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Treatment of Sleep Disordered Breathing In Acute Decompensated Heart Failure Patients

Apnea Rampant In Acute Decompensated Heart Failure II

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00804349
Acronym
ARIA-II
Enrollment
6
Registered
2008-12-08
Start date
2008-10-31
Completion date
2011-10-31
Last updated
2020-03-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Failure, Sleep Apnea Syndromes

Keywords

Heart Decompensation, Heart Failure, Congestive, Heart Failure, Left-Sided, Heart Failure, Right-Sided, Apnea, Sleep, Sleep Apnea, Mixed Central and Obstructive, Sleep Hypopnea, Sleep-Disordered Breathing

Brief summary

Heart Failure affects 5-6 million Americans and there are about 550 thousand new cases of heart failure every year. There are approximately 3 million hospital admission for acute decompensated heart failure with hospital readmission rate of 20% at 30 days and 50% at 60 day, costing up to 20 billion dollars per year. In our previous study we have discovered that sleep disordered breathing is prevalent in 70% of patients with acute decompensated heart failure. We hypothesize that, detection and treatment of sleep disordered breathing in acute decompensated heart failure patients will reduce episodic hypoxic events during acute decompensation and may decrease hospital length of stay and reduce future readmissions.

Detailed description

Background: Heart failure (HF) affects 5 to 6 million Americans and is increasing in prevalence. There are about 550,000 new cases of heart failure every year and about 3 million admissions for acute decompensated heart failure every year. Despite advances in medical care, the hospital readmission rate is 20% at one month and 50% at six months. The total cost of heart failure on the health system is upwards of 35 billion dollars per year. About half of these resources are used during acute hospitalizations. An important limitation to the current approach to the management of HF is the focus on the awake patient. This approach underestimates the mechanisms that might contribute to the pathophysiology or progression of HF. Sleep disordered breathing (SDB) is very common in congestive heart failure. Recently, the adverse implications of SDB in patients with HF have been appreciated. Intermittent apnea-induced hypoxia, hypercapnia, surges in central sympathetic outflow and left ventricular afterload, daytime hypertension, and loss of vagal heart rate regulation are potent stimuli to myocyte necrosis and apoptosis, myocardial ischemia, arrhythmias, adverse cardiac remodeling, and the resulting accelerated disease progression in HF. This makes us believe that treatment of SDB during acute decompensated heart failure in addition to standard medical therapy (SMT) would be beneficial. Study Design: 80 eligible patients admitted to Albert Einstein Medical Center with the diagnosis of Acutely Decompensated Heart Failure will be recruited for the study. Once patients have been identified, inclusion and exclusion criteria met, they will be consented to participate in the trial within 24 to 48 hours of admission to the hospital. After enrollment, the patient will be screened for SDB with NEXAN CPS system. The Sensor, a flexible data collection patch that adheres to the patient's chest, continuously records ECG, respiratory, and oximetry data and allows for future use and evaluation. Patients with SDB will be further randomized to SDB monitoring only and SDB monitoring plus Autotitratable Continuous Positive Airway Pressure (APAP) treatment arm. Patients in both arms will be treated with standard of care therapy for acute heart failure. There is a possibility that patients randomized to APAP therapy may refuse further treatment after the first night. These patients will be analyzed on the basis of intention to treat approach Once randomized, all patients will be fitted with the NEXAN Clear Path System and will continue to wear it until the time of discharge or 7 days. Those in the treatment group will be fitted with an Autotitratable Continuous Positive Airway Pressure device and will be continued on treatment until discharged or a maximum of 7 days. Follow-up of these patients will include a 15 day and 60 day phone call and a 30 day office visit. At the 30 day visit the patients will be asked to use the NEXAN sensor for that night, and return the equipment the next day. The patients that were determined to have sleep-disordered breathing will be referred for a full overnight polysomnography test.

Interventions

DEVICEAutotitrating Positive Airway Pressure

Patients will be treated with Autotitrating Positive Airway Pressure therapy

Sponsors

Nexan Inc
CollaboratorINDUSTRY
Albert Einstein Healthcare Network
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients over the age of 18 and able to consent * NYHA Class III/IV Symptoms * Objective Evidence of Heart Failure * Physical Exam consistent with Heart Failure * BNP greater than 500 * Radiographic Evidence of Heart Failure * SDB (AHI \> 5/hour) on Nexan CPS * Ability to tolerate appropriate medical therapy for Heart Failure * Willingness to follow-up as an outpatient after discharge

Exclusion criteria

* Patients with known Sleep-Disordered Breathing currently using CPAP or BiPAP * Patients with known COPD * Patients with known restrictive lung disease * Patients with tracheostomy in place * Acute MI/Acute Coronary Syndrome at time of hospitalization * Cardiogenic Shock * Troponin Leak greater than 0.08 * Patients with major multisystem disorders * Expected survival less than 6 months * End Stage Renal Disease on Dialysis * Chronic Liver Disease * Albumin level less than 3. * Patients from Nursing homes

Design outcomes

Primary

MeasureTime frameDescription
Reduction in Episodic Oxygen DesaturationConcurrent0 participants analyzed. Study closed; PI no longer at the institution. Efforts to have the PI add the required information have been unsuccessful. No study data are available.

Secondary

MeasureTime frameDescription
Readmission30 days post discharge0 participants analyzed. Study closed; PI no longer at the institution. Efforts to have the PI add the required information have been unsuccessful. No study data are available.
Length of StayConcurrent0 participants analyzed. Study closed; PI no longer at the institution. Efforts to have the PI add the required information have been unsuccessful. No study data are available.
Visual Analog Scale of Shortness of BreathConcurrent0 participants analyzed. Study closed; PI no longer at the institution. Efforts to have the PI add the required information have been unsuccessful. No study data are available.

Countries

United States

Participant flow

Recruitment details

0 participants analyzed. Study closed; PI no longer at the institution. Efforts to have the PI add the required information have been unsuccessful. No study data are available.

Pre-assignment details

0 participants analyzed. Study closed; PI no longer at the institution. Efforts to have the PI add the required information have been unsuccessful. No study data are available.

Participants by arm

ArmCount
Control
Patients will receive standard medical therapy for heart failure only and will not receive Autotitrating Positive Airway Pressure therapy. 0 participants analyzed. Study closed; PI no longer at the institution. Efforts to have the PI add the required information have been unsuccessful. No study data are available.
0
Autotitrating Positive Airway Pressure
Patients will receive Autotitrating Positive Airway Pressure therapy in addition to standard medical care for heart failure. Autotitrating Positive Airway Pressure: Patients will be treated with Autotitrating Positive Airway Pressure therapy 0 participants analyzed. Study closed; PI no longer at the institution. Efforts to have the PI add the required information have been unsuccessful. No study data are available.
0
Total0

Baseline characteristics

Characteristic
Region of Enrollment
United States
— participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 00 / 0
other
Total, other adverse events
0 / 00 / 0
serious
Total, serious adverse events
0 / 00 / 0

Outcome results

Primary

Reduction in Episodic Oxygen Desaturation

0 participants analyzed. Study closed; PI no longer at the institution. Efforts to have the PI add the required information have been unsuccessful. No study data are available.

Time frame: Concurrent

Population: 0 participants analyzed. Study closed; PI no longer at the institution. Efforts to have the PI add the required information have been unsuccessful. No study data are available.

Secondary

Length of Stay

0 participants analyzed. Study closed; PI no longer at the institution. Efforts to have the PI add the required information have been unsuccessful. No study data are available.

Time frame: Concurrent

Population: 0 participants analyzed. Study closed; PI no longer at the institution. Efforts to have the PI add the required information have been unsuccessful. No study data are available.

Secondary

Readmission

0 participants analyzed. Study closed; PI no longer at the institution. Efforts to have the PI add the required information have been unsuccessful. No study data are available.

Time frame: 30 days post discharge

Population: 0 participants analyzed. Study closed; PI no longer at the institution. Efforts to have the PI add the required information have been unsuccessful. No study data are available.

Secondary

Visual Analog Scale of Shortness of Breath

0 participants analyzed. Study closed; PI no longer at the institution. Efforts to have the PI add the required information have been unsuccessful. No study data are available.

Time frame: Concurrent

Population: 0 participants analyzed. Study closed; PI no longer at the institution. Efforts to have the PI add the required information have been unsuccessful. No study data are available.

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026