Effect of Heart Valve Replacement on Cheyne-Stokes Respiration (CSR)
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Purpose
Sleep disordered breathing, especially central sleep apnea, is common in patients with chronic heart failure. Heart valve replacement could have some effect on central sleep apnea. The aim of the study is to investigate effect of heart valve replacement on Cheyne-Stokes respiration in patients with rheumatic heart disease.
| Condition | Intervention |
|---|---|
|
Cheyne-Stokes Respiration Heart Valve Disease Central Sleep Apnea |
Procedure: heart valve replacement |
| Study Type: | Interventional |
| Study Design: | Endpoint Classification: Efficacy Study Intervention Model: Single Group Assignment Masking: Single Blind (Investigator) Primary Purpose: Screening |
| Official Title: | Effect of Heart Valve Replacement on Cheyne-Stokes Respiration in Patients With Rheumatic Heart Disease |
- Changes of CSR index before and 3, 6, 12 months following valve replacement. [ Time Frame: 1 year after cardiac surgery of each enrolled patient ] [ Designated as safety issue: Yes ]The primary goal of this study is to compare the changes of polysomnography(PSG) parameters(index of CSR, apnea hypopnea index, pulse oxygen saturation, etc)before and 3, 6, 12 months following the cardiac valve replacement surgery.
- Association of PSG parameters with cardiac function before and 3, 6, 12 months following valve replacement [ Time Frame: 1 year after cardiac surgery of each enrolled patient ] [ Designated as safety issue: Yes ]The secondary goal of this study is to determine the association of PSG parameters(index of CSR, apnea hypopnea index, pulse oxygen saturation, electrocardiogram, etc)and cardiac function (LVEF, 6-minute walk test, etc) before and 3, 6, 12 months following the cardiac valve replacement surgery. Qualities of life and sleep will also be masured before and 3, 6, 12 months after surgery. (The quality of life is assessed by reference to "The Medical Outcomes Study 36item Short-Form Health Survey"(SF-36) generic questionnaire, and sleep quality is assessed by Pittsburgh Sleep Quality Index(PSQI).)
| Enrollment: | 26 |
| Study Start Date: | September 2010 |
| Study Completion Date: | July 2012 |
| Primary Completion Date: | February 2012 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| heart valve replacement |
Procedure: heart valve replacement
The patients with heart valve disease and CSR will be received heart valve replacement
Other Name: cardiac surgery
|
Detailed Description:
Sleep apnea, especially central sleep apnea, has a high prevalence in patients with chronic heart failure. Although sleep disordered breathing (SDB) have been described in patients with heart disease, the prevalence is not known because: ①There are various forms of SDBs, including obstructive sleep apnea(OSA), central sleep apnea (CSA), and mixed forms of sleep apnea syndromes that have variable prevalence; ②Patients suffering from rheumatic valve disease usually have varying degrees of heart failure, and this variability affects estimates of prevalence; ③There are no international patient registries and SDB is underdiagnosed in many parts of the world.
The previous studies are most focusing on nonvalvular disease. We ①investigate the prevalence and the risk factors of Cheyne-Stokes respiration in patients with heart valve diseases, ②compare the changes of parameters of Cheyne-Stokes Respiration and heart function (like apnea hypopnea index, pulse oxygen saturation, blood pressure, echocardiogram, electrocardiogram, 6-minute walk test) before heart valve replacement and 3, 6, and 12 months after the surgery.
With nocturnal polysomnography (PSG) examination 30 patients typical CSR are going to be screened out from 300 patients with heart valve disease and waiting for cardiac surgery. The Comparison of 30 patients undergoing heart valve replacement will be performed before and 3, 6, and 12 months following heart valve replacement. We shall analyze the changes of CSR before and after valve replacement as well as the correlation among cardiac function and PSG parameters.
Eligibility| Ages Eligible for Study: | 18 Years to 70 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- heart valve disease with any ejection fraction
- clinical diagnosis of Cheyne-Stokes respiration
Exclusion Criteria:
- unstable heart failure
- stroke
- transient ischemic attack in last 6 months
- pacemaker, cardioverter-defibrillator or resynchronization device implanted less than 6 months before study entrance
- severe chronic obstructive pulmonary disease
Contacts and Locations| China, Jiangsu | |
| The First Affiliated Hospital of Nanjing Medical University | |
| Nanjing, Jiangsu, China, 210029 | |
| Study Director: | Shijiang Zhang, MD | The First Affiliated Hospital of Nanjing Medical University |
| Principal Investigator: | Ning Ding, Doctor | The First Affiliated Hospital of Nanjing Medical University |
More Information
Publications:
| Responsible Party: | Zhang Xilong, Department of Respirology, The First Affiliated Hospital of Nanjing Medical University, Nanjing Medical University |
| ClinicalTrials.gov Identifier: | NCT01426776 History of Changes |
| Other Study ID Numbers: | 30971319, 20092801 |
| Study First Received: | August 28, 2011 |
| Last Updated: | July 24, 2012 |
| Health Authority: | China: Ethics Committee |
Keywords provided by Nanjing Medical University:
|
Cheyne-Stokes respiration Heart valve disease Central Sleep Apnea |
Additional relevant MeSH terms:
|
Rheumatic Fever Apnea Cheyne-Stokes Respiration Heart Valve Diseases Rheumatic Heart Disease Sleep Apnea Syndromes Sleep Apnea, Central Respiration Disorders Respiratory Tract Diseases Signs and Symptoms, Respiratory |
Signs and Symptoms Heart Diseases Cardiovascular Diseases Streptococcal Infections Gram-Positive Bacterial Infections Bacterial Infections Sleep Disorders, Intrinsic Dyssomnias Sleep Disorders Nervous System Diseases |
ClinicalTrials.gov processed this record on June 17, 2013