Abstract
Intrauterine insemination (IUI) is an assisted
conception technique that involves the deposition of a
processed semen sample in the upper uterine cavity,
overcoming natural barriers to sperm ascent in the female
reproductive tract. It is a cost-effective, noninvasive first-
line therapy for selected patients with functionally normal
tubes, and infertility due to a cervical factor, anovulation,
moderate male factor, unexplained factors, immunological
factor, and ejaculatory disorders with clinical pregnancy
rates per cycle ranging from 10 to 20%. It, however, has
limited use in patients with endometriosis, severe male
factor infertility, tubal factor infertility, and advanced
maternal age C 35 years. IUI may be performed with or
without ovarian stimulation. Controlled ovarian stimula-
tion, particularly with low-dose gonadotropins, with IUI
offers significant benefit in terms of pregnancy outcomes
compared with natural cycle or timed intercourse, while
reducing associated COH complications such as multiple
pregnancies and ovarian hyperstimulation syndrome.
Important prognostic indicators of success with IUI include
Gautam N. Allahbadia is the Emeritus Editor of the Journal of
Obstetrics and Gynecology of India as well as the IVF Lite (Journal of
Minimal Stimulation IVF) and Medical Director at Rotunda—The
Center for Human Reproduction, Mumbai, India and Medcare
Fertility Center, Jumeira, Dubai, UAE.
& Gautam N. Allahbadia
[email protected]
1 Rotunda-The Center for Human Reproduction,
Bandra, Mumbai, India
Gautam Nand Allahbadia is the Emeritus Editor of the Journal of Obstetrics and Gynecology of India as well as the IVF
Lite (Journal of Minimal Stimulation IVF). He is the Medical Director of Medcare Fertility Centre, Jumeira, Dubai, UAE, as
well as Rotunda—The Center for Human Reproduction, the world-renowned Infertility clinic at Bandra, Mumbai, India. He
is a noted world authority on Ultrasound-guided Embryo Transfers and one of the pioneers in Third Party Reproduction in
Southeast Asia. Dr. Allahbadia was responsible for India’s first trans-ethnic surrogate pregnancy involving a Chinese
couple’s baby delivered by an unrelated Indian surrogate mother. He cherishes over 150 peer-reviewed publications, 140
book chapters, and 22 textbooks, the latest being a comprehensive text, entitled ‘ ‘Minimal Stimulation IVF,’ ’ and is on the
Editorial Board of several International Journals. Dr. Allahbadia has recently been elected as the Vice President of the World
Association of Reproductive Medicine (WARM), headquartered in Rome, and ‘ ‘Mumbai’s Top Doc’ ’ for 2012 by a peer nomination process.
You can read more about his work at www.gautamallahbadia.com.
The Journal of Obstetrics and Gynecology of India (November–December 2017) 67(6):385–392
DOI 10.1007/s13224-017-1060-x
123
age of patient, duration of infertility, stimulation protocol,
infertility etiology, number of cycles, timing of insemina-
tion, number of preovulatory follicles on the day of hCG,
processed total motile sperm [ 10 million, and insemina-
tion count [ 1 9 106 with [ 4% normal spermatozoa.
Alternative insemination techniques, such as Fallopian tube
sperm perfusion, intracervical insemination, and intratubal
insemination, provide no additional benefit compared to
IUI. A complete couple workup that includes patient his-
tory, physical examination, and clinical and laboratory
investigations is mandatory to justify the choice in favor of
IUI and guide alternative patient management, while
individualizing the treatment protocol according to the
patient characteristics with a strict cancelation policy to
limit multi-follicular development may help optimize IUI
pregnancy outcomes.
Introduction
Despite revolutionary advances in the field of assisted
reproduction, such as in vitro fertilization (IVF), intracy-
toplasmic sperm injection (ICSI), and subzonal insemina-
tion (SUZI), intrauterine insemination (IUI) remains an
inexpensive, noninvasive, and effective first-line therapy
for selected patients with cervical factor, moderate male
factor, unexplained infertility, immunological infertility,
and infertility due to ejaculatory disorders and is now also
proposed as a therapy for endometriosis, ovarian dysfunc-
tion, and even for tubal factor. Though the technique of IUI
has essentially remained the same, several advances in the
type of stimulation protocols, gonadotropins, sperm
preparation techniques, and ultrasound monitoring have led
to promising success rates with IUI.
Strict patient selection criteria and individualized stim-
ulation protocols tailored according to the age and etiology
of the patient with a strict cycle cancelation policy will
help to reduce the associated complications, such as mul-
tiple pregnancies and OHSS, while maximizing the overall
pregnancy outcome. Three to six IUI cycles may be offered
before considering alternate therapy. However, patients
with advanced maternal age, severe male factor infertility,
tubal pathology, or severe endometriosis will benefit from a
direct referral to IVF/ICSI.
Semen parameters that must be considered in an IUI
program include the semen processing time, processed total
motile sperm count, rapid progressive motility after pro-
cessing, sperm morphology before and after processing,
inseminating motile sperm count (IMSC), IUI insemination
time, and 24-h sperm survival. Delaying semen processing
from 30 min up to 1 h and/or delaying IUI from 90 min up
to 2 h after collection compromises the pregnancy outcome
in gonadotropin-IUI cycles [ 1]. A universal threshold level
above which IUI can be performed with acceptable preg-
nancy rates has not been determined yet [ 2]. However, IUI
success may be impaired in couples with processed total
motile sperm (PTMS) \ 10 million [ 3], sperm survival
\ 70% [ 4], \ 5% normal spermatozoa, inseminating
motile count (IMC) \ 1 9 106 [ 2], and prewash IUI-se-
men pregnancy score (IUI-SPS) \ 150 [ 5], necessitating
alternative therapy. The PTMS count has been indepen-
dently associated with fertility after IUI ( P = 0.0014) [ 3].
PTMS C 10 9 106, their 24-h sperm survival threshold
of C 70% [ 4], normal morphology before sperm separa-
tion C 15.5% [odds ratio (OR) = 2.2, ( P = 0.02)], rapid,
progressive motility C 25.5% after sperm separation
(P = 0.029), and curvilinear velocity (VCL) after sperm
separation C 102.65 lm/s ( P = 0.002) independently
predict pregnancy outcome in patients with male factor
infertility [ 6]. These variables would be helpful in coun-
seling patients for future management [ 6
].
Discussion
In couples with a cervical factor, diagnosed by a well-
timed, nonprogressive, post-coital test with normal semen
parameters [ 7], higher pregnancy rates (PRs) have been
reported following IUI compared to expectant management
(51 vs. 33%, respectively) [ 8] with acceptable pregnancy
rates even without COH (9.7%) and without an increased
risk for multiple pregnancy compared to COH (12.7%) [ 7].
Cumulative pregnancy rates of 19.7, 36.8, and 36.8% have
been reported for a maximum of three IUI cycles in
patients with a cervical factor without superovulation [ 9].
Pregnancy rates of 12.8, 29.3, and 38.3% for a maximum of
three cycles have been reported in couples with a male
factor without superovulation [ 9], 7% per cycle following
COH–IUI with clomiphene citrate (CC) and 12% per cycle
with follicle-stimulating hormone (FSH) with multiple
birth rates averaging 13% [ 10]. Despite the belief that IVF
may be a more cost-effective primary treatment option
compared to IUI in lieu of the low success rates with IUI
and the subsequent requirement for IVF in the event of
failure [ 11], the results of randomized controlled trials
(RCTs) using live birth rates rather than pregnancy rates,
and taking into account efficacy, complications, especially
multiple pregnancy rates, patient compliance, and cost-ef-
ficiency, suggest that the initial treatment for idiopathic
infertility should be IUI as opposed to IVF [ 12].
Controlled ovarian hyperstimulation with IUI is rec-
ommended in early-stage and surgically corrected
endometriosis when the pelvic anatomy is normal, while
combined surgery with gonadotropin-releasing hormone
(GnRH) analog treatment has been proposed to be a first-
line therapy followed by IVF as second-line therapy in
123
Allahbadia The Journal of Obstetrics and Gynecology of India (November–December 2017) 67(6):385–392
386
advanced cases [ 13]. Comparable clinical PRs per cycle
have been reported in women with minimal, mild
endometriosis, and unexplained infertility (21 vs. 18.9 vs.
20.5%) following COH–IUI with comparative cumulative
live birth rates within four cycles of COH and IUI (70.2,
68.2, 66.5%, respectively); CPR/cycle with or without
COH–IUI was lower in women with surgically untreated
minimal to mild endometriosis than in women with unex-
plained infertility [ 14]. However, in patients with minimal
or mild endometriosis with pathological utero-tubal trans-
port documented by hysterosalpingoscintigraphy (HSSG),
IUI yields poor pregnancy rates despite normal semen
parameters and patent Fallopian tubes, necessitating
recourse to IVF/ICSI [ 15]. Though IVF reduces time to
pregnancy in early-stage disease compared to controls, it
does not increase the chance of pregnancy after 3 years
[16]. In patients with stage IV endometriosis and in
women [ 38 years of age, significantly higher PR, fecun-
dity, and cumulative fecundity have been reported fol-
lowing IVF-ET compared to COH–IUI. Hence, IVF-ET
should be the first-line approach in the management of
infertility in such patients, and if COH–IUI is attempted, it
should not exceed 3–4 cycles [ 17].
IUI may be contraindicated in women with sperm-im-
mobilizing antibodies owing to antibodies secreted in the
female reproductive tract that might impair sperm passage,
inhibit fertilization, and prevent normal post-fertilization
processes [ 18]. The total antral follicle number is reported
to decrease with age. In women [ 35 years with antral
follicle counts (AFCs) \ 5, the application of COH/IUI
may not be indicated [ 19].
Pittrof et al. [ 20] reported a significantly higher number
of preovulatory follicles (43.6, 59.9, 12.6%, P \ 0.0001)
and significantly higher pregnancy rates ( P = 0.038) in
CC/tamoxifen ? gonadotropin—stimulated cycles com-
pared to natural cycles [ 20]. However, Chen and Liu [ 21]
concluded that though stimulated IUI is superior to natural
cycle IUI cycles in patients \ 35 years, natural cycle is
preferable for patients C 35 years. There were no signifi-
cant differences in the abortion and delivery rates between
the OI and the natural cycle insemination ( P [ 0.05) [ 21].
IUI in the spontaneous cycle carries fewer health risks than
does IUI after mild hormonal stimulation and, therefore,
should be the first-choice treatment [ 22]. Ovarian stimu-
lation by clomiphene citrate (CC) and IUI remains the first-
choice treatment for ovulatory dysfunction, unexplained
infertility, endometriosis, or male subfertility [ 23] with
pregnancy rates averaging 7% per cycle [ 10]. Though no
consensus exists about the drug of first choice to be used as
hyperstimulation and there are no significant differences in
clinical pregnancy (38 vs. 34.3%) and live birth rates (28.2
vs. 26.9%) between CC and rFSH, a randomized multi-
center parallel trial concluded that being less expensive,
CC seems the more cost-effective drug and, therefore, can
be offered as drug of first choice [ 24].
A meta-analysis of 43 trials involving 3957 women
concluded that gonadotropins might be the most effective
drugs when IUI is combined with ovarian hyperstimula-
tion, yielding higher pregnancy rates compared to antie-
strogens, comparable PRs with different types of
gonadotropins, no improvement with GnRH agonist or
antagonist but increased multiple pregnancy rates and
OHSS rates with increased doses of gonadotropins, and
significantly higher multiple pregnancy rates with the
agonist. When gonadotropins are used for ovarian stimu-
lation, low-dose protocols are advised since pregnancy
rates do not differ from those obtained with high-dose
regimens, whereas the chances to encounter negative
effects from ovarian stimulation such as multiple preg-
nancies and OHSS are limited with low-dose gonado-
tropins. Further research is needed for each comparison
made [ 25]. No significant differences have been reported
among low-dose gonadotropin protocols that differed in
gonadotropin dosage (4/6/8/ampoules of 75 IU FSH) or the
mode of administration in terms of cycle parameters,
suggesting that an individualized and more intensive
approach to ovarian stimulation is necessary for many
women with unexplained infertility [ 26]. With regard to the
mode of administration, daily recombinant FSH (follitropin
beta) stimulation has been associated with higher CPRs (42
vs. 19%, respectively), higher total recombinant FSH dose
(825 vs. 625 IU), and endometrial thickness (10.1 vs.
9.3 mm) compared to alternate-day FSH stimulation in
women with anovulatory or unexplained infertility for over
12 months who had not responded to or not conceived with
CC treatment though the duration of stimulation and the
median number of follicles over 14 mm, AFC, and day-3
serum FSH were comparable between the groups. How-
ever, prospective randomized trials would be needed to
determine whether this is indeed the case [ 27]. Mahani and
Afnan [ 28] reported the highest CPRs/cycle and CPR/pa-
tient following IUI in patients stimulated with hMG com-
pared with CC, CC ? hMG, or natural cycle.
Studies have reported a beneficial effect of the use of the
aromatase inhibitor letrozole (2.5–5 mg/day from day 3–7
of the IUI cycle) alone/co-administered with gonadotropins
compared to CC, CC ? gonadotropins, or gonadotropins
alone in terms of comparable if not higher CPR/cycle and
take home baby rates. Significantly higher serum levels of
LH, endometrial thickness, and progesterone at the time of
hCG administration have been observed despite a signifi-
cantly lower serum E2 level [ 29–31] with significantly
lower costs, risks, and patient inconvenience in patients
with unexplained infertility [ 29, 30, 32, 33] endometriosis,
and combined indications [ 34], and lower FSH dose
123
The Journal of Obstetrics and Gynecology of India (November–December 2017) 67(6):385–392 Intrauterine Insemination: Fundamentals Revisited
387
requirement and IUI cancelation rates in patients with
ovulatory infertility [ 35] and older infertile women [ 31].
Liang et al. investigated the influence of the time
interval from the end of semen processing to artificial
intrauterine insemination with husband’s sperm (AIH–IUI)
on the rate of clinical pregnancy [ 36]. This study involved
191 AIH–IUI cycles with the same ovulation induction
protocol. After Percoll density gradient centrifugation, they
divided the sperm into four groups based on the incubation
time: 0–19, 20–39, 40–59, and 60–80 min, and again into
another four groups according to the total progressively
motile sperm count (TPMC): (0–9), (10–20), (21–30),
and [ 30 9 10
6. They analyzed the correlation of the
clinical pregnancy rate with the time interval from the end
of sperm processing to AIH–IUI and with other influencing
factors, such as maternal age, infertility duration, and
semen quality. The rate of clinical pregnancy was signifi-
cantly higher in the 20–39-min group (18.3%) than in the
0–19-, 40–59-, and 60–80-min groups (12.7, 11.4 and
9.1%) (all P \ 0.05). The (10–20) 9 10
6 group achieved a
remarkably higher pregnancy rate (16.7%) than the (0–9),
(21–30), and [ 30 9 10
6 groups (0, 11.4, and 8.3%) (all
P \ 0.05). Logistic multivariate analysis showed that the
rate of clinical pregnancy was decreased with the increased
age of the women (OR 0.89, 95% CI 0.83–0.94) but sig-
nificantly elevated in the 20–39-min group (OR 2.11, 95%
CI 1.34–3.13) and of (10–20) 9 10
6 group (OR 2.06, 95%
CI 1.32–3.46). The time interval from the end of sperm
processing to AIH–IUI is a significant factor influencing
the rate of clinical pregnancy of AIH–IUI [ 36].
C¸ ok et al. reported on the comparison of the effect of
preserving prepared sperm samples at room temperature or
at 37 /C176C before intrauterine insemination (IUI) on clinical
pregnancy rate [ 37]. Clinical pregnancy rates were similar
in IUI cycles in which prepared sperm samples were pre-
served at 37 /C176C and at room temperature (9.3 vs. 8.9%).
Clinical pregnancy rates in IUI cycles with two follicles
were higher than IUI cycles with one follicle (10.8 vs.
7.6%) ( P = 0.002). Further statistical analysis after split-
ting data according to the number of the follicles revealed
that there was no statistical difference between clinical
pregnancy rates after IUI cycles in which prepared sperm
samples were preserved at 37 /C176C or at room temperature in
both one-follicle (7.6 vs. 7.6%) and two-follicle cycles
(11.5 vs. 10.1%). Preserving prepared sperm samples at
room temperature had no negative effect on clinical preg-
nancy rates when compared with preserving prepared
sperm samples at 37 /C176C during IUI cycles [ 37].
A modified application technique of intrauterine
insemination (IUI) is slow release insemination (SRI), first
described by Muharib et al. [ 38], who postulated higher
pregnancy rates with a slow release of spermatozoa for 3 h.
To investigate this approach, two randomized controlled,
crossover pilot studies were performed from 2004 to 2006
in Israel and Germany to compare SRI with the standard
bolus IUI. Marschalek et al. aimed to present the results
and perform a meta-analysis on available data for SRI [ 39].
Univariate comparisons of pregnancy rates were performed
using one-tailed z tests for method superiority. For meta-
analysis, a fixed-effect Mantel–Haenszel weighted average
of relative risk was performed. Fifty treatment cycles (IUI:
n = 25, SRI: n = 25) were performed in Germany,
achieving four pregnancies (IUI 4%, SRI 12%,
P [ 0.05). Thirty-nine treatment cycles (IUI: n = 19,
SRI: n = 20) were performed in Israel achieving six
pregnancies (IUI 10.5%, SRI 20%; P [ 0.05). Meta-
analysis of all eligible studies for SRI ( n = 3) revealed a
combined relative risk for pregnancy after SRI of 2.64
(95% CI 1.04–6.74), P = 0.02). In conclusion, these
Results
lend support to the hypothesis that the pregnancy
rate might be improved by SRI compared to the standard
bolus technique [ 39].
Multiple pregnancies are a recognized adverse effect of
assisted reproductive technologies; nevertheless, there is no
consensus on the incremental risk associated with the
ovarian stimulation (OS) used alone and intrauterine
insemination (IUI). The relationship between OS and IUI
and the risk of major congenital malformations (MCM) is
unclear. Chaabane et al. set up a study [ 40] to summarize
the literature and evaluate the risk of multiple pregnancy
and MCM associated with OS used alone and IUI used with
or without OS compared to natural conception (sponta-
neously conceived infants without any type of fertility
treatments). They carried out a systematic review to iden-
tify published papers between 1966 and 2014 in MED-
LINE, EMBASE, and the Cochrane Central Register of
Controlled Trials. They included observational studies and
randomized clinical trials related to the risk of multiple
pregnancies and MCM conceived following OS alone or
IUI compared to natural conception (spontaneously con-
ceived infants without any fertility treatments). There were
63 studies included in this review. The systematic review
suggests that the use of any OS alone was associated with
an increased risk of multiple pregnancies compared to
natural conception (pooled RR 8.80, 95% CI 5.09–15.20;
P = 0.000; 9 studies). Similar increases in the risk of
multiple pregnancies were observed following clomiphene
citrate used without assisted reproductive technologies.
Compared to natural conception, the use of IUI with or
without OS was associated with an increased risk of mul-
tiple pregnancy (pooled RR 9.73, 95% CI 7.52–12.60;
P = 0.000; 6 studies). Compared to natural conception, the
use of any OS alone was associated with an increased risk
of any MCM (RR pooled 1.18, 95% CI 1.03–1.36; 11
studies), major musculoskeletal malformations (pooled RR
1.48, 95% CI 1.21–1.81; 7 studies), and malformations of
123
Allahbadia The Journal of Obstetrics and Gynecology of India (November–December 2017) 67(6):385–392
388
the nervous system (pooled RR 1.73, 95% CI 1.15–2.61; 6
studies). Compared to natural conception, the use of IUI
was associated with an increased risk of any MCM (pooled
RR 1.23, 95% CI 1.10–1.37; 10 studies), major urogenital
(pooled RR 1.52, 95% CI 1.04–2.22; 7 studies), and mus-
culoskeletal malformations (pooled RR 1.54, 95% CI
1.20–1.98; 7 studies). The increased risk of multiple
pregnancy and certain types of MCM associated with the
use of less invasive fertility treatments, such as OS and IUI,
found in this review, highlights the importance of the
practice framing [ 40].
Heterogeneity in OS protocols, the combination with
other fertility agents, the limited number of studies, and the
methodological quality differences reduce our ability to
draw conclusions on specific treatment. More observational
studies, assessing the risk of multiple pregnancy or MCM,
as a primary outcome, using standardized methodologies,
in larger and better clinically defined populations are
needed.
Recent Advances
The transcriptome of spermatozoa used in homologous IUI
reveals profound differences between expression profiles of
sperm samples that impregnate successfully and those that
do not. These differences might improve the predictive
power of sperm evaluation to estimate IUI success by
complementing the basic sperm analysis [ 41]. Three-di-
mensional (3D) and 3D power Doppler (PD) when used
with 2D ultrasound and color Doppler for pre-hCG follic-
ular assessment improve pregnancy rates in IUI cycles by
enabling an assessment of the follicular volume, perifol-
licular resistance index, and perifollicular vascularity
index, all of which may influence the conception rates [ 42].
Abdel Razik’s study evaluated the effects of nitric oxide
donor’s treatment on the pregnancy rate and uterine blood
flow in patients with unexplained infertility undergoing
clomiphene citrate stimulation and intrauterine insemina-
tion [ 43]. A total of 120 patients were randomly allocated
to a control group who received 100 mg clomiphene citrate
daily from day 5 to 9 of cycle plus placebo vaginal tablets,
and a study group received clomiphene citrate plus
isosorbide mononitrate 10-mg vaginal tablets. Vaginal
ultrasound was done before treatment and every other day
starting from day 12 of cycle to count mature follicles, and
ovulation was triggered by IM injection of 10,000 IU hCG
when one follicle measured 18 C mm followed by
intrauterine insemination after 36 h. The endometrial
thickness, uterine arteries resistance and pulsation indices,
and endometrial vascular flow and vascular flow indices
were measured before treatment and at day of hCG injec-
tion. The study group had significant higher pregnancy
rate/cycle, higher endometrial, and lower uterine artery
blood flow indices ( P \ 0.05) [ 43].
Kutlu et al. assessed the relationship between the
estrogen–progesterone alterations before and after ovula-
tion trigger and treatment success in intrauterine insemi-
nation (IUI) cycles (54). Two hundred and fifty-one women
with infertility underwent ovulation induction followed by
IUI. For all subjects, estradiol and progesterone concen-
trations were evaluated on the trigger and IUI day. The
Results
were analyzed to assess the relationship between
hormone levels and positive pregnancy test. There were 34
women with a positive pregnancy test following controlled
ovarian stimulation and IUI cycle. Estradiol and proges-
terone levels on the trigger day and the day of IUI were
compared within groups with and without positive preg-
nancy tests. The comparison revealed significantly
increased levels of progesterone after trigger in both
groups; however, although there were estradiol level drops
in both groups, the drop in the group with negative preg-
nancy tests was statistically significant. Significant drops in
estradiol concentrations after ovulation trigger are associ-
ated with IUI cycle treatment failure [ 44].
The parameters measured in the standard semen analysis
may be insufficient for exact differentiation between fertile
and infertile men. Therefore, Boyraz et al. assumed that the
high rate of apoptotic sperm in ejaculate may play a role on
the etiology of unexplained infertility [ 45]. Couples with
unexplained infertility treated by ovulation induction and
intrauterine insemination were consecutively enrolled
(n = 94). To determine the proapoptotic sperm rate, the
ejaculate from patients was stained with annexin V. Thir-
teen of the 94 couples (13.8%) conceived after intrauterine
insemination. The annexin V-positive sperm rate was
found to be 20.0% in the whole group. In women failing to
conceive, the annexin V-positive sperm rate was 20.8%
compared to 15.7% in patients who achieved pregnancy
[45]. Although there is a trend toward higher preapoptotic
sperm rate in couples failing to get pregnant with insemi-
nation, the difference did not reach statistical significance
[45].
The advanced methods for semen preparation include
molecular sperm selection strategies such as hyaluronic
acid-mediated sperm selection, annexin V magnetic-acti-
vated cell separation (MACS) that utilizes colloidal
superparamagnetic microbeads (approximately 50 nm in
diameter) conjugated with annexin V to separate apoptotic
and nonapoptotic spermatozoa, and annexin V molecular
glass wool filtration [ 46].
123
The Journal of Obstetrics and Gynecology of India (November–December 2017) 67(6):385–392 Intrauterine Insemination: Fundamentals Revisited
389
The Future is Now
Swierkowski-Blanchard conducted an observational pilot
study to determine the impact of the frequency and inten-
sity of uterine contractions (UCs) at the time of IUI on
subsequent fertility [ 47]. One hundred volunteer women
scheduled for IUI between April 2011 and July 2013, in
whom UCs were assessed during the ultrasound before IUI
was included. A two-dimensional sagittal uterus elastog-
raphy was recorded for 5 min. The elasticity index, defined
as the mean ratio of elastographic measurements between
the subendometrial area (of interest) and the endometrial
area (control), was computed. UC frequency, endometrial
thickness and volume, and subendometrial vascularization
were also measured. These parameters, along with char-
acteristics of the IUI cycle, were entered into a logistic
regression model for predicting ongoing pregnancy. The
elasticity index was significantly higher (2.4 ± 1.3 vs.
1.5 ± 0.7, i.e., with stiffer myometrium), and the endo-
metrium was significantly less echogenic in future pregnant
women. Factors closely reaching significance were age,
previous fertility, day 3 hormonal assessments, number of
inseminated spermatozoa, endometrial thickness, and UC
count. In multivariate analysis, low UC frequency ( \ 2.8/
min; odds ratio [OR] = 0.039), high elasticity index
([ 1.7; OR 63.26), high endometrial thickness on the
ovulation triggering day ( [ 8 mm; OR 28.21), and low
patient age ( \ 32 years; OR 0.001) were predictive of
pregnancy after IUI. A low frequency and high intensity of
UCs at the day of IUI appear associated with a higher
pregnancy rate. Elastography provides a promising inno-
vative tool for IUI monitoring [ 47].
Uterine contractibility is considered a powerful prog-
nostic factor in predicting the embryo transfer outcome.
Moreover, uterine contractions are known to be stimulated
by prostaglandins, which are produced by cyclooxygenase
from arachidonic acid. As such, suppressing the inflam-
matory response and contractions using anti-inflammatory
and relaxant agents is expected to result in increased suc-
cess rate of embryo transfer and artificial insemination.
Zarei et al. investigated the effect of piroxicam adminis-
tration on the success rate in intrauterine insemination (IU)
cycles in patients presenting with unexplained infertility
[48]. This randomized, placebo-controlled clinical trial
included 260 women with unexplained infertility under-
going IUI cycles. Patients were randomly assigned to
receive either piroxicam ten mg/day on days 4–6 after IUI
or placebo (control group). The main outcome measures
were number of IUI cycles, pregnancy, abortion, and
multiple pregnancy rates. The pregnancy rate was found to
be 25 (19.2%) and 16 (12.3%) in piroxicam and control
groups, respectively ( P = 0.039). Five patients (3.8%) in
piroxicam group experienced twin pregnancy, whereas
only three patients (2.3%) in control group had twin
pregnancy ( P = 0.361). The pregnancy rate per cycle was
also significantly higher in those who received piroxicam
as compared to controls (11.16 vs. 6.66; P = 0.021).
Administration of piroxicam after IUI is associated with
decreased number of cycles, as well as increased pregnancy
rate and pregnancy rate per cycle in IUI cycles. However,
piroxicam did not have any effect on abortion, multiple
pregnancy, and ongoing pregnancy rates [ 48].
Conclusions
IUI is a simple, cost-effective, noninvasive first-line ther-
apy for cervical factor, anovulatory infertility, moderate
male factor, unexplained infertility, and immunological
infertility with clinical pregnancy rates ranging from 10 to
20%. Controlled ovarian hyperstimulation with close
monitoring of folliculogenesis and ovulation to avoid
adverse complications, such as ovarian hyperstimulation
syndrome (OHSS) and multiple pregnancies, may be used
to obtain the adequate number of follicles. IUI is the pre-
ferred conception-enhancing technique for women
\ 35 years, functional tubes, short period of infertility, and
moderate male infertility, particularly in technology-lim-
ited settings, and four to six IUI cycles may be performed
before considering alternate therapy such as IVF [ 49, 50].
It is the method of choice versus timed intercourse or
natural cycle IUI [ 51].
References
1. Yavas Y, Selub MR. Intrauterine insemination (IUI) pregnancy
outcome is enhanced by shorter intervals from semen collection
to sperm wash, from sperm wash to IUI time, and from semen
collection to IUI time. Fertil Steril. 2004;82(6):1638–47.
2. Ombelet W, Deblaere K, Bosmans E, et al. Semen quality and
intrauterine insemination. Reprod Biomed Online.
2003;7(4):485–92.
3. Miller DC, Hollenbeck BK, Smith GD, et al. Processed total
motile sperm count correlates with pregnancy outcome after
intrauterine insemination. Urology. 2002;60(3):497–501.
4. Branigan EF, Estes MA, Muller CH. Advanced semen analysis: a
simple screening test to predict intrauterine insemination success.
Fertil Steril. 1999;71(3):547–51.
5. Bedaiwy MA, Sharma RK, Alhussaini TK, et al. The use of novel
semen quality scores to predict pregnancy in couples with male-
factor infertility undergoing intrauterine insemination. J Androl.
2003;24(3):353–60.
6. Shibahara H, Obara H, Hirano Y, et al. Prediction of pregnancy
by intrauterine insemination using CASA estimates and strict
criteria in patients with male factor infertility. Int J Androl.
2004;27(2):63–8.
123
Allahbadia The Journal of Obstetrics and Gynecology of India (November–December 2017) 67(6):385–392
390
7. Steures P, van der Steeg JW, Verhoeve HR, et al. Does ovarian
hyperstimulation in intrauterine insemination for cervical factor
subfertility improve pregnancy rates? Hum Reprod.
2004;19(10):2263–6.
8. Steures P, van der Steeg JW, Hompes PG, et al. Effectiveness of
intrauterine insemination in subfertile couples with an isolated
cervical factor: a randomized clinical trial. Fertil Steril.
2007;88(6):1692–6.
9. Check JH, Bollendorf A, Zaccardo M, et al. Intrauterine insem-
ination for cervical and male factor without superovulation. Arch
Androl. 1995;35(2):135–41.
10. ESHRE Capri Workshop Group, Aboulghar M, Baird DT, Collins
J, et al. Intrauterine insemination. Hum Reprod Update.
2009;15(3):265–77.
11. Pashayan N, Lyratzopoulos G, Mathur R. Cost-effectiveness of
primary offer of IVF vs. primary offer of IUI followed by IVF
(for IUI failures) in couples with unexplained or mild male factor
subfertility. BMC Health Serv Res. 2006;6:80.
12. Homburg R. The case for initial treatment with intrauterine
insemination as opposed to in vitro fertilization for idiopathic
infertility. Hum Fertil (Camb). 2003;6(3):122–4.
13. Ozkan S, Arici A. Advances in treatment options of
endometriosis. Gynecol Obstet Invest. 2009;67(2):81–91.
14. Werbrouck E, Spiessens C, Meuleman C, et al. No difference in
cycle pregnancy rate and in cumulative live-birth rate between
women with surgically treated minimal to mild endometriosis and
women with unexplained infertility after controlled ovarian
hyperstimulation and intrauterine insemination. Fertil Steril.
2006;86(3):566–71.
15. Kissler S, Hamscho N, Zangos S, et al. Diminished pregnancy
rates in endometriosis due to impaired uterotubal transport
assessed by hysterosalpingoscintigraphy. BJOG.
2005;112(10):1391–6.
16. Hansen KA, Eyster KM. A review of current management of
endometriosis in 2006: an evidence-based approach. S D Med.
2006;59(4):153–9.
17. Dmowski WP, Pry M, Ding J, et al. Cycle-specific and cumula-
tive fecundity in patients with endometriosis who are undergoing
controlled ovarian hyperstimulation-intrauterine insemination or
in vitro fertilization-embryo transfer. Fertil Steril.
2002;78(4):750–6.
18. Shibahara H, Koriyama J, Shiraishi Y, et al. Diagnosis and
treatment of immunologically infertile women with sperm-im-
mobilizing antibodies in their sera. J Reprod Immunol.
2009;83(1–2):139–44.
19. Chang MY, Chiang CH, Chiu TH, et al. The antral follicle count
predicts the outcome of pregnancy in a controlled ovarian
hyperstimulation/intrauterine insemination program. J Assist
Reprod Genet. 1998;15(1):12–7.
20. Pittrof RU, Shaker A, Dean N, et al. Success of intrauterine
insemination using cryopreserved donor sperm is related to the
age of the woman and the number of preovulatory follicles.
J Assist Reprod Genet. 1996;13(4):310–4.
21. Chen L, Liu Q. Natural cycle versus ovulation induction cycle in
intrauterine insemination (Article in Chinese). Zhonghua Nan Ke
Xue. 2009;15(12):1112–5.
22. Goverde AJ, McDonnell J, Vermeiden JP, et al. Intrauterine
insemination or in vitro fertilisation in idiopathic subfertility and
male subfertility: a randomised trial and cost-effectiveness anal-
ysis. Lancet. 2000;355(9197):13–8.
23. Custers IM, Steures P, Hompes P, et al. Intrauterine insemination:
How many cycles should we perform? Hum Reprod.
2008;23(4):885–8.
24. Dankert T, Kremer JA, Cohlen BJ, et al. A randomized clinical
trial of clomiphene citrate versus low dose recombinant FSH for
ovarian hyperstimulation in intrauterine insemination cycles for
unexplained and male subfertility. Hum Reprod.
2007;22(3):792–7.
25. Cantineau AE, Cohlen BJ, Heineman MJ. Ovarian stimulation
protocols (anti-oestrogens, gonadotrophins with and without
GnRH agonists/antagonists) for intrauterine insemination (IUI) in
women with subfertility. Cochrane Database Syst Rev.
2007;2007(2):CD005356.
26. Hughes EG, Collins JA, Gunby J. A randomized controlled trial
of three low-dose gonadotrophin protocols for unexplained
infertility. Hum Reprod. 1998;13(6):1527–31.
27. Kabli N, Sylvestre C, Tulandi T, et al. Comparison of daily and
alternate day recombinant follicle-stimulating hormone stimula-
tion protocols for intrauterine insemination. Fertil Steril.
2009;91(4):1141–4.
28. Mahani IM, Afnan M. The pregnancy rates with intrauterine
insemination (IUI) in superovulated cycles employing different
protocols (clomiphene citrate (CC), human menopausal gonado-
tropin (HMG) and HMG ? CC) and in natural ovulatory cycle.
J Pak Med Assoc. 2004;54(10):503–5.
29. Wang CW, Horng SG, Chen CK, et al. Ovulation induction with
tamoxifen and alternate-day gonadotrophin in patients with thin
endometrium. Reprod Biomed Online. 2008;17(1):20–6.
30. Barroso G, Menocal G, Felix H, et al. Comparison of the efficacy
of the aromatase inhibitor letrozole and clomiphene citrate as
adjuvants to recombinant follicle-stimulating hormone in con-
trolled ovarian hyperstimulation: a prospective, randomized,
blinded clinical trial. Fertil Steril. 2006;86(5):1428–31.
31. Bedaiwy MA, Shokry M, Mousa N, et al. Letrozole co-treatment
in infertile women 40 years old and older receiving controlled
ovarian stimulation and intrauterine insemination. Fertil Steril.
2009;91(6):2501–7.
32. Tehrani Nejad ESh, Abediasl Z, Rashidi BH, et al. Comparison of
the efficacy of the aromatase inhibitor letrozole and clomiphene
citrate gonadotropins in controlled ovarian hyperstimulation: a
prospective, simply randomized, clinical trial. J Assist Reprod
Genet. 2008;25(5):187–90.
33. Baysoy A, Serdaroglu H, Jamal H, et al. Letrozole versus human
menopausal gonadotrophin in women undergoing intrauterine
insemination. Reprod Biomed Online. 2006;13(2):208–12.
34. Bedaiwy MA, Forman R, Mousa NA, et al. Cost-effectiveness of
aromatase inhibitor co-treatment for controlled ovarian stimula-
tion. Hum Reprod. 2006;21(11):2838–44.
35. Mitwally MF, Casper RF. Aromatase inhibition reduces the dose
of gonadotropin required for controlled ovarian hyperstimulation.
J Soc Gynecol Investig. 2004;11(6):406–15.
36. Liang JY, Li ZT, Yang XH, et al. Time interval from the end of
sperm processing to artificial intrauterine in semination with
husband’s sperm correlates to the rate of clinical pregnancy.
Zhonghua Nan Ke Xue. 2015;21(6):532–5.
37. C¸o k T , C¸a g˘lar Aytac¸P ,S¸ ims¸ek E, et al. The effect of preserving
prepared sperm samples at room temperature or at 37 /C176C before
intrauterine insemination (IUI) on clinical pregnancy rate. Turk J
Obstet Gynecol. 2015;12(1):6–10. doi: 10.4274/tjod.31644.
38. Muharib NS, Abdel Gadir A, Shaw RW. Slow release intrauterine
insemination versus the bolus technique in the treatment of
women with cervical mucus hostility. Hum Reprod.
1992;7(2):227–9.
39. Marschalek J, Franz M, Gonen Y, et al. The effect of slow release
insemination on pregnancy rates: report of two randomized
controlled pilot studies and meta-analysis. Arch Gynecol Obstet.
2017;295(4):1025–32. doi: 10.1007/s00404-017-4290-3 Epub
2017 Feb 14 .
40. Chaabane S, Sheehy O, Monnier P, et al. Ovarian stimulation,
intrauterine insemination, multiple pregnancy and major con-
genital malformations: a systematic review and meta-analysis—
the ART_Rev study. Curr Drug Saf. 2016;11(3):222–61.
123
The Journal of Obstetrics and Gynecology of India (November–December 2017) 67(6):385–392 Intrauterine Insemination: Fundamentals Revisited
391
41. Garcı´a-Herrero S, Meseguer M, Martı´nez-Conejero JA, et al. The
transcriptome of spermatozoa used in homologous intrauterine
insemination varies considerably between samples that achieve
pregnancy and those that do not. Fertil Steril. 2009;94:1360–73.
42. Panchal S, Nagori CB. Pre-hCG 3D and 3D power Doppler
assessment of the follicle for improving pregnancy rates in
intrauterine insemination cycles. J Hum Reprod Sci.
2009;2(2):62–7.
43. Abdel Razik M, El-Berry S, El-Nezamy A, et al. Nitric oxide
donors increase the pregnancy rate in patients with unexplained
infertility undergoing clomiphene citrate stimulation and
intrauterine insemination: a randomized controlled pilot study.
Gynecol Endocrinol. 2017;33(3):199–202. doi:
10.1080/09513590.2016.1240775.
44. Kutlu T, O ¨ zkaya E, S¸ anverdi I, et al. The relationship between
estradiol-progesterone alterations after ovulation trigger and
treatment success in intrauterine insemination cycles. Turk J
Obstet Gynecol. 2016;13(2):56–61. doi: 10.4274/tjod.45656.
45. Boyraz G, Selcuk I, Sokmensuer LK, et al. Evaluation of the
relation between preapoptotic sperm rate in ejaculate and
intrauterine insemination success rate in patients with unex-
plained infertility. J Obstet Gynaecol. 2016;36(8):980–3.
46. Paasch U, Grunewald S, Glander HJ. Sperm selection in assisted
reproductive techniques. Soc Reprod Fertil Suppl.
2007;65:515–25.
47. Swierkowski-Blanchard N, Boitrelle F, Alter L, et al. Uterine
contractility and elastography as prognostic factors for pregnancy
after intrauterine insemination. Fertil Steril. 2017;107(4):961–8.
doi:10.1016/j.fertnstert.2017.02.002.
48. Zarei A, Mahboubi M, Parsanezhad ME, et al. Effects of pirox-
icam administration on pregnancy outcome in intrauterine
insemination (IUI) cycles: a randomized clinical trial. Clin Exp
Obstet Gynecol. 2016;43(2):225–9.
49. Abdelkader AM, Yeh J. The potential use of intrauterine
insemination as a basic option for infertility: a review for tech-
nology-limited medical settings. Obstet Gynecol Int.
2009;2009:584837.
50. Katzorke T, Kolodziej FB. Significance of insemination in the era
of IVF and ICSI (Article in German). Urol A. 2010;49:842–6.
51. De Sutter P. Rational diagnosis and treatment in infertility. Best
Pract Res Clin Obstet Gynaecol. 2006;20(5):647–64.
123
Allahbadia The Journal of Obstetrics and Gynecology of India (November–December 2017) 67(6):385–392
392
Text is read by the "Ask this paper" AI Q&A widget below.
Extraction quality varies by source — PMC NXML preserves structure
cleanly, OA-HTML may include some navigation residue, and OA-PDF can
have broken hyphenation. The publisher copy
(via DOI)
is the canonical version.