Feasibility and Diagnostic Accuracy of Myocardial Perfusion Imaging Using Early Imaging Protocol
Status: | Completed |
---|---|
Conditions: | Peripheral Vascular Disease, Cardiology |
Therapuetic Areas: | Cardiology / Vascular Diseases |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 3/1/2014 |
Start Date: | February 2013 |
End Date: | August 2014 |
Feasibility and Diagnostic Accuracy of Myocardial SPECT Using Early Imaging Protocol: A Pilot Study
The current protocol for myocardial perfusion imaging (MPI) entails imaging within 30-45
minutes after radiotracer injection, for both rest and stress studies. We hypothesize that
early imaging 10 minutes after radiotracer injection provides high image quality and
diagnostic accuracy comparable to 30-45 minutes MPI.
minutes after radiotracer injection, for both rest and stress studies. We hypothesize that
early imaging 10 minutes after radiotracer injection provides high image quality and
diagnostic accuracy comparable to 30-45 minutes MPI.
The current MPI protocol entails imaging within 30-45 minutes after radiotracer injection
(W30 imaging), for both the rest and stress part. This delay between the radiotracer
injection and imaging is intended to limit the nonspecific liver and gut radioactivity to
the heart and allows an optimal imaging of the heart. A recent publication however indicates
that an early imaging within 10 minutes after radiotracer injection (W10 imaging) appears
feasible and may be as good as W30 imaging.
Encouraged by the recent data, we think that a waiting time of 10 minutes is feasible while
preserving the image quality; thus, we would like to assess the feasibility and accuracy of
W10 imaging compared with W30 imaging in this study. The main purpose of this study is to
obtain imaging information on the use of early imaging (W10). The feasibility of W10 imaging
will be assessed visually using a 3-point scale as well as semiquantitatively using
region-of-interest measurements. The accuracy of W10 imaging will be determined by comparing
the findings of W10 with those of coronary angiography, which will be obtained within 30
days of the MPI and serve as reference standard. The tolerability of W10 will be assessed
using 3-point scale Questionnaires.
This study will determine if early MPI imaging within 10 minutes works as well as imaging
after 30-45 minutes waiting and its role in the diagnosis of coronary artery disease. The
major advantages of this new imaging procedure include the shortening of the procedure time,
the reduction of patient discomfort and improvement of patient care.
(W30 imaging), for both the rest and stress part. This delay between the radiotracer
injection and imaging is intended to limit the nonspecific liver and gut radioactivity to
the heart and allows an optimal imaging of the heart. A recent publication however indicates
that an early imaging within 10 minutes after radiotracer injection (W10 imaging) appears
feasible and may be as good as W30 imaging.
Encouraged by the recent data, we think that a waiting time of 10 minutes is feasible while
preserving the image quality; thus, we would like to assess the feasibility and accuracy of
W10 imaging compared with W30 imaging in this study. The main purpose of this study is to
obtain imaging information on the use of early imaging (W10). The feasibility of W10 imaging
will be assessed visually using a 3-point scale as well as semiquantitatively using
region-of-interest measurements. The accuracy of W10 imaging will be determined by comparing
the findings of W10 with those of coronary angiography, which will be obtained within 30
days of the MPI and serve as reference standard. The tolerability of W10 will be assessed
using 3-point scale Questionnaires.
This study will determine if early MPI imaging within 10 minutes works as well as imaging
after 30-45 minutes waiting and its role in the diagnosis of coronary artery disease. The
major advantages of this new imaging procedure include the shortening of the procedure time,
the reduction of patient discomfort and improvement of patient care.
Inclusion Criteria:
- Men and women ≥18 years of age of any race /ethnicity
- Patient has undergone or is being scheduled for a clinically indicated cardiac
catheterization with or without angioplasty
- Patient may have suffered myocardial infarction more than 3 days before MPI
- Patient may have undergone percutaneous transluminal coronary angioplasty (PTCA) or
coronary stent placement more than 3 days prior to MPI
- Interval between T99m-MPI and cardiac catheterization is within 30 days
- Females are not pregnant and lactating
- Provide signed Informed Consent prior to undergoing the study procedures
Exclusion Criteria:
- Patients less than 18 years of age
- Female patient is pregnant or nursing
- Patient has been involved in any other investigative, radioactive research procedure
within 7 days and during the study participation period
- History of 2nd or 3rd degree AV-block, or sinus node dysfunction unless the patients
have a functioning artificial pacemaker
- Myocardial infarction within 3 days before MPI
- Percutaneous transluminal coronary angioplasty (PTCA) or stent placement within 3
days prior to MPI
- Current ventricular tachycardia, atrial fibrillation, atrial tachycardia, or atrial
flutter
- Current history of exacerbated COPD or asthma
- Known hypersensitivity or contraindication to regadenoson or aminophylline
- Use of caffeinated substance, dipyridamole-containing medication, aminophylline, or
xanthines containing medication (e.g. theophylline) within the 12 hours prior to
Lexiscan administration.
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