Congestive Heart Failure Clinical Trial
Official title:
Prevalence, Clinical Characteristics and Type of Sleep-disordered Breathing in Patients With Chronic, Symptomatic, Systolic Heart Failure
Objective target of the registry is to investigate the prevalence of SDB as well as the
clinical characteristics of patients with and without SDB as well as the predominant type of
sdb.
For this purpose data from patients suffering from chronic, symptomatic heart failure with
impaired left ventricular ejection fraction will be collected prospectively.
Despite recent advances in pharmacological treatment, congestive heart failure (CHF)
continues to cause debilitating symptoms, frequent hospital admissions and a high mortality.
Despite of therapy with beta-blockers and ACE-inhibitors many patients have persistent
symptoms and most will eventually die of cardiovascular causes, often from progressive heart
failure.
Sleep Disordered Breathing (SDB) is known to cause consequences, which have negative effects
on heart failure.
Objective target of the registry is to investigate the prevalence of SDB, clinical
characteristics, symptoms and the degree and type of SDB in patients with chronic HF.
For this purpose data from patients with chronic heart failure will be collected
prospectively.In the registry several cardiologists in private practice or hospital and
cooperating sleep laboratories shall participate.
Cardiologists screen patients with Chronic Heart Failure (chronic HF) prospectively. In case
of suffering from chronic HF for at least 12 weeks since diagnosis, with NYHA III-IV or NYHA
class II with at least one hospitalisation for HF in the last 12 months. Written informed
consent for data privacy aspects must be obtained before screening for SDB. Patients who
satisfy to all inclusion- and exclusion criteria will be included consecutively into the
registry.
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