Treating the ineligible: Disease modification in people with multiple sclerosis beyond NHS England commissioning policies.

Author: AdamsAshok, Allen-PhilbeyKimberley, BakerDavid, CampionTom, De TraneStefania, EspasandinMaria, GiovannoniGavin, GnanapavanSharmilee, MaoZhifeng, MartaMonica, MathewsJoela, SchmiererKlaus, TurnerBenjamin P, YildizOzlem, Álvarez-GonzálezCésar

Paper Details 
Original Abstract of the Article :
Label="BACKGROUND" NlmCategory="BACKGROUND">Whilst there is a broad selection of drugs licensed as disease modifying treatments (DMTs) for people with relapsing multiple sclerosis (pwRMS), access to DMTs remains restricted, particularly for people with progressive MS (pwPMS). Cladribine has shown ef...See full text at original site
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引用元:
https://doi.org/10.1016/j.msard.2018.11.001

データ提供:米国国立医学図書館(NLM)

Treating the Ineligible: Disease Modification in Multiple Sclerosis

In the ever-shifting sands of multiple sclerosis (MS) research, scientists are constantly seeking new strategies to combat this complex and often debilitating disease. This study addresses the challenges of accessing disease-modifying treatments (DMTs) for individuals with progressive MS (pwPMS), a condition that can feel like navigating a vast and unforgiving desert.

Cladribine: A Potential Oasis in the Desert of MS

The study highlights the potential of cladribine, a drug that has shown efficacy at all stages of MS. Although previously withdrawn from the market due to concerns related to lymphopenia, the authors report on the real-life safety and tolerability of subcutaneously injected cladribine in treating both pwRMS and pwPMS. This research offers a glimmer of hope for individuals with progressive MS, potentially providing a path toward more effective treatment options.

Navigating the Challenges of Access and Treatment: A Journey Through the MS Landscape

The study emphasizes the need for addressing the barriers to accessing DMTs, particularly for those with pwPMS. The authors call for a more equitable approach to treatment, ensuring that all individuals with MS have access to effective therapies.

Health Implications and Lifestyle Applications: Embracing Hope and Advocacy

This research underscores the ongoing struggle for individuals with MS to access appropriate treatments. It highlights the importance of advocacy and research efforts to expand access to DMTs for all individuals, regardless of disease stage.

Dr. Camel's Conclusion

This study reminds us that the journey through the desert of MS is often challenging, but hope can be found in the form of new research and treatment options. The authors emphasize the importance of advocating for increased access to DMTs, ensuring that all individuals with MS can benefit from the potential of these life-changing therapies.
Date :
  1. Date Completed 2019-04-16
  2. Date Revised 2019-12-10
Further Info :

Pubmed ID

30419510

DOI: Digital Object Identifier

10.1016/j.msard.2018.11.001

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.

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