Improving Care of Patients With Heart Failure
Depression, Pain, Dyspnea
About this trial
This is an interventional supportive care trial for Depression focused on measuring Palliative care, Symptom management, Heart failure
Eligibility Criteria
- HF as primary Dx or symptomatic/active HF
- During index hospitalization or within the prior 6 months
- Age > 18
- Admit from: hospital, skilled nursing, home
- Medicine, Cardiology, and Heart Failure Services
- Co-morbidities can include end-stage renal disease, metastatic cancer, ICU/CCU care patients if able to consent and complete survey
- English speaking
Exclusion Criteria:
- Non-English speaking
- Previous consult by Palliative Care Service
- Pulmonary HTN
- Right Heart Failure
- LVAD
- PCI or CABG patient within this admission
- AS with planned surgical intervention
- Pre/post heart transplant
- Pre/post organ transplant within this admission
- Dementia (unable to consent)
- Homeless
- Active drug user
- Hospice enrolled patient
- GeriTraCC patients
- Does not have a UCSF physician
- Lives outside of the SF Bay Area
Sites / Locations
- UCSF Medical Center
- University of California San Francisco Medical Center
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Symptom Management Service for heart failure
Usual cardiology care
Subjects randomized to the SMS-HF group will receive a comprehensive PC consultation by the interdisciplinary PC team at each site consisting of a nurse practitioner, physician, social worker and chaplain with 6 months of follow up. All members of the PC team are experienced PC clinicians. The SMS-HF intervention is based on National Quality Forum preferred practices and the National Consensus Project guidelines for quality PC. The SMS-HF will include assessment and management of symptoms, particularly focused on depression, pain and dyspnea, and a discussion of goals of care.
The usual cardiology care group will receive usual care provided by the HF clinic. We will assess symptoms and QoL at enrollment and symptoms, QoL, satisfaction, advance care planning documentation, and resource utilization at follow up 6 months later.