Heart Failure
Conditions
Keywords
Heart Failure, Questionnaire, ECHO, Prospective, Cross-Sectional
Brief summary
ADAPTATION HF is a prospective, observational, cross-sectional, multicenter, survey-based study. Patients who applied to the cardiology outpatient clinic with a preliminary diagnosis of HF or were hospitalized for HF and had a diagnosis of HF for at least 6 months will be included in the study.
Detailed description
ADAPTATION HF is a prospective, observational, cross-sectional, multicenter, survey-based study. Patients who applied to the cardiology outpatient clinic with a preliminary diagnosis of HF or were hospitalized for HF and had a diagnosis of HF for at least 6 months will be included in the study. Data entry staff who will be assigned to the centers for 2 weeks will apply a questionnaire consisting of different questions to the patients referred to them by clinicians with the diagnosis of HF. In addition, Pittsburg Sleep Quality Index will be applied to all cases. In addition, clinical features of HF from the current file of the cases (NYHA, comorbid conditions, comorbid diseases, blood pressure, heart rate, last drugs used, latest biochemistry (BNP/NTproBNP if available), hematology test results, most recent ECG , most recent echocardiography, coronary angiography report, if available) will be recorded. No additional examination/procedure will be performed for the study, only the data of the examinations requested by the clinician in routine clinical practice will be entered. A total of 500 patients from 10 centers will be included in this study over a six-month period.
Interventions
OTHERQuestionnaies
Data entry staff who will be assigned to the centers for 2 weeks will apply a questionnaire consisting of different questions to the patients referred to them by clinicians with the diagnosis of HF (presented in the appendix to this protocol). In addition, Pittsburg Sleep Quality Index will be applied to all cases.
Sponsors
Klinar CRO
AstraZeneca Turkey
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Outpatient or inpatient diagnosed with Heart Failure at least 6 months ago * Male or female patient aged 18 and over * Signed written informed consent form
Exclusion criteria
* newly diagnosed heart failure * CRY requiring dialysis * Serious liver and lung disease * LVAD/heart transplantation * HF due to possible temporary cause (myocarditis, peripartum CMP in the first 6 months, takotsubo etc.)
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| General Status of the patients | 6 months | At the end of the six-month recruitment period, demographic, symptoms, clinical follow-up status, disease information, treatment compliance, and awareness assessment will be performed on all included patients. |
Secondary
| Measure | Time frame |
|---|---|
| HF Percutaneous Intervention History & Operation History | 6 Months |
| Medications Used for HF | 6 Months |
| HF Risk Factors | 6 Months |
| HF ECHO Results | 6 Months |
| HF Laboratory Results | 6 Months |
| HF Comorbidities | 6 Months |
Countries
Turkey (Türkiye)
Outcome results
None listed