PET Imaging in Patients at Risk for Acute Lung Injury



Status:Recruiting
Conditions:Hospital, Pulmonary
Therapuetic Areas:Pulmonary / Respiratory Diseases, Other
Healthy:No
Age Range:Any
Updated:11/18/2012
Start Date:October 2011

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Positron Emission Tomography With [18F]Fluorodeoxyglucose in Patients at Risk for Acute Lung Injury


Despite decades of research, the mortality in acute lung injury remains very high and
treatment options are very limited. Given these facts, the best treatment modality may be in
prevention of this lethal syndrome.

Historically, imaging has played a crucial role in understanding ALI. The appearance of
chest radiography is one of the consensus criteria in defining ALI, and commuted tomography
(CT) scans further advanced the understanding of the pathoanatomy of ALI. While valuable,
these imaging modalities are nonspecific and do not incorporate functional cellular
physiology.

PET imaging measures concentrations of radioisotopes in the body. By embedding in, but not
altering molecules, the natural fate of these tracers can be studied with PET imaging.
Advances in the understanding of ALI include blood flow distribution, as well as the
response to alveolar recruitment maneuvers and prone positioning. Not all patients who are
receiving mechanical ventilation develop ALI. Inflammation in the lungs is known to play a
key early role in the development and progression of ALI. Secondary to inflammation, the
lungs develop edema and do not exchange oxygen as well. This early inflammation is in part
driven by a specific type of immune cell called the neutrophil. These cells seem to travel
and become sequestered in the lung- they are "recruited" to the lung during this
inflammatory stage. When there, these neutrophils release inflammatory substances which are
integral in the development of ALI. Neutrophils use primarily glucose as a fuel source. The
radio isotope [18F]Fluorodeoxyglucose (FDG)is a glucose analog and therefore taken
up/ingested by the neutrophils as a part of their normal metabolism. Because of this fact,
positron emission tomography (PET) using the radio isotope [18F]FDG is a highly sensitive
marker to look at the recruitment of neutrophils to the lung, therefore quantifying the
degree of pulmonary inflammation prior to the development of ALI.

The investigators seek to examine the relationship of pulmonary inflammation in patients at
risk for ALI, but without clinical evidence of the syndrome. The investigators seek to
enroll ten patients in a pilot trial.


Inclusion Criteria:

- Adults patients (age ≥ 18) presenting to the SICU after ≥ 5 hours of mechanical
ventilation in the OR or ED, without clinical evidence of ALI, and LIPS > 4 or < 4.

- Able to be positioned supine within the PET/CT scanner for ~1.25 hours

- Has legally authorized representative (LAR) available and willing to give informed
consent, or is able to give informed consent prior to initiation of mechanical
ventilation

- BMI < 35

Exclusion Criteria:

- Established ALI by accepted clinical criteria.

- Organ transplant recipient

- Treatment with immunosuppressive/immune-modulating medications

- Current corticosteroid treatment

- Chronic pulmonary or nonpulmonary inflammatory diseases

- Inability to safely travel out of the SICU (as established by regular safety
screening criteria). Patient is placed in the supine position for a minimum of 30
minutes, and on mechanical ventilator settings that will be in place for the duration
of the FDG-PET study. The patient is deemed unsafe for travel if oxygen requirement
increases or any hemodynamic instability ensues (such as increasing vasopressor
requirements).

- Glucose level > 150 mg/dl at time of PET scan

- Pregnancy (confirmed by qualitative urine hCG pregnancy test)

- Lactation

- Presence of implanted electronic medical device

- Enrollment in another research study of an investigational drug

- Prior research-related radiation exposure within the past year such that
participation in this study would result in exposures that exceed the limits as
defined by the FDA RDRC regulations (21 CFR 361.1)
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