Immune thrombocytopenic purpura Flashcards
ITP on peripheral smear
Large platelets, no schistocytes
Clinical course
VARIABLE: some do not require any treatment; others have a spontaneous remission or respond to first-line therapy with glucocorticoids; others continue to have severe thrombocytopenia necessitating additional therapy
Physical exam
Normal
Admission criteria per ASH
Platelet count <20K (ASH)
Management
If severe bleeding → IVIG FIRST
IF bleeding or platelets <30,000/mm3 → decadron 40 mg x 4 days (preferred) or prednisone 0.5-2.0 mg/kg/day (ASH)
IF cutaneous symptoms AND platelets ≥30,000/mm3 → active surveillance
Second line therapies for ITP
splenectomy, rituximab, or a thrombopoietin receptor agonist (TPO-RA) (no head to head studies)
IF surgical candidate → splenectomy + ensure immunizations
IF nonsurgical candidate → rituximab
Steroid dosing for acute treatment
decadron 40 mg x 4 days (preferred over pred)
Indications for treatment
1) bleeding
2) platelet count less than 30K
Nplate generic name
romiplostim