Table 2.
Summary of results of Safety and pharmacokinetics of pravastatin used for the prevention of preeclampsia in high-risk pregnant women: A pilot randomized controlled trial. Am J Obstet Gynecol. 2016. (ref)
| 10 mg cohort | ||
|---|---|---|
| Placebo (N= 10) | Pravastatin (N= 10) | |
| Use of low-dose aspirin | 3 (30) | 2 (20) |
| Heartburn | 3 (30) | 4 (40) |
| Musculoskeletal pain | 1 (10) | 4 (40) |
| Maternal, fetal, or infant death | 0 | 0 |
| Rhabdomyolysis | 0 | 0 |
| Liver injury | 0 | 0 |
| Myopathy (weakness without increase in CK) | 0 | 0 |
| Congenital anomalies | 2 | 2 |
| Preeclampsia (any) | 4 (40) | 0 |
| Preeclampsia with severe features | 3 (30) | 0 |
| Gestational age at delivery (wks) | 36.7± 2.1 | 37.7± 0.9 |
| Indicated preterm delivery < 37 weeks | 5 (50) | 1 (10) |
| Indicated preterm delivery < 34 weeks | 1(10) | 0 (0) |
| Total cholesterol at 34– 37 weeks (mg/dl) | 252 ± 27 | 207 ± 31 |
| LDL cholesterol at 34–37 weeks (mg/dl) | 130.8 ± 46.7 | 90.4 ± 21.9 |
| Birth weight (g) | 2,877±630 | 3,018± 260 |
| Highest level of care routine nursery | 5 (50) | 8 (80) |
| NICU length of stay ≥ 48 hours | 3 (30) | 0 |