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4-18 HYPOTHYROIDISM: Screening and
subclinical disease
Clinical and subclinical hypothyroidism are
common, especially in older women. The presence of
subclinical hypothyroidism (elevated TSH; normal
thyroxine) or thyroid antibodies increases the risk of
developing overt hypothyroidism. The risk is greater if
both are present.
"Even within the reference range of around 0.5-4.5
mU/L, a high thyroid stimulating hormone concentration
(> 2 mU/L) was associated with an increased risk of
future hypothyroidism.
Case finding in women over 40 with non-specific symptoms
is the best approach to detect unsuspected
hypothyroidism.
Modest symptomatic benefits may occur with thyroxine
treatment in some patients with subclinical
hypothyroidism. Lipid profiles may improve.
The high frequency of abnormal thyroid function tests in
acutely ill patients means that testing at this time
should be reserved for those in whom there is clinical
suspicion of thyroid dysfunction. BMJ April 19, 1997;
314: 1175-78Reference
Article
4-18 HYPOTHYROIDISM: Screening and
subclinical disease
This narrative clinical review expands on some
of the recently published consensus views on
hypothyroidism, in particular the role of screening and
the need for treatment of subclinical hypothyroidism. I
abstracted some highlights. RTJ
- Subclinical
hypothyroidism: raised thyroid stimulating
hormone (TSH) level with a normal thyroxine
level. The condition can be graded: Grade
1TSH > upper limit of reference range
(less than 10 mU/L); grade 2TSH 10-20 mU/L;
grade 3over 20 mU/L. Symptoms are
increasingly likely with higher TSH
concentrations.
- Clinical or overt
hypothyroidism: TSH is high and the thyroxine
level is low. The probability of developing overt
hypothyroidism increases steadily with age,
reaching 1 to 2/100 per year in women age 75-80.
The risk of overt hypothyroidism increases in
women with subclinical hypothyroidism: Relative
risk (RR) = 8 for those with elevated TSH or with
thyroid antibodies. RR = 38 for those with both
elevated TSH and thyroid antibodies (about 5% per
year.)
"Even within the reference range of around
0.5-4.5 mU/L, a high thyroid stimulating hormone
concentration (> 2 mU/L) was associated with
an increased risk of future hypothyroidism. The
simplest explanation is that thyroid disease is
so common that many people predisposed to thyroid
failure are included in a laboratorys
reference population, which raises the question
whether thyroxine replacement is adequate in
patients with thyroid stimulating hormone levels
above 2 mU/L"
- Screening: Screening
for hypothyroidism is as favorable as screening
for hypertension in the same age groups.
Screening may be reasonable when focused on women
over 40 visiting the doctor for non-specific
symptoms.
- Special groups: Women
with diabetes are predisposed. Ideally, all
diabetic women should have thyroid antibody
measurements in the first trimester with careful
follow-up of those with positive results. Also,
any woman who develops postpartum thyroiditis
should be offered annual follow-up, as a quarter
of these women will develop overt hypothyroidism
within the next five years.
- Treatment of
subclinical hypothyroidism: Modest symptomatic
benefits may occur with thyroxine treatment in
some patients with subclinical hypothyroidism.
Lipid profiles may improve. Thyroxine replacement
may prevent onset of overt hypothyroidism. This
is particularly persuasive for people with raised
TSH plus thyroid antibodies. Thyroxine
requirements are less in this group than in those
with overt hypothyroidism. Careful monitoring is
needed.
Disadvantages of
treatment: Providing the TSH concentrations are restored
to the reference range there are no clinical risks.
Subclinical iatrogenic hyperthyroidism must be avoided.
It is associated with risk of atrial fibrillation and
osteoporosis. On balance, the risks of properly monitored
thyroxine treatment are almost non-existent.
CONCLUSION
Clinical and subclinical hypothyroidism are common,
especially in older women.
The presence of subclinical hypothyroidism (elevated TSH)
or thyroid antibodies increases the risk of developing
overt hypothyroidism. The risk is greater if both are
present.
Case finding in women over 40 with non-specific symptoms
is the best approach to detect unsuspected
hypothyroidism.
Modest symptomatic benefits may occur with thyroxine
treatment in some patients with subclinical
hypothyroidism. Lipid profiles may improve.
The high frequency of abnormal thyroid function tests in
acutely ill patients means that testing at this time
should be reserved for those in whom there is clinical
suspicion of thyroid dysfunction. (See algorithm for
managing subclinical hypothyroidism fig. 2 p. 1178 )
BMJ April 19, 1997; 314: 1175-78 Narrative review
from Univ. Of Sheffield Clinical Sciences Centre, UK
Comment:
I believe routine TSH measurements are justifiable during
clinical encounters with older patients who present with
non-specific symptoms. (No need to do simultaneous T4
determinations.) The only additional cost would be the
cost of the test.
A new point to me was that TSH concentration above 2 mU/L
are associated with an increased risk of hypothyroidism.
We should pay particular attention to patients who have
TSH levels at the higher range of TSH reference levels.
There is a lot of information in the 4 page article. RTJ
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