Abstract
Background Firstly, to measure indicators of health-related quality of life (HRQoL) in Egyptian women with endome-
triosis; and secondly, to estimate time interval from start of symptoms until endometriosis diagnosis is made (diagnos-
tic delay) in Egyptian women with the disease.
Material and methods
Before laparoscopy for pelvic pain and/or infertility, eligible Egyptian women completed
Global Study of Women’s Health (GSWH) questionnaire and validated Arabic version of Rand SF 36 (SF-36). Accord-
ing to laparoscopic findings, participants were divided to endometriosis group and control women with no pelvic
abnormalities.
Results
Seventy women with endometriosis and 57 symptomatic controls without endometriosis were enrolled.
A diagnostic delay of 36 months (IQR 22.5–60) was observed in women with endometriosis while symptomatic
controls had a delay of 48 months (IQR 24–84). The difference was not statistically significant (P = 0.08). Bodily pain
(BP) scores were significantly lower in women with endometriosis than controls [80.0 (45.0–100.0) versus 100.0
(68.75–100.0) respectively, P is 0.01]. Women with advanced endometriosis had significantly lower scores for physical
functioning (PF), role limitation due to physical function (RP), and BP compared to women with mild endometriosis,
and to controls. Physical component summary (PCS) scores were significantly lower in women with advanced stage
endometriosis [41.51 (34.19–51.54] compared to women with early-stage disease [58.33 (50.98–60.37)] or control
group [54.72 (48.81–59.58)]. Patient’s age, intensity of noncyclical pelvic pain, and disease stage are determining fac-
tors of HRQoL in women with endometriosis.
Conclusions
Egyptian women with endometriosis experience relatively short diagnostic delay, poor bodily pain
scores, and impaired physical health for which age, disease stage, and non-cyclic pain are determinants. Multi-discipli-
nary endometriosis centers, educational programs, and patient support groups are needed in Egypt.
Keywords
Quality of life, Diagnostic delay, Endometriosis, Egypt
Open Access
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Middle East Fertility
Society Journal
†Essam R. Othman and Ahmed M. Abdelmagied contributed equally to this
work.
*Correspondence:
Essam R. Othman
[email protected]
Full list of author information is available at the end of the article
Page 2 of 9Othman et al. Middle East Fertility Society Journal (2024) 29:10
Background
Endometriosis is a menstrual cycle dependent, chronic,
inflammatory, systemic disease that presents primarily
with pelvic pain. It affects 2–10% of women of reproduc -
tive age leading to variable forms of pelvic pain, and sub -
fertility [1]. Because of the heterogeneity of symptoms,
and invasiveness of the diagnostic modality, i.e., lapa -
roscopy, women with endometriosis experience a vari -
able diagnostic delay [2]. During this time, women with
endometriosis lose days at college and/or work, suffer
from lowered self-esteem, have disturbed relationships,
and often feel their pains will never disappear, which may
erode their confidence in their physicians. These effects
negatively impact women’s productivity, professional per-
spectives, emotional wellbeing, and social lives [3].
Health-related quality of life (HRQoL) encompasses
physical health, mental state, and social wellbeing in rela-
tion to a disease or its treatment [4]. Endometriosis has
been shown in several studies to impair nearly all aspects
of HRQoL in affected women [4, 5]. However, some of the
previous studies suffered important limitations includ -
ing not using a validated HRQoL tool, an inadequately
selected control group, not considering diagnostic delay
and disease stage as factors affecting HRQoL, and focus -
ing mainly on Western populations.
Women perceive menstruation, menstrual problems,
and endometriosis symptoms in a way specific to their
culture, values, and beliefs. Arab women with endome -
triosis showed lower mental and physical health com -
ponents compared to women in other communities [6].
In a conservative society like Egypt, menstruation and
related events represent a taboo enveloped by a culture
of secrecy [7]. Similarly, infertile women are often stig -
matized by their family/ community [8]. Despite having
a special cultural background, Egyptian women, particu -
larly those in the more conservative community of the
south, were underrepresented in studies investigating
effect of endometriosis on HRQoL.
Therefore, in the current study, conducted in the south
of Egypt, we measure different domains of HRQoL in
Egyptian women with endometriosis using a validated
Arabic version of SF-36. We also assess determinant fac -
tors of HRQoL in these women. In addition, we evaluate
the diagnostic delay experienced by Egyptian Women
with endometriosis.
Material and methods
The present study was part of a larger research pro -
ject, funded by Science and Technology Development
Fund (STDF), Egyptian Ministry of Higher Education,
parts of which have already been published [9, 10]. We
recruited 70 women with endometriosis (39 women with
early-stage endometriosis, and 31 women with advanced
stage disease) and 57 symptomatic controls without
endometriosis in the period from December 2014 to May
2016.
Study design and settings
This cross-sectional survey was conducted at the Wom -
en’s Health Hospital, University of Assiut, in the South of
Egypt.
Study participants
Reproductive age women (18–45 years) scheduled for
laparoscopy to investigate their pelvic pain and/or infer -
tility, were asked to participate in the study. Exclusion
criteria were prior endometriosis diagnosis (whether
confirmed with surgery or imaging), pelvic pathology
other than endometriosis, hormonal treatment within
the last 3 months, or pregnancy/lactation in the previous
6 months before surgery.
Sample size calculation
Endometriosis is commonly associated with various
forms of chronic pelvic pains (dysmenorrhea, dys -
pareunia, non-cyclic pelvic pain, cyclic dyschezia and
dysuria). In addition, women with endometriosis have
higher risk of multi-site pain co-morbidities (fibromyal -
gia, migraines, rheumatoid arthritis, and osteoarthritis).
Moreover, bladder pain syndrome/interstitial cystitis
and irritable bowel syndrome are commonly co-occur -
ring with endometriosis [11]. We assumed that women
with endometriosis may have higher impairment in the
domain of bodily pain compared to even the sympto -
matic controls.
According to the SF-36 manual and interpretation
guide [12], detecting a 10-point difference in bodily
pain between women with endometriosis and controls
requires 71 cases per group, at a two tailed alpha of 0.05
and power of 80%.
Ethical approval
The research protocol was approved by the Science and
Technology Development Fund (STDF), which is a part
of the Egyptian Ministry of Higher Education in 2014.
Additional approval was obtained by The Institutional
Review Board at the Faculty of Medicine, University of
Assiut, (IRB# 17,400,008) in February 2018 to use the
data for publication.
Informed consent
A research team member (MYK) explained the study in
details and its objectives to the participants and obtained
their verbal informed consent to take part in the study.
Another researcher (ERO) assured participants about
Page 3 of 9
Othman et al. Middle East Fertility Society Journal (2024) 29:10
data anonymity to protect the confidentiality of their
information and double checked that participants gave
their verbal informed consent.
Interview
Early in the morning, on the day of laparoscopy, par -
ticipants were interviewed by a member of the research
team to complete two questionnaires: Global Study of
Women’s Health questionnaire (GSWH) [3], which was
completed by the researcher interviewing the patient,
and the validated Arabic version of Rand SF-36 ques -
tionnaire [13], which was completed by the patient her -
self if literate enough. Otherwise, the researcher read
and explained questions to the patient and recorded her
responses after read-back.
Questionnaires
– Global Study of Women’s Health (GSWH) question-
naire: which is a 67-item questionnaire on present -
ing symptoms, physical functioning, medical, and
reproductive history, time since start of symptoms
and health resource use [3]. The GSWH question -
naire incorporates questions and instruments previ -
ously validated for women with pelvic pains or other
symptom groups. These include Short Version-36
V2 (SF-36 v2), The Work Productivity and activity
Impairment (WPAI) questionnaire, the IRB Rome
III questionnaire to assess pelvic pain due to irritable
bowel and standardized pelvic pain symptom assess -
ment used in previous studies in Oxford [14].
– Short version-36 (SF-36) is a tool used to assess gen -
eral health related quality of life. Arabic translation of
this questionnaire is available that has already been
validated [13]. Other disease-specific questionnaires
like Endometriosis Health Profile-30 (EP-30) and
Endometriosis Health Profile-5 (EP-5) have not been
translated to Arabic Language. The SF-36 question -
naire consists of 36 questions that are grouped into 8
main domains over the last four weeks. These include
Physical functioning (FP; 10 items), Role limitation
due to physical function (RP; 4 items), Role limitation
due to emotional factors (RE; 3 items), Vitality (VT;
4 items), Mental Health (MH; 5 items), Social Func -
tioning (SF; 2 items), Bodily Pain (BP; 2 items), Gen -
eral Health (GH; 5 items), and perception of health
in comparison to the last year (1 item). Each item
response is given a raw score based on SF-36 manual.
Raw scores are then summated to give domain scores
ranging from 0 to 100 where 0 means lowest quality
of life and 100 indicates best quality of life. In addi -
tion, the 8 domain scores are combined to produce
physical component summary (PCS) score (derived
from PF, RP , BP , GH), and mental component sum -
mary (MCS) score (derived from RE, MH, SF, VT)
[12, 13]. All psychometric measures of SF-36 valida -
tion are available in the SF 36 Health Survey: Manual
and Interpretation Guide [12].
Using the GSWH questionnaire allowed us to sys -
tematically capture the demographic and clinical char -
acteristics of study participants; including structured
menstrual/reproductive history, detailed symptoms, and
the diagnostic delay. Adding SF-36 questionnaire permit-
ted the measure of different domains of the participants’
HR-QoL which were ultimately summated into PCS and
the MCS scores.
– Calculation of the diagnostic delay: Women were
asked to self-report the earliest age at which they
experienced endometriosis-related symptoms (infer -
tility or various forms of pelvic pain). Time interval
that lapsed between age at onset of symptoms and
age at which endometriosis was surgically diagnosed
represented the actual diagnostic delay [3, 6].
Surgical diagnosis of endometriosis
Endometriosis was diagnosed during laparoscopy
according to typical morphologic features of the lesions.
Women whose laparoscopic examination revealed a nor -
mal pelvis were classified as idiopathic infertility/pelvic
pain and served as the control group. Laparoscopies were
performed in the proliferative phase of the menstrual
cycle by experienced surgeons. During surgery, endo -
metriosis was scored according to the revised American
Society of Reproductive Medicine (ASRM) scoring sys -
tem. Endometriosis was rated as either minimal (stage I),
mild (stage II), moderate (stage III), or severe (stage IV).
Menstrual dates were assessed based on patient’s men -
strual history.
Statistical methods
All statistical analysis in the current study was done
using Social Package of Social Scientists (SPSS), ver -
sion 21 (IBM Corp, Armonk, NY, USA) statistical soft -
ware. Kolmogorov-Smirnov test and the Shapiro-Wilk
test were used to examine the distribution of data.
Clinical and demographic data were expressed as mean
± standard deviation (SD) except for number of liv -
ing children, duration of infertility, Numerical Rating
Score (NRS) for dysmenorrhea, deep dyspareunia, and
non-cyclic pelvic pain, and diagnostic delay in which
data were expressed as median and interquartile range
(IQR). SF-36 domain scores in women with endome -
triosis and controls were not normally distributed, so,
Page 4 of 9Othman et al. Middle East Fertility Society Journal (2024) 29:10
non-parametric statistics were used, and scores were
expressed as median ± IQR. Mann-Whitney U test
was used to compare women with endometriosis ver -
sus symptomatic controls. Kruskal-Wallis test was used
to compare scores across early-stage endometriosis,
advanced stage endometriosis, and symptomatic con -
trols. Pairwise comparisons among the 3 groups were
done with Mann-Whitney U test and Bonferroni cor -
rection. Statistical significance was considered if P
value ≤ 0.05. To identify determinants that are asso -
ciated with low PCS, and MCS in women with endo -
metriosis, a multiple logistic regression model was
developed in which both component summary scores
were dichotomized; either below or above their respec -
tive median value (given score 1 or 0, respectively), and
considered as the dependent variable. Clinical factors
(age, BMI, parity, time since start of symptoms, endo -
metriosis stage, numerical rating scale (NRS) for dys -
menorrhea, dyspareunia, and non-cyclic pelvic pain)
were incorporated in the model as independent vari -
ables [15].
Results
1. Patients’ characteristics and results of clinical/sur -
gical evaluation of recruited women are shown in
Tables 1 and 2 respectively.
2. Diagnostic delay experienced by Egyptian women
with endometriosis:
A diagnostic delay of 36 months (IQR 22.5–60) was
observed in women with endometriosis while symp -
tomatic controls had a delay of 48 months (IQR
24–84). The difference was not statistically significant
(P = 0.08), as seen in Table 2. Women complaining of
infertility represented 44.3% of endometriosis group,
and 87.7% of symptomatic control women.
3. SF-36 domain scores in women with endometriosis
and symptomatic controls:
Table 1 Characteristics of study participants
Item Endometriosis N = 70 Control women N = 57 P value
Demographics
Age (years) 28.56 ± 5.72 28.96 ± 5.7 0.690
BMI (kg/m2) 25.32 ± 4.5 27.34 ± 4.29 0.011
Urban (N, %) 9 (12.9%) 7 (12.3%) 0.922
Rural (N, %) 61 (87.1%) 50 (87.7%)
Number of living children 0.0 (0.0–1.0) 0.0 (0.0–0.0) 0.047
Marital status
Currently married 65 56 0.185
Virgin 4 0
Divorced/separated 1 1
Indication of surgery (N, %)
Infertility 31 (44.3%) 50 (87.7%) < 0.001
Pelvic pain 16 (23.0%) 6 (10.5%)
Infertility + Pelvic pain 11(15.7%) 1 (1.8%)
Ovarian cysts (N, %) 5 (7.1%) 0
Others (N, %t) 7 (10%) 0
Duration of infertility (years) 3.0 (0.0–5.0) 4.0 (2.0–7.0) 0.048
Menstrual days (N, %)
7 days 1 (1.5%) 1 (1.8%)
Cycle length
35 days) 7 (10%) 1 (1.8%)
Too irregular (metrorrhagia) 1 (1.4%) 1 (1.8%)
Page 5 of 9
Othman et al. Middle East Fertility Society Journal (2024) 29:10
As depicted in Table 3, women with endometrio -
sis had significantly lower scores for the BP domain
than symptomatic controls [80.0 (45.0–100.0) versus
100.0 (68.75–100.0) respectively, P is 0.01] indicating
poorer quality of life in this domain. No statistically
significant difference was detected between women
with endometriosis and symptomatic controls in
other domains of the SF-36.
4. SF-36 domain scores in women with endometriosis
stratified by stage of the disease:
A shown in Table 4, women with stages III/IV endo -
metriosis had significantly lower scores for PF [85.0
(50–100.0)] , RP [25.0 (0.0–75.0)], and BP [55.0
(35.0–85.0)], compared to women with stages I/II
disease [corresponding scores for PF, RP , and BP are:
95.0 (85.0–100.0), 100.0 (25.0.0–100.0), and 100.0
(70.0–100.0), respectively] and to control women
(corresponding scores are: 95.0 (82–100.0), 100.0
(0.0–100.0), and 100.0 (68.7–100.0), respectively).
For the domain of GH, women with stages III/IV
endometriosis scored significantly less than women
with stages I/II disease [60.0 (45.0–85.0) versus 85.0
(70.0–90.0) respectively, P is 0.001).
5. Physical component summary (PCS) and mental
component summary (MCS):
PCS and MCS for women with endometriosis and
symptomatic controls were calculated according to
the SF-36 manual [12]. These are standardized com -
bined scores with a mean of 50, and standard devia -
tion of 10. According to our results, neither PCS nor
MCS differed significantly between women with
endometriosis and controls (Table 3). Breaking down
endometriosis group by disease stage showed that
women with stages III/IV endometriosis had signifi -
cantly lower PCS scores compared to women with
stages I/II disease or control group (Table 4). On the
other hand, there was no significant difference in
MCS scores between different stages of endometrio -
sis or control women (Table 4).
6. Determinants of low PCS and MCS scores in women
with endometriosis:
Table 2 Clinical/surgical evaluation and diagnostic delay in study participants
NAS numerical analogue scale
Endometriosis (N = 70) Controls (N = 57) P value
Intensity of pelvic pain (NAS)
Dysmenorrhea 7.0 (0.0–9.0) 0.0 (0.0–5.0) 0.001
Dyspareunia 2.0 (0.0–6.5) 0.0 (0.0–5.0) 0.214
Non-cyclic pain 0.0 (0.0–6.0) 0.0 (0.0–6.0) 0.312
Endometriosis stage: (N, percent)
Stages I/II endometriosis 39 (56%) N/A
Stages III/IV endometriosis 31 (44%) N/A
Diagnostic delay: (months since start of symptoms)
Diagnostic delay (in months; median and IQR) 36 (22.5–60) 48 (24–84) 0.080
Table 3 SF-36 domain scores in women with endometriosis patients and controls. Data expressed as median and interquartile range
(IQR)
SF-36 items Endometriosis (N = 70) Controls (N = 57) P value
Physical Functioning (PF) 95.0 (73.75–100.0) 95.5 (82.0–100.0) 0.366
Role limitation due to physical function (RP) 62.5 (0.0–100.0) 100.0 (0.0–100.0) 0.261
Role limitation due to emotional factors (RE) 66.7 (0.0–100.0) 66.7 (0.0–100.0) 0.722
Vitality (VT) 70.0 (50.0–85.0) 70.0 (50.0–82.5) 0.850
Mental Health (MH) 62.0 (40.0–76.0) 60.0 (40.0–76.0) 0.894
Social Functioning (SF) 50.0 (50.0–50.0) 50.0 (50.0–62.0) 0.265
Bodily Pain (BP) 80.0 (45.0–100.0) 100.0 (68.75–100.0) 0.016
General Health (GH) 75.0 (60.0–86.25) 75.0 (55.0–90.0) 0.739
Physical Component Summary (PCS) 51.7 (41.34–58.99) 54.73 (48.81–59.58) 0.088
Mental Component Summary (MCS) 42.05 (30.58–48.63) 38.82 (29.47–46.03) 0.529
Page 6 of 9Othman et al. Middle East Fertility Society Journal (2024) 29:10
A multi-logistic regression model was developed
with PCS/ MCS scores are the dependent variables
(dichotomized, with score below and above their
respective median given the code 1 and 0, respec -
tively), and participants’ demographic/clinical factors
as the independent variables. Our model has shown
that age (OR: 1.22, CI: 1.01–1.49, P value: 0.036), NRS
for non-cyclic pelvic pain (OR: 1.93, CI: 1.27–2.95, P
value: 0.002), and advanced stage endometriosis (OR:
28.9, CI: 3.9–218.09, P value: 0.001) are associated
with low PCS scores in women with endometriosis.
No specific determinants were significantly associ -
ated with low MCS scores in the group of women
with endometriosis (Table 5).
Discussion
Our results show that Egyptian women with endome -
triosis experienced a relatively short diagnostic delay and
had poorer bodily pain scores compared to symptomatic
controls. Patient’s age, intensity of non-cyclic pelvic pain,
and advanced disease stage are determining factors of
physical health in Egyptian endometriosis patients.
Egyptian women were underrepresented in previous
research on endometriosis-related HRQoL. SF-36, which
performs well in evaluation of HRQoL in endometriosis,
Table 4 SF-36 domain scores in early (stages I/II) and advanced (stages III/IV) endometriosis. Data expressed as median and
interquartile range (IQR)
SF-36 items Mild Endometriosis
(Stages I and II)
N = 39
Advanced endometriosis
(Stages III and IV) N = 31
Control women N = 57 P value
Mild endo.
vs. control
Mild vs.
severe
endo
Severe
endo. vs.
control
Physical Functioning (PF) 95.0 (85.0–100.0) 85.0 (50–100.0) 95.0 (82–100.0) 1.00 0.020 0.056
Role limitation due to physical
function (RP)
100.0 (25.0.0–100.0) 25.0 (0.0–75) 100.0 (0.0–100.0) 1.00 0.002 0.011
Role limitation due to emo-
tional factors (RE)
100.0 (0.0–100.0) 33.3 (0.0–100.0) 66.6 (0.0–100.0) 0.32
Vitality (VT) 70 (55.0–90.0) 65.0 (50.0–80.0) 70.0 (50.0–82.5) 0.48
Mental Health (MH) 60.0 (40.0–76.0) 64.0 (36.0–76.0) 60.0 (40.0–76.0) 0.98
Social Functioning (SF) 50.0 (50.0–50.0) 50.0 (37.5–50.0) 50.0 (50.0–62.5) 0.24
Bodily Pain (BP) 100.0 (70.0–100.0) 55.0 (35.0–85.0) 100.0 (68.7–100.0) 1.00 < 0.001 < 0.001
General Health (GH) 85.5 (70.0–90.0) 60.0 (45.0–85.0) 75.0 (55.0–90.0) 0.145 0.003 0.260
Physical Component Summary
(PCS)
58.33 (50.98–60.38) 51.52 (34.20–51.54) 54.73 (48.81–59.59) 0.868 < 0.001 < 0.001
Mental Component Summary
(MCS)
37.8 (29.49–49.20) 43.3 (32.93–47.01) 38.82 (29.47–46.03) 0.789
Table 5 Multiple logistic regression analysis of PCS/ MCS scores (as dependent variables) and participants’ clinical/demographic
criteria (as independent variables) in Egyptian women with endometriosis
NAS numerical analogue scale
Independent variable PCS MCS
Odds ratio 95 Confidence
interval (CI)
P value Odds ratio 95 Confidence
interval (CI)
P value
Age 1.22 1.01–1.49 0.036 1.15 0.92–1.11 0.744
BMI 0.92 0.76–1.10 0.362 0.95 0.85–1.07 0.418
Time since start of symptoms 0.98 0.96–1.009 0.240 0.98 0.97–1.005 0.180
Dysmenorrhea (NAS) 0.76 0.55–1.02 0.074 0.94 0.78–1.11 0.442
Dyspareunia (NAS) 1.12 0.85–1.47 0.391 1.10 0.92–1.32 0.291
Non-cyclic pelvic pain (NAS) 1.93 1.27–2.95 0.002 1.16 0.96–1.39 0.112
Number of living children 1.31 0.63–2.74 0.464 0.83 0.50–1.36 0.466
Endometriosis stage (stages III/IV
versus stages I/II)
28.9 3.9–218.09 0.001 0.62 0.21–1.82 0.384
Page 7 of 9
Othman et al. Middle East Fertility Society Journal (2024) 29:10
was used in this study [16]. We investigated factors like
patient’s age, diagnostic delay, symptom severity, and dis-
ease stage for their influence on HRQoL. Using sympto -
matic controls likely has prevented overestimation of the
negative effect of endometriosis on HRQoL compared
to if the control group had consisted of healthy asymp -
tomatic women. A point of strength in our study is that
all endometriosis cases and symptomatic controls were
surgically evaluated.
A possible explanation of the occurrence of diagnos -
tic delay in Egyptian women with endometriosis is the
common culture of menstrual taboo, with subsequent
normalization of symptoms by families and society [7] as
well as limited availability of reproductive health educa -
tion [17], particularly knowledge about endometriosis,
among Egyptian females [18]. Therefore, educational
programs for adolescents about endometriosis as a part
of the school curriculum [19], as well as incorporating
the disease into national clinical guidelines and fostering
multi-disciplinary collaborations in endometriosis care,
may lead to more awareness for endometriosis and may
favorably impact diagnostic delay [20].
Studies addressing the length of the diagnostic delay in
women with endometriosis have reported delays up to
nearly 11 years which may vary among centers and coun -
tries [3, 21–23].
As laparoscopy is highly subsidized (and consequently
affordable) in Egyptian governmental hospitals, this may
encourage gynecologists to order it early when inves -
tigating infertility/pelvic pain as hallmarks of endome -
triosis. This practice may contribute to the relative short
delay in diagnosis of 36 months in Egyptian women with
endometriosis when compared to studies in other coun -
tries [3].
This is not in line with previous research which showed
that state-funded health care systems, compared to self-
or insurance funded counterparts, usually results in
longer diagnostic delay [3].
However, similar diagnostic delay, ranging between
2 and 3.7 years, as found in our study, were reported in
Chinese, European, and American women [3, 24, 25].
The high prevalence of infertility in our cohort of
women with endometriosis might have contributed to
the relatively short diagnostic delay. Prior studies showed
that the time to diagnosis is shorter in women with endo-
metriosis associated infertility compared to patients
with pain related symptoms for seeking medical help [2,
25, 26]. Among general practitioners, this translates as
the sense of urgency to establish a timely diagnosis and
to offer treatment of endometriosis in order to prevent
future infertility [20].
Prior studies conducted on different popula -
tions showed that women with endometriosis have
impairments in different domains of SF-36 when com -
pared to symptomatic controls [3, 27]. In addition, Nnoa-
ham and coworkers found that women with moderate/
advanced stage endometriosis had significantly lower
PCS scores than women with minimal/mild disease [3].
Our results support these findings.
Two other studies investigated Egyptian women with
endometriosis. One study found that endometriosis
patients with adhesions had lower HRQoL scores than
endometriosis women lacking them [28]. This study
included infertile women with stage III endometrio -
sis only, with no control group, and the authors used
the Global Quality of Life scale, which is not validated
for endometriosis, and does not recognize domains of
impairment. The second study used SF-12, and EHP-5 to
measure HRQoL in endometriosis patients. Again, the
study was not controlled, the Arabic version of the EHP-5
used was not validated in an independent study, the
EHP-5 results were reported only as percentages, without
actual scores, and the SF-12 scores were not mentioned
[29].
Mousa et al. [6] found that the collective PCS and MCS
were lower in Arab women with endometriosis compared
to symptomatic and asymptomatic controls. Moreover,
women with endometriosis suffered a diagnostic delay
of 11.61 years [6]. Although we could not identify a sig -
nificant difference in MCS scores between endometriosis
patients and symptomatic controls, we showed that MCS
scores in both groups were below the population average,
which is similar to Mousa et al. ’s findings. We and Mousa
et al. used the normative value of the US population for
comparison due to lack of normative values of these
scores in Egypt or the Middle East [6]. Our sample size
was much smaller than the Mousa et al. study; however,
we focused on more homogeneous population in terms of
ethnicity and cultural characteristics (Egyptian women),
rather than different Arab nationalities. Furthermore,
most recruited women in Mousa et al. ’s study were edu-
cated and employed (around 60%). In our study, 87% of
women came from rural areas. Such women are generally
less well educated or even illiterate and are housewives.
These differences in population characteristics may
account for the variability in findings. In addition, in the
Mousa et al. ’s study, 67% of women with endometriosis
had chronic pelvic pain in comparison to only 23% in our
study. This difference in clinical presentation might have
affected care seeking behavior of women in that study.
As we depended in our study on participants’ recalling of
when their symptoms started, it is also possible that the
lower level of education in our participants might have
increased their recall bias [30].
Our results showed that in Egyptian women with
endometriosis, higher patient’s age was associated
Page 8 of 9Othman et al. Middle East Fertility Society Journal (2024) 29:10
with lower PCS score of the SF-36 scale. Prior research
showed younger age was associated with poorer
domains in SF-36. However, the collective PCS and
MCS scores were not reported or correlated to age [31].
Endometriosis effects on HRQoL were not always
related to disease stage [5 ]. However, our results, in
agreement with Nnoaham and his group [3 ], showed
advanced stage disease to be significantly associated
with worse PCS scores in women with endometriosis.
The association of advanced stage endometriosis with
poor physical health might be explained by the pres -
ence of variable degrees of symptom severity or associ -
ated comorbidities in advanced endometriosis patients
[32].
We reported non-cyclic pelvic pain intensity as a sig -
nificant determinant of low PCS scores in women with
endometriosis. Prior research showed that dysmenorrhea
and non-menstrual pain negatively impacted HRQoL
in women with endometriosis [27]. On the other hand,
reduction in dysmenorrhea and non-menstrual pelvic
pain using elagolix improved HRQoL and work produc -
tivity in women with endometriosis pelvic pain [33].
Our study is not without limitations. Our sample size
was modest, as we could recruit 90% of the required
sample size as per the SF-36 Health Survey: Manual and
Interpretation Guide [12]. We did not include a control
group of healthy asymptomatic women. We could not
classify participants in our study according to their clini -
cal presentation of pelvic pain or infertility due to the
small number of pelvic pain cases in our endometriosis
(N = 16) and the symptomatic control (N = 6) groups.
Furthermore, a commonly cited disadvantage in obser -
vational studies from a methodological point of view is
the potential for recall bias as the data are collected ret -
rospectively. This represents an important limitation
for evaluating the diagnostic delay in our study as we
depended on patients memorizing when symptoms first
started. Therefore, a longitudinal cohort study would
be more suited to investigate the associations between
HRQoL and endometriosis. Finally, we could not evaluate
diagnostic delay separately at the level of general practi -
tioner or gynecologist as the Egyptian health care system
allows for patient self-selection of her health care pro -
vider [34].
In conclusion: our study has shown that Egyptian
women with endometriosis experience diagnostic delay
and exhibit impaired physical health scores for which
patient’s age, disease stage, and non-cyclic pain are sig -
nificant determining factors. Multidisciplinary endome -
triosis care centers are needed in Egypt, together with
educational programs to increase awareness about the
disease. Patient support groups are important require -
ment to empower endometriosis patients in Egypt.
Acknowledgements
The authors would like to acknowledge all the nursing team in the laparos-
copy unit at University of Assiut, Women’s Hospital for helping with recruiting
cases to the study. The authors would like to thank Dr. Ghada A Mahfouz, Fac-
ulty of Nursing, University of Assiut for providing the Arabic version of SF-36.
Authors’ contributions
ERO: conception of the idea, data collection, data analysis, manuscript
writing. AMA: data analysis, manuscript writing. MYK: data collection, data
analysis. CBL: data analysis, reviewing manuscript. VM: data analysis, reviewing
manuscript.
Funding
The study was supported by a grant from Science and Technology Develop-
ment Fund (STDF), Egypt to E.R. O. grant ID# 5525.
Availability of data and materials
The dataset used for the development of this manuscript is available from the
authors upon request.
Declarations
Ethics approval and consent to participate
The research protocol was approved by the Science and Technology
Development Fund (STDF), which is a part of the Egyptian Ministry of Higher
Education in 2014. Additional approval was obtained by The Institutional
Review Board at the Faculty of Medicine, University of Assiut, (IRB# 17400008)
in February 2018 to use the data for publication.
A research team member (MYK) explained the study in details and its objec-
tives to the participants and obtained their verbal informed consent to take
part in the study. Another researcher (ERO) assured participants about data
anonymity to protect the confidentiality of their information and double
checked that participants gave their verbal informed consent.
Consent for publication
The manuscript does not contain any individual person data. So, consent for
publication is not applicable.
Competing interests
The authors declare no competing interests.
Author details
1 OB-GYN Department, University of Assiut, Assiut, Egypt. 2 Reproductive Sci-
ence Research Center, Assiut University, Assiut, Egypt. 3 Department of Repro-
ductive Medicine, Academic Endometriosis Center, Amsterdam University
Medical Center, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Received: 10 October 2023 Accepted: 13 January 2024
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