagnostic yield once a functional diagnosis is established. 1, 3
- Relying solely on patient-reported food intolerances without objective testing causes unnecessary dietary restrictions. 1, 3
- Assuming normal CRP excludes IBD—about 20% of active Crohn's disease patients have normal CRP. 3, 5
- Ignoring continuous pain—patients with continuous (not intermittent) pain likely have "functional abdominal pain," a severe condition requiring early recognition and different management. 1
- Fragmented specialist referrals for each new symptom increase patient burden; coordinated care is preferred. 3