Smartphone-Based Grading and Rehabilitation in Patients With Facial Palsy Using Computer Vision: Prospective Validation Study
Background: Peripheral facial palsy causes significant functional and psychosocial impairments, requiring precise assessment and patient engagement for effective rehabilitation. However, conventional clinician-graded scales (eg, House-Brackmann Scale, Sunnybrook Facial Grading System, and Stennert Index) are subjective and prone to interobserver variability, limiting their reliability for tracking recovery. Smartphone-based computer vision solutions offer objective, standardized facial movement grading, and interactive home-based training to improve adherence and outcomes. Objective: This pilot study evaluated a novel iOS smartphone app (Apple Inc.) for facial palsy management. The app uses the iPhone TrueDepth 3D camera and on-device computer vision to compute a Digital Facial Index (DFI) for objective facial movement analysis, and provides guided neuromuscular facial exercises with real-time biofeedback. The study aimed to validate DFI against standard clinical grading scales and assess patient-reported outcomes and usability. Methods: A 4-week single-arm pilot included 21 patients with unilateral facial palsy. Participants used the app at home for daily facial exercises and periodic self-assessments with DFI. Clinicians, blinded to DFI, rated facial function from standardized video exams at baseline and 4 weeks using the House-Brackmann Scale, the Sunnybrook Facial Grading System, and the Stennert Index. DFI concurrent validity was evaluated via correlation with these clinician scores. Patient-reported outcomes included pre- and postintervention Facial Disability Index (FDI) physical and social scores, the System Usability Scale, and a poststudy user feedback questionnaire. Results: During the study period, strong correlations were observed between DFI and conventional clinical scores. FDI physical and social showed significant functional improvement. Mean System Usability Scale was 88.3 (SD 15.4), indicating excellent usability, and participants reported high satisfaction, preferring the app over traditional paper-based exercises. Conclusions: The app’s DFI provided objective facial function grading that correlated well with standard clinical scales. Patients’ FDI scores improved significantly over 4 weeks. High usability and patient preference support the app’s feasibility for home-based rehabilitation. This digital approach is promising for facial palsy management, and controlled studies are needed to confirm efficacy and improve long-term engagement.
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Testing a Smartphone-Based Intervention Targeting Anxiety Sensitivity Among Women Presenting for Emergency Care After Sexual Assault: Pilot Randomized Controlled Trial
Background: Anxiety sensitivity (AS), defined as the fear of anxious arousal, is a promising therapeutic target for reducing posttraumatic stress disorder (PTSD) symptom development after trauma exposure. Initial research suggests that smartphone-based AS interventions may be acceptable to sexual assault survivors at risk for PTSD symptoms and effective for symptom reduction, but only small one-arm proof-of-concept studies have been conducted. Objective: The goal of this study was to extend prior proof-of-concept work by conducting a pilot randomized controlled trial. The aims were to evaluate intervention efficacy, AS and PTSD symptom change, the acceptability and credibility of a control intervention, and the feasibility of a larger randomized controlled trial. Methods: A total of 60 women with high AS presenting for emergency care after sexual assault were recruited and randomized to either the AS intervention or a control condition, and they were followed up with for over 6 months via remote self-report questionnaires. Results: The findings indicated that the study population is at risk and in need of intervention: 88.8% (40/45) and 80.6% (29/36) of women sexual assault survivors in the sample met the criteria for probable PTSD at 7 weeks and 6 months post assault, respectively. Most (16/27, 59.3%) individuals receiving the AS intervention who completed it rated it as acceptable (eg, 18/21, 85.7% reported that the treatment was helpful). Early within-group reductions were not statistically significant, but by month 6, statistically significant reductions in AS and PTSD symptoms were observed in both conditions. Recruitment and retention data supported the feasibility of the study design, although some suggestions were noted for future research (eg, improving intervention and ecological momentary assessment compliance). Conclusions: This pilot study replicated the proof of concept and acceptability of a novel smartphone-based intervention targeting AS delivered to women sexual assault survivors presenting to emergency care. Intervention completion was in line with or better than traditional therapy but remained a challenge. Our selected control condition demonstrated a larger effect than expected, and we were unable to track its initiation or completion, causing difficulty in drawing conclusions. Overall, the results highlight the need for additional research. Trial Registration: ClinicalTrials.gov NCT05305235; https://clinicaltrials.gov/ct2/show/NCT05305235
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An In-Hospital Mortality Risk Model for Patients Undergoing Coronary Artery Bypass Grafting Based on Machine Learning: Cohort Study
Cell Therapy Shows Promise for Treating Advanced Liver Disease
A type of cell therapy made up of macrophage cells can lower risk for death or need for a liver transplant in people with cirrhosis due to advanced liver disease.
The research, published in Cell Stem Cell, was a long term follow-up study of patients recruited into an earlier Phase I/II trial and showed a 27.5% drop in risk for death or liver transplant in those who received the therapy versus usual care over up to four years of follow up.
“Cirrhosis represents a major global health burden, with substantial and rising morbidity and mortality,” write lead author Stuart Forbes, PhD, a professor at the University of Edinburgh and scientific founder of Resolution Therapeutics—the biotech developing the therapy, and colleagues.
“Apart from liver transplantation, therapeutic options for end-stage disease remain limited to supportive care and management of complications, underscoring the urgent need for innovative approaches to halt or reverse disease progression.”
The treatment used in the study involves extracting monocyte cells from the blood of patients and converting them to macrophages in the lab before injecting the macrophages into the liver to trigger repair.
The therapy is designed to overcome the tissue damage and scarring seen in people with advanced cirrhosis where the liver loses its normal ability to regenerate itself. Macrophages are able to break down scar tissue, reduce inflammation and encourage the growth of new and healthy cells in the liver.
In the initial MATCH Phase I/II study, 26 patients had macrophage therapy and 24 received standard care. After the follow up period, 30.8% of those in the treatment group had died or needed a transplant versus 58.3% of the standard care group. No serious adverse events were linked to the cell therapy.
“Liver disease is a major cause of death… Although we can use liver transplantation as a rescue treatment for a proportion of people who have advanced liver disease, this is restricted by a lack of suitable donor organs… There is therefore a desperate need for alternative treatments for patients with advanced liver disease,” commented Forbes, in a press statement.
“We hope this type of approach could one day add to our treatment choices for patients with advanced liver disease, reducing the need for liver transplants.”
Resolution has another similar Phase I/II trial to Match underway called Emerald that is building on the initial results but using macrophages modified to be more effective at tackling liver damage.
The company is also running an observational trial called Opal, a study in patients with cirrhosis and hepatic decompensation, to characterize disease trajectories and help design endpoints and inclusion criteria for future interventional trials.
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STAT+: Eli Lilly says Verve’s gene editor lowers cholesterol levels in early study
Eli Lilly said Monday that a high dose of its gene-editing therapy reduced cholesterol levels by 62% in participants in a clinical trial, an early but encouraging test of whether a one-time treatment may one day help people seeking to lower their LDL, or “bad,” cholesterol.
Lilly acquired the therapy, VERVE-102, in its $1 billion buyout of Verve Therapeutics last year. Executives tout it as a potential treatment to broadly prevent heart disease, the world’s leading killer, as many patients struggle to stay on existing, more conventional medicines for reducing cholesterol levels.
There were no treatment-related serious adverse events in the Phase 1 study — a notable finding, given that Verve had to shelve its first candidate due to safety concerns.

