Abstract
We present the first thrombelastographic descriptions of three patients with δ-storage pool deficiency, a platelet disorder that involves a deficiency of dense granules and moderate bleeding. The patients demonstrated a 49-54% loss of platelet-mediated clot strength over a 1-2-h period after normal thrombus formation. This pattern persisted, with some attenuation of loss of strength following administration of epsilon aminocaproic acid, desmopressin and platelets for tonsillectomy. Assessment of platelet function in patients with platelet granule disorders can be accomplished with thrombelastographic methods in ambulatory and perioperative settings; however, the effects of therapy for this disorder cannot be monitored with thrombelastography without obtaining a blood sample prior to prophylactic hemostatic intervention.
Original language | English (US) |
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Pages (from-to) | 610-612 |
Number of pages | 3 |
Journal | Blood Coagulation and Fibrinolysis |
Volume | 22 |
Issue number | 7 |
DOIs | |
State | Published - Oct 2011 |
Externally published | Yes |
Keywords
- platelet granule disorder
- thrombelastography
- δ-storage pool deficiency
ASJC Scopus subject areas
- Hematology