Racial and ethnic differences in reported haemophilia death rates in the United States.

Author: AntunAna, CafuirLorraine, FedewaStacey A, KemptonChristine L, PayneAmanda B, TranDuc

Paper Details 
Original Abstract of the Article :
INTRODUCTION: People with haemophilia's life expectancies have improved over time. Whether progress has been experienced equitably is unknown. AIM: To examine recorded haemophilia death (rHD) rates according to race and ethnicity in the United States (US). METHODS: In this cohort study, rHDs were ...See full text at original site
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引用元:
https://doi.org/10.1111/hae.14859

データ提供:米国国立医学図書館(NLM)

Haemophilia Mortality: Examining Racial and Ethnic Disparities in the United States

This study investigates disparities in reported haemophilia death rates in the United States based on race and ethnicity. The researchers analyzed data from the National Vital Statistics system between 1999 and 2020. They found that while reported haemophilia death rates declined over time for all racial and ethnic groups, Non-Hispanic Black males consistently experienced higher rates compared to Non-Hispanic White males. The study highlights the need for further investigation into potential contributing factors and the development of strategies to address these disparities in healthcare outcomes for individuals with haemophilia.

A Path to Equity: Addressing Disparities in Haemophilia Mortality

This study sheds light on concerning disparities in reported haemophilia death rates across racial and ethnic groups in the United States. The researchers' careful analysis reveals a persistent gap in mortality rates between Non-Hispanic Black and Non-Hispanic White males with haemophilia. It's like a desert landscape where different paths lead to uneven outcomes, a stark reminder of the need for systemic change and equity in healthcare access and treatment. This research calls for a deeper understanding of the factors contributing to these disparities and the development of targeted interventions to improve outcomes for all individuals with haemophilia.

Navigating the Desert: Ensuring Equitable Healthcare for Haemophilia

This study underscores the importance of addressing disparities in healthcare outcomes for individuals with haemophilia. The research highlights the need for targeted interventions and improved access to care for underserved communities. It's like creating a network of pathways across a vast desert, ensuring that everyone has access to the resources and support they need to thrive. We must strive to create a healthcare system that is equitable and just, ensuring that everyone has a fair chance at a healthy life.

Dr.Camel's Conclusion

This study reveals persistent racial and ethnic disparities in reported haemophilia death rates in the United States. The findings underscore the need for further investigation and targeted interventions to address these disparities and improve health outcomes for all individuals with haemophilia.
Date :
  1. Date Completed 2023-11-14
  2. Date Revised 2023-11-14
Further Info :

Pubmed ID

37718571

DOI: Digital Object Identifier

10.1111/hae.14859

Related Literature

SNS
PICO Info
in preparation
Languages

English

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