Medical Imaging

Physicians utilize medical imaging to see inside the body to diagnose and treat patients. This includes computed tomography (CT), magnetic resonance imaging (MRI), X-ray, ultrasound, fluoroscopy, angiography,  and the nuclear imaging modalities of PET and SPECT. 

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SNMMI president elect: CMS decision will discourage amyloid research

On the heels of the final decision from CMS regarding coverage for amyloid imaging, Peter Herscovitch, MD, SNMMI 2013-2014 president elect, discussed the potential impact of the new climate of coverage in an exclusive interview with Molecular Imaging.

Book alleges NFL covered up concussion risks, tainted research

The National Football League (NFL) attempted to downplay the risks of playing football and tried to influence concussion research, according to bombshell allegations in a new book, “League of Denial: The NFL, Concussions and the Battle for Truth.”

MRI catches prostate cancers missed by standard biopsy

Multiparametric MRI has high diagnostic ability for anterior prostate cancer and was able to identify lesions missed by a standard transrectal 12-core prostate biopsy, according to a study published in the September issue of The Journal of Urology.

More evidence needed to support PET imaging in AD

Current literature on amyloid-beta PET imaging for Alzheimer’s disease (AD) is insufficient to provide conclusive evidence that the test leads to better clinical outcomes, according to a review summarized online Sept. 30 in JAMA Internal Medicine.

Sofie Bio receives $1.8M SBIR grant for phase II clinical trials

Sofie Biosciences, an emerging in vivo imaging diagnostics company focused on PET probes, scanners and chemistry systems,announced today that the National Institute of Health has awarded the company a grant under the Small Business Innovation Research (SBIR) program.

FDA grants Roche’s Perjeta accelerated approval for use before surgery in people with HER2-positive early stage breast cancer

Roche (SIX: RO, ROG; OTCQX: RHHBY) today announced that the United States (U.S.) Food and Drug Administration (FDA) granted accelerated approval of a Perjeta (pertuzumab) regimen for neoadjuvant treatment (use before surgery) in people with high-risk, HER2-positive early stage breast cancer. This approval is based primarily on data from a Phase II study showing that nearly 40 percent of people receiving the combination of Perjeta, Herceptin (trastuzumab) and docetaxel chemotherapy had no evidence of tumour tissue detectable at the time of surgery (known as a pathological complete response, or pCR). The Perjeta regimen is the first neoadjuvant breast cancer treatment approved by the FDA and also the first to be approved based on pCR data.

Novel tau imaging agent takes dementia imaging to the next level

A tau-imaging agent has moved ahead of the pack to pick up strong signals of tau aggregates in the brain in patterns consistent with Alzheimer’s disease (AD), according a study published Sept. 18 in Neuron.

Soldiers with blast-related TBI at risk for pituitary dysfunction

Soldiers suffering from traumatic brain injury (TBI) caused by an explosive blast had a higher rate of anterior pituitary dysfunction than people who sustained a non-blast TBI, suggesting pituitary dysfunction is a particular problem after blast exposure, according to a study published online Sept. 24 in Annals of Neurology.

Around the web

GE HealthCare designed the new-look Revolution Vibe CT scanner to help hospitals and health systems embrace CCTA and improve overall efficiency.

Clinicians have been using HeartSee to diagnose and treat coronary artery disease since the technology first debuted back in 2018. These latest updates, set to roll out to existing users, are designed to improve diagnostic performance and user access.

The cardiac technologies clinicians use for CVD evaluations have changed significantly in recent years, according to a new analysis of CMS data. While some modalities are on the rise, others are being utilized much less than ever before.