The Journal of Obstetrics and Gynaecology of India
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VOL. 66 NUMBER 5 September-October  2016

Outcome Analysis of Day-3 Frozen Embryo Transfer v/s Fresh Embryo Transfer in Infertility: A Prospective Therapeutic Study in Indian Scenario

Neha Palo Chandel ● Vidya V. Bhat ● B. S. Bhat ● Sidharth S. Chandel

Neha Palo Chandel is a Resident at Radhakrishna Multispecialty Hospital ● Vidya V. Bhat is a Consultant at Radhakrishna Multispecialty Hospital ● B. S. Bhat is a Consultant at Radhakrishna Multispecialty Hospital ● Sidharth S. Chandel is a Resident at JLN Hospital and Research Center.

Neha Palo Chandel [neha.palo@yahoo.com]

1 Radhakrishna Multispecialty Hospital and IVF Center, Sunrise Tower, Girinagar, Bengaluru 560085, India
2 JLN Hospital and Research Center, Bhilai, Chhattisgarh, India

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About the Author


Dr. Neha Palo Chandel has been an active academician since early medical days. She graduated from the prestigious Rajiv Gandhi University in 2013; she was the college topper. She has won the best paper and poster awards in the Annual Karnataka State conference 2014. After working in top institutes and Medical College in Delhi and Chhattisgarh, she is presently undergoing ICOG advanced laparoscopic and infertility training from Radhakrishna IVF Centre Bengaluru, guided by the pioneer Dr. Vidya V. Bhat. She is currently working on laparoscopy and infertility, which is her major interest.

Abstract

Introduction: Advanced fertilization techniques like frozen embryo transfer (FET) and assisted reproductive technology have become popular and commonly used methods to treat patients suffering from infertility. Incidences of infertility are on a rise due to increased representation of females in the work place, delay in marriages, stress, and ignorance.

Methods: We performed this prospective therapeutic study to compare FET and fresh embryo transfer in the treatment of infertility in terms of conception rate, patient acceptance, complications, and patient’s compliance. A prospective screening therapeutic study on 108 patients, from September 2013 to September 2014 in Karnataka, India, randomized the patients into 2 groups (n = 54), Group-I treated with day-3 FET while Group-II was treated with fresh embryo transfer, after performing ICSI.

Results: In 108 patients, 45 % patients were within 35 years of age, 35 % were in the age group 35–39. Significantly, 22 (40.75 %) patients treated with FET conceived (P = 0.022), whereas 16 (29.63 %) patients treated with fresh embryo transfer conceived (P = 0.59).

Discussion: There is limited published literature from the subcontinent, comparing techniques like FET and embryo transfers in the treatment of infertility. Awareness and economic reforms must be formulated in India to facilitate individuals facing infertility problems to conceive.

Conclusion: FET has better and significant conception rates compared to fresh embryo transfers. FET shares an advantage of providing good quality embryos for future and subsequent implantations in cases of failure. Patient counseling and motivation play a pivotal role in the success of therapeutic procedure.

Keywords : Infertility, Frozen embryo transfer, ART, Family, Reproduction, India

Introduction

Advanced fertilization techniques like frozen embryo transfer (FET) and assisted reproductive technology (ART) have become the popular and commonly used methods to treat patients suffering from infertility. Incidences of infertility are on a rise due to increased representation of females in the work place, delay in marriages, stress, and ignorance. In India, unlike the olden days, due to increased efforts of the government and NGOs to create awareness, many couples report and seek consultation for infertility issues. However due to lack of published literature from the subcontinent, magnitude of the problem and the results of these procedures in treating infertility are unknown.

A cycle of in vitro fertilization can be completed using frozen embryos as well as fresh embryos. Good quality embryos should be frozen quickly so that they can be stored for use in future. Frozen embryos have the advantage of being stored for later use and at multiple times, avoiding repeated ovarian stimulation [1].

Cryopreservation of embryos has been an important supplementary procedure in the treatment of infertility since the advent of FET which has become an important component of ART [2–10]. FET allows controlled embryo transfer thus lowering the risk of multiple pregnancies [11]. Embryo cryopreservation provides additional clinical safety in the presence of ovarian hyper stimulation [12–16].

Following FET, pregnancy outcomes depend on the patient’s age, infertility duration, infertility type (primary or secondary), and ocyte fertilization i.e., IVF/ICSI, embryo cryopreservation timings and the endometrial thickness on the day of embryo transfer [17–20].

We performed this prospective therapeutic study to compare FET and fresh embryo transfer in the treatment of infertility in terms of conception rate, patient acceptance, complications, and patient’s compliance.

Materials and Methods

In this prospective screening therapeutic study, we prospectively treated females with infertility fromSeptember 2013 to September 2014 at our infertility center in Karnataka, India. Patients visiting gynecological outdoor with a diagnosis of infertility were explained, counseled and after obtaining consent fromthe patient and her husband were included in the study. Out of 1012 patients screened, 108 patients comprised the study population. Patients were randomized into 2 comparable groups, Group-I (n = 54) were treated with a day-3 FET while in Group-II (n = 54), patients were treated with fresh embryo transfer, after performing intracytoplasmic sperm injection (ICSI). The patients were followed up to assess the study and compare the conception rate (CR) and patient convenience and compliance.

Inclusion Criteria

1. Infertile women who were using self-embryos.
2. Male factor infertility, TESA.
3. Women who developed OHSS (ovarian hyper stimulation) in a previous IVF cycle.
4. Women known to be at high risk of OHSS.
5. All patients with> or =2 stimulated eggs/follicles, with E2 >= 2000.

Exclusion Criteria

1. Donor embryos.
2. Poor responders with < 4 stimulated follicles.
3. Subject with previous history of uterine curettage, endocrine disorders (diabetes mellitus, hypothyroidism).
4. Embryo transfer performed in a natural cycle.

Methodology

Among 1012 infertility patients attending the outpatient department, 108 patients who met the inclusion criteria were selected as the study group, following randomization 54 patients were subjected to a day-3 FET, while the other 54 patients were subjected to a day-3 fresh embryo transfer.

Controlled ovarian stimulation was achieved mainly using the gonadotropin-releasing hormone (GnRH) antagonist for pituitary suppression and recombinant FSH. The patients underwent pituitary desensitization with the use of GnRH antagonist. Immediately after the ovum pick-up, ICSI was performed for all the oocytes. The day-3 embryos were either transferred in the same cycle orwere frozen using vitrification technique and transferred in the next cycle [21].

Vitrification involved rapid freezing of the embryo to prevent any ice formation in the embryo cells. Successful conception depends upon the rapidity of freezing. Embryos are known to survive for many years once they are frozen; currently they may be stored for 10 years [22–24]. Embryos are stored in a special solution in a sterile vial/straw inside a container of liquid nitrogen at a temperature of -196 C [25]. Labeling was done very carefully, and embryos were thawed after obtaining a written informed consent from both the parents.

Procedure

On Day 2, a transvaginal baseline scan was performed with serum estradiol (E2) and LH levels to assess the hypothalamo– pituitary–ovarian status of the patient. The stimulation protocol followed for all the subjects was the antagonist protocol. From Day 2 of the cycle, gonadotropins (r-FSH 225 mg/day) were administered till Day 6. Patients were reviewed on Day 7 and a transvaginal scan, serum estradiol (E2) levels, and serum LH levels were done for follicular monitoring, assessment of the number of developing follicles, and to diagnose premature LH surge, if any, respectively.

GnRH antagonist (Cetrorelix 0.25 mg/day) was started once the follicles reached 1.4 cm and was continued until the follicles reached 1.7 cm. Once the follicles were 1.7 cm in size, r-HCG (250 micrograms stat) was given, and 34–35 h later, ovum pick-up was done under general anesthesia and antibiotic cover.

In patients who developed less than 6 matured follicles, transfer was performed in the same cycle. In these patients, immediately after ovum pick-up, progesterone (400 mg per vaginal/day) was started, and two day-3 embryos were transferred in the same cycle itself.

In patients who developed more than six matured follicles, we had let go of the ovum pick-up cycle and called the patient on the 2nd day of the next cycle. From the 2nd day of next cycle, the patient was started on estradiol valerate (4 mg/day) to prepare the endometrium for implantation [26–29]. E2 levels and TVS were done after 5 days and were performed periodically once in 3 days until the E2 reached 250 pg/ml and the endometrium was 1 cm or 10 mm [30–32]. At this stage, progesterone treatment was started (400 mg per vaginal/day) for 3 days before the embryo transfer for the final preparation and maturation of the endometrium [30]. The two best frozen embryos on day 3 were thawed and chosen for transfer[33– 36]. These Day-3 (8A celled) embryos were transferred on the 4th day of progesterone under ultrasound guidance [37, 38]. The duration of the treatment was defined as the period from embryo storage till ET.

After the ET, the woman was continued on progesterone support (400 mg per vaginal/day) [39–41]. Three weeks later, a UPT was done [42–45]. The cases in which pregnancy test was positive, progesterone support was continued until 12 weeks of pregnancy [39–41]. Thereafter, exogenous progesterone treatment was stopped as placental hormones take over. A confirmatory ultrasound was done at 7 weeks for viable gestational sac [25, 41–44]. B-HCG test was done in addition in cases of doubt.

Randomisation Protocol

Randomisation of 108 patients into two groups (n = 54) were performed according to internet-based, computer generated number by a person not involved in treating patients, who coded the numbers and sealed them in envelopes which were then given to the treating physician.

Statistical Analysis

Patient characteristics such as age and duration of infertility were represented as mean, range, and SD. For variables, x2 test and P values were calculated. The data were compiled using standard Microsoft Office Tools.

Observations

In the study population, 108 patients, 45 % patients were within 35 years of age, 35 % were in the age group 35–39, and 20 % patients > 40 years. 47 % patients had infertility of 7–9 years, followed by 42 % patients with 4–6 years of infertility with minimum of 2 years and maximum of 16 years. 70 % patients had a primary infertility. The patients in Group-1 were in the range of 25–47 with mean 33 years, SD 5. The patients in Group-2 were in the range of 24–45 with mean 31 years, SD 6. The baseline characteristics of 2 groups i.e., mean age, mean duration, and type of infertility are represented in Table 1. Causes of secondary infertility are listed in Table 2.


In Group-I, patients treated with FET, 22 (40.75 %) patients conceived significantly, 12 of them being < 35 years, followed by 8 in the group 35–39 years. 32 (59.25 %) patients had a failure (P = 0.022) with a x2 value of 7.59, Df = 2. The pregnancy rate after FET in women aged < 35 years was 63.15 % (12/19), in patients aged 35–39 years was 36.36 % (8/22), and > 40 years was 15.3 % (2/13) (see Table 3).

In Group-II, patients treated with fresh embryo transfer, 16 (29.63 %) patients conceived, nine of them being < 35 years was 31 % (9/29), followed by six in the group 35–39 years. 38 (70.37 %) patients had a failure (P = 0.59) with x2 value 1.04, Df = 2. The pregnancy rate in fresh embryo transfers in the age group < 35 years was 56.25 %, 35–39 years was 37.5 % (6/16), and in > 40 years age group was 11 % (1/9) (see Table 4). Statistical analysis showed that young (\35) and old (35–40) mothers had significant differences in pregnancy rates in FET.


Discussion

Our study compared 3-day FET with fresh embryo transfer in patients with infertility ranging from 2 to 16 years. The results reveal a significant difference between the conception rates following FET as compared to a fresh embryo transfer. Patient compliance is better with FET as the procedure stores the ovum for future purpose, minimizing unnecessary ovarian hyper stimulation, and allows the embryo transfer in a normal hormonal milieu, minimizing risks of a failure. FET has less known complications.

Due to lack of published studies from the subcontinent, the outcomes from other centers are less known. The results also suggest that in normal- and high-responder patients, it may be advantageous to cryopreserve all viable embryos and use them in a subsequent FET. Importantly, the data were extracted to allow for an intention-to-treat analysis. Patient counseling and motivation play a pivotal role in the success of the therapeutic procedure; couples who are motivated do better in terms of patient compliance, follow-up, and success rates.

The results favoring FET instead of fresh embryo transfer may be related to the adverse effects of COH on endometrial receptivity, as well as the improved results that can be achieved with current cryopreservation methods [46–48].

Embryo implantation remains an unsolved problem in ART, being responsible for 2/3 failures, whereas the embryo itself is responsible for only 1/3 of the failures [49]. Subtle increases in serum P levels (i.e., premature luteinization) show a positive correlation with FSH levels at the end of the follicular phase in COH [50–57]. With COH, the elevated P may cause advanced endometrial maturation, without affecting embryo quality which may lower implantation rates due to asynchrony between embryo and the endometrium in fresh cycles [58, 59].

Uterine receptivity is better achieved during natural cycles or with hormone replacement therapy with exogenous E2 and P, compared to stimulated cycles [26, 60, 61]. There is evidence showing that high E2 levels ( > 2500 pg/mL) may impair the endometrium maturation and implantation [62, 63]. The cryopreservation of embryos has become a vital procedure in ART. Endometrial priming for FET renders endometrium more receptive than in fresh embryo cycles [64–68]. Whereas a universal priming protocol lacks, vitrification technique has shown a higher embryo survival rate, compared to slow freezing, resulting in significantly higher implantation and pregnancy rates per transfer [69, 70].

In summary, the results of this analysis suggest that there is evidence of moderate quality that the implantation, clinical and ongoing pregnancy rates of ART cycles may be improved by performing FET compared with fresh embryo transfer. These results may be explained by improved embryo-endometrium synchrony achieved with endometrium preparation cycles instead of COH cycles. If embryos are frozen immediately after fertilization, which are still in pronuclear stage, and are being used, then the procedure differs as these embryos are literally only one cell at the point of freezing and there is no way to tell how good their quality will be. They must be thawed and cultured for at least 2–3 days in the lab until they reach a stage where they can be assessed using pre-implantation screening techniques if required. One should ensure that the embryos and the uterus are ready on the same day.

In view of the increasing incidence of infertility, keeping in mind the cost factor associated with these procedures and the failure rates, a huge economic burden may be imparted on individuals, especially the middle and low income group people who cannot sometimes afford this luxury. In India, insurances and government policies for infertility do not exist, depriving many of this privileged facility and providing a hope for parenthood. Thus, awareness and economic reforms must be formulated, especially in India, to facilitate individuals facing infertility problems with treatment options, providing them with a hope to live.

Compliance with ethical requirements and Conflict of interest The authors have no financial or other conflict of interest to declare and no financial or other relationships leading to conflict of interest. The author have adhered to the ethical requirements. Authors have no ethical issues to delcare.

Funding This research received no specific grant from any funding agency in the public, commercial or not-for-profit sectors.

References

  1. Evans J, Hannan NJ, Edgell TA, et al. Fresh versus frozen embryo transfer: backing clinical decisions with scientific and clinical evidence. Hum Reprod Update. 2014. doi:10.1093/hum upd/dmu027.
  2. Trounson A, Mohr L. Human pregnancy following cryopreservation, thawing and transfer of an eight-cell embryo. Nature. 1983;305:707–9.
  3. Zeilmaker GH, Alberda AT, van Gent I, et al. Two pregnancies following transfer of intact frozen-thawed embryos. Fertil Steril. 1984;42:293–6.
  4. Edgar DH, Bourne H, Speirs AL, et al. A quantitative analysis of the impact of cryopreservation on the implantation potential of human early cleavage stage embryos. Hum Reprod. 2000;15: 175–9.
  5. Tiitinen A, Halttunen M, Harkki P, et al. Elective single embryo transfer: the value of cryopreservation. Hum Reprod. 2001;16: 1140–4.
  6. Oehninger S, Mayer J, Muasher S. Impact of different clinical variables on pregnancy outcome following embryo cryopreservation. Mol Cell Endocrinol. 2000;169:73–7.
  7. Mandelbaum J, Belaı¨sch-Allart J, Junca AM, et al. Cryopreservation in human assisted reproduction is now routine for embryos but remains a research procedure for oocytes. Hum Reprod. 1998;13(Suppl 3):161–74.
  8. Belva F, Henriet S, Abbeel EV, et al. Neonatal outcome of 937 children born after transfer of cryopreserved embryos obtained by ICSI and IVF and comparison with outcome data of fresh ICSI and IVF cycles. Hum Reprod. 2008;23(10):2227–38.
  9. Schalkoff ME, Oskowitz SP, Powers RD. A multifactorial analysis of the pregnancy outcome in a successful embryo cryopreservation program. Fertil Steril. 1993;59:1070–4.
  10. Andersen NA, Goossens V, Bhattacharya S, et al. Assisted reproductive technology and intrauterine inseminations in Europe 2005: results generated from European registers by ESHRE: ESHRE The European IVF Monitoring Programme (EIM), for the European Society of Human Reproduction and Embryology (ESHRE). Hum Reprod. 2009;24:1267–87.
  11. Berin I, Engmann LL, Benadiva CA, et al. Transfer of two versus three embryos in women less than 40 years old undergoing frozen transfer cycles. Fertil Steril. 2010;93(2):355–9.
  12. Imudia AN, Awonuga AO, Kaimal AJ, et al. Elective cryopreservation of all embryos with subsequent cryothaw embryo transfer in patients at risk for ovarian hyperstimulation syndrome reduces the risk of adverse obstetric outcomes: a preliminary study. Fertil Steril. 2013;99:168–73.
  13. Wiener-Megnazi Z, Lahav-Baratz S, Rothschild E, et al. Impact of cryopreservation and subsequent embryo transfer on the outcome of in vitro fertilization in patients at high risk for ovarian hyperstimulation syndrome. FertilSteril. 2002;78:201–3.
  14. Awonuga AO, Dean N, Zaidi J, et al. Outcome of frozen embryo replacement cycles following elective cryopreservation of all embryos in women at risk of developing ovarian hyperstimulation syndrome. J Assist Reprod Genet. 1996;13:293–7.
  15. Pattinson HA, Hignett M, Dunphy BC, et al. Outcome of thaw embryo transfer after cryopreservation of all embryos in patients at risk of ovarian hyperstimulation syndrome. Fertil Steril. 1994;62:1192–6.
  16. Sills ES, McLoughlin LJ, Genton MG. Ovarian hyperstimulation syndrome and prophylactic human embryo cryopreservation: analysis of reproductive outcome following thawed embryo transfer. J Ovarian Res. 2008;1:7.
  17. Salumets A, Suikkari AM, Makinen S, et al. Frozen embryo transfers: implications of clinical and embryological factors on the pregnancy outcome. Hum Reprod. 2006;21:2368–74.
  18. Ashrafi M, Jahangiri N, Hassani F, et al. The factors affecting the outcome of frozen-thawed embryo transfer cycle. Taiwan J Obstet Gynecol. 2011;50:159–64.
  19. Eftekhar M, Rahmani E, Pourmasumi S. Evaluation of clinical factors influencing pregnancy rate in frozen embryo transfer. Iran J Reprod Med. 2014;12(7):513–8.
  20. Veleva Z, Orava M, Nuojua-Huttunen S, et al. Factors affecting the outcome of frozen-thawed embryo transfer. Hum Reprod. 2013;28(9):2425–31.
  21. Xie X, Zou L, Shen Y, et al. Vitrification technology in whole embryo freezing. Zhong Nan Da XueXueBao Yi Xue Ban. 2010;35(7):673–8.
  22. Papis K, Lewandowski P, Wolski JK, et al. Children born from frozen embryos stored for 10 years—analysis of 5 cases. Ginekol Pol. 2013;84(11):970–3.
  23. Aflatoonian N, Pourmasumi S, Aflatoonian A, et al. Duration of storage does not influence pregnancy outcome in cryopreserved human embryos. Iran J Reprod Med. 2013;11(10):843–6.
  24. Rato ML, Gouveia-Oliveira A, Plancha CE. Influence of postthaw culture on the developmental potential of human frozen embryos. J Assist Reprod Genet. 2012;29(8):789–95.
  25. Singh N, Begum AA, Malhotra N, et al. Role of early serum beta human chorionic gonadotropin measurement in predicting multiple pregnancy and pregnancy wastage in an in vitro ET fertilization cycle. J Hum Reprod Sci. 2013;6(3):213–8.
  26. Paulson RJ. Hormonal induction of endometrial receptivity. Fertil Steril. 2011;96(3):530–5.
  27. Check JH, Dietterich C, Cohen R, et al. Increasing the dosage of progesterone (P) supplemention from the mid-luteal phase in women not attaining a mid-luteal homogeneous hyperechogenic (HH) pattern with sonography improves pregnancy rates (PRS) following frozen embryo transfer (ET). Clin Exp Obstet Gynecol. 2010;37(1):13–4.
  28. Glujovsky D, Pesce R, Fiszbajn G, et al. Endometrial preparation for women undergoing embryo transfer with frozen embryos or embryos derived from donor oocytes. Cochrane Database Syst Rev. 2010. doi:10.1002/14651858.CD006359.pub2.
  29. Xu W, Zhou F, Li C, et al. Application of Femoston in hormone replacement treatment-frozen embryo transfer and its clinical outcomes. Zhonghua Yi Xue Za Zhi. 2013;93(47):3766–9.
  30. Kondapalli LA, Molinaro TA, Sammel MD, et al. A decrease in serum estradiol levels after human chorionic gonadotrophin administration predicts significantly lower clinical pregnancy and live birth rates in in vitro fertilization cycles. Hum Reprod. 2012;27(9):2690–7.
  31. Check JH. The importance of sonographic endometrial parameters in influencing success following embryo transfer in the modern era and therapeutic options—part 1: the importance of late proliferative phase endometrial thickness. Clin Exp Obstet Gynecol. 2011;38(3):197–200.
  32. Iyoke CA, Ugwu GO, Ezugwu FO, et al. The role of ultrasonography in in vitro fertilization and embryo transfer (IVF-ET). Niger J Med. 2013;22(3):162–70.
  33. Rhenman A, Berglund L, Brodin T, et al. Which set of embryo variables is most predictive for live birth? A prospective study in 6252 single embryo transfers to construct an embryo score for the ranking and selection of embryos. Hum Reprod. 2014;30(1): 28–36.
  34. Holte J, Berglund L, Milton K, et al. Construction of an evidencebased integrated morphology cleavage embryo score for implantation potential of embryos scored and transferred on day 2 after oocyte retrieval. Hum Reprod. 2007;22(2):548–57.
  35. Van Royen E, Mangelschots K, De Neubourg D, et al. Characterization of a top quality embryo, a step towards single-embryo transfer. Hum Reprod. 1999;14(9):2345–9.
  36. de Neubourg D. Prognostic factors of implantation. J Gynecol Obstet Biol Reprod (Paris). 2004;33(12):S21–4.
  37. Buckett WM. A meta-analysis of ultrasound-guided versus clinical touch embryo transfer. Fertil Steril. 2003;80(4):1037–41.
  38. Pandian Z, Marjoribanks J, Ozturk O, et al. Number of embryos for transfer following in vitro fertilisation or intra-cytoplasmic sperm injection. Cochrane Database Syst Rev. 2013;29:7.
  39. de Ziegler D, Fanchin R, de Moustier B, et al. The hormonal control of endometrial receptivity: estrogen (E2) and progesterone. J Reprod Immunol. 1998;39(1–2):149–66.
  40. Daya S, Gunby J. Luteal phase support in assisted reproduction cycles. Cochrane Database Syst Rev. 2004;3:CD004830.
  41. van der Linden M, Buckingham K, Farquhar C, et al. Luteal phase support for assisted reproduction cycles. Cochrane Database Syst Rev. 2011. doi:10.1002/14651858.CD009154.pub2.
  42. Sansinena M, Santos MV, Taminelli G, et al. Implications of storage and handling conditions on glass transition and potential devitrification of oocytes and embryos. Theriogenology. 2014; 82(3):373–8.
  43. Jouppila P, Huhtaniemi I, Herva R, et al. Correlation of human chorionic gonadotropin secretion in early pregnancy failure with size of gestational sac and placental histology. Obstet Gynecol. 1984;63(4):537–42.
  44. Kolte AM, Bernardi LA, Christiansen OB, et al. Terminology for pregnancy loss prior to viability: a consensus statement from the ESHRE special interest group, early pregnancy. Hum Reprod. 2014;30(3):495–8.
  45. van Oppenraaij RH, Goddijn M, Lok CA, et al. Early pregnancy: revision of the Dutch terminology for clinical and ultrasound findings. Ned Tijdschr Geneeskd. 2008;152(1):20–4.
  46. Shapiro BS, Daneshmand ST, Garner FC, et al. Evidence of impaired endometrial receptivity after ovarian stimulation for in vitro fertilization: a prospective randomized trial comparing fresh and frozen-thawed embryo transfer in normal responders. Fertil Steril. 2011;96:344–8.
  47. Aflatoonian A, Oskouian H, Ahmadi S, et al. Can fresh embryo transfers be replaced by cryopreserved-thawed embryo transfers in assisted reproductive cycles? A randomized controlled trial. J Assist Reprod Genet. 2010;27:357–63.
  48. Shapiro BS, Daneshmand ST, Garner FC, et al. Evidence of impaired endometrial receptivity after ovarian stimulation for in vitro fertilization: a prospective randomized trial comparing fresh and frozen-thawed embryo transfers in high responders. Fertil Steril. 2011;96:516–8.
  49. Achache H, Revel A. Endometrial receptivity markers, the journey to successful embryo implantation. Hum Reprod Update. 2006;12:731–46.
  50. Shapiro BS, Daneshmand ST, Garner FC, et al. Large blastocyst diameter, early blastulation, and low preovulatory serum progesterone are dominant predictors of clinical pregnancy in fresh autologous cycles. Fertil Steril. 2008;90:302–9.
  51. Shapiro BS, Daneshmand ST, Garner FC, et al. Embryo cryopreservation rescues cycles with premature luteinization. Fertil Steril. 2010;93:636–41.
  52. Al-Azemi M, Kyrou D, Kolibianakis EM, et al. Elevated progesterone during ovarian stimulation for IVF. Reprod Biomed Online. 2012;24:381–8.
  53. Venetis CA, Kolibianakis EM, Papanikolaou E, et al. Is progesterone elevation on the day of human chorionic gonadotrophin administration associated with the probability of pregnancy in in vitro fertilization? A systematic review and meta-analysis. Hum Reprod Update. 2007;13:343–55.
  54. Ubaldi F, Bourgain C, Tournaye H, et al. Endometrial evaluation by aspiration biopsy on the day of oocyte retrieval in the embryo transfer cycles in patients with serum progesterone rise during the follicular phase. Fertil Steril. 1997;67:521–5.
  55. Filicori M, Cognigni GE, Pocognoli P, et al. Modulation of folliculogenesis and steroidogenesis in women by graded menotrophin administration. Hum Reprod. 2002;17:2009–15.
  56. Andersen AN, Devroey P, Arce JC. Clinical outcome following stimulation with highly purified hMG or recombinant FSH in patients undergoing IVF: a randomized assessor-blind controlled trial. Hum Reprod. 2006;21:3212–27.
  57. Bosch E, Escudero E, Crespo J, et al. Serum luteinizing hormone in patients undergoing ovarian stimulation with gonadotropinreleasing hormone antagonists and recombinant follicle-stimulating hormone and its relationship with cycle outcome. Fertil Steril. 2005;84:1529–32.
  58. Bourgain C, Devroey P. The endometrium in stimulated cycles for IVF. Hum Reprod Update. 2003;9:515–22.
  59. Santos MA, Kuijk EW, Macklon NS. The impact of ovarian stimulation for IVF on the developing embryo. Reproduction. 2010;139:23–34.
  60. Simon C, Velasco JJG, Valbuena D, et al. Increasing uterine receptivity by decreasing estradiol levels during the preimplantation period in high responders with the use of a follicle-stimulating hormone step-down regimen. Fertil Steril. 1998;70:234–9.
  61. Paulson RJ, Sauer MV, Lobo RA. Embryo implantation after human in vitro fertilization: importance of endometrial receptivity. Fertil Steril. 1990;53:870–4.
  62. Simon C, Cano F, Valbuena D, et al. Clinical evidence for a detrimental effect on uterine receptivity of high serum estradiol levels in high and normal responders patients. Hum Reprod. 1995;10:2432–7.
  63. Groothuis PG, Dassen HH, Romano A, et al. Estrogen and the endometrium: lessons learned from gene expression profiling in rodents and human. Hum Reprod Update. 2007;13:405–17.
  64. Abdel Hafez FF, Desai N, Abou-Setta AM, et al. Slow freezing, vitrification and ultra-rapid freezing of human embryos: a systematic review and metaanalysis. Reprod Biomed Online. 2010;20:209–22.
  65. Guerif F, Bidault R, Cadoret V, et al. Parameters guiding selection of best embryo for transfer after cryopreservation: a reappraisal. Hum Reprod. 2002;17:1321–6.
  66. Mandelbaum J. Embryo and oocyte cryopreservation. Hum Reprod. 2000;15:43–7.
  67. Martı´nez-Conejero JA, Simo´n C, Pellicer A, et al. Is ovarian stimulation detrimental to the endometrium? Reprod Biomed Online. 2007;15:45–50.
  68. Horcajadas JA, Riesewijk A, Polman J, et al. Effect on controlled ovarian hyperstimulation in IVF on endometrial gene expression profiles. Mol Hum Reprod. 2005;11:195–205.
  69. Glujovsky D, Pesce R, Fiszbajn G, et al. Endometrial preparation for women undergoing embryo transfer with frozen embryos or embryos derived from donor oocytes. Cochrane Database Syst Rev. 2010;20:CD006359.
  70. Saragusty J, Arav A. Current progress in oocyte and embryo cryopreservation by slow freezing and vitrification. Reproduction. 2011;141:1–19.
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