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Clinical Trials/NCT06487468
NCT06487468
Completed
Not Applicable

A Study on Risk Factors in Heart Failure Patients With Preserved Ejection Fraction After Hospital Discharge

Xiangtan Central Hospital0 sites9,419 target enrollmentMay 1, 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Heart Failure With Preserved Ejection Fraction
Sponsor
Xiangtan Central Hospital
Enrollment
9419
Primary Endpoint
All-cause death(people)
Status
Completed
Last Updated
last year

Overview

Brief Summary

This study aimed to identify the independent risk factors associated with heart failure readmission, cardiac mortality and all-cause death among patients discharged from Xiangtan Central Hospital with heart failure and preserved ejection fraction (HFpEF). Understanding related risk factors might add future clinical decision making for individualized post discharge management of HFpEF patients aiming to improve the outcome of discharged HFpEF patients.

Detailed Description

This study sought to determine the independent risk factors linked to endpoint events (which include all-cause mortality or readmission for heart failure, cardiovascular death) among hospitalized patients with heart failure and preserved ejection fraction (HFpEF) at Xiangtan Central Hospital during the period from May 1, 2014, to January 31, 2023. The clinical follow up ended on January 31, 2024. The study examined the risk factors associated with the endpoint outcome (cardiovascular death and death from any cause and readmission due to heart failure) to provide clinical evidence for intervening discharged HFpEF patients, with the objective of improving patient outcomes in future clinical practice. The clinical features of hospitalized heart failure with preserved ejection fraction (HFpEF, EF≥50%) are analyzed retrospectively by reviewing the patient's demographic, clinical data, including patient medical history, initial clinical evaluations, and therapeutic interventions, as well as echocardiographic data in the hospital's electronic health records and relevant databases. The clinical outcome of enrolled patients are obtained through a team of three experienced cardiologists and twelve nursing professionals through outpatient consultations, telephone follow-ups, and community visit. The primary endpoint events are all-cause mortality, the second endpoints are the composite cardiovascular death and heart failure readmission.

Registry
clinicaltrials.gov
Start Date
May 1, 2014
End Date
January 31, 2024
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Jianping Zeng

Director of Cardiovascular Department of Xiangtan Central Hospital,Clinical Professor

Xiangtan Central Hospital

Eligibility Criteria

Inclusion Criteria

  • Patients discharged with diagnosis of heart failure were screened and met definition of heart failure with preserved ejection fraction (HFpEF) according to the 2021 European Society of Cardiology (ESC) guidelines at final analysis.
  • 1)Heart failure signs and symptoms; 2)LVEF\>50%;

Exclusion Criteria

  • age under 18 years; 2) life expectancy of less than one year due to non-cardiac conditions.

Outcomes

Primary Outcomes

All-cause death(people)

Time Frame: The patients are clinically followed up until January 31, 2024, per clinical visit or telephone call or community visit.

Risk factors of all-cause death are analyzed(Increase the factors that contribute to the occurrence of endpoint events)

Secondary Outcomes

  • Cardiovascular death and Heart failure readmission(people)(The patients are clinically followed up until January 31, 2024, per clinical visit or telephone call or community visit.)

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