Literature DB >> 24571597

Temporal leukocyte numbers and granulocyte activation in pulsatile and rotary ventricular assist device patients.

Joshua R Woolley1, Jeffrey J Teuteberg, Christian A Bermudez, Jay K Bhama, Kathleen L Lockard, Robert L Kormos, William R Wagner.   

Abstract

Individual ventricular assist device (VAD) design may affect leukocytes and impact immunity. Few studies have presented leukocyte and infection profiles in VAD patients over the course of the implant period. CD11b (MAC-1) expression on granulocytes is an indicator of activation during inflammation, mediating extravasation and the release of reactive oxygen species in tissue. No reported studies have presented MAC-1 expression on circulating granulocytes in VAD patients. Fifty-six patients implanted at a single center with a HeartMate II (HMII; n = 32), HeartWare (HW; n = 12), or Thoratec pneumatic VAD (PVAD; n = 12) between 1999 and 2011 were followed for 120 days of support. The leukocyte profiles and infectious events of all patients were evaluated; additionally, a subset had MAC-1 expression on circulating granulocytes was measured (HMII n = 9; HW n = 7; PVAD n = 4). All groups exhibited a significant peak in leukocyte numbers at postoperative day (POD) 14 while simultaneously experiencing a significant decrease in hematocrit. HMII patients exhibited a 3.2-fold increase in granulocyte MAC-1 expression at POD 14, and the temporal trend over the implant period differed from that experienced by HW patients. Further, HW patients experienced significantly fewer infection events. Alterations in leukocyte profiles and granulocyte activation experienced by VAD patients appear to be device-specific. Elevations in leukocyte activation may be related to an increased risk for infection, although the specific relationship between these phenomena in this patient group is not known.
Copyright © 2013 International Center for Artificial Organs and Transplantation and Wiley Periodicals, Inc.

Entities:  

Keywords:  Artificial organs; Circulatory assist devices; Immunology; Inflammatory cells; Left ventricular assist devices; Neutrophils; Systemic inflammation

Mesh:

Substances:

Year:  2013        PMID: 24571597      PMCID: PMC4010558          DOI: 10.1111/aor.12200

Source DB:  PubMed          Journal:  Artif Organs        ISSN: 0160-564X            Impact factor:   3.094


  25 in total

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Authors:  Stefan Klotz; Christian Vahlhaus; Christian Riehl; Christiane Reitz; Juergen R Sindermann; Hans H Scheld
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4.  Hyporesponsiveness of T cell subsets after cardiac surgery: a product of altered cell function or merely a result of absolute cell count changes in peripheral blood?

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Authors:  M C Deng; M Erren; T D Tjan; N Tamminga; B Werntze; P Zimmermann; M Weyand; D Hammel; C Schmidt; H H Scheld
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8.  Activation-induced T-cell death and immune dysfunction after implantation of left-ventricular assist device.

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9.  Infection in permanent circulatory support: experience from the REMATCH trial.

Authors:  William L Holman; Soon J Park; James W Long; Alan Weinberg; Lopa Gupta; Anita R Tierney; Robert M Adamson; John D Watson; Edward P Raines; Gregory S Couper; Francis D Pagani; Nelson A Burton; Leslie W Miller; Yoshifumi Naka
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10.  Time course of beta 2-integrin CD11b/CD18 (Mac-1, alpha M beta 2) upregulation on neutrophils and monocytes after coronary artery bypass grafting. CD11b upregulation after CABG surgery.

Authors:  A J Takala; I T Jousela; O S Takkunen; S E Jansson; K T Kyösola; K T Olkkola; M Leirisalo-Repo; H Repo
Journal:  Scand J Thorac Cardiovasc Surg       Date:  1996
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2.  Visualization and analysis of biomaterial-centered thrombus formation within a defined crevice under flow.

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4.  Temporal expression of cytokines and B-cell phenotypes during mechanical circulatory support.

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