Abstract:This review has demonstrated that no significant coagulation factor deficiency would be left undiagnosed if the protocol was followed. This would have considerably reduced the cost and time spent performing these assays.
“…The reagents for APTT (Dade Actin FS) and PT (Dade innovin) used on the CS5100 showed a higher sensitivity toward factor deficiencies compared with the reagents used on the STA‐R Evolution instrument. The factor sensitivity was comparable with data from the literature where the same APTT reagent was used . Ideally, reagents should have factor sensitivities between 30 and 45% .…”
Section: Resultssupporting
confidence: 75%
“…For APTT, the higher sensitivity toward factor deficiencies may lead to prolonged APTT's in the presence of only mildly reduced factor concentrations or even normal concentrations. These prolonged APTT's should be interpreted with care and may trigger the need for (unnecessary) specific factor assays to be performed . On the other hand, in FXI deficient patients, the FXI concentration is not correlated with the bleeding phenotype and a reagent with higher factor sensitivity is useful to diagnose these patients .…”
“…The reagents for APTT (Dade Actin FS) and PT (Dade innovin) used on the CS5100 showed a higher sensitivity toward factor deficiencies compared with the reagents used on the STA‐R Evolution instrument. The factor sensitivity was comparable with data from the literature where the same APTT reagent was used . Ideally, reagents should have factor sensitivities between 30 and 45% .…”
Section: Resultssupporting
confidence: 75%
“…For APTT, the higher sensitivity toward factor deficiencies may lead to prolonged APTT's in the presence of only mildly reduced factor concentrations or even normal concentrations. These prolonged APTT's should be interpreted with care and may trigger the need for (unnecessary) specific factor assays to be performed . On the other hand, in FXI deficient patients, the FXI concentration is not correlated with the bleeding phenotype and a reagent with higher factor sensitivity is useful to diagnose these patients .…”
“…When individuals with prolonged APTT arising out of routine screening are investigated, FXI deficiency was approximately five times more common than either FVIII of FIX deficiency [17] though this finding is likely to be dependent on the reagent used for screening.…”
Section: Prothrombin Time and Activated Partial Thromboplastin Time Dmentioning
“…Urine and blood cultures were negative. Since 1988 in Airedale the possibility of a bleeding disorder was tested by comparing the clotting times of two aPTT reagents, currently Synthesil (IL) as the reagent sensitive to factor inhibitors and deficiencies and Actin FS (Dade) as the reagent insensitive to factor inhibitors and deficiencies but sensitive to factor XII deficiency [2]. Unbeknown to the laboratory personnel the same comparison can be used to detect a lupus anticoagulant [3].…”
Simultaneous or sequential haemorrhage and thrombosis in the presence of a prolonged activated partial thromboplastin time (aPTT) is a rare occurrence: we describe the case a 37 year old lady who developed post-delivery deep vein thrombosis treated with low molecular heparin and warfarin followed a week later by extensive bruising over legs and forearms, a significant drop in haemoglobin and a very prolonged aPTT. Further tests revealed an acquired factor VIII inhibitor at 35 Bethesda Units. We discuss the clinical and laboratory implications and provide a literature review of simultaneous thrombophilia and haemophilia in the presence of a prolonged aPTT.
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