Treatment of Dysmotility-Like Dyspepsia
Target treatment at the patient's most bothersome symptom using prokinetic agents for nausea/vomiting/constipation, acid suppression for epigastric pain/burning, and optimize glycemic control in diabetics, while avoiding long-term metoclopramide due to tardive dyskinesia risk. 1
Initial Assessment and Diagnosis
Before initiating treatment, establish the diagnosis and exclude organic disease:
- Document the patient's single most bothersome symptom (pain, nausea, vomiting, early satiety, bloating) as this predicts treatment response 1
- Perform endoscopy if age ≥55 years with dyspepsia, or if alarm symptoms present (weight loss, vomiting, bleeding, anemia, dysphagia) 1
- Test for H. pylori in younger patients without alarm symptoms and eradicate if positive 1
- Screen for diabetes, hypothyroidism, and celiac disease as these commonly cause secondary dysmotility 1
Critical Pitfall: Drug-Induced Dysmotility
Review and discontinue medications that impair motility, particularly opioids, anticholinergics (including cyclizine), and tricyclic antidepressants, as these are frequently overlooked contributors 1
Treatment Algorithm by Primary Symptom
For Nausea and Vomiting (Prokinetic Therapy)
First-line prokinetic options:
- Domperidone (D2 antagonist): Use with caution and QTc monitoring due to cardiac arrhythmia risk; avoid long-term use 1
- Metoclopramide: DO NOT use for more than 12 weeks due to risk of irreversible tardive dyskinesia (1 in 500 patients), especially in elderly women and diabetics 2. If used acutely, maximum 30-40 mg/day 2
- Erythromycin 900 mg/day (motilin agonist): Preferred for acute presentations but subject to tachyphylaxis; useful if absent migrating motor complexes 1, 3
- Prucalopride (5-HT4 agonist): Safer cardiac profile than withdrawn agents (cisapride, tegaserod); does not prolong QT interval 1
For Epigastric Pain/Burning
- Proton pump inhibitors (PPIs) are first-line empirical therapy after H. pylori testing 1
- Antispasmodics for colicky pain: dicycloverine, hyoscine butylbromide, mebeverine, or peppermint oil 1
- Low-dose tricyclic antidepressants (amitriptyline) for visceral hypersensitivity and pain modulation 1
For Early Satiety and Postprandial Fullness
- Dietary modifications: Small, frequent meals; avoid trigger foods including coffee 4
- Prokinetic agents as above to improve gastric accommodation 1
Special Consideration: Diabetic Gastroparesis
Optimize glycemic control aggressively as hyperglycemia directly impairs gastric motility:
- Target normoglycemia (fasting <7.8 mmol/L, postprandial <9.7 mmol/L) as this alone improves gastroparesis in many cases 1, 5, 6
- Consider insulin pump therapy for tight control 1
- Prokinetics are needed in up to 80% of diabetic patients despite optimal glucose control 5
- Erythromycin is first choice for acute symptoms; cisapride was effective but withdrawn 3, 7
Diabetic Gastroparesis Prevalence
Note that 55-75% of type 1 diabetics and 15-20% of type 2 diabetics with long-standing disease develop impaired gastric emptying, though many are asymptomatic 5, 6
Medications to Avoid
Never use these drugs long-term or in combination:
- Metoclopramide >12 weeks: Risk of permanent tardive dyskinesia increases with duration and cumulative dose 2
- Opioids: Cause narcotic bowel syndrome with worsening pain despite escalating doses; consider supervised withdrawal with pain specialist 1
- Cyclizine and anticholinergics: Directly impair motility 1
Adjunctive Treatments
- Antibiotics for bacterial overgrowth: rifaximin, amoxicillin-clavulanate, or ciprofloxacin if suspected 1
- Antiemetics: ondansetron (5-HT3 antagonist) for refractory nausea 1
- Nutritional support: Oral supplements first; if inadequate, consider nasojejunal feeding, then parenteral nutrition if jejunal feeding fails 1
When to Refer to Gastroenterology
Refer for specialist evaluation when:
- Symptoms are severe or refractory to first-line treatments 1
- Diagnostic uncertainty exists 1
- Need for physiologic testing (gastric emptying scintigraphy, manometry, accommodation studies) 1, 8
- Consideration of full-thickness jejunal biopsy to diagnose myopathy or neuropathy 1
Key Clinical Pearls
- Symptom subgroups (ulcer-like, reflux-like, dysmotility-like) do NOT predict underlying pathology in uninvestigated dyspepsia and should not guide initial management 1
- Most patients with objectively measured dysmotility are asymptomatic, while symptomatic patients usually have demonstrable motor disturbances 6
- Hyperglycemia and hyperinsulinemia both impair motility independent of neuropathy 6
- Psychosocial factors significantly impact treatment success; address these early 1