Acute Kidney Injury in Patients Undergoing Contrast Exposure: VQ vs. CT



Status:Recruiting
Conditions:Renal Impairment / Chronic Kidney Disease, Cardiology, Cardiology, Hospital, Nephrology
Therapuetic Areas:Cardiology / Vascular Diseases, Nephrology / Urology, Other
Healthy:No
Age Range:18 - Any
Updated:12/27/2018
Start Date:July 1, 2017
End Date:December 31, 2022
Contact:Alice Mitchell, MD
Email:alimitch@iu.edu
Phone:(317) 880-3900

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1 R01 HL132358: The Contribution of Contrast Media Exposure to Acute Kidney Injury in Patients Evaluated for Pulmonary Embolism in the Emergency Care Setting: a Prospective, Randomized Trial

Both, CT scans and VQ scans, are used by doctors to look for pulmonary embolism. The most
common reason to order a VQ scan is to avoid the IV dye. The IV dye used for CT scans can
cause kidney problems in some patients, called contrast-induced nephropathy or "CIN." This is
a kidney problem that usually does not make patients feel any differently or change how they
urinate. Most of the time, it can only be found by testing blood several days later. This
kind of kidney problem can be very mild and some patients will never have any symptoms,
rarely these problems can be severe. Some patients can also have similar kidney problems for
many other reasons (reactions to medications, blood pressure problems, etc.) and can even
happen in patients that do not get IV dye. That is why doctors are not sure exactly who will
have these problems or if using a test that does not use IV dye can prevent this kidney
problem. The VQ scan uses a different medication through the IV that is not IV dye and has
not been linked to kidney problems. The purpose of this study is to learn if using the test
that does not use IV dye (the "VQ scan") instead of a CT scan in some patients can help to
prevent kidney problems.

Before the study begins, research personnel will do the following to be sure that patients
can be in the study:

- research personnel will talk to the treating physician.

- research personnel will review the patient medical records, blood and urine tests
already done for as usual medical care, and chest X-ray.

- research personnel will ask the patients some questions about their health.

- If it has not already been done for usual medical care, patients will be asked to give a
urine sample to test for medical conditions that may result in a higher risk of having
kidney problems such as having glucose (sugar) in the urine.

If the patient is eligible to continue in the study, the following will also happen at the
initial day of enrollment:

- research personnel may draw about 4 tablespoons of blood from the vein or, if from the
IV that was (or will be) placed for usual medical care.

- If one of the 100 patients who are at low risk of kidney problems, they will have a CT
scan of the chest that was ordered by the doctor.

- Otherwise, the potential subject will be randomly assigned to have either a CT scan of
the chest, which will include dye given in an IV, or a VQ scan, that does not use IV
dye. One half will have the CT scan and one half will have the VQ scan.

- Potential subjects will also have an ultrasound (a painless sound wave test of the legs
to look for a clot in the legs that can cause a clot in the lungs), if the doctor thinks
that one is needed, or if the VQ scan is "indeterminate." Indeterminate means that the
radiologist, the doctor reading the VQ scan, cannot tell if there is a pulmonary
embolism (a clot in your lung). Research personnel expect that less than 5% (5 out of
100) patients will have a VQ scan that is indeterminate. Some patients who have a VQ
scan that is indeterminate, may also need to have a CT scan of their chest to be sure
that they do or do not have a clot in their lungs.

- research personnel will also save blood and urine samples. Later, these samples will be
used to test for electrolytes (salts) and proteins (that may help better predict who
will get kidney problems. Subjects will not have to pay for these tests because they
will not be used for usual medical care. To protect privacy, research personnel will use
a code instead of name to label samples. For this reason, research personnel will not be
able to tell the results of these tests.

- If you are not found to be eligible for this study, the reason will be discussed with
you and your treating provider. If you are eligible to continue in the study, the
following will happen later:

- Subjects will be given an appointment to return to the hospital between 2 and 7 days
from the initial visit. As a reminder, research personnel will give subjects a reminder
card; research personnel will call and/or text the subjects, and/or email with
reminders. If subjects are still in the hospital during this time, research personnel
will visit the subjects in the hospital.

- At this appointment research personnel will ask some questions about the health, will
take about 4 tablespoons of blood and a urine sample. Blood and urine will be used to
test for kidney problems. If these tests do show a kidney problems after having IV dye,
research personnel will send a letter to notify subjects and the treating physician.

- In 30 days, research personnel will make 3 attempts to call and ask some questions about
the subject's health. If research personnel cannot follow up by telephone, they will
also try to contact by text, and/or by mail.

- research personnel will also review medical records in 7 days, 30 days, and in 1 year.

Inclusion Criteria:

1. Age≥18 years

2. CTPA ordered by the treating provider to evaluate PE.

3. Pre-test probability of PE ≤20% (defined using the PE Pretest Consult Score)

4. For Randomization to CTPA or VQ imaging: Pre-imaging CIN risk ≥25% (CINRisk Score ≥2
points) • A lower-risk subset of 100 patients (CINRisk Score <2) will be enrolled and
followed. These patients will complete the CTPA as ordered by their provider (not
randomized). Data from this lower-risk subset, along with high-risk patients
randomized to CTPA will be used will be used to validate the CINRisk Score, alone and
in combination with NGAL and eGFRCYS (Study Aims 1 and 3).

Exclusion Criteria:

1. History of pulmonary surgery or pulmonary infiltrate, mass or effusion on chest
radiograph.

2. Inability to provide written informed consent.

3. Inability to obtain venous blood for baseline creatinine measurement

4. Clinical instability preventing randomization to CTPA or VQ imaging.

5. Pregnancy or ≤48 hours post-partum

6. Subject unavailability for reasonable follow-up including biological sample
collection, serum creatinine measurement, and interview, such as an insecure
residence, planned travel or absence, personal or professional obligations,
incarceration, and/or other reason preventing follow-up, identified at enrollment.

7. Active renal replacement therapy (hemodialysis or peritoneal dialysis) within 30-days
of enrollment or previous physician-directed plans to initiate dialysis within 30-days
of the index visit.

8. Prior renal transplant or planned within 30-days of enrollment.

9. Intravascular contrast administration within 14 days prior to enrollment or planned
within 7 days of enrollment.
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Indianapolis, Indiana 46202
Phone: 317-963-5177
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