FDA Approves ZOLL remedē System for MRI Conditional Use

The United States Food and Drug Administration (FDA) has approved the remedē System, marketed by ZOLL Medical Corporation, for conditional use with magnetic resonance imaging (MRI). ZOLL’s remedē System is an implantable transvenous phrenic nerve stimulation therapy for the treatment of adults with moderate to severe central sleep apnea. Full-body MRI approval applies to all…

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Women’s Silent Battle with Mild OSA

Interview by Alyx Arnett Women with obstructive sleep apnea (OSA) often present with lower apnea-hypopnea indexes (AHI) and fewer oxygen desaturations than men, as well as atypical symptoms like fatigue and insomnia—differences that put them at risk of being underdiagnosed and undertreated.1  Alison Wimms, PhD But despite its subtler appearance, research suggests that the negative…

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