Management of Thrombocytopenia in Pregnancy
Pregnant patients with thrombocytopenia should be managed based on platelet count thresholds and trimester, with corticosteroids and IVIg as first-line treatments when intervention is needed, and the mode of delivery should be determined by obstetric indications alone—not by maternal platelet count.
Diagnosis and Initial Evaluation
The diagnosis of immune thrombocytopenic purpura (ITP) in pregnancy requires exclusion of pregnancy-specific causes 1:
- Rule out these pregnancy-specific conditions: gestational thrombocytopenia, preeclampsia, HELLP syndrome, DIC, folate deficiency, massive obstetrical hemorrhage, acute fatty liver, and antiphospholipid antibody syndrome 1
- Bone marrow examination is NOT required to diagnose ITP in pregnancy 1
- Antiplatelet antibody testing has no value in routine diagnosis 1
- Blood pressure and liver function tests should be obtained to exclude preeclampsia 1
Key distinction: Gestational thrombocytopenia (the most common cause) typically presents with platelet counts >70,000/μL, no history of thrombocytopenia before pregnancy, and no bleeding symptoms 2, 3. ITP patients often have a history of thrombocytopenia prior to pregnancy or lower platelet counts 3.
Treatment Thresholds by Trimester
First and Second Trimesters
Treatment is indicated when 1:
- Platelet count <20,000-30,000/μL (even if asymptomatic)
- Any symptomatic bleeding regardless of platelet count
- Need for procedures requiring higher platelet counts
Patients with platelets ≥30,000/μL do NOT routinely require treatment in the first two trimesters 1.
Third Trimester and Delivery Planning
- Increase monitoring frequency as delivery approaches, since platelet counts may fall in the third trimester 1
- Target platelet count ≥50,000/μL for vaginal delivery or cesarean section 1
- Target platelet count ≥75,000/μL for neuraxial (epidural/spinal) anesthesia per anesthesiologists, though hematologists consider ≥50,000/μL adequate 1
First-Line Treatment Options
Corticosteroids
- Prednisone 10-20 mg/day initially, adjusted to minimum dose maintaining hemostatic platelet count 1
- Avoid aggressive tapering in the final weeks before delivery due to risk of worsening thrombocytopenia 1
- After delivery, taper slowly to prevent rapid platelet count decline and monitor mental state 1
- Caution: High doses may affect the fetus, though prednisone is largely metabolized by placental 11-beta-hydroxylase 1
Intravenous Immunoglobulin (IVIg)
- Use when: corticosteroids are ineffective, significant side effects occur, or more rapid platelet increase is required 1
- Dosing: Single infusions can be repeated as needed to maintain safe platelet counts for delivery 1
- Response rates similar to non-pregnant patients 1
- Appropriate for platelets <10,000/μL in third trimester 1
IV Anti-D (Rh-Positive Patients Only)
- Dose: 50-75 μg/kg in non-splenectomized Rh(D)-positive patients 1
- Effective and safe in second and third trimesters 1
- Often requires augmentation with corticosteroids or IVIg to achieve target platelet count of 50,000/μL 1
- Monitor neonate for jaundice, anemia, and positive direct antiglobulin test 1
Second-Line and Refractory Treatment
For patients failing first-line therapy 1:
- Combine first-line treatments (corticosteroids + IVIg) in weeks before delivery 1
- High-dose methylprednisolone (1000 mg) possibly with IVIg or azathioprine 1
- Azathioprine: Safe during pregnancy based on SLE and transplant data, but response is slow 1
- Cyclosporin A: Not associated with significant maternal or fetal toxicity 1
- Splenectomy: If necessary, best performed in second trimester; may be done laparoscopically but difficult beyond 20 weeks 1
Medications to AVOID During Pregnancy
These are contraindicated due to teratogenicity 1, 4:
- Vinca alkaloids
- Rituximab
- Danazol
- TPO-receptor agonists (eltrombopag has insufficient safety data) 5
- Most immunosuppressive drugs except azathioprine
Management of Delivery
Mode of Delivery
The mode of delivery should be determined by obstetric indications alone—NOT by maternal platelet count 1. This is critical to understand:
- No evidence that cesarean section is safer for thrombocytopenic fetuses than uncomplicated vaginal delivery 1
- Cesarean section is actually riskier for the mother in most cases 1
- Most neonatal hemorrhagic events occur 24-48 hours after delivery at the nadir of platelet count, not during delivery itself 1
- Neonatal mortality rate is <1% in babies born to mothers with ITP 1
- Severe neonatal thrombocytopenia occurs in only 8.9-14.7% of cases, with intracranial hemorrhage in 0-1.5% 1
Platelet Transfusions
Prophylactic platelet transfusions before delivery are appropriate when 1:
- Platelets <10,000/μL with planned cesarean section
- Platelets <10,000/μL with epistaxis or mucous membrane bleeding and expected vaginal delivery
- Unnecessary when platelets >30,000/μL without bleeding symptoms 1
Hospitalization Criteria
Hospitalize patients with 1:
- Platelets <20,000/μL with significant mucous membrane bleeding
- Severe, life-threatening bleeding: Treat with high-dose parenteral corticosteroids, IVIg, and platelet transfusions 1
Neonatal Management
Monitoring
- Check neonatal platelet count for 3-4 days after birth 1
- Brain imaging (ultrasound) if platelet count at birth is <20,000/μL 1
- Consider brain imaging even if platelets 20,000-50,000/μL, even without neurologic abnormalities 1
Neonatal Treatment
- IVIg appropriate if infant's platelets <20,000/μL without evidence of intracranial hemorrhage 1
- Platelets 20,000-50,000/μL do not necessarily require IVIg 1
- Do NOT treat with IVIg or corticosteroids if platelets >50,000/μL 1
Important: Fetal/neonatal platelet count cannot be reliably predicted by maternal platelet count or antibody levels 1, 6.
Common Pitfalls to Avoid
- Do not perform routine cesarean sections based solely on maternal ITP diagnosis—this outdated practice increases maternal risk without proven fetal benefit 1
- Do not use fetal scalp sampling for platelet counts to guide delivery mode, as this is no longer recommended practice 1
- Do not aggressively taper corticosteroids in the final weeks before delivery 1
- Do not assume gestational thrombocytopenia is ITP—most asymptomatic pregnant patients with mild thrombocytopenia (>70,000/μL) have benign gestational thrombocytopenia 2, 3
- Do not use teratogenic medications like rituximab or TPO-receptor agonists 1, 4, 5
Multidisciplinary Collaboration
Optimal management requires collaboration among 1:
- Obstetrician experienced in ITP management
- Hematologist
- Obstetric anesthetist
- Neonatologist