Heart Failure, Sleep Apnea, Central
Conditions
Brief summary
The study objectives are to demonstrate the ease and safety of bilateral cervically implanted phrenic nerve stimulators for Central Sleep Apnea in patients with Heart Failure. To demonstrate the efficacy, both in the short and long term, of implanted phrenic nerve stimulators in patients with Central Sleep Apnea and Heart Failure. Central Sleep Apnea is a form of hypoventilation syndrome, for which this device is FDA approved. We will also determine if the patient's quality and duration of life is improved by using the PNS to treat CSA in heart failure patients.
Detailed description
This is a multi-center prospective cohort study to monitor the effect of bilateral phrenic nerve stimulation for treatment of central sleep apnea (CSA) in patients with heart failure. There will be 2 groups of study patients, both with CSA and heart failure. One group will receive the phrenic nerve pacer, and one will not. Both groups will have the same medical oversight, management, and assessment of heart health whether they receive the pacer or not. Subjects will have a physical exam, review of medications, New York Heart Association (NYHA) functional classification assessment for heart failure, Minnesota Living With Heart Failure (MLWHF) Questionnaire for quality of live assessment and blood test for Pro-BNP. In-lab sleep study will be required if subject haven't had one within 3 months, and Echocardiogram, if subjects haven't had one within 30 days. If subjects are willing to have stimulator placement procedure, they'll have an ENT consult. Subjects in the procedure arm will have Phrenic Nerve Stimulator placement procedure, and 3 weeks after procedure follow up visit with ENT doctor to activate the device and have sleep study to confirm proper settings.
Interventions
DEVICEPhrenic nerve stimulator
Implantation of phrenic nerve stimulator
Sponsors
Steward St. Elizabeth's Medical Center of Boston, Inc.
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
Yes
Inclusion criteria
* 1\. Male or female, age 18 to 80 years inclusive. 2\. New York Heart Association (NYHA) class III or IV, or NYHA class II with an episode of heart failure requiring hospitalization in the past 24 months. 3\. Stable on guide line directed medical therapy (GDMT) for 30 days prior to enrollment. 4\. Moderate or severe sleep apnea, that is an Apnea Hypopnea Index (AHI) of \>15/hour with \>50% being central apneas. 5\. Willing and able to provide written informed consent in compliance with the regulatory requirements. If a subject is unable to provide written informed consent, written informed consent may be obtained from the subject's legal representative.
Exclusion criteria
1. Phrenic nerve palsy. 2. Baseline hypoxia (oxygen saturation \<90% on room air). 3. On supplemental oxygen. 4. Severe COPD. 5. Unstable angina, MI or cardiac procedure within 3 months of phrenic nerve stimulator placement. 6. Unwilling or unable to comply with the requirements of this protocol, including the presence of any condition (physical, mental, or social) that is likely to affect the subject's ability to comply with the protocol. 7. Any other reasons that, in the opinion of the Investigator, the candidate is determined to be unsuitable for entry into the study. \-
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Number of participants with treatment related adverse events as assessed by CTCAEv40 | 2 years | Visual Analog Score for pain, BMI in Kg/m \^2 |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Improvement in quality of life with phrenic nerve stimulation in patients with central sleep apnea and heart failure | 2 years | Physicians Global Assessments to measure quality of life, |
Countries
United States
Outcome results
None listed