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Thyroid Disorders in Pregnancy

RCOG Green-top Guideline No. 76 Management of Thyroid Disorders in Pregnancy. Last reviewed: Apr 2025.

Implications / Complications

Scenario Maternal risk Fetal / newborn risk
Untreated / undertreated hypothyroidism Increased risk of:

  • Miscarriage
  • Pre-eclampsia
  • Pregnancy-induced hypertension
  • Postpartum haemorrhage
Increased risk of:

  • Perinatal death
  • Preterm birth
  • Low birth weight

Major implication: impaired fetal neurodevelopment and lower IQ

Untreated / poorly controlled hyperthyroidism Increased risk of:

  • Pre-eclampsia
  • Maternal heart failure
  • Maternal admission to ICU
Increased risk of:

  • Fetal growth restriction
  • Preterm birth
  • Stillbirth
  • Low birth weight

In contrast, treating maternal hyperthyroidism can risk neonatal hypothyroidism (as the drug can cross the placenta)

Pre-Existing Thyroid Disorders

Graves’ Hyperthyroidism

Pre-Conception

Discuss the option of definitive treatment with radioactive iodine or thyroidectomy prior to conception, especially in those with severe disease.

Following definitive treatment, wait at least 6 months before attempting to conceive and only when 2 measurements (3 months apart) are within the reference range.

Early Pregnancy Management

Management aspect Key principles
Anti-thyroid drugs In 1st trimester: propylthiouracil is preferred

  • If the patient conceives while taking carbimazole → switch to propylthiouracil
  • Rationale: Carbimazole carries a higher teratogenic risk during the 1st trimester

In 2nd and 3rd trimester: switch back to carbimazole

  • Rationale: to avoid risk of maternal hepatotoxicity associated with prolonged use of propylthiouracil
Tests and monitoring Monitor:

  • TFT every 2-4 weeks (4-8 weekly TFT after 20 weeks)
  • TSH receptor antibody level in 1st trimester
    • If elevated / woman is taking antithyroid drugs → further measurement at 20 and 28 weeks

Treatment aim: maintain free T4 at the upper half of normal

Fetal monitoring Serial ultrasound with umbilical artery Doppler monthly at 26-28 weeks is recommended if:

  • Required antithyroid drug treatment
  • Uncontrolled Graves’ disease at any time during pregnancy
  • TSH receptor antibody level 3x above threshold

ROCG recommends considering discontinuing antithyroid drugs with close TFT monitoring if:

  • Euthyroid prior to conception, and
  • On low-dose antithyroid drug for ≥6 months

Hypothyroidism

Pre-Conception

Aim for TSH ≤2.5 mU/L before conception.

Management During Pregnancy

Upon pregnancy confirmation → increase the existing levothyroxine dose by 25-30%

  • Double the dose on 2 days of each week, or
  • Increase 25 mcg per day (if taking <100 mcg) or 50 mcg per day (if taking >100 mcg)

Postpartum Management

Following birth: revert to pre-conception dose of levothyroxine at 2 weeks postpartum

Newly Diagnosed Thyroid Disorders During Pregnancy

Overt Hypothyroidism

Definition

  • ↑ TSH
  • ↓ Free T4

Management During Pregnancy

Start levothyroxine immediately and continue throughout pregnancy

  • Initial dose: 1.6 mcg/kg/day
  • Aim: TSH ≤2.5 mU/L
  • TFT every 4-6 weeks until 20 weeks, then repeat once at 28 weeks

Postpartum Management

  • Stop levothyroxine following birth
  • Check TFT 6 weeks postpartum to determine if long-term treatment is necessary

Subclinical Hypothyroidism

Definition

  • ↑ TSH (above pregnancy-specific reference range)
  • Normal free T4

Management During Pregnancy

Management depends on TSH level:

TSH level (mU/L) Management
>10 Start levothyroxine immediately (treat as overt hypothyroidism)
<10 Consider levothyroxine treatment (especially if +ve anti-TPO antibodies or IVF pregnancy), or

No treatment + TFT every 4-6 weeks until 20 weeks, then again at 28 weeks

Postpartum Management

  • Stop levothyroxine following birth
  • Check TFT 6 weeks postpartum to determine if long-term treatment is necessary

Hyperthyroidism

Definition

  • ↓ TSH
  • ↑ T4

Management During Pregnancy

Initiate antithyroid drugs, choice of drug depends on when the diagnosis is made:

  • 1st trimester: propylthiouracil (if still necessary beyond 20 weeks → switch to carbimazole)
  • 2nd and 3rd trimester: carbimazole

Start with the lowest effective dose to maintain free T4 at the upper half of normal. Monitor TFT every 2-4 weeks during the first half of the pregnancy

Because maternal thyroid autoimmunity naturally subsides as the pregnancy progresses, many women will be able to gradually reduce their dose.

Most women can safely discontinue treatment entirely in the late second or early third trimester.

Radioactive iodine should be avoided during pregnancy.

Surgery is rarely performed during pregnancy; it is reserved for severe cases, such as when a woman has severe adverse reactions to antithyroid drugs or a large goitre that could compromise the airway.

Postpartum Management

Maternal management:

  • Check TFT 6-8 weeks after birth
  • If treatment is still required, both carbimazole and propylthiouracil are safe for breastfeeding (use the lowest effective dose during lactation)

The newborn must have their TFTs monitored soon after birth and again at 1–2 weeks post-birth

  • This is critical to check for neonatal hyperthyroidism (caused by the mother’s stimulating antibodies crossing the placenta) or neonatal hypothyroidism (caused by maternal antithyroid drug treatment)

References

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