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Understanding the mechanism of radiation induced fibrosis and therapy options

Always check first, adjust safely, and let evidence lead the way

The FDA reviewed Medical Device Reports (MDRs) and literature reports which describe adverse events, such as neurological deficits (e.g., focal motor deficits, aphasia, cognitive changes), increased intracerebral edema or pressure, intracranial bleeding, and/or visual changes (e.g., visual field deficits, blurry vision) when these devices were used to treat intra-cranial lesions

DSIPs ability to enhance sleep quality during whatever window is available makes it potentially valuable for this population

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