Effects of Nocturnal Nasal Oxygen on Biomarkers in Sleep Apnea Patients With Heart Failure
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Purpose
Sleep apnea syndrome is clinically defined by frequent pauses in breathing during sleep and symptoms, such as being tired. It can decrease the restfulness of sleep and decreases the level of oxygen in the blood. Sleep apnea patients suffer from daytime sleepiness, hypertension, coronary artery disease (CAD), stroke, ischemic heart disease, arrhythmias, pulmonary hypertension, heart failure, and premature death. There is significant evidence suggesting that nighttime decreases in blood oxygen levels are the primary cause of many of the abnormalities associated with this disease.
Epidemiological studies have demonstrated a surprisingly high prevalence of sleep apnea. Mild sleep apnea is present in 17% of adults in the general population and moderate to severe sleep apnea is present in 5.7% of adults. Among patients with heart failure the prevalence skyrockets. Multiple studies have found the prevalence of moderate to severe sleep apnea to be anywhere from 11-53% in heart failure patients.
Continuous positive airway pressure (CPAP) therapy is currently the standard of care for sleep apnea sufferers regardless of the severity of their disease. In patients without heart failure, CPAP therapy has numerous benefits and several long term studies have reported that CPAP causes less cardiovascular disease as well as a long term improvement in cardiovascular symptoms and mortality among patient with severe sleep apnea.
In heart failure patients, CPAP has shown some beneficial short term effects but evidence of long term improvements in symptoms and mortality are lacking. Compliance with CPAP therapy reduces systolic blood pressure, improves cardiac function, raises oxygen levels, and increases exercise tolerance. On the other hand, CPAP has not been shown to affect survival or number of hospitalizations in heart failure patients. Moreover, compliance with CPAP is often poor and many people cannot tolerate it. This further limits the therapeutic effectiveness of this intervention.
The purpose of this study is to assess whether nocturnal oxygen administration via nasal cannula alone can improve outcomes in congestive heart failure patients with moderate to severe sleep apnea. The effects of nocturnal oxygen administration will be assessed by using biomarkers of heart stress and markers of whole body inflammation.
| Condition | Intervention |
|---|---|
|
Sleep Apnea Heart Failure |
Procedure: Nocturnal nasal oxygen Other: No nasal oxygen |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Crossover Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Effects of Nocturnal Nasal Oxygen on Biomarkers in Sleep Apnea Patients With Heart Failure |
- BNP (a blood test which is a biomarker for heart failure) [ Time Frame: 1 month ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 20 |
| Study Start Date: | November 2011 |
| Estimated Primary Completion Date: | October 2013 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Active Comparator: Nasal oxygen
Nocturnal nasal oxygen
|
Procedure: Nocturnal nasal oxygen
Nasal oxygen at 2 l/min will be given at night
|
| Placebo Comparator: No nasal oxygen |
Other: No nasal oxygen
Patients will have no intervention for sleep apnea
|
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- RDI > 15
- Symptomatic Heart failure
- Oxygen saturation < 88% during apnea
- Not currently be on nocturnal oxygen therapy, CPAP, or other PAP therapy
Exclusion Criteria:
- Hypoxemia requiring oxygen supplementation
- serum creatinine > 2.5 or on chronic dialysis
- blood pressure > 160
- pregnant
- chronic physical disability that would prevent subjects from participating in any aspect of the trial
Contacts and Locations| Contact: Stephen Gottlieb, MD | 410-328-8788 | sgottlie@medicine.umaryland.edu |
| United States, Maryland | |
| University of Maryland | Recruiting |
| Baltimore, Maryland, United States, 21201 | |
| Contact: Stephen Gottlieb, MD 410-328-8788 sgottlie@medicine.umaryland.edu | |
| Principal Investigator: Stephen Gottlieb, MD | |
| Baltimore VA Medical Center | Not yet recruiting |
| Baltimore, Maryland, United States, 21201 | |
| Contact: Stephen S Gottlieb, MD 410-328-8788 sgottlie@medicine.umaryland.edu | |
More Information
No publications provided
| Responsible Party: | Steve Gottlieb, Professor, University of Maryland |
| ClinicalTrials.gov Identifier: | NCT01431157 History of Changes |
| Other Study ID Numbers: | HP-00049080 |
| Study First Received: | September 7, 2011 |
| Last Updated: | May 11, 2012 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by University of Maryland:
|
Sleep Apnea Syndrome Heart Failure Oxygen Inhalation Therapy |
Additional relevant MeSH terms:
|
Apnea Heart Failure Sleep Apnea Syndromes Respiration Disorders Respiratory Tract Diseases Signs and Symptoms, Respiratory Signs and Symptoms |
Heart Diseases Cardiovascular Diseases Sleep Disorders, Intrinsic Dyssomnias Sleep Disorders Nervous System Diseases |
ClinicalTrials.gov processed this record on June 17, 2013