Treatment Options for Gastroparesis
The first-line treatment for gastroparesis is metoclopramide at a dose of 10 mg orally, 30 minutes before meals and at bedtime, as it is the only FDA-approved medication for this condition. 1
Pharmacological Management
Prokinetic Agents
Metoclopramide: 10 mg orally, 30 minutes before meals and at bedtime 1, 2
- FDA-approved specifically for gastroparesis
- Limited to 12 weeks of use due to risk of tardive dyskinesia
- For severe symptoms, may begin with injectable form before transitioning to oral 2
Erythromycin: 40-250 mg orally 3 times daily 1
- Alternative first-line agent
- Limitations include antibiotic resistance and tachyphylaxis (diminishing response with continued use)
Antiemetic Medications
5-HT3 receptor antagonists:
- Ondansetron: 4-8 mg 2-3 times daily
- Granisetron: 1 mg twice daily or 34.3 mg patch weekly 1
Phenothiazines:
- Prochlorperazine: 5-10 mg 4 times daily
- Chlorpromazine: 10-25 mg 3-4 times daily 1
Antihistamines:
- Meclizine: 12.5-25 mg 3 times daily
- Scopolamine: 1.5 mg patch every 3 days 1
NK-1 receptor antagonists:
- Aprepitant: 80 mg daily
- Tradipitant: 85 mg daily (particularly effective for nausea in idiopathic gastroparesis) 1
Neuromodulators for Pain and Symptom Control
Tricyclic antidepressants:
- Amitriptyline: 25-100 mg daily
- Nortriptyline: 25-100 mg daily (secondary amines have fewer side effects) 1
SNRIs:
- Duloxetine: 60-120 mg daily 1
Anticonvulsants:
- Gabapentin: >1200 mg daily in divided doses
- Pregabalin: 100-300 mg daily in divided doses 1
Nutritional and Dietary Management
Dietary Modifications
- Eat small, frequent meals (5-6 per day) that are low in fat and fiber 1
- Increase liquid calories and foods with small particle size
- Focus on complex carbohydrates for sustained energy
- Avoid carbonated beverages, alcohol, and smoking
- Consider energy-dense liquids for easier digestion 1
Stepwise Nutritional Approach
- Start with solid food with modifications
- Progress to blended/pureed foods if needed
- Transition to liquid diet with oral nutritional supplements
- Consider enteral nutrition via jejunostomy tube for severe cases 1
Interventional Therapies
Gastric electrical stimulation: Consider for medication-refractory symptoms
- Goals: Reduce weekly vomiting frequency and need for nutritional supplementation 1
- Based on moderate strength of evidence from clinical trials
Enteral feeding: Via jejunostomy tube when oral intake is inadequate 1, 3
Venting gastrostomy: Second-line approach for symptom relief 3
Management of Comorbid Conditions
Diabetes Management
- Optimize glycemic control 1
- Consider DPP-4 inhibitors (neutral effect on gastric emptying) 1
- Insulin therapy with appropriate dose adjustments 1
- Consider metformin or SGLT-2 inhibitors if not contraindicated 1
- Avoid GLP-1 receptor agonists and pramlintide as they can worsen gastroparesis 1
Medications to Avoid or Minimize
- Opioids
- Anticholinergics
- Tricyclic antidepressants (when used for other conditions)
- GLP-1 receptor agonists
- Pramlintide
- Possibly dipeptidyl peptidase 4 inhibitors 1
Monitoring and Follow-up
- Monitor electrolytes, especially with persistent vomiting 1
- Consider multivitamin supplementation to prevent nutritional deficiencies 1
- For severe cases requiring hospitalization, provide:
- IV hydration
- Electrolyte replacement
- Vitamin supplementation
- Parenteral nutrition if necessary 1
Special Considerations
Renal or hepatic impairment: For patients with creatinine clearance below 40 mL/min, initiate metoclopramide at approximately half the recommended dosage 2
Acute dystonic reactions: If they occur with metoclopramide, inject 50 mg diphenhydramine hydrochloride intramuscularly 2
Important Caveats
- Diagnosis must be confirmed with gastric emptying scintigraphy, not based solely on symptoms 1
- Gastric emptying scintigraphy is considered abnormal if >10% retention at 4 hours 1
- Partial gastrectomy and pyloroplasty should be used rarely and only in carefully selected patients 3
- Intrapyloric botulinum toxin injection has not been shown to be effective in randomized controlled trials 3