Geburtshilfe Frauenheilkd 2012; 72(8): 710-715
DOI: 10.1055/s-0032-1315059
Review
GebFra Science
Georg Thieme Verlag KG Stuttgart · New York

Endometrial Receptivity and its Predictive Value for IVF/ICSI-Outcome

Die endometriale Rezeptivität in der IVF-Therapie
A. Heger
1   Obstetrics and Gynecology, Medical University of Vienna, Vienna, Austria
,
M. Sator
1   Obstetrics and Gynecology, Medical University of Vienna, Vienna, Austria
2   Fertility Center Doebling, Ambulatorium Doebling, Vienna, Austria
,
D. Pietrowski
1   Obstetrics and Gynecology, Medical University of Vienna, Vienna, Austria
2   Fertility Center Doebling, Ambulatorium Doebling, Vienna, Austria
› Author Affiliations
Further Information

Correspondence

Dr. Detlef Pietrowski
Medical University of Vienna, Obstetrics and Gynecology
1090 Vienna
Austria

Publication History

received 29 March 2012
revised 12 June 2012

accepted 26 June 2012

Publication Date:
28 August 2012 (online)

 

Abstract

Endometrial receptivity plays a crucial role in the establishment of a healthy pregnancy in cycles of assisted reproduction. The endometrium as a key factor during reproduction can be assessed in multiple ways, most commonly through transvaginal grey-scale or 3-D ultrasound. It has been shown that controlled ovarian hyperstimulation has a great impact on the uterine lining, which leads to different study results for the predictive value of endometrial factors measured on different cycle days. There is no clear consensus on whether endometrial factors are appropriate to predict treatment outcome and if so, which one is suited best. The aim of this review is to summarize recent findings of studies about the influence of endometrial thickness, volume and pattern on IVF- and ICSI-treatment outcome and provide an overview of future developments in the field.


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Zusammenfassung

Die endometriale Rezeptivität spielt eine entscheidende Rolle für den Beginn und den Erhalt einer Schwangerschaft. Die physiologische Ausbildung eines implantationsfördernden und -erhaltenden Endometriums wird daher als Schlüsselfaktor bei allen fertilitätsunterstützenden therapeutischen Behandlungen angesehen. Dabei wird in der Praxis der Zustand des Endometriums mithilfe des Einsatzes des transvaginalen Ultraschalls bestimmt. Die kontrollierte ovarielle Überstimulation, wie sie im Rahmen einer IVF-Therapie angewandt wird, kann einen erheblichen Einfluss auf den Zustand des Endometriums zum Zeitpunkt der Untersuchung haben. Bislang gibt es allerdings keinen klaren Konsens darüber, ob endometriale Faktoren geeignet sind, um das Behandlungsergebnis einer IVF-Therapie verlässlich vorhersagen zu können. Das Ziel dieser Übersichtsarbeit ist es daher, die aktuellen wissenschaftlichen Ergebnisse über den Einfluss der mithilfe von Ultraschallmessungen gewonnenen endometrialen Parametern im Rahmen der IVF-Behandlung zusammenzufassen und einen Überblick über zukünftige Entwicklungen auf diesem Gebiet zu geben.


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Introduction

A multitude of variables play a major part in successful implantation and pregnancy, nonetheless in cycles of assisted reproduction. It is established that the endometrium is a key factor during the so-called “implantation window”, a short period of time of maximal endometrial receptivity to blastocyst signals [1], [2], during which the human embryo is nearing the endometrium in secretory phase in order to attach and invade. This embryo-maternal dialogue is crucial for the establishment of a healthy pregnancy [3]. During the natural menstrual cycle the endometrium is under constant influence of hormones, estradiol (E2) from the maturing follicles and later progesterone (P) from the corpus luteum [4]. These hormones lead directly and indirectly to endometrial proliferation, transformation and secretion [5], and this process becomes apparent as a change in thickness and pattern. During the proliferative phase the endometrium thickens and thus provides an ideal site for attachment and nourishment for an implanting embryo in the first few weeks until the development of the placenta is completed [6]. This post-ovulatory state of the endometrium is therefore of great importance to the success of IVF and ICSI treatments [7].

In this review we will elaborate on the hormonal levels during assisted reproduction techniques (ART) as well as their deviation from levels during natural menstrual cycles and how that may potentially lead to changes to the endometrium. Furthermore, sonographically measureable endometrial parameters like thickness, volume and pattern will be examined in regard to their predictive value for positive treatment outcome.


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Hormonal Influence During ART

In order to establish an endometrium that is able to offer the blastocyst a site for attachment and nourishment, it has to undergo certain proliferative changes [6]. Changes to the endometrium occur as an answer to hormonal signals [5]. During natural cycles these signals are estradiol and progesterone but in assisted cycles these hormones are substituted by controlled ovarian hyperstimulation (COH), using gonadotropins in various different protocols in order to induce multiple follicular growth [8]. This may lead to differing hormone levels to those in natural cycles and may potentially alter endometrial development and receptivity. Moreover, it was shown by other authors that different stimulation protocols used for COH severely affected the ART outcome with regards to pregnancy rates [9], [10].

Recently these stimulation protocols consist mostly of either hMG [11], [12], [13] or recombinant FSH [13], [14], [15] injections alone or, if the serum E2 levels are initially too low and further stimulation of follicular growth is needed, a combination of both [13], [15], [16], [17].

Some authors have also added GnRH antagonists after at least one follicle was > 14 mm in diameter [14] or gave their patients GnRH agonists for pituitary downregulation prior to COH [11], [12], [13], [15], [18].

The protocols used until the late 1990s containing clomiphene citrate (CC) [19], [20] have long since become obsolete, because CC is claimed to have a negative influence on uterine receptivity [21], [22], [23]. This is very likely due to its partly antiestrogenic effect [24].

The effects of these pharmacological treatments on the endometrial quality may be one of the reasons for decreased implantation rates [25]. Following COH supraphysiological levels of estradiol are achieved during follicular phase and consecutively supraphysiological levels of estradiol and progesterone are being produced by multiple corpora lutea [6], [25], [26], [27].

Abnormally high E2 levels in the early luteal phase may result in irregular endometrial structure [28]. Furthermore, changes in estrogen to progesterone ratio, growth factor concentrations and cell adhesion molecule profiles, possibly induced by ovarian stimulation, may potentially affect endometrial receptivity [26]. It was also established that under COH the endometrial pinopod expression occurred at an earlier state of endometrial maturation, which could lead to a time shift of the implantation window [29].

Valbuena et al. [25] showed in their study that there was a decline in both implantation and pregnancy rates as serum E2 concentrations increased on days 4–6 after oocyte retrieval, implying that this abnormal endocrine level could lead to impaired implantation. Sharara et al. [30] on the other hand found no detrimental effect of high E2 levels on pregnancy rates.


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Endometrial Assessment

Endometrial receptivity is the ability of the endometrium to successfully attach the blastocyst, to nourish it and keep it alive. This can only be achieved after the endometrium underwent a number of histological changes while also increasing in thickness [4]. While histological changes can only be examined by biopsy, transvaginal ultrasound is a non-invasive, easy and reliable method to measure parameters like thickness and pattern [2], [31]. Practitioners performing in vitro fertilization (IVF) or any other ART method (e.g. intracytoplasmatic sperm injection, ICSI) are in need of an objective measurement to determine the probability of a successful pregnancy. Therefore, using a simple and accurate measuring tool like grey-scale ultrasound and evaluating endometrial thickness, pattern or volume as surrogate parameters for endometrial receptivity seems appropriate [4]. These parameters are likely to be indirect indications of the receptive quality of the endometrium and we are going to discuss some recent findings on each of these factors and examine if any one of them can be used to predict the chances of a positive outcome.

Endometrial thickness

Endometrial thickness is commonly measured in the midsagittal plane, from the outer edge of the endometrial-myometrial junction to the outer edge of the thickest part of the endometrium by two-dimensional ultrasonography [11], [12], [13], [14], [16], [32], [33].

The measurement of endometrial thickness and its predictive value is, above all, a question of timing. Most authors have used the thickness as measured on the day of ovulation induction (triggered by hCG administration) for their analyses. But since the endometrium is under constant influence of hormones it changes incessantly and still increases its thickness after ovulation in natural cycles [34]. This may suggest that the exact day of ultrasound evaluation has a great influence on the results of studies. [Table 1] shows an overview over the main study results for the respective dates of endometrial assessment.

Table 1 Studies regarding endometrial thickness.

Day of endometrial assessment

Number of cycles analysed

Study design

Main study results

Abbreviations: retro: retrospective; pro: prospective; EMT: endometrial thickness; PR: pregnancy rates; IR: implantation rates; ART: assisted reproduction techniques; v.s.: vide supra

Before induction of ovulation

414

retro

statistically significant relationship between EMT and total PR

Bozdag et al. (2009)

758

retro

IR & PR significantly higher if EMT > 14 mm

Induction of ovulation

Okohue et al. (2009)

251

pro, cohort study

significantly more pregnancies occured in patients with an EMT of 7–14 mm

Kinay et al. (2010)

40

pro, cohort study

no significant difference in mean EMT between pregnant and non-pregnant groups

Mercé et al. (2008)

80

pro, clinical study

v.s.

Corbacioglu et al. (2009)

241

retro

v.s.

Laasch et al. (2004)

155

retro

v.s.

Yoeli et al. (2004)

1 218

pro, clinical study

v.s.

Rashidi et al. (2004)

150

pro

v.s.

Coulam et al. (1994)

405

pro, case-control

v.s.

Sharara et al. (1999)

86

pro

v.s.

Lesny et al. (1999)

60

retro

v.s.

Al-Ghamdi et al. (2008)

2 464

retro, cohort study

significant difference in mean EMT between pregnant and non-pregnant groups

Chen et al. (2010)

2 896

retro

PR was significantly higher with increasing EMT

Richter et al. (2007)

1 294

retro

significant difference in mean EMT between pregnant and non-pregnant groups

Traub et al. (2009)

114

retro, cohort study

patients achieving clinical pregnancy had a thicker endometrial stripe

Amir et al. (2007)

2 339

retro

a thicker endometrium is correlated with a higher PR only for patients > 35 years of age

Zhang et al. (2005)

897

retro

PR was positively associated with increased EMT

Rinaldi et al. (1996)

158

pro

PR was positively associated with increased EMT ≥ 10 mm for IVF cycles only

Before oocyte aspiration

Bergh et al. (1992)

100

pro

significantly thicker endometrium in pregnant patients

Gonen & Casper (1990)

123

pro, cohort study

v.s.

Oocyte retrieval

Welker et al. (1989)

190

pro

no relationship between EMT and IR

Lesny et al. (1999)

60

retro

no significant difference in mean EMT between pregnant and non-pregnant groups

Bassil et al. (2001)

153

pro, case-control

v.s.

Järvelä et al. (2005)

35

pro

v.s.

Schild et al. (2001)

135

pro, clinical study

no relationship between EMT and IR

Kumbak et al. (2009)

175

retro

≤ 7 mm not necessarily a negative predictor

Quintero et al. (2004)

2

case report

two successful twin pregnancies with an EMT of 16 and 20 mm

Embryo transfer

Kovacs et al. (2003)

1 228

retro

mean EMT significantly higher in pregnant patients

Kinay et al. (2010)

40

pro, cohort study

no significant difference in mean EMT between pregnant and non-pregnant groups

Bassil et al. (2001)

153

pro, case-control

v.s.

Kovachev et al. (2005)

58

pro, clinical study

endometrial volume is a better predictor for ART outcome

A statistically significant association between total pregnancy rate (PR) and endometrial thickness, measured before induction of ovulation, has been found by Kehila et al. [35]. They argue that the chances of a successful pregnancy are about three times higher if the endometrium is more than 12 mm wide [35]. The study of Bozdag et al. [36] reaches roughly the same conclusion, as they found a significantly higher clinical PR in patients with an endometrial thickness of > 14 mm on the day of hCG administration.

In some studies there was neither a correlation between pregnancy rates and endometrial thickness on the day of hCG application [37], [38], [39], [40] nor a significant difference in mean endometrial thickness between pregnant and non-pregnant groups [12], [14], [15], [37], [38], [39], [40], [41], [42], [43].

Others on the contrary did find that an increasing endometrial thickness on hCG day led to a higher probability of establishing a healthy pregnancy [11], [13], [16], [17], [33], [44].

In the report of Rinaldi et al. [45] there was a significantly higher PR with a thickness of > 10 mm, but only for IVF and not for ICSI cycles.

As for the day before oocyte aspiration, Bergh et al. [46] found a significantly thicker endometrium in patients who were able to conceive when compared to those who were not. Gonen & Casperʼs study [19] reached the same conclusion.

The endometrial thickness measured on the day of oocyte retrieval proved to be no reliable predictor of conception in some cases [20], [43], [47], [48], [49].

Kumbak et al. [50] examined the outcome in patients with a thin endometrium (7 mm or less) on the day of ovum pick-up and concluded that it was not necessarily a negative predictor, especially when the patient age was < 35 years and the number of transferred embryos was three or more. As for the other side of the spectrum, Quintero et al. [51] reported two successful twin pregnancies with an endometrial lining of 16 and 20 mm, respectively, also measured on the day of oocyte retrieval.

The latest possible date to examine the thickness of the uterine lining is during embryo transfer (ET). Kovacs et al. [52] showed that the mean endometrial thickness was significantly higher in pregnant patients. Others found no statistically significant difference when comparing endometrial thickness between conception and non-conception groups [14], [47].

Kovachev et al. [53] compared the predictive value of endometrial thickness on the day of ET to that of endometrial volume on the same day. Their results imply that volume is a better predictor for ART outcome [53].


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Endometrial volume

Some authors tried to distinguish a better predictor for endometrial receptivity than thickness alone. Kovachev et al. [53] examined the predictive value of endometrial volume as assessed by 3-D ultrasound on the day of ET and found that a volume of < 2 ml resulted in significantly lower implantation rates, whereas an endometrial volume of > 2 ml was a positive predictor for successful ART outcome. One investigator showed that endometrial volume decreased significantly after the administration of hCG in women who succeeded to conceive, but not in those who failed to do so [48]. Also, endometrial volume on the day of oocyte aspiration did not differ between conception and non-conception cycles [48], confirming findings from previous studies [49], [54]. Mercé et al. [15], however, have found a significantly higher endometrial volume in patients that became pregnant ([Table 2]).

Table 2 Studies regarding endometrial volume.

Day of endometrial assessment

Number of cycles analysed

Study design

Main study results

Abbreviations: retro: retrospective; pro: prospective; EV: endometrial volume; hCG: human chorionic gonadotropin; IR: implantation rates; v.s.: vide supra

Induction of ovulation

Mercé et al. (2008)

80

pro, clinical study

significantly higher EV in pregnant patients

Järvalä et al. (2005)

35

pro

EV decreased significantly after hCG administration in patients who conceived

Oocyte retrieval

Järvelä et al. (2005)

35

pro

no difference in EV between pregnant and non-pregnant patients

Schild et al. (2001)

135

pro, clinical study

v.s.

Schild et al. (1999)

47

pro

v.s.

Embryo transfer

Kovachev et al. (2005)

58

pro, clinical study

EV of < 2 ml resulted in significantly lower IR


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Endometrial pattern

The ultrasonic appearance of endometrial pattern has been described by Smith et al. [55] as a “qualitative change in grey-scale appearance or reflectivity”. In most studies two distinct patterns have been defined, one of “homogeneous” echogenicity and one of a “multi-layered” or “triple-line” echogenicity [13], [19], [20], [46], [48], [56], [57].

Welker et al. [20] found that endometrial pattern on the day of oocyte retrieval positively influenced implantation, whereas no such correlation was found for endometrial thickness of the same day. Another study also showed that pregnant women had a significantly higher rate of multi-layered patterns [19].

The report of Sher et al. [56] further supports those results, as they found a much higher clinical PR in patients with a multi-layered pattern and an endometrial thickness of ≥ 9 mm in comparison to those with homogeneous echogenicity and/or a thickness of < 9 mm. Other investigators produced similar results, finding a significantly higher PR in women with a triple-line pattern compared to those with a homogeneous one, both after FSH stimulation and on the day of ovum pick-up [48].

However, there are also various studies showing no statistically significant relationships between the different echogenic patterns and pregnancy rates [13], [40], [46], [47], [57], and Kuc et al. [58] found out that endometrial echogenicity significantly influenced treatment outcome only in the long GnRH agonist protocol.

Sharara et al. [42] could confirm a significantly lower implantation rate in patients who had a homogeneous, hyperechogenic pattern compared to those with a triple-line pattern on the day of oocyte retrieval. ([Table 3]) Furthermore, they evaluated the endometrium on the day of hCG application as well as on the day of oocyte retrieval and noted a change from a more receptive triple-line pattern to one of homogenous echogenicity between those two dates in 12,6 % of cycles [42]. A similar change in pattern was noted by Bassil et al. [47], as they recorded an alteration from a multilayered to a homogeneous, hyperechogenic pattern between the day of oocyte retrieval and the day of embryo transfer in 22.2 % of cycles. This suggests that the evaluation of endometrial receptivity is probably more accurate the closer it is performed to the actual implantation of the embryo.

Table 3 Studies regarding endometrial pattern.

Day of endometrial assessment

Number of cycles analysed

Study design

Main study results

Abbreviations: retro: retrospective; pro: prospective; IR: implantation rates; EP: endometrial pattern; PR: pregnancy rates; v.s.: vide supra

Induction of ovulation

Sharara et al. (1999)

86

pro

significantly lower IR in patients with a homogeneous, hyperechogenic pattern

Rashidi et al. (2005)

150

pro

no significant relationship between different EP and PR

Chen et al. (2010)

2 896

retro

v.s.

Singh et al. (2011)

101

pro, clinical study

v.s.

Before oocyte aspiration

Bergh et al. (1992)

100

pro

v.s.

Gonen & Casper (1990)

123

pro, cohort-study

significantly higher rate of multi-layered patterns in pregnant patients

Oocyte retrieval

Welker et al. (1989)

190

pro

EP influences implantion

Järvelä et al. (2005)

35

pro

significantly higher PR in women with a triple-line pattern

Bassil et al. (2001)

153

pro, case-control

no significant relationship between different EP and PR

Embryo transfer

Bassil et al. (2001)

153

pro, case-control

v.s.


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Discussion

While it is widely accepted that the endometrium is a key factor for successful implantation and for establishing a healthy pregnancy [11], [13], [14], opinions are divided as to which parameter is suited best for predicting a positive outcome during cycles of assisted reproduction.

Many authors have tried to identify a simple method to evaluate the quality of the uterine lining. The overall consensus is that transvaginal ultrasound scan fits the criteria the best, the crucial questions are: What parameters can be obtained through grey-scale ultrasound of the endometrium? And are the ascertained parameters suitable for predicting treatment outcome [59]?

The first question is easily answered. Four distinct factors can be measured: endometrial thickness, endometrial pattern, endometrial volume (measured by 3-D ultrasound) and subendometrial blood flow (measured by power Doppler sonography). All of these have been examined in many different studies, but the results vary from author to author.

Even though a lot of studies have shown no significant correlation between either endometrial thickness [14], [37], [38], [39], [40], [43], [47], [48], [49] or pattern [13], [40], [46], [47], [57] and pregnancy rates, there are many who did prove that a statistical connection between these parameters and PR existed [11], [13], [16], [17], [18], [19], [20], [35], [36], [42], [44], [45], [46], [48], [52], [56]. The same goes for endometrial volume, where both positive [15], [53] and negative [48], [49], [54] study results have been published.

The endometrial vascularity determined by three-dimensional power Doppler ultrasound was proposed to have a predictive value on the implantation rate in IVF cycles irrespective of the morphological appearance of the endometrium [57]. However, the number of studies dealing with this topic is rather low.


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Conclusions

The different and partly conflicting results of the studies may be due to varying study designs and population sizes ([Tables 1] to [3]), as well as the specific hormonal stimulation protocols used for COH. In spite of the abundance of studies on that subject with varying results and of the individual restrictions of these studies we suggest that prediction of successful implantation with the help of ultrasound examinations of the endometrium does not seem to be an exact science yet. However, in practice it is a possibility of getting at least some information about endometrial receptivity during ART. There is still a need for a more reliable measurement technique to predict the probability of pregnancy prior to embryo transfer to influence the decision if embryos should be transferred or rather cryopreserved for later ART cycles.


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Acknowledgements

The help of the physicians and staff members of the Fertility Center Döbling, Vienna is greatfully acknowledged.


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Conflict of Interest

The authors report no conflicts of interest. The authors alone are responsible for the content and writing of the paper.

  • References

  • 1 Bourgain C, Devroey P. The endometrium in stimulated cycles for IVF. Hum Reprod Update 2003; 9: 515-522
  • 2 Makker A, Singh MM. Endometrial receptivity: clinical assessment in relation to fertility, infertility, and antifertility. Med Res Rev 2006; 26: 699-746
  • 3 Senturk LM, Erel CT. Thin endometrium in assisted reproductive technology. Curr Opin Obstet Gynecol 2008; 20: 221-228
  • 4 Rogenhofer N, Bohlmann MK, Thaler CJ et al. Habituelle Abortneigung: Evidenzbasierte Diagnostik und Therapie. Geburtsh Frauenheilk 2010; 70: 544-552
  • 5 Beier HM, Beier-Hellwig K. Molecular and cellular aspects of endometrial receptivity. Hum Reprod Update 1998; 4: 448-458
  • 6 Cittadini E, Palermo R. The endometrium in human assisted reproduction. Ann N Y Acad Sci 1991; 622: 230-235
  • 7 Sterzik K, Grab D, Rosenbusch B et al. [Receptivity of the endometrium: comparison of ultrasound and histologic findings after hormonal stimulation]. Geburtsh Frauenheilk 1991; 51: 554-558
  • 8 Cohen J. A short review of ovarian stimulation in assisted reproductive techniques. Reprod Biomed Online 2003; 6: 361-366
  • 9 Manno M, Cervi M, Zadro D et al. Different ART outcomes at increasing peak estradiol levels with long and antagonist protocols: retrospective insights from ten years experience. J Assist Reprod Genet 2011; 28: 693-698
  • 10 Ye H, Huang GN, Zeng PH et al. IVF/ICSI outcomes between cycles with luteal estradiol (E2) pre-treatment before GnRH antagonist protocol and standard long GnRH agonist protocol: a prospective and randomized study. J Assist Reprod Genet 2009; 26: 105-111
  • 11 Al-Ghamdi A, Coskun S, Al-Hassan S et al. The correlation between endometrial thickness and outcome of in vitro fertilization and embryo transfer (IVF-ET) outcome. Reprod Biol Endocrinol 2008; 6: 37
  • 12 Okohue JE, Onuh SO, Ebeigbe P et al. The effect of endometrial thickness on in vitro fertilization (IVF) – embryo transfer/intracytoplasmic sperm injection (ICSI) outcome. Afr J Reprod Health 2009; 13: 113-121
  • 13 Chen SL, Wu FR, Luo C et al. Combined analysis of endometrial thickness and pattern in predicting outcome of in vitro fertilization and embryo transfer: a retrospective cohort study. Reprod Biol Endocrinol 2010; 8: 30
  • 14 Kinay T, Tasci Y, Dilbaz S et al. The relationship between endometrial thickness and pregnancy rates in GnRH antagonist down-regulated ICSI cycles. Gynecol Endocrinol 2010; 26: 833-837
  • 15 Merce LT, Barco MJ, Bau S et al. Are endometrial parameters by three-dimensional ultrasound and power Doppler angiography related to in vitro fertilization/embryo transfer outcome?. Fertil Steril 2008; 89: 111-117
  • 16 Richter KS, Bugge KR, Bromer JG et al. Relationship between endometrial thickness and embryo implantation, based on 1,294 cycles of in vitro fertilization with transfer of two blastocyst-stage embryos. Fertil Steril 2007; 87: 53-59
  • 17 Traub ML, Van Arsdale A, Pal L et al. Endometrial thickness, Caucasian ethnicity, and age predict clinical pregnancy following fresh blastocyst embryo transfer: a retrospective cohort. Reprod Biol Endocrinol 2009; 7: 33
  • 18 Müller A, Bals-Pratsch M, Oppelt PG et al. Kultur von mehr als 3 2-PN-Stadien in der täglichen Praxis – eine Pilotstudie in Kongruenz mit dem Embryonenschutzgesetz. Geburtsh Frauenheilk 2011; 71: 779-783
  • 19 Gonen Y, Casper RF. Prediction of implantation by the sonographic appearance of the endometrium during controlled ovarian stimulation for in vitro fertilization (IVF). J In Vitro Fert Embryo Transf 1990; 7: 146-152
  • 20 Welker BG, Gembruch U, Diedrich K et al. Transvaginal sonography of the endometrium during ovum pickup in stimulated cycles for in vitro fertilization. J Ultrasound Med 1989; 8: 549-553
  • 21 Eden JA, Place J, Carter GD et al. The effect of clomiphene citrate on follicular phase increase in endometrial thickness and uterine volume. Obstet Gynecol 1989; 73: 187-190
  • 22 Fleischer AC, Pittaway DE, Beard LA et al. Sonographic depiction of endometrial changes occurring with ovulation induction. J Ultrasound Med 1984; 3: 341-346
  • 23 Yagel S, Ben-Chetrit A, Anteby E et al. The effect of ethinyl estradiol on endometrial thickness and uterine volume during ovulation induction by clomiphene citrate. Fertil Steril 1992; 57: 33-36
  • 24 Csemiczky G, Wramsby H, Johannisson E et al. Endometrial evaluation is not predictive for in vitro fertilization treatment. J Assist Reprod Genet 1999; 16: 113-116
  • 25 Valbuena D, Jasper M, Remohi J et al. Ovarian stimulation and endometrial receptivity. Hum Reprod 1999; 14 (Suppl. 02) 107-111
  • 26 Macklon NS, Fauser BC. Impact of ovarian hyperstimulation on the luteal phase. J Reprod Fertil Suppl 2000; 55: 101-108
  • 27 Van Der Gaast MH, Beckers NG, Beier-Hellwig K et al. Ovarian stimulation for IVF and endometrial receptivity – the missing link. Reprod Biomed Online 2002; 5 (Suppl. 01) 36-43
  • 28 Dockery P, Rogers AW. The effects of steroids on the fine structure of the endometrium. Baillieres Clin Obstet Gynaecol 1989; 3: 227-248
  • 29 Kolb BA, Paulson RJ. The luteal phase of cycles utilizing controlled ovarian hyperstimulation and the possible impact of this hyperstimulation on embryo implantation. Am J Obstet Gynecol 1997; 176: 1262-1267 discussion 1267–1269
  • 30 Sharara FI, McClamrock HD. High estradiol levels and high oocyte yield are not detrimental to in vitro fertilization outcome. Fertil Steril 1999; 72: 401-405
  • 31 Pöhls UG, Meurer B, Schälicke M et al. 3D Sonographie in der Gynäkologie. Geburtsh Frauenheilk 2005; 65: R85-R104
  • 32 Dickey RP, Olar TT, Curole DN et al. Endometrial pattern and thickness associated with pregnancy outcome after assisted reproduction technologies. Hum Reprod 1992; 7: 418-421
  • 33 Amir W, Micha B, Ariel H et al. Predicting factors for endometrial thickness during treatment with assisted reproductive technology. Fertil Steril 2007; 87: 799-804
  • 34 Sakamoto C, Yoshimitsu K, Nakamura G et al. Sonographic study of the endometrial responses to ovarian hormones in patients receiving ovarian stimulation. Int J Gynaecol Obstet 1988; 27: 407-414
  • 35 Kehila M, Kebaili S, Bougmiza I et al. [Endometrial thickness in in vitro fertilization. A study of 414 cases]. Tunis Med 2010; 88: 928-932
  • 36 Bozdag G, Esinler I, Yarali H. The impact of endometrial thickness and texture on intracytoplasmic sperm injection outcome. J Reprod Med 2009; 54: 303-311
  • 37 Corbacioglu A, Baysal B. Effects of endometrial thickness and echogenic pattern on assisted reproductive treatment outcome. Clin Exp Obstet Gynecol 2009; 36: 145-147
  • 38 Laasch C, Puscheck E. Cumulative embryo score, not endometrial thickness, is best for pregnancy prediction in IVF. J Assist Reprod Genet 2004; 21: 47-50
  • 39 Yoeli R, Ashkenazi J, Orvieto R et al. Significance of increased endometrial thickness in assisted reproduction technology treatments. J Assist Reprod Genet 2004; 21: 285-289
  • 40 Rashidi BH, Sadeghi M, Jafarabadi M et al. Relationships between pregnancy rates following in vitro fertilization or intracytoplasmic sperm injection and endometrial thickness and pattern. Eur J Obstet Gynecol Reprod Biol 2005; 120: 179-184
  • 41 Coulam CB, Bustillo M, Soenksen DM et al. Ultrasonographic predictors of implantation after assisted reproduction. Fertil Steril 1994; 62: 1004-1010
  • 42 Sharara FI, Lim J, McClamrock HD. Endometrial pattern on the day of oocyte retrieval is more predictive of implantation success than the pattern or thickness on the day of hCG administration. J Assist Reprod Genet 1999; 16: 523-528
  • 43 Lesny P, Killick SR, Tetlow RL et al. Ultrasound evaluation of the uterine zonal anatomy during in-vitro fertilization and embryo transfer. Hum Reprod 1999; 14: 1593-1598
  • 44 Zhang X, Chen CH, Confino E et al. Increased endometrial thickness is associated with improved treatment outcome for selected patients undergoing in vitro fertilization-embryo transfer. Fertil Steril 2005; 83: 336-340
  • 45 Rinaldi L, Lisi F, Floccari A et al. Endometrial thickness as a predictor of pregnancy after in-vitro fertilization but not after intracytoplasmic sperm injection. Hum Reprod 1996; 11: 1538-1541
  • 46 Bergh C, Hillensjo T, Nilsson L. Sonographic evaluation of the endometrium in in vitro fertilization IVF cycles. A way to predict pregnancy?. Acta Obstet Gynecol Scand 1992; 71: 624-628
  • 47 Bassil S. Changes in endometrial thickness, width, length and pattern in predicting pregnancy outcome during ovarian stimulation in in vitro fertilization. Ultrasound Obstet Gynecol 2001; 18: 258-263
  • 48 Jarvela IY, Sladkevicius P, Kelly S et al. Evaluation of endometrial receptivity during in-vitro fertilization using three-dimensional power Doppler ultrasound. Ultrasound Obstet Gynecol 2005; 26: 765-769
  • 49 Schild RL, Knobloch C, Dorn C et al. Endometrial receptivity in an in vitro fertilization program as assessed by spiral artery blood flow, endometrial thickness, endometrial volume, and uterine artery blood flow. Fertil Steril 2001; 75: 361-366
  • 50 Kumbak B, Erden HF, Tosun S et al. Outcome of assisted reproduction treatment in patients with endometrial thickness less than 7 mm. Reprod Biomed Online 2009; 18: 79-84
  • 51 Quintero RB, Sharara FI, Milki AA. Successful pregnancies in the setting of exaggerated endometrial thickness. Fertil Steril 2004; 82: 215-217
  • 52 Kovacs P, Matyas S, Boda K et al. The effect of endometrial thickness on IVF/ICSI outcome. Hum Reprod 2003; 18: 2337-2341
  • 53 Kovachev E, Ganchev Z, Cherneva S et al. [Measurement of endometrial volume and endometrial thickness for assessment of endometrial receptivity in assisted reproductive techniques]. Akush Ginekol 2005; 2: 27-33
  • 54 Schild RL, Indefrei D, Eschweiler S et al. Three-dimensional endometrial volume calculation and pregnancy rate in an in-vitro fertilization programme. Hum Reprod 1999; 14: 1255-1258
  • 55 Smith B, Porter R, Ahuja K et al. Ultrasonic assessment of endometrial changes in stimulated cycles in an in vitro fertilization and embryo transfer program. J In Vitro Fert Embryo Transf 1984; 1: 233-238
  • 56 Sher G, Herbert C, Maassarani G et al. Assessment of the late proliferative phase endometrium by ultrasonography in patients undergoing in-vitro fertilization and embryo transfer (IVF/ET). Hum Reprod 1991; 6: 232-237
  • 57 Singh N, Bahadur A, Mittal S et al. Predictive value of endometrial thickness, pattern and sub-endometrial blood flows on the day of hCG by 2D doppler in in-vitro fertilization cycles: A prospective clinical study from a tertiary care unit. J Hum Reprod Sci 2011; 4: 29-33
  • 58 Kuc P, Kuczynska A, Topczewska M et al. The dynamics of endometrial growth and the triple layer appearance in three different controlled ovarian hyperstimulation protocols and their influence on IVF outcomes. Gynecol Endocrinol 2011; 27: 867-873
  • 59 Diedrich K, Strowitzki T, Kentenich H. The state of reproductive medicine in Germany. Geburtsh Frauenheilk 2012; 72: 225-234

Correspondence

Dr. Detlef Pietrowski
Medical University of Vienna, Obstetrics and Gynecology
1090 Vienna
Austria

  • References

  • 1 Bourgain C, Devroey P. The endometrium in stimulated cycles for IVF. Hum Reprod Update 2003; 9: 515-522
  • 2 Makker A, Singh MM. Endometrial receptivity: clinical assessment in relation to fertility, infertility, and antifertility. Med Res Rev 2006; 26: 699-746
  • 3 Senturk LM, Erel CT. Thin endometrium in assisted reproductive technology. Curr Opin Obstet Gynecol 2008; 20: 221-228
  • 4 Rogenhofer N, Bohlmann MK, Thaler CJ et al. Habituelle Abortneigung: Evidenzbasierte Diagnostik und Therapie. Geburtsh Frauenheilk 2010; 70: 544-552
  • 5 Beier HM, Beier-Hellwig K. Molecular and cellular aspects of endometrial receptivity. Hum Reprod Update 1998; 4: 448-458
  • 6 Cittadini E, Palermo R. The endometrium in human assisted reproduction. Ann N Y Acad Sci 1991; 622: 230-235
  • 7 Sterzik K, Grab D, Rosenbusch B et al. [Receptivity of the endometrium: comparison of ultrasound and histologic findings after hormonal stimulation]. Geburtsh Frauenheilk 1991; 51: 554-558
  • 8 Cohen J. A short review of ovarian stimulation in assisted reproductive techniques. Reprod Biomed Online 2003; 6: 361-366
  • 9 Manno M, Cervi M, Zadro D et al. Different ART outcomes at increasing peak estradiol levels with long and antagonist protocols: retrospective insights from ten years experience. J Assist Reprod Genet 2011; 28: 693-698
  • 10 Ye H, Huang GN, Zeng PH et al. IVF/ICSI outcomes between cycles with luteal estradiol (E2) pre-treatment before GnRH antagonist protocol and standard long GnRH agonist protocol: a prospective and randomized study. J Assist Reprod Genet 2009; 26: 105-111
  • 11 Al-Ghamdi A, Coskun S, Al-Hassan S et al. The correlation between endometrial thickness and outcome of in vitro fertilization and embryo transfer (IVF-ET) outcome. Reprod Biol Endocrinol 2008; 6: 37
  • 12 Okohue JE, Onuh SO, Ebeigbe P et al. The effect of endometrial thickness on in vitro fertilization (IVF) – embryo transfer/intracytoplasmic sperm injection (ICSI) outcome. Afr J Reprod Health 2009; 13: 113-121
  • 13 Chen SL, Wu FR, Luo C et al. Combined analysis of endometrial thickness and pattern in predicting outcome of in vitro fertilization and embryo transfer: a retrospective cohort study. Reprod Biol Endocrinol 2010; 8: 30
  • 14 Kinay T, Tasci Y, Dilbaz S et al. The relationship between endometrial thickness and pregnancy rates in GnRH antagonist down-regulated ICSI cycles. Gynecol Endocrinol 2010; 26: 833-837
  • 15 Merce LT, Barco MJ, Bau S et al. Are endometrial parameters by three-dimensional ultrasound and power Doppler angiography related to in vitro fertilization/embryo transfer outcome?. Fertil Steril 2008; 89: 111-117
  • 16 Richter KS, Bugge KR, Bromer JG et al. Relationship between endometrial thickness and embryo implantation, based on 1,294 cycles of in vitro fertilization with transfer of two blastocyst-stage embryos. Fertil Steril 2007; 87: 53-59
  • 17 Traub ML, Van Arsdale A, Pal L et al. Endometrial thickness, Caucasian ethnicity, and age predict clinical pregnancy following fresh blastocyst embryo transfer: a retrospective cohort. Reprod Biol Endocrinol 2009; 7: 33
  • 18 Müller A, Bals-Pratsch M, Oppelt PG et al. Kultur von mehr als 3 2-PN-Stadien in der täglichen Praxis – eine Pilotstudie in Kongruenz mit dem Embryonenschutzgesetz. Geburtsh Frauenheilk 2011; 71: 779-783
  • 19 Gonen Y, Casper RF. Prediction of implantation by the sonographic appearance of the endometrium during controlled ovarian stimulation for in vitro fertilization (IVF). J In Vitro Fert Embryo Transf 1990; 7: 146-152
  • 20 Welker BG, Gembruch U, Diedrich K et al. Transvaginal sonography of the endometrium during ovum pickup in stimulated cycles for in vitro fertilization. J Ultrasound Med 1989; 8: 549-553
  • 21 Eden JA, Place J, Carter GD et al. The effect of clomiphene citrate on follicular phase increase in endometrial thickness and uterine volume. Obstet Gynecol 1989; 73: 187-190
  • 22 Fleischer AC, Pittaway DE, Beard LA et al. Sonographic depiction of endometrial changes occurring with ovulation induction. J Ultrasound Med 1984; 3: 341-346
  • 23 Yagel S, Ben-Chetrit A, Anteby E et al. The effect of ethinyl estradiol on endometrial thickness and uterine volume during ovulation induction by clomiphene citrate. Fertil Steril 1992; 57: 33-36
  • 24 Csemiczky G, Wramsby H, Johannisson E et al. Endometrial evaluation is not predictive for in vitro fertilization treatment. J Assist Reprod Genet 1999; 16: 113-116
  • 25 Valbuena D, Jasper M, Remohi J et al. Ovarian stimulation and endometrial receptivity. Hum Reprod 1999; 14 (Suppl. 02) 107-111
  • 26 Macklon NS, Fauser BC. Impact of ovarian hyperstimulation on the luteal phase. J Reprod Fertil Suppl 2000; 55: 101-108
  • 27 Van Der Gaast MH, Beckers NG, Beier-Hellwig K et al. Ovarian stimulation for IVF and endometrial receptivity – the missing link. Reprod Biomed Online 2002; 5 (Suppl. 01) 36-43
  • 28 Dockery P, Rogers AW. The effects of steroids on the fine structure of the endometrium. Baillieres Clin Obstet Gynaecol 1989; 3: 227-248
  • 29 Kolb BA, Paulson RJ. The luteal phase of cycles utilizing controlled ovarian hyperstimulation and the possible impact of this hyperstimulation on embryo implantation. Am J Obstet Gynecol 1997; 176: 1262-1267 discussion 1267–1269
  • 30 Sharara FI, McClamrock HD. High estradiol levels and high oocyte yield are not detrimental to in vitro fertilization outcome. Fertil Steril 1999; 72: 401-405
  • 31 Pöhls UG, Meurer B, Schälicke M et al. 3D Sonographie in der Gynäkologie. Geburtsh Frauenheilk 2005; 65: R85-R104
  • 32 Dickey RP, Olar TT, Curole DN et al. Endometrial pattern and thickness associated with pregnancy outcome after assisted reproduction technologies. Hum Reprod 1992; 7: 418-421
  • 33 Amir W, Micha B, Ariel H et al. Predicting factors for endometrial thickness during treatment with assisted reproductive technology. Fertil Steril 2007; 87: 799-804
  • 34 Sakamoto C, Yoshimitsu K, Nakamura G et al. Sonographic study of the endometrial responses to ovarian hormones in patients receiving ovarian stimulation. Int J Gynaecol Obstet 1988; 27: 407-414
  • 35 Kehila M, Kebaili S, Bougmiza I et al. [Endometrial thickness in in vitro fertilization. A study of 414 cases]. Tunis Med 2010; 88: 928-932
  • 36 Bozdag G, Esinler I, Yarali H. The impact of endometrial thickness and texture on intracytoplasmic sperm injection outcome. J Reprod Med 2009; 54: 303-311
  • 37 Corbacioglu A, Baysal B. Effects of endometrial thickness and echogenic pattern on assisted reproductive treatment outcome. Clin Exp Obstet Gynecol 2009; 36: 145-147
  • 38 Laasch C, Puscheck E. Cumulative embryo score, not endometrial thickness, is best for pregnancy prediction in IVF. J Assist Reprod Genet 2004; 21: 47-50
  • 39 Yoeli R, Ashkenazi J, Orvieto R et al. Significance of increased endometrial thickness in assisted reproduction technology treatments. J Assist Reprod Genet 2004; 21: 285-289
  • 40 Rashidi BH, Sadeghi M, Jafarabadi M et al. Relationships between pregnancy rates following in vitro fertilization or intracytoplasmic sperm injection and endometrial thickness and pattern. Eur J Obstet Gynecol Reprod Biol 2005; 120: 179-184
  • 41 Coulam CB, Bustillo M, Soenksen DM et al. Ultrasonographic predictors of implantation after assisted reproduction. Fertil Steril 1994; 62: 1004-1010
  • 42 Sharara FI, Lim J, McClamrock HD. Endometrial pattern on the day of oocyte retrieval is more predictive of implantation success than the pattern or thickness on the day of hCG administration. J Assist Reprod Genet 1999; 16: 523-528
  • 43 Lesny P, Killick SR, Tetlow RL et al. Ultrasound evaluation of the uterine zonal anatomy during in-vitro fertilization and embryo transfer. Hum Reprod 1999; 14: 1593-1598
  • 44 Zhang X, Chen CH, Confino E et al. Increased endometrial thickness is associated with improved treatment outcome for selected patients undergoing in vitro fertilization-embryo transfer. Fertil Steril 2005; 83: 336-340
  • 45 Rinaldi L, Lisi F, Floccari A et al. Endometrial thickness as a predictor of pregnancy after in-vitro fertilization but not after intracytoplasmic sperm injection. Hum Reprod 1996; 11: 1538-1541
  • 46 Bergh C, Hillensjo T, Nilsson L. Sonographic evaluation of the endometrium in in vitro fertilization IVF cycles. A way to predict pregnancy?. Acta Obstet Gynecol Scand 1992; 71: 624-628
  • 47 Bassil S. Changes in endometrial thickness, width, length and pattern in predicting pregnancy outcome during ovarian stimulation in in vitro fertilization. Ultrasound Obstet Gynecol 2001; 18: 258-263
  • 48 Jarvela IY, Sladkevicius P, Kelly S et al. Evaluation of endometrial receptivity during in-vitro fertilization using three-dimensional power Doppler ultrasound. Ultrasound Obstet Gynecol 2005; 26: 765-769
  • 49 Schild RL, Knobloch C, Dorn C et al. Endometrial receptivity in an in vitro fertilization program as assessed by spiral artery blood flow, endometrial thickness, endometrial volume, and uterine artery blood flow. Fertil Steril 2001; 75: 361-366
  • 50 Kumbak B, Erden HF, Tosun S et al. Outcome of assisted reproduction treatment in patients with endometrial thickness less than 7 mm. Reprod Biomed Online 2009; 18: 79-84
  • 51 Quintero RB, Sharara FI, Milki AA. Successful pregnancies in the setting of exaggerated endometrial thickness. Fertil Steril 2004; 82: 215-217
  • 52 Kovacs P, Matyas S, Boda K et al. The effect of endometrial thickness on IVF/ICSI outcome. Hum Reprod 2003; 18: 2337-2341
  • 53 Kovachev E, Ganchev Z, Cherneva S et al. [Measurement of endometrial volume and endometrial thickness for assessment of endometrial receptivity in assisted reproductive techniques]. Akush Ginekol 2005; 2: 27-33
  • 54 Schild RL, Indefrei D, Eschweiler S et al. Three-dimensional endometrial volume calculation and pregnancy rate in an in-vitro fertilization programme. Hum Reprod 1999; 14: 1255-1258
  • 55 Smith B, Porter R, Ahuja K et al. Ultrasonic assessment of endometrial changes in stimulated cycles in an in vitro fertilization and embryo transfer program. J In Vitro Fert Embryo Transf 1984; 1: 233-238
  • 56 Sher G, Herbert C, Maassarani G et al. Assessment of the late proliferative phase endometrium by ultrasonography in patients undergoing in-vitro fertilization and embryo transfer (IVF/ET). Hum Reprod 1991; 6: 232-237
  • 57 Singh N, Bahadur A, Mittal S et al. Predictive value of endometrial thickness, pattern and sub-endometrial blood flows on the day of hCG by 2D doppler in in-vitro fertilization cycles: A prospective clinical study from a tertiary care unit. J Hum Reprod Sci 2011; 4: 29-33
  • 58 Kuc P, Kuczynska A, Topczewska M et al. The dynamics of endometrial growth and the triple layer appearance in three different controlled ovarian hyperstimulation protocols and their influence on IVF outcomes. Gynecol Endocrinol 2011; 27: 867-873
  • 59 Diedrich K, Strowitzki T, Kentenich H. The state of reproductive medicine in Germany. Geburtsh Frauenheilk 2012; 72: 225-234