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PUBLISHER: GlobalData | PRODUCT CODE: 1100966

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PUBLISHER: GlobalData | PRODUCT CODE: 1100966

Cardiomyopathies Epidemiology Forecast, 2021-2031

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PAGES: 38 Pages
DELIVERY TIME: 1-2 business days
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Cardiomyopathy is a general term for a collection of diverse conditions of the heart muscle that inhibit the heart muscle's ability to pump blood. The main forms of cardiomyopathy are dilated cardiomyopathy (DCM), hypertrophic cardiomyopathy (HCM), restrictive cardiomyopathy (RCM), and arrhythmogenic right ventricular cardiomyopathy (ARCM). Cardiomyopathies can eventually lead to irregular heartbeats, the backup of blood into the lungs or rest of the body, and heart failure, which can result in sudden cardiac arrest (CDC, 2019).

GlobalData epidemiologists relied on the most robust country-specific data for each segmentation covered in this forecast, obtained from scientific studies published in peer-reviewed academic journals, international healthcare agency publications, nationwide registries, and national disease surveillance agencies available at the time of publication. The report includes a 10-year epidemiological forecast for the diagnosed prevalent cases of these cardiomyopathies segmented by subtype, sex, and age (under 18 years, 18-29 years, and by 10-year age groups for ages 30 years up to 80 years and older) in these markets. The diagnosed prevalent cases are further segmented by causes (acquired versus inherited) and ischemic cases (DCM only).

In the 7MM, the diagnosed prevalent cases of cardiomyopathies will increase from 2,268,240 cases in 2021 to 2,852,506 cases in 2031, at an annual growth rate (AGR) of 2.58% per year. The diagnosed prevalent cases of cardiomyopathies in the five major European markets (5EU) (France, Germany, Italy, Spain, and the UK) will increase at an AGR of 1.43%, from 366,582 cases in 2021 to 419,183 cases in 2031. When examining the AGR by individual markets, GlobalData estimates that the US will have the highest number of cases of cardiomyopathies in 2031, with 2,385,118 cases at an AGR of 2.87%. Conversely, Japan will have the least number of cases by 2031, with 48,205 cases at a negative AGR of 0.10%.

Scope

  • The cardiomyopathies epidemiology report provides an overview of the risk factors, comorbidities, and global and historical trends for cardiomyopathies (DCM, HCM, RCM, and ARCM) in the seven major markets (7MM) (US, France, Germany, Italy, Spain, UK, and Japan).
  • The report includes a 10-year epidemiological forecast for the diagnosed prevalent cases of cardiomyopathies segmented by subtype, sex, and age (under 18 years, 18-29 years, and by 10-year age groups for ages 30 years up to 80 years and older) in these markets. The diagnosed prevalent cases are further segmented by causes (acquired versus inherited) and ischemic cases (DCM only).
  • The epidemiology report provides additional clinically relevant segmentations for the diagnosed prevalent cases of cardiomyopathies including subtype specific etiology
  • The cardiomyopathies epidemiology report is written and developed by Masters- and PhD-level epidemiologists.
  • The Epidemiology Report is in-depth, high quality, transparent and market-driven, providing expert analysis of disease trends in cardiomyopathies.

Reasons to Buy

The Cardiomyopathies Epidemiology series will allow you to -

  • Develop business strategies by understanding the trends shaping and driving the global cardiomyopathies markets.
  • Quantify patient populations in the global cardiomyopathies markets to improve product design, pricing, and launch plans.
  • Organize sales and marketing efforts by identifying the age groups and sex that present the best opportunities for cardiomyopathies therapeutics in each of the markets covered.
  • Understand magnitude of the population with cardiomyopathies by age, sex, etiology, and ischemia (DCM only).
Product Code: GDHCER296-22

Table of Contents

Table of Contents

1 Cardiomyopathies: Executive Summary

  • 1.1 Related Reports
  • 1.2 Upcoming Reports

2 Epidemiology

  • 2.1 Disease Background
    • 2.1.1 Risk Factors and Comorbidities
  • 2.2 Global and Historical Trends
  • 2.3 Forecast Methodology
    • 2.3.1 Sources
    • 2.3.2 Forecast Assumptions and Methods
    • 2.3.3 Diagnosed Prevalent Cases of Dilated Cardiomyopathy
    • 2.3.4 Diagnosed Prevalent Cases of Hypertrophic Cardiomyopathy
    • 2.3.5 Diagnosed Prevalent Cases of Restrictive Cardiomyopathy
    • 2.3.6 Diagnosed Prevalent Cases of Arrhythmogenic Cardiomyopathy
    • 2.3.7 Diagnosed Prevalent Cases of Cardiomyopathies by Etiology
    • 2.3.8 Diagnosed Prevalent Cases of Dilated Cardiomyopathy with Ischemia
  • 2.4 Epidemiological Forecast for Cardiomyopathies (2021-2031)
    • 2.4.1 Diagnosed Prevalent Cases of Cardiomyopathies
    • 2.4.2 Diagnosed Prevalent Cases of Cardiomyopathies by Subtype
    • 2.4.3 Age-Specific Diagnosed Prevalent Cases of Cardiomyopathies
    • 2.4.4 Sex-Specific Diagnosed Prevalent Cases of Cardiomyopathies
    • 2.4.5 Diagnosed Prevalent Cases of Cardiomyopathies by Etiology
    • 2.4.6 Diagnosed Prevalent Cases of Dilated Cardiomyopathy with Ischemia
  • 2.5 Discussion
    • 2.5.1 Epidemiological Forecast Insight
    • 2.5.2 COVID-19 Impact
    • 2.5.3 Limitations of the Analysis
    • 2.5.4 Strengths of the Analysis

3 Appendix

  • 3.1 Bibliography
  • 3.2 Primary Research - Prescriber Survey
  • 3.3 About the Authors
    • 3.3.1 Epidemiologist
    • 3.3.2 Reviewers
    • 3.3.3 Global Director of Therapy Analysis and Epidemiology
    • 3.3.4 Global Head and EVP of Healthcare Operations and Strategy
  • Contact Us
Product Code: GDHCER296-22

List of Tables

List of Tables

  • Table 1: Risk factors and comorbidities for cardiomyopathies
  • Table 2: High-prescribing physicians (non-KOLs), surveyed by country, 2022

List of Figures

List of Figures

  • Figure 1: 7MM, diagnosed prevalent cases of cardiomyopathies, both sexes, all ages, N, 2021 and 2031
  • Figure 2: 7MM, diagnosed prevalence of cardiomyopathies (%), men and women, all ages, 2021
  • Figure 3: Sources used and not used for diagnosed prevalent cases of dilated cardiomyopathy
  • Figure 4: Sources used and not used for diagnosed prevalent cases of hypertrophic cardiomyopathy
  • Figure 5: Sources used for diagnosed prevalent cases of restrictive cardiomyopathy
  • Figure 6: Sources used for diagnosed prevalent cases of arrhythmogenic cardiomyopathy
  • Figure 7: Sources used for diagnosed prevalent cases of dilated cardiomyopathy by etiology
  • Figure 8: Sources used for diagnosed prevalent cases of hypertrophic cardiomyopathy by etiology
  • Figure 9: Sources used for diagnosed prevalent cases of restrictive cardiomyopathy by etiology
  • Figure 10: Sources used for diagnosed prevalent cases of arrhythmogenic cardiomyopathy by etiology
  • Figure 11: 7MM, diagnosed prevalent cases of cardiomyopathies in 2021, men and women, N, all ages
  • Figure 12: 7MM, diagnosed prevalent cases of cardiomyopathies by subtype, men and women, all ages, N, 2021
  • Figure 13: 7MM, age-specific diagnosed prevalent cases of cardiomyopathies, men and women, all ages, N, 2021
  • Figure 14: 7MM, diagnosed prevalent cases of cardiomyopathies by sex, all ages, N, 2021
  • Figure 15: 7MM, Diagnosed Prevalent Cases of Cardiomyopathies by Etiology, Men and Women, All Ages, N, 2021
  • Figure 16: 7MM, diagnosed prevalent cases of ischemic dilated cardiomyopathy, men and women, all ages, N, 2021
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