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Pi Is 0015028212014069
Pi Is 0015028212014069
OBJECTIVE: To evaluate the effects of barusiban on uterine cont- P-244 Tuesday, October 23, 2012
ractions (UC).
DESIGN: Double-blind RCT (ClincalTrial.gov NCT01043120). EFFECT OF TAKING A ONE TIME INJECTION OF 1MG LEUPRO-
MATERIALS AND METHODS: Oocyte donors were randomized LIDE ACETATE 3 DAYS AFTER EMBRYO TRANSFER ON PREG-
to receive barusiban (IV bolus 20 mg, IV infusion 19 mg; total duration NANCY OUTCOME AND LEVEL OF FIRST BETA HUMAN
60 min) (N¼49) or placebo (saline) (N¼50) two days after oocyte re- CHORIONIC GONADOTROPIN (b-hCG) LEVEL. J. H. Check,a,b
trieval. Transvaginal ultrasound (TVU) recordings of a continuous cine- J. K. Choe,a D. Brasile,a R. Cohen,c D. Summers-Chase.a aDept. OB/
loop image of at least 5 min were obtained pre-dosing, 30 min after start GYN, Div. Repro. Endo. & Infertility, UMDNJ, Robert Wood Johnson
of dosing (30 min; main time point), immediately after a mock Med. School at Camden, Camden, NJ; bDept. OB/GYN, Div. Repro.
embryo transfer (MET0min) performed 40 min after start of dosing, and Endo. & Infertility, Cooper Medical School of Rowen University, Camden,
10 min and 1h after end of dosing. Frequency of UC, direction of the NJ; cDept. OB/GYN, Philadelphia College of Osteopathic Medicine,
waves and ability to complete uterine wave propagation were determined Philadelphia, PA.
by a blinded assessor, using a computer-assisted time series motion anal-
ysis software. OBJECTIVE: To determine if injecting 1mg leuprolide acetate (LA) in the
RESULTS: At 30 min, a significant mean decrease in frequency of 0.58 mid-luteal phase will improve pregnancy outcome following embryo trans-
UC/min was found with barusiban vs placebo (P¼0.014). The proportion fer.
of subjects with ability to complete wave propagation was similar for baru- DESIGN: Prospective cohort comparison.
siban and placebo at pre-dosing (95% vs 98%), but significantly lower with MATERIALS AND METHODS: 1 of 3 in vitro fertilization-embryo trans-
barusiban compared to placebo at 30 min (39% vs 70%, P¼0.006) and at fer (IVF-ET) cycles using a gonadotropin releasing hormone antagonist pro-
MET0min (29% vs 60%, P¼0.004). There was no significant difference be- tocol was supplemented with 1mg LA 3 days after ET. There was no
tween groups in direction of wave at any time point. The predominant direc- restriction for day 3 follicle stimulating hormone (FSH) levels. The data
tion of the wave at pre-dosing was cervical (from fundus to cervix) (73%), were stratified according to 4 age groups. Chi-square analysis was used for
rather than convergent/focal (8%), no activity (5%), fundal (2%) or not evalu- comparison.
able (12%). The direction of the wave changed progressively as a result of the RESULTS: The clinical and ongoing/delivered pregnancy rates (PRs) ac-
TVU with primarily cervical (41%) or convergent/focal (39%) at 30 min after cording to age up to%42 is seen in Table 1. For age>43 the clinical and live
start of dosing, and mainly convergent/focal at MET0min (64%), at 10 min pregnancy rates were 8.7% (2/23) and 4.3% without LA vs. 25% (2/8) and
(63%) and 1h (53%) after end of dosing. 12.5% with LA. The average 1st beta-hCG was 192.5 without and 137.3
CONCLUSION: Barusiban modifies uterine contractility in the luteal with LA. Implantation rates were 3.4% and 8.3%, respectively. The clinical
phase after controlled ovarian stimulation by reducing the frequency of uter- and live delivered PRs were higher in all 4 age groups in those using LA.