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Friday, Dec 20 2024

Full Issue

FDA Approves ARC-EX Device For Non-Invasive Spinal Cord Stimulation

Meanwhile, synthetic gel aids in recovery after spinal surgery; Pittsburgh researchers create helper robots for people with ALS; a study finds nerve stimulation is effective against treatment-resistant depression; and more.

Spinal cord injuries dramatically reduce a person鈥檚 mobility and independence, but a new device could aid rehabilitation efforts. Onward Medical received Food and Drug Administration clearance on Thursday for its non-invasive spinal cord stimulator, the ARC-EX. In a recent trial, the stimulator boosted hand sensation and strength in 72% of participants. While the treatment cannot replace rehabilitative therapy, device users rave about its effects. (Broderick, 12/19)

For those recovering from spinal surgery, the process can be lengthy and precarious, as patients try to circumvent infection and regain mobility. A key hiccup? The ever-present risk of a herniated disc. Now, Swedish researchers may have identified an unlikely solution in the form of a slime, inspired by the slick coating that covers parasites in the stomach of cows. This slimy coating helps the parasites duck the immune system and prevents immune cells from recognizing them. (Hagmajer, 12/19)

A University of Pittsburgh research group is reaching new limits and perfecting a robot to help people with ALS live better lives. Stretch, a robot by the company Hello Robot, looks like a Roomba from the future. Researchers in Pitt's Accessible Smart-Tech Research Group teamed up with Hello Robot and the ALS Association to work on advancing Stretch.聽(Guay, 12/19)

Nick Fournie was 24 years old when severe depression upended his life. Fournie had been married to his longtime sweetheart for two years, and had no reason to suspect he had any mental health issues. 鈥淚 just thought to myself, 鈥業f this is it, if this is all there is to life 鈥 if it ended now, I鈥檇 be OK with it,鈥欌 Nick, now 62 and based in Illinois, said of that fateful day outdoors nearly 40 years ago. (Rogers, 12/19)

Also 鈥

Reaching the end of a long road to approval, the first mesenchymal stromal cell (MSC) therapy for steroid-refractory acute graft-versus-host disease (GVHD) finally reached the FDA green light. The approval of remestemcel-L (Ryoncil) specifies use in pediatric patients 2 months or older with steroid-refractory acute GVHD. The cellular therapy received a vote of confidence from the Oncologic Drugs Advisory Committee in 2020, despite questions regarding the product's consistency and the approval request's reliance on data from a single-arm clinical trial. (Bankhead, 12/19)

Major cardiovascular event risk in patients with inflammatory bowel disease (IBD) was no greater with Janus kinase (JAK) inhibitors than with tumor necrosis factor (TNF) inhibitors, according to a retrospective single-center study. ... Despite the effectiveness of JAK inhibitors for IBD, the authors noted that concerns about cardiovascular safety have circulated since the 2022 ORAL Surveillance study found a higher risk of major adverse cardiovascular events in rheumatoid arthritis (RA) patients who took tofacitinib compared with those on TNF inhibitors. (Haelle, 12/19)

Two studies published yesterday in the New England Journal of Medicine聽show that 6 months of preventive treatment with levofloxacin in children and adults with household exposure to multidrug-resistant tuberculosis (TB) resulted in statistically non-significant reductions in TB incidence compared with placebo. But an additional analysis of individual data from the two trials, which were conducted in Vietnam and South Africa, found that preventive levofloxacin led to a much larger relative reduction in cumulative incidence of TB than was initially observed. (Dall, 12/19)

This is part of the Morning Briefing, a summary of health policy coverage from major news organizations. Sign up for an email subscription.
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