ITP , TTP vs. HUS vs. DIC Flashcards
(21 cards)
Autoantibodies against GPIIb/IIIa receptors
Immune Thrombocytopenia (ITP)
Secondary (Associated Conditions) of immune thrombocytopenia
o Autoimmune: Lupus (SLE)
o Hematologic: CLL
o Infectious: HIV, Hepatitis C, CMV, Varicella
Treatment of Immune thrombocytopenia
In children:
Often self-resolving, monitor unless severe
Treatment of Immune thrombocytopenia
Adult : Often chronic, requires treatment if platelets <30,000/µL
o First-line: Corticosteroids
o Second-line: IVIG
o Refractory cases: Splenectomy
o Platelet transfusion only for severe bleeding
Deficiency of ADAMTS13 (vWF-cleaving protease)
Thrombotic Thrombocytopenic Purpura
(TTP)
Accumulation of large vWF multimers → platelet aggregation
Thrombotic Thrombocytopenic Purpura
(TTP)
Clinical Features (Pentad) of TTP
- Thrombocytopenia (petechiae, purpura)
- Microangiopathic Hemolytic Anemia (MAHA) (schistocytes, ↑ LDH, ↓
haptoglobin) - Neurologic symptoms (confusion, seizures, stroke)
- Fever
- Renal dysfunction (mild)
Diagnosis of TTP
CBC + Peripheral Smear: Schistocytes
ADAMTS13 Activity: Severe deficiency (<10%) (Not required before starting
treatment)
Normal PT/PTT (Unlike DIC)
Treatment of TTI
Plasma Exchange (PEX) → Lifesaving
Glucocorticoids
Platelet transfusion is contraindicated (worsens thrombosis)
Platelet-rich thrombi in small vessels
TTP
Platelet-rich thrombi in renal vasculature
Hemolytic Uremic Syndrome (HUS)
Shiga-like toxin from E. coli O157:H7 → endothelial damage
HUS
Clinical Features (Triad) of HUS
- Thrombocytopenia
- MAHA (schistocytes)
- Acute kidney injury (↑ creatinine)
Diagnosis of HUS
CBC + Peripheral Smear: Schistocytes
Kidney Function: ↑ Creatinine, ↑ BUN
Stool culture for E. coli O157:H7
Treatment of HUS
Supportive care (fluids, dialysis if needed)
No plasma exchange (unlike TTP)
Uncontrolled clotting activation → microthrombi + bleeding
DIC
Consumption of platelets & coagulation factors
DIC
Common Causes Of DIC
Sepsis (bacterial endotoxins)
Obstetric emergencies (amniotic fluid embolism)
Malignancy (APL, adenocarcinomas)
Clinical Features of DIC
Thrombocytopenia + MAHA (schistocytes)
Diffuse bleeding (IV sites, mucosa)
Organ dysfunction (kidney failure, ARDS)
Diagnosis of DIC
↑ PT, ↑ PTT, ↑ INR
↑ D-dimer (fibrin degradation product)
↓ Fibrinogen
Peripheral smear: Schistocytes
Treatment of DIC
Treat underlying cause
Supportive care (blood, platelet transfusions)
Fresh frozen plasma (clotting factor replacement)