Epidemiology, treatment and burden of Wilson disease in France: A 10-year analysis of the national health insurance database.

Author: BleinCécile, BénichouBernard, CombalJean-Philippe, Daniel-RobinThomas, LeboucherClaire

Paper Details 
Original Abstract of the Article :
Wilson disease (WD) is a rare hereditary, debilitating disease that is fatal if untreated. Given its low prevalence, collecting longitudinal information on large cohorts of patients is challenging. Analysis of health insurance databases offers an approach to meet this challenge. The aim of this stud...See full text at original site
Dr.Camel IconDr.Camel's Paper Summary Blogラクダ博士について

ラクダ博士は、Health Journal が論文の内容を分かりやすく解説するために作成した架空のキャラクターです。
難解な医学論文を、専門知識のない方にも理解しやすいように、噛み砕いて説明することを目指しています。

* ラクダ博士による解説は、あくまで論文の要点をまとめたものであり、原論文の完全な代替となるものではありません。詳細な内容については、必ず原論文をご参照ください。
* ラクダ博士は架空のキャラクターであり、実際の医学研究者や医療従事者とは一切関係がありません。
* 解説の内容は Health Journal が独自に解釈・作成したものであり、原論文の著者または出版社の見解を反映するものではありません。


引用元:
https://doi.org/10.1016/j.clinre.2022.101992

データ提供:米国国立医学図書館(NLM)

Epidemiology, Treatment, and Burden of Wilson Disease in France: A 10-Year Analysis

Wilson disease (WD), a rare genetic disorder, is like a hidden oasis in the vast desert of human health. This research, like a team of explorers, delves into the epidemiology, treatment, and burden of WD in France, using a decade's worth of data from the national health insurance database. The study aims to provide a comprehensive understanding of this complex condition, shedding light on its presentation, management, and impact on patients' lives.

Unveiling the Oasis: Understanding Wilson Disease

The study, like a meticulous mapmaker, meticulously analyzes the data, revealing trends in the presentation and management of WD patients. The research highlights the importance of early diagnosis and treatment, as well as the need for ongoing monitoring and management to prevent serious complications, a process akin to carefully nurturing a fragile oasis in a harsh desert environment.

Navigating the Challenges: Addressing the Burden of Wilson Disease

This research underscores the significant burden of WD on patients and healthcare systems, highlighting the need for improved access to specialized care and resources. It's like building a network of roads and infrastructure that can connect isolated oases and facilitate access to essential resources. This effort is essential for improving the lives of individuals with WD, a condition that can significantly impact their physical and cognitive abilities.

Dr.Camel's Conclusion

This research provides valuable insights into the epidemiology, treatment, and burden of Wilson disease in France. It underscores the importance of early diagnosis, ongoing management, and access to specialized care for individuals with this complex genetic disorder. By working together, we can create a more supportive and accessible landscape for those affected by WD, helping them thrive despite the challenges they face. This study serves as a reminder that even in the vast and often unforgiving desert of rare diseases, there are still ways to create oases of hope and well-being for those in need.

Date :
  1. Date Completed 2022-11-29
  2. Date Revised 2022-12-23
Further Info :

Pubmed ID

35793759

DOI: Digital Object Identifier

10.1016/j.clinre.2022.101992

Related Literature

SNS
PICO Info
in preparation
Languages

English

Positive IndicatorAn AI analysis index that serves as a benchmark for how positive the results of the study are. Note that it is a benchmark and requires careful interpretation and consideration of different perspectives.

This site uses cookies. Visit our privacy policy page or click the link in any footer for more information and to change your preferences.