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HSR&D Study


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IIR 06-082
 
 
Depression and CHF in Outpatients
Carolyn L Turvey PhD MS
VA Medical Center, Iowa City
Iowa City, IA
Funding Period: January 2007 - February 2010

BACKGROUND/RATIONALE:
Background/Rationale: Heart failure affects 4 to 5 million Americans and is the number one cause of hospitalization in people aged 65 and older. People with heart failure also suffer significant depressive morbidity, with an estimated 11 to 36% meeting criteria for major or minor depression. Comorbid depression in heart failure is associated with greater morbidity, services use, and a two-fold increase in mortality. In 1998, an estimated $5 billion of the $20 billion total cost for heart failure was associated with psychological distress and depression. Several multidisciplinary care management programs have been developed to improve the medical outcomes of heart failure. However, none have addressed the psychological impact of the illness.

OBJECTIVE(S):
Objective: This study aims to demonstrate greater effectiveness of a comorbid illness management program that addresses both depressive symptoms and the medical management of heart failure when compared to a standard single illness management heart failure program. We hypothesize that the comorbid illness management program will yield superior psychological AND medical outcomes. We propose that the comorbid illness management program will also lead to better self care in heart failure patients than a single illness management program.

METHODS:
Methods: Study design: This is a two-arm randomized controlled trial. We anticipate recruiting 110-115 patients per treatment arm. Sample characteristics: Veterans aged 45 and older being treated for heart failure at the Iowa City Veteran’s Administration Primary Care clinic and the Cardiology clinic and at the Columbia Missouri Veteran’s Administration Medical Center will be screened for participation. Inclusion criteria are NYHA Class II, III or IV heart failure, absence of major psychiatric illness such as schizophren; bipolar disorder and substance abuse disorder. Veterans with PTSD will be eligible to participate in the study. Intervention: Participants in the standard illness management program will receive a 12-week, 8-session intervention designed to help them improve daily weighing, salt-restriction, medication management, etc. This intervention will be conducted in a combination of home visits and phone visits. They will also receive interactive, telephone-based daily monitoring that assesses daily weight, dyspnea, fatigue and medication compliance. Patients in the comorbid illness management program will receive the same illness management program PLUS education and behavioral techniques designed to help them cope emotionally with the illness. The comorbid illness management home monitoring will include a twice-monthly screen for depression. Major Variables: The major outcomes will be depressive symptoms, health-related quality of life, functional status, heart failure symptom severity, and self-care behaviors in heart failure. Main types of analyses: The main study hypotheses will be tested using random mixed effects models comparing the two treatment conditions on main outcomes while controlling for key covariates.

FINDINGS/RESULTS:
No results to report.

IMPACT:
Impact Statement: This novel intervention aims to improve psychological and cardiac health, reduce cost, and improve quality of life for VA patients in the later stages of heart failure. Once implemented, the comorbid illness management model may be applied to other major chronic illnesses in the VA population such as comorbid depression and pulmonary disease or arthritis.

PUBLICATIONS:

Journal Articles

  1. Klein DM, Turvey CL, Pies CJ. Relationship of coping styles with quality of life and depressive symptoms in older heart failure patients. Journal of Aging and Health. 2007; 19(1): 22-38.


DRA: Aging and Age-Related Changes, Chronic Diseases, Health Services and Systems
DRE: Treatment, Quality of Care, Prevention
Keywords: Cardiovasc’r disease, Telemedicine, Care Management
MeSH Terms: none