Demographic and Clinical Characteristics, Treatment Patterns and Clinical Outcomes of Heart Failure Patients in China

May 18, 2019 updated by: China Cardiovascular Association

Real World Demographic and Clinical Characteristics, Treatment Patterns and Clinical Outcomes of Heart Failure Patients in China: a Retrospective Non-Interventional Nationwide Study

This is a non-interventional, multicenter, retrospective study assessing demographic characteristics, clinical characteristics, management and outcome of patients with a HF (heart failure) diagnosis utilizing real world data derived from HF Center Database. This database collects the data of HF from patients hospitalized between March 2010 to Dec 2018 in more than 300 hospitals across China.

Study Overview

Status

Completed

Conditions

Detailed Description

Research question and objectives Primary objective

  • Describe the demographic and clinical characteristics of HF patients at HF index hospitalization admission Secondary objective
  • Assess the HF diagnosis and evaluation patterns and treatment patterns during index hospitalization and after discharge compare with guideline (2018 China HF Guideline) recommendations
  • Describe the demographic characteristics, clinical characteristics, diagnostic pattern, treatment pattern of HF patients stratified by LVEF (left ventricular ejection fraction) and region Exploratory objectives Describe the demographic and clinical characteristics, sac/val start dose and titration pattern among chronic HF patients prescribed sac/val

Study design This is a non-interventional, multicenter, retrospective study assessing demographic characteristics, clinical characteristics, management and outcome of patients with a HF diagnosis utilizing real world data derived from HF Center Database. This database collects the data of HF from patients hospitalized between March 2010 to Dec 2018 in more than 300 hospitals across China.

Setting and study population This study will include the data from all patients who were enrolled in the HF Center database. The study population consists of adult inhospital patients (18+ years) being diagnosed with HF at discharge.

Inclusion criteria

  • Aged 18 years and older
  • Patients with confirmed diagnosis of HF
  • Diagnosis is made by the treating physicians according to local practices and their clinical judgement Exclusion criteria Concomitant participation in a clinical study with any investigational treatment during the index hospitalization

Variables

Collection at index hospitalization:

Demography Comorbidities and Medical History Patient presentation at admission (including signs and symptoms) Vital Status In-hospital evaluation tests (laboratories, function tests, etc) Medication at discharge

Collection at follow-up (1 month, 3months and 1year):

Vital status Evaluation tests (laboratories, function tests, etc) Medication at follow-up Clinical outcomes (mortality and re-hospitalization events where feasible)

Data sources The data from this study will be retrieved from the HF Center database provided by CHH (China Heart House). All data were collected from more than 300 collaborative hospitals of China, including approximately 60,000 patients of HF. The information was collected during index hospitalization, 1 month, 3 months, 1 year after discharge by trained coordinators using a standardized case report form, entered into the HF Center database.

Study size This study will be conducted based on existing database and no formal sample size calculation is necessary for this type of descriptive retrospective observational research. In HF Center database, there is around 60,000 patients in total planned to be analyzed in this study.

Data analysis Descriptive data analyses will be focus on: (1) Continuous variables: mean, standard error, median, first quartile, third quartile, ranges for continuous variables; (2) Categorical variables: frequencies, and percentages for categorical variables. Summaries will be presented together with estimates and corresponding 95% confidence intervals (CI) as appropriate.

For the endpoints that stratified by LVEF and region, differences will be assessed by the p-values of corresponding tests. Categorical variables will be compared using chi-square tests; continuous variables will be compared using unequal variance two-sample t-test; for continuous variables with skewed data Mann-Whitney U test will be used, or Wilcoxon signed-rank test in case of paired data. 95% confidence intervals (CIs) and two tailed p-value will be reported for the parameter estimated in the multivariable models.

The number and proportion of patients with missing data will be presented. Detailed description will be provided in the SAP (Statistical Analysis Plan).

Study Type

Observational

Enrollment (Actual)

60000

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Beijing
      • Beijing, Beijing, China, 100034
        • Peking University First Hospital
      • Beijing, Beijing, China, 100730
        • Beijing Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

The demographic and clinical characteristics were collected from patients' medical records during their in-patients treatment period, and the follow-up data were collected from face-to-face interview at outpatient clinics or phone interview after discharge.

Description

Inclusion Criteria:

  • Aged 18 years and older
  • Patients with confirmed diagnosis of HF
  • Diagnosis is made by the treating physicians according to local practices and their clinical judgement

Exclusion Criteria:

• Concomitant participation in any/a clinical trial with any investigational treatment during the index hospitalization

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Patients' demographics at index hospitalization admission.
Time Frame: 1 years
Patients' demographics at index hospitalization admission.
1 years
Patients' medical history at index hospitalization admission.
Time Frame: 1 years
Patients' medical history at index hospitalization admission.
1 years
Patients' comorbidities (i.e. diabetes, renal insufficiency, chronic obstructive pulmonary disease, anemia, obesity, hypertension) at index hospitalization admission.
Time Frame: 1 years
Patients' comorbidities (i.e. diabetes, renal insufficiency, chronic obstructive pulmonary disease, anemia, obesity, hypertension) at index hospitalization admission.
1 years

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The percentage of patients who received the guideline (2018 China HF Guideline) recommended tests during the indexed hospitalization.
Time Frame: 1 years
The percentage of patients who received the guideline (2018 China HF Guideline) recommended tests (i.e. echocardiography, electrocardiogram, brain natriuretic peptide (BNP)/n-terminal pro-brain natriuretic Peptide (NT-proBNP)) during the indexed hospitalization.
1 years
The percentage of HF patients who received the guideline (2018 China HF Guideline) recommended HFrEF (Hear failure with reduced ejection fraction) pharmacological and device treatments (i.e. ICD, CRT) at the discharge of the index hospitalization.
Time Frame: 1 years
The percentage of HF patients who received the guideline (2018 China HF Guideline) recommended HFrEF pharmacological (i.e. Angiotensin-converting enzyme inhibitors (ACEIs), angiotensin receptor blockers (ARBs), ARNI, β-blockers, aldosterone antagonists, diuretics) and device treatments (i.e. ICD, CRT) at the discharge of the index hospitalization.
1 years
The percentage of HF patients adherent to guideline.
Time Frame: 1 years
The percentage of HF patients adherent to guideline (2018 China HF Guideline) recommended HFrEF pharmacological treatments including ACEIs, ARBs, β-blockers, aldosterone antagonists and diuretics at 1 month, 3 months and 1 year after discharge from the indexed hospitalization.
1 years
Follow-up rate at 1month, 3 months and 1 year after discharge from indexed hospitalization.
Time Frame: 1 years
Follow-up rate at 1month, 3 months and 1 year after discharge from indexed hospitalization.
1 years
In-hospital mortality rate at 1month, 3 months and 1 year after discharge from indexed hospitalization.
Time Frame: 1 years
In-hospital mortality rate at 1month, 3 months and 1 year after discharge from indexed hospitalization.
1 years
Re-hospitalization rate at 1month, 3 months and 1 year after discharge from indexed hospitalization.
Time Frame: 1 years
Re-hospitalization rate at 1month, 3 months and 1 year after discharge from indexed hospitalization.
1 years
Demographic characteristics among HF patients stratified by LVEF (<40%/40-49%/≥50%).
Time Frame: 1 years
Demographic characteristics among HF patients stratified by LVEF (<40%/40-49%/≥50%).
1 years
Medical history among HF patients stratified by LVEF (<40%/40-49%/≥50%).
Time Frame: 1 years
Medical history among HF patients stratified by LVEF (<40%/40-49%/≥50%).
1 years
Diagnostic pattern among HF patients stratified by LVEF (<40%/40-49%/≥50%).
Time Frame: 1 years
Diagnostic pattern among HF patients stratified by LVEF (<40%/40-49%/≥50%).
1 years
Treatment pattern among HF patients stratified by LVEF (<40%/40-49%/≥50%).
Time Frame: 1 years
Treatment pattern among HF patients stratified by LVEF (<40%/40-49%/≥50%).
1 years
Outcomes among HF patients stratified by LVEF (<40%/40-49%/≥50%).
Time Frame: 1 years
Outcomes among HF patients stratified by LVEF (<40%/40-49%/≥50%).
1 years
Demographic characteristics comparing HF patients in Shanghai vs the whole of China and Shanghai vs the rest of China.
Time Frame: 1 years
Demographic characteristics comparing HF patients in Shanghai vs the whole of China and Shanghai vs the rest of China.
1 years
Medical history comparing HF patients in Shanghai vs the whole of China and Shanghai vs the rest of China.
Time Frame: 1 years
Medical history comparing HF patients in Shanghai vs the whole of China and Shanghai vs the rest of China.
1 years
Diagnostic pattern comparing HF patients in Shanghai vs the whole of China and Shanghai vs the rest of China.
Time Frame: 1 years
Diagnostic pattern comparing HF patients in Shanghai vs the whole of China and Shanghai vs the rest of China.
1 years
Treatment pattern comparing HF patients in Shanghai vs the whole of China and Shanghai vs the rest of China.
Time Frame: 1 years
Treatment pattern comparing HF patients in Shanghai vs the whole of China and Shanghai vs the rest of China.
1 years
Outcomes comparing HF patients in Shanghai vs the whole of China and Shanghai vs the rest of China.
Time Frame: 1 years
Outcomes comparing HF patients in Shanghai vs the whole of China and Shanghai vs the rest of China.
1 years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

April 30, 2019

Primary Completion (ACTUAL)

May 18, 2019

Study Completion (ACTUAL)

May 18, 2019

Study Registration Dates

First Submitted

April 15, 2019

First Submitted That Met QC Criteria

April 25, 2019

First Posted (ACTUAL)

April 30, 2019

Study Record Updates

Last Update Posted (ACTUAL)

May 21, 2019

Last Update Submitted That Met QC Criteria

May 18, 2019

Last Verified

April 1, 2019

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • GUSU19002

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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