Release date: 2014-09-12
According to Mobihealthnews, a wearable device for monitoring and treating Parkinson's disease has recently obtained FDA approval. According to Global Dynamics, based in Melbourne, Australia, the company's product, KinetiGraph, provides comprehensive, automated reports of exercise in patients with Parkinson's disease, allowing neurologists and other physicians to more easily identify changes in motor symptoms to assist in their decision making. Optimize treatment.
The company's CEO said monitoring changes in patient motor symptoms is key to the treatment of Parkinson's and other sports-related diseases. But it is difficult for patients and doctors to identify and assess effective monitoring of changes in their movements, but individual KinetiGraph can provide clinicians with a clear and accurate assessment of patient conditions beyond the examination.
The wristband device has been released in Australia but was previously not available for sale in the United States. The device can be administered to a Parkinson patient by a clinician who can be used at home after obtaining the device. It collects and stores 10 days of athletic data. Shorthand can be downloaded by a doctor for more accurate assessment of a patient's athletic ability, which is more accurate than an assessment made at the clinic.
The device can also be used as a drug compliance tool for levodopa with Parkinson's symptomatic treatment. The device can set a preset number of vibrations to remind the patient to take medication on time.
Dr. Robert Griffith, chief scientific officer of one of the founders of Global Dynamics, which developed the technology, said the technology has enabled clinicians to reach a whole new level of accurate assessment of Parkinson's disease for more effective and timely treatment.
This summer, the FDA has approved two wristband motion monitoring devices from Camntech, UK. The device cannot be connected to a smartphone, mainly for clinical use, and the device is highly accurate. In July, Australia's DrosaVi followed, and its ViMove sensor system for fine motion tracking was also approved by the FDA. At the same time, Orthocare Innovations, its equipment StepwWatch equipment has long-term FDA license, created the spin-off company Modus health to operate its equipment, currently used for clinical research.
Source: Kexun Medical Network
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