Biohemijska i funkcionalna ispitivanja kvaliteta koncentrata trombocita

  • Nebojša Vacić Clinical Center Niš, Clinic for Haematology, Niš, Serbia
  • Ana Antić Blood Transfusion Institute Niš, Niš, Serbia
  • Zoran Stanojković Blood Transfusion Institute Niš, Niš, Serbia
  • Miodrag Vučić Clinical Center Niš, Clinic for Haematology, Clinic for Vascular Surgery, Niš, Serbia
  • Milan Lazarević Clinical Center Niš, Department of Cardiac Surgery, Niš, Serbia
Ključne reči: trombociti, referentni standardi, krv, hemijske analize, trombociti, agregacija, trombociti, broj

Sažetak


Uvod/Cilj. Priprema koncentrata trombocita (KT) iz jedinice cele krvi je metoda uslovljena velikim brojem faktora koji pojedinačno ili udruženo mogu imati značajan uticaj na kvalitet konačnog proizvoda. Kvalitet koncentrata trombocita određen je kriterijumima definisanim u Vodiču za pripremu, korišćenje i obezbeđenje kvaliteta Evropskog komiteta za transfuziju krvi Saveta Evrope. Cilj istraživanja bio je da se ispita kvalitet KT dobijenih izdvajanjem iz “buffy coat”-a (BC) i izdvojiti faktore koji doprinose poboljšanju kvaliteta i standardizaciji KT. Metode. Ispitivanje je obuhvatilo ukupno 80 KT izdvojenih iz BC prema standardnoj proceduri pripreme u Zavodu za transfuziju krvi u Nišu. Kvalitet KT određivan je na osnovu zapremine produkta i laboratorijskih testiranja prvog (KT1), trećeg (KT3) i petog dana skladištenja (KT5). Određivan je broj trombocita, zaostalih eritrocita i leukocita, parcijalni pritisak kiseonika i ugljen-dioksida (pO2, pCO2), pH, sterilnost i agregacija trombocita izazvana dodavanjem 3,2; 6,4 i 9,6 μg kolagena/mL (impedantna agregometrija). Rezultati. Nađen je statistički značajno manji broj trombocita, pO2, pCO2 i pH u uzorcima KT3 i KT5 (p < 0,001). Osim ispu-njenosti kriterijuma za broj trombo­cita, svi ostali parametri bili su u saglasnosti sa preporukama Vodiča. Agregacija trombocita za sve kon­cen­tracije kolagena pokazala je pad tokom skladištenja, sa statistički značajnom razlikom za uzorke KT3 i KT5 u odnosu na uzorak KT1 (p < 0,01). Postojala je statistički značajna razlika u smanjenju aktivnosti uzoraka KT aktiviranih primenom visokih koncentracija kolegena (6,4 i 9,6 μg kolagena/mL) u odnosu na nižu koncentraciju kolagena (3,2 μg kolagena/mL). Zaključak. Broj trombocita, posmatrani biohemijski parametri i funkcija trombocita statistički se zna­čajno menjaju tokom perioda skladištenja. U cilju po­boljšanja kvaliteta KT važno je skladištiti KT u propisanim uslovima, promeniti vrstu kese za skladištenje KT i koristiti aditivni rastvor za čuvanje trombocita umesto plazme.

Reference

Balint B, Todorović M. From hematopoiesis to clinical applica-tion of haemoproduct. In: Balint B, Trkluljic M, Todorovic M. Basic principles of chemotherapy. Belgrade: Institute of Trans-fusion Medicine, Military Medical Academy; 2010. p.126–31. (Serbian)

Tynngård N. Preparation, storage and quality control of plate-let concentrates. Transfus Apher Sci 2009; 41(2): 97–104.

Hess JR. Conventional blood banking and blood component storage regulation: opportunities for improvement. Blood Transfus 2010; 8 (Suppl 3): s9–s15.

Stanojković Z, Antić A, Stanojević G, Stanojković M, Jelić M. Cur-rent principles of preparation and improvement of storage conditions of platelet concentrates. Bilt Transfuziol 2012; 58(1): 13–9. (Serbian)

Singh RP, Marwaha N, Malhotra P, Dash S. Quality assessment of platelet concentrates prepared by platelet rich plasma-platelet concentrate, buffy coat poor-platelet concentrate (BC-PC) and apheresis-PC methods. Asian J Transfus Sci 2009; 3(2): 86–94.

Antić A, Stanojković Z, Jelić M, Stanojković M. Quality assessment of platelet concentrates prepared using top&bottom blood bags. Bilt Transfuziol 2013; 59(1–2): 9–13. (Serbian)

Mokhtar MB, Hashim HB, Joshi SR. Assessment of quality of platelets preserved in plasma and platelet additive solution: A Malaysian experience. Asian J Transfus Sci 2016; 10(1): 84–7.

Council of Europe. Guide to preparation, use and quality assur-ance of blood components.19th ed. Strasbourg, France: Eu-ropean Directorate for the Quality of Medicines & HealthCare; 2017.

Paniccia R, Priora R, Liotta AA, Abbate R. Platelet function tests: a comparative review. Vasc Health Risk Manag 2015; 11: 133–48.

Panzer S, Jilma P. Methods for testing platelet function for transfusion medicine. Vox Sang 2011; 101(1): 1–9.

Kehrel E, Brodde FM. State of the Art in Platelet Function Testing.Transfus Med Hemother 2013; 40(2): 73–86.

Gulliksson H. Platelets from platelet-rich-plasma versus buffy-coat-derived platelets: what is the difference? Rev Brasil He-matol Hemoter 2012; 34(2): 76–7.

Vucetić D, Balint B, Taseski J, Mandić-Radić S, Regović V. Bio-chemical changes in thrombocyte concentrates stored for 5 day. Vojnosanit Pregl 2000; 57(5): 29–36. (in Serbian)

Rinalducci S, Zolla L. Biochemistry of storage lesions of red cell and platelet concentrates: A continuous fight implying oxida-tive/nitrosative/phosphorylative stress and signaling. Transfus Apher Sci 2015; 52(3): 262–9.

Kshitija M, Ravneet K. Platelet storage lesion: An update. Asian J Transfus Sci 2015; 9(1): 1–3.

Balint B, Todorović M. From haematopoesis to clinical use of haemoproducts. In: Balint B, editor. The basic principles of haemotherapy. Belgrade: Čigoja; 2010. p. 128-31. (Serbian)

Stanojković Z, Antić A, Stanojković M. Rational use of platelet transfusion. Proceedings of the Fifth Annual Spring Scientific Symposium in Anaesthesiology and Intensive Care Unit. Niš: University of Niš, Faculty of Medicine; 2013. p. 206–11.

Mathai J. Problem of bacterial contamination in platelet con-centrates. Transfus Apher Sci 2009; 41(2): 139–44.

Doescher A, Müller TH. Noninvasive pH Monitoring in Platelet Concentrates. Transfus Med Hemother 2013; 40(2): 88–92.

Riugwald I, Zimmermann R, Strasser E, Weiss D, Eckstein R. Masuring the pH of platelet concentrates. Transfusion 2006; 46(5): 870–1.

Gupta A, Chandra T, Kumar A. Evaluation of random donor platelets at different temperatures for an extended shelf life. Biomed Res 2010; 21(4): 433–6.

Coêlho MJ, Monteiro Tde C, Vasquez FG, Silva KL, Dos Santos KS, de Oliveira VM, et al. Platelet aggregation and quality con-trol of platelet concentrates produced in the Amazon Blood Bank. Rev Bras Hematol Hemoter 2011; 33(2): 110–4.

Neiva T, Machado M, Hoehn M, Hermes E, Vituri C, Ferreira J, et al. Evaluation of platelet aggregation in platelet concen-trates: storage implications. Rev Brasil Hematol Hemoter 2003; 25(4): 207–12.

Shabani NR, Baqir H. Quality Assessment of Platelet Concen-trates Prepared after Whole Blood Overnight Storage. J Med Bioeng 2014; 3(2): 87–92.

Mallhi RS, Kumar S, Philip J. A Comparative Assessment of Quality of Platelet Concentrates Prepared by Buffy Coat Poor Platelet Concentrate Method and Apheresis Derived Platelet Concentrate Method. Indian J Hematol Blood Transfus 2015; 31(4): 453–9.

Stanojković Z, Antić A, Stanojković M, Jelić M. The use of addi-tive solution for preparation and storage of platelets. Bilt Transfuziol 2014; 60(1–2): 43–5.

van der Meer PF. PAS or plasma for storage of platelets? A concise review. Transfus Med 2016; 26(5): 339–42.

Gulliksson H. Platelet storage media. Vox Sang 2014; 107(3): 205–12.

Rebulla P, Vaglio S, Beccaria F, Bonfichi M, Carella A, Chiurazzi F, et al. Clinical effectiveness of platelets in additive solution treated with two commercial pathogen-reduction technolo-gies. Transfusion 2017; 57(5): 1171–83.

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2021/08/19
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