Parkinson’s AI Proves Accuracy In Clinical Studies Reports PD Neurotechnology

Study shows wearable Parkinson’s monitor, which uses machine learning to detect and assess motor symptoms, is more than 95 per cent accurate when compared to expert evaluation

The results of a multi-site clinical study analysing the performance of PDMonitor, a pioneering Parkinson’s Disease monitoring device from PD Neurotechnology that uses wearables and Artificial Intelligence (AI) to track and assess symptoms, have been published in Frontiers in Neurology, a leading peer-reviewed clinical neurology journal.

The study compared PDMonitor’s automated assessments of Parkinson’s patients at three European hospitals with physicians’ clinical evaluations and symptom diaries to help determine whether the device provided a reliable and feasible means of informing treatment plans. PDMonitor uses five sensors worn on the patient’s trunk and limbs to gather data about the timing and severity of symptoms, and machine learning algorithms to complete its assessments.

Statistical analysis demonstrated a high level of accuracy in symptom detection and a strong correlation with expert evaluation when assessing their severity. PDMonitor achieved accuracy and specificity levels of 99 per cent or more when detecting mild to severe dyskinesia, gait impairment, wrist and leg tremor, and at least 96 per cent when detecting ‘Off’ periods when Parkinson’s symptoms re-emerge between medication doses.

A second study, details of which were also published in Frontiers in Neurology, confirmed that PDMonitor can be used effectively and easily by patients and caregivers, taking just five minutes, on average, to attach the sensors, even for patients at later stages of the disease. Automatic recording and identification of each sensor’s location on the patient’s body were found to further improve the ease of using the device.

These peer-reviewed papers are part of a growing body of evidence highlighting the accuracy and efficacy of PDMonitor. Preliminary findings from the analysis of data about 267 patients in Greece provide evidence that continuous telemonitoring in clinical practice can lead to the alleviation of Parkinson’s symptoms. The average ‘Off’ time experienced by patients in this study fell for two consecutive quarters following the introduction of PDMonitor.

In January 2023, PDMonitor was one of five devices to be conditionally recommended for remote monitoring of Parkinson’s disease to inform treatment by NICE, the National Institute for Health and Care Excellence. This decision opened the door to the use of PDMonitor by NHS patients and their physicians in the UK.

Nikos Moschos, Managing Director of PD Neurotechnology, comments:

“Our monitoring device is a game-changer in the fight against Parkinson’s. Studies confirm that it is effective and easy to use, and we have seen time and again how it facilitates better treatment decisions for patients based on real-world data. By providing accurate and continuous data on symptoms, together with an ecosystem to collect and present effectively, we are always aiming to help improve the management of Parkinson’s and hopefully enhance patients’ quality of life.”

Professor K Ray Chaudhuri, Head of Parkinson’s Foundation Centre of Excellence at King’s College Hospital, who has been piloting PDMonitor with private patients since March 2022, comments:

“Parkinson’s is the world’s second most common neurodegenerative disease and a significant cause of disability at a huge societal cost.  Patients’ quality of life and wellness strongly depend on the consistent, prompt monitoring of disease progression and optimal timing and dosing of the prescribed therapy.”

“PDMonitor is supporting an emerging paradigm shift in Parkinson’s care by moving from traditional short lived face to face consultations to be augmented by home monitoring which has many advantages similar to monitoring in diabetes and cardiac disorders.

“Monitoring patients at home, continuously while they conduct everyday activities, allows treatment decisions to be made more frequently and physicians to respond faster to changing symptoms.

“A major advantage of PDMonitor is its ability to provide a self-monitoring platform for patients in addition to monitoring gait and risk of falls, gait, and bone health being a major feature in the recently described ‘dashboard of vitals’ of Parkinson’s Disease.

“While you cannot reverse Parkinson’s, one can delay the deterioration of symptoms and possibly decrease the risk of falling. Mobility falls and related fractures remain a major cause of morbidity and hospitalisation in Parkinson’s Disease. Prudent use of PD Monitor data, therefore, means accurate assessment with a snapshot of home activities so as to provide a dashboard based bespoke personalised care.”

Hot this week

Cartessa Aesthetics Partners with Classys to Bring EVERESSE to the U.S. Market

Classys, which is listed on the KOSDAQ, is one of South Korea's most distinguished aesthetic technology manufacturers, with devices distributed in 80+ markets globally. This partnership marks Classys's official entry into the American marketplace, with Cartessa Aesthetics as the exclusive distributor for EVERESSE, launched under the Volnewmer brand in current global markets.

Stryker Launches Next-Generation of SurgiCount+

Now integrated with Stryker's Triton technology, SurgiCount+ addresses two key challenges: retained surgical sponges and blood loss assessment. Integrating these previously separate digital solutions provides the added benefit of a more efficient, streamlined workflow for hospitals notes Stryker.

Nevro Receives CE Mark In Europe for It’s HFX iQ™ Spinal Cord Stimulation System

Nevro notes HFX iQ is the first and only SCS system with artificial intelligence (AI) technology that combines high-frequency (10 kHz) therapy built on landmark evidence that uses ongoing cloud data insights to deliver personalized pain relief

Recor Medical Reports: CMS Grants Distinct TPT Device Code and Category to Recor Medical for Ultrasound Renal Denervation

The approval of TPT offers incremental reimbursement payments for outpatient procedures performed with ultrasound renal denervation for Medicare fee-for-service beneficiaries. It becomes effective January 1, 2025, and is expected to remain effective for up to three years notes Recor Medical.

Jupiter Endovascular Reports | 1st U.S. Patient Treated with Jupiter Shape-shifting Thrombectomy Device

“Navigation challenges during endovascular procedures are often underappreciated and have led to under-adoption of life-saving procedures, such as pulmonary embolectomy. We have purpose-built our Endoportal Control technology to solve these issues and make important endovascular procedures accessible to more clinicians and their patients who can benefit from them,” said Carl J. St. Bernard, Jupiter Endovascular CEO. “This first case in the U.S. could not have gone better, and appears to validate the safety and performance we are seeing in our currently-enrolling European SPIRARE I study.”
Exit mobile version