Assessment of Immediate Adverse Reactions From Dotarem in Children Under 2 Years of Age

Our primary outcome is to assess the safety of Dotarem in these patients up to 24 hours after
Dotarem injection. The patients will be monitored in the hospital for at least 2 hours
following the completion of the MRI exam. Many of these patients will have received sedation
for the MRI and would be monitored normally for up to 1 hour after the exam is completed.
Patients will be monitored for any adverse events that occurred during the observation
period. The type of event, time of onset, duration of symptoms, intensity of the reaction
(mild, moderate, severe), causality (not related, probably related, related, definitely
related, unclassifiable), and subsequent outcome (required treatment, favorable outcome,
recovery with sequela, or death) will be documented. Parents will be given an information
sheet prior to discharge indicating the possible adverse events that may occur related to the
administration of Dotarem with instructions on what to do and who to call, if necessary,
should any of them occur. Parents will be called by the radiology department the next day to
identify any adverse events that occurred during the first 24 hours after discharge from the
hospital.

Our secondary outcome is to assess image quality of the exam. The pre-contrast images will be
compared to the combined pre- and post-contrast images following administration of Dotarem by
radiologists who are blinded to the patients' clinical information to assess for improvement
of image quality and delineation of structures with contrast.

200 patients are expected to be enrolled in this study over the course of 18 months.

Exclusion criteria: Patients 2 years of age or older. Patients receiving an MRI exam without
contrast. Patients with a GFR <30. Patients with known renal failure or prior gadolinium
based contrast agent hypersensitivity reaction. Patients who receive an MRI exam using a
different gadolinium-based contrast agent. Patients who are not accompanied by a parent will
not be included. Patients who are unable to complete the MRI exam prior to contrast
administration will be excluded.

Inclusion criteria: Any patient under 2 years of age undergoing an MRI exam of the neuraxis
or body with and without contrast as part of their standard of care. Included patients may be
scheduled with simultaneous sedation for the MRI. Nonsedated patients also qualify for the
study.

Patients who qualify for Dotarem administration are usually preselected by the radiologist
depending on the type of exam and the reason for the study. While, the use of Dotarem is not
approved by the FDA in this patient population, off-label use of the agent is routinely
performed during routine clinical care of patients in this age group in our practice. Those
patients who would be given Dotarem as part of routine standard of care will be asked to
enroll. Written consent will be obtained from the parents. Patients will be recruited over an
18 month period of time.

All MRI exams will be performed on our 3T GE Discovery 750W or 1.5T GE Signa HDXT 23.0.

All patients will have the following information recorded: age, sex, weight, risk factors
(renal disease, cardiac disease, autoimmune disease, dehydration, other medical conditions),
reason for exam, type of exam, dose of Dotarem, route of injection (manual or power
injection), a premedication regimen (i.e. steroids), and tolerance to injection. In addition,
when applicable, the types of medications used for sedation will be recorded as well as the
route of sedation: deep sedation, laryngeal mask airway, or general endotracheal anesthesia.

Patients will be given a weight-based dose of Dotarem of 0.2mL/kg (0.1 mmol/kg) body weight.
It will be administered as an intravenous bolus injection at a flow rate of approximately 1-2
mL/second either by manual or power injection.

During the MRI exam, all patients will undergo continuous monitoring of heart rate and
peripheral oxygen saturation. Sedated patients will be monitored similarly until they reach
an Aldrete score >6. After this the monitoring devices will be removed. The patients will
then be observed off the monitors until a total of 2 hours after the exam has elapsed.

All adverse drug events (ADEs) will be documented including nausea, headache, injection site
pain, injection site coldness, burning sensation, heart arrhythmia, allergic reactions
(cardiac or respiratory arrest, laryngeal edema, angioedema, urticarial, seizures, syncope,
tremors, muscle spasms or weakness, diarrhea, drooling, and fever. If an ADE occurs, the
timing related to the injection of Dotarem will be recorded.

A crash cart is available directly across the hallway from the MRI suite in the
Sedation/Nursing area in radiology. Nursing staff and a staff radiologist are available at
all times for immediate reactions. If a severe anaphylactic or bronchospasm reaction occurs,
the patient will be brought to the Emergency Department. Management and treatment of acute
reactions to contrast media will follow the guidelines outlined in Table 4 of the ACR Manual
on Contrast Media Version 10.1 (2015).

Aldrete Scoring System:

Activity Voluntary movement of all limbs to command 2 Voluntary movement of 2 extremities to
command 1 Unable to move 0 Respiration Able to breathe deeply and cough 2 Dyspnea,
hypoventilation 1 Apnea 0 Circulation B/P + 20% of pre-anesthetic level 2 B/P + 20%-50% of
pre-anesthetic level 1 B/P + 50% of pre-anesthetic level 0 Consciousness Fully awake 2
Arousable 1 Unresponsive 0 Color Pink 2 Pale, dusky, blotchy, jaundice, other 1 Cyanotic 0

Phone Call: The follow up phone call to the parents the next day (>24 hours) will include
asking the parents the following questions:

Did your child experience any of the following after being discharged from the hospital from
the MRI exam? Headache Y/N Nausea Y/N Dizziness Y/N Dysgeusia Y/N Feeling Hot Y/N Injection
site reactions Y/N Vomiting Y/N Rash (includes generalize, macular, popular, pruritic) Y/N
Erythema Y/N Hypersensitivity/Anaphylactoid (i.e. urticarial, facial edema, eyelid edema,
flushing, cough, sneezing, wheezing, chest pain, cyanosis) Y/N Dyspnea Y/N Paresthesia Y/N

Following your child's discharge from MRI, did he/she have any other clinic appointments or
tests/exams in the hospital? If so, what were they?

Our secondary outcome is to assess the image quality of the exam. Patients will initially
undergo a pre-contrast MRI examination followed by the administration of Dotarem. The
pre-contrast images will be compared to the combined pre- and post-contrast images
independently by 3 radiologists blinded to the clinical information. The three primary
imaging components judged will be contrast enhancement, border delineation, and internal
morphology. In addition, within each of these components, the radiologist will assign a
result based on a pre-defined scoring scale. These include the following:

Pre-contrast images vs. Paired pre-post contrast images:

Border delineation: better, same, not better, missing Internal morphology: better, same, not
better, missing Contrast enhancement: better, same, not better, missing

Better is defined as those patients in which the combined pre- and post-contrast exam images
were greater than the pre-contrast images alone. Same is defined as those patients in which
the characteristics of a lesion or disease did not change following contrast administration
because of the inherent characteristics of the lesion/disease in which enhancement is not
expected. Missing identifies those patients in which a score was not assigned.

Inclusion Criteria:

- Any patient under 2 years of age undergoing an MRI exam of the neuraxis or body with
or without and with contrast as part of their standard of care.

- Included patients may be scheduled with simultaneous sedation for the MRI.

- Nonsedated patients also qualify for the study.

Exclusion Criteria:

- Patients 2 years of age or older.

- Patients receiving an MRI exam without contrast.

- Patients with a GFR <30.

- Patients with known renal failure or prior gadolinium based contrast agent
hypersensitivity reaction.

- Patients who receive an MRI exam using a different gadolinium-based contrast agent.

- Patients who are not accompanied by a parent will not be included.

- Patients who are unable to complete the MRI exam prior to contrast administration will
be excluded.