Performance of the platelet function analyser PFA-100® in testing abnormalities of primary haemostasis

The PFA-100® device is a new instrument for the in-vitro testing of platelet function. Primary haemostasis is stimulated by recording the closure time taken for platelets to seal a 150 μm aperture in the centre of a membrane coated with collagen and either epinephrine or ADP. Patients with type 3 vo...

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Veröffentlicht in:Blood coagulation & fibrinolysis 1999-01, Vol.10 (1), p.25-32
Hauptverfasser: Harrison, P, Robinson, M S. C, Mackie, I J, Joseph, J, McDonald, S J, Liesner, R, Savidge, G F, Pasi, J, Machin, S J
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container_end_page 32
container_issue 1
container_start_page 25
container_title Blood coagulation & fibrinolysis
container_volume 10
creator Harrison, P
Robinson, M S. C
Mackie, I J
Joseph, J
McDonald, S J
Liesner, R
Savidge, G F
Pasi, J
Machin, S J
description The PFA-100® device is a new instrument for the in-vitro testing of platelet function. Primary haemostasis is stimulated by recording the closure time taken for platelets to seal a 150 μm aperture in the centre of a membrane coated with collagen and either epinephrine or ADP. Patients with type 3 von Willebrandʼs disease (n = 4) all had infinitely prolonged closure times (> 200 s) with both types of cartridge. A patient with afibrinogenemia exhibited only slightly prolonged closure times of 111 and 166 s for the ADP and epinephrine membranes, respectively. Patients with Glanzmannʼs thrombasthenia (n = 6) and Bernard Soulier syndrome (n = 2) had grossly prolonged closure times (> 200 s) with both types of cartridges. These results confirmed that the PFA-100® system was highly dependent on normal von Willebrand factor, glycoprotein lb and glycoprotein IIb/IIIa levels but not on plasma fibrinogen. Patients with storage pool disease (n = 6) and Hermansky Pudlak syndrome (n = 7) had prolonged closure times with the epinephrine cartridge. There was no evidence of enhanced platelet function in patients with antiphospholipid syndrome, in sickle-cell disease or thalassemia. However, ingestion of aspirin resulted in a near consistent and significant prolongation of the closure time for the epinephrine cartridge but not for the ADP cartridge in both normal subjects and patients. The test offers a reliable, reproducible, rapid and simple means of assessing high-shear platelet function in vitro.
doi_str_mv 10.1097/00001721-199901000-00004
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Patients with Glanzmannʼs thrombasthenia (n = 6) and Bernard Soulier syndrome (n = 2) had grossly prolonged closure times (&gt; 200 s) with both types of cartridges. These results confirmed that the PFA-100® system was highly dependent on normal von Willebrand factor, glycoprotein lb and glycoprotein IIb/IIIa levels but not on plasma fibrinogen. Patients with storage pool disease (n = 6) and Hermansky Pudlak syndrome (n = 7) had prolonged closure times with the epinephrine cartridge. There was no evidence of enhanced platelet function in patients with antiphospholipid syndrome, in sickle-cell disease or thalassemia. However, ingestion of aspirin resulted in a near consistent and significant prolongation of the closure time for the epinephrine cartridge but not for the ADP cartridge in both normal subjects and patients. 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source MEDLINE; Journals@Ovid Complete
subjects Biological and medical sciences
Blood Platelets - physiology
Hematologic and hematopoietic diseases
Hematologic Diseases - blood
Hemostasis
Humans
Medical sciences
Platelet diseases and coagulopathies
Platelet Function Tests - instrumentation
Platelet Function Tests - methods
title Performance of the platelet function analyser PFA-100® in testing abnormalities of primary haemostasis
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