Vitamin A Dosing for Suspected Deficiency
For adults with suspected vitamin A deficiency, initiate treatment with 10,000-25,000 IU oral vitamin A daily for 1-2 weeks, then recheck levels at 3 months and transition to maintenance dosing based on underlying risk factors. 1, 2
Age-Specific Treatment Dosing
Adults (≥18 years)
- Treatment dose: 10,000-25,000 IU oral vitamin A daily for 1-2 weeks when deficiency is clinically suspected based on symptoms (night blindness, dry eyes) or risk factors (malabsorption, dietary restriction) 1, 2
- Recheck vitamin A levels at 3 months after initiating treatment 1, 2
- Monitor for clinical improvement in night vision and other symptoms within 1-2 weeks 1, 2
Children with Clinical Deficiency (Xerophthalmia)
For children with eye signs of vitamin A deficiency (xerosis, Bitot's spots, keratomalacia, corneal ulceration), use the following emergency treatment schedule: 3
- Day 1: 200,000 IU oral vitamin A 3, 2
- Day 2: 200,000 IU oral vitamin A 3, 2
- 1-4 weeks later: 200,000 IU oral vitamin A 3, 2
- Infants <12 months: Use half doses (100,000 IU per dose) 3, 2
Children with Severe Malnutrition
- All children with severe malnutrition (weight-for-height Z-score <-3) should receive the full treatment schedule above, even without eye signs 3
Preventive Supplementation in High-Risk Populations
Children in Endemic Areas
- Children 12 months to 5 years: 200,000 IU every 3 months 3, 2
- Infants <12 months: 100,000 IU every 3 months (total 400,000 IU in first year) 3, 2
- Alternative if 3-month dosing impractical: 200,000 IU every 6 months 3
Postpartum Women
- 200,000 IU within 2 months of giving birth to provide adequate vitamin A in breast milk 3, 2
- If postpartum dosing not feasible: 100,000 IU during third trimester of pregnancy 3
Maintenance Dosing After Treatment
Standard Maintenance
- After initial 1-2 week treatment course: 6,000 IU daily as part of a multivitamin for patients with confirmed deficiency but no ongoing malabsorption 1, 4
Malabsorption Disorders
- Post-bariatric surgery (RYGB, BPD/DS): 10,000 IU daily long-term 3, 1, 4
- Start at 10,000 IU (3,000 μg) daily and adjust based on monitoring 3
- Consider water-miscible forms of vitamin A to improve absorption after malabsorptive procedures 3
High-Risk Populations Requiring Screening and Supplementation
Actively seek vitamin A deficiency in the following populations: 3
Liver Disease
- Chronic liver disease patients show high prevalence of deficiency, with severity correlating to disease progression 3
- Liver transplant candidates have 69.8% prevalence of deficiency 3
- Chronic alcohol consumption depletes liver stores despite potentially normal serum levels 3
Malabsorption Syndromes
- Short bowel syndrome, cystic fibrosis, celiac disease, chronic diarrhea all increase deficiency risk 3
- Fat malabsorption from any cause warrants screening and supplementation 3
Chronic Kidney Disease
- Do NOT routinely supplement in CKD - these patients often have elevated serum retinol levels 3
- Monitor regularly as liver stores can become depleted despite elevated serum levels 3
Administration Considerations
Optimizing Absorption
- Administer vitamin A with lipid-containing meals or lipid emulsion to optimize absorption 1, 4
- For parenteral nutrition, use light-protecting material as vitamin A is photosensitive 3, 4
- Avoid adsorption losses to infusion bags during IV administration 3
Special Populations
- Women of childbearing age: Exclude pregnancy or use beta-carotene form instead of retinol if pregnancy is possible 1, 4
- Upper limit for women of childbearing age is 10,000 IU daily 3, 4
Treatment Failure and Specialist Referral
If no response to oral treatment after 1-2 weeks, refer to specialist for: 1, 2
- Assessment of underlying causes of persistent deficiency 2
- Consideration of intramuscular vitamin A injections 1, 2
- Investigation for severe malabsorption or other complicating factors 2
Safety Thresholds and Toxicity
Acute Toxicity
- Occurs with >300,000 IU (adults) or >60,000 IU (children) within hours to days 3
- Symptoms: increased intracranial pressure, nausea, headaches, joint/bone pain 3
Chronic Toxicity
- Daily amounts >25,000 IU for >6 years or >100,000 IU for >6 months 3, 4
- Hepatotoxic effects occur above 14,000 mg/day for prolonged periods 3
- Upper limit set at 10,000 IU daily for women of childbearing age 3, 4
Treatment Dose Safety
- The recommended treatment dose of 10,000-25,000 IU for 1-2 weeks is safe for short-term use 1, 2
- No recognized treatment for vitamin A toxicity exists - stop supplementation if toxicity occurs 3
Common Pitfalls to Avoid
Underdosing
- Do not use prophylactic doses (6,000 IU daily) when deficiency is clinically suspected - this underdoses the patient and delays recovery 1
- Treatment requires 10,000-25,000 IU daily, not maintenance doses 1, 2
Prolonged High-Dose Use
- Avoid prolonged high-dose supplementation beyond 1-2 weeks without reassessment 1
- Transition to maintenance dosing after initial treatment course 1, 4
Pregnancy Risk
- Never give >10,000 IU daily to pregnant women or those who may become pregnant due to teratogenic effects 4, 5
- Use beta-carotene form for women of childbearing age when pregnancy cannot be excluded 1, 4
Drug Interactions
- Excessive vitamin A can exacerbate vitamin K deficiency and affect coagulation 4
- Monitor patients on anticoagulants more closely 4
Inappropriate Supplementation
- Do not routinely supplement patients with chronic kidney disease - they often have elevated serum levels despite potential total body deficiency 3, 4