Filter survival time and requirement of blood products in patients with severe sepsis receiving drotrecogin alfa (activated) and requiring renal replacement therapy.docVIP
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Filter survival time and requirement of blood products in patients with severe sepsis receiving drotrecogin alfa (activated) and requiring renal replacement therapy
Available online /content/12/6/R163
Research
Open Access
Vol 12 No 6
Filter survival time and requirement of blood products in patients
with severe sepsis receiving drotrecogin alfa (activated) and
requiring renal replacement therapy
Luigi Camporota, Eleonora Corno, Eleonora Menaldo, John Smith, Katie Lei, Richard Beale and
Duncan Wyncoll
Adult Intensive Care Unit, Guys and St Thomas NHS Foundation Trust, St Thomas Hospital, 1st Floor East Wing, Lambeth Palace Road. London
SE1 7EH, UK
Corresponding author: Duncan Wyncoll, duncan.wyncoll@gstt.nhs.uk
Received: 10 Sep 2008 Revisions requested: 14 Oct 2008 Revisions received: 10 Nov 2008 Accepted: 18 Dec 2008 Published: 18 Dec 2008
Critical Care 2008, 12:R163 (doi:10.1186/cc7163)
This article is online at: /content/12/6/R163
? 2008 Camporota et al.; licensee BioMed Central Ltd.
This is an open access article distributed under the terms of the Creative Commons Attribution License (/licenses/by/2.0),
which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract
Introduction Drotrecogin alfa (activated) (DrotAA) is licensed in
the United States and the European Union for the treatment of
severe sepsis with multiple organ failure. Patients with severe
sepsis on renal replacement therapy (RRT), who typically
receive additional anticoagulation to prevent circuit clotting, may
be at higher risk of bleeding when DrotAA is administered in
addition to standard anticoagulation. However, the effects of
DrotAA on filter duration in the absence of additional
anticoagulation have not been established. The aim of this study
was to analyse the filter survival time (FST), and to quantify the
requirement of packed red cells (PRC) and blood products
during DrotAA infusion.
standard anticoagulation after the DrotAA infusion had been
completed (post-DrotAA).
Results The proportion of filter changes due to
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