Presented byBRezvankhah In 2011 the American Thyroid Association ATA first published guidelines on the diagnosis and management of thyroid disease during pregnancy and postpartum ATA 2011 Recommendations76 ID: 932179
Download Presentation The PPT/PDF document "In the Name of God What Is New?" is the property of its rightful owner. Permission is granted to download and print the materials on this web site for personal, non-commercial use only, and to display it on your personal computer provided you do not modify the materials and that you retain all copyright notices contained in the materials. By downloading content from our website, you accept the terms of this agreement.
Slide1
In the Name of God
Slide2What Is New?
Presented
by:B.Rezvankhah
Slide3In 2011, the American Thyroid Association (ATA) first published guidelines on
the diagnosis
and management of thyroid disease during pregnancy and
postpartum.
ATA 2011 Recommendations:76
ATA 2017 Recommendations:97
Slide4In addition
to evidence-based updates of traditional content areas, the task force also sought
to expand
the prior document to address topics such as thyroid disease during lactation,
the treatment
of thyroid illness in infertile women and those undergoing assisted
reproductive techniques
(ART), as well as the approach to thyroid disease in the newborn.
Slide5Slide6Slide7III
. Thyroid Function Testing and Pregnancy
Slide8THYROID FUNCTION
TESTS DURING PREGNANCY
The
reference ranges for the most widely applied tests, TSH and
FT4,
may vary significantly in different populations
.
TSH below
the
nonpregnant
lower limit of 0.4
mU
/L is observed in as many as 15% of
healthy
women during
1th
trimester of
pregnancy.
The
fraction
of women
with a suppressed TSH falls to about 10% in the second trimester, and 5% in the
third trimester
Slide9Measurement of free T4 (FT4) concentration by automated immunoassays results in
a significant
and assay dependent reduction in the measured serum FT4 concentrations in
3th trimester.
FT4 automated
immunoassays,
are complicated in pregnant women by the increase in TBG and decrease
in albumin concentrations.
Other
methods of direct measurement, such as measurement
by equilibrium
dialysis, ultrafiltration, or liquid chromatography/tandem mass
spectrometry (LC/MS/MS
), are less influenced by the pregnancy-associated changes in serum proteins, but
are significantly
more expensive and less widely
available.
Slide10Recommendation 1
When possible, population-based trimester-specific reference ranges for serum TSH should
be defined
through assessment of local population data representative of a healthcare
provider’s practice
. Reference range determinations should only include pregnant women with no
known thyroid
disease, optimal iodine intake, and negative
TPOAb
status.
(
Strong recommendation
, Moderate quality evidence)
Slide11NL RANGE
FOR TSH IN
EACH TRIMESTER
Although the downward shift in TSH reference ranges is seen
in essentially all populations
, the extent of this reduction
varies significantly
between different racial and
ethnic groups.
Serum TSH reference range determinations should take into account iodine intake, TPO positivity, and according to some studies, body mass index (BMI).
Slide12Design:
We screened 4800 pregnant women in the first trimester and 2000 women who
planned to
become pregnant and evaluated 535
pregnant women in
follow-up visits during the second
and third
trimester.
Results:
Median concentrations of serum TSH decreased significantly from the seventh week
of gestation
. The median of TSH from 4 to 6 weeks was significantly higher than from 7 to 12
weeks (2.15
[0.56 –5.31]
mIU
/L vs 1.47 [0.10–4.34]
mIU
/L,
P
.001
).
The median
of free
T4 was not significantly altered in the first trimester. The prevalence of subclinical
hypothyroidism in
the 4800 pregnant women was 27.8% on the diagnostic criteria of TSH 2.5
mIU/L and 4.0% using the reference interval derived by our laboratory (0.14–4.87 mIU/L).
J
Clin
Endocrinol
Metab
2014
Slide13Slide14Methods
. The serum of 215 cases was analyzed for measurement of thyroid function
tests by
immunoassay method of which 152 iodine-sufficient pregnant women without thyroid autoantibodies and history of
thyroid disorder
or goiter were selected for final analysis. Reference intervals were defined as 5th and 95th percentiles.
Results
.
Reference intervals
in the first, second, and third trimesters were as follows: TSH (0.2–3.9, 0.5–4.1, and 0.6–4.1
mIU
/l), TT4 (8.2–18.5,
10.1–20.6
, and 9–19.4 𝜇g/dl), and TT3 (137.8–278.3, 154.8–327.6, and 137–323.6 ng/dl), respectively
Journal
of Thyroid Research 2013
Slide15Table 4.
Slide16Recommendation 2
The accuracy of serum Free T4 measurement by the indirect analog immunoassays
is influenced
by pregnancy and also varies significantly by manufacturer. If measured
in pregnant
women, assay method-specific and trimester-specific pregnancy reference
ranges should
be applied
.
(
Strong recommendation, Moderate quality evidence)
Slide17Recommendation 3
In lieu of measuring freeT4, total T4 measurement (with a pregnancy-adjusted
reference range
), is a highly reliable means of estimating hormone concentration during the last part
of pregnancy
. Accurate estimation of the free T4 concentrations can also be done by
calculating a
free thyroxine index.
(
Strong recommendation, Moderate quality evidence)
Slide18RECOMMENDATION
3
The
optimal method to assess serum FT4 during
pregnancy is
measurement of T4 in the dialysate or
ultrafiltrate
of serum
samples employing on-line
extraction/liquid chromatography/tandem
mass spectrometry (
LC/MS/MS
). Level A-USPSTF
RECOMMENDATION
4
If FT4 measurement by LC/MS/MS is not available,
clinicians should
use whichever measure or estimate of FT4
is available
in their laboratory, being aware of the
limitations of
each method. Serum TSH is a more accurate indication
of thyroid
status in pregnancy than any of these
alternative methods
. Level A-USPSTF
Slide19OPTIMAL METHOD TO ASSESS T4 CONCENTRATION
Serum total T4 concentrations are measured in the
nanomolar
range,while
FT4 concentrations are measured in the
picomolar
range.
Indirect
analog immunoassays is prone to inaccuracy in the setting
of pregnancy
because of disruption of the original equilibrium – a process dependent upon
dilution, temperature
, buffer composition, affinity,
and the
concentration of the T4 antibody reagent
and the
T4-binding capacity within the serum
sample.
Slide20TT4 measurements may be superior
to immunoassay
measurement of FT4 measurements in pregnant women.
Reference
values should take the 50% increase in TBG witnessed during pregnancy by calculating the
FT4 index
using a serum thyroid hormone uptake test
into account
.
An
increase in total
T4 concentration
from weeks 7-16 of
gestation is seen,
ultimately reaching ~50% above the
prepregnancy
level and
then sustained through
pregnancy.
Slide21If a T4 measurement is required
before
weeks 7-16 of
pregnancy,a
calculation
can be made for the upper reference
range based on increasing
the
non-pregnant
upper reference limit by 5% per
week, beginning with week
7
.(For
example, at 11 weeks of gestation (4
weeks beyond
week 7), the upper
reference range
for T4 is increased by 20
%)
Slide22Slide23Slide24We have
demonstrated
that the measurement of free thyroxine by 2 different immunoassays did not reflect the expected physiological
hCG
mediated rise in the first trimester. In addition, the expected return to
nonpregnant
concentrations in the second and third trimesters was not seen. Instead, a continued decline in FT4 was identified, resulting in 57-68% of women falling into a range that would be classified as
hypothyroxinemic
by the manufacturer’s recommended ranges.
In contrast, the FT4I performed as expected, with a physiologic increase in the first trimester with normalization to
nonpregnant
levels in the second and third trimesters
Slide25Methods: A total of 466 healthy pregnant women were evaluated. After exclusion of women with
history,
ultrasonographic
, or laboratory evidence of any thyroid disorder or iodine deficiency and those who
were positive
for thyroid autoantibodies, 152 women entered the study. Serum thyrotropin (TSH), TT4,
and triiodothyronine-
resine
uptake were measured by an immunoassay method. Reference intervals were
defined as
5th and 95th percentiles, using the bootstrap-based
procedure.
Slide26Slide27IV
. Iodine Status and Nutrition
Slide28Recommendation 4
Median urinary iodine concentrations can be used to assess the iodine status of
populations,but
single spot or 24-hour urine iodine concentrations are not a valid marker for the
iodine nutritional
status of individual patients
.
(
Strong recommendation, High quality evidence
)
Slide29Kozing
et al (2011):
In
a prospective, longitudinal, 15-mo study, healthy Swiss women (n = 22) aged 52–77 y collected repeated 24-h urine samples (total n = 341) and corresponding fasting, second-void, morning spot urine samples (n = 177). From the UIC in spot samples, 24-h urinary iodine excretion (UIE) was extrapolated based on the age- and sex-adjusted
iodine:creatinine
ratio
.
The CV tended to be higher for the spot UIC (38%) than for the estimated 24-h UIE (33%) (P = 0.12). In this population, 10 spot urine samples or 24-h urine samples were needed to assess individual iodine status with 20% precision.
Slide30Recommendation
5
All
pregnant women should ingest approximately 250
μg
iodine daily. To achieve a total
of 250
μg
iodine ingestion daily, strategies may need to be varied based on country of origin
.
(
Strong recommendation, High-quality evidence)
Recommendation 6
In most regions, including the United States, women who are planning pregnancy or
currently pregnant
, should supplement their diet with a daily oral supplement that contains 150
μg
of iodine
in the form of potassium iodide.
This is optimally started 3 months in advance
of planned
pregnancy
.
(Strong recommendation, Moderate-quality evidence)
Slide31Recommendation 7
In low-resource countries and regions where neither salt iodization nor daily iodine supplements are feasible, a single annual dose of ~400 mg iodized oil for pregnant
women and
women of childbearing age can be used as a temporary measure to protect
vulnerable populations
. This should not be employed as a long-term strategy or in regions where
other options
are available
.
(
Weak Recommendation, Moderate-quality evidence
).
Recommendation
8
There is no need to initiate iodine supplementation in pregnant women who are being treated for hyperthyroidism or who are taking LT4.
(Weak recommendation, Low quality evidence)
Slide32Current Medical Research & Opinion 2015
Methods:
a total of 460 pregnant
women belonging
to non-goiter areas (group 1; n=156) and endemic areas
without (group
2; n=154) and with iodine supplementation (group 3; n=150),
and their
respective
newborns,Women
of group 3 with visible goiter were
administered 2 capsules of iodized oil orally each containing
200mg of
iodine, between 6-8 weeks of pregnancy. Blood samples were
obtained from
all groups during each trimester, at parturition (umbilical cord
blood) and
after delivery.
T3,T4
and
TSH
levels were measured by specific enzyme immunoassays.
Results
:
In group 2, serum T4 concentrations were low while T3 and TSH levels were high which showed hypothyroidism in the women of endemic areas. Goiter size decreased in most of the subjects who received a single dose of iodized oil
and resulted
in increase in serum concentrations of thyroid hormones; whereas, TSH levels decreased.
Iodinesupplementation
also
resulted in raised T4 and low TSH levels in the cord-blood of neonates.
Slide33Slide34Recommendation 10
Sustained iodine intake from diet and dietary supplements
exceeding 500
μg
daily
should be avoided during pregnancy due to concerns about the potential for fetal thyroid dysfunction.
(Strong recommendation, Moderate quality
evidence)
(
RECOMMENDATION 40
:Sustained
iodine intake from diet and dietary
supplements exceeding
500–1100
mcg
daily
should be avoided due to
concerns about
the potential for fetal
hypothyroidism.
Level
C
-USPSTF)
Slide35Method:
7190
pregnant women at 4–8 weeks gestation
were investigated
and their UIC, serum thyroid stimulating hormone (TSH), free thyroxine (FT4),
thyroidperoxidase
antibody
(
TPOAb
), thyroglobulin antibody (
TgAb
), and thyroglobulin (
Tg
)
were measured
.
Results
:
The prevalence of overt hypothyroidism was lowest in the group with UIC 150–249
mcg/L.
Prevalences
of
subclinical hypothyroidism
(2.4%) and isolated hypothyroxinemia (1.7%) were lower in the group with
UIC 150–249 mcg/L. Multivariate logistic regression indicated that excessive iodine intake (UIC 500 mcg/L
)
was
associated
with
a 2.17-fold increased risk of subclinical
hypothyroidism.
Meanwhile,
excessive iodine
intake was associated with a 2.85-fold increased risk of isolated hypothyroxinemia.
J
Clin
Endocrinol
Metab
2015
Slide36Slide37METHODS:
In this cohort study, we assessed a total of 203 pregnant women in the first trimester of pregnancy
and followed
them in the second and third trimesters. They were divided into two groups, group I with urinary iodine excretion (
UIE)<150
mg/l, and group II with UIE
>=150
mg/l. Serum samples from women were assayed for levels of total T4, T3, FT4I and
thyroidstimulating
hormone
(TSH), thyroid peroxidase antibody (
TPOAb
) and thyroglobulin antibody (
TgAb
) only once in each
trimester. Urinary
iodine concentration was measured three times and the median was considered as UIE in the first trimester, but it
was measured
only once in the second and third
trimesters.
Slide38Slide39V
. Thyroid Auto-Antibodies & Pregnancy Complications
Slide40P
REVALENCE
OF THYROID
AUTO-AB
IN
PREGNANCY?
Anti-
thyroperoxidase
or anti-thyroglobulin
thyroid autoantibodies
are present in 2 to
17% of
unselected pregnant
women.
In
U.S.populations
, thyroid antibodies are most frequent
in Caucasian
and Asian women and least frequent in
African-Americans.
Slide41A recent study from Belgium in women seeking fertility treatment showed that
both
TPOAb
and
TgAb
were present in 8% of women, while 5% demonstrated isolated
Tg
antibodies, and
4% demonstrated isolated
TPOAb
concentrations.
Those women with isolated
TgAb
positivity
had a significantly higher serum TSH than women without thyroid
autoimmunity.
While
testing
thyroid autoimmunity using only
TPOAb
would
likely miss a small proportion of women with isolated
Tg antibodies,the vast majority of studies investigating thyroid autoimmunity and clinical outcomes used only TPOAb measurements.
Slide42Recommendation 11
Euthyroid
, but TPO or
Tg
antibody positive pregnant women should have measurement
of serum
TSH concentration performed at time of pregnancy confirmation, and every 4
weeks through
mid-pregnancy.
(
Strong recommendation, High quality
evidence
)
(RECOMMENDATION 20
Euthyroid
women (not receiving LT4) who are
TAb
+ require monitoring
for hypothyroidism during
pregnancy. Serum
TSH should be evaluated every 4 weeks during
the first
half of pregnancy and
at least once between 26 and
32 weeks
gestation. Level B-USPSTF)
Slide43A
clear association
between thyroid autoimmunity and miscarriage
was observed
with a pooled odds ratio of
2.55
(95% CI
1.42–4
.
57, P
=
0.002
) in eight case–control studies and a pooled relative
risk of 2.31
(95% CI
1.90–2
.
82
, P <
0.000
01) in 14 cohort
studies. Women
with TAI were found to have slightly higher age [age
difference, 1
.
29
years] (95% CI 0.43–2.16, P = 0.003) and TSH levels [TSH difference, 0.61
mIU
/l] (
95% CI 0.51–0
.
71
, P <
0.000
01) compared with those without TAI.
Slide44Although a clear association has been demonstrated between thyroid antibodies
and spontaneous
pregnancy loss, this does not prove causality and the underlying mechanisms
for such
an association remain
unclear.
Several
mechanistic hypotheses have been proposed,
including
increased fetal resorption in active immunization murine models
antibody_mediated
mild
thyroid
hypofunction
, cross-reactivity of anti-thyroid antibodies with
hCG
receptors
on the zona
pellucida
, the presence of concurrent non-organ specific
autoimmunity, and
increased levels of endometrial cytokines in women with thyroid
autoimmunity.
Slide45ASSOCIATION BETWEEN THYROID
ANTIBODIES AND
RECURRENT SPONTANEOUS PREGNANCY LOSS IN EUTHYROID
WOMEN
The
data for an association between thyroid antibodies and recurrent pregnancy
loss are
less robust than for sporadic loss. This may be because recurrent pregnancy loss has
many potential
causes, and endocrine dysfunction may only account for 15-20 % of all such
cases.
One study
reported an apparent interaction of anti-phospholipid
antibodies (APAS
) and anti-thyroid antibodies in the risk for recurrent pregnancy
loss.
In support
of this
, Kim and colleagues reported that women with recurrent pregnancy loss who were
antithyroid
antibody
positive also demonstrated higher levels of
anticardiolipin
Ab and other
nonorgan
-specific antibodies.
Slide46Recommendation 13
Intravenous immunoglobulin treatment of
euthyroid
women with a history of
recurrent pregnancy
loss is not recommended
.
(
Weak recommendation, Low quality evidence)
Recommendation
14
There is insufficient evidence to conclusively determine whether levothyroxine
therapy decreases
pregnancy loss risk in
TPOAb
positive,
euthyroid
women who are newly
pregnant. However
, administration of levothyroxine to
TPOAb
positive,
euthyroid
pregnant
women
with a prior history of loss may be considered given its potential benefits in comparison to its minimal risk. In such cases, 25-50 mcg of levothyroxine is a typical starting dose. (Weak recommendation, Low quality evidence)(RECOMMENDATION 42 There is insufficient evidence to recommend for or against screening for thyroid antibodies, or treating in the
first trimester
of pregnancy with LT4 or IVIG, in
euthyroid
women
with sporadic or recurrent abortion or in
women undergoing
in vitro fertilization (IVF). Level
I-USPSTF)
Slide47DOES TREATMENT WITH LT4 OR IVIG DECREASE THE
RISK FOR
PREGNANCY LOSS IN EUTHYROID WOMEN WITH
THYROID AUTOIMMUNITY
?
Lepoutre
et al(
Gynecol
Obstet
Invest 2012);
In a non-randomized
, retrospective
study,analyzed
data
from 65
TPOAb
positive pregnant women with serum TSH values of 1-3.5
mU
/L at the first
mantenatal
visit
,Thirty-four of these women were treated with 50
μg LT4 daily starting at a mean 10 weeks gestation, while the others were not treated. None of the levothyroxine treated women miscarried, but 5 of 31 untreated women (16%) experienced pregnancy loss.
Slide48Methods
:
In a prospective study,
A total of 984 pregnant women were
enrolled;11.7
% were thyroid peroxidase
antibody positive
(
TPOAb
).
TPOAb
patients were divided into two groups:
group A
(
n=57
) was treated with LT4, and group B (
n=58
) was not
treated. The
869
TPOAb
patients (group C) served as a
normal population control group.
Slide49Slide50Slide51VI
. The Impact of Thyroid illness upon Infertility
&
Assisted Reproduction
Slide52Recommendation
18
There
is insufficient evidence to determine if levothyroxine therapy improves fertility
in sub clinically
hypothyroid, thyroid auto-antibody negative women who are attempting
natural conception
(not undergoing ART). However, administration of levothyroxine may
be considered
in this setting given its ability to prevent progression to more
significant hypothyroidism
once pregnancy is achieved. Furthermore, low dose levothyroxine
therapy (25-50
mcg daily) carries minimal risk
.
(Weak recommendation, Low quality evidence
)
Slide53Recommendation 19
There is insufficient evidence to determine if levothyroxine therapy improves fertility in
nonpregnant
,
euthyroid
, thyroid autoantibody positive women who are attempting natural conception (not undergoing ART). Therefore, no recommendation can be made for levothyroxine therapy in this setting.
(No recommendation, Insufficient evidence
)
Slide54IS
SUBCLINICAL HYPOTHYROIDISM
ASSOCIATED WITH INFERTILITY
IN WOMEN?
Different
definitions of subclinical hypothyroidism have been used in different
studies examining
this question, and results have been
inconsistent.
Some studies showed,
the prevalence of TSH elevations was 2.3%, similar to background
rates in
the general
population or was slightly higher.
However
, in a retrospective study, higher rates of subclinical hypothyroidism (13.9%
vs. 3.9
%) were reported in infertile women as compared to fertile
controls.
Slide55METHOD:
We
examined 69 female infertile
patients with SCH (TSH>3)
and the effects of levothyroxine
(LT4
) therapy on pregnancy rates and pregnancy outcomes were observed.
RESULTS:
Fifty-eight
(84.1%) patients successfully conceived during the T4 treatment period (Group A), although 17 patients (29.3
%) had
miscarriage afterward. The remaining 11 patients continued to be infertile (Group B). The median TSH value in
Group A
before the T4 treatment was 5.46
μIU
/mL (range 3.1-13.3) and this significantly decreased to 1.25
μIU
/mL (range
0.02-3.75
) during the treatment (
p
< 0.001). The estimated duration of infertility before the T4 treatment was 2.8±1.7 years
and the
duration until pregnancy after the treatment was significantly shorter at 0.9±0.9 years (
p
< 0.001). Anti-thyroid autoantibodies were identified in 42.0% of all patients and no significant difference was observed in positivity between Group A and Group BEndocrine Journal 2015
Slide56Slide57IS THYROID AUTOIMMUNITY LINKED TO INFERTILITY
IN WOMEN
?
Limited
evidence suggests that women with female-factor infertility are more likely
to have
positive
TPOAb
than age-matched women who are not infertile, even if
euthyroid
.
The
prevalence of anti-thyroid antibodies may be higher in women with
polycystic ovarian
syndrome (PCOS) than in age-matched
controls. (
Antithyroid
antibodies
are detectable
in the ovarian follicles of women with thyroid autoimmunity, and correlate with
serum antibody levels).
Among
infertile women with PCOS, the presence of
antithyroid
antibodies has been associated with a decreased likelihood of developing ovarian follicles in response to treatment with clomiphene citrate.
Slide58IS
MATERNAL SUBCLINICAL HYPOTHYROIDISM
ASSOCIATED WITH
WORSE ART OUTCOMES?
DOES
TREATMENT OF SUBCLINICALLY
HYPOTHYROID WOMEN
IMPROVE ART OUTCOMES
?
IS
MATERNAL ANTITHYROID AB POSITIVITY
ASSOCIATED WITH
POORER OUTCOMES FOLLOWING ASSISTED
REPRODUCTIVE TECHNOLOGY
?
Slide59Recommendation
20
Subclinically
hypothyroid women undergoing IVF or ICSI should be treated
with levothyroxine
. The goal of treatment is to achieve a TSH concentration <2.5
mU
/L.
(Strong recommendation
, Moderate quality evidence)
Slide60The
majority of evidence suggests that there is no difference in IVF outcomes
between women
with serum TSH <2.5
mU
/L and those with very mild TSH elevations, defined as a
TSH between
2.5-5
mU
/L.
Slide61Clinical Endocrinology 2014
METHODS:
A total of 627 women without past or current history
of thyroid disorder undergoing their first IVF
cycle.Pre
-IVF
archived blood serum samples
were tested
for TAI and thyroid function tests.
Main outcome measure
live
birth rate.
RESULTS:
The clinical pregnancy rate, live birth rate and miscarriage
rate were similar among women with or without TAI and/
or subclinical hypothyroidism using a TSH threshold
4.5
mIU
/l.
Thyroid autoantibody level did not affect these IVF outcomes
Slide62Method(s
):
Prospective, randomized trial
.A
total of 64 infertile patients with
SCH.
Patients were randomized into an LT4 treatment group or control group. For the LT4
treatment group
, 50 mg LT4 was administered from the first day of controlled ovarian stimulation for
IVF/ICSI.
Result(s):
There were no differences in patient characteristics between the two groups.
There
was no
significant difference
in the clinical pregnancy rate per cycle between the two groups
. However, the miscarriage rate
was significantly
lower in the LT4 treatment group than in the control group. Embryo implantation rate and live
birth rate
were significantly higher in the LT4 treatment group. In the control group, both thyroid peroxidase antibody
and thyroglobulin
antibody levels were significantly higher in the miscarried subgroup than in the delivered subgroup.
Slide63Human Reproduction
Update,2013
Slide64Slide65Slide66Recommendation
21
There
is insufficient evidence to determine whether levothyroxine therapy improves
the success
of pregnancy following ART in
TPOAb
positive,
euthyroid
women.
However,administration
of levothyroxine to
TPOAb
positive,
euthyroid
women undergoing ART
may be
considered given its potential benefits in comparison to its minimal risk.
In such cases,
25-50
mcg of levothyroxine is a typical starting dose.
(
Weak Recommendation, Low
quality evidence)
Recommendation 22
Glucocorticoid therapy is not recommended for euthyroid, thyroid auto-antibody positive women undergoing ART. (Weak recommendation, Moderate quality evidence)
Slide67Methods:
194
patients including 60 positive for
antithyroid
antibodies (
ATA) underwent
the ovarian stimulation in the standard long protocol for IVF and 30 women received the
low-dose prednisolone
from the day of oocyte retrieval.
Results
:
The overall, clinical pregnancy and live birth rate in ATA-positive patients receiving
prednisolone supplementation
was significantly higher when confronted with ATA-positive untreated subjects (60.0%
vs 30.0
%,
P
= 0.02; 46.6% vs 16.6%,
P
= 0.03; and 46.6% vs 20.0%,
P
= 0.05, respectively).
Slide68Slide69DOES OVARIAN HYPERSTIMULATION ALTER
THYROID FUNCTION?
The
presumed mechanism for this effect relates to
the rise
in TBG associated with high estrogen levels, which reduce free
thyroid hormone concentrations
and, in turn, feed back to cause serum TSH elevations. In addition,
the administered
hCG
can directly stimulate thyroidal TSH receptors, causing increases in
thyroid hormone
and subsequent
decreases
in
TSH.
Slide702011
American Society for Reproductive Medicine
Slide71Slide72The
current evidence is inconclusive regarding
OS effect
on thyroid function or
TAI.
Serum
TSH concentrations
may be
increased during or within 1 month after
OS.
In
some
women, TSH
concentrations after OS exceeded 2.5
mU
/L, which has
been proposed
as a threshold above which thyroid
hormone replacement
therapy has to be
offered.
Slide73Recommendation
23
When possible, thyroid function testing should be performed either before or 1-2 weeks
after controlled
ovarian
hyper stimulation
, since results obtained during the course of
controlled ovarian
stimulation may be difficult to interpret.
(
Weak recommendation, Moderate
quality evidence
)
Recommendation 24
In women who achieve pregnancy following controlled ovarian
hyperstimulation
,
TSH elevations
should be treated according to the recommendations outlined in Section VII.
In non-pregnant
women with mild TSH elevations following controlled ovarian
stimulation, serum
TSH measurements should be repeated in 2-4 weeks, since levels may normalize.
(Weak recommendation, Moderate quality evidence)
Slide74VII
. Hypothyroidism and Pregnancy
Slide75Several investigations report that at least 2-3% of healthy, non-pregnant women of
childbearing age
have an elevated serum
TSH.
When
iodine nutrition is adequate, the most frequent cause of hypothyroidism
is autoimmune
thyroid disease (Hashimoto’s thyroiditis).
Thyroid autoantibodies
can be detected in ~30-60% of pregnant women with an elevated
TSH concentration.
Slide76Recommendation
25
In
the setting of pregnancy, maternal hypothyroidism is defined as a TSH
concentration elevated
beyond the upper limit of the pregnancy-specific reference range
.
(
Strong recommendation
, High quality evidence)
Slide77Recommendation 26
The pregnancy-specific TSH reference range should be defined as follows:
When
available, population and trimester-specific reference ranges for serum TSH
during pregnancy
should be defined by a provider’s institute / laboratory, and should represent
the typical
population for whom care is provided. Reference ranges should be defined
in healthy
,
TPOAb
-negative pregnant women with optimal iodine intake and without
thyroid illness.
(
Strong recommendation, High quality evidence
)
Slide78…
When this is not feasible, pregnancy-specific TSH reference ranges obtained from similar patient populations, and performed using similar TSH assays should be substituted.
(Strong recommendation, High quality evidence)
If
internal or transferable pregnancy-specific TSH reference ranges are not available, an upper reference limit of ~ 4.0mU/l may be used. For most assays, this represents a reduction in the non-pregnant TSH upper reference limit of ~0.5
mU
/L.
(Strong recommendation, Moderate quality evidence
)
Slide79SHOULD
WOMEN WITH
SUBCLINICAL HYPOTHYROIDISM BE TREATED
IN PREGNANCY?
Many
prospective and retrospective studies have demonstrated an increased risk
of pregnancy
complications associated with mildly elevated maternal TSH
concentrations,especially
in
TPOAb
positive women. However, only a small number of studies
have investigated
the impact of LT4 treatment on pregnancy complications in such
women.
Slide80Recommendation
28
Pregnant
women with TSH concentrations >2.5
mU
/L should be evaluated for TPO
antibody status.
Slide81Recommendation 29
Subclinical
hypothyroidism in pregnancy should be approached as follows:
a)
Levothyroxine therapy is recommended for:
TPO
antibody positive women with a TSH greater than the pregnancy specific
reference range
(Strong recommendation, Moderate quality
evidence)
TPO
antibody negative women with a TSH greater than 10.0
mU
/L.
(Strong recommendation, Low quality evidence)
b
)
Levothyroxine therapy may be considered for:
TPO antibody positive women with TSH concentrations > 2.5
mU
/L and below
the upper
limit of the pregnancy specific reference range.
(Weak recommendation, Moderate quality evidence)
TPO
antibody negative women with TSH concentrations greater than the pregnancy specific reference range and below 10.0 mU/L. (Weak recommendation, Low quality evidence)
Slide82…
c)
Levothyroxine therapy is not recommended for:
TPO antibody negative women with a normal TSH (TSH within the pregnancy specific reference range, or < 4.0
mU
/L if unavailable).
(Strong recommendation, High quality evidence).
(RECOMMENDATION 8
SCH
has been associated with adverse maternal and
fetal outcomes
. However, due to the lack of randomized
controlled trials
there is insufficient evidence to recommend
for or
against
universal
LT4 treatment in
TAb
(-)
pregnant
women with
SCH.Level
I-USPSTF)
(
RECOMMENDATION 9 Women who are positive for TPOAb and have SCH should be treated with LT4. Level B-USPSTF)
Slide83Slide84Thyroid 2014
Slide85Slide86The
results revealed
that, through the eighth week of pregnancy,
women whose
TSH values were above the upper limit of the
pregnancy-specific
interval (SCH 2 with 5.22
<
TSH < 10
mIU
/L) and
women with isolated TAI had an elevated risk of
miscarriage,but
women with TSH values within the
reference range
for the pregnant population (SCH 1 with 2.5
<
TSH
<5.22
mIU
/L) did not have an increased risk of
miscarriage.
The
high risk of miscarriage in both SCH and
TAI-positive subjects
is highly associated with an early gestational age of miscarriage.
Slide87Slide88Gynecologic & Obstetric investigation 2012
Slide89Slide90Slide91BMJ 2017
Design:
Retrospective
cohort
study.US
administrative
database 2010-2014 5405
pregnant women with
subclinical hypothyroidism(defined
as untreated
TSH
concentration
2.5-10
mIU
/L) were treated by LT4
Results:
843 pregnant women
with a
mean TSH
of 4.8 (SD 1.7)
mIU
/L were treated
with thyroid hormone.
Compared
with the untreated group,
treated women had lower adjusted odds of pregnancy loss but higher odds of preterm delivery, gestational diabetes,and
pre-eclampsia.
The adjusted odds of pregnancy loss were lower in treated women than in untreated women if their pre-treatment TSH concentration was 4.1-10
mIU
/L (odds ratio 0.45, 0.30 to 0.65) but not if it was
2.5-4.0 mIU/L (0.91, 0.65 to 1.23) (P<0.01).
Slide92Slide93Recommendation
32
In parallel to the treatment of hypothyroidism in a general population, it is reasonable to
target a
TSH in the lower half of the trimester specific reference range. When this is not available,
it is
reasonable to target maternal TSH concentrations below 2.5
mU
/L.
(Weak recommendation, Moderate quality evidence)
(
RECOMMENDATION 11 The
goal of LT4 treatment is to normalize maternal
serum TSH
values within the trimester-specific
pregnancy reference
range (first trimester, 0.1–2.5
mIU
/L;
second trimester
, 0.2–3.0
mIU
/L; third trimester, 0.3–3.0
mIU
/L
). Level
A-USPSTF
Slide94Recommendation
37
Following
delivery, LT4 should be reduced to the patient’s preconception dose.
Additional thyroid
function testing should be performed at approximately 6 weeks postpartum
.
(Strong recommendation
, Moderate quality evidence)
Recommendation 38
Some
women in whom LT4 is initiated during pregnancy may not require LT4
postpartum. Such
women are candidates for discontinuing LT4,
especially when the LT4 dose is ≤50
mcg daily
. The decision to discontinue LT4, if desired, should be made by the patient and
their caregiver
. If LT4 is discontinued, serum TSH should be evaluated in ~ 6 weeks.
(Weak recommendation
, Moderate quality evidence)
Slide95HOW
SHOULD LT4 BE ADJUSTED POSTPARTUM?
F
ollowing
delivery, maternal LT4 dosing should be reduced to
prepregnancy
levels
and
a serum TSH assessed 6 weeks thereafter.
However
, a study demonstrated that more
than 50
% of women with Hashimoto’s thyroiditis required an increase in the
pregestational
thyroid hormone
dose in the postpartum period, presumably due an exacerbation of autoimmune
thyroid dysfunction postpartum.
In
women started on LT4 during pregnancy for
thyroid autoimmunity
in the absence of TSH elevation, the LT4 can be stopped at delivery, with
serum TSH
assessment at 6 weeks postpartum.
Slide96Recommendation 39
In the care of women with adequately treated hypothyroidism, no other maternal or
fetal testing
(such as serial fetal ultrasounds, antenatal testing, and/or umbilical blood sampling)
is recommended
beyond measurement of maternal thyroid function unless needed due to
other
circumstances
of pregnancy
.
An exception to this is women with Graves’ disease
effectively treated
with 131I ablation or surgical resection, who require
TRAb
monitoring
.
(Strong recommendation
, Moderate quality evidence)
Slide97VIII
.
Thyrotoxicosis in Pregnancy
Slide98Recommendation
42
The
appropriate management of abnormal maternal thyroid tests attributable to
gestational transient
thyrotoxicosis and/or hyperemesis
gravidarum
includes supportive
therapy,management
of dehydration, and hospitalization if needed.
Antithyroid
drugs are
not recommended
,
though beta-blockers may be considered.
(
Strong recommendation,
Moderate quality
evidence)
Slide99J
Clin
Endocrinol Metab,
2013
E
xposure
to
either MMI/CMZ
or PTU or to both in
early pregnancy was associated
with an increased prevalence of birth
defects.
The overall prevalence of birth defects was not
significantly different
for PTU vs MMI/CMZ
exposure.
The prevalence of birth defects was high in children exposed to ATD in early
pregnancy (PTU
, 8.0%; MMI/CMZ, 9.1%; MMI/CMZ and PTU, 10.1%; no ATD, 5.4%;
nonexposed
, 5.7%;
P
<.
001).
MMI/CMZ
and PTU were associated with urinary system malformation, and PTU with malformations in the face and neck region. Choanal atresia
, esophageal atresia,
omphalocele
, omphalomesenteric duct anomalies, and aplasia
cutis were
common in MMI/CMZ-exposed
children.
Slide100Slide101SHOULD ANTITHYROID MEDICATION BE WITHDRAWN
OR MODIFIED
IN EARLY PREGNANCY?
Only
a small fraction of patients who have become
TRAb
negative
during therapy will become hyperthyroid within the first
months
(
Nedrebo
et al 2002
;5
%
of
TRAb
negative patients became hyperthyroid within 8 weeks after ATD
withdrawal)
One
option when pregnancy is diagnosed in a woman receiving ATD therapy
for GD
and who, based on clinical and biochemical findings appears to be in remission, is
to withdraw
ATD medication and perform repeated thyroid function testing during the
first trimester
of pregnancy.
Slide102The risk
of rapid relapse of hyperthyroidism after medication
withdrawal
is high in
patients;
who have been treated for a
short period
(< 6 months), who have suppressed or low serum TSH while on medication
prepregnancy
, who
require >5-10 mg of MMI per day to stay
euthyroid
, who have
active
orbitopathy
or large goiter, and those who have high levels of
TRAb
Slide103Thyroid 2015
Slide104Slide105Recommendation 46
a.
In a newly-pregnant woman with Graves’ disease, who is
euthyroid
on a low dose of
MMI (
≤5-10 mg/day) or PTU (≤ 100-200 mg/day), the physician should consider discontinuing
all
antithyroid
medication given
potential teratogenic effects. The decision to stop
medication should
take into account the disease history, goiter size, duration of therapy, results of
recent thyroid
function tests,
TRAb
measurement, and other clinical factors
.
(Weak recommendation
, Low quality evidence)
Slide106…
b.
Following cessation of
antithyroid
medication, maternal thyroid function testing (TSH,
and FT4
or TT4) and clinical examination should be performed every 1-2 weeks to
assess maternal
and fetal thyroid status. If the pregnant woman remains clinically and
biochemically
euthyroid
, test intervals may be extended to 2-4 weeks during the 2
nd
and 3
rd
trimester
.
(Weak recommendation
, Low quality evidence)
c
.
At each assessment, the decision to continue conservative management (
withholding
antithyroid
medication) should be guided both by the clinical and the biochemical
assessment of maternal thyroid status. (Weak recommendation, Low quality evidence)
Slide107RECOMMENDATION 86
We suggest that the physician contacted according to recommendation 85 evaluate whether ATD withdrawal in the first trimester of pregnancy is likely to cause relapse of hyperthyroidism or not. Evaluation should be based on patient records, especially the severity of GD at time of diagnosis and current disease activity, duration of ATD therapy, current ATD dose requirement, and results of recent thyroid function and
TRAb
testing. If risk of relapse is considered low, therapy can be withdrawn, and followed by weekly thyroid function testing during the 1
st
trimester.
Weak
recommendation, low-quality evidence
Slide108Recommendation 47
In pregnant women with a high risk of developing thyrotoxicosis if
antithyroid
drugs were to be discontinued, continued
antithyroid
medication may be necessary. Factors predicting high clinical risk include being currently hyperthyroid, or requirement of> 5-10 mg/day MMI or > 100-200 mg/day PTU to maintain a
euthyroid
state. In such cases:
a.
PTU
is recommended for the treatment of maternal hyperthyroidism through 16 weeks of pregnancy.
(Strong recommendation, Moderate quality evidence)
Slide109…
b
.Pregnant women receiving MMI who are in need of continuing therapy during pregnancy should be switched to PTU as early as possible.
(Weak Recommendation, Low quality evidence)
c.
When
shifting from MMI to PTU, a dose ratio of approximately 1:20 should be used (e.g. MMI 5 mg daily = PTU 100 mg twice daily).
(Strong recommendation, Moderate quality evidence)
Slide110…
d
.
If ATD therapy is required after 16 weeks gestation, it remains unclear whether
PTU should
be continued or therapy changed to MMI. As both medications are associated
with potential
adverse effects and shifting potentially may lead to a period of less-tight control,
no recommendation
regarding switching
antithyroid
drug medication
can be
made at this time.
(No recommendation, Insufficient evidence
)
(
RECOMMENDATION 28
PTU is preferred for the treatment of hyperthyroidism in the first trimester. Patients on MMI should be switched to PTU if pregnancy is confirmed in the first trimester. Following the first trimester, consideration should be given to switching to MMI. Level I-USPSTF)
Slide111RECOMMENDATION 83
Women with hyperthyroidism caused by GD who are well controlled on MMI and desire pregnancy have several options:
a) Patients could consider definitive therapy before they become pregnant.
b) Patients could switch to PTU before trying to conceive.
c) Patients could switch to PTU as soon as pregnancy is diagnosed.
d) Appropriately selected patients could withdraw from ATD therapy as soon as pregnancy is diagnosed. If ATD therapy is withdrawn, thyroid function should be assessed weekly throughout the first trimester, then monthly.
Weak
recommendation, low-quality evidence.
Slide112In the first trimester of pregnancy some women with GD experience an exacerbation
of symptoms,
which is parallel to the moderate increase in incidence of GD in
early pregnancy.
By
the 3rd trimester the incidence of GD becomes very low
corresponding
to the general decrease in thyroid autoimmunity, with a decrease in
TRAb
.
Discontinuation
of all ATD therapy is feasible in 20-30% of patients in the last
trimester of gestation.
Maternal
serum TSH well within the reference range is a sign that the
ATD dose
has to be reduced to avoid fetal overtreatment.
Slide113Altogether 3673 women (0.9%) were identified with an onset of hyperthyroidism from 1997 to 2010, and the overall IR of maternal hyperthyroidism was 65.0/100 000/year.
The incidence rate of hyperthyroidism in and around pregnancy varied widely and was high in the first 3 months of pregnancy [(IRR): 1.50 (95% CI 1.09–2.06) ], very low in the last 3 months of pregnancy [(0.26 (0.15–0.44)], and reached the highest level 7–9 months postpartum [3.80 (2.88–5.02)].
J
Clin
Endocrinol
Metab
2015
Slide114Slide115Recommendation
50
Thyroidectomy in pregnancy may be indicated for unique scenarios. If required, the optimal time for thyroidectomy is in the second trimester of pregnancy.
If
maternal
TRAb
concentration
is high (> 3x upper reference for the assay) the fetus should be
carefully monitored
for development of fetal hyperthyroidism throughout pregnancy, even if the
mother is
euthyroid
post-thyroidectomy
.
(
Strong recommendation, High quality evidence)
Slide116The
fetal
potential complications depend
on several
factors:
poor
control of hyperthyroidism throughout pregnancy may
induce transient central hypothyroidism.
2
) excessive amounts of ATDs may be responsible for
fetal and
neonatal hypothyroidism, even if the mother is biochemically
euthyroid
.
3) high
levels of thyroid stimulating antibodies in the 2nd half of pregnancy may induce fetal
and neonatal hyperthyroidism.
The
incidence of fetal and neonatal hyperthyroidism is between 1-5% in all women with active or a past history of Graves’ hyperthyroidism.
Slide117Recommendation 52
a
.
If
the patient has a past history of Graves’ disease treated with ablation (radioiodine or surgery), a maternal serum determination of
TRAb
is recommended at initial thyroid function testing during early pregnancy.
(Strong recommendation, Moderate quality evidence)
b
.
If maternal
TRAb
concentration is elevated in early pregnancy, repeat testing should occur at weeks 18-22.
(
Strong recommendation, Moderate quality evidence)
Slide118…
c
.
If maternal
TRAb
is undetectable or low in early pregnancy, no further
TRAb
testing
is needed
.
(
Weak recommendation, Moderate quality evidence)
d
.
If a patient is taking ATDs for treatment of Graves’ hyperthyroidism when pregnancy
is confirmed
, a maternal serum determination of
TRAb
is recommended.
(
Weak recommendation
, Moderate quality evidence
)
Slide119…
e
.
If the patient requires treatment with ATDs for Graves’ disease through mid pregnancy,
a repeat
determination of
TRAb
is again recommended at weeks 18-22
.
(
Strong recommendation
, Moderate quality evidence
)
f
.
If elevated
TRAb
is detected at weeks 18-22 or the mother is taking ATD in the
third trimester
, a
TRAb
measurement should again be performed in late pregnancy (weeks
30-34
) to evaluate the need for neonatal and postnatal monitoring.
(Strong recommendation, High quality evidence)(RECOMMENDATION 32 If the patient has a past or present history of Graves’ disease,a maternal serum determination of TRAb should be obtained at 20–24 weeks gestation. Level
B-USPSTF)
Slide120RECOMMENDATION 93
Patients who were treated with RAI or thyroidectomy for GD prior to pregnancy should have
TRAb
levels measured using a sensitive assay initially during the first trimester thyroid function testing and, if elevated, again at 18-22 weeks of gestation.
Strong
recommendation, low-quality evidence.
Slide121RECOMMENDATION 95
Patients with elevated
TRAb
levels at 18-22 weeks of gestation should have
TRAb
remeasured
in late pregnancy (weeks 30-34) to guide decisions regarding neonatal monitoring. An exception to this is a woman with an intact thyroid who is no longer in need of ATD therapy
.
Strong recommendation, low-quality evidence.
Slide122European Journal of Endocrinology 2014
Methods: Sixty-eight neonates born to mothers with GD were managed from birth and divided into three groups
based on
thyrotropin receptor antibody (
TRAb
) and anti-thyroid drug (ATD) status in the mother:
TRAb
-/ATD-, n=27;
TRAb
-
/ATD
+
, n=8
; and
TRAb
+
/ATD
+
, n=33
.
The
main outcome measures were clinical examination,
thyroid function
tests (TSH, free thyroxine (FT
4), free triiodothyronine, and TRAb) echocardiography, thyroid ultrasonography, and
bone maturation assessment
Slide123Slide124HOW SHOULD HYPERTHYROIDISM CAUSED BY AUTONOMOUS
THYROID NODULES BE HANDLED IN
PREGNANCY?
In pregnancy, a major difference from GD is that no
TRAb
is produced by the
mother, and
consequently the fetal thyroid is not stimulated as it is in
GD.
ATD therapy
to make
the mother
euthyroid
would significantly increase the risk of hypothyroidism and goiter
in the fetus.
The early pregnancy
high
hCG
level may theoretically activate non-affected normal thyroid tissue
and increase
thyroid secretion in early
pregnancy.
Women
with
such disease
should probably refrain from taking iodine-containing supplements in
pregnancy.
Slide125Recommendation
55
If
ATD therapy is given for hyperthyroidism caused by autonomous nodules, the fetus
should be
carefully monitored for goiter and signs of hypothyroidism during the 2
nd
half
of pregnancy
. A low dose of ATD should be administered with the goal of maternal FT4 or
TT4 concentration
at or moderately above the reference range.
(
Strong recommendation,
Low quality
evidence)
Slide126IX
. Thyroid Nodules and Thyroid Cancer during
Pregnancy
Slide127Recommendation
60
Pregnant
women with
cytologically
benign thyroid nodules do not require special
surveillance strategies
during pregnancy, and should be managed according to the 2015 ATA
Management Guidelines
for Adult Patients with Thyroid Nodules and Differentiated Thyroid Cancer.
(Strong recommendation, Moderate quality evidence
)
Recommendation
61
Pregnant women with
cytologically
indeterminate (AUS/FLUS, SFN, or SUSP) nodules,
in the
absence of
cytologically
malignant lymph nodes or other signs of metastatic disease,
do not
routinely require surgery while pregnant.
(
Strong recommendation, Moderate
quality evidence
)
Slide128
Recommendation 62
During pregnancy
,
if there is clinical suspicion of an aggressive behavior in
cytologically
indeterminate
nodules, surgery may be considered.
(
Weak recommendation, Low
quality evidence
)
RECOMMENDATION 57
Thyroid hormone therapy may be considered in pregnant women who have deferred surgery for well differentiated thyroid carcinoma until postpartum. The goal of LT4 therapy is a serum TSH level of 0.1–1.5mIU/
L.Level
I-USPSTF
Slide129X
. Fetal and Neonatal Considerations
Slide130Recommendation 71
A history of maternal thyroid illness, use of
antithyroid
medications (PTU, MMI)
during gestation
, or measurements of abnormal maternal thyroid function or
TRAb
during
gestation should
be communicated to the newborn’s neonatologist or pediatrician
.
(Strong recommendation
, Moderate quality evidence)
Recommendation 72
The
severity of maternal and fetal thyroid illness should guide the timing of
communication. Severe
, progressive, or complex thyroid illness during pregnancy mandates
communication with
the neonatologist or pediatrician before birth and consideration of consultation with
a pediatric
endocrinologist. Most other illness is optimally communicated shortly after birth.
(Strong recommendation, Moderate quality evidence)
Slide131HOW
IS
NEONATAL HYPOTHYROIDISM
TREATED?
In women receiving
antithyroid
drugs,transfer
of the
medication can potentially induce neonatal hypothyroidism.
In
such cases,
neonatal metabolism
removes the remaining MMI or PTU from the newborn circulation. This results
in the
return of normal thyroid function
,
within 3 to 5 days.
For
neonates with
congenital hypothyroidism
, levothyroxine must be administered. The recommended starting dose for
fullterm
infants
is 10 to 15 mcg/kg/day,depends on the severity.In premature hypothyroid infants a lower dose is generally utilized. For optimal cognitive outcomes, therapy should be initiated within two weeks of life.
Slide132Age-dependent normative values for TSH and T4 should be used to guide therapy. Until further information becomes available, infants with severe congenital hypothyroidism (i.e. - initial serum TSH concentration >100
mU
/L) should remain on a single formulation of L-thyroxine without substitution
.
The
presence of a goiter in a newborn should prompt referral to a pediatric endocrinologist. An ultrasound examination should be performed to evaluate the patency of the trachea.
A
goiter may reflect a hypothyroid or hyperthyroid state in response to maternal thyroid illness, or overtreatment with
antithyroid
medications.
Slide133HOW
IS
NEONATAL HYPERTHYROIDISM
TREATED?
Most neonatal hyperthyroidism is caused by maternal transfer of
TRAb
to the
fetus.
Typically
, neonatal Graves’ disease does not present until the end of the first week of life
when maternal
antithyroid
drug, but not the
TRAb
, have been cleared from the neonatal
circulation.
This
may be delayed in babies born to mothers with a mixture of stimulating and
blocking antibodies
. Thus, results on newborn screening may be paradoxically
normal.
Slide134The conventional treatment for neonatal hyperthyroidism is PTU 5 to10 mg/kg administered in divided doses
However
recent evidence of rare hepatotoxicity due to this agent has led to a switch to MMI therapy (0.5 to 1 mg/day) by many pediatric endocrinologists.
Propranolol
(2 mg/kg) may be added if the hyperthyroidism is severe
.
Close follow up of the affected newborn is important, with downward adjustment in the dose of
antithyroid
drug required as the hyperthyroidism resolves.
Slide135The
usual duration of neonatal Graves’ disease is 1 – 3 months, but depends on antibody potency.
Separate
from neonatal Graves’ disease (which is
selflimited
),neonatal hyperthyroidism may rarely be caused by a gain-of-function mutation in the TSH receptor, or by McCune-Albright syndrome. In such cases, newborn hyperthyroidism may be
permanent.
Slide136XI
.
Thyroid Disease and Lactation
Slide137Abnormal maternal thyroid hormone concentrations (both hypothyroidism
and hyperthyroidism
) can impact milk letdown and the ability to successfully
breastfeed
While there
are no controlled or randomized human
trials interventional
trials in non-human mammals corroborate
these findings
Slide138Recommendation
74
As
maternal hypothyroidism can adversely impact lactation, women experiencing
poor lactation
without other identified causes should have TSH measured to assess for
thyroid dysfunction
.
(
Weak recommendation, Low quality evidence)
Recommendation
75
Given its adverse impact upon milk production and letdown
, subclinical and
overt hypothyroidism
should be treated in lactating women seeking to breastfeed
.
(Weak recommendation
, Low quality evidence
)
Slide139Recommendation 76
The impact of maternal hyperthyroidism upon lactation is not well understood. Therefore, no recommendation to treat maternal hyperthyroidism on the grounds of improving lactation can be made at this time.
(No recommendation, Insufficient Evidence)
Slide140Recommendation 77
The use of
131
I
is contraindicated during lactation. If required
,
123
I
can be used if breast milk is pumped and discarded for 3-4 days before breastfeeding is resumed. Similarly, Tc-99m
pertechnetate
administration requires breast milk to be pumped and discarded during the day of testing.
(Strong recommendation, Moderate quality evidence)
Slide141Recommendation 78
Excepting treatment decisions specifically made on the grounds of improving
lactation (discussed
above), the decision to treat hyperthyroidism in lactating women should be
guided by
the same principles applied to non-lactating women
.
(
Strong recommendation,
Low quality
evidence)
Slide142ARE
ANTITHYROID MEDICATIONS (PTU,
MMI) TRANSFERREDIN TO
BREAST MILK, AND WHAT ARE THE CLINICAL CONSEQUENCES TO
THE BREASTFED INFANT?
Using PTU only
a very small amount of the drug is transferred from maternal serum into breast
milk (
0.007-0.077% of the ingested
dose)
Some studies report
elevated TSH within one week of birth, however, these values
normalized thereafter
despite continued breastfeeding. This suggests the cause of neonatal
hypothyroidism in
these infants was
transplacental
passage of PTU before birth, as opposed to any adverse
effect of
PTU transferred via breast
milk.
Studies
of MMI or CM, confirm a 4-7 fold higher proportion of the
medication transferred
into maternal milk in comparison to PTU.
Slide143Study A
. Twelve women with thyrotoxicosis
received
methimazole
therapy during pregnancy and were
permitted to
breast-feed exclusively after delivery. Mothers were
taking 5
mg maintenance doses of
methimazole
daily.
Clinical status
and
T4,T3,TSH,
and resin T3 uptake in their infants were
evaluated after
1 month of lactation.
Study
B. Seventeen women in whom thyrotoxicosis
had developed
2 to 8 months after delivery were given
methimpazole,5 mg BID
and allowed to continue
breastfeeding exclusively
, with supplements given to infants
older than 6 months of age. Clinical status and serum investigation were evaluated in both mothers and infants were evaluated before and after 4 weeks of treatment with methimazoleStudy C:…J Pediatr 1996
Slide144Study C
Slide145Recommendation 79
When
antithyroid
medication is indicated for women who are lactating, both MMI (up
to maximal
dose of 20 mg daily) and PTU (up to maximal dose of 450 mg daily) can
be administered
. Given a small, but detectable amount of both PTU and MMI transferred
into breast
milk, the lowest effective does of MMI/CM or PTU should always be administered
.
(Strong recommendation, Moderate quality evidence)
Slide146Recommendation
80
Breastfed children of women who are treated with
antithyroid
drugs should be monitored for appropriate
growth and development during routine pediatric health and wellness
evaluations. Routine
assessment of serum thyroid function in the child is not recommended.
(Weak recommendation
, Moderate quality evidence)
Slide147XII
.
Postpartum thyroiditis
Slide148Recommendation 86
During the
thyrotoxic
phase of PPT, symptomatic women may be treated with
beta-
blockers.A
beta-blocker which is safe for lactating women, such as Propranolol or
Metoprolol
, at
the lowest
possible dose to alleviate symptoms is the treatment of choice. Therapy is
typically required
for a few weeks
.
(
Strong recommendation, Moderate quality evidence)
Slide149Recommendation 90
If levothyroxine is initiated for PPT, discontinuation of therapy should be attempted
after
12
months
. Tapering of levothyroxine should be avoided when a woman is actively
attempting pregnancy
or is pregnant.
(Weak
recommendation
, Low quality evidence
)
(RECOMMENDATION 69; …Tapering of
LT4 should be avoided when a woman is
actively attempting
pregnancy,
is breastfeeding
, or is
pregnant)
Slide150XIII
. Screening for Thyroid Dysfunction Before or
During Pregnancy
Slide151A survey
to study current practices in the screening and management of hypothyroidism in pregnancy. We
collected completed
questionnaire survey based on clinical case scenarios from 321 members of the Asia-Oceania
Thyrpid
Association (AOTA
). Responses from 310 clinician members (from 21 Asian countries) were analyzed.
Slide152Slide153In the recent 2014 ETA guidelines, the majority
of authors
recommended universal screening because of the beneficial effects of treatment for
overt hypothyroidism
, and the fact that the targeted approach will miss a large percentage of
women with
subclinical
hypothyroidism.
American Society for Reproductive Medicine
recommends TSH
testing in all infertile women attempting pregnancy and in “high-risk women” in
early pregnancy.
Slide154M
any have argued
that screening for thyroid dysfunction must occur very early in pregnancy (e.g. 4-7
weeks of
gestation) to maximize potential benefits of levothyroxine treatment upon pregnancy loss
rates and
possibly neurocognitive development.
The
largest prospective screening studies thus
far have
provided data most translatable to typical pregnancy care currently provided
worldwide, with
initial evaluation between 10-15 weeks of gestation. This is important to consider, as
the feasibility
of any screening earlier in gestation is unclear.
Slide155Thank you