Abstract
Platelet apheresis units are transfused into patients to mitigate or prevent bleeding. In a hospital, platelet apheresis units are transported from the transfusion service to the healthcare teams via two methods: a pneumatic tubing system (PTS) or ambulatory transport. Whether PTS transport affects the activity and utility of platelet apheresis units is unclear. We quantified the gravitational forces and transport time associated with PTS and ambulatory transport within our hospital. Washed platelets and supernatants were prepared from platelet apheresis units prior to transport as well as following ambulatory or PTS transport. For each group, we compared resting and agonist-induced platelet activity and platelet aggregate formation on collagen or von Willebrand factor (VWF) under shear, platelet VWF-receptor expression and VWF multimer levels. Subjection of platelet apheresis units to rapid acceleration/deceleration forces during PTS transport did not pre-activate platelets or their ability to activate in response to platelet agonists as compared to ambulatory transport. Platelets within platelet apheresis units transported via PTS retained their ability to adhere to surfaces of VWF and collagen under shear, although platelet aggregation on collagen and VWF was diminished as compared to ambulatory transport. VWF multimer levels and platelet GPIb receptor expression was unaffected by PTS transport as compared to ambulatory transport. Subjection of platelet apheresis units to PTS transport did not significantly affect the baseline or agonist-induced levels of platelet activation as compared to ambulatory transport. Our case study suggests that PTS transport may not significantly affect the hemostatic potential of platelets within platelet apheresis units.
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Abbreviations
- PTS:
-
Pneumatic tubing system
- AMB:
-
Ambulatory transport
- PRP:
-
Platelet rich plasma
- cPRP:
-
Concentrated platelet rich plasma
- VWF:
-
von Willebrand factor
- GPIb:
-
Glycoprotein Ib
- CD62P:
-
P-selectin
- ECM:
-
Extracellular matrix
References
AABB. Standards for Blood Banks and Transfusion Services (29th ed.). Bethesda: American Association of Blood Banks, 2014.
Amann, G., C. Zehntner, F. Marti, and G. Colucci. Effect of acceleration forces during transport through a pneumatic tube system on ROTEM® analysis. Clin. Chem. Lab. Med. 50:1335–1342, 2012.
Auton, M., C. Zhu, and M. A. Cruz. The mechanism of VWF-mediated platelet GPIbalpha binding. Biophys. J. 99:1192–1201, 2010.
Baker-Groberg, S. M., S. Lattimore, M. Recht, O. J. T. McCarty, and K. M. Haley. Assessment of neonatal platelet adhesion, activation, and aggregation. J. Thromb. Haemost. 14:815–827, 2016.
Bartels, A., Y. Sarpong, J. Coberly, et al. Failure of the Platelet Function Assay (PFA)-100 to detect antiplatelet agents. Surgery 158:1012–1018, 2015; (discussion 1018–1019).
Baurand, A., A. Eckly, N. Bari, C. Léon, B. Hechler, J. P. Cazenave, and C. Gachet. Desensitization of the platelet aggregation response to ADP: differential down-regulation of the P2Y1 and P2cyc receptors. Thromb. Haemost. 84:484–491, 2000.
Bolliger, D., M. D. Seeberger, K. A. Tanaka, S. Dell-Kuster, M. Gregor, U. Zenklusen, M. Grapow, D. A. Tsakiris, and M. Filipovic. Pre-analytical effects of pneumatic tube transport on impedance platelet aggregometry. Platelets 20:458–465, 2009.
Boomgaard, M. N., C. W. Gouwerok, C. H. Homburg, G. de Groot, M. J. IJsseldijk, and D. de Korte. The platelet adhesion capacity to subendothelial matrix and collagen in a flow model during storage of platelet concentrates for 7 days. Thromb. Haemost. 72:611–616, 1994.
Canault, M., D. Duerschmied, A. Brill, L. Stefanini, D. Schatzberg, S. M. Cifuni, W. Bergmeier, and D. D. Wagner. p38 mitogen-activated protein kinase activation during platelet storage: consequences for platelet recovery and hemostatic function in vivo. Blood 115:1835–1842, 2010.
Cardigan, R., C. Turner, and P. Harrison. Current methods of assessing platelet function: relevance to transfusion medicine. Vox Sang. 88:153–163, 2005.
Chen, W., X. Liang, A. K. Syed, P. Jessup, W. R. Church, J. Ware, C. D. Josephson, and R. Li. Inhibiting GPIbα shedding preserves post-transfusion recovery and hemostatic function of platelets after prolonged storage. Arterioscler. Thromb. Vasc. Biol. 36:1821–1828, 2016.
Das, S. S., R. Chaudhary, S. K. Verma, S. Ojha, and D. Khetan. Determinants of transfusion decisions in a mixed medical-surgical intensive care unit—a prospective cohort study. Blood Transfus. 7:188–192, 2009.
De Rossi, S. S., and M. Glick. Bleeding time: an unreliable predictor of clinical hemostasis. J. Oral Maxillofac. Surg. 54:1119–1120, 1996.
Devine, D. V., and K. Serrano. The platelet storage lesion. Clin. Lab. Med. 30:475–487, 2010.
Dyszkiewicz-Korpanty, A., R. Quinton, J. Yassine, and R. Sarode. The effect of a pneumatic tube transport system on PFA-100 trade mark closure time and whole blood platelet aggregation. J. Thromb. Haemost. 2:354–356, 2004.
Enko, D., H. Mangge, A. Münch, T. Niedrist, E. Mahla, H. Metzler, and F. Prüller. Pneumatic tube system transport does not alter platelet function in optical and whole blood aggregometry, prothrombin time, activated partial thromboplastin time, platelet count and fibrinogen in patients on anti-platelet drug therapy. Biochem. Med. 27:217–224, 2017.
Favaloro, E. J. Diagnosing von Willebrand disease: a short history of laboratory milestones and innovations, plus current status, challenges, and solutions. Semin. Thromb. Hemost. 40:551–570, 2014.
Gitz, E., C. A. Koekman, D. J. van den Heuvel, H. Deckmyn, J. W. Akkerman, H. C. Gerritsen, and R. T. Urbanus. Improved platelet survival after cold storage by prevention of glycoprotein Ibα clustering in lipid rafts. Haematologica 97:1873–1881, 2012.
Glas, M., D. Mauer, H. Kassas, T. Volk, and S. Kreuer. Sample transport by pneumatic tube system alters results of multiple electrode aggregometry but not rotational thromboelastometry. Platelets 24:454–461, 2013.
Hardy, A. R., P. B. Conley, J. Luo, J. L. Benovic, A. W. Poole, and S. J. Mundell. P2Y1 and P2Y12 receptors for ADP desensitize by distinct kinase-dependent mechanisms. Blood 105:3552–3560, 2005.
Harrison, P., I. Mackie, A. Mumford, C. Briggs, R. Liesner, M. Winter, S. Machin, and British Committee for Standards in Haematology. Guidelines for the laboratory investigation of heritable disorders of platelet function. Br. J. Haematol. 155:30–44, 2011.
Hess, J. R., K. Brohi, R. P. Dutton, et al. The coagulopathy of trauma: a review of mechanisms. J. Trauma 65:748–754, 2008.
Holme, S. Storage and quality assessment of platelets. Vox Sang. 74:207–216, 1998.
Hübner, U., N. Böckel-Frohnhöfer, B. Hummel, and J. Geisel. The effect of a pneumatic tube transport system on platelet aggregation using optical aggregometry and the PFA-100. Clin. Lab. 56:59–64, 2010.
Jackson, S. P. The growing complexity of platelet aggregation. Blood 109:5087–5095, 2007.
Jackson, S. P., W. S. Nesbitt, and S. Kulkarni. Signaling events underlying thrombus formation. J. Thromb. Haemost. 1:1602–1612, 2003.
Jain, A., A. D. van der Meer, A.-L. Papa, et al. Assessment of whole blood thrombosis in a microfluidic device lined by fixed human endothelium. Biomed. Microdevices 18:73, 2016.
Javela, K., J. Eronen, S. Sarna, and R. Kekomäki. Soluble glycoprotein V as a quality marker of platelet concentrates stressed by transportation. Transfusion (Paris) 45:1504–1511, 2005.
Jeger, V., H. Zimmermann, and A. K. Exadaktylos. The role of thrombelastography in multiple trauma. Emerg. Med. Int. 2011:1–4, 2011.
Jurk, K., and B. E. Kehrel. Platelets: physiology and biochemistry. Semin. Thromb. Hemost. 31:381–392, 2005.
Kanaji, S., S. A. Fahs, Q. Shi, S. L. Haberichter, and R. R. Montgomery. Contribution of platelet vs. endothelial VWF to platelet adhesion and hemostasis. J. Thromb. Haemost. 10:1646–1652, 2012.
Kauvar, D. S., R. Lefering, and C. E. Wade. Impact of hemorrhage on trauma outcome: an overview of epidemiology, clinical presentations, and therapeutic considerations. J. Trauma 60:S3–11, 2006.
Kelly, A. M., S. F. Garner, T. Foukaneli, et al. The effect of variation in donor platelet function on transfusion outcome: a semirandomized controlled trial. Blood 130:214–220, 2017.
Kicken, C., S. V. Poucke, A. E. Marcus, M. D. Lancé, and Y. Henskens. Response of platelet concentrates to pressure and temperature changes without impairment of the in vitro function. Thromb. Res. 135:679–683, 2015.
Kicken, C. H., M. Roest, Y. M. C. Henskens, B. de Laat, and D. Huskens. Application of an optimized flow cytometry-based quantification of Platelet Activation (PACT): Monitoring platelet activation in platelet concentrates. PloS ONE 12:e0172265, 2017.
Kreuger, A. L., C. Caram-Deelder, J. Jacobse, J.-L. Kerkhoffs, J. G. van der Bom, and R. A. Middelburg. Effect of storage time of platelet products on clinical outcomes after transfusion: a systematic review and meta-analyses. Vox Sang 112:291–300, 2017.
Lancé, M. D., M. A. E. Marcus, R. van Oerle, H. M. S. Theunissen, and Y. M. C. Henskens. Platelet concentrate transport in pneumatic tube systems—does it work? Vox Sang. 103:79–82, 2012.
Lenting, P. J., and C. V. Denis. Platelet von Willebrand factor: sweet resistance. Blood 122:4006–4007, 2013.
Leytin, V., D. J. Allen, A. Gwozdz, B. Garvey, and J. Freedman. Role of platelet surface glycoprotein Ibalpha and P-selectin in the clearance of transfused platelet concentrates. Transfusion (Paris) 44:1487–1495, 2004.
Li, R., H. Elmongy, C. Sims, and S. L. Diamond. Ex vivo recapitulation of trauma-induced coagulopathy and preliminary assessment of trauma patient platelet function under flow using microfluidic technology. J. Trauma Acute Care Surg. 80:440–449, 2016.
Liang, X., S. R. Russell, S. Estelle, L. H. Jones, S. Cho, M. L. Kahn, M. C. Berndt, S. T. Bunting, J. Ware, and R. Li. Specific inhibition of ectodomain shedding of glycoprotein Ibα by targeting its juxtamembrane shedding cleavage site. J. Thromb. Haemost. 11:2155–2162, 2013.
Liang, X., A. K. Syed, S. R. Russell, J. Ware, and R. Li. Dimerization of glycoprotein Ibα is not sufficient to induce platelet clearance. J. Thromb. Haemost. 14:381–386, 2016.
Ling, L.-Q., J. Liao, Q. Niu, X. Wang, J. Jia, C.-H. Zuo, H. Jiang, and J. Zhou. Evaluation of an automated light transmission aggregometry. Platelets 28:712, 2017.
Luo, G.-P., B. Ni, X. Yang, and Y.-Z. Wu. von Willebrand factor: more than a regulator of hemostasis and thrombosis. Acta Haematol. 128:158–169, 2012.
Magnette, A., M. Chatelain, B. Chatelain, H. Ten Cate, and F. Mullier. Pre-analytical issues in the haemostasis laboratory: guidance for the clinical laboratories. Thromb. J. 14:49, 2016.
McCarty, O. J. T., S. D. J. Calaminus, M. C. Berndt, L. M. Machesky, and S. P. Watson. von Willebrand factor mediates platelet spreading through glycoprotein Ib and alpha(IIb)beta3 in the presence of botrocetin and ristocetin, respectively. J. Thromb. Haemost. 4:1367–1378, 2006.
McGrath, R. T., M. van den Biggelaar, B. Byrne, J. M. O’Sullivan, O. Rawley, R. O’Kennedy, J. Voorberg, R. J. S. Preston, and J. S. O’Donnell. Altered glycosylation of platelet-derived von Willebrand factor confers resistance to ADAMTS13 proteolysis. Blood 122:4107–4110, 2013.
Moore, H. B., E. E. Moore, M. P. Chapman, et al. Viscoelastic measurements of platelet function, not fibrinogen function, predicts sensitivity to tissue-type plasminogen activator in trauma patients. J Thromb Haemost 13:1878–1887, 2015.
Mullins, G. R., J. H. Harrison, and D. E. Bruns. Smartphones can monitor medical center pneumatic tube systems. Clin. Chem. 62:891–893, 2016.
Nybo, M., M. E. Lund, K. Titlestad, and C. U. Maegaard. Blood sample transportation by pneumatic transportation systems: a systematic literature review. Clin. Chem. 64:782, 2017.
Ozaki, Y., N. Asazuma, K. Suzuki-Inoue, and M. C. Berndt. Platelet GPIb-IX-V-dependent signaling. J. Thromb. Haemost. 3:1745–1751, 2005.
Perkins, J. G., A. P. Cap, C. P. Andrew, et al. An evaluation of the impact of apheresis platelets used in the setting of massively transfused trauma patients. J. Trauma 66:S77–S84, 2009; (discussion S84–S85).
Pidcoke, H. F., J. K. Aden, A. G. Mora, M. A. Borgman, P. C. Spinella, M. A. Dubick, L. H. Blackbourne, and A. P. Cap. Ten-year analysis of transfusion in Operation Iraqi Freedom and Operation Enduring Freedom: increased plasma and platelet use correlates with improved survival. J. Trauma Acute Care Surg. 73:S445–452, 2012.
Ruggeri, Z. M. Platelets in atherothrombosis. Nat Med 8:1227–1234, 2002.
Sandgren, P., S. Larsson, P. Wai-San, and B. Aspevall-Diedrich. The effects of pneumatic tube transport on fresh and stored platelets in additive solution. Blood Transfus. 12:85–90, 2014.
Sauaia, A., F. A. Moore, E. E. Moore, K. S. Moser, R. Brennan, R. A. Read, and P. T. Pons. Epidemiology of trauma deaths: a reassessment. J. Trauma 38:185–193, 1995.
Schoner, A., C. Tyrrell, M. Wu, J. M. Gelow, A. A. Hayes, J. R. Lindner, K. L. Thornburg, and W. Hasan. Endocardial endothelial dysfunction progressively disrupts initially anti then pro-thrombotic pathways in heart failure mice. PloS ONE 10:e0142940, 2015.
Schreiber, M. A., J. Differding, P. Thorborg, J. C. Mayberry, and R. J. Mullins. Hypercoagulability is most prevalent early after injury and in female patients. J. Trauma 58:475–480, 2005; (discussion 480–481).
Singh, I., E. Themistou, L. Porcar, and S. Neelamegham. Fluid shear induces conformation change in human blood protein von Willebrand factor in solution. Biophys. J. 96:2313–2320, 2009.
Sobrino, J., and S. Shafi. Timing and causes of death after injuries. Proc. Bayl. Univ. Med. Cent. 26:120–123, 2013.
Stanworth, S. J., L. J. Estcourt, G. Powter, et al. A no-prophylaxis platelet-transfusion strategy for hematologic cancers. N. Engl. J. Med. 368:1771–1780, 2013.
Streichert, T., B. Otto, C. Schnabel, G. Nordholt, M. Haddad, M. Maric, A. Petersmann, R. Jung, and C. Wagener. Determination of hemolysis thresholds by the use of data loggers in pneumatic tube systems. Clin. Chem. 57:1390–1397, 2011.
Tao, Y., X. Zhang, X. Liang, J. Zang, X. Mo, and R. Li. Structural basis for the specific inhibition of glycoprotein Ibα shedding by an inhibitory antibody. Sci. Rep. 6:24789, 2016.
Tenorio, G. C., R. G. Strauss, M. J. Wieland, T. A. Behlke, and G. A. Ludwig. A randomized comparison of plateletpheresis with the same donors using four blood separators at a single blood center. J. Clin. Apheresis 17:170–176, 2002.
Thalén, S., I. Forsling, J. Eintrei, L. Söderblom, and J. P. Antovic. Pneumatic tube transport affects platelet function measured by multiplate electrode aggregometry. Thromb. Res. 132:77–80, 2013.
Tisherman, S. A., R. H. Schmicker, K. J. Brasel, E. M. Bulger, J. D. Kerby, J. P. Minei, J. L. Powell, D. A. Reiff, S. B. Rizoli, and M. A. Schreiber. Detailed description of all deaths in both the shock and traumatic brain injury hypertonic saline trials of the Resuscitation Outcomes Consortium. Ann. Surg. 261:586–590, 2015.
Wallin, O., J. Söderberg, K. Grankvist, P. A. Jonsson, and J. Hultdin. Preanalytical effects of pneumatic tube transport on routine haematology, coagulation parameters, platelet function and global coagulation. Clin. Chem. Lab. Med. 46:1443–1449, 2008.
Watson, S. P., J. M. Auger, O. J. T. McCarty, and A. C. Pearce. GPVI and integrin αIIbβ3 signaling in platelets. J. Thromb. Haemost. 3:1752–1762, 2005.
Winters, J. L. Complications of donor apheresis. J. Clin. Apheresis 21:132–141, 2006.
Yonge, J. D., and M. A. Schreiber. The pragmatic randomized optimal platelet and plasma ratios trial: what does it mean for remote damage control resuscitation? Transfusion (Paris) 56(Suppl 2):S149–156, 2016.
Zilberman-Rudenko, J., A. Itakura, J. Maddala, S. M. Baker-Groberg, R. Vetter, E. I. Tucker, A. Gruber, C. Gerdes, and O. J. T. McCarty. Biorheology of platelet activation in the bloodstream distal to thrombus formation. Cell. Mol. Bioeng. 9:496–508, 2016.
Zilberman-Rudenko, J., A. Itakura, C. P. Wiesenekker, R. Vetter, C. Maas, D. Gailani, E. I. Tucker, A. Gruber, C. Gerdes, and O. J. T. McCarty. Coagulation factor XI promotes distal platelet activation and single platelet consumption in the bloodstream under shear flow. Arterioscler Thromb. Vasc. Biol. 36:510–517, 2016.
Acknowledgments
We thank the staff of the OHSU Transfusion Service, the American Red Cross, Pacific Northwest Blood Services Region, and Fenwal Inc., A Fresenius Kabi Company, producer of Amicus separator, for technical help with procurement of platelet apheresis units and preparation of fresh cPRP. O.J.T. McCarty is an American Heart Association Established Investigator (13EIA12630000).
Funding
This study was funded by grants from the National Institutes of Health (R01HL101972, R01GM116184 and F31HL13623001). O.J.T. McCarty is an American Heart Association Established Investigator (13EIA12630000).
Conflict of interest
J. Zilberman-Rudenko, F. Z. Zhao, S. E. Reitsma, A. Mitrugno, J. Pang, J. J. Shatzel, B. Rick, C. Tyrrell, W. Hasan, O. J. T. McCarty, and M. A. Schreiber have no conflicts of interests.
Ethical Approval
All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. Informed consent was received from all human participants. This article does not contain any studies with animals performed by any of the authors.
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Associate Editors Keefe B. Manning and Ajit P. Yoganathan oversaw the review of this article.
J. Zilberman-Rudenko and F. Zhao are co-first authors. O. J. T. McCarty and M. A. Schreiber and are co-senior authors.
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13239_2018_361_MOESM1_ESM.jpg
Supplementary material 1 (JPEG 1832 kb) Supplemental Figure 1. Integration of an accelerometer. From left to right: an iPod is attached to the standard cushioning sponge using silk tape; subsequently, the iPod attached to the sponge is inserted into a transport capsule and is protected by additional layer of sponge prior to insertion of a platelet apheresis units.
13239_2018_361_MOESM2_ESM.tif
Supplementary material 2 (TIFF 548 kb) Supplemental Figure 2. Fresh platelet activation and microaggregation. Freshly prepared washed platelets were incubated with indicated agonists for 30 minutes, immunostained and evaluated by fluorescence-activated cell sorting (FACS) cytometry for percent platelet activation (CD41+/CD31+/CD62P+ events; A) or platelet microaggregate formation (high fluorescence intensity CD41+/CD31+ events; B). Mean ± SEM, n = 3.
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Zilberman-Rudenko, J., Zhao, F.Z., Reitsma, S.E. et al. Effect of Pneumatic Tubing System Transport on Platelet Apheresis Units. Cardiovasc Eng Tech 9, 515–527 (2018). https://doi.org/10.1007/s13239-018-0361-2
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DOI: https://doi.org/10.1007/s13239-018-0361-2