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Intermediate AMD - Epidemiology Forecast - 2034

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    Report

  • 60 Pages
  • February 2024
  • Region: Global
  • DelveInsight
  • ID: 6027157
UP TO OFF until Dec 31st 2024

Key Highlights

  • Aplastic anemia is a rare and severe nonmalignant disease characterized by autoimmune destruction of early hematopoietic cells. Its global incidence rate ranges from 0.7 to 7.4 cases per million inhabitants per year, with higher rates in Asia compared to Europe and the United States.
  • According to the Aplastic Anemia and MDS International Foundation, about 600-900 patients of aplastic anemia are diagnosed each year in the US.
  • According to the Aplastic Anemia Trust and Leukemia Care, it is estimated that between 100 and 150 people will be diagnosed across the UK every year, i.e., around 2 people for every 1,000,000 of the population.
  • Based on severity, severe and very severe aplastic anemia patients contributes roughly 65%-80% of the total aplastic anemia patient population.
This report delivers an in-depth understanding of aplastic anemia, historical and forecasted epidemiology trends in the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, and Japan.

Geography Covered

  • The United States
  • EU4 (Germany, France, Italy, and Spain) and the United Kingdom
  • Japan

Study Period: 2020-2034

Aplastic Anemia Disease Understanding

Aplastic Anemia Overview

Aplastic anemia refers to the syndrome of chronic primary hematopoietic failure from injury leading to diminished or absent hematopoietic precursors in the bone marrow and attendant pancytopenia. The symptoms of aplastic anemia occur because the bone marrow fails to produce enough blood cells. Some individuals may have mild symptoms that remain stable for many years; others may have serious symptoms that can progress to life-threatening complications. Individuals with anemia may experience tiredness, increased need for sleep, weakness, lightheadedness, dizziness, irritability, headaches, pale skin color, difficulty breathing, and cardiac symptoms like chest pain.

Aplastic Anemia Diagnosis

The rarity of aplastic anemia, coupled with its overlap with other bone marrow failure syndromes, poses a diagnostic challenge. Except for findings related to bleeding or infections, the examination presents mainly negative characteristics: absence of lymphadenopathy, no enlarged spleen or liver, and no infiltration of any other organ. Bone marrow (BM) aspiration and biopsy are essential procedures for diagnosing aplastic anemia. Cytogenetic abnormalities can be detected in up to 12-15% of otherwise typical aplastic anemia patients, making systematic cytogenetic investigations essential for all aplastic anemia patients. Molecular analysis, including next-generation sequencing (NGS), has become increasingly instrumental in comprehending the pathophysiology of diseases.

Aplastic Anemia Epidemiology

The aplastic anemia epidemiology chapter in the report provides historical as well as forecasted epidemiology segmented by total incident cases of aplastic anemia, severity-specific cases of aplastic anemia, and age-specific cases of aplastic anemia in the 7MM covering the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, and Japan from 2020 to 2034.
  • The total incident cases of aplastic anemia in the 7MM comprised ~2,500 cases in 2023 and are projected to increase during the forecast period.
  • Among the 7MM, Japan accounted for the highest number of incident cases of aplastic anemia, i.e., ~800 cases in 2023.
  • According to estimates, aplastic anemia is more common in the older population; the highest incident cases were in the age group of =60 years, accounting for ~60% of cases, and ~40% were < 60 in 2020 in the 7MM.
  • In 2023, among EU4 and the UK, Germany accounted for the largest number of aplastic anemia cases, whereas Spain occupied the bottom of the ladder.

KOL Views

To keep up with current epidemiology trends, we take KOLs and SMEs’ opinions working in the domain through primary research to fill the data gaps and validate our secondary research. Industry experts contacted for insights on the aplastic anemia evolving treatment landscape, patient reliance on conventional therapies, patient’s therapy switching acceptability, and drug uptake, along with challenges related to accessibility, including Medical/scientific writers, Professors; MD, FACS, Head of the Universities, and others.

The analysts connected with 30+ KOLs to gather insights; however, interviews were conducted with 10+ KOLs in the 7MM. Centers such as the East Tennessee State University, Düsseldorf Clinics Association, Duke University School of Medicine, etc., were contacted. Their opinion helps understand and validate aplastic anemia epidemiology trends.

Scope of the Report

  • The report covers a segment of key events, an executive summary, descriptive overview of aplastic anemia, explaining its causes, signs and symptoms, pathogenesis, and currently available therapies.
  • Comprehensive insight into the epidemiology segments and forecasts of disease progression has been provided.
  • The report provides an edge while developing business strategies, understanding trends, and expert insights in the 7MM.
  • A detailed review of current challenges in establishing the diagnosis.

Aplastic Anemia Report Insights

  • Patient Population
  • Country-wise Epidemiology Distribution

Aplastic Anemia Report Key Strengths

  • Eleven Years Forecast
  • The 7MM Coverage
  • Aplastic Anemia Epidemiology Segmentation

Aplastic Anemia Report Assessment

  • Current Diagnostic Practices
  • Unmet Needs

FAQs

  • What are the disease risks, burdens, and unmet needs of aplastic anemia? What will be the growth opportunities across the 7MM concerning the patient population with aplastic anemia?
  • What is the historical and forecasted aplastic anemia patient pool in the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, and Japan?
  • What is the severity-specific distribution of aplastic anemia in the 7MM?
  • What is the age-specific rate of aplastic anemia?

Reasons to Buy

  • Insights on patient burden/disease, evolution in diagnosis, and factors contributing to the change in the epidemiology of the disease during the forecast years.
  • To understand the diagnosed cases of aplastic anemia in varying geographies over the coming years.
  • To understand the perspective of key opinion leaders around the current challenges with establishing the diagnosis and insights on the recurrent and treatment-eligible patient pool.
  • Detailed insights on various factors hampering disease diagnosis and other existing diagnostic challenges.

Table of Contents

1. Key Insights2. Report Introduction3. Executive Summary of Intermediate Amd4. Epidemiology Methodology
5. Intermediate Amd Epidemiology Overview at a Glance in the 7MM
5.1. Patient Share (%) Distribution of Intermediate Amd in 2023
5.2. Patient Share (%) Distribution of Intermediate Amd in 2034
6. Disease Background and Overview
6.1. Introduction
6.1.1. Classification and Clinical Manifestation
6.1.2. Signs and Symptoms of Amd
6.1.3. Risk Factors
6.1.4. Pathophysiology of Amd
6.2. Diagnosis
6.2.1. Biomarkers for the Progression of Intermediate Amd
6.2.2. Diagnostic Test
6.3. Diagnostic Guidelines
6.3.1. Nice Guidelines
6.3.2. American Academy of Ophthalmology
7. Epidemiology and Patient Population
7.1. Key Findings
7.2. Assumption and Rationale
7.3. Total Prevalent Cases of Intermediate Amd in the 7MM
7.4. Total Diagnosed Prevalent Cases of Intermediate Amd in the 7MM
7.5. the United States
7.5.1. Total Prevalent Cases of Intermediate Amd in the US
7.5.2. Total Diagnosed Prevalent Cases of Intermediate Amd in the US
7.5.3. Age-Specific Cases of Intermediate Amd in the United States
7.6. EU4 and the UK
7.6.1. Total Prevalent Cases of Intermediate Amd in EU4 and the UK
7.6.2. Total Diagnosed Prevalent Cases of Intermediate Amd in EU4 and the UK
7.6.3. Age-Specific Cases of Intermediate Amd in EU4 and the UK
7.7. Japan
7.7.1. Total Prevalent Cases of Intermediate Amd in Japan
7.7.2. Total Diagnosed Prevalent Cases of Intermediate Amd in Japan
7.7.3. Age-Specific Cases of Intermediate Amd in Japan
8. Appendix
8.1. Bibliography
8.2. Report Methodology
9. Publisher Capabilities10. Disclaimer11. About the Publisher
List of Tables
Table 1: Summary of Intermediate AMD Epidemiology (2020-2034)
Table 2: The Beckman Clinical Classification of AMD
Table 3: AMD Classification in NICE Guidance
Table 4: Environmental risk factors for AMD, divided into no modifiable and modifiable factors
Table 5: Prevalence of Non-vision Threatening AMD in 2019 by Age
Table 6: Total Prevalent Cases of Intermediate AMD in the 7MM, in thousand (2020-2034)
Table 7: Total Diagnosed Prevalent Cases of Intermediate AMD in the 7MM, in thousand (2020-2034)
Table 8: Total Prevalent Cases of Intermediate AMD in the US, in thousand (2020-2034)
Table 9: Total Diagnosed Prevalent Cases of Intermediate AMD in the US, in thousand (2020-2034)
Table 10: Age-specific Cases of Intermediate AMD in the US, in thousand (2020-2034)
Table 11: Total Prevalent Cases of Intermediate AMD in EU4 and the UK, in thousand (2020-2034)
Table 12: Total Diagnosed Prevalent Cases of Intermediate AMD in EU4 and the UK, in thousand (2020-2034)
Table 13: Age-specific Cases of Intermediate AMD in EU4 and the UK, in thousand (2020-2034)
Table 14: Total Prevalent Cases of Intermediate AMD in Japan, in thousand (2020-2034)
Table 15: Total Diagnosed Prevalent Cases of Intermediate AMD in Japan, in thousand (2020-2034)
Table 16: Age-specific Cases of Intermediate AMD in Japan, in thousand (2020-2034)
List of Figures
Figure 1: Anatomy of the Fundus and Macula
Figure 2: Clinical Manifestations and Pathology of AMD from the Early to Late Stage
Figure 3: Cellular Senescence Contributing to AMD
Figure 4: Biomarkers Used to Assess the Progression of Intermediate AMD
Figure 5: The Royal College of Ophthalmologists Commissioning Diagnostic Guidelines on AMD
Figure 6: Total Prevalent Cases of Intermediate AMD in the 7MM (2020-2034)
Figure 7: Total Diagnosed Prevalent Cases of Intermediate AMD in the 7MM (2020-2034)
Figure 8: Total Prevalent Cases of Intermediate AMD in the US (2020-2034)
Figure 9: Total Diagnosed Prevalent Cases of Intermediate AMD in the US (2020-2034)
Figure 10: Age-specific Cases of Intermediate AMD in the US (2020-2034)
Figure 11: Total Prevalent Cases of Intermediate AMD in EU4 and the UK (2020-2034)
Figure 12: Total Diagnosed Prevalent Cases of Intermediate AMD in EU4 and the UK (2020-2034)
Figure 13: Age-specific Cases of Intermediate AMD in EU4 and the UK (2020-2034)
Figure 14: Total Prevalent Cases of Intermediate AMD in Japan (2020-2034)
Figure 15: Total Diagnosed Prevalent Cases of Intermediate AMD in Japan (2020-2034)
Figure 16: Age-specific Cases of Intermediate AMD in Japan (2020-2034)