Cryopreserved stem cell products containing dimethyl sulfoxide lead to activation of the coagulation system without any impact on engraftment. Issue 6 (4th December 2013)
- Record Type:
- Journal Article
- Title:
- Cryopreserved stem cell products containing dimethyl sulfoxide lead to activation of the coagulation system without any impact on engraftment. Issue 6 (4th December 2013)
- Main Title:
- Cryopreserved stem cell products containing dimethyl sulfoxide lead to activation of the coagulation system without any impact on engraftment
- Authors:
- Holbro, Andreas
Graf, Lukas
Topalidou, Maria
Bucher, Christoph
Passweg, Jakob R.
Tsakiris, Dimitrios A. - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="trf12511-sec-0001" sec-type="section"> <title>Background</title> <p>Dimethyl sulfoxide (DMSO) is extensively used as a cryoprotectant in stem cell preservation. Little is known on direct hemostatic changes in recipients of hematopoietic stem cell transplantation (HSCT), immediately after DMSO administration. The objectives of the current study were to measure hemostatic changes during HSCT.</p> </sec> <sec id="trf12511-sec-0002" sec-type="section"> <title>Study Design and Methods</title> <p>In this prospective analysis, changes in plasma biomarkers, platelets (PLTs), or endothelial cells (D‐dimers, thrombin–antithrombin complex [TAT], microparticle activity as thrombin‐generation potential [MPA], whole blood aggregation, von Willebrand factor) were measured before and immediately after HSCT. Furthermore, associations with clinical complications were recorded.</p> </sec> <sec id="trf12511-sec-0003" sec-type="section"> <title>Results</title> <p>A total of 54 patients were included in the study. Mean MPA and TAT increased significantly immediately after HSCT, returning to baseline the day after the procedure (p &lt; 0.01). No significant differences in engraftment for neutrophils and PLTs were found in patients presenting a high increase of TAT or MPA compared with those presenting with a smaller increase. Patients with a high increase in TAT and MPA had received a greater number of<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="trf12511-sec-0001" sec-type="section"> <title>Background</title> <p>Dimethyl sulfoxide (DMSO) is extensively used as a cryoprotectant in stem cell preservation. Little is known on direct hemostatic changes in recipients of hematopoietic stem cell transplantation (HSCT), immediately after DMSO administration. The objectives of the current study were to measure hemostatic changes during HSCT.</p> </sec> <sec id="trf12511-sec-0002" sec-type="section"> <title>Study Design and Methods</title> <p>In this prospective analysis, changes in plasma biomarkers, platelets (PLTs), or endothelial cells (D‐dimers, thrombin–antithrombin complex [TAT], microparticle activity as thrombin‐generation potential [MPA], whole blood aggregation, von Willebrand factor) were measured before and immediately after HSCT. Furthermore, associations with clinical complications were recorded.</p> </sec> <sec id="trf12511-sec-0003" sec-type="section"> <title>Results</title> <p>A total of 54 patients were included in the study. Mean MPA and TAT increased significantly immediately after HSCT, returning to baseline the day after the procedure (p &lt; 0.01). No significant differences in engraftment for neutrophils and PLTs were found in patients presenting a high increase of TAT or MPA compared with those presenting with a smaller increase. Patients with a high increase in TAT and MPA had received a greater number of total mononucleated cells (p &lt; 0.001) and higher transplant volumes (p = 0.002).</p> </sec> <sec id="trf12511-sec-0004" sec-type="section"> <title>Conclusions</title> <p>Infusion of stem cells containing DMSO reversibly activated coagulation, measured as thrombin generation. This finding was not associated with acute adverse events and did not influence engraftment. Further studies are needed to compare variable DMSO concentrations as well as DMSO‐free products, to better address the influence of DMSO on hemostasis.</p> </sec> </abstract> … (more)
- Is Part Of:
- Transfusion. Volume 54:Issue 6(2014)
- Journal:
- Transfusion
- Issue:
- Volume 54:Issue 6(2014)
- Issue Display:
- Volume 54, Issue 6 (2014)
- Year:
- 2014
- Volume:
- 54
- Issue:
- 6
- Issue Sort Value:
- 2014-0054-0006-0000
- Page Start:
- 1508
- Page End:
- 1514
- Publication Date:
- 2013-12-04
- Subjects:
- Hematology -- Periodicals
Blood -- Transfusion -- Periodicals
Blood Group Antigens -- Periodicals
Blood Preservation -- Periodicals
Blood Transfusion -- Periodicals
615 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1537-2995 ↗
http://www.blackwell-synergy.com/member/institutions/issuelist.asp?journal=trf ↗
http://www.transfusion.org ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/trf.12511 ↗
- Languages:
- English
- ISSNs:
- 0041-1132
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 9020.704000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3864.xml