Lomotil (Diphenoxylate/Atropine) Dosing for High-Output Ostomy
Lomotil is not the preferred antimotility agent for high-output ostomy—loperamide should be used instead as first-line therapy due to superior safety profile, lack of addiction potential, and absence of fat malabsorption. 1, 2, 3
Why Loperamide Over Lomotil
- Loperamide is explicitly preferred over diphenoxylate/atropine (Lomotil) because it is not sedative, not addictive, and does not cause fat malabsorption 2, 3
- The atropine component in Lomotil can cause significant adverse effects that are problematic in ostomy patients already dealing with fluid and electrolyte disturbances 4
- All major guidelines (AGA, ESPEN, British Society of Gastroenterology) recommend loperamide as the antimotility drug of choice for high-output ostomy management 1, 2, 3
Loperamide Dosing Algorithm (The Correct Approach)
Initial Dosing
- Start with 2-4 mg (1-2 tablets) taken 30 minutes before each meal and at bedtime to reduce postprandial intestinal output 2, 3
- Timing is critical—administer before meals as intestinal output rises after eating, especially in net "secretors" 2
High-Output Situations Requiring Dose Escalation
- For patients with disrupted enterohepatic circulation (common with ileal resection), doses of 12-24 mg at a time may be required 2, 3
- Total daily doses up to 32 mg (16 tablets) are frequently needed in short bowel syndrome patients without an ileum, as loperamide enters enterohepatic circulation which is disrupted 1
- Expected reduction in output is approximately 20-30% in water and sodium losses 2, 3
Critical Administration Considerations
- If tablets emerge unchanged in stoma output, crush them or open capsules and mix with water or food to improve absorption 2, 3
- Avoid sustained-release or delayed-release formulations as absorption is compromised in short bowel syndrome 1, 2
When Loperamide Alone Is Insufficient
Add Antisecretory Agents
- Combine with proton pump inhibitors or H2-receptor antagonists to reduce gastric hypersecretion, particularly if output exceeds 2 L/day 1, 3, 5
- These are as effective as octreotide in reducing stomal output volume and should be tried before escalating to octreotide 5
Consider Combination Antimotility Therapy
- Codeine phosphate (60 mg three times daily) may have synergistic effects when combined with loperamide in refractory cases 1, 6
- Codeine reduces mean total weight of ileostomy output and losses of water, sodium, and potassium but increases faecal fat and slows transit (risk of obstruction) 6
Reserve Octreotide for Severe Cases
- Octreotide 50 mcg subcutaneously twice daily should be reserved for very high-output stomas (>3 L/24 hours) when fluid and electrolyte management remains problematic despite conventional treatments 1, 3, 5
- Octreotide can reduce stomal output by 1-2 L/24 hours but does not improve absorption and may inhibit pancreatic enzymes 1, 5
Essential Non-Pharmacologic Measures (Must Be Implemented Concurrently)
- Restrict oral hypotonic fluids (water, tea, coffee, juice) to <500 mL daily as these paradoxically increase stomal sodium losses 1
- Replace fluid deficit with glucose-saline oral rehydration solution containing 90-100 mmol/L sodium to enhance coupled sodium-glucose absorption 1, 2
- Separate solids and liquids (no drink for 30 minutes before/after food) though evidence for this is limited 1
Monitoring and Duration
- Measure 24-hour stomal output volumes regularly to assess objective benefit and guide dose adjustments 2, 3
- Continue loperamide indefinitely as long as it provides objective benefit—this is maintenance therapy, not short-term intervention 3
- Goal is to maintain output <1-1.5 L/day for ileostomy 3
Common Pitfalls to Avoid
- Do not encourage patients to drink large quantities of water—this creates a vicious cycle of increased output and worsening dehydration 1
- Do not use Lomotil as first-line therapy when loperamide is safer and more effective 2, 3, 4
- Do not abruptly discontinue antimotility agents—this can precipitate high-output crisis requiring IV resuscitation 3
- Exclude other causes of high output first (intra-abdominal sepsis, partial obstruction, C. difficile, Crohn's recurrence) before escalating therapy 1