IUCD Insertion During Cesarean Section in a Patient with Cerebral Venous Thrombosis
Intrauterine contraceptive device (IUCD) insertion during cesarean section is safe and recommended for women with a history of cerebral venous thrombosis (CVT), as it provides effective non-hormonal contraception without increasing thrombotic risk.
Safety of IUCD Insertion During Cesarean Section
General Safety Profile
- Postplacental IUCD insertion during cesarean section has been shown to be safe and effective with high continuation rates and low expulsion rates 1
- A prospective study demonstrated that intracesarean Copper T 380A insertion had:
- 91% continuation rate at one year
- Only 5.33% expulsion rate
- Low complication rates (2% febrile morbidity) 1
- Another study confirmed that women undergoing cesarean section who desire long-term reversible contraception should be offered IUCD insertion during the same procedure 2
Specific Considerations for CVT Patients
Thrombotic Risk Assessment
- Cerebral venous thrombosis is a serious condition with increased risk during pregnancy and postpartum period 3
- The postpartum period, especially after cesarean delivery, represents a high-risk time for CVT development 4
- Cesarean delivery itself is identified as a risk factor for CVT, with onset typically within the first 3 weeks postpartum (mean 9.6 days) 4
Contraceptive Options for Women with CVT
- For women with a history of CVT, non-hormonal contraception is preferred to avoid additional thrombotic risk
- The Copper IUD (Cu-IUD) is classified as Category 1 (no restriction) for women with a history of VTE, making it an ideal choice 5
- Combined hormonal contraceptives (CHCs) would be contraindicated (Category 4) in women with a history of CVT due to increased thrombotic risk 5
Thromboprophylaxis Management
Postpartum Anticoagulation
- Women with a history of VTE (including CVT) should receive postpartum prophylaxis for 6 weeks with prophylactic or intermediate-dose LMWH or vitamin K antagonists 5
- The Society for Maternal-Fetal Medicine recommends that women with previous VTE who undergo cesarean delivery receive both mechanical and pharmacologic prophylaxis for 6 weeks postoperatively 5
Compatibility with IUCD
- There is no contraindication to IUCD insertion in women receiving anticoagulation therapy
- The timing of IUCD insertion during cesarean (immediately after delivery of placenta) avoids the need for a separate procedure while the patient is anticoagulated
Practical Approach
- Timing of insertion: Insert the IUCD within 10 minutes after delivery of the placenta during cesarean section 5
- Device selection: Copper T 380A is preferred for women with CVT as it provides non-hormonal contraception
- Technique: Place the IUCD at the uterine fundus before closure of the uterine incision
- Anticoagulation management: Continue prescribed thromboprophylaxis as recommended (typically 6 weeks of LMWH) 5
- Follow-up: Schedule a follow-up visit at 6 weeks postpartum to:
- Verify IUCD placement
- Check for visible strings
- Assess for any complications
Potential Complications and Management
- Bleeding: Minimal risk of increased bleeding with copper IUCD even with anticoagulation
- Infection: Low risk (2%) of postoperative infection 1
- Expulsion: Approximately 5% risk of expulsion within the first year 1
- Perforation: Extremely rare during cesarean insertion due to direct visualization
Common Pitfalls to Avoid
- Delaying contraception: Waiting for a separate procedure after cesarean increases risk of short interpregnancy interval
- Using hormonal IUDs: Levonorgestrel IUDs may be less preferable than copper IUDs in women with history of thrombosis
- Failing to counsel about strings: Inform the patient that strings may not be visible immediately and require checking at follow-up
- Neglecting thromboprophylaxis: Ensure proper anticoagulation is maintained regardless of IUCD insertion
In conclusion, intracesarean IUCD insertion provides a safe, effective, and convenient contraceptive option for women with a history of cerebral venous thrombosis, while appropriate thromboprophylaxis should be continued as indicated by the patient's risk profile.