Ovarian stimulation: today and tomorrow.

@article{Fatemi2012OvarianST,
  title={Ovarian stimulation: today and tomorrow.},
  author={Human M. Fatemi and Christophe Blockeel and Paul Devroey},
  journal={Current pharmaceutical biotechnology},
  year={2012},
  volume={13 3},
  pages={
          392-7
        }
}
In assisted reproductive technology, medications and ovarian stimulation play a crucial role. The availability of gonadotrophins and GnRH analogues has allowed the tailoring of several stimulation schemes. The two most commonly used gonadotrophin forms are urinary hMG and recombinant FSH in combination with GnRH agonists or GnRH antagonists. Cycles stimulate with recombinant FSH appear to have a higher risk of premature progesterone rise in the late follicular phase, if not triggered on time… 
Influence of controlled ovarian stimulation protocols on ovarian hyperstimulation syndrome patterns during in vitro fertilization programs
TLDR
OHSS that has developed after the GnRH agonists protocol of controlled ovarian stimulation is associated with higher risks of complications and lower chances of successful pregnancy, which is explained by hyperestrogenic state, elevated progesterone levels, marked hypercoagulation, and higher incidence of early OHSS, which leads to the necessity of embryo transfer cancellation.
Random-start GnRH antagonist for emergency fertility preservation: a self-controlled trial
TLDR
GnRH antagonists can be effectively used for random-start controlled ovarian hyperstimulation with an ovarian response similar to that of standard protocols, and the antagonists appear suitable for emergency fertility preservation in cancer patients.
Medroxyprogesterone acetate used in ovarian stimulation is associated with reduced mature oocyte retrieval and blastocyst development: a matched cohort study of 825 freeze-all IVF cycles
TLDR
Flexible-start MPA co-treatment OS was as effective in freeze-all IVF cycles as GnRH-ant co- treatment, with similar LB per transfer rates; however, increased cycle cancellation and reduced blastocyst numbers reduced LB per treatment rates significantly.
Recombinant versus urinary human chorionic gonadotrophin for final oocyte maturation triggering in IVF and ICSI cycles.
TLDR
The evidence for different comparisons ranged from very low to high quality: limitations were poor reporting of study methods and imprecision.
Female fertility preservation: past, present and future.
TLDR
It is expected that the risk of reimplantation of malignant cells with ovarian grafts will be overcome with the putative development of an artificial ovary and an efficient follicle class- and species-dependent in vitro system for culturing primordial follicles.
Ovarian stimulation protocols for IVF: is more better than less?
Expression of long-acting human follicle-stimulating hormone analog from Chinese hamster ovary cells and functional characterization
TLDR
Chinese hamster ovary (CHO-K1) cell expression of a novel long-acting human FSH single chain analog consisting of the native a and â subunit indicates that this recombinant FSH analog could serve as a long- acting FSH preparation.
Dydrogesterone versus medroxyprogesterone acetate co-treatment ovarian stimulation for IVF: a matched cohort study of 236 freeze-all-IVF cycles
TLDR
Flexible-start DYG co-treatment OS was as effective in blastocyst freeze-all-IVF cycles as MPA co- treatment, with similar ongoing pregnancy rates; however, mature oocyte retrieval was significantly decreased and cycle cancellation increased in DyG cycles.
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