Differences in Activated Partial Thromboplastin Time (APTT) measures depending on the device used in blood samples drawn (direct Vacutainer® versus Butterfly needle): A Randomized Comparative Study
Abstract
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Background. Most laboratory errors occur during the pre-analytical phase and are often related to the blood drawn equipment. No studies have evaluated yet the influence of the most common vein puncture devices on activated partial thromboplastin time (APTT). We aimed to compare APTT when venous blood samples are drawn with two different needle devices (direct Vacutainer® versus butterfly needle).Â
Methods. Consecutive adult healthy volunteers were prospectively enrolled and assigned to receive two antecubital peripheral blood punctures from both arms, using the two devices. The blood drawn sequence (i.e. right or left arm first) and the first device to be used (i.e. direct vacuntainer® or butterfly needle first) were randomly established.
Results. Forty healthy volunteers (mean age 42.9 years; SD 7.5; range 27-58), comprising 25 (62.5%) women, were recruited. APTT obtained with the two blood drawn devices significantly and positive correlated (Spearman rho=0.943; p<0.001). However, mean APTT was significantly more prolonged in blood samples drawn with butterfly needles than in those obtained with direct vacutainer® (34.01 ± 4.4 vs. 33.63 ± 3.8 seconds, respectively; p=0.013). No differences in APTT were found when samples obtained from right and left arms were compared.
Discussion. The type of blood drawn equipment significantly influences APTT, which is prolonged when a butterfly needle is used. An increased contact time between blood and butterfly tube plastic material would favor a premature consumption of plasma coagulation factors before mixing with anticoagulants in the collection tube. The appropriately chosen blood drawn device is thus essential to avoid pre-analytical errors.
KEY WORDS: Activated partial thromboplastin time, Phlebotomy; Quality control; Blood Specimen Collection; Pre-analytical quality; Laboratory techniques and procedures
References
Jackups R Jr, Szymanski JJ, Persaud SP. (2017).Clinical decision support for hematology laboratory test utilization. Int J Lab Hematol;39.Suppl 1:128-135.
McHugh J, Holt C, O'Keeffe D. (2011). An assessment of the utility of unselected coagulation screening in general hospital practice. Blood Coagul Fibrinolysis;22(2): 106-9.
Chee YL. (2014). Coagulation. J R Coll Physicians Edinb;44(1):42-5.
Zehnder JL, Leung LLK, Tirnauer JS.(2015). Clinical use of coagulation tests. Uptodate. Topic last updated Nov 09.
Barrio J, Peris V, Asensio I, Molina I, López F. (2002). Tiempo de tromboplastina parcial activado prolongado no sospechado en cirugÃa de urgencia. Orientación diagnóstica y terapéutica. GarcÃa. Rev. Esp. Anestesiol. Reanim.; 49: 424-427.
Chng WJ, Sum C, Kuperan P. (2005). Causes of isolated prolonged activated partial thromboplastin time in an acute care general hospital. Singapore Med J; 46(9): 450-6.
Munro J, Booth A, Nicholl J. (1997). Routine preoperative testing: a systematic review of the evidence. Health Technol Assess; 1: i-iv; 1-62.
Capoor MN, Stonemetz JL, Baird JC, et al. (2015). Prothrombin time and activated partial thromboplastin time testing: a comparative effectiveness study in a million-patient sample. PLoS One.;10(8): e0133317.
Chng WJ, Sum C, Kuperan P 2005). Causes of isolated prolonged activated partial thromboplastin time in an acute care general hospital. Singapore Med J.;46(9):450-6.
Mccraw A, Hillarp A, Echenagucia M, et al. Considerations in the laboratory assessment of haemostasis. Haemophilia Centre & Thrombosis Unit, Royal Free Hospital, London, UK; University and Regional Laboratories Region Skane, Department of Clinical Chemistry, Malmo University Hospital, Malmo, Sweden; and Banco Metropolitano de Sangre del D.C. Escuela de Bioanalisis, Universidad Central de Venezuela, Caracas, Venezuela.
Lippi G, Salvagno GL, Brocco G, Guidi GC. ( 2005). Preanalytical variability in laboratory testing: influence of the blood drawing technique. Clin Chem Lab Med.;43(3):319-25.
Lippi G, Salvagno GL, Montagnana M, Brocco G, Cesare Guidi G. (2006). Influence of the needle bore size used for collecting venous blood samples on routine clinical chemistry testing. Clin Chem Lab Med.;44(8):1009-14.
Lippi G, Salvagno GL, Montagnana M, Lima-Oliveira G, Guidi GC, Favaloro EJ. (2012). Quality standards for sample collection in coagulation testing. Semin Thromb Hemost.;38(6):565-75.
Grant MS. (2003). The effect of blood drawing techniques and equipment on the hemolysis of ED laboratory blood samples. J Emerg Nurs;29(2):116-21.
WHO Guidelines on Drawing Blood: Best Practices in Phlebotomy.(2010) Geneva: World Health Organization;.
Jennifer Downing, Linda H. Yoder, and Kenn M. Kirksey. (2011). A Qualitative Study of Phlebotomy Device Selection. Medsurg Nurs. Nov-Dec;20(6):291-5.
Bonini P, Plebani M, Ceriotti F, Rubboli F. (2002). Errors in laboratory medicine. Clin Chem; 48: 691–8.
Triachini Codagnone F; Mattos Flores Alencar S, Wet S et al. (2014). The use of indicators in the pre-analytical phase as a laboratory management tool. Bras Patol Med Lab, v. 50, n. 2, p. 100-104.
Plebani M. ( 2012). Quality Indicators to Detect Pre-Analytical Errors in Laboratory Testing. Clin Biochem Rev.; 33(3): 85–88.
Lippi G, Chance JJ, Church S. et al. (2011). Preanalytical quality improvement: from dream to reality. Clin Chem Lab Med.;49(7):1113-26.
Lip¬pi G., Si¬mun¬dic A. M., Mat¬tiuz¬zi C. (2010). Overview on patient safety in healthcare and laboratory diagnostics.Special issue: Quality in laboratory diagnostics: from theory to practice. Biochemia Medica;20(2):131-43.
Mäkitalod O, Liikanen E.( 2013). Improving quality at the preanalytical phase of blood sampling: literature review. International Journal of Biomedical Laboratory Science (IJBLS) Vo1. 2, No. 1:7-16
Narang V., Kaur H., Kaur Selhi P., Sood N., Singh A. (2016). Preanalytical Errors in Hematology Labortory- an Avoidable Incompetence. Iranian Journal of Pathology.:11(2):151-154.
Satyavati V. (2012). No Preanalytical Errors in Laboratory Testing: A Beneficial Aspect for Patients. Indian J Clin Biochem.; 27(4): 319–321.
Martin, H., Metcalfe, S. & Whichello, R (2015). Specimen Labeling Errors: A Retrospective Study. OJNI Volume 19, Number 2. Online Journal of Nursing Informatics (OJNI), 19 (2).
Halm MA, Gleaves M.(2009). Obtaining Blood Samples From Peripheral Intravenous Catheters: Best Practice? Am J Crit Care;18(5):474-478.
Aznar J, Núñez Roldán A, de Haro Muñoz T, et al (2009). Manual de Obtención y Manejo de Muestras para el Laboratorio de Análisis ClÃnico. Plan de Laboratorios ClÃnicos y Bancos Biológicos. Servicio Andaluz de Salud..
Pérez Zenn J. RÃos Tamayo R, GarcÃa Ruiz A et al.(2011). Guia del Laboratorio del Servicio de HematologÃa y Hemoterapia. Hospital Universitario Virgen de las Nieves. Servicio Andaluz de Salud. Edición 01/11.
Koscielny J1, Ziemer S, Radtke H, Schmutzler M, Pruss A, Sinha P, Salama A, Kiesewetter H, Latza R.(2004). A practical concept for preoperative identification of patients with impaired primary hemostasis. Clin Appl Thromb Hemost;10(3):195-204.
Scielny J1, Ziemer S, Radtke H, Schmutzler M, Pruss A, Sinha P, Salama A, Kiesewetter H, Latza R.(2004). A practical concept for preoperative identification of patients with impaired primary hemostasis. Clin Appl Thromb Hemost;10(3):195-204.
Bowen RAR, Remaley AT. (2014). Interferences from blood collection tube components on clinical chemistry assays. Biochem Med (Zagreb).;24(1):31–44.
Green SF. (2013). The cost of poor blood specimen quality and errors in preanalytical processes. Clin Biochem;46 (13-14):1175-9.
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