Abstract
Background: Endometriosis could be present among women without any symptoms, accounting for as
many as fifty percent of women seeking infertility treatment . Antral follicle count (AFC) as well as serum
anti-Mullerian hormone (AMH) levels are often utilized as accurate quantitative ovarian reserve indicators.
This work was aimed at assessing different endometrioma surgical treatment modalities’ impact on ovarian
reserve.
Methods
Our prospective comparative study involved 40 cases whose ages fall between 20 and 35 years,
female patients who are married, nullipara with unilateral endometrioma > 4 cm. Subject underwent a
random equal allocation into two equal groups according to patient's condition intra -operative, hence
decision of the operator: Group A (n=20): treated by laparoscopic excision of endometrioma and Group B
(n=20): treated laparoscopically by evacuation of the cyst then by cyst wall’s cauterization utilizing Bipolar
Diathermy.
Results
A significantly variance among AMH levels was documented within group A as well as between
AFC in group A and B and AMH in group B during various follow -up periods ( p<0.05). AMH within
group A during various follow -up periods was significantly different between base line and after 6 months
(P2 < 0.05). There was a significantly difference between base line with after 6 months, between base line
with after 3 months and between 3 months with 6 months (P1, P2, P3 < 0.05) regarding of AFC within
group A as well as AMH within group B during various follow -up periods. Pregnancy rate exhibited
significant variances among both groups (p<0.05).
Conclusions
Both techniques, complete laparoscopic cystectomy and partial cystectomy with bipolar
coagulation of the cyst wall have adverse effect as regards ovarian reserve determined with serum AMH
level. However, AFC increased after both techniques. No significant variance was documented among both
groups as regards the ovarian reserve’s degree of reduction.
Keywords
Ovarian reserve, laparoscopic excision, endometrioma, antral follicle count, anti -mullerian
hormone
Introduction
Endometriosis represents a chronic inflammatory condition linked to persistent pelvic pain,
affecting six to ten percent of females within their reproductive age. The endometriosis
diagnosis remains definitive only while confirming endometrial like tissue lesions outside the
uterus following the surgical procedure. Endometriosis could be present among women without
any symptoms, accounting for as many as fifty percent of women seeking infertility treatment.
The predominant endometriosis symptoms involve discomfort, gastrointestinal as well as urinary
issues, along with exhaustion and sadness resulting from the persistent pain . There could be a
delay while diagnosis such a condition since symptoms, involving pelvic discomfort and/or
infertility, may or may not be oberverd among all individuals. Additionally, they could also
be linked to other medical disorders [1].
The current therapies for this condition involve the surgical lesions' excision along with
administering medicines, inhibiting the ovarian hormones synthesis. More than fifty percent of
individuals going through surgery will need an additional surgical operation withi n five years.
Additionally, several medical therapies have adverse side effects. Surveys conducted on
cases regularly emphasize the symptoms alleviation along with enhancing medical treatments
that do not have any negative impact on fertility [2].
Ovarian reserve refers to the reproductive capacity determined by the quantity and quality of
resting primordial follicles that have the ability to mature into primary, antral, as well
International Journal of Clinical Obstetrics and Gynaecology https://www.gynaecologyjournal.com
~ 61 ~
as ovulatory follicles. Antral follicle count (AFC) as well
as serum anti -Mullerian hormone (AMH) levels are often
utilized as accurate quantitative ovarian reserve indicators.
Publications in the literature present comparative analysis
studies between different surgical techniques used in the
treatment of endometrioma [3].
AMH exhibits a crucial role as regards the physiology
of ovaries. It is produced by the granulosa cells of developing
follicles, starting from the early stages of follicle growth until
cyclic selection. AMH has a detrimental effect on the
recruitment of primor dial follicles [4]. The AMH level is a
dependable and valuable indicator of ovarian reserve, since it
consistently decreases as a person ages and becomes
undetectable during the perimenopause stage. It is widely agreed
that cases developing endometrioma ha ve a more rapid fall in
serum AMH levels as opposed to healthy women.
Endometrioma may mechanically impact ovarian reserve
via compressing the adjacent ovarian cortex, which hinders
vascular circulation, resulting in follicles loss [5].
Endometriotic cyste ctomies lead to a significant decrease in
serum AMH levels, but do not affect the AFC. The negative
impact on AMH levels could be reliably seen at several time
points, involving early, intermediate, as well as late
postoperative periods. Among women having endometrioma, the
AMH level could be a more precise marker, assessing the risk
for the ovarian reserve’s iatrogenic depletion [6].
This work was aimed at assessing different endometrioma
surgical treatment modalities’ impact on ovarian reserve.
Patients and Methods
Our prospective comparative study involved 40 cases whose
ages fall between 20 and 35 years, female patients who are
married, nullipara with unilateral endometrioma > 4 cm. The
research commenced following the Ethical Committee’s
approval at Ta nta University Hospitals, Tanta, Egypt. All
subjects were allowed to sign an informed consent.
We excluded polycystic ovarian syndrome based on the
Rotterdam criteria, prior ovarian surgical procedures, any
ovarian mass either benign or malignant, known en docrinal
disorders or other chronic conditions along with consuming oral
contraceptives or gonadotropin releasing hormone (GnRH)
agonist or antagonist or any other medicines affecting ovarian
function within a minimum of three months prior to the research.
Subject underwent a random equal allocation into two equal
groups according to patient's condition intra -operative, hence
decision of the operator: Group A (n=20): treated by
laparoscopic excision of endometrioma and Group B (n=20):
treated laparoscopical ly by evacuation of the cyst then by cyst
wall’s cauterization utilizing Bipolar Diathermy.
All subjects underwent a comprehensive medical history taking,
general assessment and ovarian reserve evaluation prior to
surgical procedure and at three, six month s postoperatively by:
[serum AMH and AFC by transvaginal ultrasonography
(TV/US).
Evaluation of ovarian reserve prior to the surgical
procedure, at three, and six months postoperatively by
Serum Anti- Mullerian Hormone (AMH)
During the time frame of 8 t o 9 AM, blood samples were
obtained via venipuncture then underwent storage within tubes
containing heparin. They were then placed on ice till
being centrifuged. The plasma obtained following centrifugation
(With a force of 1200 times the acceleration due to gravity for a
duration of 10 minutes) was separated into smaller portions and
kept at a temperature of -20 °C until it was examined for AMH
levels. The plasma concentrations of AMH were measured
utilizing a commercially available ELISA kit (MOFA Global
AMH ELISA, Verona, WI) based on the instructions provided
by the manufacturer. This analysis was specifically to quantify
AMH levels within serum and plasma samples. The absorbance
at 450 and 630 nm was measured employing a microplate
spectrophotometer (BioTek Powerwave HT, Winooski, VT).
Antral Follicular Count (AFC) by TV/US
Transvaginal sonography was employed on cycle day 1, 2, 3, or
4 to examine the ovaries. The same observer conducted
sonography measures, G.S., utilizing a 7.5 MHz transvaginal
probe on a Toshiba Capasee SSA -220A. The ovary's
examination was conducted via scanning from the outside to
inner edge. Every follicle with a size falling between two and
ten mm was measured then counted within both ovaries. The
total of both numbers equated to the AFC. The follicle size was
determined by taking two or three perpendicular measures,
according to the follicle's diameter (6 mm). Each follicle's
volume was determined utilizing the equation for the volume of
an ellipsoid, which is L3W3D3p/6. The tota l follicular volume
was calculated via summing the all follicles volumes measuring
up to 10 mm in size within both ovaries. The mean follicular
volume was determined through dividing the total follicular
volume by the follicles' number counted. Ovarian vol ume was
determined via measuring the ovarian contour's diameter in three
perpendicular directions, employing the formula for the volume
of an ellipsoid (D13D23D33p/6). The total ovarian volume was
calculated through adding together the left as well as right
ovary's volumes. Prior research have shown intra - as well as
inter-observer variability while evaluatng AFC as well
as ovarian volume.
The primary outcome was assessed by measurement of serum
AMH and AFC by TV/US before surgery and after surgery by 3
m and 6 m and secondary outcome: was assessed by occurrence
of pregnancy.
Statistical analysis
Data underwent a statistical analysis utilizing SPSS v26 (IBM
Inc., Chicago, IL, USA). Quantitative variables were exhibited
as mean and SD then a comparison amon g both groups was
employed with unpaired Student's t - test. Qualitative variables
were exhibited as frequency and percentage (%) then underwent
analysis with the Chi -square test or Fisher's exact test when
appropriate. A two tailed P value of below 0.05 de emed to
exhibit a statistically significance.
Results
There was insignificantly variance among both groups as regards
demographic data as well as size of endometrioma (p>0.05).
Table 1: Comparison among both groups as regards demographic data
as well as size of endometrioma
Group A (n=20) Group B (n=20) P
Age (Years) 26.3±4.52 28±5.29 0.141
BMI (kg/m2) 26.235±3.51 26.435±3.65 0.430
Size of endometrioma 5.02±0.62 4.925±0.59 0.311
Data are exhibited as mean ± SD. BMI: Body mass index.
A significa ntly variance between levels of AMH was
documented within group A within various follow -up periods
(p<0.05). There was a significantly difference between base line
and after 6 months (P2 < 0.05) while there was insignificant
International Journal of Clinical Obstetrics and Gynaecology https://www.gynaecologyjournal.com
~ 62 ~
difference between base line w ith after 3 months and between 3
months with 6 months (P1, P3 > 0.05) regarding levels of AMH
in group A within various follow -up periods. There was a
significantly different between AFC within group A as well as B
and AMH within group B during various fol low-up periods
(p<0.05). There was a significantly different between base line
with after 6 months, between base line with after 3 months and
between 3 months with 6 months (P1, P2, P3 < 0.05) regarding
of AFC within group A as well as AMH within group B during
different periods of follow up. Table 2
Table 2: Comparison between levels of AMH and AFC in group A and
B within various follow-up periods
At base line After 3 months After 6 months P
Group A
AMH 3.5±1.2 3±1 2.5±0.8 0.005* P1=0.069, P2=0.002*, P3=0.061
AFC 4.8±0.7 7.1±1.1 10.5±1.4 0.001* P1=0.006*, P2=0.001*, P3=0.042*
Group B
AMH 3.79±1.32 3.28±1.13 2.85±1.01 0.036* P1=0.089, P2=0.002*, P3=0.061
AFC 4.68±0.62 6.83±1.18, 9.38±2.14 0.001* P1=0.021*, P2=0.001*, P3=0.003*
Data are exhibited as mean ± SD. *significant p value < 0.05, P1
comparison among base line as well as following three months, P2
comparison among base line and following six months, P3 comparison
among three as well as six months, AMH: Anti -Mullerian hormone,
AFC: Antral follicle count.
There was insignificant variance among both groups as regards
AMH within various follow -up periods ( p>0.05) and AFC at
base line and after 3 months ( p>0.05) while a significantly
variance was documented after six months (p<0.5). Table 3
Table 3: Comparison among both groups regarding AMH and AFC
within various follow-up periods
Group A (n=20) Group B (n=20) P
AMH
At base line 3.5±1.2 3.79±1.32 0.328
After 3 months 3.0±1.0 3.28±1.13 0.310
After 6 months 2.5±0.8 2.85±1.01 0.098
AFC
At base line 4.8±0.7 4.68±0.62 0.328
After 3 months 7.1±1.1 6.83±1.18 0.209
After 6 months 10.5±1.4 9.38±2.14 0.046*
Data are exhibited as mean ± SD. *significant p value < 0.05, AMH:
Anti-Mullerian hormone, AFC: Antral follicle count.
Patients who had pregnancy rate in group A were 14(70%) and
in group B were 7(35%) while patients who had not pregnancy
rate were 6(30%) and 13(65%) in both groups respectively.
There was a significantly variance among both groups as regards
pregnancy rate (p<0.05). Table 4
Table 4: Comparison among both groups as regards pregnancy rate
Group A (n=20) Group B (n=20) P
Pregnancy rate No 6(30.0%) 13(650%) 0.026* Yes 14(70.0%) 7(35.0%)
Data are exhibited as frequency (%). *Significant p value < 0.05.
Discussion
Endometriosis is through to be a factor in infertility due to
increased the disease incidence among sub -fertile women
(Reaching fifty percent) as opposed to other women having a
history of proven fertility (Five to ten percent) [7].
Recently, a marked rise as regards the infertile patients’ number
developing endometriosis have been documented. It is uncertain
if this indicates a rise in numbers or just signifies the higher
frequency of laparoscopy use. The dysmenorrhea prevalence
among women is e stimated to fall between forty and sixty
percent, whereas the subfertility prevalence is estimated to fall
between twenty and thirty percent among women [8].
Endoscopic surgery adheres to the essential microsurgical
principles of delicate tissue manipulat ion, continuous irrigation,
cautious bleeding control, as well as accurate tissue dissection.
The choice of operative procedures for endometriosis depends
on the lesions type as well as extent. Several technologies could
be utilized, with hydrodissection a s well as CO2 laser being the
most effective methods [9].
In our study the results showed that the hormonal assay in this
study showed no significant variance among both groups as
regards AMH. In group A and B, a significant decrease within
AMH level was documented following 6 as opposed to base line
level.
Our findings supported a meta -analysis by Raffi et al . [10]
suggesting a negative effect linked to endometriomas’ excision
on ovarian reserve, involving a marked decline as regards
circulating AMH post operatively, which could occur as a result
of comparable mean age group as well as sample size.
Biacchiardi et al . [11] documented no significant variance
between AMH level among both laparoscopic excision group as
well as bipolar diathermy.
In the result s of our study the AFC shows insignificant
difference among both groups at base line and following three
months, while after six months the AFC was significantly
greater within group A as opposed to group B. Within group A
and B, a significant rise as rega rds AFC was documented after
three months and following 6 months compared to base line
value. Celik et al. [12] addressed significant drop of serum AMH
at the sixth month (61%) post operatively after laparoscopic
endometrioma stripping. The AMH level exhib ited a significant
reduction among cases having the cyst below 5 cm as well as
among those having bilateral endometrioma. Raffi et al . [10]
reported a statistically significant decline (thirty percent) as
regards serum AMH post operatively in patients with unilateral
endometrioma. This indicates a significant ovarian reserve
damage following ovarian cystectomy for endometrioma.
The ovarian endometrioma’s laparoscopic treatment has been
linked to worsening ovarian reserve in several different ways.
These in clude surgical -related local inflammation, heat injury
from adhering cyst wall or bleeding arteries, and unintentional
healthy ovarian cortex removal [13].
Our research addressed that pregnancy rate in group A were 14
(70%) and in group B were 7 (35%). A statistically significant
rise as regards pregnancy rate was documented among patients
treated by laparoscopic excision of endometrioma more than the
patients treated laparoscopically by evacuation of the cyst then
by cauterization of the cyst wall by Bipo lar Diathermy.
Supporting our research, Pais et al . [14] investigated the
pregnancy chances following endometriomas’ laparoscopic
excision fell between 30% and 67%, addressing an overall
weighted mean around fifty oercent. Zhou et al. [15] performed a
prospective study involving 124 cases aligned with such
findings, addressing a total spontaneous pregnancy rate reaching
50.49% at twenty -four months following excisional surgical
procedure.
The procedure utilized for hemostasis following cysts'
excision is one of the factors, probably inducing harm to ovarian
reserve. Common methods for achieving hemostasis involve
utilizing sutures, haemostatic gel, or bipolar cauterization (BC).
International Journal of Clinical Obstetrics and Gynaecology https://www.gynaecologyjournal.com
~ 63 ~
The drawbacks of suturing involve the need for specialized skills
as well as ischemia possibilities induced by elevated intraovarian
pressure during suture tightening. Hemostatic gels are costly
along with potentially causing severe complications such as
bowel obstruction or thrombosis. BC, or cryotherapy,
represents a cost -effective, uncomplicated, as well as efficient
method. However, caution must be implemented
for minimizing thermal damage risks [16].
Limitations
involve a single -senter study with a relatively
modest sample size. Therefore, more research should be
implemented for calrifying issues associated with ovarian
reserve with the ovarian endometrioma’s conservative treatment,
specifically in terms of medical or expectant care. Research on
the effect of surgery for endometrioma on ovarian reserve
should continue to be prior itized in the field of reproductive
medicine.
Conclusions
Both techniques, complete laparoscopic cystectomy and partial
cystectomy with bipolar coagulation of the cyst wall have
adverse effect as regards ovarian reserve determined with serum
AMH level. Ho wever, AFC increased after both techniques. No
significant variance was documented among both groups as
regards the ovarian reserve’s degree of reduction.
Financial support and sponsorship: Nil
Conflict of Interest: Nil
References
1. Saunders PTK, Horne AW . Endometriosis: Etiology,
pathobiology, and therapeutic prospects. Cell.
2021;184:2807-2824.
2. Samartzis K, Kathopoulis N, Loutradis D, Protopapas A. Do
techniques of surgical management of ovarian
endometrioma affect ovarian reserve? A narrative review. J
Obstet Gynaecol. 2022;42:778-784.
3. Park SJ, Seol A, Lee N, Lee S, Kim HS. A randomized
controlled trial of ovarian reserve preservation and
hemostasis during ovarian cystectomy. Sci . Rep.
2021;11:8495-84510.
4. Zhou Y. The effect of anti -Müllerian hormone (AMH) on
ovarian follicle development: University of Otago; c2023.
5. Keikhaie R, Kaveh M, Bahrami F, Sadegi K, Kamali A,
Afshari M. Comparing the Changes of AMH Level
Following Two Methods of Laparoscopic Cystectomy for
Evaluating Ovarian Reserve in Patients with Endo metrioma.
JOGCR. 2021;6:110-115.
6. Younis JS, Shapso N, Ben -Sira Y, Nelson SM, Izhaki I.
Endometrioma surgery -a systematic review and meta -
analysis of the effect on antral follicle count and anti -
Müllerian hormone. Am J Obstet Gynecol. 2022;226:33-51.
7. Fadhlaoui A, Jolinière J, Feki A. Endometriosis and
infertility: How and when to treat? Front Surg.
2014;18:710-5.
8. Gałczyński K, Jóźwik M, Lewkowicz D, Semczuk -Sikora
A, Semczuk A. Ovarian endometrioma - a possible finding
in adolescent girls and young women: A mini-review. J
Ovarian Res. 2019;12:104-110.
9. Ghosh P, Kochhar PK. A comparative study of the use of
different energy sources in laparoscopic management of
endometriosis-associated infertility. World J Laparosc Surg.
2013;4:89-95.
10. Raffi F, Metwally M, Amer S. The impact of excision of
ovarian endometrioma on ovarian reserve: A systematic
review and meta -analysis. J Clin Endocrinol Metab.
2012;97:3146-3154.
11. Biacchiardi CP, Piane LD, Camanni M, Deltetto F,
Delpiano EM, Marchino GL, et al . Laparoscopic stripping
of endometriomas negatively affects ovarian follicular
reserve even if performed by experienced surgeons. Reprod
Biomed Online. 2011;23:740-746.
12. Celik HG, Dogan E, Okyay E, Ulukus C, Saatli B, Uysal S,
et al. Effect of laparoscopic excision of endometriomas on
ovarian reserve: serial changes in the serum antimüllerian
hormone levels. Fertil Steril. 2012;97:1472-148.
13. Var T, Batioglu S, Tonguc E, Kahyaoglu I. The effect of
laparoscopic ovarian cystectomy versus coagulation in
bilateral endometriomas on ovarian reser ve as determined
by antral follicle count and ovarian volume: A prospective
randomized study. Fertil Steril. 2011;95:2247-2250.
14. Pais AS, Flagothier C, Tebache L, Almeida Santos T,
Nisolle M. Impact of surgical management of
endometrioma on amh levels and pre gnancy rates: A review
of recent literature. J Clin Med. 2021;10:310-315.
15. Zhou Y, Chen C, Hu C, Wang Y, Zhang X, Wu R.
Predictive value of the serum anti -Müllerian level for
spontaneous pregnancy in women after endometriosis
surgery. J Int Med Res. 2019;47:5643-5649.
16. Mısırlıoğlu S, Türkgeldi E, Yağmur H, Urman B, Ata B.
Use of a gelatin -thrombin hemostatic matrix in obstetrics
and gynecological surgery. Turk J Obstet Gynecol.
2018;15:193-199.
How to Cite This Article
El-Baiomy HF, Elhamamy NM, Othman AM, Abozeid EH. Evaluation of
ovarian reserve after different surgical techniques in management of
endometrioma. International Journal of Clinical Obstetrics and
Gynaecology. 2024;8(4):60-63.
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