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INVESTIGATION OF PLATELET FUNCTIONS IN PSEUDOTHROMBOCYTOPENIA
Author(s): ,
Birgul Onec
Affiliations:
Hematology,Duzce University Faculty Of Medicine,Duzce,Turkey
,
Sinem Cesur
Affiliations:
Internal Medicine,Duzce University Faculty Of Medicine, Duzce,Turkey
,
Kursad Onec
Affiliations:
Internal Medicine,Duzce University Faculty Of Medicine,Duzce,Turkey
,
Emel Caliskan
Affiliations:
Medical Microbiology,Duzce University Faculty Of Medicine,Duzce,Turkey
Sengul Cangur
Affiliations:
Biostatistics,Duzce University Faculty Of Medicine,Duzce,Turkey
(Abstract release date: 05/18/17) EHA Library. Onec B. 05/18/17; 182836; PB2123
Dr. Birgul Onec
Dr. Birgul Onec
Contributions
Abstract

Abstract: PB2123

Type: Publication Only

Background

Pseudothrombocytopenia (pseudoTCP)), is incorrectly detection of low platelet counts in automatic blood counter devices and is most frequently caused by ethylene diamine tetra-aseticacid (EDTA) induced platelet clumping and in vitro agglutination. Therefore, pseudoTCP which accounts 15-30 of thrombocytopenic admissions, actually is not associated with a bleeding tendency. This situation may be detected with a careful investigation of peripheral blood smears (PBS) by experienced clinicians but in centers which does not have these facilities; misleading of worried patients through advanced centers or even unnecessery treatments with steroids and platelet transfusions often occurs.

Aims
In theory, formation of platelet clusters in the presence of EDTA requires functional adhesion molecules, so platelet adhesion and aggregation tests are expected to be in normal range. We aimed to investigate the capacity of simple platelet function analizers for making the distinction between pseudo TCP and real thrombocytopenia.

Methods
Platelet functions were measured as collagen-ADP and collagen-epinephrine closure times (ColADP and ColEPI) by Platelet Function Analyzer (PFA-200™) for all patients who are referred to our clinic as thrombocytopenia (TCP, plt <150 x103/µL) and value of this new method for determining peseudoTCP is compared with PBS which is accepted as the gold standard by using Receiver Operating Characteristic (ROC) curve analysis. PFA-200 system closure time is expected to be longer in true thrombocytopenia and normal in pseudoTCP, but there is no study investigated this system for this purpose. Descriptive analyses were presented using means ±standard deviations for normally distributed variables or median and interquartile range (IQR) for nonparametric continuous variables. An overall p-value of less than 0.05 was considered to show a statistically significant result. This study is supported by Duzce University with project number of 2015.04.03.370 and these are preliminary results.

Results
We included 59 patients who were referred to our clinic with thrombocytopenia (TCP, Plt<150 x103/µL) and 11 healthy controls (Plt>150 x103/µL). Median age was 54 (IQR:37-68) for thrombocytopenic subjects and 37 (%63) of them were female. Median Plt count was 61 x103/µL (IQR:30-90) in TCP group but WBC and Hb were not different from control subjects. Subjects referred with TCP were grouped with PBS as pseudo-TCP and real-TCP. There was no difference in terms of Plt, MPV, PCT, WBC or Hb between these groups but age was younger (median age 46 vs 62, p<0.05) and PDW was higher in pseudoTCP group (med 17.6 vs 16.8, p<0.01). ColEPI and ColADP measures were significantly lower (med 125 vs 287 for ColEPI, med 84 vs 224 for ColADP, p<0.001 for both) at pseudoTCP group.

The capacity of ColEPI and ColADP values in predicting pseudoTCP were analyzed using ROC curve analysis. We found that, when the manufacturer's recommended cut-off value (150 s) was used, the sensitivity and specificity were 74.4% and 95%, with overall accuracy of 81.4% for ColEPI (AUC 0.813, SD:0.061, p<0.001, %95CI: 0.694-0.933). Similarly sensitivity and specificity were 79.5%, and 95%, with overall accuracy of 84.7% for ColADP using manufacturer's cut-off value of 100 s (AUC 0.878, SD:0.055, p<0.001, %95CI: 0.770-0.986).

Conclusion
We concluded that, running PFA tests for everybody with thrombocytopenic counts, could be used for differentiate pseudoTCP and realTCP in centers which does not have conditions for proper BS. Especially long closure times excludes pseudoTCP with a high specificity and could make clinicians quick decisions for further investigations.

Session topic: 32. Platelets disorders

Keyword(s): Thrombocytopenia, Platelet function, Anticoagulants, Aggregation

Abstract: PB2123

Type: Publication Only

Background

Pseudothrombocytopenia (pseudoTCP)), is incorrectly detection of low platelet counts in automatic blood counter devices and is most frequently caused by ethylene diamine tetra-aseticacid (EDTA) induced platelet clumping and in vitro agglutination. Therefore, pseudoTCP which accounts 15-30 of thrombocytopenic admissions, actually is not associated with a bleeding tendency. This situation may be detected with a careful investigation of peripheral blood smears (PBS) by experienced clinicians but in centers which does not have these facilities; misleading of worried patients through advanced centers or even unnecessery treatments with steroids and platelet transfusions often occurs.

Aims
In theory, formation of platelet clusters in the presence of EDTA requires functional adhesion molecules, so platelet adhesion and aggregation tests are expected to be in normal range. We aimed to investigate the capacity of simple platelet function analizers for making the distinction between pseudo TCP and real thrombocytopenia.

Methods
Platelet functions were measured as collagen-ADP and collagen-epinephrine closure times (ColADP and ColEPI) by Platelet Function Analyzer (PFA-200™) for all patients who are referred to our clinic as thrombocytopenia (TCP, plt <150 x103/µL) and value of this new method for determining peseudoTCP is compared with PBS which is accepted as the gold standard by using Receiver Operating Characteristic (ROC) curve analysis. PFA-200 system closure time is expected to be longer in true thrombocytopenia and normal in pseudoTCP, but there is no study investigated this system for this purpose. Descriptive analyses were presented using means ±standard deviations for normally distributed variables or median and interquartile range (IQR) for nonparametric continuous variables. An overall p-value of less than 0.05 was considered to show a statistically significant result. This study is supported by Duzce University with project number of 2015.04.03.370 and these are preliminary results.

Results
We included 59 patients who were referred to our clinic with thrombocytopenia (TCP, Plt<150 x103/µL) and 11 healthy controls (Plt>150 x103/µL). Median age was 54 (IQR:37-68) for thrombocytopenic subjects and 37 (%63) of them were female. Median Plt count was 61 x103/µL (IQR:30-90) in TCP group but WBC and Hb were not different from control subjects. Subjects referred with TCP were grouped with PBS as pseudo-TCP and real-TCP. There was no difference in terms of Plt, MPV, PCT, WBC or Hb between these groups but age was younger (median age 46 vs 62, p<0.05) and PDW was higher in pseudoTCP group (med 17.6 vs 16.8, p<0.01). ColEPI and ColADP measures were significantly lower (med 125 vs 287 for ColEPI, med 84 vs 224 for ColADP, p<0.001 for both) at pseudoTCP group.

The capacity of ColEPI and ColADP values in predicting pseudoTCP were analyzed using ROC curve analysis. We found that, when the manufacturer's recommended cut-off value (150 s) was used, the sensitivity and specificity were 74.4% and 95%, with overall accuracy of 81.4% for ColEPI (AUC 0.813, SD:0.061, p<0.001, %95CI: 0.694-0.933). Similarly sensitivity and specificity were 79.5%, and 95%, with overall accuracy of 84.7% for ColADP using manufacturer's cut-off value of 100 s (AUC 0.878, SD:0.055, p<0.001, %95CI: 0.770-0.986).

Conclusion
We concluded that, running PFA tests for everybody with thrombocytopenic counts, could be used for differentiate pseudoTCP and realTCP in centers which does not have conditions for proper BS. Especially long closure times excludes pseudoTCP with a high specificity and could make clinicians quick decisions for further investigations.

Session topic: 32. Platelets disorders

Keyword(s): Thrombocytopenia, Platelet function, Anticoagulants, Aggregation

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