Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

The Healthcare Amyloidosis European Registry (HEAR): study design and methods

View through CrossRef
Abstract Background Cardiac amyloidosis (CA) is a rare disease that can lead to poor quality of life, conduction disorders, arrhythmia, heart failure, and even death. Fortunately, specific treatments that can modify the natural history of the disease and the disease outcomes are now available. However, data on the prevailing patient management procedures and long-term outcomes of CA are scarce. Objective In order to gather more information on the diagnosis and management of CA, we created the Healthcare Amyloidosis European Registry (HEAR). The registry’s primary objective is to describe the demographic, clinical, laboratory and imaging characteristics of patients with CA. The secondary objectives are to (i) describe the different types of CA and their progression, (ii) describe the prevailing disease management procedures and any changes in these procedures, (iii) evaluate tools and quality of life questionnaires, (iv) describe the prognosis for patients with CA; (v) describe the management of CA by cardiologists, and (vi) assess hospital admissions and treatments and any changes in these factors. The HEAR will give us an opportunity to share good practice and to evaluate and optimize the quality of care for patients with CA. Methods HEAR is a noninterventional, longitudinal, multicentre registry initiated in France but which has been designed with a view to extension to other European countries. It includes cohorts of patients referred for suspected CA or with a confirmed diagnosis of CA. Since July 2021, 34 hospitals across France have joined the HEAR project. We expect to include 6500 patients in the HEAR between January 2021 and December 2027. At baseline, we use a structured e-case report form to collect data on demographics, clinical, laboratory and imaging variables, the management of CA by cardiologists, specific treatments, quality of life, and diagnostic data. Lastly, we intend to collect in-hospital data on outcomes (deaths, cause of death, and hospital readmissions) annually. Conclusions HEAR is dedicated to suspected and confirmed cases of CA. It will provide crucial information on the prevailing aetiologies, prevalence, and CA management to optimize patient care.
Title: The Healthcare Amyloidosis European Registry (HEAR): study design and methods
Description:
Abstract Background Cardiac amyloidosis (CA) is a rare disease that can lead to poor quality of life, conduction disorders, arrhythmia, heart failure, and even death.
Fortunately, specific treatments that can modify the natural history of the disease and the disease outcomes are now available.
However, data on the prevailing patient management procedures and long-term outcomes of CA are scarce.
Objective In order to gather more information on the diagnosis and management of CA, we created the Healthcare Amyloidosis European Registry (HEAR).
The registry’s primary objective is to describe the demographic, clinical, laboratory and imaging characteristics of patients with CA.
The secondary objectives are to (i) describe the different types of CA and their progression, (ii) describe the prevailing disease management procedures and any changes in these procedures, (iii) evaluate tools and quality of life questionnaires, (iv) describe the prognosis for patients with CA; (v) describe the management of CA by cardiologists, and (vi) assess hospital admissions and treatments and any changes in these factors.
The HEAR will give us an opportunity to share good practice and to evaluate and optimize the quality of care for patients with CA.
Methods HEAR is a noninterventional, longitudinal, multicentre registry initiated in France but which has been designed with a view to extension to other European countries.
It includes cohorts of patients referred for suspected CA or with a confirmed diagnosis of CA.
Since July 2021, 34 hospitals across France have joined the HEAR project.
We expect to include 6500 patients in the HEAR between January 2021 and December 2027.
At baseline, we use a structured e-case report form to collect data on demographics, clinical, laboratory and imaging variables, the management of CA by cardiologists, specific treatments, quality of life, and diagnostic data.
Lastly, we intend to collect in-hospital data on outcomes (deaths, cause of death, and hospital readmissions) annually.
Conclusions HEAR is dedicated to suspected and confirmed cases of CA.
It will provide crucial information on the prevailing aetiologies, prevalence, and CA management to optimize patient care.

Related Results

Anemia and outcome in cardiac amyloidosis
Anemia and outcome in cardiac amyloidosis
Abstract Background Anemia is a common comorbidity in patients with cardiac amyloidosis, yet its prognostic significance ...
Perceptions of Telemedicine and Rural Healthcare Access in a Developing Country: A Case Study of Bayelsa State, Nigeria
Perceptions of Telemedicine and Rural Healthcare Access in a Developing Country: A Case Study of Bayelsa State, Nigeria
Abstract Introduction Telemedicine is the remote delivery of healthcare services using information and communication technologies and has gained global recognition as a solution to...
Comparative Histopathological Characteristics of Duodenal Involvement in Different Types of Amyloidosis
Comparative Histopathological Characteristics of Duodenal Involvement in Different Types of Amyloidosis
Background/Objectives: The duodenum is commonly involved in systemic amyloidosis. This retrospective observational study describes histoanatomical distributions of different types ...
A Pilot Study of Rare Renal Amyloidosis Based on FFPE Proteomics
A Pilot Study of Rare Renal Amyloidosis Based on FFPE Proteomics
Renal amyloidosis typically manifests albuminuria, nephrotic-range proteinuria, and ultimately progresses to end-stage renal failure if diagnosed late. Different types of renal amy...
Updates on Emerging Therapies in Cardiac Light Chain (AL) Amyloidosis
Updates on Emerging Therapies in Cardiac Light Chain (AL) Amyloidosis
Introduction: Amyloidosis is a disorder where misfolded proteins get deposited in different tissues. The most common of them is immunoglobulin light chain (AL) depos...
SAA1 α/α alleles in amyloidosis
SAA1 α/α alleles in amyloidosis
Abstract: Background: Amyloidosis, mainly AA type, is one of the common diseases in nephrology clinics in Turkey. AA type amyloidosis is a complication of various...
Cardiomyopathies with left ventricular hypertrophy phenotype: prevalence of cardiac amyloidosis and clinical characteristics of patients
Cardiomyopathies with left ventricular hypertrophy phenotype: prevalence of cardiac amyloidosis and clinical characteristics of patients
Cardiac amyloidosis was long considered a rare disease, primarily affecting the elderly. However, recent studies have demonstrated a higher prevalence, highlighting the need for fu...
Tổng quan bệnh tim thoái hóa dạng bột trong thực hành lâm sàng
Tổng quan bệnh tim thoái hóa dạng bột trong thực hành lâm sàng
Amyloidosis là một bệnh lý ảnh hưởng đến nhiều cơ quan do sự lắng đọng bất thường của các protein trong các mô khác nhau. Biểu hiện lâm sàng phụ thuộc vào thể bệnh và vị trí lắng đ...

Back to Top