Sleep Disordered Breathing in Acute Congestive Heart Failure

NCT ID: NCT03804827

Last Updated: 2021-08-05

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 19 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2019-01-14
• Study Completion Date: 2021-08-03

Brief Summary

The goal of this study is to determine if sleep disordered breathing results in a measurable degree of overnight myocardial stress/injury in patients with acutely decompensated congestive heart failure. A secondary goal is to determine of a period of medical management attenuates this sleep disordered breathing-induced cardiac injury in this patient population.

Detailed Description

Consecutive patients admitted to the hospital with acutely decompensated heart failure will be identified for potential enrollment in this study. Enrolled patients will first be asked to complete questionnaires to assess their symptoms and risk of having sleep apnea.

Relevant information will be obtained from the electronic medical record (age, gender, body mass index, co-morbidities, medications, prior echocardiography results). Subjects will then undergo a "type III" portable monitoring sleep study on the first or second night of their hospital admission, which measures respiratory effort, nasal airflow, oxyhemoglobin saturation, and heart rate. Blood samples will be collected on the evening before (08:00 PM +/- 2 hours), and the morning after (06:00 AM +/-2 hours) sleep apnea testing. If not otherwise obtained clinically, echocardiography will be obtained within 48 hours of admission. After a period of medical management for acutely decompensated heart failure, subjects will then have a second portable sleep apnea study (with associated pre and post-sleep blood draws) on the evening prior to discharge (approximately hospital day 5 or 6). Later, clinical outcomes such as incidence of renal dysfunction, hospital length of stay etc. will be collected from the electronic medical record. Blood samples will be processed, stored, and subsequently analyzed for high-sensitivity cardiac troponin T and I.

Conditions

Obstructive Sleep Apnea; Heart Failure; With Decompensation

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

Heart Failure With Sleep Disordered Breathing

AHI3% \>/= 5 events per hour of sleep.

No interventions assigned to this group

Heart Failure without Sleep Disordered Breathing

AHI3% \< 5 events per hour of sleep.

No interventions assigned to this group

Eligibility Criteria

Inclusion Criteria

• Patients age 18-80 years admitted to University of California San Diego La Jolla campus (Sulpizio Cardiovascular Center, Jacobs Medical Center, and Thornton Hospital) with acute decompensated heart failure will be identified in the emergency department, or upon admission to the cardiology or inpatient general medical services.

Exclusion Criteria

• Known diagnosis of sleep disordered breathing and on treatment while hospitalized.
• Suspected acute coronary syndrome as determined by the primary clinical team.
• Intensive care unit level care.
• Requiring advanced heart failure therapy such as inotrope infusion, mechanical circulatory support etc.
• Intolerance of study procedures.
• Clinical attending physician refusal

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University of California, San Diego

OTHER

Sponsor Role: lead

Responsible Party

Robert L. Owens

Assistant Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Altman Clinical and Translational Research Institute

San Diego, California, United States

University of California San Diego

San Diego, California, United States

Countries

United States

Other Identifiers

181121

Identifier Type: -

Identifier Source: org_study_id