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    <title>Bustion, S.</title>
    <link>http://repub.eur.nl/res/aut/4743/</link>
    <description>List of Publications</description>
    <language>en</language>
    <image>
      <url>http://repub.eur.nl/static-eur/img/logo.png</url>
      <title>RePub, Erasmus University Rotterdam</title>
      <link>http://repub.eur.nl</link>
    </image>
    <item>
      <title>Nonsupplemented luteal phase characteristics after the administration of recombinant human chorionic gonadotropin, recombinant luteinizing hormone, or gonadotropin-releasing hormone (GnRH) agonist to induce final oocyte maturation in in vitro fertilization patients after ovarian stimulation with recombinant follicle-stimulating hormone and GnRH antagonist cotreatment (Article)</title>
      <link>http://repub.eur.nl/res/pub/10221/</link>
      <pubDate>2003-01-01T00:00:00Z</pubDate>
      <description>Replacing GnRH agonist cotreatment for the prevention of a premature rise
      in LH during ovarian stimulation for in vitro fertilization (IVF) by the
      late follicular phase administration of GnRH antagonist may render
      supplementation of the luteal phase redundant, because of the known rapid
      recovery of pituitary function after antagonist cessation. This randomized
      two-center study was performed to compare nonsupplemented luteal phase
      characteristics after three different strategies for inducing final oocyte
      maturation. Forty patients underwent ovarian stimulation using recombinant
      (r-)FSH (150 IU/d, fixed) combined with a GnRH antagonist (antide; 1 mg/d)
      during the late follicular phase. When at least one follicle above 18 mm
      was observed, patients were randomized to induce oocyte maturation by a
      single injection of either r-human (h)CG (250 microg) (n = 11), r-LH (1
      mg) (n = 13), or GnRH agonist (triptorelin; 0.2 mg) (n = 15). Retrieved
      oocytes were fertilized by either IVF or intracytoplasmatic sperm
      injection, depending on sperm quality. Embryo transfer was performed 3-4 d
      after oocyte retrieval. No luteal support was provided. Serum
      concentrations of FSH, LH, estradiol (E(2)), progesterone (P), and hCG
      were assessed at fixed intervals during the follicular and luteal phase.
      The median duration of the luteal phase was 13, 10, and 9 d for the r-hCG,
      the r-LH, and the GnRH agonist group, respectively (P = 0.005). The median
      area under the curve per day (from 4 d post randomization until the onset
      of menses) for LH was 0.50, 2.34, and 1.07 for the r-hCG, the r-LH, and
      the GnRH agonist group, respectively (P = 0.001). The median area under
      the curve per day for P was 269 vs. 41 and 16 for the r-hCG, the r-LH, and
      the GnRH agonist group, respectively (P &lt; 0.001). Low pregnancy rates
      (overall, 7.5%; range, 0-18% per started cycle) were observed in all
      groups. In conclusion, the nonsupplemented luteal phase was insufficient
      in all three groups. In the patients receiving r-hCG, the luteal phase was
      less disturbed, compared with both other groups, presumably because of
      prolonged clearance of hCG from the circulation and the resulting extended
      support of the corpus luteum. Despite high P and E(2) concentrations
      during the early luteal phase in all three groups, luteolysis started
      prematurely, presumably because of excessive negative steroid feedback
      resulting in suppressed pituitary LH release. Hence, support of corpus
      luteum function remains mandatory after ovarian stimulation for IVF with
      GnRH antagonist cotreatment.</description>
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