Rheumatoid Arthritis Pregnancy Management
Pre-Conception Planning
Women with rheumatoid arthritis planning pregnancy must achieve optimal disease control before conception, discontinue teratogenic medications at least 1-3 months prior, and transition to pregnancy-compatible DMARDs. 1
Disease Activity Optimization
- Postpone conception until optimal disease control is reached 1
- Target clinical remission or low disease activity before attempting pregnancy
- Recent evidence shows women treated with a treat-to-target approach had median time to pregnancy of 91 days versus 251 days in those without this approach 2
- Women achieving remission had even shorter time to pregnancy (65 days) 2
Medication Adjustments Before Conception
Discontinue these teratogenic medications:
- Methotrexate: Stop 1-3 months before conception 3
- Leflunomide: Stop 24 months prior OR check serum metabolite levels and perform cholestyramine washout if detectable 3
- Mycophenolate/mycophenolic acid: Stop >6 weeks prior to assess disease stability 3
- Cyclophosphamide: Stop 3 months prior 3
Continue these pregnancy-compatible medications:
- Hydroxychloroquine: Strongly recommended to continue 1, 3
- Sulfasalazine: Continue (up to 2g/day) with daily folic acid supplementation 1, 3
- Azathioprine: Continue (up to 2mg/kg/day) 1, 3
- Colchicine: Continue (1-2mg/day) 1, 3
- Cyclosporine/Tacrolimus: Continue at lowest effective dose 1, 3
TNF inhibitors:
- Certolizumab: Strongly recommended to continue throughout pregnancy (minimal placental transfer) 3
- Infliximab, etanercept, adalimumab, golimumab: Can continue through conception and pregnancy 3
NSAIDs: Discontinue if difficulty conceiving due to unruptured follicle syndrome 3
During Pregnancy
First and Second Trimesters
Maintain pregnancy-compatible medications to control disease activity:
- Continue hydroxychloroquine, sulfasalazine, azathioprine, colchicine 1, 3
- Continue certolizumab throughout pregnancy 3
- Continue other TNF inhibitors (infliximab, etanercept, adalimumab, golimumab) 3
- NSAIDs: Can use in first and second trimesters (nonselective preferred over COX-2 inhibitors) 3
Glucocorticoids:
- Continue low-dose prednisone (≤10mg/day) if needed 3
- Taper doses >20mg/day by adding pregnancy-compatible glucocorticoid-sparing agents 3
Discontinue at positive pregnancy test:
- Rituximab, belimumab, anakinra, abatacept, tocilizumab, secukinumab, ustekinumab 3
- Exception: Rituximab can be used for life-threatening or organ-threatening disease 3
Third Trimester
Critical medication adjustments:
- Discontinue NSAIDs completely (risk of premature ductus arteriosus closure) 3
- TNF inhibitors (except certolizumab): May discontinue several half-lives before delivery if disease well-controlled, OR continue through delivery if disease active 3
- Note: Continuing through delivery results in significant neonatal drug levels but accumulated evidence suggests no adverse effects 3
Monitoring
- Monitor disease activity throughout pregnancy
- Laboratory monitoring at least once per trimester 3
- Adjust medications as needed to maintain disease control
Delivery Planning
Glucocorticoid stress dosing:
- Do NOT give stress-dose steroids for vaginal delivery 3
- DO give stress-dose steroids for cesarean delivery 3
Postpartum and Breastfeeding
Encourage breastfeeding while maintaining disease control with compatible medications 1, 3
Breastfeeding-Compatible Medications
Strongly compatible:
- Hydroxychloroquine 3
- TNF inhibitors: infliximab, etanercept, adalimumab, golimumab, certolizumab 3
- Rituximab 3
- Prednisone <20mg/day 3
Conditionally compatible:
- NSAIDs (ibuprofen preferred) 3
- Sulfasalazine 3
- Colchicine 3
- Azathioprine 3
- Cyclosporine, tacrolimus 3
- Anakinra, belimumab, abatacept, tocilizumab, secukinumab, ustekinumab 3
For prednisone ≥20mg/day: Discard breast milk obtained within 4 hours of medication 3
NOT compatible with breastfeeding:
Neonatal Considerations
- Infants exposed to biologic medications in utero can receive all recommended vaccinations 3
- Monitor for disease flare postpartum and adjust medications accordingly
Critical Principles
The risk of untreated maternal disease must be weighed against potential medication risks 1. Untreated RA is associated with:
- Prolonged time to pregnancy 2
- Increased adverse pregnancy outcomes 1
- Higher rates of pregnancy complications 4, 5
Shared decision-making is essential throughout the preconception, pregnancy, and postpartum periods 1. Comprehensive counseling should enable informed decisions and reduce concerns about medication use during these critical periods.