Abstract
Background ART in women with endometriosis is associated with poor quality of the retrieved oocytes and lower
fertilization and pregnancy rates, reflecting that endometriosis may influence fertility by altering the quality
of both the oocyte and embryo quality and also by impairing the endometrial receptivity. On comparing endometri-
osis-affected patients to healthy counterparts, many differences were demonstrated at the endometrial level. Thus,
choosing the appropriate method of embryo transfer is of utmost importance, particularly for patients with advanced
endometriosis.
Objective
The aim of the present study was to compare the reproductive outcomes between fresh and frozen
embryo transfer cycles in women with advanced endometriosis.
Material and methods
A retrospective cohort study was conducted in the period from January 2018 until Decem-
ber 2021 for patients recruited from two IVF centers, Alexandria, Egypt. Careful review of paper and electronic
medical records of infertile women (primary, relative, or secondary infertility) aged 18–37 years who were diagnosed
with advanced endometriosis by means of laparoscopy and were scheduled for ICSI followed by either fresh embryo
transfer (group I) or freeze-all embryos and deferred embryo transfer (group II) of day 5 embryo(s) was included
in the study.
Results
Two-hundred and eleven women were eligible and included in the study. Women in each study group were
matched regarding baseline characteristics. Clinical pregnancy, implantation, and ongoing pregnancy rates were sta-
tistically significantly higher in the group of frozen embryo transfer (p < 0.001). Miscarriage rate was found to be higher
in the group of fresh transfer compared to FET group but without a statistical significance (20.9% vs 9.2%, p = 0.072).
Conclusion
In women with advanced endometriosis, freeze-all policy seems to be associated with better implanta-
tion, ongoing pregnancy rates.
Keywords
Endometriosis, Freeze all, Frozen embryo transfer, Ongoing pregnancy rate
Introduction
Endometriosis is defined as a disease characterized by
the presence of endometrium resembling epithelium
and/or stroma outside the endometrium and myome -
trium, usually in association with an inflammatory pro -
cess [1]. It roughly affects 10% (approximately 190 million
women worldwide) of girls and women of reproductive
age globally.
Open Access
© The Author(s) 2024. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which
permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the
original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or
other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line
to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory
regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this
licence, visit http://creativecommons.org/licenses/by/4.0/.
Middle East Fertility
Society Journal
*Correspondence:
Ahmed Shoukry
[email protected]
1 Obstetrics and Gynecology, Department of Obstetrics and Gynecology,
Faculty of Medicine, Alexandria University, Alexandria, Egypt
2 Obstetrics and Gynecology, Alexandria University Hospitals, Alexandria,
Egypt
Page 2 of 8Shoukry et al. Middle East Fertility Society Journal (2024) 29:41
Endometriosis-infertility relationship has been a point
of debate for decades. The fecundity ranges from 15 to
20% per month in normal couples and declines with age.
Patients with endometriosis have a decreased monthly
fecundity of about 0.2–1% each month [2, 3]. Moreover,
endometriosis is associated with decline in the live birth
rate (LBR) [4]. Although ART remain the most effective
treatment modality for infertile women with endometrio-
sis, it still yields poor outcomes as ART could not over -
come all the substantial effects of endometriosis [5, 6].
Endometriosis-affected women have declined pregnancy
and implantation rates in comparison to women without
endometriosis [7].
It was noticed that endometriosis has undesirable
effect on the pregnancy, miscarriage, and live birth rates.
It was found that ART outcomes, as the quality of the
retrieved oocytes and fertilization rate, are negatively
influenced by the existence of endometriosis, reflect -
ing that endometriosis influence fertility by altering the
quality of both the oocyte and embryo quality and by
impairing the endometrial receptivity [6]. On comparing
endometriosis-affected patients to healthy counterparts,
many differences were demonstrated at the endometrial
level [8], which define the decline in the receptivity of the
endometrium. Thus, choosing the appropriate method of
embryo transfer is of utmost importance, particularly for
patients with advanced endometriosis.
In the view of the impact of the supraphysiological level
of hormones associated with stimulation in fresh embryo
transfer on the uterine environment during early peri-
implantation, it was demonstrated that flowing of blood
in the endometrium and sub-endometrium is reduced
in stimulated cycles in comparison to natural cycles as
evaluated by three-dimensional power Doppler ultra -
sonography [9]. Furthermore, histopathologic alterations
of the stimulated endometrium were reported, and this
includes advancement in the maturation of the endome -
trium [10] and premature development of channel sys -
tems in the nucleolus [11].
On the other hand, in frozen embryo transfer (FET)
cycles, endometrial growth can be more controlled than
in fresh cycles [12]. Based on that, the use of frozen
embryos avoided the supraphysiological hormone level
found during ovarian hyperstimulation in in vitro fertili -
zation (IVF)/ICSI with fresh embryo transfer, which leads
to an unfavorable environment for implantation and has
been found to have detrimental effects on the endome -
trial receptivity, irrespective of the amount of retrieved
oocytes or levels of progesterone (P) [13–16].
Therefore, the aim of the present study was to com -
pare the reproductive outcomes between fresh and fro -
zen embryo transfer cycles in women with advanced
endometriosis.
Study design and setting
A retrospective cohort study was conducted in the
period from January 2018 until December 2021 for
patients recruited from two IVF centers (Agial Fertility
Center & Dar-Elkhosoba Center), Alexandria, Egypt.
Materials and methods
Careful review of paper and electronic medical records
of infertile women (primary, relative, or secondary
infertility) aged 18–37 years who were diagnosed with
advanced endometriosis, stage III/IV r-ASRM clas -
sification [17], by means of laparoscopy and were
scheduled for intracytoplasmic sperm injection (ICSI)
followed by either fresh embryo transfer or freeze-
all embryos and deferred embryo transfer of day 5
embryo(s) was included in the study.
Couples with abnormal semen analysis of the male
partner, recurrent implantation failure in previous ICSI
trials, and women with uterine lesions such as fibroids,
adenomyosis, polypi, uterine septum, and women with
no available follow up data were excluded from the
study. The study protocol was approved from the Eth -
ics Committee of Faculty of Medicine, Alexandria
University.
Ovarian stimulation
All the women enrolled in the study underwent con -
trolled ovarian stimulation via the fixed GnRH antago -
nist protocol. Before ovarian stimulation, women were
pretreated with combined oral contraceptive pills for
2–3 weeks. On day 2 of the menstrual cycle (stimula -
tion day 1), patients received a fixed daily dose of recom -
binant FSH or combination of rec-FSH and human
menopausal gonadotropins. Starting on day 5 of stimu -
lation, patients underwent monitoring with transvaginal
ultrasound and serial assessment of estradiol every 2–3
days as required. A daily subcutaneous dose of 0.25 mg
of GnRH antagonist cetrorelix was initiated on day 6 of
ovarian stimulation and continued up to the day of trig -
ger administration. When at least three follicles reached
17 mm in diameter, final oocyte maturation was trig -
gered using 10,000 IU of human chorionic gonadotropin
(hCG). Ovum pickup (OPU) was performed 35–36 h of
hCG administration. Mature oocytes were inseminated
by means of intracytoplasmic sperm injection and cul -
tured to blastocyst stage.
Group I: Women who underwent fresh embryo transfer (ET)
Combined vaginal suppositories (400 mg twice daily)
and intramuscular progesterone in oil (50 mg once daily)
Page 3 of 8
Shoukry et al. Middle East Fertility Society Journal (2024) 29:41
injections were started on day of OPU, and ET was per -
formed 5 days after P administration.
Group II: Women who underwent frozen embryo
transfer after endometrial preparation through artificial
or programmed cycle
After vitrification of the available embryos, in the sub -
sequent cycle, women underwent ovarian suppression
by combined pills for 2–3 weeks, and then endometrial
preparation was achieved with a daily dose of 8 mg of
estradiol valerate for at least 12–14 days. When endome -
trium thickness was at least 8 mm and E2 level reached
at least 200 pg/dl, progesterone as vaginal suppositories
(400 mg twice daily) and intramuscular in oil (50 mg
once daily) injection was administered, and ET of thawed
embryos was performed after 5 days of P therapy.
Outcome variables
The primary outcome of the study was the ongoing
pregnancy rate (OPR) defined as pregnancy progressed
beyond 14 weeks’ gestation. Secondary outcomes include
the following: implantation rate, defined as the num -
ber of intrauterine gestational sacs observed by trans -
vaginal ultrasound divided by the number of transferred
embryos; clinical pregnancy rate (CPR), calculated by
considering clinical pregnancy and determined by the
visualization of a viable gestational sac within the uter -
ine cavity by ultrasound 3–4 weeks after embryo transfer;
and miscarriage rate, defined as the number of cases who
aborted (after a confirmed clinical pregnancy) divided by
the total number of pregnant cases.
Statistical analysis
Data were fed to the computer and analyzed using IBM
SPSS software package version 20.0. (Armonk, NY: IBM
Corp.). Qualitative data were described using number
and percent. The Kolmogorov-Smirnov test was used to
verify the normality of distribution. Quantitative data
were described using range (minimum and maximum),
mean, standard deviation, median, and interquartile
range (IQR). Significance of the obtained results was
judged at the 5% level. The used tests were chi-square test
for categorical variables, to compare between different
groups; Student t-test for normally distributed quantita -
tive variables, to compare between two studied groups;
and Mann-Whitney test for abnormally distributed
quantitative variables, to compare between two studied
groups.
Results
Over the 4-year study period, there were 237 women with
advanced endometriosis who underwent either fresh or
frozen embryo transfer cycles; out of them, 211 women
were eligible and included in the study, and Fig. 1 dem-
onstrates the flow chart of the study. The study included
211 patients divided into two groups as follows: Group
I includes 103 patients who underwent fresh embryo
transfer, and Group II includes 108 patients who under -
went frozen embryo transfer.
Regarding the baseline characteristics of both groups
(Table 1), patients in the two study groups were matched
regarding mean age, infertility duration, type of infertil -
ity (primary or secondary), body mass index, and AMH
level.
Fig. 1 Study flowchart
Page 4 of 8Shoukry et al. Middle East Fertility Society Journal (2024) 29:41
Table 2 shows that the number of retrieved oocytes,
MII (metaphase II) oocyte number, and the number
of available blastocysts for transfer on day 5 were sig -
nificantly higher in the group of frozen embryo transfer
(p < 0.001).
As shown in Table 3, the number of embryos trans -
ferred was either a single embryo or two embryos, and
there was no statistical significant difference between
the two groups (p 0.473); for the quality of the embryos
transferred that were either high-quality embryos alone
or low -quality embryos alone or both of them together,
both groups showed no statistically significant difference
(p 0.325).
The clinical pregnancy rate was significantly higher in
the frozen embryo transfer group than the fresh group
(82 patients (75.9%) vs 46 patients (44.7%) (p < 0.001));
again, the FET group showed a significantly higher
Table 1 Comparison between the two studied groups according to the baseline characteristics
Baseline characteristics Fresh ET (n = 103) Frozen ET (n = 108) Test of sig P
Mean age (years) 31.22 ± 4.94 30.87 ± 4.45 t = 0.546 0.586
Median infertility duration (IQR)
years
4.0 (3.0–7.0) 4.25 (3.0–8.0) U = 5266.50 0.502
Mean BMI (kg/m2) 25.83 ± 3.26 25.01 ± 3.04 t = 1.903 0.058
Infertility type No % No % χ2 = 3.987 0.136
Primary 76 73.8 71 65.7
Secondary 17 16.5 16 14.8
Relative 10 9.7 21 19.4
Mean AMH 1.91 ± 1.11 2.21 ± 1.31 t = 1.813 0.071
AFC U = 5064.5 0.258
Mean 7.74 ± 2.93 8.18 ± 2.96
Median (IQR) 7.0 (6.0–10.0) 8.0 (6.0–10.0)
Chocolate cyst before OI χ2 = 0.021 0.884
Absent 87 (84.5%) 92 (85.2%)
Present 16 (15.5%) 16 (14.8%)
Table 2 Comparison between the two groups regarding the
number of oocyte retrieved, mature oocytes, and available
embryos number at day 5
* : statistically significant
Fresh (n = 103) Frozen (n = 108) U p
Oocyte retrieved
Min.–max 2.0–10.0 3.0–12.0 3710.5* < 0.001*
Mean ± SD 5.29 ± 2.08 6.56 ± 1.93
Median (IQR) 5.0 (4.0–7.0) 6.0 (6.0–8.0)
MII oocytes
Min.–max 1.0–7.0 2.0–9.0 3546.5* < 0.001*
Mean ± SD 3.78 ± 1.62 4.87 ± 1.46
Median (IQR) 4.0 (2.0–5.0) 5.0 (4.0–6.0)
Embryo no. on day 5
Min.–max 1.0–5.0 1.0–7.0 3612.0* < 0.001*
Mean ± SD 2.55 ± 0.96 3.22 ± 1.06
Median (IQR) 2.0 (2.0–3.0) 3.0 (2.0–4.0)
Table 3 Comparison between the two studied groups according to the embryos transferred
Embryos transferred Fresh ET (n = 103) Frozen ET (n = 108) χ2 P
No % No %
Number
Single embryo 47 45.6 44 40.7 0.514 0.473
Two embryos 56 54.4 64 59.3
Quality
Low 26 25.2 22 20.4 2.246 0.325
High 73 70.9 77 71.3
High + low 4 3.9 9 8.3
Page 5 of 8
Shoukry et al. Middle East Fertility Society Journal (2024) 29:41
implantation rate in comparison to the fresh group as
illustrated in Table 4 (30.8% vs 54.1% (p < 0.001)).
Out of the 128 pregnant females in the study, 3 preg -
nant patients dropped out from the fresh group, and 6
pregnant patients dropped out from the frozen group;
those 9 patients were excluded from our statistical
Results
while estimating the miscarriage rate. The mis -
carriage rate was higher in the fresh ET group than
in the frozen ET group; however, the difference did
not reach statistical significance (9 (20.9%) vs 7 (9.2%)
(p = 0.072).
As for the primary outcome of the study, the ongo -
ing pregnancy rate, out of the 211 patients included
in our study, there was no available data for 9 pregnant
patients, 3 patients in group 1, and 6 patients in group
2; those 9 patients were excluded from our statistical
analysis while estimating the ongoing pregnancy rate.
Sixty-nine patients in the frozen embryo transfer group
(69/102 = 67.6%) continued their pregnancy beyond
14 weeks, while 33 patients (34/100 = 34%) of the fresh
embryo transfer group continued their pregnancy
beyond 14 weeks, and the OPR was significantly higher
in the frozen embryo transfer group (p < 0.001) (Table 5).
Furthermore, a subgroup analysis was performed
to compare the pregnancy rates between women who
underwent single embryo transfer (SET) and those to
whom two embryos were transferred (Table 6). It was
observed that the clinical and ongoing pregnancy rates
in women who underwent SET and who have under -
went double embryo transfer are not significantly dif -
ferent (in the group of fresh ET, the group of FET, and
for the total sample).
Discussion
The present study showed that OPR in women with
advanced endometriosis is significantly higher in the
group of frozen embryo transfer compared to the fresh
embryo transfer group (67.6% vs. 34%, respectively).
Regarding the secondary outcomes, there was a statisti -
cally significant higher implantation and clinical preg -
nancy rates also in the frozen embryo transfer group.
To the best of our knowledge, only few studies have
addressed the issue of freeze-all policy in women with
advanced endometriosis.
In agreement with the findings of the current study,
Wu et al. [18] conducted a retrospective study that
Table 4 Comparison between the two studied groups according clinical pregnancy and implantation rates
* : statistically significant
Fresh ET (n = 103) Frozen ET (n = 108) χ2 p
No % No %
Clinical pregnancy rate 46 44.7 82 75.9 21.597* < 0.001*
Number of GS seen by TVU (after 3–5 weeks) 49 93 < 0.001*
Number of transferred embryos 159 172
Implantation rate 30.8% 54.1%
Table 5 Comparison between the two studied groups
according to the ongoing pregnancy
* : statistically significant
Fresh ET Frozen ET χ2 p
No. (%) No. (%)
Ongoing pregnancy (n = 100) (n = 102) 22.876* < 0.001*
34 (34.0%) 69 (67.6%)
Table 6 Relation between numbers of embryos transferred with
clinical and ongoing pregnancy rates
a Not available cases were excluded
Number χ2 p
1 2
Clinical pregnancy rate
Fresh (n = 103) (n = 47) (n = 56)
Negative 30 (63.8%) 27 (48.2%) 2.521 0.112
Positive 17 (36.2%) 29 (51.8%)
Frozen (n = 108) (n = 44) (n = 64)
Negative 9 (20.5%) 17 (26.6%) 0.532 0.466
Positive 35 (79.5%) 47 (73.4%)
Total (n = 211) (n = 91) (n = 120)
Negative 39 (42.9%) 44 (36.7%) 0.831 0.362
Positive 52 (57.1%) 76 (63.3%)
Ongoing pregnancy rate
Fresh (n = 100)a (n = 47) (n = 53)
Negative/miscarriage 35 (74.5%) 31 (58.5%) 2.834 0.092
Positive 12 (25.5%) 22 (41.5%)
Frozen (n = 102)a (n = 43) (n = 59)
Negative/miscarriage 14 (32.6%) 19 (32.2%) 0.001 0.970
Positive 29 (67.4%) 40 (67.8%)
Total (n = 202)a (n = 90) (n = 112)
Negative/miscarriage 49 (54.4%) 50 (44.6%) 1.918 0.166
Positive 41 (45.6%) 62 (55.4%)
Page 6 of 8Shoukry et al. Middle East Fertility Society Journal (2024) 29:41
encompassed 1651 women with advanced stages of endo-
metriosis performing ICSI. After matching, 506 women
and 255 women were eligible in the freeze-all group and
the fresh group, respectively. In their matched cohort
study, the implantation, CPR, and LBR were significantly
higher in the FET group in comparison to the fresh
groups. Those results coincide with the current study in
all perspectives except for the LBR as it was not included
in the outcomes for the study.
However, the present study differs from Wu et al.,
where in their study the development of the embryo was
accessed on day 3, and the embryos selected to be trans -
ferred were high-quality cleavage-stage embryos only (at
least six blastomeres with ≤ 20% fragmentation based
on the Cummins’ criteria). In the fresh embryo transfer
group, patients were arranged for a day 3 fresh embryo
transfer and vitrification of the extra embryos. For the
FET group, vitrification on day 3 of the entire cohort
of good quality embryos. While in the present study,
embryo development was assessed on day 5, and patients
performing fresh transfer were scheduled for a day-5
ET, while in the frozen group, the embryos were vitri -
fied on day 5, and embryo transfer was not exclusively
for high-quality embryos, but in some cases, average or
low-quality embryos were transferred either alone or in
combination with a high-quality embryo.
Again, the results of the present study coincided with
a matched cohort prospective study conducted by Bour -
don et al. [19], and they compared the results of FET to
fresh ET in women having endometriosis, where the FET
group involved 135 women and the fresh group involved
424 matched women. CPR was of higher significance
toward the FET group in comparison to the fresh group;
also, the ongoing pregnancy rate showed greater statisti -
cal significance in the FET group (34.8%) in comparison
to the fresh-ET group (17.8%) (p = 0.005), and the live
birth rate as well was of higher significance in FET in
comparison to fresh embryo transfer group.
Another interesting study conducted by Mohamed
et al. [20] is a retrospective, database-searched cohort
study. The study included two groups: the first group had
freshly transferred embryos, while the second group per -
formed frozen embryo transfer. The primary outcome for
the study was the live birth rate, while the secondary out-
comes included the clinical pregnancy rate and the mis -
carriage rate. Out of the total number of cases, 415 (5.7%)
had infertility attributed to endometriosis, in whom fro -
zen ET cycles were associated with a relatively similar
clinical pregnancy rate and live birth rate, in comparison
to the clinical pregnancy rate and live birth rate of fresh
ET cycles, showing no significant difference. Neverthe -
less, the study of Mohamed et al. differs from the present
study as they considered other causes of infertility rather
than endometriosis alone as a sole factor of infertility,
and it also concluded that there was no significant differ -
ence between FET over the fresh ET in cases of endome -
triosis concerning CPR (18.2 vs. 20.2%, respectively) and
LBR (16.9% vs. 15.5%, respectively).
In accordance, a recent systematic review and meta-
analysis conducted by Chang et al. [21] aimed at evaluat -
ing if FET has the ability to reimpose optimal receptivity
targeting better ART results in patients with endometrio-
sis. A total of six studies with moderate methodological
quality were included in the meta-analysis. Three-thou -
sand and ten patients with endometriosis who under -
went ICSI were included in the studies: 1777 performed
FET, and 1233 performed fresh ET. LBR was significantly
higher in the FET group in comparison to the fresh
group. Although that CPR was similar between the two
study groups, there was a significantly higher miscarriage
rate in the fresh group.
The endometrium of endometriosis-affected women
is different from that of healthy, unaffected women [8],
which could be the main reason for the decline in endo -
metrial receptivity quality. Thus, it is crucial to select the
right embryo transfer technique, particularly for women
who have severe endometriosis. The effects of ovarian
stimulation in fresh ET cycles on the early peri-implan -
tation uterine milieu have been documented in a number
of studies, and three-dimensional power Doppler ultra -
sonography measurements have revealed that stimulated
cycles have reduced endometrial and subendometrial
blood flow in comparison to normal cycles [9]. Further -
more, certain pathologic alterations of the stimulated
endometrium have been verified, such as the progression
of endometrial maturation [10], as well as the early estab-
lishment of nucleolar channel systems [11].
Additionally, a number of researchers have demon -
strated that during fresh embryo transfer cycles, there
are abnormalities in the transcriptional activity of genes
related to endometrial receptivity [22–24]. The altera -
tions indicated above are linked to the hyperestrogenic
environment created during fresh IVF, which might sub -
sequently hinder early embryonic adhesion [18, 25] and,
consequently, the embryos’ capacity to implant. It follows
that the current study’s findings regarding implantation,
clinical pregnancy, and ongoing pregnancy are better in
FET cycles.
Our study has the advantage of being one of the few
studies that addressed the role of FET in endometriosis-
affected women and was conducted for a fair number
of patients; moreover, this study focused on advanced
endometriosis being the sole factor of infertility in the
studied patients, excluding any other infertility-related
factors; however, the main study limitation was being a
retrospective analysis depending on the availability of
Page 7 of 8
Shoukry et al. Middle East Fertility Society Journal (2024) 29:41
complete medical records, and the follow-up stopped at
14 weeks of gestation.
Conclusions
The findings of the present study suggest that frozen
embryo transfer policy in cases of advanced endometrio -
sis would result in better reproductive outcomes in com -
parison to fresh embryo transfer in terms of clinical and
ongoing pregnancy rates. Further, randomized controlled
studies are needed for confirmation of such findings.
Abbreviations
ART Assisted reproductive technologies
LBR Live birth rate
FET Frozen embryo transfer
ASRM American Society of Reproductive Medicine
CPR Clinical pregnancy rate
OPR Ongoing pregnancy rate
IVF In vitro fertilization
ICSI Intracytoplasmic sperm injection
GnRH Gonadotropin-releasing hormone
AMH Anti-Mullerian hormone
Acknowledgements
Not applicable.
Authors’ contributions
HA and AS were the main authors responsible of the research and writing the
paper. MK was responsible for the data collection, and WEG was responsible
for reviewing and revising the paper. All authors read and approved the final
manuscript.
Funding
The authors received no external funds.
Availability of data and materials
The datasets used and/or analyzed during the current study are available from
the corresponding author on reasonable request.
Declarations
Ethical approval and consent to participate
The study protocol was approved by the ethical committee of the Faculty of
Medicine, Alexandria University, Egypt. No informed consent was required due
to the retrospective design of the study.
Consent for publication
Not applicable.
Competing interests
The authors declare that they have no competing interests.
Received: 27 April 2024 Accepted: 4 August 2024
References
1. Zegers-Hochschild F, Adamson GD, Dyer S, Racowsky C, De Mouzon J,
Sokol R, Cooke ID (2017) The international glossary on infertility and fertil-
ity care, 2017. Hum Reprod 32(9):1786–1801
2. Navot D, Drews MR, Bergh PA, Guzman I, Karstaedt A, Scott RT Jr,
Hofmann GE (1994) Age-related decline in female fertility is not due to
diminished capacity of the uterus to sustain embryo implantation. Fertil
Steril 61(1):97–101
3. Hughes EG, Fedorkow DM, Collins JA (1993) A quantitative overview
of controlled trials in endometriosis-associated infertility. Fertil Steril
59(5):963–970
4. Collins JA, Burrows EA, Willan AR (1995) The prognosis for live birth
among untreated infertile couples. Fertil Steril 64(1):22–28
5. Somigliana E, Vigano P , Benaglia L, Busnelli A, Berlanda N, Vercellini P
(2017) Management of endometriosis in the infertile patient. Semin
Reprod Med 35(1):31–37
6. Barnhart K, Dunsmoor-Su R, Coutifaris C (2002) Effect of endometriosis
on in vitro fertilization. Fertil Steril 77(6):1148–1155
7. Pellicer A, Oliveira N, Ruiz A, Remohí J, Simón C (1995) Exploring the
mechanism (s) of endometriosis-related infertility: an analysis of
embryo development and implantation in assisted reproduction. Hum
Reprod 10(suppl_2):91–97
8. SHARPE-TIMMS, K. L. (2001) Endometrial anomalies in women with
endometriosis. Ann N Y Acad Sci 943(1):131–147
9. Ng EHY, Chan CCW, Tang OS, Yeung WSB, Ho PC (2004) Comparison
of endometrial and subendometrial blood flow measured by three-
dimensional power Doppler ultrasound between stimulated and
natural cycles in the same patients. Hum Reprod 19(10):2385–2390
10. Kolibianakis E, Bourgain C, Albano C, Osmanagaoglu K, Smitz J, Van
Steirteghem A, Devroey P (2002) Effect of ovarian stimulation with
recombinant follicle-stimulating hormone, gonadotropin releas-
ing hormone antagonists, and human chorionic gonadotropin on
endometrial maturation on the day of oocyte pick-up. Fertil Steril
78(5):1025–1029
11. Zapantis G, Szmyga M, Rybak E, Meier U (2013) Premature formation of
nucleolar channel systems indicates advanced endometrial matura-
tion following controlled ovarian hyperstimulation. Hum Reprod
28(12):3292–3300
12. Basirat Z, Rad HA, Esmailzadeh S, Jorsaraei SGA, Hajian-Tilaki K, Pasha
H, Ghofrani F (2016) Comparison of pregnancy rate between fresh
embryo transfers and frozen-thawed embryo transfers following ICSI
treatment. Int J Reprod Biomed 14(1):39
13. Shapiro BS, Daneshmand ST, Garner FC, Aguirre M, Hudson C, Thomas
S (2011) Evidence of impaired endometrial receptivity after ovar -
ian stimulation for in vitro fertilization: a prospective randomized
trial comparing fresh and frozen–thawed embryo transfer in normal
responders. Fertil Steril 96(2):344–348
14. Singh N, Lata K, Naha M, Malhotra N, Tiwari A, Vanamail P (2014) Effect
of endometriosis on implantation rates when compared to tubal
factor in fresh non donor in vitro fertilization cycles. J Hum Reprod Sci
7(2):143–147
15. Simon C, Domínguez F, Valbuena D, Pellicer A (2003) The role of
estrogen in uterine receptivity and blastocyst implantation. Trends
Endocrinol Metab 14(5):197–199
16. Kao L, Germeyer A, Tulac S, Lobo S, Yang J, Taylor R, Giudice L (2003)
Expression profiling of endometrium from women with endometriosis
reveals candidate genes for disease-based implantation failure and
infertility. Endocrinology 144(7):2870–2881
17. Canis M, Donnez JG, Guzick DS, Halme JK, Rock JA, Schenken RS, Ver -
non MW (1997) Revised American Society for reproductive medicine
classification of endometriosis. Fertil Steril 67(5):817–821
18. Wu J, Yang X, Huang J, Kuang Y, Wang Y (2019) Fertility and neona-
tal outcomes of freeze-all vs. fresh embryo transfer in women with
advanced endometriosis. Front Endocrinol. 10:770
19. Bourdon M, Santulli P , Maignien C, Gayet V, Pocate-Cheriet K, Marcellin
L, Chapron C (2018) The deferred embryo transfer strategy improves
cumulative pregnancy rates in endometriosis-related infertility: a
retrospective matched cohort study. PLoS One 13(4):e0194800
20. Mohamed AM, Chouliaras S, Jones CJ, Nardo LG (2011) Live birth rate in
fresh and frozen embryo transfer cycles in women with endometriosis.
Eur J Obstet Gynecol Reprod Biol 156(2):177–180
21. Chang Y, Shen M, Wang S, Li X, Duan H (2022) Association of embryo
transfer type with infertility in endometriosis: a systematic review and
meta-analysis. J Assist Reprod Genet 39(5):1033–1043
22. Mirkin S, Nikas G, Hsiu J-G, Díaz J, Oehninger S (2004) Gene expression
profiles and structural/functional features of the peri-implantation
endometrium in natural and gonadotropin-stimulated cycles. J Clin
Endocrinol Metab 89(11):5742–5752
Page 8 of 8Shoukry et al. Middle East Fertility Society Journal (2024) 29:41
23. Horcajadas JA, Riesewijk A, Polman J, van Os R, Pellicer A, Mosselman S,
Simón C (2004) Effect of controlled ovarian hyperstimulation in IVF on
endometrial gene expression profiles. Mol Hum Reprod 11(3):195–205
24. Haouzi D, Assou S, Mahmoud K, Tondeur S, Rème T, Hedon B, Hamamah
S (2009) Gene expression profile of human endometrial receptivity: com-
parison between natural and stimulated cycles for the same patients.
Hum Reprod 24(6):1436–1445
25. Valbuena D, Martin J, de Pablo JL, Remohı́, J., Pellicer, A., & Simón, C.
(2001) Increasing levels of estradiol are deleterious to embryonic implan-
tation because they directly affect the embryo. Fertil Steril 76(5):962–968
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in pub-
lished maps and institutional affiliations.
Text is read by the "Ask this paper" AI Q&A widget below.
Extraction quality varies by source — PMC NXML preserves structure
cleanly, OA-HTML may include some navigation residue, and OA-PDF can
have broken hyphenation. The publisher copy
(via DOI)
is the canonical version.