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Day-care Unit for Patients With Refractory Heart Failure

Day-care Unit for Patients With Refractory Heart Failure - a Single-centre Study

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03056651
Acronym
DayCare-HF
Enrollment
200
Registered
2017-02-17
Start date
2016-04-30
Completion date
2022-12-31
Last updated
2020-05-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiovascular Diseases, Heart Diseases, Heart Failure

Keywords

heart failure, day care, prognosis

Brief summary

The Day-Care Unit for Patients With Refractory Heart Failure (DayCare-HF) is an observational study on selected patients with advanced refractory heart failure. The purpose of the study was to examine the comprehensive management of HF in the day-care unit in terms of the safety and its impact on the rehospitalization and mortality rates in patients with advanced refractory HF.

Detailed description

The Day-Care Unit for Patients With Refractory Heart Failure (DayCare-HF) is a single-center observational study conducted in the 3rd Department of Cardiology, School of Medicine with the Division of Dentistry in Zabrze, Medical University of Silesia in Katowice, Silesian Centre for Heart Disease in Zabrze, Poland. The main objective of the DayCare-HF is to verify the hypothesis that comprehensive and multidisciplinary day-care management of patients with refractory heart failure (HF) is safe and beneficial in terms of hospital readmission due to HF and al cause mortality. The study population is formed by selected patients with heart failure, hospitalized in cardiology wards and intensive cardiac care unit of Silesian Centre for Heart Disease, who fulfilled eligibility criteria. During the scheduled visits comprehensive medical service is provided, including education, diagnostic tools (electrocardiography, transthoracic echocardiography, implanted cardioverter defibrillator (ICD) / cardiac resynchronization therapy device (CRT) interrogation and additional treatment (intravenous loop diuretic, dobutamine, vasodilators administration). The patients are under constant follow-up for major adverse events, heart transplantation, hospital readmissions due to HF and all cause mortality.

Interventions

OTHERtreatment in day-care heart failure unit

Sponsors

Silesian Centre for Heart Diseases
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Optimally decongested heart failure in New York Heart Association (NYHA) class II-IV, treated for at least 6 months 2. Performance of all possible reparative procedures if indications were present (cardiac revascularization, correction of valvular heart disease, cardiac ablation, cardiac resynchronization therapy) 3. Implantation of cardioverter-defibrillator (ICD) if applicable 4. At least two unplanned hospitalizations for heart failure during preceding 6 months

Exclusion criteria

1. Inability to travel to the unit 2. Non-compliance with the medical recommendations

Design outcomes

Primary

MeasureTime frame
Number of participants with rehospitalization due to heart failure decompensationFrom date of inclusion until the date of death from any cause, assessed up to 1 year

Secondary

MeasureTime frame
Number of participants with major adverse cardiovascular eventFrom date of inclusion until the date of death from any cause, assessed up to 1 year
Number of participants with reported deaths from any causeFrom date of inclusion until the date of death from any cause, assessed up to 1 year

Countries

Poland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026