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Should Surgeons Postpone Airway Evaluation During DISE?

For DISE to determine sleep apnea therapy candidacy, the first 10+ minutes may not be representative of airway collapse.

United statesRajcc dedhiaAlyx arnettAsim royDavid kentAlanr schwartzAmerican academy of otolaryngologyDivision of sleep surgeryUniversity of pennsylvaniaVanderbilt university medical centerOhio sleep medicine instituteInspire medicalNeck surgerySleep surgeryScientific orals

One Less Worry About Neurostimulators

What MRI compatibility means for neurostimulator referrals for sleep apnea. Inspire, remede, and Genio are all MRI compatible.

United statesDavid kentSeamus jacksonB tucker woodsonAsim royNyxoah genioSree royOhio sleep medicine instituteVanderbilt university medical centerDrug administrationOhio sleep medicineInspire modelInspire medical systemsVanderbilt university medical

FDA Approves ZOLL remedē System for MRI Conditional Use

Full-body MRI approval applies to all models of remedē System, covering new remedē patients as well as those who already have a remedē device.

United statesCollin andersonAsim royOhio sleep medicine instituteDrug administrationUnited states food

FDA approves Zoll therapy for sleep apnea with MRI

Zoll Medical announced that it received FDA approval for its Remedē system for conditional use with magnetic resonance imaging (MRI).

United statesAsim royZoll respicardiaCollin andersonOhio sleep medicine instituteMassachusetts based zoll

FDA Grants De Novo Status for Wearable System to Treat RLS

The FDA granted Noctrix Health its De Novo request for the NTX100 Tonic Motor Activation System for certain restless legs syndrome patients.

United statesAsim royShri raghunathanMark buchfuhrerNoctrix healthStanford university school of medicineDrug administrationOhio sleep medicine instituteMotor activation systemBreakthrough device designationStanford university school

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