Gestational Diabetes - Sweet Baby, Sour Mom
- Pathophysiology: Human placental lactogen (hPL) and other placental hormones ↑ insulin resistance in the mother.
- Screening & Diagnosis: Standard two-step approach.

- Maternal Risks: ↑ risk of preeclampsia, C-section, and future Type 2 DM.
- Fetal Risks: Macrosomia, neonatal hypoglycemia, polycythemia, respiratory distress.
⭐ High-Yield: Fetal macrosomia results from fetal hyperinsulinemia (insulin as a growth factor). After birth, persistent hyperinsulinemia with loss of maternal glucose supply causes profound neonatal hypoglycemia.
Thyroid Disorders - Bumps, Babies, & Butterflies
- Physiologic Changes: ↑ Estrogen → ↑ Thyroxine-binding globulin (TBG) → ↑ Total T4. hCG can weakly stimulate TSH receptors, causing transient hyperthyroidism.
- Maternal Hypothyroidism: Key risk is impaired fetal neurodevelopment (cretinism). Requires ↑ levothyroxine dose.
- Maternal Hyperthyroidism (Graves'):
- 📌 Propylthiouracil (PTU) for Primary (1st) trimester.
- Methimazole for 2nd/3rd trimesters to avoid PTU hepatotoxicity.
⭐ TSH-receptor antibodies (TSI) are IgG and can cross the placenta, causing fetal/neonatal thyrotoxicosis.
Preeclampsia & HELLP - When Pregnancy Gets Pressured
- Preeclampsia: New-onset hypertension (BP >140/90 mmHg) after 20 weeks gestation PLUS proteinuria or signs of end-organ damage.
- Pathophysiology: Defective spiral artery remodeling → placental ischemia → release of anti-angiogenic factors (e.g., sFlt-1) → systemic endothelial dysfunction.
- HELLP Syndrome: A severe manifestation of preeclampsia.
- Hemolysis (schistocytes on smear, ↑LDH)
- Elevated Liver enzymes (AST, ALT)
- Low Platelets (<100,000/μL)
- Management:
- Definitive cure: Delivery of the placenta.
- Seizure prophylaxis: Magnesium sulfate (MgSO₄).
- BP control: Hydralazine, Labetalol, Nifedipine.
⭐ The definitive treatment for preeclampsia/HELLP syndrome is delivery of the fetus and placenta, which resolves the underlying pathology.

Pituitary & Adrenal Issues - The Other Endocrine Players
- Sheehan Syndrome: Postpartum pituitary necrosis due to severe hemorrhage & hypotension.
- Presents with failure to lactate (↓ prolactin), amenorrhea, adrenal insufficiency (↓ ACTH), and hypothyroidism (↓ TSH).
- Onset is often gradual.
- Lymphocytic Hypophysitis: Autoimmune pituitary inflammation, usually in late pregnancy or postpartum.
- Can mimic a pituitary adenoma, causing headaches, visual defects, and hypopituitarism.
- Adrenal Insufficiency (Addison's): Requires increased glucocorticoid doses during pregnancy and stress-dose steroids for labor to prevent adrenal crisis.
⭐ Failure to lactate is the most common initial sign of Sheehan syndrome.

High‑Yield Points - ⚡ Biggest Takeaways
- Gestational diabetes is driven by hPL-induced insulin resistance; screen at 24-28 weeks.
- Maternal hyperglycemia → fetal hyperinsulinemia → macrosomia & neonatal hypoglycemia.
- hCG stimulates TSH receptors, raising total T4; free T4 and TSH levels remain normal.
- Graves' disease often improves during pregnancy; maternal anti-TSH receptor antibodies can cause fetal thyrotoxicosis.
- Postpartum thyroiditis presents as transient hyperthyroidism, often followed by a hypothyroid phase.
- Sheehan syndrome is postpartum pituitary necrosis causing failure to lactate and hypopituitarism.
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