Management of Functional Dyspepsia and Functional Abdominal Pain Disorders
Functional dyspepsia should be diagnosed clinically when patients present with bothersome epigastric pain or burning, early satiation, and/or postprandial fullness lasting more than 8 weeks without alarm features, and managed with a stepwise approach starting with H. pylori testing and eradication, followed by proton pump inhibitors, and then tricyclic antidepressants if first-line therapies fail. 1
Understanding the Condition
Functional dyspepsia is a disorder of gut-brain interaction (DGBI), not a diagnosis of exclusion or psychological condition. 1 The condition follows a chronic, fluctuating course in approximately two-thirds of patients, with no increased mortality risk but substantial impact on quality of life and work productivity. 2
Key Pathophysiologic Mechanisms to Explain to Patients:
- Altered gut-brain axis communication affecting gastric sensitivity 1
- Postinfectious changes (threefold increased odds after gastroenteritis) 2
- Impact of diet, stress, and emotional responses on symptoms 1
- Disordered gastrointestinal motility and visceral hypersensitivity 3, 4
Diagnostic Approach
Initial Clinical Diagnosis
Diagnose functional dyspepsia clinically without extensive testing when symptoms of epigastric pain/burning, early satiation, or postprandial fullness persist >8 weeks without alarm features. 1
Age-Stratified Investigation Strategy:
For patients <55 years without alarm features:
- Perform non-invasive H. pylori testing ("test and treat") 1
- Check coeliac serology only if overlapping IBS-type symptoms present 1
- Avoid routine endoscopy, gastric emptying studies, or 24-hour pH monitoring 1
For patients ≥55 years:
- Full blood count is mandatory 1
- Urgent endoscopy only if: weight loss present, OR age >40 years with family history of gastro-oesophageal cancer, OR from high-risk gastric cancer area 1, 2
- Non-urgent endoscopy if: treatment-resistant dyspepsia, raised platelet count, or persistent nausea/vomiting 1
For patients ≥60 years with abdominal pain AND weight loss:
- Urgent abdominal CT scan to exclude pancreatic cancer 1
Treatment Algorithm
Step 1: Establish Therapeutic Relationship and Lifestyle Modifications
Create an empathic doctor-patient relationship with shared understanding of the chronic nature—this reduces healthcare utilization and improves quality of life. 1, 2
- Prescribe regular aerobic exercise for all patients (strong recommendation) 1
- Advise frequent small meals and low-fat diet 5
- Recommend cessation of smoking, limiting alcohol and coffee intake 5
- Do not routinely recommend low FODMAP diet (insufficient evidence) 1
Step 2: First-Line Pharmacotherapy
H. pylori-positive patients:
- Eradicate H. pylori—this is the only therapy that may change the natural history of functional dyspepsia (strong recommendation, high-quality evidence) 1, 2, 6
- Counsel patients that adverse events are more common than control therapy 1
- Confirm eradication only in patients at increased gastric cancer risk 1
H. pylori-negative patients or persistent symptoms after eradication:
- Initiate proton pump inhibitors (PPIs) at the lowest effective dose (strong recommendation, high-quality evidence) 1, 2, 6
- No dose-response relationship exists, so avoid dose escalation 1
- Alternative: Histamine-2 receptor antagonists (weaker evidence, but well-tolerated) 1, 5
For postprandial distress syndrome (PDS) symptoms:
- Consider prokinetics after H. pylori and PPI trials 6
- Acotiamide 100 mg three times daily (weak recommendation, low-quality evidence) 6
- Alternatives: itopride (weak evidence), tegaserod (stronger evidence but limited availability) 1, 6
Step 3: Second-Line Therapy (After 4-8 Weeks of Failed First-Line Treatment)
Initiate tricyclic antidepressants (TCAs) as gut-brain neuromodulators (strong recommendation, moderate-quality evidence) 1, 2, 6
Specific dosing protocol:
- Start amitriptyline 10 mg once daily at bedtime 1, 5
- Titrate slowly to maximum 30-50 mg once daily 1
- Provide careful explanation of rationale (neuromodulation, not depression treatment) and counsel about side effects 1
Alternative second-line options:
- Sulpiride 100 mg four times daily or levosulpiride 25 mg three times daily (with careful counseling about antipsychotic side effects) 1
Step 4: Refractory or Severe Disease Management
Refer to gastroenterology when:
- Diagnostic doubt exists 1
- Symptoms are severe or refractory to first-line treatments 1
- Patient requests specialist opinion 1
For severe/refractory functional dyspepsia:
- Involve multidisciplinary support team (strong recommendation) 1
- Screen for eating disorders including avoidant restrictive food intake disorder (ARFID) if weight loss and food restriction present 1, 2
- Arrange early dietitian involvement to prevent overly restrictive diets 1, 2
- Consider cognitive behavioral therapy or other gut-brain behavioral therapies 1, 3
Critical Pitfalls to Avoid
Never prescribe opioids for functional dyspepsia—this causes iatrogenic harm (strong recommendation) 1, 2
Avoid surgery for refractory symptoms (strong recommendation) 1, 2
Do not perform repetitive or extensive investigations without alarm features—this reinforces illness behavior and provides no diagnostic yield. 1, 4
Do not dismiss symptoms as "psychological"—functional dyspepsia has demonstrable pathophysiologic mechanisms involving gut-brain interaction. 1, 3
Functional Abdominal Pain Syndrome
Functional abdominal pain syndrome represents a distinct entity from functional dyspepsia, characterized by chronic abdominal pain without specific localization to the epigastrium and without the meal-related symptoms of dyspepsia. 3
Management approach:
- Establish effective patient-physician relationship 3
- Avoid opioids entirely 3
- Consider low-dose tricyclic antidepressants for visceral hypersensitivity 3, 5
- Implement behavioral and psychological approaches, particularly cognitive behavioral therapy 3
- Utilize multidisciplinary pain management programs for chronic cases 3
Prognosis Counseling
Inform patients that functional dyspepsia follows a chronic, fluctuating course rather than progressive deterioration, with no mortality risk. 2 Even when symptoms improve, they often fluctuate to other disorders of gut-brain interaction rather than completely resolving. 2 This realistic expectation-setting, combined with empathic communication, reduces healthcare utilization and improves quality of life outcomes. 1, 2