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DEPARTMENT OF ANESTHESIOLOGY ANNUAL REPORT

DEPARTMENT OF ANESTHESIOLOGY ANNUAL REPORT

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the country. The division added two<br />

active NIH grants during the year, for a<br />

combined total of 8 NIH grants within<br />

the division. The research efforts of the<br />

division are supported by our entire faculty<br />

and eight full-time research coordinators<br />

Aimee Butler, Wayne Cohen,<br />

Kelli Cozart, Bonnie Funk, Vince Gaver,<br />

Malissa Harris, Jason Hawkins and Jerry<br />

Kirchner. Additionally, research technicians<br />

Chonna Campbell, Amanda<br />

Cheek, Mary Currier, E. D. Derilus,<br />

Tanya Kagarise, Satarah (Torie) Latiker,<br />

Erich Lauff, Kenya Lee, Scott Lee, Colin<br />

Macdonnell, Terri Moore, Beverly Perry,<br />

Melanie Tirronen, Erin Ward, and<br />

Jonathan Williams have significantly<br />

extended the capabilities of divisional<br />

research.<br />

Clinical Research<br />

The Neurologic Outcome Research<br />

Group added one National Institutes of<br />

Health grant, for a total of 5 NIH grants<br />

supporting ongoing work as well as<br />

receiving the first American Heart<br />

Association Roundtable grants awarded<br />

at Duke. Under the direction of Drs.<br />

Mark Newman, Jerry Reves, and Jim<br />

Blumenthal, with the assistance of all<br />

cardiac division members, the division<br />

is continuing to investigate neurologic<br />

and neuropsychologic outcome after<br />

cardiac surgery, as well as interventions<br />

to improve these perioperative complications.<br />

The group recently published<br />

studies in the New England Journal of<br />

Medicine and Stroke documenting the<br />

long-term impact of perioperative cognitive<br />

decline on long-term cognitive<br />

function. This is a first hopeful step<br />

in prevention or treatment of these<br />

untoward events. The group has also<br />

continued its investigation of the association<br />

of Apolipoprotein ε4 and cognitive<br />

dysfunction and stroke after cardiac<br />

surgery. This research has led to an<br />

important collaboration with the Department<br />

of Neurology to further assess<br />

a patient's genetic predisposition to<br />

neuronal injury or potential recovery<br />

from neuronal injury.<br />

In conjunction with the Department<br />

of Neurology and Duke Clinical<br />

Research Institute, the newest focus<br />

of the neurologic outcomes research<br />

group is the development of the Multicenter<br />

"Perioperative Organ Protection<br />

Consortium." This is a collection of 25<br />

Academic Sites in the United States and<br />

Canada. The group is submitting two<br />

multicenter interventional NIH grants<br />

in early 2000 evaluating the impact<br />

of clinical practice on neurocognitive<br />

outcome.<br />

Laboratory and<br />

Translational Research<br />

The cardiac anesthesiology division has<br />

spent considerable resources, time, and<br />

energy over the last 5-10 years developing<br />

physician scientists and basic<br />

researchers in areas related to cardiovascular<br />

medicine. Examples of individuals<br />

include Debra Schwinn, M.D.,<br />

Hilary Grocott, M.D., FRCP(C) and<br />

Madan Kwatra, Ph.D. We are now<br />

pleased to report that basic science<br />

projects originating from each of these<br />

investigator's laboratories have resulted<br />

in publications in major scientific journals<br />

and national peer reviewed funding<br />

(NIH, FAER, AHA).<br />

The Molecular Pharmacology<br />

Laboratory, under the direction of Dr.<br />

Debra Schwinn has continued its investigation<br />

of adrenergic receptors, with an<br />

additional NIH RO1 grant awarded this<br />

year. In addition, translational research<br />

has also begun, with investigators bridging<br />

clinical and basic science areas<br />

with new hypothesis-driven research<br />

projects designed to elucidate mechanisms<br />

underlying acute myocardial<br />

beta-adrenergic receptor desensitization,<br />

G protein-coupling in human<br />

heart, and mechanisms underlying<br />

brain injury during cardiopulmonary<br />

bypass.<br />

Dr. Debra Schwinn initiated a NIH<br />

sabbatical in January of 2000 to gather<br />

additional expertise into genetic and<br />

genetic translational research. Our goal<br />

is to develop a perioperative outcome<br />

CLINICAL ACTIVITIES<br />

and genetics database that will be a<br />

resource for the entire world.<br />

A new laboratory initiative was<br />

begun in 1999 in the Cardiothoracic<br />

Anesthesia division. A laboratory<br />

focused on the pathophysiology and<br />

adverse outcomes (particularly neurologic)<br />

after cardiopulmonary bypass<br />

(CPB) was established under the direction<br />

of Dr. Hilary Grocott. This laboratory,<br />

The Anesthesiology Cardiopulmonary<br />

Bypass Laboratory, used a pig CPB<br />

model to investigate intermediate cerebral<br />

outcomes (glial and neuronal<br />

derived proteins released into the CSF<br />

and serum following brain injury) after<br />

CPB. In order to make the most of a relatively<br />

expensive animal preparation as<br />

well as to capitalize on other expertise<br />

in the division and department, the<br />

model was also used to examine issues<br />

related to myocardial (-adrenergic<br />

desensitization and renal ultrasound<br />

imaging employing intravenous contrast.<br />

Concurrent with the pig CPB<br />

model, a second, more economical<br />

CPB model was developed in the rat.<br />

This work, performed with the collaborative<br />

support of cardiothoracic anesthesia<br />

fellow Dr. Burkhard Mackensen,<br />

took place in the neuroanesthesia laboratory<br />

with space generously donated<br />

by Dr. David Warner. This new laboratory<br />

has been unique, thus far in the<br />

field, with its ability to successfully perform<br />

complete CPB in rats with subsequent<br />

recovery. The coming year’s<br />

focus will continue with the further<br />

development of a model of neurocognitive<br />

impairment after CPB in the rat<br />

in order to investigate both the mechanisms<br />

of injury as well as potential pharmacologic<br />

neuroprotection. In conjunction<br />

with Dr. Warner, neurology,<br />

neurosciences and other related fields,<br />

the Duke Multidisciplinary Neuroprotection<br />

Laboratory has been developed to<br />

facilitate these important investigations.<br />

CLINICAL ACTIVITIES 45

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