Trends in mortality due to aplastic anemia in the United States, 1999-2020: a center for disease control wonder analysis
BACKGROUND: Acquired aplastic anemia is a rare, life-threatening hematologic disorder characterized by immune-mediated bone marrow failure. Despite therapeutic advancements that have increased survival, evaluating contemporary mortality trends in the United States remains important to inform clinical practice and health policy. OBJECTIVES: This study examined aplastic anemia-related mortality trends, demographic disparities, and geographic variation among United States adults from 1999 to 2020. METHODS: Death certificate data from the Centers for Disease Control and Prevention Wide-Ranging Online Data for Epidemiologic Research database were analyzed for adults aged 25 years and older. Age-adjusted mortality rates per 100,000 persons and annual percent changes were calculated across years, sex, race, ethnicity, and geographic regions. Place of death and state-level social vulnerability index correlations were also evaluated. RESULTS: Aplastic anemia was recorded in 107,975 deaths from 1999 to 2020. The national age-adjusted mortality rate decreased initially from 1999 to 2002, remained stable until 2015, and increased through 2020. Men consistently demonstrated higher age-adjusted mortality rates than women. Non-Hispanic Black or African American individuals had the highest mortality rates among racial groups. Mortality was higher in non-metropolitan areas and the Midwest region. Mortality varied widely across states, whereas state-level social vulnerability was not associated with mortality rates. CONCLUSIONS: Following a period of stability, aplastic anemia-related mortality has increased in the United States since 2015. Disparities persist across sex, race, urbanization, and geographical region.
Authors
- Ayman Irshad (ORCID: https://orcid.org/0009-0009-6158-4429)
- Muhammad Sohaib (ORCID: https://orcid.org/0000-0003-1749-1945)
- Hamza Sohail (ORCID: https://orcid.org/0000-0002-8673-152X)
- Talha Khalid (ORCID: https://orcid.org/0009-0007-9295-511X)
- Noor Fatima (ORCID: https://orcid.org/0000-0002-8201-0645)
- Saif Ali Malik (ORCID: https://orcid.org/0009-0002-1950-3815)
- Zaima Afzaal (ORCID: https://orcid.org/0009-0000-2600-9474)
- Fatima Aslam (ORCID: https://orcid.org/0009-0002-8396-5328)
- Sahil Jairamani (ORCID: https://orcid.org/0009-0009-5160-8191)
- Ibrahim Zulfiqar Ali (ORCID: https://orcid.org/0009-0003-9330-570X)
- Amnah Khan
- Hafiz Zerak Naseer (ORCID: https://orcid.org/0009-0003-3721-7131)
Institutions
- Our Lady of Lourdes Hospital (IE)
- Karachi Medical and Dental College (PK)
- Liaquat University of Medical & Health Sciences (PK)
- Shifa Tameer-e-Millat University (PK)
- Tucson Medical Center (US)
- Bahawal Victoria Hospital (PK)
- Shaikh Zayed Postgraduate Medical Institute (PK)
- Amna Inayat Medical College (PK)
Publication Details
- Journal
- Hematology Transfusion and Cell Therapy
- Published
- 2026-11-02
- DOI
- https://doi.org/10.1016/j.htct.2026.108556
- Primary Topic
- Hematological disorders and diagnostics
- Type
- article
- Field-Weighted Citation Impact
- 0.00