VASCULAR DILATION OF THE BRACHIAL ARTERY IN PREECLAMPTIC AND NORMOTENSIVE WOMEN INNA LANDRES, MARIA SMALL, ADESH SIRJUSINGH, SAMUEL RAMSAWAK, KEITH WILLIAMS, Yale University, Obstetrics & Gynecology, New Haven, Connecticut, Yale University, OB/GYN, New Haven, Connecticut, University of the West Indies, Mount Hope, Port of Spain, Trinidad and Tobago OBJECTIVE: Flow mediated dilation of the Brachial artery is impaired with endothelial dysfunction. We previously identified that brachial artery waveforms were changed in preeclamptic women. We therefore sought to compare Doppler waveform analysis with Flow Mediated Vascular Dilation (FMVD) measurements in Preeclamptic and Normotenstive women. STUDY DESIGN: We conducted a nestled case-control of 12 preeclamptic vs 20 normotensive women, matched for gestational age, maternal age and ethnicity. Research was conducted at three hospitals and two geographic settings; (1) YaleNew Haven Hospital in New Haven CT, (2) Mount Hope Maternity and (3) Port of Spain General Hospital in, Trinidad. Brachial artery doppler waveform measurements were done at baseline and 90s post cuff-release. From the doppler waveforms we assessed % change in Peak Systolic Velocity, systolic acceleration and acceleration time and compared them with % change in (FMVD). Statistical analysis using student t tests, chi squared analysis and correlation coefficient was done as necessary. RESULTS: The % change PSV at 90s in normotensives vs preeclamptics was (13.5% G 22.7 vs 20.5% G 27.8) (P = .432). The % change in mean FMVD in the normotensives vs the preeclamptics was (4.3% G 4.7 vs -0.52% G 2.2) (P = .031). Correlation between the % change in the doppler waveform parameters and % change in mean FMVD identified only % change in peak systolic velocity (P = .040) as significant. CONCLUSION: FMVD remains the gold standard for assessment of endothelial dysfunction .A correlation was observed between the doppler measured % change in Peak Systolic Velocity and flow mediated vascular dilation. Although % change in the other doppler waveforms parameters did not correlate with flow mediated dilation they were done at 90 s and may need to be more appropriately measured earlier, corresponding to the peak of flow mediated vascular dilation. 111 A RANDOMIZED PLACEBO-CONTROLLED TRIAL OF PROLONGED PREDNISOLONE ADMINISTRATION TO PATIENTS WITH HELLP SYNDROME REMOTE FROM TERM: MATERNAL AND NEONATAL COMPLICATIONS P.J. VAN RUNNARD HEIMEL, A. J. M. HUISJES, A. FRANX, C. KOOPMAN, M. L. BOTS, H. W. BRUINSE, University Medical Center Utrecht, Obstetrics and Gynaecology, Utrecht, The Netherlands, Netherlands, Gelre Ziekenhuizen Apeldoorn, Obstetrics and Gynaecology, Apeldoorn, The Netherlands, Netherlands, Erasmus University Medical Centre Rotterdam, Obstetrics and Gynaecology, Rotterdam, The Netherlands, Netherlands, University Medical Center Utrecht, Neonatology, Utrecht, The Netherlands, Netherlands, University Medical Center Utrecht, Julius Center for Health Science and Primary Care, Utrecht, The Netherlands, Netherlands OBJECTIVE: Several reports have shown a beneficial effect of corticosteroids on HELLP syndrome. However, there is a lack of RCTs of corticosteroids in HELLP syndrome in the antepartum period for more than 48 hours. Prednisolone is a glucocorticoid with limited transplacental passage. This randomized, double-blind, placebo-controlled study was undertaken to evaluate the effect of prolonged administration of high-dose prednisolone on maternal, perinatal and neonatal outcome in patients suffering early onset HELLP syndrome. STUDY DESIGN: 31 pregnant women were included suffering HELLP syndrome with an onset prior to 30 weeks gestation. Prior to inclusion all women received 2 intramuscular doses of betamethasone 11.4 mg 24 hours apart to promote fetal lung maturation. Patients received either prednisolone (n = 15) or placebo (n = 16) 50 mg intravenously twice a day. Maternal outcome measures were presence of liver hematoma and rupture, pulmonary oedema, renal failure and placental abruption. Perinatal outcome measures were gestational age at delivery, occurrence of perinatal death, birth weight and Apgar score. Neonatal outcome measures were occurrence of neonatal complications during admission at the neonatal intensive care unit (NICU) and the duration of admission at the NICU. Long-term neonatal follow-up was also performed at 6, 15 and 24 months. RESULTS: In the placebo group two liver hematomas and one liver rupture occurred, the latter resulting in maternal death. In both treatment groups a placental abruption occurred. Four perinatal deaths occurred in the placebo group versus three neonatal deaths in the prednisolone group. No further differences were found in perinatal and neonatal outcome measures. At longterm neonatal follow-up no differences could be demonstrated. CONCLUSION: Although administration of prednisolone to patients suffering early onset HELLP syndrome did not significantly improve maternal, perinatal and neonatal outcome measures, a trend towards a beneficial effect on the occurrence of maternal complications could be shown.