Table 2.
Test | Information obtained |
Potential implications |
---|---|---|
CBC with
peripheral smear |
Platelet count Platelet size Platelet granularity |
Thrombocytopenia: ITP, marrow infiltration, consumption, DIC Macro-thrombocytopenia: MYH-9, BSS. Micro-thrombocytopenia: WAS Hypo-granularity: Gray platelet syndrome |
PFA-100 ® | Closure time for Collagen/ADP or Collagen/Epi |
↑coll/ADP alone: ADP receptor disorder ↑coll/Epi alone: Aspirin/NSAIDs, MYH-9 related disorders ↑both: BSS, GT, VWD, Gray platelet syndrome |
Platelet
aggregation |
Aggregation response to various agonists (i.e. ADP, collagen, thrombin, ristocetin) |
Impaired ristocetin aggregation: VWD, BSS Impaired aggregation to everything except ristocetin: Glanzmann’s thrombasthenia, afibrinogenemia Primary aggregation only with ADP, Epi, collagen: storage pool disorder |
Flow Cytometry | Quantification of platelet surface markers |
Low or absent GPIb: BSS Low or absent GPIIb/IIIa: GT Low or absent P-selectin: alpha granule dysfunction |
Electron
Microscopy |
Dense granule content |
Low dense granule content: storage pool deficiency |
ITP: Immune Thrombocytopenic Purpura, DIC: Disseminated Intravascular Coagulation, BSS: Bernard Soulier Syndrome, WAS: Wiskott Aldrich Syndrome, NSAIDs: Non-Steroidal Anti-Inflammatory Drugs, GT: Glanzmann’s Thrombasthenia, VWD: Von Willebrand disease.