Aprotinin Use and Renal Outcome in Hypothermic Bypass and Circulatory Arrest for Surgical Repair of Thoracic Aorta.
Information source: Weill Medical College of Cornell University
Information obtained from ClinicalTrials.gov on November 03, 2008 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Circulatory Arrest
Phase: N/A
Status: Recruiting
Sponsored by: Weill Medical College of Cornell University Official(s) and/or principal investigator(s): Manuel Fontes, MD, Principal Investigator, Affiliation: Associate Professor
Overall contact: Manuel Fontes, MD, Phone: 212-746-0395, Email: maf2029@med.cornell.edu
Summary
Primary Objective: The aim of this study is to assess the effects of Aprotinin (an
antifibrinolytic drug used to reduce bleeding during cardiac surgery) on renal function in
patients undergoing surgery with use of hypothermic bypass and circulatory arrest for repair
of the thoracic aorta.
Secondary Objective: To compare the effects of Aprotinin and Amicar on major vascular
outcomes following thoracic aorta surgery with use of hypothermic bypass and circulatory
arrest.
Clinical Details
Official title: Aprotinin Use and Renal Outcome in Hypothermic Bypass and Circulatory Arrest for Surgical Repair of Thoracic Aorta. A Retrospective Study.
Study design: Case-Only, Retrospective
Detailed description:
Significance:
Complex surgery of the ascending thoracic aorta and the aortic arch requires use of
cardiopulmonary bypass (CPB) with moderate or profound total body hypothermia and circulatory
arrest. As expected, coagulation disorder can be common and severe requiring multiple
transfusions of blood product, which, in turn, is associated with increased risk of morbidity
and mortality. Over the years, many techniques have been employed to ameliorate CPB- related
bleeding with some agents such as aprotinin proving to be efficacious but centered in
controversy either because of high cost or due to safety concerns.
Aprotinin is a serine protease inhibitor, intended to limit blood loss in patients undergoing
surgery, was approved for use 13 years ago, and now administered in more than 250,000 surgery
patients per year. Although its mechanism of action is not entirely known, it is shown to
interfere with contact activation, preserve platelet function, inhibit fibrinolysis, and
having some anti-inflammatory effects. Multiple studies have shown its superiority for
reducing blood loss over other antifibrinolytics while other studies showing safety concerns
regarding early graft closure causing myocardial infarction (following coronary bypass
surgery), renal failure, vascular thrombosis, and death. Of note, several other studies have
addressed such safety concerns- finding that the risk of the aforementioned vascular
complications are comparable to results utilizing placebo or other antifibrinolytics such as
aminocaproic acid. For example, the associated renal dysfunction was attributed to a
competitive excretion process involving creatinine. That is, aprotinin competes with
creatinine for elimination by the kidneys such that the apparent renal dysfunction is
transient and a false marker of renal injury. However, the issue of renal injury has
recently re-emerged as a serious problem in a multicenter study on patients undergoing
coronary revascularization, whereby more than two fold increase in postoperative renal
dysfunction as well as a nearly two fold rise in postoperative stroke was reported.
Much of the controversy and many of the conflicting results arise from either inadequate
information (i. e., the definitive prospective study has not been done), from inadequately
powered studies for the intended outcome, inclusion of multi-institution and multi-surgeon
outcomes, or from studies involving patients with advanced ischemic heart disease whose
ventricular function may have been compromised perioperatively. To overcome the mentioned
limitations, and to better characterize to postoperative renal outcomes, we propose to
investigate the safety of aprotinin in a single institution, single surgeon, and very large
homogenous surgical cohort who underwent surgical repair of the ascending and aortic arch
with use of hypothermic CPB.
Methods:
This will be a retrospective review of data collected between 1998 and present (nearly 900
patients) on adult patients having had ascending aorta and or aortic arch surgery at the
NewYork Presbyterian Hospital. Data on demographics, preoperative, intraoperative, and
postoperative clinical events will be extracted from the patient's electronic record and
recorded on a database (Variables to be collected are presented in Appendix 1). A renal
event will be comprised of renal dysfunction; defined by a serum creatinine level of at least
2. 0 mg/dL (177 µmol/L), accompanied by an increase of at least 0. 70 mg/dL (62 µmol/L) from
baseline or renal failure; defined need for renal replacement therapy. Creatinine values
and creatinine clearance will be recorded/calculated preoperatively and postoperatively until
hospital discharge.
Statistical Analysis Include analysis for association between potential preoperative,
intraoperative, and early postoperative variables with postoperative renal dysfunction by
univariate analysis (student's t test and Fisher's exact test). The variables identified by
univariate testing (p< 0. 15) will be entered into a multivariate logistic regression.
Significance will be set a P < 0. 05 and odds ratio will be calculated where applicable.
Eligibility
Minimum age: N/A.
Maximum age: N/A.
Gender(s): Both.
Criteria:
Inclusion Criteria:
1. Adult male and female patients having surgery of ascending and aortic arch
2. Use of Antifibrinolytic agents (Aprotinin and Aminocaproic Acid)
Exclusion Criteria:
1. Emergency surgery for ruptured aorta
2. Pre-Existing Renal Failure or Renal dysfunction (creatinine >2. 0 mg/dl)
3. Moderate or Severe Ventricular Dysfunction
Locations and Contacts
Manuel Fontes, MD, Phone: 212-746-0395, Email: maf2029@med.cornell.edu
The New York Presbyterian Hospital - Weill Medical College of Cornell University, New York, New York 10021, United States; Recruiting Manuel Fontes, MD, Phone: 212-746-0395, Email: maf2029@med.cornell.edu Manuel Fontes, MD, Principal Investigator
Additional Information
Starting date: July 2006
Ending date: July 2008
Last updated: February 21, 2008
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