Oral contraceptive pretreatment does not improve outcome in microdose gonadotrophin-releasing hormone agonist protocol among poor responder intracytoplasmic sperm injection patients
Abstract:Purpose To compare oral contraceptive (OC) pretreatment plus microdose GnRH-a in flare-up protocol and non-OC microdose GnRH-a in flare-up protocol among poor responder ICSI patients. Methods A retrospective analysis of poor responder ICSI patients. Patients were divided into two groups according to used microdose protocol. Precycle treatment with OC followed by follicular phase administration of 40 μg sc leuprolide acetate (LA) every 12 h beginning on after 2 day pill-free period and rFSH administration was b… Show more
“…Furthermore, implantations and pregnancy rates per embryo transfer were similar. As a result of our previous study, we thought that this preference should not affect the outcomes of the microdose protocol negatively (34). The major weakness of our study is the limited number of couples undergoing the ICSI procedures investigated.…”
Objective: To determine the potential effect of the ultrashort gonadotropin-releasing hormone (GnRH) agonist/GnRH antagonist protocol versus the microdose GnRH agonist protocol in poor responders undergoing intracytoplasmic sperm injection (ICSI).
Material and Methods:The patients in the Agonist-Antagonist Group (n=41) were administered the ultrashort GnRH-agonist/ antagonist protocol, while the patients in the Microdose Group (n=41) were stimulated according to the microdose flare-up protocol. The mean number of mature oocytes retrieved was the primary outcome measure. Fertilization rate, implantation rate per embryo and clinical pregnancy rates were secondary outcome measures.
Results:There was no differenc between the mean number of mature oocytes retrieved in the two groups. There were also no statistical differences between the two groups in terms of peak serum E 2 level, canceled cycles, endometrial thickness on hCG day, number of 2 pronucleus and number of embryos transferred. However, the total gonadotropin consumption and duration of stimulation were significantly higher with the Agonist-Antagonist Group compared with the Microdose Group. The implantation and clinical pregnancy rates were similar between the two groups.
Conclusion:Despite the high dose of gonadotropin consumption and longer duration of stimulation with the ultrashort GnRH agonist/ antagonist protocol, it seems that the Agonist-Antagonist Protocol is not inferior to the microdose protocol in poor responders undergoing ICSI. (J Turkish-German Gynecol Assoc 2010; 11: 187-93) Key words: Poor responder, mature oocytes, Agonist-Antagonist protocol, microdose flare-up protocol Received: 11 August, 2010 Accepted: 19 November, 2010 Amaç: ICSI uygulanan zayıf over cevaplı hastalarda ultra kısa GnRH agonist/GnRH antagonist protokolünün mikrodoz GnRH agonist protokolüne karşı potansiyel etkisini belirlemek.
Gereç ve Yöntemler:Mikrodoz grubundaki (n=41) hastalar mikrodoz flare up protokolüne uygun olarak stimüle edilirken AgonistAntagonist grubundaki (n=41) hastalara da ultra kısa GnRH-agonist/ antagonist protokolü uygulandı. Bu çalışmanın primer sonuç değeri toplanan ortalama matür oosit sayısı iken, fertilizasyon oranı, embryo başına implantasyon oranı ve klinik gebelik oranı da sekonder sonuç değerleriydi.
Bulgular:İki grup arasındaki toplanan ortalama matür oosit sayıla-rı arasında fark yoktu. Serum E 2 düzeyleri, iptal edilen sikluslar, hCG günü endometrial kalınlığı, 2 pronukleus sayıları ve transfer edilen embryo sayılarında da iki grup arasında istatistiksel farklılıklar yoktu. Bununla birlikte Agonist-Antagonist grubunda total gonadotropin tüketimi ve stimülasyon süresi Mikrodoz grubuyla karşılaştırıldığında belirgin olarak daha yüksekti. İki grup arasındaki implantasyon ve klinik gebelik oranları ise birbirine benzerdi.
Sonuç:
Abstract ÖzetOriginal Investigation 187
“…Furthermore, implantations and pregnancy rates per embryo transfer were similar. As a result of our previous study, we thought that this preference should not affect the outcomes of the microdose protocol negatively (34). The major weakness of our study is the limited number of couples undergoing the ICSI procedures investigated.…”
Objective: To determine the potential effect of the ultrashort gonadotropin-releasing hormone (GnRH) agonist/GnRH antagonist protocol versus the microdose GnRH agonist protocol in poor responders undergoing intracytoplasmic sperm injection (ICSI).
Material and Methods:The patients in the Agonist-Antagonist Group (n=41) were administered the ultrashort GnRH-agonist/ antagonist protocol, while the patients in the Microdose Group (n=41) were stimulated according to the microdose flare-up protocol. The mean number of mature oocytes retrieved was the primary outcome measure. Fertilization rate, implantation rate per embryo and clinical pregnancy rates were secondary outcome measures.
Results:There was no differenc between the mean number of mature oocytes retrieved in the two groups. There were also no statistical differences between the two groups in terms of peak serum E 2 level, canceled cycles, endometrial thickness on hCG day, number of 2 pronucleus and number of embryos transferred. However, the total gonadotropin consumption and duration of stimulation were significantly higher with the Agonist-Antagonist Group compared with the Microdose Group. The implantation and clinical pregnancy rates were similar between the two groups.
Conclusion:Despite the high dose of gonadotropin consumption and longer duration of stimulation with the ultrashort GnRH agonist/ antagonist protocol, it seems that the Agonist-Antagonist Protocol is not inferior to the microdose protocol in poor responders undergoing ICSI. (J Turkish-German Gynecol Assoc 2010; 11: 187-93) Key words: Poor responder, mature oocytes, Agonist-Antagonist protocol, microdose flare-up protocol Received: 11 August, 2010 Accepted: 19 November, 2010 Amaç: ICSI uygulanan zayıf over cevaplı hastalarda ultra kısa GnRH agonist/GnRH antagonist protokolünün mikrodoz GnRH agonist protokolüne karşı potansiyel etkisini belirlemek.
Gereç ve Yöntemler:Mikrodoz grubundaki (n=41) hastalar mikrodoz flare up protokolüne uygun olarak stimüle edilirken AgonistAntagonist grubundaki (n=41) hastalara da ultra kısa GnRH-agonist/ antagonist protokolü uygulandı. Bu çalışmanın primer sonuç değeri toplanan ortalama matür oosit sayısı iken, fertilizasyon oranı, embryo başına implantasyon oranı ve klinik gebelik oranı da sekonder sonuç değerleriydi.
Bulgular:İki grup arasındaki toplanan ortalama matür oosit sayıla-rı arasında fark yoktu. Serum E 2 düzeyleri, iptal edilen sikluslar, hCG günü endometrial kalınlığı, 2 pronukleus sayıları ve transfer edilen embryo sayılarında da iki grup arasında istatistiksel farklılıklar yoktu. Bununla birlikte Agonist-Antagonist grubunda total gonadotropin tüketimi ve stimülasyon süresi Mikrodoz grubuyla karşılaştırıldığında belirgin olarak daha yüksekti. İki grup arasındaki implantasyon ve klinik gebelik oranları ise birbirine benzerdi.
Sonuç:
Abstract ÖzetOriginal Investigation 187
“…Apart from the above-mentioned studies, available experience with leuprolide acetate and OCP is limited to studies evaluating hyperresponder [12] or poor responder [13,14] cohorts of women. Among high responder patients, premedication with an OCP might decrease the cancellation rate and increase both the clinical and ongoing pregnancy rates when compared with their previous IVF cycle without OCP pretreatment [12].…”
Section: Discussionmentioning
confidence: 99%
“…leuprolide acetate may enhance the follicular response to exogenous gonadotropin in patients who presented a poor response in the long leuprolide acetate protocol in their initial attempt [14]. However, according to a recent trial [13], this positive effect seems to be related with low-dose leuprolide acetate usage rather than OCP itself. The pregnancy rate among OCP pretreated (n = 26) and untreated (n = 27) groups is not statistically significant (15 vs. 14%, respectively) when all patients underwent a microdose flare-up protocol [13].…”
Section: Discussionmentioning
confidence: 99%
“…However, according to a recent trial [13], this positive effect seems to be related with low-dose leuprolide acetate usage rather than OCP itself. The pregnancy rate among OCP pretreated (n = 26) and untreated (n = 27) groups is not statistically significant (15 vs. 14%, respectively) when all patients underwent a microdose flare-up protocol [13]. …”
Background: To analyze the influence of oral contraceptive pill (OCP) pretreatment in intracytoplasmic sperm injection cycles among normoresponders in whom leuprolide acetate is preferred for that kind of gonadotropin-releasing hormone agonist. Methods: Between March 2001 and January 2010, a total of 821 cycles were pretreated with OCP in luteal-long leuprolide acetate in the IVF Center, Faculty of Medicine, University of Hacettepe. Of these, a total of 169 consecutive patients were selected for the final analyses according to the selection criteria (OCP group) and compared with 349 age-matched controls (Control group). The normoresponders were defined by the presence of 6–15 antral follicles in both ovaries. Results: Female age, body mass index, duration of infertility and antral follicle count were similar among both groups. Although the total dose of FSH used and duration of stimulation were similar, the maximal serum estradiol concentrations were higher in the OCP group than in the Control group (2,630.3 ± 1,568.0 vs. 2,166.5 ± 1,259.7 pg/ml, p = 0.001). The mean numbers of metaphase-II oocytes were 11.0 ± 6.2 versus 9.4 ± 5.2 in the OCP and Control groups, respectively (p = 0.004). The mean number of available day 3 embryos having ≧7 blastomeres was also higher in the OCP group (4.4 ± 3.3 vs. 3.5 ± 3.1, p = 0.013). However, the embryo transfer cancellation rate was noted to be higher in the OCP group, which is mainly due to fertilization failure and arrest during embryogenesis (6.5 vs. 2.9%, p = 0.049). The clinical pregnancy (36.7 vs. 38.3%) and implantation rates (21.8 vs. 20.6%) were comparable. Conclusion: These findings suggest that although pretreatment with an OCP might exaggerate ovarian response, the pregnancy rate does not fluctuate in leuprolide acetate cycles among normoresponders.
“…Cette situation concernant neuf à 24 % des cycles selon les études [1,2]. Différentes prises en charge ont été proposées dans la littérature pour optimiser les réponses à la stimulation ovarienne chez les patientes ayant eu une annulation pour mauvaise réponse : la fécondation in vitro en cycle naturel modifié (FIVnm) [3], l'utilisation des antagonistes [4][5][6][7], des supplémentassions de la phase lutéale par de la LH [8], le prétraitement par pilule oestroprogestative [9], l'utilisation de l'aspirine à faibles doses (81 mg/j) [10], ou l'augmentation des doses de gonadotrophines [11,12], la prolongation de la stimulation ovarienne [13], ou l'utilisation de facteurs de croissance [14,15]. Mais, aucune de ces propositions n'a démontré sa supé-riorité dans le cas des mauvaises répondeuses [16].…”
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