TY - JOUR
T1 - Time-dependent cellular population of textured-surface left ventricular assist devices contributes to the development of a biphasic systemic procoagulant response
AU - Spanier, T. B.
AU - Chen, J. M.
AU - Oz, M. C.
AU - Stem, D. M.
AU - Rose, E. A.
AU - Schmidt, A. M.
AU - Pennington, D. G.
AU - Hetzer, R.
PY - 1999
Y1 - 1999
N2 - Objective: Textured-surface left ventricular assist devices (LVAD) have been shown to enhance ventricular function and survival in patients with end- stage heart failure. Furthermore, we have described a procoagulant physiology in our LVAD population with sustained thrombin generation (elevated thrombin- antithrombin III complex and prothrombin fragment 1+2) and fibrinolysis (D- dimers), even up to 335 days after LVAD placement. To explain such sustained activation of coagulation, we speculated that the LVAD surface selectively adsorbed and promoted activation of circulating blood cells. Methods: In a prospective study of 20 patients with LVADs, we examined samples of peripheral blood as well as cells harvested from the surface of the LVADs at the time of their explantation for procoagulant proinflammatory markers. Results: Analysis of the cells populating the LVAD surface revealed the presence of pluripotent hematopoietic CD34+ cells, as well as cells bearing monocyte (CD14)/macrophage (CD68) markers, which also expressed procoagulant tissue factor. Reverse transcriptase-polymerase chain reaction confirmed cellular activation on the LVAD surface, revealing transcripts for interleukin 1α, interleukin 2, and tumor necrosis factor α, in addition to vascular cell adhesion molecule-1 consistent with their capacity to continually recruit and activate circulating cells, thereby propagating their response. In the periphery, elevated levels of tissue factor were found in the plasma of patients with LVADs, along with enhanced procoagulant activity. Conclusion: These observations suggest that the LVAD surface selectively absorbs and activates circulating hematopoietic precursor and monocytic cells, thereby creating a sustained prothrombotic and potentially proinflammatory systemic environment.
AB - Objective: Textured-surface left ventricular assist devices (LVAD) have been shown to enhance ventricular function and survival in patients with end- stage heart failure. Furthermore, we have described a procoagulant physiology in our LVAD population with sustained thrombin generation (elevated thrombin- antithrombin III complex and prothrombin fragment 1+2) and fibrinolysis (D- dimers), even up to 335 days after LVAD placement. To explain such sustained activation of coagulation, we speculated that the LVAD surface selectively adsorbed and promoted activation of circulating blood cells. Methods: In a prospective study of 20 patients with LVADs, we examined samples of peripheral blood as well as cells harvested from the surface of the LVADs at the time of their explantation for procoagulant proinflammatory markers. Results: Analysis of the cells populating the LVAD surface revealed the presence of pluripotent hematopoietic CD34+ cells, as well as cells bearing monocyte (CD14)/macrophage (CD68) markers, which also expressed procoagulant tissue factor. Reverse transcriptase-polymerase chain reaction confirmed cellular activation on the LVAD surface, revealing transcripts for interleukin 1α, interleukin 2, and tumor necrosis factor α, in addition to vascular cell adhesion molecule-1 consistent with their capacity to continually recruit and activate circulating cells, thereby propagating their response. In the periphery, elevated levels of tissue factor were found in the plasma of patients with LVADs, along with enhanced procoagulant activity. Conclusion: These observations suggest that the LVAD surface selectively absorbs and activates circulating hematopoietic precursor and monocytic cells, thereby creating a sustained prothrombotic and potentially proinflammatory systemic environment.
UR - http://www.scopus.com/inward/record.url?scp=0032888117&partnerID=8YFLogxK
U2 - 10.1016/S0022-5223(99)70176-5
DO - 10.1016/S0022-5223(99)70176-5
M3 - Article
C2 - 10469951
AN - SCOPUS:0032888117
SN - 0022-5223
VL - 118
SP - 404
EP - 413
JO - Journal of Thoracic and Cardiovascular Surgery
JF - Journal of Thoracic and Cardiovascular Surgery
IS - 3
ER -