High-Output Ostomy/High-Output Stoma (HOS)
High-Output Ostomy/High-Output Stoma (HOS)
David Ray Velez, MD
Table of Contents
Definition
High-Ostomy Output Definition: > 1,500 cc/Day Output
Normal Output: 600-1,200 cc/Day
Risk Factors
Risk After Ostomy Creation: 16-31%
- Most Common After Ileostomy and Rare After Colostomy Creation (1-3% Risk)
Risk Factors
- Short Bowel
- Sepsis
- Diabetes
- Medications/Prokinetics
- Inflammatory Bowel Disease
- Clostridioides difficile Enteritis
- Opiate Withdrawal
- Internal Fistula
- Small Bowel Diverticula
- Intermittent/Partial Obstruction (Stricture) with Bacterial overgrowth
Complications
Dehydration/Acute Kidney Injury (AKI)
- Dehydration is the Most Common and Most Clinically Significant Complication of High-Output Stomas
- Due to Large Fluid Loss within the High Stoma Output
- Pre-Renal AKI Caused by High Fluid Loss
- Fluid Replacement:
- Oral Rehydration is Preferred
- Limit Hypotonic Drinks (Water, Tea, Coffee, Juice, Soda) – Can Worsen Stoma Losses by Drawing Sodium Out of the Body and into the Bowel
- Use High Sodium Oral Rehydration Solutions (ORS) Such as Double-Strength Pedialyte with Sodium 90-120 mEq/L
- Replace Losses ≥ 1:1
- Add IV Fluid Resuscitation if Oral Replacement is Insufficient (Severe Dehydration, Poor Oral Intake, AKI, etc.)
Electrolyte Abnormalities
- Hyponatremia
- High Sodium Loss in Stoma Effluent
- Patinets Often Drink Large Volumes of Hypotonic Fluid (Water, Tea, Juice) Which Further Worsens Sodium Depletion
- Dehydration Stimulates ADH Release Causing Water Retention and Further Diluting Serum Sodium
- Hypokalemia
- High Potassium Loss in Stoma Effluent
- Dehydration Stimulates a Secondary Hyperaldosteronism in Which the Kidneys Retain Sodium but Excrete Potassium Further
- Hypomagnesemia
- Due to Poor Absorption, Direct GI Losses, and Renal Wasting by Secondary Hyperaldosteronism
- Non-Anion Gap Metabolic Acidosis (NAGMA)
- Primarily from High Bicarbonate Losses
Wound Issues
- Due to Constant Exposure to Large Volumes of Fluid Rich in Digestive Enzymes, Electrolytes, and Bile Salts
- Causes Skin Irritation and Peristomal Dermatitis
- Can Lead to Ulceration and Infection
- Risk for Long-Term Scarring and Fistula
- Requires Proper Fitting Appliance with Vigilant Monitoring and Protective Skin Barriers
Malabsorption
- Due to High Transit Times Causing Decreased Absorption
- Can Cause Malnutrition
- Can Cause Impaired Medication Absorption – Particularly in Extended-Release Formulations
Management
Initial Immediate Management Consists of Fluid Resuscitation and Electrolyte Replacement Due to Excessive Losses
First-Line: Soluble Fiber Supplement (Psyllium/Metamucil)
- Absorbs Water to Slow Transit Time
- Often Dosed as “Packets” in the Hospital EMR
- Each Packet Generally Contains ~ ½ Tbsp (~ 4 g Fiber)
- Starting Dose: 1 Packet 2-3x/Day
- Max Dose: 2 Packets 4x/Day
- *Avoid Insoluble Fiber Supplements (Wheat Bran) – Can Speed Up Transit Time
Second-Line: Common Antimotility Drugs
- Loperamide (Imodium)
- MOA: A Peripherally Acting Mu-Opioid Receptor Agonist to Reduce GI Motility
- Generally the Preferred First Antimotility Medication (Lower Side Effects Than Diphenoxylate-Atropine)
- Starting Dose: 2 mg 4x/Day
- Max Dose: 8 mg 4x/Day
- Caution: High Doses > 16 mg/Day Can Prolong QTc with Risk for Cardiac Arrhythmias
- Diphenoxylate-Atropine (Lomotil)
- MOA: A Centrally Acting Opioid Derivative to Reduce GI Motility
- Atropine Added to Discourage Misuse
- Starting Dose: 2.5 mg (One Tablet) 4x/Day
- Max Dose: 5 mg (Two Tablets) 4x/Day
- MOA: A Centrally Acting Opioid Derivative to Reduce GI Motility
Tertiary Options:
- Tincture of Opium
- MOA: Binds Mu-Opioid Receptors in the GI Tract to Slow Motility
- Uncommonly Available in Patient
- Dose: 6 mg (0.6 mL) 4x/Day (Max: 6.0 mL/Day)
- Codeine
- MOA: Binds Mu-Opioid Receptors in the GI Tract to Slow Motility
- Dose: 15 mg 2x-4x/Day
- Octreotide
- MOA: Synthetic Somatostatin Analog Decreases GI Secretions and Slows Motility
- Dose: 100 mcg 3x/Day or 12.5-50 mcg/hr Continuous Infusion
- Cholestyramine
- MOA: A Resin that Sequesters Bile Acids to Decrease Bile Acid Secretion and Diarrhea
- Generally Only Used for a High-Output Colostomy with Terminal Ileum Resection in Which there is Concern for a Bile Acid Etiology
- Avoided in End Ileostomies Due to Worsened Fat Absorption and No Improvement in Output
- PPI/H2-Blockers
- Anti-Secretory Effects
- Pantoprazole Dose: IV 80 mg 2x/Day or PO 40 mg 2x/Day
- Famotidine Dose: 20-40 mg 2x/Day (PO or IV)
“Start Low and Go Slow” When Increasing Pharmacologic Regimens
Persistent Difficulty May Be Considered for Early Ostomy Reversal if Appropriate