Intro
Polycystic ovary syndrome (PCOS) was initially
reported by Stein and Leventhal ( 1 ) in modern medical
texts when they described seven women who suffered
from amenorrhea, hirsutism, and enlarged ovaries that
contained several cysts. This syndrome is now considered
to be a common, heterogeneous, and hereditary disorder
which can affect women of reproductive age. The
prevalence of PCOS may vary based on the applied
diagnostic criteria ( 2 , 3 ). The highest rate of PCOS has
been reported at 52% among West Asian women having
migrated to England ( 4 ); in other references, this figure
has been reported as 2-26% ( 3 ). Infertility involves 40%
of the cases affected by PCOS ( 5 ).
Clomiphene citrate is the first treatment option for
inducing ovulation in these women ( 6 - 8 ); however,
drug resistance has been observed in around 20% of
such cases ( 8 ). Clomiphene resistance is defined as
three cycles of ovulation failure or six cycles without
pregnancy ( 9 ). One of the alternatives used among
clomiphene-resistant women is laparoscopic ovarian
drilling (LOD); particularly, in cases which the patient
has other surgical indications or when she is unable to attend the frequent visits required for treatment with
gonadotropins ( 10 ).
Historically, the surgical treatment of infertile PCOS
women reported by Stein and Leventhal ( 1 ) in 1935
was ovarian wedge resection via laparotomy, and it
showed promising results. However, three decades later,
this method was abandoned due to the risk of pelvic
adhesions following surgery and has been replaced by
ovulation-inducing medications such as clomiphene and
gonadotropins ( 11 ). In 1984, the surgical treatment of
infertile PCOS women improved remarkably with the
introduction of LOD that had an ovulation success rate
of 92% and pregnancy success rate of 80% ( 12 ). LOD,
as a less harmful and less-invasive method compared to
ovarian wedge resection, uses electrocautery (diathermy)
or laser beam and has played a significant role in the
treatment of infertile PCOS women ( 11 ).
The beneficial effects of this method seem to be related
to the destruction of the androgen generating stroma,
which results in reduced production of androgens in
the ovary and its reduced concentration in the blood
circulation. Clomiphene citrate-resistant women may
respond better to medical therapy after this type of
surgery. Sensitivity to exogenic gonadotropins also
increase in such cases ( 13 ).
Several studies have evaluated ovarian cauterization.
In the initial studies, it was hypothesized that a higher
energy level would result in a more efficient procedure.
Subsequently, lower temperatures with a fixed
number of drilled points, regardless of the ovary’s
size or unilateral ovarian cautery have been reported
with the intent to reduce a possible risk of ovarian
atrophy and adnexal adhesions. With such fixed doses
of temperature, the optimal amount of ovulation may
not be achieved or the clinical manifestations of the
disease may persist in individuals with enlarged ovaries
( 14 ). Armar et al. ( 15 ) reported the first descriptive
research on ovarian drilling with 4 drills at a dose of
640 joules per ovary; this method was later widely
accepted and used in various studies. Many authors
subsequently examined and compared the effects and
consequences of changes in the number of ovarian
drills or the appropriate thermal dose based on the
ovarian size during laparoscopic ovarian cauterization
( 14 - 22 ). However, in some studies, the relationship
between the number of ovarian drills and adnexal
adhesion was not confirmed ( 23 ). Nevertheless, the
optimal amount of electrosurgical energy required
during LOD to achieve the maximal fertility outcome
without causing any risk to the follicles and ovaries
has not been established ( 24 ).
We designed this study because of the inadequate
number of studies in this area (particularly in Iran) and
by taking into consideration the influence of genetic,
regional and nutritional factors on PCOS. We sought
to compare the effect of ovarian cauterization between
the standard and dose-adjusted (based on the ovarian
volume) methods in Iranian women with infertile
clomiphene-resistant PCOS.
Ethical
At study initiation, the study protocol was fully
described to each patient and they were free to withdraw
from the study at any time. Their data was regarded as
confidential. All patients signed a written informed
consent to participate in the study. The Ethics Committee
of Mashhad University of Medical Sciences approved
this study (IR.MUMS.fm.REC.1395.335). The study
was registered in the Iranian Registry for Clinical Trials
(IRCT20171210037820N1).
The inclusion criteria were: all women aged 18 to 35
years, not pregnant despite two years without contraception,
diagnosed with PCOS based on the Rotterdam criteria,
having ruled out other reasons of infertility except
for ovulation disorder (normal sperm analysis of the
spouse, normal uterine tubes in hysterosalpingography or
laparoscopy), clomiphene-resistant, and provided consent
to participate in this study.
Exclusion criteria were: withdrawal during the study,
patients lost to follow-up, presence of any other pathology
during laparoscopy (e.g., endometriosis or adhesion)
suggestive of other aetiologies for infertility.
Initially, we recorded the patients’ demographic
characteristics and paraclinical data by means of an
interview and the patient’s records. We divided the patients
into two groups according to a table of random number
generator with equal sizes of groups: standard method
(group A) and ovarian cautery based on the ovarian
volume or the dose-adjusted method (group B). One
radiologist performed the transvaginal ultrasonography
(TVS) for group B patients by using a Honda sonography
device (Honda Electronics, Japan) to measure ovarian
volume. This volume was measured on the basis of a
cubic centimetre and at three perpendiculars.
A gynaecology laparoscopist performed each
laparoscopy via an Olympus laparoscopic machine
(Olympus Europa SE & Co., Germany) in the
gynaecology theatre of Imam Reza Hospital with patients
under general anaesthesia and in the lithotomy position.
Abdominal entry was done by the closed technique and via a Veress needle. Only patients who had any history of
abdominal surgery had an open laparoscopic procedure. A
triple puncture laparoscopy was performed with 3 trocars.
The abdominal and pelvic environment, and the patency
of the tubes were examined. Patients with adhesions,
endometriosis, or any pathology in the pelvic area were
excluded from the study.
Next, the ovarian cautery was performed. The uteroovarian ligament was caught with an Atraumatic
Grasper (Aesculape Inc., USA) and the ovary was
separated from the intestines. Afterwards, the ovarian
cautery was carried out with a 4-millimetre monopolar
needle electrode (with a straight needle) and with a
Vallylab generator that had a voltage of 30 (in both
groups) as follows: using the CUT energy, a puncture
with the depth of 4 millimetres was initially created
on the ovarian capsule and then the coagulation button
was activated. After the cautery of each ovary and
before releasing the utero-ovarian ligament, the ovary
was rinsed with cold normal saline serum to prevent
any adhesion or injury to the adjacent viscera. The
ligament was then released and examined with regards
to the possibility of mechanical injury.
In group B (on the basis of ovarian volume), the
measurement of energy was based on the following model
( 15 , 16 , 18 , 25 ) that used 640, 450, 600, and 800 joules for
each ovary (mean: 625 joules) and ovarian volume means
of 8 and 10 cm 3
. The dose of 60 joules was chosen for
each cubic centimetre of the ovarian mass. The ovarian
mass was multiplied by 60 joules. In order to achieve
the correct time, we multiplied the ovarian volume by
2 and measured the number and time of each puncture
as follows: Energy=Power (voltage)×Time (number of
punctures×time of each puncture) and by taking into
account that the generator’s energy for all individuals was
30 joules.
In group A, based on the size of the ovary, we created
either 4 drills of 5 s or 5 drills of 4 s with a voltage of
30 in order to achieve an energy of 600 joules per ovary
(4×5×30=600).
The patients were followed for six months from the
first menstrual cycle after the operation. Hormonal
levels of anti-Müllerian hormone (AMH), testosterone,
dehydroepiandrosterone sulphate (DHEAS), and
progesterone were obtained on the third day of the first
menstrual cycle after the operation and the progesterone
level was measured at the mid-luteal phase of the same
cycle. All tests were performed in the same laboratory and
without charge.
TVS was also performed from the sixth day of the first
menstrual cycle after the operation, every three days up
to the 16 th day or until the observation of a dominant
follicle. Ovulation was confirmed by the observation
of an 18 mm dominant follicle or pregnancy. TVS was
performed by the same radiologist as before the LOD. In
the event of anovulation, subsequent sonographies were
not performed. Cycle regularity and the occurrence of
pregnancy were examined after six months.
Patients who did not menstruate until a month after
ovarian cautery (menstrual cycle over 35 days) were
administered 100 mg of intramuscular micronized
progesterone to re-establish the menstrual cycle, and the
investigations were performed though most of these cases
had no ovulation.
Results
In this study, 60 infertile clomiphene-resistant PCOS
women received LOD by two methods: standard and
dose-adjusted on the basis of the ovarian volume. The
demographic, clinical and sonographic characteristics
did not differ between the two study groups ( Table 1 , Fig.1
Comparison of demographic, clinical, and sonographic data of infertile clomiphene-resistant PCOS women between the two treatment groups
Data represented as mean ± SD or frequency (%) as appropriate. PCOS; Polycystic ovary syndrome, AMH; Anti-Müllerian hormone, AFC; Antral follicle count, and DHEAS; Dehydroepiandrosterone sulphate.
Flowchart.
Mean numbers of points and cautery time per ovary in the dose-dependent group
Data are presented as mean ± SD.
Table 3 shows a comparison of the mean AFC and
serum levels of AMH, testosterone, and DHEAS between
the two groups, before and after the operation.
Table 4 displays the mean changes in the AFC and
serum levels of AMH, testosterone, and DHEAS before
and after the operation in each of the studied groups.
Repeated measure ANOVA revealed that there was no
interaction, nor any difference between the two study
groups in terms of AFC (P=0.14), AMH (P=0.71),
testosterone (P=0.67), and DHEAS (P=0.12).
The number of antral follicles before the operation
was not significantly different between the two
groups (independent t test, P=0.43). The same result
was obtained after the operation (P=0.10). Intra-group
comparisons showed that the decrease in the number
of antral follicles was significant in the standard
treatment group (paired t test, P=0.02); however, we
did not observe any difference in the dose-adjusted
group (P=0.24).
Before the intervention, the two groups were matched
in terms of AMH level (independent t test, P=0.73).
We observed the same result after the intervention
(Mann-Whitney test, P=0.94). In the intra-group
comparison, there was a significant decrease in the
AMH level in the dose-adjusted group (paired t test,
P=0.04); however, this difference was not observed in
the standard treatment group (paired t test, P=0.17).
Before the intervention, the testosterone level was
similar in the two groups (independent t test, P=0.91).
The same result was obtained after the intervention
(P=0.46). However, the decrease in testosterone
level in the standard treatment group was meaningful
(paired t test, P=0.02), but this difference was not
observed in the dose-adjusted group (paired t test,
P=0.14).
Comparison of the hormone profile and AFC between the study groups
AFC; Antral follicle count, AMH; Anti-Müllerian hormone, and DHEAS; Dehydroepiandrosterone sulphate. Data represented as mean ± SD.
A comparison of the changes in the hormone profile and AFC before and after the operation in the two groups
AFC; Antral follicle count, AMH; Anti-Müllerian hormone, and DHEAS; Dehydroepiandrosterone sulphate. Data represented as mean ± SD.
In addition, both at study initiation and study termination,
the level of DHEAS did not significantly differ between
the two studied groups (independent t test, P=0.16 at
study initiation, P=0.12 at study termination). In the intragroup comparisons, the level of DHEAS decrease was
not significant in either group (paired t test, P=0.16 in the
standard group and P=0.08 in the dose-adjusted group).
The status of cycle regularity and the occurrence of
ovulation and pregnancy among patients were examined
from the first post-surgical cycle up to six months. The
obtained results are presented in Table 5.
There were regular menstrual cycles reported in 25
(83.3%) patients in the standard treatment group and 21
(70%) patients in the dose-adjusted group. Accordingly,
there was no statistically significant difference observed
between the two groups (chi-square test, P=0.22).
Ovulation occurred in 26 (86.7%) patients in the
standard group and in 21 (70%) patients from the doseadjusted group, which was not statistically significant
(chi-square test, P=0.11).
Finally, 11 (36.7%) patients in the standard group and
8 (26.7%) patients in the dose-adjusted group became
pregnant during 6 months, which indicated no meaningful
difference between the two groups (chi-square test, P=0.40).
Intragroup comparisons on cycle regularity indicated a
significant increase after the operation compared to before
the operation in the standard treatment (30 vs. 83.3%) and
dose-adjusted (26.7 vs. 70%, P<0.001) groups.
No case of premature ovarian failure was observed in
our study population. Cycle regularity was experienced in
9 (30%) patients in the standard group before the operation
and in 25 (83.3%) patients after the operation. In the dosedependent group 8 (26.7%) patients had cycle regularity
before the operation and 21 (70%) had cycle regularity
after the operation. This was a significant change in both
groups (P<0.001).
A comparison of cycle regularity, ovulation, and pregnancy between the study groups
Data represented as frequency (%).
We measured progesterone levels in both groups in
the first postoperative menstrual cycle. There was no
significant difference between the two groups (P=0.11).
However, the mean progesterone level in patients with
(12.44 ± 2.20) and without ovulation (2.93 ± 0.20) was
significantly different (P<0.001). No case of early ovarian
failure was observed in the studied subjects.
Discussion
The results of our study indicated no difference in the
number of antral follicles after the operation in both
groups. However, the decrease in the number of antral
follicles was significant in the standard treatment group.
Such results corresponded to those reported by Nasr et al.
( 26 ) who observed a meaningful decrease in the number
of antral follicles in the ovarian cautery group that had
a fixed dose. However, no decrease in the numbers of
follicles and the ovarian volume was observed in the
ovarian cautery performed with a Harmonic scalpel
group. The authors believe that the decrease in the
number of antral follicles or the ovarian volume is caused
by the adjacent thermal destruction created by the use of
electrocautery. The creation of one puncture destroys the
ovarian tissue as deep as 4 mL; thus if 4 punctures are
made in each ovary, 3.2 mL of the ovarian tissue will be
destroyed. The Harmonic scalpel minimizes the amount
of ovarian tissue destruction (0.50 mL), which is about
1/8 of the destruction done by the electrocautery. Salem
et al. ( 27 ) have considered the decrease in the number
of follicles as the undesired consequence of LOD. They
indicated that the amount of AMH and numbers of antral
follicles were reliable indicators of the ovarian reserve.
Their measurement in clomiphene-resistant PCOS women
without ovulation could be a useful indicator to assess the
treatment outcome of LOD. In our study, the dependency
of the energy used by the cautery to the ovarian volume
might have led to the selection of a more appropriate
amount of energy for the ovarian cautery, and therefore
caused less damage to the ovarian tissue.
AMH is one of the new predictive indicators of ovarian
reserve ( 28 ). This hormone can be used as a substitute
for determining the age of ovaries because it is related
to the number of initial antral follicles, which can reflect
the number of residually stored follicles ( 29 ). The
current study findings indicated a decrease in the AMH,
testosterone, and DHEAS levels in both the standard and
dose-adjusted groups. The decrease in the amount of
AMH in the dose-adjusted group and the decrease in the
amount of testosterone in the standard treatment group
were statistically significant. These findings did not fully
correspond to the results of similar studies. This could
be due to the difference in study design, sample size,
or genetic and regional differences among the studied
patients. Sunj et al. ( 30 ) had a vast inclusion criteria that
included variables such as weight, acceptable hormonal
range, infertility period, etc. in selection of their study
population. This could result in decreased generalizability
of the achieved results. In their study, only women with
an infertility period of fewer than 3 years participated
in the research, while the mean infertility period in our
study was 4.7 years. Therefore, one of the reasons for
the heterogeneity of the results might be the difference in
patient selection due to differences in the inclusion criteria.
The results of another study on the changes in AMH,
testosterone, and free androgen index by unilateral (doseadjusted) and bilateral (fixed dose) ovarian diathermy
revealed a significant decrease in AMH, testosterone,
and LH levels in both treatment groups. Amer et al. ( 31 ) and Elmashad ( 32 ) also reported significant decreases in
AMH levels following LOD. However, Farzadi et al. ( 33 )
reported no such relationship. The meaningful decreases
in serum levels of FSH, LH, AMH, testosterone, and free
androgen index following LOD were also reported in the
study by Salem et al. ( 27 ).
Given that the increase in androgens in PCOS is the
result of the insulin’s ability to increase the secretion of
androgens in ovarian theca cells, the remarkable decrease
in the level of androgens after drilling among patients who
receive cauterization with a volume dependent dose might
be justified by the hypothesized destruction of androgen
generating stromal cells. It is believed that the effects of
LOD on androgen levels are influenced by the amount of
energy entrapped by the ovaries and, for this reason, low
doses may be less successful ( 13 ).
Both groups had a nonsignficant decrease in DHEAS
levels. A review of previous literature has revealed
that the existing data on DHEAS are ambiguous. LOD
seems to have a minimal effect on adrenal function, even
among women affected by hyperinsulinemia, and the
improvement of hyperandrogenism is probably secondary
to the decrease in LH concentration and reduced androgen
production by the ovarian stroma ( 34 ).
In our study, the regularity of menstrual cycles
increased from 30 to 83.3% in the standard treatment
group. The regularity of menstrual cycles in the doseadjusted group increased from 26.7 to 70%. This was
a significant increase in both groups. The intra-group
changes were different compared to the Zakherah et al.
( 14 ) study. In their study, the cycle’s regularity was higher
in the dose-adjusted cautery group (87.9%) compared to
the fixed-dose cautry group (75.4%); however, similar to
our study, its effect on the regulation of the cycles was
significant.
In a study by Nasr et al. ( 26 ), the occurrence of regular
cycles after LOD was similar in both groups (92.8%) and
higher than our study results. Takeuchi et al. ( 35 ) reported
that a regular menstrual pattern was established in 94%
of the patients and the rate of oligomenorrhea decreased
to 6%. Felemban et al. ( 16 ) observed that the occurrence
of regular cycles was 80.4% and oligomenorrhea was
19.6% in patients after ovarian cautery. However, Salem
et al. ( 27 ) reported that among 37 clomiphene-resistant
PCOS patients, the cycles regularization was 16.22%
three months after the ovarian cautery and 54.06% after
six months. Some authors believe that such differences
could be due to the different definitions used for the
diagnosis of PCOS or the differences in the study
populations ( 26 ).
In our study, ovulation occurred in 86.7% of patients
in the standard treatment group and 70% of those in the
dose-adjusted group; 36.7% of patients in the standard
treatment group and 26.7% in the dose-adjusted group
became pregnant. The findings of our study contradicted
those reported by Zakherah et al. ( 14 ). In the latter study,
the rate of ovulation (81.8 vs. 62.2%) and pregnancy
(51.7 vs. 36.8%) in the volume-dependent ovarian cautery
group was significantly higher than the fixed thermal
dose group. The authors concluded that the adjusted
thermal dose on the basis of ovarian volume (60 joules/
cm3) in LOD resulted in improved fertility consequences
in comparison to the fixed thermal dose (600 joules per
ovary) among clomiphene-resistant PCOS patients.
The difference between the results of this study and our
research might be due to the differences in sample size or
racial and regional characteristics. As with our study, the
measurement of the ovarian volume was not done in the
standard treatment group. Possibly, the ovarian volume
of these patients was more or identical to the patients of
the dose-adjusted group; therefore, the same intervention
might have been done for the patients in both groups.
In a study by Salem et al. ( 27 ), 4 (10.81%) pregnancies
occurred after three months and 18 (48.65%) after six
months, which were less than our study. They mentioned
various reasons for the low rate of pregnancy occurrence
among their study patients, which included the existence
of subtle aetiologies such as hyperprolactinemia, minor
anatomical problems, and male reasons such as varicocele.
He also mentioned inadequate drilling to induce optimal
changes in fertility parameters.
Ramezani et al. ( 36 ) examined the cumulative effect
of pregnancy after cauterization of polycystic ovaries in
clomiphene-resistant patients at Imam Khomeini Hospital
in Karaj, Iran, with the following pregnancy rates after
surgery: 14.7% (6 months), 36.8% (12 months), 58.8% (18
months), and 76.6% (24 months). However, in this study,
the fixed dose method was used for ovarian cauterization in
all patients. Although the rate of pregnancy after 6 months
(14.7%) was less than the pregnancy rate achieved in our
study (26.7% for the dose-adjusted group and 36.7% for
the standard group), the rate of pregnancy after 12 months
was very close to that of our standard treatment group
after 6 months.
Our study had certain limitations; the small sample
size which led to a low power, decreased cooperation of
patients for the ultrasound study and the postoperative lab
tests, as well as the impossibility of performing TVS in all
subjects due to limited facilities in this center.
Conclusions
The results of this study indicated a significant decrease
in antral follicles and testosterone in the standard treatment
group in comparison to the dose-adjusted group along with
a significant decrease in AMH level in the dose-adjusted
group. The changes in DHEAS were insignificant in both
groups.
Cycle regulation, and the occurrence of ovulation
and pregnancy showed that both methods were
efficient; however, there were no statistically significant
differences. In terms of the effects of ovarian cautery on
these variables, neither of the two methods was superior.
It is possible that the small number of samples examined
and the differences in the sample selection method or
the racial and regional differences might have led to
the difference in the results of our study with previous
researches. Therefore, conducting similar regional studies
with a larger sample sizes are highly recommended.
Statistical
We performed SPSS software (version 16)
analyses of te raw data. If the quantitative variables
were normally distributed, we used the t test and
paired t test; for non-normally distributed data, the
corresponding non-parametrical tests were used.
The chi-square test was used to examine qualitative
variables. Repeated measure ANOVA was performed
to assess the interaction and overall effect of before/
after assessments in the two groups. The significance
level was set at P<0.05.
Materials Methods
This randomized clinical trial was conducted in the
Gynaecology Department of Imam Reza Hospital,
Mashhad, Iran from 2016 to 2017. All infertile clomipheneresistant PCOS women who visited the Gynaecology
Department enrolled in this study. The sample size
of this study was calculated at 30 women according to
the following formula and by taking into consideration
information from a previously published study ( 14 ), with
an alfa error=0.05, beta error=0.8, P1=0.6, and P2=0.9.
The achieved power of this study was 37% based on the
antral follicle count (AFC).
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