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Practical tips for monitoring
of an IUI cycle
Dr. Jyoti Agarwal

Alumini of Lady Harding Medical College
Presently Director of :- Lifecare Centre
: - Lifecare IVF
- Consultant : Pushpanjali Crosslay Hospital
- Secretary of East Delhi Gynaecologist Forum
- Treasurer Delhi Gynaecologist Forum
- Member of WOW India
- Special interest in Infertility & Ultrasound
Introduction
• Ovulation induction though sounds simple but
there are many obstacles ,
as each patient behaves in a different fashion.
Variety of drugs and protocols are available.

• Every center has its own pattern of COH
but the basic concept of monitoring
remains the same.
Who should monitor?
Why add to the burden ?

Do it yourself
“Vision is the art of seeing invisible ”
Jonathan swift
• It is difficult to think of managing an infertile
couple without resorting to this versatile and
easy to use technology.
• All the modalities of ultrasound ranging from
basic black and white to the most complex ,
real time 3 – D and colour doppler have a role
to play in managing these infertile patients .
Five Reasons To Monitor
To evaluate if the dose being used is optimal
To adjust the dose of the drug as some patients
are hyper responsive and some are poor
responders.
To find the optimal time for inducing ovulation
To time IUI
To avoid excessive stimulation , to prevent OHSS
and multiple pregnancy

All patients to be monitored
Monitoring Should Be

•
•
•
•
•

Easy
Reliable
Patient friendly
Not expensive
Can be done by self
How to monitor ?
•
•
•
•
•

BY E 2 ALONE
BY ULTRASOUND ALONE
BY BOTH
BY COLOR POWER DOPPLER
BY OTHER HORMONES

MINIMUM MONITORING
Monitoring
Ultrasound states the morphological
growth of the follicles
Hormones indicates the functional
activity of the follicles
TVS is the accepted method by all
ART centers.
Why TVS ?
•
•
•
•
•
•
•
•

Simple
Easy
Reproducible
Reliable
Cheap
Can be done repeatedly
Patient friendly
Antral count/ovarian volume /color doppler/ 3 D

An transvaginal probe is an extension of
clinician’s fingers
Importance of D -2 scan
TVS is performed on day 2 of the cycle to see for
•
•
•
•

Antral follicle count
To rule out any cyst.( > 3 cm)
Endometrial shedding
Or any other pelvic pathology
We expect normal sized ovaries with very small follicles
(3—5 mm in diameter)

Follicles are of clinical importance only when their
size is 10 mm
Follicular size is measured by taking mean of 2 or 3
largest perpendicular diameters of each follicle .
Ultrasound follicular
monitoring
Serial USG follicular monitoring is started from
day 7 or 8 of the cycle
But in case of gonadotrophins we start scanning
from 6th day of stimulation.
Assessing the follicular maturity
• The follicles normally grow at a rate of
2- 3 mm / day in a stimulated cycle.
• Definitive size of the follicle which
confirms the maturity of oocytes is still
controversial.
• A follicle measuring 18—20 mm has
been found to contain a mature oocyte.
Corelation with serum
oestradiol levels
• Plasma estradiol levels correlates
closely with the stage of development of
the dominant follicle
• Serum estradiol levels >200 pg / ml on
day 8 of stimulation indicates adequate
dose of gonadotropins.

Ultrasound monitoring has totally
replaced estradiol monitoring in most
centers.
Predicting the risk of OHSS
If there are
more than 4 follicles larger than 16 mm
or more than 8 follicles larger than 12 mm
It is best not to give hCG so as to prevent
OHSS and high order multiple births.
In case of doubt do serum estradiol levels
Estradiol levels of > 1500 – 2000 pg/ml
indicates risk of OHSS and is advisable to
withhold hCG trigger.
Follicular doppler flow studies
• A mature follicle shows
vascularity in atleast ¾
th of the follicular
circumference &
• PSV is 10 cm/sec.
• At this time LH surge
starts and
• This is the right time to
give hCG trigger
Interpretation of ovarian indices
• Rising PSV & steady low RI suggests follicle is
close to rupture
• Decreasing PSV & rising RI suggests follicle is
likely to become LUF.
• Fertilisation of a follicle with PSV of less than
10 cm /sec may result in an embryo with
chromosomal abnormality.
Perifollicular vascularisation

Grade 1 : < 10%

Grade 2 : 10-25%

Grade 3 : 25-50%

Grade 4 : > 50%
Predictors of poor ovarian
response are :
•
•
•
•
•

Ovarian volume <3 cc
< 3 antral follicles
Ovarian RI > 0.6
Ovarian PSV < 5 cm / sec
Stromal flow index < 11

• Suggest poor ovarian response &
• Higher doses of gonadotropins will
be required for stimulation.
ENDOMETRIAL EVALUATION
Clear
association
between
endometrial
growth and the
circulating
estrogen &
progesterone
levels.
Endocrine implantation
ET – 8 – 14 mm
BEST ENDOMETRIUM ON THE DAY OF HCG TRIGGER

ET > 16 mm or < 7mm
Is not associated with good prognosis
•
•
•
•

Proliferative phase : 4- 7 mm
Periovulatory period : 6-10 mm
Secretory phase
: 8-12 mm
Postmenopausal pd. : < 4 mm

Thickest part of the endometrium should
be measured
D-2
Can show
 anechoic
collection of
blood.
 thick echogenic
endometrial
echo .
 a very thin
endometrium
1-3 mm thick.
D3-7
• Increase in
oestrogenic
biosynthesis leads to
stimulation and
growth of
endometrial glands
and stroma.
• Double line
endometrium is
seen which is
usually < 6 mm.
D-7 onwards
• Proliferative
endometrium
continues to grow in
size and thickens
and is seen as a
triple layer or triple
line.
• Middle layer
echogenic—Lumen
• Hypoechoic area
surrounding the
lumen—
Endometrium
functionalism
• Hyperechoic ring
outside—
Endometrium
In Periovulatory Phase

characteristic changes start only 24 hrs post
ovulation.
Triple line progressively becomes thicker, homogenous
and hyperechoic
Applebaum’s uterine scoring system for
reproduction (USSR)
Cyclical Endometrial Changes
Power Doppler evaluation
Endometrial evaluation
Conception rates according to zones of
vascularity
• Zone 1 5.2 %
• Zone 2 28 %
• Zone 3 52 %
• Zone 4
74%
COLOR DOPPLER
UT.ARTERY DAY 2
DAY 7-9
PERIOVULATORY UT A.
Uterine Artery Doppler
The chance for
pregnancy is
almost zero if the PI
is more than 3.019
on the day of hCG
administration
Patients who get
pregnant have a lower
RI (0.53 vs 0.64)
Doppler study for uterine
receptivity
Uterine artery RI 0.60 – 0.80
PI 2.22 –3.16
No pregnancy if
VI < 1.0,
FI < 31 and
VFI < 0.25

Smoking is associated with significantly lower VI and VFI.
Subendometrial Vascularisation
• Presence of
subendometrial flow
is an indicator of
good endometrial
receptivity
•

If pregnancy occurs in
patients with absent
subendometrial flow
more than half of these
pregnancies will result in
abortion
3 D power doppler for
endometrial receptivity
• Endometrial volume is a more reliable
parameter than endometrial thickness
• Favourable endometrial volume is 4.28 –
1.9 ml.
• No pregnancy occurred if endometrial
volume is <1 ml.
• 3D tells us also about global vascularity
of the endometrium
Cervix and follicular
monitoring
On D – 13 scan
Good cervical mucus
• E2 > 100 pg
• 2 follicles
• ET 7-8 mm
Application of 3 D us for
follicular assessment
• Cumulus may be seen
in almost 90 % of the
follicles using 3 D usg
rendering. Where as it
is seen only in 25 % of
follicles by 2D usg.
• On the day of hCG if
cumulus is not seen in
all the three planes by
3D usg , it is less likely
to be mature follicle.
Infolding of inner cell mass
of granulosa layers
hCG timing

ALWAYS TIME HCG WITH FOLLICLE SIZE
Ovulation trigger
The end point of any ovulation induction
protocol is to indentify the best time for
triggering ovulation.
most crucial step

In a gonadotrophin

In clomiphene

Leading follicle is
18 – 20 mm in diameter.

Leading follicle is
20 – 22 mm in size
Ovulation to be confirmed by
• Disappearance of the follicle
• Presence of free fluid in the cul-de-sac.
• Presence of hyperechoic , smooth
secretary endometrium.
Timing of insemination
IUI is done 24 hrs. after LH surge is
detected
IUI is done 36 - 38 hrs. after hCG
injection
serum progesterone and
implantation
• Periovulatory progesterone levels are
used as a predictor of outcome.
• Elevated levels of serum progesterone in
the late follicular phase is associated
with diminshed chances of conception.
Premature LH surge
• Premature LH surge is known to occur in
approx 15-25 % of patients once the
leading follicle is 16 mm.
• Urinary LH kits are available to detect LH
surge.

A blood level of >10 IU /L correlates with the LH surge
Premature LH surge
• If an LH surge is detected , injection hCG
is given immediately.
• The hCG injection is required to
supplement the LH secreted by the body
as it is not adequate enough to induce
the final maturational changes in all the
follicles .
• IUI is done 24 hrs after the LH surge
Luteal phase scan
• A healthy corpus luteum shows a good
vascular ring on colour doppler
• RI of 0.35 – 0.50
• PI of 0.70 – 0.80
• PSV of 10 – 15 cm / sec.
• RI of corpus luteum corelates well with
plasma progesterone level which is an
index of luteal function.
To conclude
“ In the hands of experienced
operators , ultrasound and
ultrasound alone suffices for cycle
monitoring , with no necessity for
additional hormonal estimations.”
NEED OF EXTENSIVE HORMONAL
MONITORING IS NO LONGER NEEDED
All The Best to all of you to
design your own Minimal
Monitoring Protocol

THANK YOU FOR HEARING ME OUT

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Practical tips for monitoring of an iui cycle Dr. Jyoti Agarwal

  • 1. Practical tips for monitoring of an IUI cycle Dr. Jyoti Agarwal Alumini of Lady Harding Medical College Presently Director of :- Lifecare Centre : - Lifecare IVF - Consultant : Pushpanjali Crosslay Hospital - Secretary of East Delhi Gynaecologist Forum - Treasurer Delhi Gynaecologist Forum - Member of WOW India - Special interest in Infertility & Ultrasound
  • 2. Introduction • Ovulation induction though sounds simple but there are many obstacles , as each patient behaves in a different fashion. Variety of drugs and protocols are available. • Every center has its own pattern of COH but the basic concept of monitoring remains the same.
  • 3. Who should monitor? Why add to the burden ? Do it yourself
  • 4. “Vision is the art of seeing invisible ” Jonathan swift • It is difficult to think of managing an infertile couple without resorting to this versatile and easy to use technology. • All the modalities of ultrasound ranging from basic black and white to the most complex , real time 3 – D and colour doppler have a role to play in managing these infertile patients .
  • 5. Five Reasons To Monitor To evaluate if the dose being used is optimal To adjust the dose of the drug as some patients are hyper responsive and some are poor responders. To find the optimal time for inducing ovulation To time IUI To avoid excessive stimulation , to prevent OHSS and multiple pregnancy All patients to be monitored
  • 6. Monitoring Should Be • • • • • Easy Reliable Patient friendly Not expensive Can be done by self
  • 7. How to monitor ? • • • • • BY E 2 ALONE BY ULTRASOUND ALONE BY BOTH BY COLOR POWER DOPPLER BY OTHER HORMONES MINIMUM MONITORING
  • 8. Monitoring Ultrasound states the morphological growth of the follicles Hormones indicates the functional activity of the follicles TVS is the accepted method by all ART centers.
  • 9. Why TVS ? • • • • • • • • Simple Easy Reproducible Reliable Cheap Can be done repeatedly Patient friendly Antral count/ovarian volume /color doppler/ 3 D An transvaginal probe is an extension of clinician’s fingers
  • 10. Importance of D -2 scan TVS is performed on day 2 of the cycle to see for • • • • Antral follicle count To rule out any cyst.( > 3 cm) Endometrial shedding Or any other pelvic pathology We expect normal sized ovaries with very small follicles (3—5 mm in diameter) Follicles are of clinical importance only when their size is 10 mm Follicular size is measured by taking mean of 2 or 3 largest perpendicular diameters of each follicle .
  • 11. Ultrasound follicular monitoring Serial USG follicular monitoring is started from day 7 or 8 of the cycle But in case of gonadotrophins we start scanning from 6th day of stimulation.
  • 12. Assessing the follicular maturity • The follicles normally grow at a rate of 2- 3 mm / day in a stimulated cycle. • Definitive size of the follicle which confirms the maturity of oocytes is still controversial. • A follicle measuring 18—20 mm has been found to contain a mature oocyte.
  • 13. Corelation with serum oestradiol levels • Plasma estradiol levels correlates closely with the stage of development of the dominant follicle • Serum estradiol levels >200 pg / ml on day 8 of stimulation indicates adequate dose of gonadotropins. Ultrasound monitoring has totally replaced estradiol monitoring in most centers.
  • 14. Predicting the risk of OHSS If there are more than 4 follicles larger than 16 mm or more than 8 follicles larger than 12 mm It is best not to give hCG so as to prevent OHSS and high order multiple births. In case of doubt do serum estradiol levels Estradiol levels of > 1500 – 2000 pg/ml indicates risk of OHSS and is advisable to withhold hCG trigger.
  • 15. Follicular doppler flow studies • A mature follicle shows vascularity in atleast ¾ th of the follicular circumference & • PSV is 10 cm/sec. • At this time LH surge starts and • This is the right time to give hCG trigger
  • 16. Interpretation of ovarian indices • Rising PSV & steady low RI suggests follicle is close to rupture • Decreasing PSV & rising RI suggests follicle is likely to become LUF. • Fertilisation of a follicle with PSV of less than 10 cm /sec may result in an embryo with chromosomal abnormality.
  • 17. Perifollicular vascularisation Grade 1 : < 10% Grade 2 : 10-25% Grade 3 : 25-50% Grade 4 : > 50%
  • 18. Predictors of poor ovarian response are : • • • • • Ovarian volume <3 cc < 3 antral follicles Ovarian RI > 0.6 Ovarian PSV < 5 cm / sec Stromal flow index < 11 • Suggest poor ovarian response & • Higher doses of gonadotropins will be required for stimulation.
  • 19. ENDOMETRIAL EVALUATION Clear association between endometrial growth and the circulating estrogen & progesterone levels.
  • 20. Endocrine implantation ET – 8 – 14 mm BEST ENDOMETRIUM ON THE DAY OF HCG TRIGGER ET > 16 mm or < 7mm Is not associated with good prognosis
  • 21. • • • • Proliferative phase : 4- 7 mm Periovulatory period : 6-10 mm Secretory phase : 8-12 mm Postmenopausal pd. : < 4 mm Thickest part of the endometrium should be measured
  • 22. D-2 Can show  anechoic collection of blood.  thick echogenic endometrial echo .  a very thin endometrium 1-3 mm thick.
  • 23. D3-7 • Increase in oestrogenic biosynthesis leads to stimulation and growth of endometrial glands and stroma. • Double line endometrium is seen which is usually < 6 mm.
  • 24. D-7 onwards • Proliferative endometrium continues to grow in size and thickens and is seen as a triple layer or triple line. • Middle layer echogenic—Lumen • Hypoechoic area surrounding the lumen— Endometrium functionalism • Hyperechoic ring outside— Endometrium
  • 25. In Periovulatory Phase characteristic changes start only 24 hrs post ovulation. Triple line progressively becomes thicker, homogenous and hyperechoic
  • 26.
  • 27. Applebaum’s uterine scoring system for reproduction (USSR)
  • 29. Endometrial evaluation Conception rates according to zones of vascularity • Zone 1 5.2 % • Zone 2 28 % • Zone 3 52 % • Zone 4 74%
  • 33. Uterine Artery Doppler The chance for pregnancy is almost zero if the PI is more than 3.019 on the day of hCG administration Patients who get pregnant have a lower RI (0.53 vs 0.64)
  • 34. Doppler study for uterine receptivity Uterine artery RI 0.60 – 0.80 PI 2.22 –3.16 No pregnancy if VI < 1.0, FI < 31 and VFI < 0.25 Smoking is associated with significantly lower VI and VFI.
  • 35. Subendometrial Vascularisation • Presence of subendometrial flow is an indicator of good endometrial receptivity • If pregnancy occurs in patients with absent subendometrial flow more than half of these pregnancies will result in abortion
  • 36. 3 D power doppler for endometrial receptivity • Endometrial volume is a more reliable parameter than endometrial thickness • Favourable endometrial volume is 4.28 – 1.9 ml. • No pregnancy occurred if endometrial volume is <1 ml. • 3D tells us also about global vascularity of the endometrium
  • 37. Cervix and follicular monitoring On D – 13 scan Good cervical mucus • E2 > 100 pg • 2 follicles • ET 7-8 mm
  • 38. Application of 3 D us for follicular assessment • Cumulus may be seen in almost 90 % of the follicles using 3 D usg rendering. Where as it is seen only in 25 % of follicles by 2D usg. • On the day of hCG if cumulus is not seen in all the three planes by 3D usg , it is less likely to be mature follicle. Infolding of inner cell mass of granulosa layers
  • 39. hCG timing ALWAYS TIME HCG WITH FOLLICLE SIZE
  • 40. Ovulation trigger The end point of any ovulation induction protocol is to indentify the best time for triggering ovulation. most crucial step In a gonadotrophin In clomiphene Leading follicle is 18 – 20 mm in diameter. Leading follicle is 20 – 22 mm in size
  • 41. Ovulation to be confirmed by • Disappearance of the follicle • Presence of free fluid in the cul-de-sac. • Presence of hyperechoic , smooth secretary endometrium.
  • 42. Timing of insemination IUI is done 24 hrs. after LH surge is detected IUI is done 36 - 38 hrs. after hCG injection
  • 43. serum progesterone and implantation • Periovulatory progesterone levels are used as a predictor of outcome. • Elevated levels of serum progesterone in the late follicular phase is associated with diminshed chances of conception.
  • 44. Premature LH surge • Premature LH surge is known to occur in approx 15-25 % of patients once the leading follicle is 16 mm. • Urinary LH kits are available to detect LH surge. A blood level of >10 IU /L correlates with the LH surge
  • 45. Premature LH surge • If an LH surge is detected , injection hCG is given immediately. • The hCG injection is required to supplement the LH secreted by the body as it is not adequate enough to induce the final maturational changes in all the follicles . • IUI is done 24 hrs after the LH surge
  • 46. Luteal phase scan • A healthy corpus luteum shows a good vascular ring on colour doppler • RI of 0.35 – 0.50 • PI of 0.70 – 0.80 • PSV of 10 – 15 cm / sec. • RI of corpus luteum corelates well with plasma progesterone level which is an index of luteal function.
  • 47. To conclude “ In the hands of experienced operators , ultrasound and ultrasound alone suffices for cycle monitoring , with no necessity for additional hormonal estimations.” NEED OF EXTENSIVE HORMONAL MONITORING IS NO LONGER NEEDED
  • 48. All The Best to all of you to design your own Minimal Monitoring Protocol THANK YOU FOR HEARING ME OUT

Editor's Notes

  1. 3 D