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. Author manuscript; available in PMC: 2015 Sep 1.
Published in final edited form as: Pediatr Res. 2014 Jun 18;76(3):230–237. doi: 10.1038/pr.2014.87

Table 2.

Clinically used tests of platelet function and the potential clinical implications of abnormal results.

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.