Cardiac Function After CPAP Therapy in Patients With Chronic Heart Failure and Sleep Apnea. A Multicenter Study

The role of continuous positive airway pressure (CPAP) in cardiac function in patients with CSA and OSA has been studied with varying results. Nevertheless, it is not clear whether CPAP treatment for respiratory sleep disorders in CHF could slow down deterioration or improve the cardiovascular function.

In an attempt to yield further insight into this subject, we undertook a multicentre study to analyze the role of CPAP therapy (optimal vs sham) in the LVEF and in other cardiac measurements in patients with CHF.Aim. We evaluated in a randomized multicentre placebo (sham-CPAP) controlled study the effect of CPAP treatment on the left ventricle ejection fraction (LVEF) among other cardiological related variables.

Study Overview

• Status: Terminated
• Conditions: Cardiovascular Diseases; Heart Failure; Sleep Apnea
• Intervention / Treatment: Device: CPAP(Continuous Positive Airway Pressure)

Detailed Description

From the Cardiologist Department of eight university hospitals CHF patients were referred to the Sleep Units with the sole condition of having a LVEF < 45%. After an interview and some clinical explorations, 127 out of 245 fulfilled the rigid inclusion and exclusion criteria in order to have CHF subjects without obvious comorbidity (see flowchart of figure 1). These subjects went to full (polysomnography) PSG. Fifty seven per cent of them (n: 73) had an apnea hypopnea index (AHI) > 10. Forty three per cent (n:54) had an AHI < 10. Only 17% of the patients had CSA. The selection and inclusion criteria used for recruitment were the following: 1) referral of patients with chronic heart failure to the sleep laboratory; 2) diagnosis of heart failure with at least one episode of cardiac failure; 3) LVEF less than 45% using radionuclide ventriculography; 4) clinical stability for at least one month prior to inclusion; 5) optimum treatment with diuretics and/or beta-blockers and/or digoxin and/or ACE inhibitors according to tolerance 6) no change in treatment for one month prior to inclusion; and 7) an Apnea-Hypopnea Index (AHI) greater than 10 measured by conventional polysomnography. The exclusion criteria were as follows: 1) patients that had a previous diagnosis of OSA or had been exposed to CPAP therapy. 2) uncontrolled arterial hypertension; 3) valvular or congenital cardiopathy, unstable angina, acute myocardial infarction or cardiac surgery in the three months prior to enrolment; 4) severe somnolence defined as severe sleepiness in situations of activity; 5) present or past medical history of clinically significant renal, liver or pulmonary disease; 6) untreated hypothyroidism; 7) clinically significant kyphoscoliosis; 8) morbid obesity with a body mass index (BMI)> 41 Kg/m2; and 9) concomitant use of the following drugs: morphine, hypnotics and sedatives, theophylline, acetazolamide or home oxygen therapy. Informed written consent was obtained from all subjects. This study was approved by the Human Ethics Committee of the 8 centres.

The subjects selected were randomized to receive CPAP or sham CPAP (Figure 1). They were evaluated at baseline (before any intervention) and after three months of follow-up. The assessment was performed on the basis of a LVEF. In addition, hypertension, subjective daytime sleepiness(sleepiness scale [ESS] (17), quality of life questionnaire according to the Spanish version of the SF-36 were also studied (18) The answers of the SF-36 were codified and divided into two groups, physical (PCS) and mental (MCS) with eight subclasses (physical function, physical role, bodily pain, general health, vitality, social function, emotional role, mental health). Other measurements were: dyspnea using the Borg scale (19), the New York Heart Association scale (NYHA scale), and the 6-minute walking test (20-21). The obstructive group accounting for 83% of all the patients were also studied. CPAP and sham CPAP compliance were recorded by a built-in device in the machine and registered at 4 weeks and at the end of the treatment period. After one month of treatment, another PSG was performed to re-assess the AHI. All visits were registered in a database on an encrypted website of the homepage of the Basque Health Service

• Study Type: Interventional
• Enrollment: 245
• Phase: Not Applicable

Contacts and Locations

Study Locations

• Spain
  • Alava
    • Vitoria Gasteiz, Alava, Spain, 01009
      • Hospital Universitario Txagorritxu

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 30 years to 85 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

1. referral of patients with chronic heart failure to the sleep laboratory;
2. diagnosis of heart failure with at least one episode of cardiac failure;
3. LVEF less than 45% using radionuclide ventriculography;
4. clinical stability for at least one month prior to inclusion;
5. optimum treatment with diuretics and/or beta-blockers and/or digoxin and/or ACE inhibitors according to tolerance
6. no change in treatment for one month prior to inclusion; and
7. an Apnea-Hypopnea Index (AHI) greater than 10 measured by conventional polysomnography

Exclusion Criteria:

1. patients that had a previous diagnosis of OSA or had been exposed to CPAP therapy.
2. uncontrolled arterial hypertension;
3. valvular or congenital cardiopathy, unstable angina, acute myocardial infarction or cardiac surgery in the three months prior to enrolment;
4. severe somnolence defined as severe sleepiness in situations of activity;
5. present or past medical history of clinically significant renal, liver or pulmonary disease;
6. untreated hypothyroidism;
7. clinically significant kyphoscoliosis;
8. morbid obesity with a body mass index (BMI)> 41 Kg/m2; and
9. concomitant use of the following drugs: morphine, hypnotics and sedatives, theophylline, acetazolamide or home oxygen therapy

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Single

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Ejection fraction

Secondary Outcome Measures

Outcome Measure
Quality of life (SF-36)
Daytime sleepiness
Hypertension
NewYork Heart Scale (NYHA score),
Dyspnea (by using the Borg scale)
Exercise tolerance (6-min WT

Collaborators and Investigators

• Sponsor: Sociedad Española de Neumología y Cirugía Torácica
• Collaborators: Fondo de Investigacion Sanitaria; Sociedad Vasco-Navarra de Patología Respiratoria; RESPIRA
• Investigators: Principal Investigator: Carlos Egea-Santaolalla, MD, Hospital Universitario Txagorritxu. Vitoria Gasteiz. Spain

Study record dates

Study Major Dates

• Study Start: January 1, 2001
• Study Completion: June 1, 2004

Study Registration Dates

• First Submitted: November 28, 2006
• First Submitted That Met QC Criteria: November 28, 2006
• First Posted (Estimate): November 29, 2006

Study Record Updates

• Last Update Posted (Estimate): November 29, 2006
• Last Update Submitted That Met QC Criteria: November 28, 2006
• Last Verified: November 1, 2006

More Information

Terms related to this study

• Keywords: cardiovascular diseases; Continuous positive airway pressure; sleep apnea syndromes; sleep breathing disorders; sham CPAP
• Additional Relevant MeSH Terms: Heart Diseases; Nervous System Diseases; Respiratory Tract Diseases; Respiration Disorders; Sleep Disorders, Intrinsic; Dyssomnias; Sleep Wake Disorders; Signs and Symptoms, Respiratory; Heart Failure; Sleep Apnea Syndromes; Cardiovascular Diseases; Apnea
• Other Study ID Numbers: PI 01009