2011
DOI: 10.4045/tidsskr.10.0489
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Bruk av GnRH-antagonist ved in vitro-fertilisering

Abstract: Stimulation with a GnRH-antagonist instead of a GnRH-agonist in IVF, is less physically and psychologically demanding for the patients and maintains the same birth rate.

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Cited by 3 publications
(4 citation statements)
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“…This substantially lowers the number of injections required during IVF, and may improve drug compliance and/or prevent errors during drug administration [12]. The use of GnRH-a and GnRH-antagonists in assisted fertility treatments has been the focus of considerable comparative research [1,13-16]. Reproductive outcomes, as well as safety and efficacy, between these two treatment approaches are thought to be similar [8,17-20] and GnRH-antagonists have joined alongside GnRH-a as mainstream therapeutic agents used widely at infertility units worldwide.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…This substantially lowers the number of injections required during IVF, and may improve drug compliance and/or prevent errors during drug administration [12]. The use of GnRH-a and GnRH-antagonists in assisted fertility treatments has been the focus of considerable comparative research [1,13-16]. Reproductive outcomes, as well as safety and efficacy, between these two treatment approaches are thought to be similar [8,17-20] and GnRH-antagonists have joined alongside GnRH-a as mainstream therapeutic agents used widely at infertility units worldwide.…”
Section: Discussionmentioning
confidence: 99%
“…GnRH-antagonists can serve an important role in advanced reproductive treatments, because this pharmacological approach enables the IVF sequence to be reduced from 4-5wks to <2wks, and lower overall gonadotropin consumption [1]. The attenuated stimulation associated with GnRH-antagonists also has been shown to minimize OHSS risk [2-4].…”
Section: Introductionmentioning
confidence: 99%
“…Second, the attribute (safety) ‘risks of developing OHSS' was selected and described by the levels 2.6% (resembling a GnRH antagonist) and 4.2% (resembling a GnRH agonist). The 3 latter aspects were selected in order to reflect treatment burden and included the following: (1) ‘side effects' (such as headaches, hot flushes, insomnia) described by ‘present' (GnRH agonist) or ‘not present' (GnRH antagonist) [7,8], (2) ‘importance of compliance' described by the levels ‘very important' (GnRH antagonist) or ‘important' (GnRH agonist) [9,15,16] and (3) ‘treatment duration' described by the 2 levels ‘short' (GnRH antagonist) and ‘long' (GnRH agonist) [9,17]. …”
Section: Methodsmentioning
confidence: 99%
“…less headaches, hot flushes and insomnia, shorter treatment duration [7,8] and more safety (lesser chance of ovarian hyperstimulation syndrome, OHSS [7,9]). GnRH antagonists have limited treatment effectiveness (lower ongoing pregnancy rates [7,9]).…”
Section: Introductionmentioning
confidence: 99%