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VERIFICATION OF BLOOD COLLECTION SYSTEM GIAN LUCA SALVAGNO, MD, PhD University of Verona, Italy.

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Presentation on theme: "VERIFICATION OF BLOOD COLLECTION SYSTEM GIAN LUCA SALVAGNO, MD, PhD University of Verona, Italy."— Presentation transcript:

1 VERIFICATION OF BLOOD COLLECTION SYSTEM GIAN LUCA SALVAGNO, MD, PhD University of Verona, Italy

2 HUB Spoke START

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5 Laboratory’ s errors Lundberg’s loop.

6 Laboratory testing

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8 Errors and patient’s outcome

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11 Pre- analytica l errors

12 Preanalytical:56% Analytical:21% Postanalytical:18% Multiple: 5% Preanalytical:56% Analytical:21% Postanalytical:18% Multiple: 5% ……….and in laboratory?

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14 Pre-analytical phase: Where? Patient identification Critical s point Blood specimen collection Specimen identification Specimen transport Time of specimen arrival Check-in Centrifugation decaping Aliquoting and labeling of the secondary specimen Outside LaboratoryLaboratoryLaboratoryLaboratory Within

15 Phlebotomist?

16 Blood collection device

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18 Blood drawing technique

19 VENOUS STASIS

20 Venous Stasis:Tourniquet time

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23 1)Tourniquet time: Clinical Chemistry

24 GLS 2) Tourniquet time: Coagulation testing

25 3) Tourniquet time: Hematological testing

26 BLOOD CONTAINER

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31 GLS Anticoagulants

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35 VENOUS ACCESS

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37 Hemolysis: Clinical Chemistry

38 GLS Hemolysis: Coaguation testing

39 GLS VisuallyundetectablehemolysisVisuallyundetectablehemolysis Percentage RBC lysate on the total RBC mass. 0 0.1 0.2 0.4 0.8 1.6 3.3 6.8 14.7 Hemolysis :clinical chemistry testing

40 NEEDLE SIZE

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42 Recommendations for Collection of a Quality Specimen for Coagulation Testing

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44 Influence of under-filling of 3.2% buffered sodium citrate blood tubes on results of activated partial thromboplastin time (APTT), prothrombin time (PT), fibrinogen, activated protein C resistance (APCR), and coagulation factor VIII. The dotted lines designate the desirable bias for each parameter.

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46 GLS The JCAHO has recently given priority within the 2007 National Patient Safety Goals to the improvement of the accuracy of patient identification and it applies to all JCAHO-accredited healthcare organizations and those seeking JCAHO accreditation. Failure to comply can result in a special Type I recommendation and jeopardize a facility’s accreditation status.

47 GLS The International Organization for Standardization 15189:2003 clause 5.4 “Pre-examination procedures'” includes requirements for traceability of primary samples to an identified individual.

48 GLS

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51 What’s next?

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55 “Which is the best choice?” Or……

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57 …and I am ready to start!

58 The End Take a home message


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