Steroid Safety During Periconception Period
Prednisolone is the safest systemic corticosteroid for use during the periconception period, as only 10% of maternal concentration reaches fetal blood, and it has the most extensive safety data in pregnancy. 1
Systemic Corticosteroids
First-Line Choice: Prednisolone
- Prednisolone (and prednisone) are classified as Category A by the Australian TGA, indicating the highest safety profile during periconception and pregnancy. 1
- Only 10% of maternal prednisolone/prednisone concentration crosses to fetal blood, providing a protective barrier for the developing fetus. 1
- Multiple studies demonstrate no increase in birth defects when used at therapeutic doses, though some data suggest a 3-fold increased risk of isolated cleft lip ± cleft palate specifically during first trimester exposure. 1
- Despite conflicting data on cleft palate risk, the major benefit of systemic corticosteroids in severe disease exceeds the possible fetal risk. 1
Alternative: Hydrocortisone
- Hydrocortisone is also classified as Category A and represents a safe alternative to prednisolone during periconception. 1
- Hydrocortisone may be necessary when parenteral administration is required. 1
Avoid: Betamethasone and Dexamethasone
- These fluorinated corticosteroids cross the placenta more readily and are specifically used when fetal treatment is intended (such as for fetal lung maturation). 2
- They should not be used for maternal indications during periconception unless specifically treating the fetus. 2
Inhaled Corticosteroids
Preferred Agents
- Budesonide is the preferred inhaled corticosteroid, classified as Category A, with the most extensive pregnancy safety data. 1
- Beclomethasone is also well-studied and considered safe (Category B3), representing an acceptable alternative. 1
- At usual doses, inhaled corticosteroids have not been associated with increased risk of major malformations, intrauterine growth restriction, preterm delivery, or low birthweight. 1
Acceptable Alternatives
- Fluticasone, triamcinolone, ciclesonide, and mometasone are classified as "probably safe" (Category B3) but have less pregnancy data than budesonide or beclomethasone. 1
- If a woman is already well-controlled on another inhaled corticosteroid pre-pregnancy, she can continue it during the periconception period. 1
Critical Dosing Considerations
Minimize Dose While Maintaining Control
- Use the lowest effective dose necessary to maintain disease control during periconception. 1
- One study showed doses >1000 µg/day beclomethasone were associated with a small risk of congenital malformation. 1
High-Dose Systemic Steroids
- If high-dose systemic corticosteroids continue until birth, monitor the newborn for adrenal insufficiency. 1
- With prolonged treatment at high maternal doses, delay breastfeeding for 3-4 hours after the dose to minimize transfer to breast milk. 1
Common Pitfalls to Avoid
- Do not switch a well-controlled patient to a different corticosteroid solely based on pregnancy category if disease control might be compromised. Disease exacerbation poses greater risk than continuing effective therapy. 1
- Do not use fluorinated corticosteroids (betamethasone, dexamethasone) for maternal indications during periconception, as these are reserved for fetal treatment. 2
- Do not prescribe topical corticosteroids at high potency or over large surface areas during periconception, as some studies suggest a relationship with intrauterine growth restriction. 1
- Avoid abrupt discontinuation of chronic corticosteroid therapy during periconception, as this may precipitate adrenal crisis. 1
Clinical Algorithm for Selection
- Determine route needed: Systemic vs. inhaled vs. topical
- For systemic therapy: Choose prednisolone or hydrocortisone (Category A)
- For inhaled therapy: Choose budesonide first-line, beclomethasone as alternative (both well-studied)
- For topical therapy: Use lowest potency that controls disease, limit surface area
- Optimize dose: Use minimum effective dose while maintaining disease control
- Monitor: Assess disease control and adjust as needed, avoiding both under-treatment and over-treatment