medicina

Article
Pregnancy Rates after Hysteroscopic Endometrial Polypectomy
versus Endometrial Curettage Polypectomy: A
Retrospective Study
Mikiko Nishioka 1,2,3 , Tadashi Maezawa 2,3, *, Hiroki Takeuchi 1,3 , Katsuyuki Hagiwara 4 , Sachiyo Tarui 5 ,
Mito Sakamoto 1,2,3 , Erina Takayama 2,3 , Hideaki Yajima 1,2,3 , Eiji Kondo 1,2 , Hiroaki Kawato 6,7 ,
Hiroyuki Minoura 7 , Ken Sugaya 8 , Aisaku Fukuda 5 and Tomoaki Ikeda 1,2,3

1 Department of Obstetrics and Gynecology, Graduate School of Medicine, Mie University, 2-174 Edo-bashi,
Tsu, Mie 514-8507, Japan; [email protected] (M.N.); [email protected] (H.T.);
[email protected] (M.S.); [email protected] (H.Y.); [email protected] (E.K.);
[email protected] (T.I.)
2 Department of Obstetrics and Gynecology, Mie University Hospital, 2-174 Edo-bashi, Tsu,
Mie 514-8507, Japan; [email protected]
3 Center of Advanced Reproductive Medicine, Mie University Hospital, 2-174 Edo-bashi, Tsu, Mie 514-8507,
Japan
4 Faculty of Education, Mie University, 1577 Kurima-Machiya-cho, Tsu,
Mie 514-8507, Japan; [email protected]
5 Department of Obstetrics and Gynecology, IVF Osaka Clinic, 1-1-14 Nagatahigashi, Higashiosaka,
Osaka 577-0012, Japan; [email protected] (S.T.); [email protected] (A.F.)
6 Department of Obstetrics and Gynecology, Kawato Ladies Clinic, 1-16-11 Betsumei, Yokkaichi, Mie 510-0007,
Japan; [email protected]
7 Department of Obstetrics and Gynecology, Minoura Ladies Clinic, 3-9-17 Isoyama, Suzuka, Mie 510-0256,
Japan; [email protected]
8 Department of Obstetrics and Gynecology, Saiseikai Matsusaka General Hospital, 15-6 asahimachiichiku,
Matsusaka, Mie 515-8557, Japan; [email protected]
* Correspondence: [email protected]; Tel.: +81-59-232-1111
Citation: Nishioka, M.; Maezawa, T.;
Takeuchi, H.; Hagiwara, K.; Tarui, S.;
Sakamoto, M.; Takayama, E.; Yajima, Abstract: Background and Objectives: A relationship between endometrial polypectomy and in vitro
H.; Kondo, E.; Kawato, H.; et al. fertilization (IVF) pregnancy outcomes has been reported; however, only a few studies have compared
Pregnancy Rates after Hysteroscopic polyp removal techniques and pregnancy rates. We investigated whether different polypectomy
Endometrial Polypectomy versus techniques with endometrial curettage and hysteroscopic polypectomy for endometrial polyps
Endometrial Curettage Polypectomy: affect subsequent pregnancy outcomes. Materials and Methods: Data from 434 patients who had
A Retrospective Study. Medicina 2023, undergone polypectomy for suspected endometrial polyps using transvaginal ultrasonography
59, 1868. https://doi.org/10.3390/
before embryo transfer in IVF at four institutions between January 2017 and December 2020 were
medicina59101868
retrospectively analyzed. Overall, there were 157 and 277 patients in the hysteroscopic (mean age:
Academic Editor: 35.0 years) and curettage (mean age: 37.3 years) groups, respectively. Single-blastocyst transfer
Dimitrios Papandreou cases were selected from both groups and age-matched to unify background factors. Results: In
the single-blastocyst transfer cases, 148 (mean age: 35.0 years) and 196 (mean age: 35.9 years) were
Received: 25 August 2023
Revised: 2 October 2023
in the hysteroscopic and curettage groups, respectively, with the 148 cases matched by age. In
Accepted: 16 October 2023 these cases, the pregnancy rates for the first embryo transfer were 68.2% (odds ratio (OR): 2.14)
Published: 20 October 2023 and 51.4% (OR: 1.06) in the hysteroscopic and curettage groups, respectively; the resulting OR
was 2.03. The pregnancy rates after up to the second transfer were 80.4% (OR: 4.10) and 68.2%
(OR: 2.14) in the hysteroscopic and curettage groups, respectively, in which the OR was 1.91. The
live birth rates were 66.2% (OR: 1.956) and 53.4% (OR: 1.15) in the hysteroscopic and curettage
Copyright: © 2023 by the authors.
groups, respectively, in which the odds ratio was 1.71. These results show the effectiveness of
Licensee MDPI, Basel, Switzerland.
hysteroscopic endometrial polypectomy compared to polypectomy with endometrial curettage. No
This article is an open access article
distributed under the terms and
significant difference was found regarding the miscarriage rates between the two groups. Conclusions:
conditions of the Creative Commons Hysteroscopic endometrial polypectomy resulted in a higher pregnancy rate in subsequent embryo
Attribution (CC BY) license (https:// transfer than polypectomy with endometrial curettage. Therefore, establishing a facility where
creativecommons.org/licenses/by/ polypectomy can be performed hysteroscopically is crucial.
4.0/).

Medicina 2023, 59, 1868. https://doi.org/10.3390/medicina59101868 https://www.mdpi.com/journal/medicina

Medicina 2023, 59, 1868 2 of 11

Keywords: endometrial polypectomy; pregnancy; IVF-ET; snare; curettage

1. Introduction
Endometrial polyps, which cause irregular bleeding and infertility, occur in 7.8–34.9%
of women [1] and reportedly in 15–24% of infertile patients [2,3]. They are localized, adher-
ent, or stalked projections of the uterine mucosa that result from abnormal hyperplastic
growth of the glands and stroma around the vascular core [4,5]. Histologically, an endome-
trial polyp comprises endometrial glands and stroma around the vascular axis of the spiral
artery [6]. Although estrogen receptors are overexpressed in the glandular epithelium of
polyps [7] and exposure has been suggested to be involved in the etiology of endometrial
polyps [8], the exact etiology of endometrial polyps has not been determined.
Endometrial polyps are categorized as macropolyps (visible on transvaginal ultra-
sonography) and micropolyps (1–2 mm in diameter and recognized hysteroscopically).
Micropolyps have been reported to coexist with chronic endometritis at a high rate [9] and
are effectively treated with antibiotics [10]. Treatment with antibiotics also dramatically
improves in vitro fertilization (IVF) pregnancy rates by approximately 65% [11–13]. How-
ever, most infertile patients with macropolyps develop endometritis, and polypectomy
has been reported to improve endometritis [2]. Additionally, the pregnancy rate after
macropolypectomy is reportedly 23–65% [14–16], and polypectomy is expected to improve
pregnancy rates.
Endometrial polypectomy is performed using endometrial curettage under anesthesia.
However, because endometrial curettage involves the non-visual excision of polyps using
placental forceps or curettes, potential damage to endometrial tissue other than the polyps
exists, and some patients may experience a decreased pregnancy rate postoperatively due to
endometrium thinning [17]. Therefore, the hysteroscopic resection of confirmed polyps has
recently been widely used. Various hysteroscopic methods have been reported, including
excision using a snare [18], a slender resectoscope [19], and a transvaginal morcellator [20].
Compared to curettage, which removes many endometrial tissues, hysteroscopic resection
only partly resects endometrial polyps. However, snare resection has drawbacks, such
as the time required to learn the technique and the installation and running costs of the
slender resectoscope and transvaginal morcellator. Therefore, if the main focus is on
pregnancy rates, the effects and benefits are significant and can be expected to increase
pregnancy rates.
Hysteroscopy before IVF is expected to increase pregnancy outcomes [21]. Specifically,
performing hysteroscopy in the cycle preceding the ovarian stimulation cycle could improve
IVF outcomes in asymptomatic patients with normal transvaginal ultrasound findings
undergoing their first IVF attempt. A previous review revealed that clinical pregnancy and
live birth rates were higher in the hysteroscopy group than in the controls [21].
To begin with, uterine abnormalities can cause increased miscarriage rates because of
the poor implantation environment and their impact on the developmental environment
of the fetus. Appropriate uterine surgery has been reported to result in high pregnancy
rates and favorable birth rates [22]. Therefore, minimally invasive surgery, including la-
paroscopic surgery, for infertile patients is expected to improve favorable IVF outcomes
and pregnancy rates without IVF [23]. Surgery has recently become increasingly mini-
mally invasive, and many techniques have proven to be relatively effective and safe [24].
Therefore, surgical treatment should be considered an option for organic abnormalities that
cause infertility.
Infertility frequently results from uterine or ovarian disease without symptoms in
infertile patients, and abnormalities may be noted for the first time during infertility testing.
The prevalence of unsuspected intrauterine abnormalities identified at hysteroscopy in the
asymptomatic IVF population is as high as 50% [25–27], and their early detection would
Medicina 2023, 59, 1868 3 of 11

likely contribute to improved pregnancy outcomes. Therefore, reproductive facilities

should incorporate more hysteroscopies as a tool to detect the causes of infertility early.
Although a relationship between endometrial polypectomy and IVF pregnancy out-
comes has been reported, only a few studies have compared polyp removal techniques
and pregnancy rates. Therefore, this study aimed to retrospectively compare IVF outcomes
after non-visual polypectomy with endometrial curettage and hysteroscopic polypectomy
and evaluate the results with respect to the surgical method of choice.

2. Materials and Methods

2.1. Ethical Approval
This retrospective observational study was approved by the Ethics Committee of Mie
University Hospital (approval number: H2021-104), and information was provided to
patients through an opt-out method. The Ethics Committee waived the need for informed
consent since opt-out consent was deemed acceptable.

2.2. Study Population

Patients with suspected endometrial polyps on transvaginal ultrasonography before
embryo transfer in IVF who had undergone polypectomy at four facilities (Mie University
Hospital, IVF Osaka Clinic, Saiseikai Matsusaka General Hospital, and Minoura Ladies
Clinic) between January 2017 and December 2020 were included in this study.

2.3. Study Design

This was a retrospective observational study. Patients with endometrial polyps sched-
uled for IVF at the four facilities were included during the study period. The inclusion
criteria included patients who were diagnosed with endometrial polyps before IVF, who
had undergone endometrial polypectomy, who had subsequently undergone IVF embryo
transfer, and whose subsequent progress was confirmed in their medical records. The exclu-
sion criteria included patients who had not undergone embryo transfer after endometrial
polyp excision and those whose progress after embryo transfer could not be confirmed.
Three facilities performed hysteroscopic polypectomy for endometrial polyps. Based
on polyp size and location findings, some cases were resected through snare polypectomy
using a flexible speculum, while others were resected without energization using a re-
sectoscope. Endometrial polyps were excised at one facility using endometrial curettage
after they were identified through hysteroscopy (Figure 1). The primary endpoints were
pregnancy, miscarriage, and live birth rates after polypectomy. After the pregnancy rates
of all embryo transfers were evaluated, single-blastocyst transfer cases were re-evaluated.
Pregnancy rates were first evaluated for patients who became pregnant during the first
embryo transfer, and those who did not were followed up until the second embryo transfer.
Patients who became pregnant during the second embryo transfer and those who became
pregnant during the first embryo transfer were collectively evaluated as patients who be-
came pregnant up to the second embryo transfer. Single-blastocyst transfers were matched
by age to eliminate the effects of age, and pregnancy, miscarriage, and live birth rates were
evaluated after polypectomy. As a secondary endpoint, the endometrial thickness in each
group was evaluated after polypectomy.
Medicina 2023,59,
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12

Figure 1.
Figure 1. There
There were
were 434
434cases
caseswith
withpolyps
polypsbefore
beforeininvitro
vitrofertilization
fertilization(IVF) and
(IVF) 157
and with
157 hyster-
with hys-
oscopic polypectomy. Of these, 103 and 54 cases were resected using a snare and resectoscope,
teroscopic polypectomy. Of these, 103 and 54 cases were resected using a snare and resectoscope, re-
spectively. Polypectomy with endometrial cure age was performed in 277 cases. Single-blastocyst
respectively. Polypectomy with endometrial curettage was performed in 277 cases. Single-blastocyst
transfer was performed in 148 hysteroscopic and 196 endorectal cure age cases. Among these, 148
transfer was performed in 148 hysteroscopic and 196 endorectal curettage cases. Among these, 148
were matched by age.
were matched by age.
2.4. Surgical
2.4. Surgical Procedure
Procedure
At one
At one institution,
institution, polyp
polyp excision
excision was was performed
performed using using endometrial
endometrial curettage
cure age afterafter
confirming the presence and location of the polyps using a flexible
confirming the presence and location of the polyps using a flexible hysteroscope (curettage hysteroscope (curet-
tage group).
group). A flexible
A flexible hysteroscope
hysteroscope is a endoscope
is a flexible flexible endoscope
with a camerawith a(Figure
camera 2b)(Figure
whose 2b)tip
whose tip can be moved up and down manually [28]. It
can be moved up and down manually [28]. It allows for observation of the uterus whileallows for observation of the
uterus while
refluxing water refluxing
throughwater through
the uterus andthedoesuterus and does
not require not require
cervical dilationcervical
because dilation
of its
becausetip.
narrow of its
Fornarrow tip. Forcurettage,
endometrial endometrial cure
after age, afterthe
confirming confirming the polyp’s
polyp’s location usinglocation
a hys-
using a hysteroscope,
teroscope, the cervix was thedilated
cervix using
was dilated
a Hegar using a Hegar
dilator, dilator, and
and curettage wascure age was
performed per-
using
formed using
placental forceps placental forceps
or curettage or cure
either blindage eitherconfirming
or while blind or while throughconfirming through
transabdominal
transabdominal
ultrasound. Finally,ultrasound. Finally,
the procedure wastheterminated
procedureafter was confirmation
terminated after confirmation via
via hysteroscopy.
hysteroscopy.
At the remaining three institutions, after the polyps were identified using a flexible
At the remaining
hysteroscope, the polypthree stem institutions,
was removed after
usingthea polyps
snare and were identified using
subsequently removed a flexible
from
hysteroscope,
the the polyp the
body. Alternatively, stem was removed
polyp using using
was identified a snarea and subsequently
resectoscope, andremoved
a loop orfromball
the body.was
electrode Alternatively,
used without the polyp was identified
energization to remove using
theapolyp,
resectoscope,
which was andsubsequently
a loop or ball
removed
electrodefromwas theused body (hysteroscopic
without energization group). The snares
to remove were made
the polyp, whichusing
was the Lin snare
subsequently
system ® (Hakko Medical Co., Tokyo, Japan) by inserting a wire with a looped tip into the
removed from the body (hysteroscopic group). The snares were made using the Lin snare
threaded portion Medical
system® (Hakko of a flexibleCo.,hysteroscope.
Tokyo, Japan) Next, the polypa was
by inserting wireremoved by squeezing
with a looped tip into the
the
loop after portion
threaded hookingofit aatflexible
its basehysteroscope.
and moving the wire
Next, theback
polypandwasforth while passing
removed water
by squeezing
from the side
the loop afterofhooking
the wire.itAatresectoscope
its base anduses movinga 9 mmtherigid
wirespeculum
back and to remove
forth while lesions
passingin
the uterus
water from bythe
moving
side ofa loop- or ball-shaped
the wire. A resectoscope instrument
uses a back
9 mm and forth
rigid using a hand-held
speculum to remove
control
lesions [29].
in theAdditionally,
uterus by moving the instrument
a loop- or is connectedinstrument
ball-shaped to an electrode back and
and energized
forth usingtoa
perform incision and coagulation. The diameter of the camera
hand-held control [29]. Additionally, the instrument is connected to an electrode is large, and the procedure
and en-
requires cervical dilation and anesthesia. In this study, the
ergized to perform incision and coagulation. The diameter of the camera is large, electrodes were not connected
and the
when the resectoscope
procedure requires cervical was used;
dilation therefore, the polyps
and anesthesia. were
In this excised
study, thebluntly.
electrodes Finally,
were the
not
excised
connectedpolyps
when werethe looped aroundwas
resectoscope theused;
polyp’s largest diameter
therefore, the polyps and placed
were on the
excised body
bluntly.
with the the
Finally, hysteroscope
excised polypsand polyp
were in close contact
looped around (Figure 2). largest diameter and placed
the polyp’s
on the body with the hysteroscope and polyp in close contact (Figure 2).
Medicina
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Figure 2. (a) Lin snare®® , which consists of a wire with a looped end, a tube that passes water from
Figure 2. (a) Lin snare , which consists of a wire with a looped end, a tube that passes water from
theside,
the side,and
andaadevice
devicethat
thatholds
holdsthe
thewire
wireininplace;
place;(b)
(b)hysteroscope
hysteroscopewithwithsnare
snareaattached; (c)changes
ached; (c) changes
with the snare in and out; (d) schematic of polypectomy with snare: the ring portion
with the snare in and out; (d) schematic of polypectomy with snare: the ring portion of the wire of the wireisis
hookedaround
hooked aroundthethebase
baseofofthe
thepolyp,
polyp,andandthe
thewire
wireisispulled
pulledwith
withthetheinstrument
instrumentatathand
handtotoreduce
reduce
the
thesize
sizeofofthe
thering
ring and
and remove the polyp;
polyp; (e)
(e) use
useofofsnare:
snare:on
onthe
theleft
leftisiswhere
wherethe
the wire
wire is hooked
is hooked up,
up,
andand
on on
thethe right
right is how
is how thethe polyp
polyp is removed.
is removed.

2.5.Embryo
2.5. EmbryoTransfer
Transferafter
afterEndometrial
EndometrialPolypectomy
Polypectomy
Embryotransfer
Embryo transferafter
afterpolypectomy
polypectomywas wasperformed
performedaccording
accordingtotoeach
eachinstitution’s
institution’s
endometrial adjustment method (hormone replacement or natural
endometrial adjustment method (hormone replacement or natural cycle). It was cycle). It wasusually
usually
performed within at least two cycles after treatment. If the first embryo
performed within at least two cycles after treatment. If the first embryo transfer did transfer didnot
not
result in a pregnancy, the embryos were transferred in successive cycles or one
result in a pregnancy, the embryos were transferred in successive cycles or one cycle apart. cycle apart.
Forcases
For caseswhere
wherethe
thefirst
firstpregnancy
pregnancywas wassuccessful
successfulbut butresulted
resultedininmiscarriage,
miscarriage,the thenext
next
embryotransfer
embryo transferwas
wasperformed
performedafter
afterthe
thesecond
secondmenstrual
menstrualperiod.
period.Embryos
Embryosthat thatwere
were
transferred during the second time point after polypectomy were included
transferred during the second time point after polypectomy were included in this study. in this study.
Thetransferred
The transferredembryos
embryoscouldcouldbe
beeither
eitherembryos
embryosororblastocysts.
blastocysts.Additionally,
Additionally,the
thetransfer
transfer
method is independent of whether it involves a single-embryo (blastocyst),
method is independent of whether it involves a single-embryo (blastocyst), double-em- double-embryo
(blastocysts),
bryo or two-step
(blastocysts), or two-step embryo
embryo (transfer
(transferofofananembryo
embryoandandaa blastocyst
blastocyst inin the
thesame
same
cycle) transfer. However, only single-blastocyst transfers were analyzed after all cases were
cycle) transfer. However, only single-blastocyst transfers were analyzed after all cases
evaluated. Transfers were performed on embryos that were grade III or higher according to
were evaluated. Transfers were performed on embryos that were grade III or higher ac-
Veeck’s classification, which is an index used to prioritize the transfer of split-stage embryos.
cording to Veeck’s classification, which is an index used to prioritize the transfer of split-
The uniformity of the blastomere and the number and rate of fragments determine the grade
stage embryos. The uniformity of the blastomere and the number and rate of fragments
(Figure S1). Blastocysts were transferred from viable blastocysts with an inner cell mass
determine the grade (Figure S1). Blastocysts were transferred from viable blastocysts with
(ICM) grade of C or higher according to the Gardner classification, which is an index used
an inner cell mass (ICM) grade of C or higher according to the Gardner classification,
to prioritize the transfer of blastocysts. Furthermore, the degree of blastocyst expansion
which is an index used to prioritize the transfer of blastocysts. Furthermore, the degree of
and the number and rate of ICM and trophectoderm cells determine the grade (Figure S1).
blastocyst expansion and the number and rate of ICM and trophectoderm cells determine
the
2.6.grade (Figure
Statistical S1).
Analysis
The data are presented as means. R software was used to analyze the data. The
2.6. Statistical Analysis
Mann–Whitney U test was used to examine the differences in mean age and endometrial
The data
thickness are presented
between as means.
the two groups. R software
Regarding clinicalwas used tomiscarriage,
pregnancy, analyze the anddata.
live The
birth
Mann–Whitney U test wasZ-test
rates, the two-proportion used (pooled)
to examine
wasthe differences
used in mean
to compare items.age
Theand endometrial
significance level
thickness
was set atbetween
<5%. In the
this two groups.
study, Regarding transfer
single-blastocyst clinical cases
pregnancy, miscarriage,
were selected and live
for background
birth rates, the
uniformity, andtwo-proportion Z-test (pooled)
subsequently, matching was used factors
by confounding to compare items. Thetosignifi-
was performed derive
cance level was set at <5%. In this study, single-blastocyst transfer cases were selected for
Medicina 2023, 59, 1868 6 of 11

test results that excluded confounders, if any, between each group for the present results.
For matching, one-to-one nearest neighbor matching based on Euclidean distance was
employed, and the post-matching samples were tested for differences in proportions (using
normal approximation) between each group, with the significance level set at <5%.

3. Results
3.1. Pregnancy, Miscarriage, and Live Birth Rates from Embryo Transfer after
Endometrial Polypectomy
Table 1 summarizes the number of cases, age, endometrial thickness, and clinical
outcomes after polypectomy in each group for all cases. Table 1 also includes the p-values
of the statistical tests. During the study period, 434 patients with endometrial polyps were
scheduled for IVF at the four facilities. The number of patients in the hysteroscopic group
was 157, with a median age of 35 (24–46) years. Of these, 103 and 54 cases were resected
using snare polypectomy and Trans Cervical Resection (TCR), respectively. Additionally,
the number of patients in the curettage group was 277. Specifically, the patients in the curet-
tage group were significantly older than those in the hysteroscopic group, with a median
age of 37 (25–47) years. Of the cases where a single-blastocyst transfer was performed, 148
and 196 were hysteroscopic and endometrial curettages, respectively (Figure 1).

Table 1. Comparison of results between the hysteroscopic and curettage groups in endometrial
polypectomy and the effect of age on this data. (a) All cases. (b) SBT cases.

Curettage
Hysteroscopic Group
Variable Group p-Value
(n = 157)
(n = 277)
Age [years], median (range) 35 (24–46) 37 (25–47) <0.0001 *
Endometrial thickness [mm], 11.0 11.2
0.0278 *
median (range) (6.0–19.0) (7.4–19.1)
Clinical pregnancies/first embryo 106 118
<0.0001 †
transfer, frequency [%] (67.5) (42.6)
Clinical pregnancies/up to the second 128 153
<0.0001 †
embryo transfer, frequency [%] (81.5) (55.2)
26 42
Miscarriages, frequency [%] 0.7002 †
(16.6) (15.2)
102 111
Live births, frequency [%] <0.0001 †
(65.0) (40.1)
Curettage
Hysteroscopic group
Variable group p-value
(n = 148)
(n = 196)
Age [years], median (range) 35 (24–46) 36 (25–45) 0.0211 *
Endometrial thickness [mm], median 11.0 11.4
0.0260 *
(range) (6.0–19.0) (7.4–17.6)
Clinical pregnancies/first embryo 101 102
0.0025 †
transfer, frequency [%] (68.2) (52.0)
Clinical pregnancies/up to the second 119 128
0.0021 †
embryo transfer, frequency [%] (80.4) (65.3)
24 32
Miscarriages, frequency [%] 0.9781 †
(16.2) (16.3)
98 97
Live births, frequency [%] 0.0019 †
(66.2) (49.5)
Data are reported as mean and (range) for age and endometrial thickness, and as frequency and (percentage) for
the other variables. * Mann–Whitney’s test; † two-proportion Z-test. SBT: single-blastocyst transfer.

The initial endometrial thicknesses after polypectomy were 11.0 and 11.2 mm in the
hysteroscopic and curettage groups, respectively, both in the 11 mm range, although the en-
dometrium was significantly thicker in the curettage group than in the hysteroscopic group.
Medicina 2023, 59, 1868 7 of 11

One (0.6%), two (1.3%), and six (3.8%) cases of single-embryo, double-embryo, and
two-step embryo transfers, respectively, were performed in the hysteroscopy group. In
the curettage group, 61 (22.0%) embryo and 20 (7.2%) two-step embryo transfers were
performed. The pregnancy rate for the first embryo transfer in the hysteroscopic group
(67.5%) was significantly higher than that in the curettage group (42.6%). In contrast, the
pregnancy rate after up to the second embryo transfer was higher in the hysteroscopy
group (81.5%) than in the curettage group (55.2%). The live birth rate in the hysteroscopy
group (65.0%) was higher than that in the curettage group (40.1%). However, no significant
difference was found in the miscarriage rates between the two groups (Table 1).

3.2. Pregnancy, Miscarriage, and Live Birth Rates for the Single-Blastocyst Transfer Only
Table 1 presents the results for the cases with single-blastocyst transfer after endome-
trial polypectomy. Regarding the single-blastocyst transfer after endometrial polypectomy,
the median ages in the hysteroscopic and curettage groups were 35 (24–46) years in 148
patients and 36 (25–45) in 196, respectively, indicating that the curettage group was signifi-
cantly older than the hysteroscopic group.
The initial endometrial thicknesses after polypectomy were 11.0 and 11.4 mm in the
hysteroscopic and curettage groups, respectively, suggesting that the endometrium was
thicker in the curettage group than in the hysteroscopic group; however, both were within
the 11 mm range.
The pregnancy rate in the first embryo transfer in the hysteroscopic group (68.2%) was
significantly higher than that in the curettage group (52.0%). In contrast, the pregnancy
rates after up to the second attempts were 80.4% and 65.3% in the hysteroscopic and
curettage groups, respectively, signifying that they were higher in the hysteroscopic group
than in the curettage group. The live birth rates were 66.2% and 49.5% in the hysteroscopic
and curettage groups, respectively, with a higher rate in the hysteroscopic group than in
the curettage group. However, no significant difference was found in the miscarriage rates
between the two groups (Table 1).

3.3. Pregnancy, Miscarriage, and Live Birth Rates after Matching by Confounding Factors
This study’s results showed that the pregnancy rate was significantly higher in the
hysteroscopic group than in the curettage group; however, the age of the hysteroscopic
group was lower than that of the curettage group. Since pregnancy rates are generally
higher in younger women, the effect of age on each of these results is discussed below.
In the single-blastocyst transfer cases, the standardized mean difference (SMD) was
0.459 for patients who became pregnant and those who did not after the first embryo transfer
(mean age: 34.6 and 36.6 years). The SMDs were 0.729 (mean age: 34.6 and 37.6 years, 0.846
(mean age: 34.0 and 37.3 years), and −0.398 (mean age: 36.8 and 35.2 years) for patients
who became pregnant and those who did not up to the second transfer, patients with and
those without live births, and patients with and those without miscarriages, respectively
(Table S1). Since the absolute values of SMDs were all >0.1, which was the standard for
significant differences, the pregnancy, live birth, and miscarriage rates were considered to
be influenced by age. Particularly, the finding that younger age groups are more likely to
conceive and have live births was valid. However, the mean ages were 34.8 and 35.9 years
for the hysteroscopic and curettage groups, respectively, with an SMD of 0.261, indicating
an age bias between the groups. Therefore, since age was likely to be a confounding factor
when considering the association between the method of polypectomy and pregnancy,
miscarriage, and live birth rates, matching by age was performed between the hysteroscopic
and curettage groups for single-blastocyst transfer cases.
For the single-blastocyst transfer cases with matching by age, the number of cases,
age, endometrial thickness, and clinical outcomes after polypectomy in each group are
summarized in Table 2. In the single-blastocyst transfer cases, the sample size after matching
was 148 cases (sample size of the hysteroscopic group), and the SMD after matching was
0.067, suggesting that the age bias among the groups was almost eliminated. In the
Medicina 2023, 59, 1868 8 of 11

hysteroscopic group, the pregnancy rate after the first embryo transfer and that after up
to the second embryo transfer were 68.2% and 80.4%, respectively; the miscarriage rate
was 16.2%, and the live birth rate was 66.2%. In contrast, the pregnancy rate after the first
embryo transfer and that after up to the second embryo transfer in the curettage group were
51.4% and 68.2%, respectively; the miscarriage rate was 15.5%, and the production rate was
53.4%. Both pregnancy and live birth rates were significantly higher in the hysteroscopic
group, whereas no significant differences were found in the miscarriage rates (Table 2).

Table 2. Tests for differences between proportions and ratios in the SBT group matched by age.

Hysteroscopic
Curettage Group
Variable Group p-Value
(n = 148)
(n = 148)
Age [years], median (range) 35 (24–46) 35 (25–45) 0.6049 *
Endometrial thickness [mm], 11.0 11.2
0.1093 *
median (range) (6.0–19.0) (7.4–17.6)
Clinical pregnancies/first 101 76
0.0030 †
embryo transfer, frequency [%] (68.2) (51.4)
Clinical pregnancies/up to the
119 101
second embryo transfer, 0.0166 †
(80.4) (68.2)
frequency [%]
24 23
Miscarriages, frequency [%] 0.8736 †
(16.2) (15.5)
98 79
Live births, frequency [%] 0.0243 †
(66.2) (53.4)
Data are reported as mean and (range) for age and endometrial thickness, and as frequency and (percentage) for
the other variables.* Mann–Whitney test; † two-proportion Z-test.

4. Discussion
Endometrial polyps are a relatively frequent infertility disorder, recently linked to
chronic endometritis [20]. Polypectomy is frequently performed when small polyps are sus-
pected to cause implantation failure [13]. It was previously performed non-visually under
anesthesia using placental forceps or curettes and hysteroscopically using a resectoscope
for large polyps. However, both procedures require anesthesia and are burdensome for
patients. Additionally, non-visual endometrial curettage frequently involves the curettage
of normal endometrial tissue around the polyp, which may result in infertility in some cases
because of endometrial thinning-induced embryo implantation failure [30]. Polypectomy
using a snare has been reported to have minimal impact on the endometrial tissue [17].
A snare is considered to have little effect on the endometrium because only polyps can
be removed using a hysteroscope with visualization of the inside of the uterus. However,
only a few reports have compared subsequent pregnancy outcomes in patients treated with
curettage and hysteroscopic polypectomy.
In this study, we compared the postoperative IVF outcomes between patients in
whom endometrial curettage was performed after polyps were identified using a flexible
hysteroscope and those in whom endometrial polyps were removed using a hysteroscope.
Single-blastocyst transfer cases were also extracted and examined to unify the background
factors. Because a significant difference was found in age between the groups in these
results, matching by age was performed to remove age bias. The pregnancy rate was
significantly higher in patients who had undergone hysteroscopic resection of endometrial
polyps than in those who had undergone curettage.
Endometrial polyps have a high recurrence rate [18], and embryo transfer should be
performed immediately after polypectomy. Therefore, pregnancy rates after the second
embryo transfer were used for comparison in this study. The pregnancy rates were 80.4%
and 68.2% in the hysteroscopic and curettage groups, respectively, when matched by age,
with the hysteroscopic group having a significantly higher pregnancy rate than the curettage
group (Table 2). This may be due to a certain degree of removal of normal endometrial
Medicina 2023, 59, 1868 9 of 11

tissue through curettage. Since no difference was found between the two groups regarding
the miscarriage rate, the polypectomy technique appeared to have no effect.
A relationship between endometrial thickness and pregnancy rate has long been
reported [31], and endometrial curettage reportedly causes endometrium thinning [32,33].
Cases with an endometrium of <7 mm did not result in pregnancy [34]. In this study,
the endometrial thickness before embryo transfer was greater in the curettage group than
in the hysteroscopic group, although both groups were in the 11 mm range, and neither
group showed obvious endometrium thinning; therefore, the effect of polypectomy on
endometrial thickness was considered low. However, differences were observed in the
pregnancy rates during embryo transfer after polypectomy, possibly due to inflammation or
other effects of the endometrium caused by endometrial curettage. Intrauterine adhesions
caused by endometrial curettage or infection have been suggested to cause infertility [35]. If
the basal layer of the endometrium is damaged during curettage, inflammation is triggered
during the wound-healing process [36,37]. Patients with healed chronic endometritis
have higher pregnancy and live birth rates than those with persistent inflammation [11];
therefore, healed inflammation in the uterus is important for improving pregnancy rates.
These events may prevent embryo implantation by affecting endometrial formation.
Although there are various devices and techniques for hysteroscopic endometrial
polypectomy, performing endometrial polypectomy using these methods is useful for early
pregnancy in infertile patients. Hysteroscopic endometrial polypectomy, which has less
impact on the endometrium, is a useful procedure that leads to earlier patient pregnancy,
as suggested by this study’s results. We examined cases at multiple institutions because
of the limited number of cases at one institution. However, biases, such as differences in
polypectomy techniques and embryo transfer methods at each institution, could not be
eliminated. Additionally, perinatal risks, such as diabetes, hypertension, and obesity, were
excluded from this study; therefore, including these factors in future analyses is necessary.

5. Conclusions
This study showed that hysteroscopic endometrial polypectomy resulted in a signifi-
cantly higher pregnancy rate than endometrial curettage polypectomy.

Supplementary Materials: The following supporting information can be downloaded at: https:
//www.mdpi.com/article/10.3390/medicina59101868/s1, Table S1: Study of the effect of age on
pregnancy, live birth, and miscarriage rates in each of the outcomes of single-blastocyst transfer;
Figure S1: Veeck and Gardner classifications.
Author Contributions: Conceptualization, T.M. and H.T.; methodology, T.M. and H.T.; validation,
T.M. and H.T.; formal analysis, T.M. and K.H.; investigation, M.N. and T.M.; resources, S.T., H.K.,
H.M., K.S. and A.F.; data curation, M.N. and T.M.; supervision, M.S., E.T., H.Y., E.K. and T.I.; writing—
original draft preparation, M.N. and T.M.; writing—review and editing, H.T. and K.H.; project
administration, T.M. and H.T.; funding acquisition, M.N. and H.T. All authors have read and agreed
to the published version of the manuscript.
Funding: This work was supported by the JSPS KA-KENHI (grant numbers: 20K18164 (M. Nishioka)
and 20K18188 (H. Takeuchi)).
Institutional Review Board Statement: This research was approved by the Ethics Committee of Mie
University Hospital (approval number: H2021-104, 10/6/2021).
Informed Consent Statement: Since this study was retrospective and based on medical record
information, we used the opt-out method as consent.
Data Availability Statement: The data supporting the results of this study are available from the
corresponding author upon reasonable request.
Acknowledgments: We thank Midori Uemura, Seiya Higashimoto, Eri Magara, Megumi Fukui, and
Sayaka Okuhara-Terasawa for their technical assistance.
Conflicts of Interest: The authors declare no conflict of interest.
Medicina 2023, 59, 1868 10 of 11

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