3 to 5.8; patients referred for bleeding disorder assessments: −3.0 to 13.7), with native samples showing more variability with ristocetin [3]. For detecting reduced MA from bleeding disorders (with two or more agonists), native PRP were non-inferior, whereas adjusted PRP were superior, despite their wider RI with weak agonists [3]. While this study validates using either native or adjusted PRP for LTA assessments of bleeding disorders, adjusted PRP were superior to native PRP for detecting impaired LTA from bleeding disorders [3]. Furthermore, native PRP (which show more variable responses

to ristocetin) have not been validated for ristocetin induced platelet aggregation assessments selleck screening library of von Willebrand disease [3]. North American guidelines recommend that laboratories consider a single abnormal agonist response by LTA as a potential false positive findings (except with collagen and ristocetin) as such abnormalities are not predictive of platelet function disorders [1,3,10]. On the other hand, evidence to date indicates that LTA abnormalities

with multiple agonists are strongly associated with bleeding disorders (OR ≥23) and inherited platelet secretion defects (OR ≥91), which are the most common type of platelet function disorder [1,3]. Studies on the reproducibility of LTA indicate that most results (be they normal or abnormal) are confirmed on repeat testing [4]. Nonetheless, it is considered good practice to confirm

abnormalities RGFP966 cost on another sample to exclude preexamination or analytical artifacts [10]. Abnormalities with learn more multiple agonists should be considered suspicious of a platelet function disorder [10]. Like LTA, assays of dense granule adenosine triphosphate (ATP) release using Chronolume® (Chronolog Corporation, Haverston, PA, USA), a commercial luciferin–luciferase reagent containing magnesium, are helpful to detect impaired platelet function due to a bleeding disorder (OR: 17; diagnosis based on clinical opinion, not laboratory tests) or an inherited platelet disorder (OR: 128). ROC analyses indicate that like LTA, ATP release has high specificity and moderate sensitivity for inherited platelet disorders [2], with most function defects detected by the combination of: 6 μM epinephrine, 5.0 μg mL−1 Horm collagen, and 1 μM thromboxane analogue U46619 [2]. ATP release abnormalities are predictive of platelet disorders, regardless of LTA findings (respective OR: if LTA abnormal: 261; if LTA normal: 105) [2]. However, the predictive power could been overestimated for subjects with normal LTA findings as ATP release was considered in the definition of platelet disorders [2]. Because ATP release findings show significant variability [2], abnormalities in platelet function should be confirmed on another sample.