Abstract
Background: Endometrial ablation is a safe and effective minimally invasive surgical procedure. Despite the high success rate of
endometrial ablation for heavy uterine bleeding management, some patients experience persistent symptoms after the procedure, ne-
cessitating a hysterectomy. The aim of this study is to determine the pre-operative clinical predictive factors of failure of endometrial
ablation in the management of uterine bleeding. Methods: Retrospective cohort study of endometrial ablation procedures performed
for treating heavy uterine bleeding. Results: Ninety five patients were included in the study. The failure rate was 24.2%. There was a
statistically significant association between ablation failure and fluid deficit ( p = 0.002) and intra-operative blood loss ( p = 0.047). There
was a statistically significant moderate association between adenomyosis (p = 0.003, φ = 0.37) and failed endometrial ablation. However,
the age, body mass index (BMI), parity, number of miscarriages, number of cesarean sections, uterine length, endometrial thickness and
procedure duration had no significant association with endometrial ablation. There was no significant relationship between the uterine
abnormalities in general and the outcome of the endometrial ablation ( p = 0.637). However, patients with combined adenomyosis and
dysmenorrhea had a statistically significant association with outcome of the endometrial ablation ( p = 0.016, φ = 0.28) and were more
likely to have a failed endometrial ablation (crude odds ratio (COR) = 4.67, 95% confidence interval (CI), 1.35–16.09). Logistic regres-
sion to adjust for related factors revealed that the adenomyosis (adjusted odds ratio (AOR) = 50.83, 95% CI, 3.64–706.75, p = 0.003)
and fluid deficit (AOR = 1.003, 95% CI, 1.000–1.006, p = 0.044) had a higher likelihood of an unsuccessful outcome. Hysterectomy
was performed in 47.8% of patients who had failure of the ablation. Conclusions: Among pre-operative factors, adenomyosis, fluid
deficit and combined adenomyosis and dysmenorrhea were found to predict failure of hysteroscopic endometrial ablation. Clinical Trial
Registration: It was registered in https://www.clinicaltrials.gov database with Identifier: NCT05483348.
Keywords
endometrial; ablation; hysteroscopic; rollerball; uterine; adenomyosis
1. Introduction
Endometrial ablation (EA) is a safe and efficacious
endoscopic surgical procedure that has become a well-
established alternative option in selected women with heavy
and abnormal uterine bleeding [1]. In the United Kingdom,
hysterectomy rates were significantly reduced over the past
20 years due to both improved medical treatment and in-
creased use of EA techniques [ 2]. EA improves treatment
access for those women who have abnormal uterine bleed-
ing (AUB) and provides an alternative to radical procedures
such as hysterectomy [ 3]. Hysterectomy was found to be
associated with a higher risk than endometrial ablation of
surgery for pelvic floor repair and stress urinary inconti-
nence [3].
Despite the high success rate of endometrial ablation
for uterine bleeding management, some patients experi-
ence persistent symptoms after the procedure, necessitat-
ing a hysterectomy. The characteristics of patients whose
endometrial ablation fails had been studied by Kristin A Ri-
ley in a cohort study of 51 patients who had multiple vari-
ants assessed, including age, body mass index (BMI), parity
and tubal ligation. The only statistically significant vari-
ant was age; it also revealed that endometriosis was the
most common finding among patients who presented for
hysterectomy after endometrial ablation; other findings in-
cluded adenomyosis and leiomyomata [ 4]. Another retro-
spective cohort study of 968 women who had endometrial
ablation between January 2007 and July 2009 compared the
risk of treatment failure between women who had regular
and irregular heavy uterine bleeding, concluding that pre-
operative bleeding pattern has no effect on failure rates or
the need for gynecological procedures after endometrial ab-
lation [5]. A study that included 128 women who had en-
dometrial ablation or resection was conducted to determine
the perioperative factors that influenced the success of this
hysteroscopic intervention It was found that the presence of
submucosal myoma was found to increase the risk of sub-
sequent surgery [6].
The first-generation hysteroscopic techniques namely,
roller ball ablation, bipolar endometrial resection and laser
ablation, all required visualization of the cavity for the en-
tirety of the procedure [ 7]. Second generation techniques
have been developed which do not require hysteroscopy
and can be easily performed without requiring high lev-
els of skill include bipolar radiofrequency, microwave and
thermal balloon ablation, endometrial cryotherapy, and hy-
drothermal ablation [8].
The success of endometrial ablation was seen in
80.6% of cases [ 9]. On the other hand, failure rates of en-
dometrial ablation, which were manifested as persistence
of pain or bleeding, have reached 10–20% that required pa-
tients to undergo further interventions to handle their mal-
ady [10].
The objective of our study was to determine additional
patient characteristics and the clinical predictive factors of
failure of endometrial ablation and the need of subsequent
gynecological procedure.
The primary outcomes were to determine the pre-
operative clinical predictive factors of failure of endome-
trial ablation in the management of uterine bleeding. Sec-
ondary outcomes were to search for any intra-operative pre-
dictive factors of failure of the procedure. Better under-
standing of the predictive factors of success or failure will
help in proper counselling of patients and in decreasing the
incidence of endometrial ablation failure and avoid further
re-ablation or hysterectomy.
2. Methods
2.1 Study Design
A retrospective cohort study was conducted in a single
tertiary center, Jordan University Hospital (JUH). Such a
design enabled us to compare two populations of similar
baseline characteristics for the exception of the one studied.
2.2 Population
Patients with heavy menstrual bleeding for 6 months
who had trans-cervical hysteroscopic endometrial ablation
in the period September 2016 to September 2021 and fol-
lowed up for at least one year. Heavy bleeding was sub-
jectively indicated by the patient as having prolonged cy-
cles, using excessive pads, staining her underwear, affect-
ing her usual activities, taking supplements to correct her
low hemoglobin and the presence of clots. This bleeding
pattern should be experienced by the patient for at least 3
months. Patients with hemoglobin of less than 10.5 g/dL
were considered anemic.
2.3 Data Collection
Clinical data included age, BMI, parity, tubal liga-
tion, uterine size/length (in weeks as determined by biman-
ual examination and uterine sound), endometrial thickness
(in millimeters as measured by transvaginal ultrasound scan
(U/S)), procedure duration, fluid deficits, presence of uter-
ine abnormality as endometriosis, adenomyosis, leiomy-
omata and polyps or history of dysmenorrhea, menorrha-
gia, number of cesarean sections, history of uterine surgery;
myomectomy, dilatation and curettage (D&C).
Patients who had resection or subsequently had a diag-
nosis of endometrial cancer or hyperplasia (both simple and
those with atypia), those with intramural fibroids, patients
with submucosal fibroids larger than 5 cm, patients with
previous ablation, patients who had ablation using bipolar
diathermy and those with incomplete or missing records or
follow up were excluded from the study’s target population.
2.4 Ethical Considerations
Patients’ data was treated with the utmost of confi-
dentiality. Moreover, all records were accessed through
JUH’s computers and under JUH’s medical staff supervi-
sion ensuring that no data was copied or transferred to pri-
vate storage sources. Any and all data that contributes to
the recognition of patients’ identities, such as names, phone
numbers or addresses were either turned into codes or not
be used at all. The study obtained approval of the insti-
tutional review board (IRB) committee at JUH (decision
number 58/2022, dated 17/02/2022). It was also registered
in https://www.clinicaltrials.gov database with Identifier:
NCT05483348.
All women had general and gynecologic examination
preoperatively and either had diagnostic hysteroscopy or
trans-vaginal ultrasound (U/S) scan done by consultant gy-
necologists to accurately measure the uterine size, endome-
trial thickness and the size of the fibroids or polyps, or both
before the hysteroscopic ablation.
A written informed consent was obtained from all pa-
tients included in this study. The consent included full
explanation of the procedure, benefits, potential complica-
tions and risks.
2.5 Surgical Technique
Hysteroscopic ablation was performed in the post-
menstrual period when the endometrium was very thin. In
our practice, we not use pre-operative endometrial thin-
ning agents. The operative hysteroscopy in our study was
done using rigid, with 30 degrees angulated continuous
flow hysteroscopy utilizing a monopolar rollerball. This
necessitated the use of glycine 1.5% as a uterine distending
medium in 3.0 Liter-bags. The monopolar resectoscope was
sterilizable and reusable while the bipolar one was a single-
use instrument, thus minimizing financial costs. The flow
rate used was at 250 mL/minute. Myomectomy cases were
performed using angled wire cutting loop electrodes. All
patients had standardized 80 millimeter mercury (mmHg)
of intra-uterine pressure during surgery with the use of the
same automated glycine infusion pump. Patients had cervi-
cal dilatation done to 10 mm using Hegar dilators unless the
cervix was already found to be dilated. Patients with uterine
polyps or fibroids (submucosal (SM) type 0 and 1 only) [11]
2
Table 1. Comparison of failed and successful endometrial ablations in relation to different factors.
V ariables Failure Success p value Effect size
Mean Standard deviation Mean Standard deviation
Age 45.39 8.45 46.36 6.68 0.431 -
BMI 30.75 3.47 29.8 6.71 0.413 -
Parity 4.1 2.49 4.43 2.27 0.283 -
Miscarriage 0.81 0.87 1.23 1.6 0.51 -
N of cesarean sections 2 1.66 1.31 1.55 0.135 -
Uterine length (weeks) 9.57 2.48 8.59 1.91 0.057 -
Endometrial thickness (mm) 10.77 5.21 11.02 7.04 0.935 -
Procedure duration (min) 36.3 14.94 35.42 13.63 0.893 -
Fluid deficit (cc) 575 298.33 335.3 203.99 0.002 0.34
Blood loss (cc) 65.22 49.35 49.93 46.09 0.047 0.21
Notes: p values for the Parity and uterine length were calculated by independent sample t-test. All other items were
subjected to Mann-Whitney Utest or Mann–Whitney–Wilcoxon (MWW/MWU) test. BMI, body mass index; mm,
millimeter; min, minute; cc, cubic centimeter; N, number.
had their lesions first resected using a resectoscope loop fol-
lowed by rollerball endometrial ablation (REA). Before the
REA, all patients had curettage of the whole endometrial
cavity to obtain tissue for histopathological examination
and to thin the endometrial to enhance the thermal effect
of the ablation. There were selected cases that had bipo-
lar ablation and they were excluded from the study to have
a homogenous study population. All procedures were per-
formed by the same consultant gynecologist. Data was ex-
tracted from patients’ clinical notes in the clinic, operative
notes, admission and follow up visits’ notes.
Data was extracted by using relevant International
Classification of Diseases—Ninth revision (ICD-9) codes
as well as Current Procedural Terminology (CPT) codes
[12].
Patients included in this study experienced heavy uter-
ine bleeding and underwent endometrial ablation. Success-
ful cases were defined as patients’ satisfaction with the pro-
cedure as indicated by amenorrhea or very light menstrual
bleeding for 12 months at least. Failure was defined as
patients’ un-satisfaction necessitating subsequent gyneco-
logical procedures such as hysterectomy or repeat ablation
within 12 months after the endometrial ablation. We did
not assess the effect of the ablation on the post-operative
hemoglobin level. We then determined those who were
unsatisfied (recurrent heavy bleeding, dysmenorrhea) and
those who ended up with repeated ablation, hormonal treat-
ment and those who had hysterectomy after the ablation.
2.6 Statistical Analysis
Data analysis was performed using the IBM SPSS,
version 28.0 (IBM Corp., Armonk, NY , USA) developed
by Norman H. Nie, Dale H. Bent and C. Hadlai Hull. Cate-
gorical variables were summarized as frequencies and per-
centages. Participants were categorized into two groups ac-
cording to their failure or success of the primary endome-
trial ablation. Pearson’s Chi-square ( χ2) test and Fischer’s
exact test with crude odds ratios (COR) (95% confidence in-
terval (CI)) was used to determine the association between
categorical data. The phi coefficient ( φ) was used as a mea-
sure of the strength of association.
Normality was assessed using the Shapiro-Wilk test.
Independent samples t-test and Mann-Whitney U tests were
used to determine the association between continuous data.
The effect size was calculated depending on the test use by
effect size r for Mann-Whitney U. V ariables that showed
potentially interesting associations from the univariate anal-
ysis were included in the binary logistic regression model
in order to control for possible confounding factors, which
were summarized using adjusted odds ratios (AOR) (95%
CI). Statistical significance was defined as a p-value of less
than 0.05.
3. Results
In total, there were 138 procedures were done in the
study period. Ninety-five patients were included in this
study; the age ranged from 29 to 52 years, with a mean age
of 46.13 ± 7.11 years. Among the participants, the mean
BMI was 29.97 ± 6.23, ranged from 18 to 56. Participants
were categorized into two groups according to their fail-
ure or success of the primary endometrial ablation. Overall,
24.2% (n = 23) had a failed endometrial ablation with a sub-
sequent gynecological procedure and 75.8% (n = 72) had a
successful endometrial ablation with no further procedures
required. Tables 1,2 show a comparison between patients
with successful and those with failed endometrial ablation
groups.
Our results showed a significant difference between
patients with successful and failed endometrial ablations in
regard to fluid deficit ( p = 0.002) and blood loss during the
surgery ( p = 0.047); however, the age, BMI, parity, num-
ber of miscarriages, number of cesarean sections, uterine
length, endometrial thickness and procedure duration had
no significant difference between the two groups (p > 0.05).
3
Table 2. A comparison between the clinical characteristics of failed and successful endometrial ablation.
V ariables Total number (%) Endometrial ablation OR (95% CI) p value
Failure Success
Smoker (yes) 3/78 (3.8) 2/18 (11.1) 1/60 (1.7) 7.38 (0.63–86.60) 0.131
History of coagulation disorders (yes) 1/92 (1.1) 0/22 (0) 1/70 (1.4) 0.99 (0.96–1.01) 1
Use of anticoagulants (yes) 1/92 (1.1) 0/22 (0) 1/70 (1.4) 0.99 (0.96–1.01) 1
Previous tubal ligation (yes) 9/95 (9.5) 2/23 (8.7) 7/72 (9.7) 0.88 (0.17–4.59) 1
Uterine abnormalities 1.55 (0.26–9.16) 0.637
Polyps 43/84 (51.2) 7/21 (33.3) 36/63 (57.1)
Fibroids 42/84 (50) 14/21 (66.7) 28/63 (44.4)
Adenomyosis 6/84 (7.1) 5/21 (23.8) 1/63 (1.6)
No abnormalities 6/84 (7.1) 2/21 (9.5) 4/63 (6.3)
Endometriosis 3/84 (3.6) 0/21 (0) 3/63 (4.8)
Thickened endometrium 3/84 (3.6) 0/21 (0) 3/63 (4.8)
Leiomyomata 1/84 (1.2) 1/21 (4.8) 0/63 (0)
Menstrual abnormalities 0.38 (0.08–1.83) 0.349
Menorrhagia 79/89 (88.8) 18/21 (85.7) 61/68 (89.7)
Dysmenorrhea 7/89 (7.9) 2/21 (9.5) 5/68 (7.4)
Intermenstrual spotting 1/89 (1.1) 0/21 (0) 1/68 (1.5)
History of uterine surgery 0.66 (0.23–1.90) 0.440
Dilation and curettage 51/91 (56) 15/22 (68.2) 36/69 (52.2)
Evacuations 7/91 (7.7) 0/22 (0) 7/69 (10.1)
Myomectomy 4/91 (4.4) 0/22 (0) 4/69 (5.8)
Other 7/91 (7.7) 0/22 (0) 7/69 (10.1)
No 31/91 (34.1) 6/22 (27.3) 25/69 (36.2)
Indication for primary endometrial ablation
Menorrhagia 36/95 (37.9) 12/23 (52.2) 24/72 (33.3) 2.18 (0.84–5.66) 0.139
Heavy menstrual bleeding 31/95 (32.6) 4/23 (17.4) 27/72 (37.5) 0.35 (0.11–1.14) 0.081
Fibroid 17/95 (17.9) 8/23 (34.8) 9/72 (12.5) 3.73 (1.24–11.29) 0.026
Irregular vaginal bleeding 14/95 (14.7) 2/23 (8.7) 12/72 (16.7) 0.48 (0.10–2.30) 0.506
Polyps 10/95 (10.5) 0/23 (0) 10/72 (13.9) – 0.112
Postmenopausal bleeding 9/95 (9.5) 2/23 (8.7) 7/72 (9.7) 0.88 (0.17–4.59) 1
Infertility 3/95 (3.2) 1/23 (4.3) 2/72 (2.8) 1.59 (0.14–18.40) 0.569
There might be more than one indication. OR, odds ratio; CI, confidence interval.
Table 1 shows the details of the successful and failed en-
dometrial ablations.
There was no significant relationship between the
uterine abnormalities in general and the outcome of the en-
dometrial ablation ( p = 0.637); however, there was a sta-
tistically significant, moderate association between adeno-
myosis and the outcome of the endometrial ablation ( p =
0.003, φ = 0.37) and were more likely to have a failed
endometrial ablation COR = 19.38, 95% CI, 2.11–177.73)
(Table 2). In addition, patients with combined adenomyosis
and dysmenorrhea had a statistically significant association
with the outcome of the endometrial ablation ( p = 0.016, φ
= 0.28) and were more likely to have a failed endometrial
ablation (COR = 4.67, 95% CI, 1.35–16.09).
Menorrhagia and heavy irregular menstrual bleeding
were among the most common indications for endometrial
ablation in 37.9% and 32.6% of the patients, respectively.
Moreover, the patients who underwent endometrial ablation
due to fibroids (17.9%) had a significant weak relationship
with the outcome of the endometrial ablation ( p = 0.26, φ
= 0.25), they were more likely to have a failed endometrial
ablation (COR = 3.73, 95% CI, 1.24–11.29). Other indi-
cations included irregular vaginal bleeding, polyps, post-
menopausal bleeding, and infertility and they no longer
sought pregnancy and would only treat their heavy periods.
We also found that patients who had both adenomyosis
and dysmenorrhea were at higher statistically significant
risk to have ablation failure than those with adenomyosis
alone, p value = 0.016, 95% CI, 1.51–50.69 and p value=
0.003, φ = 0.37, respectively.
Overall, 24.2% had a failed endometrial ablation and
had to undergo an additional procedure to alleviate the
symptoms. The most common were repeated hysteroscopic
ablation and hysterectomy, in 15 and 11 patients, respec-
tively (Table 3).
In order to account for any confounding effects, the
variables having significant associations at the p < 0.1 level
from the univariate analysis were included in the logistic
4
Table 3. Subsequent gynecological procedures after failed
ablation (N = 23).
Surgeries N (%)
Hysterectomy 11 (47.8)
Hysteroscopy and repeated ablation 15 (65.2)
Dilation and curettage (endometrial biopsy) 9 (39.1)
Other 5 (21.7)
Some patients underwent more than one procedure. N, number.
regression model. These were the uterine length in weeks,
fluid deficit, blood loss, diagnosis of adenomyosis, heavy
menstrual bleeding and fibroid(s). The significant pre-
dictors for endometrial ablation failure were adenomyosis
(AOR = 50.83, 95% CI, 3.64–706.75, p = 0.003) and fluid
deficit (AOR = 1.003, 95% CI, 1.000–1.006, p = 0.044).
The uterine length in weeks, blood loss, indication for pri-
mary endometrial ablation being heavy menstrual bleed-
ing, or presence of fibroid were not significant predictors
in the regression model, which had a Pseudo Nagelkerke R
Squared of 0.49. Table 4 demonstrates the regression model
Results
for an endometrial ablation failure prediction.
Table 4. The results of regression model for endometrial
ablation failure.
V ariables AOR 95% CI p value
Uterine length (weeks) 1.069 0.704–1.622 0.755
Fluid deficit (mL/cc) 1.003 1.000–1.006 0.044
Blood loss (mL/cc) 1.004 0.991–1.018 0.505
Adenomyosis 50.825 3.655–706.745 0.003
Heavy menstrual bleeding 0.295 0.043–2.015 0.213
Fibroid 3.224 0.585–17.754 0.179
AOR, adjusted odds ratios; CI, confidence interval; mL, milliliter;
cc, cubic centimeter.
4. Discussion
The overall success rate of our endometrial ablation
procedures using the firstly generation rollerball ablative
technique, REA, was very much good, acceptable and very
helpful in a third world country with limited resources.
When compared with hysterectomy, the treatment of AUB
with endometrial ablation has been associated with reduced
operative time, decreased morbidity, and cost effectiveness
[13,14].
Over half of patients treated with microwave endome-
trial ablation (MEA) achieved amenorrhea, and the proce-
dure was suitable for women with myomas and irregular
uterine cavities and the success rate of MEA at 12 months
(87.0%; 95% CI, 81.7%–91.2%) did not differ significantly
(p = 0.40) from that of REA (83.2%; 95% CI, 74.7%–
89.7%) [15].
Our study showed an overall failure rate of 24.2%. All
patients were operated upon using either general or spinal
anesthesia with no reported serious complications like per-
foration, bleeding or significant fluid absorption. When
second-generation versus first-generation techniques were
compared, there was no evidence of differences in amen-
orrhea at 1 year and 2 to 5 years’ follow-up and there was
subjective improvement at 1 year follow-up based on a Pic-
torial Blood Assessment Chart (PBAC) [ 16]. Moreover,
patient satisfaction was not different between second- and
first-generation techniques at 1 year, 2 years and 5 years’
follow-up. Second-generation ablation techniques were as-
sociated with shorter operating times and more often were
performed under local instead of general anaesthesia [ 16].
There was uncertainty whether perforation rates differed
between second- and first-generation techniques [ 16]. Tri-
als reported little or no difference between second- and first-
generation techniques in requirement for additional surgery
(ablation or hysterectomy) at 1 and 5 years’ follow-up [ 16].
These findings support our practice in using first genera-
tion ablation as newer generations (second and third) are
expensive and not readily available in our country. Simi-
larly, levonorgestrel intra-uterine system (LNG-IUS) is still
expensive in Jordan and not covered by many medical in-
surance companies. In a meta-analysis in 2020, endome-
trial ablation and LNG-IUS were found to be two excellent
treatment options for heavy menstrual bleeding, although
women treated with the LNG-IUS were at higher risk of
experiencing side effects compared to women treated with
endometrial ablation/resection [17]. This is very encourag-
ing to us to further implement endometrial ablation in our
practice taking into consideration the global and, particu-
larly, the local economic restrictions. Similarly, in a re-
view, when compared to endometrial ablation, it was not
clear whether the LNG IUS offered any benefits with re-
gard to reduced heavy bleeding while satisfaction rates and
quality of life measures were found to be similar. In the
same review, some minor adverse effects were more com-
mon with the LNG IUS but it appeared to be more cost
effective than endometrial ablation techniques [ 18]. Hys-
terectomy was found to cause serious complications for a
minority of women and most women might be well advised
to try a less radical treatment as first-line therapy and it was
found that both LNG-IUS and conservative surgery (abla-
tion/resection) appeared to be safe, acceptable and effective
[19]. Unfortunately, there were no studies in Jordan that
compared these different modalities regarding particularly
cost-effectiveness and patient satisfaction. There is an on-
going a multicenter randomized controlled trial to evaluate
if the combination of endometrial ablation and an LNG-IUS
is superior to endometrial ablation alone in terms of reduc-
ing subsequent rates of hysterectomy at two years following
the initial ablative procedure [ 20].
Our study found a significant association between
greater operative blood loss and fluid absorption (fluid
deficit), as independent factors, with endometrial ablation
5
failure. The presence of adenomyosis and uterine fibroids
as indication of endometrial ablation was also found to
be significantly associated with the outcome of the en-
dometrial ablations. However, the patient’s age, BMI, par-
ity, miscarriage, previous cesarean sections, uterine length
(in weeks), endometrial thickness (in millimeters mm),
dysmenorrhea and procedure duration (minutes) were not
found to influence the effectiveness of the procedure. Some
but not all of these findings were consistent with previous
studies. Previous Cesarean delivery was not associated with
an increased risk of failure of endometrial ablation, but dys-
menorrhea, a submucous myoma and longer uterine depth
are [21]. Their definition of failure was those patients who
had ablation and hysterectomy. In our study, we did not
specify hysterectomy as the only destination for failure def-
inition. Moreover, dysmenorrhea cases in our study were
only seven in both failed and successful cases. This low
number might have influenced the statistical result.
We had a total of 6 cases of adenomyosis who had ab-
lation; one was successful while the remaining 5 were a fail-
ure. There was no statistically significant difference in the
outcome in our study concerning the success or failure of
ablation. This might be due to the low number of cases
or to the degree of junctional zone changes. In fact, the
effect of transcervical endometrial resection might depend
upon the degree of junctional zone changes, and patients
with intrinsic adenomyosis were more likely to undergo re-
intervention surgery than patients with either linear or ser-
rated junctional zone [ 22]. However, hysteroscopic roller-
ball endometrial ablation as a surgical management in pa-
tients with adenomyosis associated with menorrhagia was
found to be an effective and safe procedure which could
reduce the need for the unnecessary major surgery of hys-
terectomy [23].
In a systemic review and meta-analysis [ 10], younger
age, prior tubal ligation and preexisting dysmenorrhea were
found to be associated with failure of endometrial ablation.
Obesity and large submucous fibroids showed conflicting
Results
and there was a need for further research to estimate
the influence of these factors. This meta-analysis involved
studies that were different from ours. The studies involved
in this meta-analysis were using second generation endome-
trial ablation [10].
Our study did not show a statistically significant dif-
ference in ablation failure or success regarding preoperative
menstrual irregularities and intermenstrual spotting. These
findings were similar to a retrospective cohort study of a
relatively large number of patients (968) [ 5].
As the first- and second- generation ablation tech-
niques are effective and safe, we can expand our hystero-
scopic endometrial ablation service to decrease the need
for hysterectomy and particularly useful for patients with
contraindications for medical therapy [ 24]. Both seem to
be equally effective in reducing heavy bleeding and there
was no evidence that rates of satisfaction differed signif-
icantly [ 25]. Despite second-generation techniques were
often found to be easier to perform with shorter operative
times with the ability to use local rather than general anes-
thesia and complications appeared to be less after second-
generation techniques, the easiness of use can be a pitfall
[25]. In fact, our experience with the first-generation tech-
nique showed that in expert hands and with strict adherence
to energy settings and fluid management, significant com-
plications could almost be eliminated.
Endometrial resection and ablation were effective al-
ternative to hysterectomy for heavy menstrual bleeding and
both were shown to have high satisfaction rates. Hysterec-
tomy was associated with longer operating time, longer re-
covery period and higher rates of postoperative complica-
tions [26]. These features further support the incorporation
of endometrial ablation service particularly in developing
and under-resourced countries with limited financial, tech-
nical and medical capabilities to deal with complications.
In our practice, for endometrial ablation, we use the
monopolar rollerball rather than the resectoscope. For bipo-
lar resectoscope, in a randomized clinical trial, no sig-
nificant difference was found in the postoperative PBAC
score, amenorrhea rates, patient satisfaction, and need for
re-intervention between ball endometrial ablation and trans-
cervical resection of the endometrium using resectoscope
[27]. This might have further explained the success and
low complication rates in our study.
We did not assess post-ablation pain in our study as we
followed patients for one year. It was reported in 20.8% of
cases and the median number of days for the development
of pain after ablation was 301 days [ 28].
The strengths of our study lied in the consistency of
the study population and of the surgical technique. More-
over, the low cost of the procedure was a feature as no pre-
operative thinning agents were used and, instead, whole en-
dometrial cavity curettage was utilized to obtain tissue for
assessment and to mechanically and instantly thin the en-
dometrium to increase the effectiveness of the thermal dam-
age on the endometrium.
Study Limitations
The study was limited by its retrospective nature and
being a single-center study. The post-operative follow up
was another limiting feature.
5. Conclusions
Among pre-operative factors, adenomyosis, fluid
deficit and combined adenomyosis and dysmenorrhea were
found to predict failure of hysteroscopic endometrial abla-
tion.
Abbreviations
BMI, body mass index; EA, endometrial ablation;
AUB, abnormal uterine bleeding; JUH, Jordan university
hospital; g, gram; mL, milliliter; dL, deciliter; D&C, dilata-
6
tion and curettage; IRB, institutional review board; U/S, ul-
trasound; mmHg, millimeter mercury; REA, rollerball en-
dometrial ablation; ICD, international classification of dis-
eases; CPT, current procedural terminology; COR, crude
odds ratio; AOR, adjusted odds ratio; CI, confidence in-
terval; mm, millimeter; min, minute; cc, cubic centime-
ter; MEA, microwave endometrial ablation; PBAC, picto-
rial blood assessment chart; LNG-IUS, levonorgestrel intra-
uterine system; SM, submucosal.
Availability of Data and Materials
All data are available from the corresponding author
on reasonable request.
Author Contributions
NA—design, concept and writing the manuscript;
AA—statistical analysis and extraction of data; RN—
statistical analysis and extraction of data; LA—statistical
analysis and extraction of data; MA—statistical analysis
and extraction of data; HA—drafting and revision. All au-
thors read and approved the final manuscript.
Ethics Approval and Consent to Participate
The study was conducted in accordance with the Dec-
laration of Helsinki, and the protocol was approved by the
Ethics Committee of Jordan University hospital decision
number 58/2022, dated 17/02/2022.
Acknowledgment
Not applicable.
Funding
This research received no external funding.
Conflict of Interest
The authors declare no conflict of interest.
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