Abstract
Anticoagulation therapy during pregnancy in women with prosthetic cardiac valves is a therapeutic challenge. The use of vitamin K antagonists such as warfarin during pregnancy carries the potential for serious risks to the fetus, especially if these drugs are administered during the first trimester or at term. Between 6 and 12 weeks' gestation, fetal synthesis of proteins crucial for bone and cartilage formation may be impaired by warfarin, resulting in the well-defined "warfarin embryopathy." One of the most commonly suggested regimens involves the substitution of heparin for warfarin between 6 and 12 weeks' gestation to minimize the risk of warfarin embryopathy. Warfarin has a long half-life; following a single dose, the terminal elimination half-life is about one week, with a mean effective half-life of 40 hours. To date, all existing guidelines have ignored this long elimination half-life. If a policy of substituting heparin for warfarin between 6 and 12 weeks' gestation is followed, we suggest that substitution should begin at a much earlier gestational age. Substitution starting at 6 weeks' gestation may be too late to avoid embryopathy.
| Original language | English |
|---|---|
| Pages (from-to) | 988-989 |
| Number of pages | 2 |
| Journal | Journal of Obstetrics and Gynaecology Canada |
| Volume | 32 |
| Issue number | 10 |
| DOIs | |
| State | Published - 1 Jan 2010 |
| Externally published | Yes |
Keywords
- Anticoagulation
- Pregnancy
- Prosthetic valve
- Warfarin
- Warfarin embryopathy
ASJC Scopus subject areas
- Obstetrics and Gynecology